Crystallography Open Database

Result: there are 1640 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)

Searching journal of publication like 'Chemical Communications' volume of publication is 60

Left arrow Left arrow First | Left arrow Previous 1000 | of 2 | Next 1000 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1571152 CIFC26 H42 Cl2 N2 Si2I 1 2/m 110.53; 10.929; 12.931
90; 96.525; 90		1478.5Hüßler, Christopher; Dietl, Martin C.; Kahle, Justin; Lopes, Eric F.; Kawamura, Miku; Krämer, Petra; Rominger, Frank; Rudolph, Matthias; Hachiya, Iwao; Hashmi, A Stephen K
Synthesis and structural properties of <i>para</i>-diselenopyrazines.
Chemical communications (Cambridge, England), 2024, 60, 3786-3789
1571153 CIFC10 H6 Cl2 N2P 1 21/n 18.833; 4.114; 14.134
90; 106.095; 90		493.5Hüßler, Christopher; Dietl, Martin C.; Kahle, Justin; Lopes, Eric F.; Kawamura, Miku; Krämer, Petra; Rominger, Frank; Rudolph, Matthias; Hachiya, Iwao; Hashmi, A Stephen K
Synthesis and structural properties of <i>para</i>-diselenopyrazines.
Chemical communications (Cambridge, England), 2024, 60, 3786-3789
1571154 CIFC8 H4 N2 Se2P 1 21/n 14.1984; 8.1335; 12.0157
90; 96.9877; 90		407.26Hüßler, Christopher; Dietl, Martin C.; Kahle, Justin; Lopes, Eric F.; Kawamura, Miku; Krämer, Petra; Rominger, Frank; Rudolph, Matthias; Hachiya, Iwao; Hashmi, A Stephen K
Synthesis and structural properties of <i>para</i>-diselenopyrazines.
Chemical communications (Cambridge, England), 2024, 60, 3786-3789
1571155 CIFC26 H44 N2 Se2 Si2P 1 21/c 114.408; 16.0163; 12.9816
90; 97.694; 90		2968.7Hüßler, Christopher; Dietl, Martin C.; Kahle, Justin; Lopes, Eric F.; Kawamura, Miku; Krämer, Petra; Rominger, Frank; Rudolph, Matthias; Hachiya, Iwao; Hashmi, A Stephen K
Synthesis and structural properties of <i>para</i>-diselenopyrazines.
Chemical communications (Cambridge, England), 2024, 60, 3786-3789
1571156 CIFC30 H32 N2 Se2P -14.7908; 9.1049; 15.3497
75.701; 89.134; 80.513		639.7Hüßler, Christopher; Dietl, Martin C.; Kahle, Justin; Lopes, Eric F.; Kawamura, Miku; Krämer, Petra; Rominger, Frank; Rudolph, Matthias; Hachiya, Iwao; Hashmi, A Stephen K
Synthesis and structural properties of <i>para</i>-diselenopyrazines.
Chemical communications (Cambridge, England), 2024, 60, 3786-3789
1571172 CIFC38 H27 O2 PP 1 21/c 110.0902; 20.276; 14.0678
90; 104.978; 90		2780.3Li, Yang; Yan, Xiao-Long; Hu, Li-Yan; Luo, Kai; Zhu, Jie; Wu, Lei
Pd-catalyzed divergent regioselective annulation of phosphinyl allenes accessing polyarylfurans and 2<i>H</i>-chromenes.
Chemical communications (Cambridge, England), 2024, 60, 3814-3817
1571173 CIFC30 H27 O4 PP -18.9061; 10.4242; 14.312
74.291; 76.463; 86.731		1243.5Li, Yang; Yan, Xiao-Long; Hu, Li-Yan; Luo, Kai; Zhu, Jie; Wu, Lei
Pd-catalyzed divergent regioselective annulation of phosphinyl allenes accessing polyarylfurans and 2<i>H</i>-chromenes.
Chemical communications (Cambridge, England), 2024, 60, 3814-3817
1571174 CIFC45 H26 OP -18.7621; 10.6742; 16.727
80.613; 82.954; 70.163		1448.1Yang, Guang; Zhao, Wen-Xuan; Cao, Jing-Yi; Xue, Zeng-Min; Lin, Hong-Tao; Chen, Shu-Hai; Yamato, Takehiko; Redshaw, Carl; Wang, Chuan-Zeng
Regulable high-contrast mechanofluorochromic enhancement behaviour based on substituent effects.
Chemical communications (Cambridge, England), 2024, 60, 3966-3969
1571187 CIFC30 H28 N2 O4 S2P 1 21/n 18.2168; 12.1811; 28.132
90; 93.702; 90		2809.8Sun, Haoyany; Pan, Junhong; Zhao, Wenying; Zhou, Tong; Song, Xizhong; Lin, Jun; Jin, Yi
Scandium-catalyzed chemoselective carbene insertion into N-H over S-H: access to <i>o</i>-alkylamine-diaryl disulfides.
Chemical communications (Cambridge, England), 2024, 60, 3798-3801
1571188 CIFC33 H32 N2 O2P 1 21/n 114.474; 12.9605; 14.8707
90; 110.226; 90		2617.6Xu, Lihua; Zhao, Jiang
Bromine atom introduction improves the F<sup>-</sup> sensing ability of an indolo[3,2-<i>b</i>]carbazole-salicylaldehyde-based fluorescence turn-on sensor.
Chemical communications (Cambridge, England), 2024, 60, 3830-3833
1572878 CIFC24 H18 N2 O3P 21 21 218.6718; 9.0165; 24.3506
90; 90; 90		1903.96Weng, Rui; Zhou, Yuqiao; Zhang, Yaqin; Feng, Xiaoming; Liu, Xiaohua
Catalytic asymmetric Michael and Nef-type sequential reaction of nitroolefin with azlactone to construct oxazole-fused succinimide.
Chemical communications (Cambridge, England), 2024, 60, 13384-13387
1572879 CIFC24 H15 Cl O4P 1 21/n 111.941; 8.391; 19.4783
90; 107.214; 90		1864.24Dey, Sovan; Das, Arindam; Yadav, Ram Naresh; Boruah, Palash Jyoti; Sarkar, Koushik; Paul, Amit Kumar; Hossain, Md Firoj
Electron donor-acceptor complex enabled photocascade strategy for the synthesis of <i>trans</i>-dihydrofuro[3,2-<i>c</i>]chromen-4-one scaffolds <i>via</i> radical conjugate addition of pyridinium ylide.
Chemical communications (Cambridge, England), 2024, 60, 14384-14387
1572880 CIFC26 H20 Br N O4P -15.0399; 14.26675; 15.137
82.4456; 83.3581; 85.9012		1069.96Dey, Sovan; Das, Arindam; Yadav, Ram Naresh; Boruah, Palash Jyoti; Sarkar, Koushik; Paul, Amit Kumar; Hossain, Md Firoj
Electron donor-acceptor complex enabled photocascade strategy for the synthesis of <i>trans</i>-dihydrofuro[3,2-<i>c</i>]chromen-4-one scaffolds <i>via</i> radical conjugate addition of pyridinium ylide.
Chemical communications (Cambridge, England), 2024, 60, 14384-14387
7132357 CIFC47 H48 O P SbP 1 21/c 117.478; 18.488; 12.2139
90; 100.786; 90		3877Zhou, Benyu; Bedajna, Shantabh; Gabbaï, François P
Pnictogen bonding at the service of gold catalysis: the case of a phosphinostiborane gold complex.
Chemical communications (Cambridge, England), 2023, 60, 192-195
7132358 CIFC47 H48 Au Cl O P SbP 1 21/n 117.3843; 10.5399; 24.0882
90; 107.186; 90		4216.6Zhou, Benyu; Bedajna, Shantabh; Gabbaï, François P
Pnictogen bonding at the service of gold catalysis: the case of a phosphinostiborane gold complex.
Chemical communications (Cambridge, England), 2023, 60, 192-195
7132359 CIFC65 H78 Au Cl O4 P SbP -110.8607; 14.1687; 20.185
77.272; 80.912; 86.225		2990.2Zhou, Benyu; Bedajna, Shantabh; Gabbaï, François P
Pnictogen bonding at the service of gold catalysis: the case of a phosphinostiborane gold complex.
Chemical communications (Cambridge, England), 2023, 60, 192-195
7132360 CIFC61 H68 O3 P SbP -110.577; 15.3832; 16.6017
91.68; 101.133; 96.861		2627.6Zhou, Benyu; Bedajna, Shantabh; Gabbaï, François P
Pnictogen bonding at the service of gold catalysis: the case of a phosphinostiborane gold complex.
Chemical communications (Cambridge, England), 2023, 60, 192-195
7132361 CIFC26 H25 N O3 SP n a 2115.5963; 8.0239; 17.6239
90; 90; 90		2205.51He, Jiwen; Li, Xiaohua; He, Qiuqin; Fan, Renhua
Cascade alkyl migration in 2-alkynylanilines for the synthesis of benzenoid ring multi-functionalized indoles.
Chemical communications (Cambridge, England), 2023, 60, 71-74
7132362 CIFC25 H23 N O3 SP 1 21/n 117.6632; 6.9882; 18.3317
90; 116.15; 90		2031.15He, Jiwen; Li, Xiaohua; He, Qiuqin; Fan, Renhua
Cascade alkyl migration in 2-alkynylanilines for the synthesis of benzenoid ring multi-functionalized indoles.
Chemical communications (Cambridge, England), 2023, 60, 71-74
7132363 CIFC27.5 H28 Cl N O3 SC 1 2/c 118.9459; 9.6231; 28.0552
90; 107.401; 90		4880.9He, Jiwen; Li, Xiaohua; He, Qiuqin; Fan, Renhua
Cascade alkyl migration in 2-alkynylanilines for the synthesis of benzenoid ring multi-functionalized indoles.
Chemical communications (Cambridge, England), 2023, 60, 71-74
7132364 CIFC27 H35 Cl2 N O3 SP 1 n 110.5744; 11.146; 23.328
90; 99.659; 90		2710.5He, Jiwen; Li, Xiaohua; He, Qiuqin; Fan, Renhua
Cascade alkyl migration in 2-alkynylanilines for the synthesis of benzenoid ring multi-functionalized indoles.
Chemical communications (Cambridge, England), 2023, 60, 71-74
7132365 CIFC27 H27 N O3 SP -19.2045; 10.3746; 12.3389
105.482; 102.087; 92.734		1103.62He, Jiwen; Li, Xiaohua; He, Qiuqin; Fan, Renhua
Cascade alkyl migration in 2-alkynylanilines for the synthesis of benzenoid ring multi-functionalized indoles.
Chemical communications (Cambridge, England), 2023, 60, 71-74
7132369 CIFC17 H26 O5 SiP -17.9252; 9.8381; 12.6943
98.475; 107.944; 106.441		872.76Kawamoto, Yuichiro; Nishitani, Ayaka; Yoshimura, Yukari; Kobayashi, Toyoharu; Ito, Hisanaka
Total synthesis of highly oxygenated phomopsol B <i>via</i> acid-induced etherification to construct a bridged structure.
Chemical communications (Cambridge, England), 2023, 60, 95-97
7132370 CIFB2 Cl Rb S6 Sr3P b c a11.082; 7.9064; 29.1239
90; 90; 90		2551.8Yun, Yihan; Hou, Xueling; Yang, Zhihua; Li, Guangmao; Pan, Shilie
[RbSr<sub>3</sub>X][(BS<sub>3</sub>)<sub>2</sub>] (X = Cl, Br): two salt-inclusion thioborates with large birefringence and structure transformation from centrosymmetric to asymmetric.
Chemical communications (Cambridge, England), 2023, 60, 118-121
7132371 CIFB2 Br Rb S6 Sr3C m c 2115.044; 10.978; 7.8706
90; 90; 90		1299.9Yun, Yihan; Hou, Xueling; Yang, Zhihua; Li, Guangmao; Pan, Shilie
[RbSr<sub>3</sub>X][(BS<sub>3</sub>)<sub>2</sub>] (X = Cl, Br): two salt-inclusion thioborates with large birefringence and structure transformation from centrosymmetric to asymmetric.
Chemical communications (Cambridge, England), 2023, 60, 118-121
7132377 CIFC37 H44 N4 O6 ZnP -111.5986; 12.6596; 13.1983
78.37; 64.275; 76.951		1688.91Di Zazzo, Lorena; Nardis, Sara; Caroleo, Fabrizio; Pizzoli, Francesco; Fronczek, Frank R.; Smith, Kevin M.; Berna, Beatrice Berionni; Paolesse, Roberto
5- and 10-oxocorroles from β-octaalkylcorroles.
Chemical communications (Cambridge, England), 2023, 60, 102-105
7132378 CIFC37 H44 N4 O6 ZnP -110.2436; 11.0056; 15.7208
91.07; 101.638; 105.968		1663.7Di Zazzo, Lorena; Nardis, Sara; Caroleo, Fabrizio; Pizzoli, Francesco; Fronczek, Frank R.; Smith, Kevin M.; Berna, Beatrice Berionni; Paolesse, Roberto
5- and 10-oxocorroles from β-octaalkylcorroles.
Chemical communications (Cambridge, England), 2023, 60, 102-105
7132379 CIFC8 H7 Cs OP b c a6.7766; 8.3061; 29.6225
90; 90; 90		1667.37Wacker, Jakoba; Lynch, Jennifer R.; Banerjee, Sumanta; Macdonald, Peter A.; Kennedy, Alan R.; Sarkar, Biprajit; Mulvey, Robert E.
Isolable rubidium and caesium derivatives of common organic carbonyl compounds.
Chemical communications (Cambridge, England), 2023, 60, 91-94
7132380 CIFC14 H12 N O RbP 1 21/c 112.6999; 8.7124; 12.2028
90; 113.878; 90		1234.63Wacker, Jakoba; Lynch, Jennifer R.; Banerjee, Sumanta; Macdonald, Peter A.; Kennedy, Alan R.; Sarkar, Biprajit; Mulvey, Robert E.
Isolable rubidium and caesium derivatives of common organic carbonyl compounds.
Chemical communications (Cambridge, England), 2023, 60, 91-94
7132381 CIFC14 H12 Cs N OP c a 2118.6607; 6.0929; 22.6838
90; 90; 90		2579.1Wacker, Jakoba; Lynch, Jennifer R.; Banerjee, Sumanta; Macdonald, Peter A.; Kennedy, Alan R.; Sarkar, Biprajit; Mulvey, Robert E.
Isolable rubidium and caesium derivatives of common organic carbonyl compounds.
Chemical communications (Cambridge, England), 2023, 60, 91-94
7132382 CIFC57 H57 O5.25 Rb3C 1 2/c 125.4358; 15.8158; 26.622
90; 92.424; 90		10700.1Wacker, Jakoba; Lynch, Jennifer R.; Banerjee, Sumanta; Macdonald, Peter A.; Kennedy, Alan R.; Sarkar, Biprajit; Mulvey, Robert E.
Isolable rubidium and caesium derivatives of common organic carbonyl compounds.
Chemical communications (Cambridge, England), 2023, 60, 91-94
7132383 CIFC20.76 H22.51 Cs O2.19P -113.3301; 16.647; 28.3794
73.521; 83.579; 80.046		5934.82Wacker, Jakoba; Lynch, Jennifer R.; Banerjee, Sumanta; Macdonald, Peter A.; Kennedy, Alan R.; Sarkar, Biprajit; Mulvey, Robert E.
Isolable rubidium and caesium derivatives of common organic carbonyl compounds.
Chemical communications (Cambridge, England), 2023, 60, 91-94
7132384 CIFC12 H12 O3 SP 1 21/n 19.6096; 8.767; 14.39
90; 104.067; 90		1176Bhat, Showkat Ahmad; Ahmed, Qazi Naveed; Bhat, Khursheed Ahmad
DMSO-KOH mediated stereoselective synthesis of <i>Z</i>-enamides: an expeditious route to <i>Z</i>-enamide bearing natural products.
Chemical communications (Cambridge, England), 2023, 60, 114-117
7132385 CIFC42 H66 Ni P2P b c a18.802; 17.9299; 22.3674
90; 90; 90		7540.45Lin, Lirong; Tresp, David S.; Spasyuk, Denis M.; Lalancette, Roger A.; Prokopchuk, Demyan E.
Accessing Ni(0) to Ni(IV) <i>via</i> nickel-carbon-phosphorus bond reorganization.
Chemical communications (Cambridge, England), 2024, 60, 674-677
7132386 CIFC90 H66 B2 F40 Ni P2P -114.818; 16.711; 19.124
94.76; 90.21; 90.44		4719.04Lin, Lirong; Tresp, David S.; Spasyuk, Denis M.; Lalancette, Roger A.; Prokopchuk, Demyan E.
Accessing Ni(0) to Ni(IV) <i>via</i> nickel-carbon-phosphorus bond reorganization.
Chemical communications (Cambridge, England), 2024, 60, 674-677
7132387 CIFC102 H225 N2 O42 Si21 U3P -118.0726; 19.32; 25.3604
98.4318; 90.6353; 110.969		8159.7Tricoire, Maxime; Jori, Nadir; Fadaei Tirani, Farzaneh; Scopelliti, Rosario; Z Ivković, Ivica; Natrajan, Louise S.; Mazzanti, Marinella
A trinuclear metallasilsesquioxane of uranium(III).
Chemical communications (Cambridge, England), 2023, 60, 55-58
7132388 CIFC93 H21 O36 Si21 U3P -114.7163; 22.3387; 24.009
65.307; 87.504; 78.555		7021.6Tricoire, Maxime; Jori, Nadir; Fadaei Tirani, Farzaneh; Scopelliti, Rosario; Z Ivković, Ivica; Natrajan, Louise S.; Mazzanti, Marinella
A trinuclear metallasilsesquioxane of uranium(III).
Chemical communications (Cambridge, England), 2023, 60, 55-58
7132389 CIFC112 O48 Si28 U4C 1 2/c 133.7165; 33.7274; 35.24
90; 101.864; 90		39217.8Tricoire, Maxime; Jori, Nadir; Fadaei Tirani, Farzaneh; Scopelliti, Rosario; Z Ivković, Ivica; Natrajan, Louise S.; Mazzanti, Marinella
A trinuclear metallasilsesquioxane of uranium(III).
Chemical communications (Cambridge, England), 2023, 60, 55-58
7132390 CIFC19 H17 N2 O3I 1 2/a 111.6169; 15.6243; 23.3222
90; 94.169; 90		4221.9Zhu, Zhi-Qiang; Hu, Jia-Yu; Xie, Zong-Bo; Le, Zhang-Gao
Visible-light-enabled cascade cross-dehydrogenative-coupling/cyclization to construct α-chromone substituted α-amino acid derivatives.
Chemical communications (Cambridge, England), 2023, 60, 106-109
7132391 CIFC24 H18 Br N3 O3P 21 21 2110.11185; 13.81714; 15.0875
90; 90; 90		2107.98Chen, Xiangjie; Zhao, Yujie; Huang, Cheng; Zhao, Zhifei; Zhao, Weiwei; Li, Shi-Wu
Catalytic asymmetric conjugate addition of coumarins to unsaturated ketones catalyzed by a chiral-at-metal Rh(III) complex.
Chemical communications (Cambridge, England), 2023, 60, 236-239
7132392 CIFC35 H41.5 Cu N5.5P b c n14.32746; 12.45283; 34.81445
90; 90; 90		6211.5Gridneva, Tatiana; Karimata, Ayumu; Bansal, Richa; Fayzullin, Robert R.; Vasylevskyi, Serhii; Bruhacs, Andrew; Khusnutdinova, Julia R.
Deep-red photoluminescent mechanoresponsive polymers with dynamic Cu<sup>I</sup>-arylamide mechanophores.
Chemical communications (Cambridge, England), 2023, 60, 212-215
7132393 CIFC35 H40 Cu N5 OP 1 21/n 111.89392; 15.29071; 17.47129
90; 100.826; 90		3120.9Gridneva, Tatiana; Karimata, Ayumu; Bansal, Richa; Fayzullin, Robert R.; Vasylevskyi, Serhii; Bruhacs, Andrew; Khusnutdinova, Julia R.
Deep-red photoluminescent mechanoresponsive polymers with dynamic Cu<sup>I</sup>-arylamide mechanophores.
Chemical communications (Cambridge, England), 2023, 60, 212-215
7132394 CIFC48 H32 Cu4 N4P -19.5755; 9.91553; 10.19785
89.3747; 75.0262; 86.676		933.79Gridneva, Tatiana; Karimata, Ayumu; Bansal, Richa; Fayzullin, Robert R.; Vasylevskyi, Serhii; Bruhacs, Andrew; Khusnutdinova, Julia R.
Deep-red photoluminescent mechanoresponsive polymers with dynamic Cu<sup>I</sup>-arylamide mechanophores.
Chemical communications (Cambridge, England), 2023, 60, 212-215
7132395 CIFC36 H44 Cu N5 O2P -112.7194; 13.23166; 20.6802
106.722; 106.808; 90.6783		3173.69Gridneva, Tatiana; Karimata, Ayumu; Bansal, Richa; Fayzullin, Robert R.; Vasylevskyi, Serhii; Bruhacs, Andrew; Khusnutdinova, Julia R.
Deep-red photoluminescent mechanoresponsive polymers with dynamic Cu<sup>I</sup>-arylamide mechanophores.
Chemical communications (Cambridge, England), 2023, 60, 212-215
7132396 CIFC100 H88 Cu4 N4 O5P -111.9543; 12.2544; 15.0509
99.545; 104.493; 110.466		1920.37Gridneva, Tatiana; Karimata, Ayumu; Bansal, Richa; Fayzullin, Robert R.; Vasylevskyi, Serhii; Bruhacs, Andrew; Khusnutdinova, Julia R.
Deep-red photoluminescent mechanoresponsive polymers with dynamic Cu<sup>I</sup>-arylamide mechanophores.
Chemical communications (Cambridge, England), 2023, 60, 212-215
7132397 CIFC42 H44 Cu N5P 1 21/n 115.29636; 13.67332; 17.78811
90; 114.721; 90		3379.45Gridneva, Tatiana; Karimata, Ayumu; Bansal, Richa; Fayzullin, Robert R.; Vasylevskyi, Serhii; Bruhacs, Andrew; Khusnutdinova, Julia R.
Deep-red photoluminescent mechanoresponsive polymers with dynamic Cu<sup>I</sup>-arylamide mechanophores.
Chemical communications (Cambridge, England), 2023, 60, 212-215
7132398 CIFC50 H72 Cu N5 O2P n m a17.1539; 20.3189; 13.4474
90; 90; 90		4687.07Gridneva, Tatiana; Karimata, Ayumu; Bansal, Richa; Fayzullin, Robert R.; Vasylevskyi, Serhii; Bruhacs, Andrew; Khusnutdinova, Julia R.
Deep-red photoluminescent mechanoresponsive polymers with dynamic Cu<sup>I</sup>-arylamide mechanophores.
Chemical communications (Cambridge, England), 2023, 60, 212-215
7132399 CIFC58 H52 Cl4 Cu4 N4 O8P -110.2104; 10.755; 13.3061
70.726; 79.185; 79.171		1342.23Gridneva, Tatiana; Karimata, Ayumu; Bansal, Richa; Fayzullin, Robert R.; Vasylevskyi, Serhii; Bruhacs, Andrew; Khusnutdinova, Julia R.
Deep-red photoluminescent mechanoresponsive polymers with dynamic Cu<sup>I</sup>-arylamide mechanophores.
Chemical communications (Cambridge, England), 2023, 60, 212-215
7132400 CIFC42 H44 Cu N5P b c a18.82101; 16.82525; 21.49677
90; 90; 90		6807.34Gridneva, Tatiana; Karimata, Ayumu; Bansal, Richa; Fayzullin, Robert R.; Vasylevskyi, Serhii; Bruhacs, Andrew; Khusnutdinova, Julia R.
Deep-red photoluminescent mechanoresponsive polymers with dynamic Cu<sup>I</sup>-arylamide mechanophores.
Chemical communications (Cambridge, England), 2023, 60, 212-215
7132401 CIFC34 H42 Cu N5P b c a15.10177; 19.65119; 20.19471
90; 90; 90		5993.14Gridneva, Tatiana; Karimata, Ayumu; Bansal, Richa; Fayzullin, Robert R.; Vasylevskyi, Serhii; Bruhacs, Andrew; Khusnutdinova, Julia R.
Deep-red photoluminescent mechanoresponsive polymers with dynamic Cu<sup>I</sup>-arylamide mechanophores.
Chemical communications (Cambridge, England), 2023, 60, 212-215
7132402 CIFC46 H54 Cu N5 OP 1 21/c 113.72164; 14.80305; 18.99296
90; 95.9445; 90		3837.15Gridneva, Tatiana; Karimata, Ayumu; Bansal, Richa; Fayzullin, Robert R.; Vasylevskyi, Serhii; Bruhacs, Andrew; Khusnutdinova, Julia R.
Deep-red photoluminescent mechanoresponsive polymers with dynamic Cu<sup>I</sup>-arylamide mechanophores.
Chemical communications (Cambridge, England), 2023, 60, 212-215
7132403 CIFC36 H33 N O2 SP -111.0196; 11.9729; 12.4127
68.202; 71.011; 87.557		1432.13Gharpure, Santosh J.; Kumari, Sanyog
Cascade radical cyclization on 3-propargyl-2-alkenyl indole gives stereoselective access to cyclohepta[<i>b</i>]indole over carbazole.
Chemical communications (Cambridge, England), 2024, 60, 538-541
7132404 CIFC41 H35 N O4 S2P 1 21/c 119.4285; 11.6342; 16.4121
90; 113.21; 90		3409.5Gharpure, Santosh J.; Kumari, Sanyog
Cascade radical cyclization on 3-propargyl-2-alkenyl indole gives stereoselective access to cyclohepta[<i>b</i>]indole over carbazole.
Chemical communications (Cambridge, England), 2024, 60, 538-541
7132405 CIFC35 H30 N2 O2 SP 1 21/n 113.651; 8.9231; 22.78
90; 95.384; 90		2762.6Gharpure, Santosh J.; Kumari, Sanyog
Cascade radical cyclization on 3-propargyl-2-alkenyl indole gives stereoselective access to cyclohepta[<i>b</i>]indole over carbazole.
Chemical communications (Cambridge, England), 2024, 60, 538-541
7132406 CIFC32 H25 N SP -110.4151; 11.5788; 12.6011
95.743; 112.337; 116.102		1195.11Gharpure, Santosh J.; Kumari, Sanyog
Cascade radical cyclization on 3-propargyl-2-alkenyl indole gives stereoselective access to cyclohepta[<i>b</i>]indole over carbazole.
Chemical communications (Cambridge, England), 2024, 60, 538-541
7132407 CIFC41 H35 N O4 S2P -110.5565; 17.7776; 19.8243
72.058; 79.538; 73.177		3370.5Gharpure, Santosh J.; Kumari, Sanyog
Cascade radical cyclization on 3-propargyl-2-alkenyl indole gives stereoselective access to cyclohepta[<i>b</i>]indole over carbazole.
Chemical communications (Cambridge, England), 2024, 60, 538-541
7132408 CIFC44 H33 F5 N2 O4 S2P 1 21/n 110.3514; 27.898; 15.1231
90; 101.799; 90		4275Gharpure, Santosh J.; Kumari, Sanyog
Cascade radical cyclization on 3-propargyl-2-alkenyl indole gives stereoselective access to cyclohepta[<i>b</i>]indole over carbazole.
Chemical communications (Cambridge, England), 2024, 60, 538-541
7132409 CIFC48 H42 N2P -112.669; 12.856; 13.378
95.35; 113.56; 111.6		1781.6Gentile, Giuseppe; Bartolomei, Beatrice; Dosso, Jacopo; Demitri, Nicola; Filippini, Giacomo; Prato, Maurizio
Synthesis of a novel tetra-phenol π-extended phenazine and its application as an organo-photocatalyst.
Chemical communications (Cambridge, England), 2024, 60, 602-605
7132410 CIFC51 H48.75 Cl0.75 N2P 1 21/n 119.373; 17.608; 23.058
90; 92.25; 90		7859Gentile, Giuseppe; Bartolomei, Beatrice; Dosso, Jacopo; Demitri, Nicola; Filippini, Giacomo; Prato, Maurizio
Synthesis of a novel tetra-phenol π-extended phenazine and its application as an organo-photocatalyst.
Chemical communications (Cambridge, England), 2024, 60, 602-605
7132411 CIFC19 H18 Cl N O3P b c a11.0033; 15.9828; 19.388
90; 90; 90		3409.64Takeda, Norihiko; Maeda, Ryoya; Yasui, Motohiro; Ueda, Masafumi
Synthesis of oxime ethers <i>via</i> a formal reductive O-H bond insertion of oximes to α-keto esters.
Chemical communications (Cambridge, England), 2023, 60, 172-175
7132412 CIFC16 H10 N2 OP -18.0807; 11.4488; 13.0502
75.453; 79.894; 79.458		1138.21Nipate, Dhananjay S.; Meena, Neha; Swami, Prakash N.; Rangan, Krishnan; Kumar, Anil
Rh(III)-catalyzed oxidative [4+2] annulation of 2-arylquinoxalines and 2-aryl-2<i>H</i>-indazoles with allyl alcohols.
Chemical communications (Cambridge, England), 2024, 60, 344-347
7132413 CIFC30 H26 O2P -16.0915; 10.7543; 17.1562
100.087; 92.581; 102.264		1077.32Garbini, Mauro; Brunetti, Andrea; Pedrazzani, Riccardo; Monari, Magda; Marcaccio, Massimo; Bertuzzi, Giulio; Bandini, Marco
Reductive cyclodimerization of chalcones: exploring the "self-adaptability" of galvanostatic electrosynthesis.
Chemical communications (Cambridge, England), 2024, 60, 404-407
7132414 CIFC33 H34 O3P 1 21/n 120.754; 5.945; 24.1084
90; 112.709; 90		2744Garbini, Mauro; Brunetti, Andrea; Pedrazzani, Riccardo; Monari, Magda; Marcaccio, Massimo; Bertuzzi, Giulio; Bandini, Marco
Reductive cyclodimerization of chalcones: exploring the "self-adaptability" of galvanostatic electrosynthesis.
Chemical communications (Cambridge, England), 2024, 60, 404-407
7132415 CIFB4 O9 Pb TeP -16.574; 6.7445; 9.8903
70.105; 78.877; 61.726		362.88Zhang, Ruonan; Tudi, Abudukadi; Yang, Xia; Wang, Xuping; Yang, Zhihua; Han, Shujuan; Pan, Shilie
PbTeB<sub>4</sub>O<sub>9</sub>: a lead tellurium borate with unprecedented fundamental building block [B<sub>4</sub>O<sub>10</sub>] and large birefringence.
Chemical communications (Cambridge, England), 2024, 60, 340-343
7132418 CIFC52 H60 D12 I2 Mo3 S4 UP -113.3084; 13.3384; 17.3783
90.036; 109.162; 110.969		2696.47Patra, Kamaless; Brennessel, William W.; Matson, Ellen M.
Molybdenum sulphide clusters as redox-active supports for low-valent uranium.
Chemical communications (Cambridge, England), 2024, 60, 530-533
7132419 CIFC59 H78 Mo3 N2 S4 UP 21 21 2111.0151; 20.2686; 24.6766
90; 90; 90		5509.31Patra, Kamaless; Brennessel, William W.; Matson, Ellen M.
Molybdenum sulphide clusters as redox-active supports for low-valent uranium.
Chemical communications (Cambridge, England), 2024, 60, 530-533
7132420 CIFC40 H60 I Mo3 S4 UP -111.2243; 20.51803; 21.54896
79.9966; 75.1189; 87.6951		4723.32Patra, Kamaless; Brennessel, William W.; Matson, Ellen M.
Molybdenum sulphide clusters as redox-active supports for low-valent uranium.
Chemical communications (Cambridge, England), 2024, 60, 530-533
7132421 CIFC14 H15 Cl3 N2 O4 SP 1 21 111.978; 9.923; 14.449
90; 96.646; 90		1705.8Trinh, Tuan Anh; Fu, Yue; Hu, Derek B.; Zappia, Soren A.; Guzei, Ilia A.; Liu, Peng; Schomaker, Jennifer M.
Chemo- and enantioselective intramolecular silver-catalyzed aziridinations of carbamimidates.
Chemical communications (Cambridge, England), 2023, 60, 224-227
7132423 CIFC30 H25 Br2 N3 O4 SI 1 2/a 120.8975; 9.037; 31.2449
90; 108.922; 90		5581.8Feng, Guang-Chao; Li, Jun-Chi; Huang, Xiang; Liu, Ji-Kai; Wu, Bin; Yang, Jin-Ming
Cascade hydroarylation/Diels-Alder cycloaddition of alkynylindoles with electron-deficient alkynes and alkenes.
Chemical communications (Cambridge, England), 2024, 60, 328-331
7132424 CIFC24 H21 Cl N2 O2 SI 41/a :224.2953; 24.2953; 16.7274
90; 90; 90		9873.5Zhou, Pan; Wu, Senhui; Niu, Kaikai; Song, Hongjian; Liu, Yuxiu; Zhang, Jingjing; Wang, Qingmin
Intramolecular trapping of an iminium salt: rapid construction of quindoline derivatives.
Chemical communications (Cambridge, England), 2024, 60, 292-295
7132425 CIFC56.5 H47 Cl F6 N4 O5.5 P RuP -113.7564; 17.4685; 25.0576
86.19; 81.914; 67.772		5517.96Wang, Rui; Pan, Yunling; Feng, Sushan; Liang, Chenyi; Xie, Jianhui; Lau, Tai-Chu; Liu, Yingying
Structure and reactivity of a seven-coordinate ruthenium acylperoxo complex.
Chemical communications (Cambridge, England), 2024, 60, 312-315
7132426 CIFC24 H23 N3 OP 1 21/c 16.459; 26.872; 13.342
90; 98.252; 90		2291.7Chen, Longkun; Zhang, Mingshuai; Liu, Meichen; Liu, Zhuoyuan; Qiu, Yuetong; Zhang, Zhilai; Yu, Fuchao; Huang, Jiuzhong
Rh(III)-catalyzed selective mono- and dual-functionalization/cyclization of 1-aryl-5-aminopyrazoles with iodonium ylides.
Chemical communications (Cambridge, England), 2024, 60, 432-435
7132427 CIFC33 H36 Br N3 O4 SP -19.915; 13.033; 14.176
113.225; 97.316; 101.109		1609.3Chen, Longkun; Zhang, Mingshuai; Liu, Meichen; Liu, Zhuoyuan; Qiu, Yuetong; Zhang, Zhilai; Yu, Fuchao; Huang, Jiuzhong
Rh(III)-catalyzed selective mono- and dual-functionalization/cyclization of 1-aryl-5-aminopyrazoles with iodonium ylides.
Chemical communications (Cambridge, England), 2024, 60, 432-435
7132428 CIFC19 H47 O4 P3 WP 1 21/n 111.0303; 16.4864; 15.3533
90; 92.425; 90		2789.5Ju, Shaoying; Zhang, Chi; Tang, Beili; Liu, Liu Leo; Stephan, Douglas W.; Wu, Yile
The Lewis superacidic aluminium cation: [(NHC)Al(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 698-701
7132429 CIFC39 H36 Al F11 N2P c a 2114.4808; 12.6637; 20.244
90; 90; 90		3712.4Ju, Shaoying; Zhang, Chi; Tang, Beili; Liu, Liu Leo; Stephan, Douglas W.; Wu, Yile
The Lewis superacidic aluminium cation: [(NHC)Al(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 698-701
7132430 CIFC77 H52 Al B F30 N2P -112.8701; 14.0245; 21.8859
75.193; 78.87; 70.815		3581.2Ju, Shaoying; Zhang, Chi; Tang, Beili; Liu, Liu Leo; Stephan, Douglas W.; Wu, Yile
The Lewis superacidic aluminium cation: [(NHC)Al(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 698-701
7132431 CIFC75.45 H48.2 Al B F31 N2P 1 21/c 118.2366; 12.6216; 30.5952
90; 94.208; 90		7023.3Ju, Shaoying; Zhang, Chi; Tang, Beili; Liu, Liu Leo; Stephan, Douglas W.; Wu, Yile
The Lewis superacidic aluminium cation: [(NHC)Al(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 698-701
7132432 CIFC123 H96 Al2 B F40 N7C 1 2/c 158.9625; 12.3783; 42.5423
90; 132.777; 90		22790.6Ju, Shaoying; Zhang, Chi; Tang, Beili; Liu, Liu Leo; Stephan, Douglas W.; Wu, Yile
The Lewis superacidic aluminium cation: [(NHC)Al(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 698-701
7132433 CIFC8 H30 B20P n n m9.5876; 11.2736; 10.0616
90; 90; 90		1087.53Chen, Feijing; Guo, Wenjing; Ma, Yan-Na; Chen, Xuenian
9,9'-Bis-<i>o</i>-carboranes: synthesis and exploration of properties.
Chemical communications (Cambridge, England), 2024, 60, 614-617
7132434 CIFC4 H20 B20 Cl2 O0.06C 2 2 2113.41936; 25.17; 25.1694
90; 90; 90		8501.35Chen, Feijing; Guo, Wenjing; Ma, Yan-Na; Chen, Xuenian
9,9'-Bis-<i>o</i>-carboranes: synthesis and exploration of properties.
Chemical communications (Cambridge, England), 2024, 60, 614-617
7132435 CIFC4 H22 B20 O2P 1 21/c 112.3573; 12.905; 13.124
90; 112.213; 90		1937.57Chen, Feijing; Guo, Wenjing; Ma, Yan-Na; Chen, Xuenian
9,9'-Bis-<i>o</i>-carboranes: synthesis and exploration of properties.
Chemical communications (Cambridge, England), 2024, 60, 614-617
7132436 CIFC2 H11 B10P 1 21/n 16.9432; 10.0433; 12.6587
90; 97.066; 90		876.02Chen, Feijing; Guo, Wenjing; Ma, Yan-Na; Chen, Xuenian
9,9'-Bis-<i>o</i>-carboranes: synthesis and exploration of properties.
Chemical communications (Cambridge, England), 2024, 60, 614-617
7132437 CIFC20 H34 B20P 1 2/c 120.2379; 7.7225; 18.3961
90; 96.014; 90		2859.25Chen, Feijing; Guo, Wenjing; Ma, Yan-Na; Chen, Xuenian
9,9'-Bis-<i>o</i>-carboranes: synthesis and exploration of properties.
Chemical communications (Cambridge, England), 2024, 60, 614-617
7132438 CIFC16 H54 B20 Si4P 1 21/n 19.2397; 17.1741; 12.2399
90; 109.52; 90		1830.64Chen, Feijing; Guo, Wenjing; Ma, Yan-Na; Chen, Xuenian
9,9'-Bis-<i>o</i>-carboranes: synthesis and exploration of properties.
Chemical communications (Cambridge, England), 2024, 60, 614-617
7132439 CIFC24 H84 B38 N2P -110.7318; 13.0844; 18.4673
89.977; 78.418; 88.417		2539.36Chen, Feijing; Guo, Wenjing; Ma, Yan-Na; Chen, Xuenian
9,9'-Bis-<i>o</i>-carboranes: synthesis and exploration of properties.
Chemical communications (Cambridge, England), 2024, 60, 614-617
7132440 CIFC20 H62 B18 N2P -111.2612; 17.2885; 18.0579
85.761; 87.21; 82.019		3469.5Chen, Feijing; Guo, Wenjing; Ma, Yan-Na; Chen, Xuenian
9,9'-Bis-<i>o</i>-carboranes: synthesis and exploration of properties.
Chemical communications (Cambridge, England), 2024, 60, 614-617
7132441 CIFC23 H32 N5 O14.5P -17.0876; 9.0701; 22.1771
93.434; 95.177; 94.89		1411.39Almuhana, Asia R. Y.; Orton, Georgia R. F.; Rosenberg, Callum; Champness, Neil R.
Photoinduced radical formation in hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 452-455
7132442 CIFC54 H78 N13 O36P -17.843; 19.3052; 23.3588
88.568; 81.294; 86.534		3489.2Almuhana, Asia R. Y.; Orton, Georgia R. F.; Rosenberg, Callum; Champness, Neil R.
Photoinduced radical formation in hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 452-455
7132443 CIFC27 H29 N6 O11P -17.1361; 9.0655; 20.9919
88.41; 87.473; 83.432		1347.44Almuhana, Asia R. Y.; Orton, Georgia R. F.; Rosenberg, Callum; Champness, Neil R.
Photoinduced radical formation in hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 452-455
7132444 CIFC24 H18 N2 OP -16.3722; 13.4572; 14.9777
66.406; 89.765; 84.766		1171.35Bhoi, Saswat Ranjan; Debnath, Chhanda; Gandhi, Shikha
Pd/Brønsted acid catalysed intramolecular <i>N</i>-allylation of indoles and pyrroles with alkynes for the synthesis of N-fused heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 428-431
7132445 CIFC15 H12 O2P 1 21 18.0868; 6.9699; 10.0387
90; 90.595; 90		565.79Zhang, Xu; Wang, Di; Chang, Mengfan; Xu, Xuefeng; Li, Wenguang; Wang, Wanya
Pd(II)-Catalyzed tandem selective dehydrogenative [4+2] annulation of 2-methyl-1,3-cycloalkanediones with olefins.
Chemical communications (Cambridge, England), 2024, 60, 594-597
7132446 CIFC22 H16 O2P 1 21/c 115.586; 21.146; 9.659
90; 90.83; 90		3183.1Zhang, Xu; Wang, Di; Chang, Mengfan; Xu, Xuefeng; Li, Wenguang; Wang, Wanya
Pd(II)-Catalyzed tandem selective dehydrogenative [4+2] annulation of 2-methyl-1,3-cycloalkanediones with olefins.
Chemical communications (Cambridge, England), 2024, 60, 594-597
7132447 CIFC18 H13 Cl2 N O3C 1 2/c 130.7988; 4.6614; 22.7529
90; 94.524; 90		3256.4Liu, Jing; Liu, Deng-Yin; Yang, Qian; Zeng, Yao-Fu; Wang, Xiao-Li; Wang, Peng-Fei; Ruan, Yu-Jun; Wen, Miao-Miao; Zhang, Shang-Shi; Du, Li-da; Liu, Xu-Ge
Cp*Rh(III)-catalyzed regioselective cyclization of aromatic amides with allenes.
Chemical communications (Cambridge, England), 2024, 60, 598-601
7132448 CIFC20 H15 Br N2 O3P 1 21/c 15.3629; 17.7232; 18.1847
90; 94.638; 90		1722.8Liu, Jing; Liu, Deng-Yin; Yang, Qian; Zeng, Yao-Fu; Wang, Xiao-Li; Wang, Peng-Fei; Ruan, Yu-Jun; Wen, Miao-Miao; Zhang, Shang-Shi; Du, Li-da; Liu, Xu-Ge
Cp*Rh(III)-catalyzed regioselective cyclization of aromatic amides with allenes.
Chemical communications (Cambridge, England), 2024, 60, 598-601
7132449 CIFC28 H36 Cl2 Ge N4P 1 21/c 19.1689; 16.185; 22.5667
90; 94.33; 90		3339.3Eisner, Teresa; Kostenko, Arseni; J Kiefer, Fiona; Inoue, Shigeyoshi
Synthesis and isolation of a cyclic bis-vinyl germylene <i>via</i> a diazoolefin adduct of germylene dichloride.
Chemical communications (Cambridge, England), 2024, 60, 558-561
7132450 CIFC68 H92 Cl4 N8 O3 Sn2C 1 c 131.096; 12.7331; 18.1401
90; 94.162; 90		7163.6Eisner, Teresa; Kostenko, Arseni; J Kiefer, Fiona; Inoue, Shigeyoshi
Synthesis and isolation of a cyclic bis-vinyl germylene <i>via</i> a diazoolefin adduct of germylene dichloride.
Chemical communications (Cambridge, England), 2024, 60, 558-561
7132451 CIFC56 H72 Ge N6C 1 2/c 139.42; 12.489; 22.5821
90; 111.047; 90		10375.8Eisner, Teresa; Kostenko, Arseni; J Kiefer, Fiona; Inoue, Shigeyoshi
Synthesis and isolation of a cyclic bis-vinyl germylene <i>via</i> a diazoolefin adduct of germylene dichloride.
Chemical communications (Cambridge, England), 2024, 60, 558-561
7132452 CIFC26 H16 OP 1 21/c 15.8787; 25.8705; 12.0671
90; 101.194; 90		1800.31Calikyilmaz, Eylul; Karaoglu, Gozde; Demir, Mete; Şahin, Onur; Ulgut, Burak; Akdag, Akin; Türkmen, Yunus Emre
Intramolecular through-space charge transfer between benzofuran and ynone groups on a naphthalene spacer.
Chemical communications (Cambridge, England), 2024, 60, 550-553
7132453 CIFC55 H48 Cl2 N6 O2P 21 21 217.015; 17.56; 7.712
90; 90; 90		2304.2Yamanomoto, Ken; Yamamoto, Kota; Yoshida, Satoshi; Sato, Sota; Akiyama, Takahiko
Enantioselective synthesis of 3-(<i>N</i>-indolyl)quinolines containing axial and central chiralities.
Chemical communications (Cambridge, England), 2024, 60, 582-585
7132454 CIFC35 H34 B F4 N O1.5 PP 1 c 18.3585; 14.7884; 25.0191
90; 90.077; 90		3092.6Litle, Elishua D.; Gabbaï, François P
Double axial stabilization of a carbenium ion <i>via</i> convergent PO → C<sup>+</sup> tetrel bonding.
Chemical communications (Cambridge, England), 2024, 60, 690-693
7132455 CIFC45 H38 B F4 N O2 P2C 1 2/m 112.224; 25.959; 12.87
90; 91.755; 90		4082Litle, Elishua D.; Gabbaï, François P
Double axial stabilization of a carbenium ion <i>via</i> convergent PO → C<sup>+</sup> tetrel bonding.
Chemical communications (Cambridge, England), 2024, 60, 690-693
7132456 CIFC33 H30 N O2 PP 1 21/c 115.3105; 10.7158; 15.7073
90; 92.104; 90		2575.3Litle, Elishua D.; Gabbaï, François P
Double axial stabilization of a carbenium ion <i>via</i> convergent PO → C<sup>+</sup> tetrel bonding.
Chemical communications (Cambridge, England), 2024, 60, 690-693
7132457 CIFC45 H40 N O3.5 P2P -112.0136; 12.8997; 13.449
71.834; 71.445; 67.41		1781Litle, Elishua D.; Gabbaï, François P
Double axial stabilization of a carbenium ion <i>via</i> convergent PO → C<sup>+</sup> tetrel bonding.
Chemical communications (Cambridge, England), 2024, 60, 690-693
7132458 CIFC61 H56 Cl2 N O P2P -113.849; 13.924; 14.623
115.72; 90.378; 96.195		2521.1Litle, Elishua D.; Gabbaï, François P
Double axial stabilization of a carbenium ion <i>via</i> convergent PO → C<sup>+</sup> tetrel bonding.
Chemical communications (Cambridge, England), 2024, 60, 690-693
7132459 CIFC32 H31 Br O6P 1 21 110.845; 11.7874; 11.0385
90; 97.286; 90		1399.71Liu, Zi-Hao; Xiao, Jian; Zhai, Qian-Qian; Tang, Xi; Xu, Li-Jun; Zhuang, Zhi-Yuan; Wang, Ya-Wen; Peng, Yu
Intramolecular Ni-catalyzed reductive coupling enables enantiodivergent synthesis of linoxepin.
Chemical communications (Cambridge, England), 2024, 60, 694-697
7132460 CIFC22 H22 O6P 21 21 218.41567; 11.8302; 18.4063
90; 90; 90		1832.51Liu, Zi-Hao; Xiao, Jian; Zhai, Qian-Qian; Tang, Xi; Xu, Li-Jun; Zhuang, Zhi-Yuan; Wang, Ya-Wen; Peng, Yu
Intramolecular Ni-catalyzed reductive coupling enables enantiodivergent synthesis of linoxepin.
Chemical communications (Cambridge, England), 2024, 60, 694-697
7132461 CIFC21 H18 O6P 21 21 217.60702; 8.8987; 25.627
90; 90; 90		1734.76Liu, Zi-Hao; Xiao, Jian; Zhai, Qian-Qian; Tang, Xi; Xu, Li-Jun; Zhuang, Zhi-Yuan; Wang, Ya-Wen; Peng, Yu
Intramolecular Ni-catalyzed reductive coupling enables enantiodivergent synthesis of linoxepin.
Chemical communications (Cambridge, England), 2024, 60, 694-697
7132462 CIFC9 H15 F3 O3P 6311.4469; 11.4469; 4.7028
90; 90; 120		533.66Haridas, Shyamkumar V.; von Delius, Max
Synthesis and supramolecular properties of all-<i>cis</i>-2,4,6-trifluorocyclohexane-1,3,5-triol.
Chemical communications (Cambridge, England), 2024, 60, 606-609
7132463 CIFC6 H11 F3 O4P n m a17.1696; 9.4705; 4.8298
90; 90; 90		785.35Haridas, Shyamkumar V.; von Delius, Max
Synthesis and supramolecular properties of all-<i>cis</i>-2,4,6-trifluorocyclohexane-1,3,5-triol.
Chemical communications (Cambridge, England), 2024, 60, 606-609
7132464 CIFC15 H15 F3 O3C 1 2/c 118.1588; 9.2165; 16.7115
90; 92.384; 90		2794.43Haridas, Shyamkumar V.; von Delius, Max
Synthesis and supramolecular properties of all-<i>cis</i>-2,4,6-trifluorocyclohexane-1,3,5-triol.
Chemical communications (Cambridge, England), 2024, 60, 606-609
7132465 CIFC10 H15 F3 O4P 1 21/n 16.4778; 8.9049; 19.2107
90; 98.964; 90		1094.62Haridas, Shyamkumar V.; von Delius, Max
Synthesis and supramolecular properties of all-<i>cis</i>-2,4,6-trifluorocyclohexane-1,3,5-triol.
Chemical communications (Cambridge, England), 2024, 60, 606-609
7132466 CIFC18 H7 Ag3 F12 N4P -18.2213; 12.3633; 12.5168
116.455; 95.181; 102.301		1087.63Titov, Aleksei A.; Smol'yakov, Alexander F.; Chernyadyev, Andrey Yu; Godovikov, Ivan A.; Filippov, Oleg A.; Shubina, Elena S.
Pyrazolate <i>vs.</i> phenylethynide: direct exchange of the anionic bridging ligand in a cyclic trinuclear silver complex.
Chemical communications (Cambridge, England), 2024, 60, 847-850
7132467 CIFC33 H10 Ag6 F30 N10P -113.3037; 15.8607; 16.964
90.382; 106.152; 109.675		3217.5Titov, Aleksei A.; Smol'yakov, Alexander F.; Chernyadyev, Andrey Yu; Godovikov, Ivan A.; Filippov, Oleg A.; Shubina, Elena S.
Pyrazolate <i>vs.</i> phenylethynide: direct exchange of the anionic bridging ligand in a cyclic trinuclear silver complex.
Chemical communications (Cambridge, England), 2024, 60, 847-850
7132468 CIFC33 H29 F N2 O5 S2P -18.3017; 13.9812; 14.6108
112.009; 98.334; 104.508		1467.25Liu, Xiao-Li; Ji, Shun-Jun; Cai, Zhong-Jian
Palladium-catalyzed carbomonofluoromethylation of unactivated alkenes: rapid access to γ-monofluoromethyl carboxylic acid derivatives.
Chemical communications (Cambridge, England), 2024, 60, 730-733
7132469 CIFC5 Cl3.4 F43.4 N O13.8 S3.4 Sb Te7 XeP -19.9625; 13.7996; 20.0668
102.386; 95.157; 93.654		2673.8Toraman, Ahmet N.; Fischer, Lukas; Pérez-Bitrián, Alberto; Wiesner, Anja; Hoffmann, Kurt F.; Riedel, Sebastian
[Xe(OTeF<sub>5</sub>)(py<sup>F</sup>)]<sup>+</sup>: a strong oxidizing xenonium(II) teflate cation with N-donor bases.
Chemical communications (Cambridge, England), 2024, 60, 1711-1714
7132470 CIFC5 H3 N8 Na O7C 1 2/c 111.421; 9.3158; 21.599
90; 96.498; 90		2283.3Balaraju, Muntha; Kommu, Nagarjuna; Vangara, Srinivas; Sahoo, Aswini K.; Thaltiri, Vikranth; Sahoo, Akhila K.
Synthetic manifestation of trinitro-pyrazolo-2<i>H</i>-1,2,3-triazoles (TNPT) as insensitive energetic materials.
Chemical communications (Cambridge, England), 2024, 60, 827-830
7132471 CIFC5 H2 N8 O6P 1 21/c 111.9516; 8.6036; 10.7241
90; 104.501; 90		1067.6Balaraju, Muntha; Kommu, Nagarjuna; Vangara, Srinivas; Sahoo, Aswini K.; Thaltiri, Vikranth; Sahoo, Akhila K.
Synthetic manifestation of trinitro-pyrazolo-2<i>H</i>-1,2,3-triazoles (TNPT) as insensitive energetic materials.
Chemical communications (Cambridge, England), 2024, 60, 827-830
7132472 CIFC5 H4 N6 O2P 1 21 16.6812; 7.0171; 7.8472
90; 104.571; 90		356.06Balaraju, Muntha; Kommu, Nagarjuna; Vangara, Srinivas; Sahoo, Aswini K.; Thaltiri, Vikranth; Sahoo, Akhila K.
Synthetic manifestation of trinitro-pyrazolo-2<i>H</i>-1,2,3-triazoles (TNPT) as insensitive energetic materials.
Chemical communications (Cambridge, England), 2024, 60, 827-830
7132473 CIFC6 H4 N8 O6P 1 21/n 19.1552; 8.1515; 15.7139
90; 106.884; 90		1122.16Balaraju, Muntha; Kommu, Nagarjuna; Vangara, Srinivas; Sahoo, Aswini K.; Thaltiri, Vikranth; Sahoo, Akhila K.
Synthetic manifestation of trinitro-pyrazolo-2<i>H</i>-1,2,3-triazoles (TNPT) as insensitive energetic materials.
Chemical communications (Cambridge, England), 2024, 60, 827-830
7132474 CIFC5 H3 N9 O6P 1 21/n 18.8502; 7.3093; 16.7588
90; 98.44; 90		1072.37Balaraju, Muntha; Kommu, Nagarjuna; Vangara, Srinivas; Sahoo, Aswini K.; Thaltiri, Vikranth; Sahoo, Akhila K.
Synthetic manifestation of trinitro-pyrazolo-2<i>H</i>-1,2,3-triazoles (TNPT) as insensitive energetic materials.
Chemical communications (Cambridge, England), 2024, 60, 827-830
7132475 CIFC5 H5 N9 O6P -15.1838; 9.1275; 12.3907
107.311; 99.537; 102.736		528.83Balaraju, Muntha; Kommu, Nagarjuna; Vangara, Srinivas; Sahoo, Aswini K.; Thaltiri, Vikranth; Sahoo, Akhila K.
Synthetic manifestation of trinitro-pyrazolo-2<i>H</i>-1,2,3-triazoles (TNPT) as insensitive energetic materials.
Chemical communications (Cambridge, England), 2024, 60, 827-830
7132476 CIFC42 H37 B2 Co Fe2 N24 O3.5P -112.176; 13.726; 16.323
68.781; 86.578; 79.806		2502.9Kharel, Ranjan; Yadav, Jyoti; Konar, Sanjit
Modulation of single-chain magnet behaviour in a heterometallic Fe<sub>2</sub>Co cyanide-bridged 2D sheet.
Chemical communications (Cambridge, England), 2024, 60, 839-842
7132477 CIFC42.5 H40 B2 Fe2 N24 O4 ZnP -112.358; 13.8278; 16.4558
68.011; 86.398; 78.696		2556.72Kharel, Ranjan; Yadav, Jyoti; Konar, Sanjit
Modulation of single-chain magnet behaviour in a heterometallic Fe<sub>2</sub>Co cyanide-bridged 2D sheet.
Chemical communications (Cambridge, England), 2024, 60, 839-842
7132478 CIFC42 H34 B2 Co Fe2 N24P -111.9253; 13.8081; 16.3778
68.189; 86.117; 80.393		2468.6Kharel, Ranjan; Yadav, Jyoti; Konar, Sanjit
Modulation of single-chain magnet behaviour in a heterometallic Fe<sub>2</sub>Co cyanide-bridged 2D sheet.
Chemical communications (Cambridge, England), 2024, 60, 839-842
7132479 CIFC42 H35 B2 Co Fe2 N24 O3.5P -112.328; 13.811; 16.392
68.709; 86.93; 79.551		2557Kharel, Ranjan; Yadav, Jyoti; Konar, Sanjit
Modulation of single-chain magnet behaviour in a heterometallic Fe<sub>2</sub>Co cyanide-bridged 2D sheet.
Chemical communications (Cambridge, England), 2024, 60, 839-842
7132480 CIFC74 H65 Cu F6 Fe N8 O7 P2 S2P -111.046; 18.14; 20.185
81.621; 86.362; 82.139		3959.9Rickmeyer, Kerstin; Huber, Matthias; Hess, Corinna R.
Influence of a neighbouring Cu centre on electro- and photocatalytic CO<sub>2</sub> reduction by Fe-Mabiq.
Chemical communications (Cambridge, England), 2024, 60, 819-822
7132481 CIFC38 H39 F3 Fe N10 O3 SP 1 21/c 112.8059; 16.387; 20.403
90; 105.269; 90		4130.4Rickmeyer, Kerstin; Huber, Matthias; Hess, Corinna R.
Influence of a neighbouring Cu centre on electro- and photocatalytic CO<sub>2</sub> reduction by Fe-Mabiq.
Chemical communications (Cambridge, England), 2024, 60, 819-822
7132482 CIFC21 H28 Co N2 S2P b c a15.9232; 15.0712; 16.8379
90; 90; 90		4040.8Jana, Manish; Quiroz, Manuel; Darensbourg, Marcetta Y.
A single carbon atom controls the geometry and reactivity of Co<sup>II</sup>(N<sub>2</sub>S<sub>2</sub>) complexes.
Chemical communications (Cambridge, England), 2024, 60, 1128-1131
7132483 CIFC40 H52 Co2 N4 S4I 1 2/a 117.8761; 13.6323; 15.8821
90; 102.083; 90		3784.6Jana, Manish; Quiroz, Manuel; Darensbourg, Marcetta Y.
A single carbon atom controls the geometry and reactivity of Co<sup>II</sup>(N<sub>2</sub>S<sub>2</sub>) complexes.
Chemical communications (Cambridge, England), 2024, 60, 1128-1131
7132484 CIFC31 H43 Co N3 O6 S2 WP 1 21/c 113.2062; 14.533; 18.5933
90; 105.716; 90		3435.1Jana, Manish; Quiroz, Manuel; Darensbourg, Marcetta Y.
A single carbon atom controls the geometry and reactivity of Co<sup>II</sup>(N<sub>2</sub>S<sub>2</sub>) complexes.
Chemical communications (Cambridge, England), 2024, 60, 1128-1131
7132485 CIFC54 H70 Co2 N6 O8 S4 W2P 1 21/n 124.5425; 11.5431; 24.7944
90; 115.177; 90		6356.9Jana, Manish; Quiroz, Manuel; Darensbourg, Marcetta Y.
A single carbon atom controls the geometry and reactivity of Co<sup>II</sup>(N<sub>2</sub>S<sub>2</sub>) complexes.
Chemical communications (Cambridge, England), 2024, 60, 1128-1131
7132486 CIFC34 H28 N2 O6P 21 21 219.2858; 10.8685; 27.6229
90; 90; 90		2787.8Zhang, Xuan; Song, Xiaoxiao; Ni, Qijian
Organocatalytic regio- and enantioselective C1-arylation of β,γ-alkynyl-α-imino esters with pyrrolo[2,1-<i>a</i>]isoquinolines.
Chemical communications (Cambridge, England), 2024, 60, 831-834
7132487 CIFC31 H30 N2 O6P -110.1018; 11.4504; 13.7104
105.43; 99.759; 108.874		1388.58Zhang, Xuan; Song, Xiaoxiao; Ni, Qijian
Organocatalytic regio- and enantioselective C1-arylation of β,γ-alkynyl-α-imino esters with pyrrolo[2,1-<i>a</i>]isoquinolines.
Chemical communications (Cambridge, England), 2024, 60, 831-834
7132488 CIFC55.5 H60 B Cl N6 NiP 1 21/c 117.9362; 11.3297; 24.0854
90; 96.57; 90		4862.3Audsley, Gabrielle; Carpentier, Ambre; Pécharman, Anne-Frédérique; Wright, James; Roseveare, Thomas M.; Clark, Ewan R.; Macgregor, Stuart A.; Riddlestone, Ian M.
Contrasting reactivity of B-Cl and B-H bonds at [Ni(IMes)<sub>2</sub>] to form unsupported Ni-boryls.
Chemical communications (Cambridge, England), 2024, 60, 874-877
7132489 CIFC41 H40 B2 N6P 1 21/c 112.5356; 7.8928; 33.1689
90; 92.781; 90		3277.9Audsley, Gabrielle; Carpentier, Ambre; Pécharman, Anne-Frédérique; Wright, James; Roseveare, Thomas M.; Clark, Ewan R.; Macgregor, Stuart A.; Riddlestone, Ian M.
Contrasting reactivity of B-Cl and B-H bonds at [Ni(IMes)<sub>2</sub>] to form unsupported Ni-boryls.
Chemical communications (Cambridge, England), 2024, 60, 874-877
7132490 CIFC54 H56 B N4 Ni O4P 1 21/c 112.2169; 15.9479; 24.7366
90; 98.364; 90		4768.27Audsley, Gabrielle; Carpentier, Ambre; Pécharman, Anne-Frédérique; Wright, James; Roseveare, Thomas M.; Clark, Ewan R.; Macgregor, Stuart A.; Riddlestone, Ian M.
Contrasting reactivity of B-Cl and B-H bonds at [Ni(IMes)<sub>2</sub>] to form unsupported Ni-boryls.
Chemical communications (Cambridge, England), 2024, 60, 874-877
7132491 CIFC55.2 H57 B F0.2 N4 Ni2 O4P -112.0673; 13.458; 15.2235
91.823; 99.146; 97.973		2413.63Audsley, Gabrielle; Carpentier, Ambre; Pécharman, Anne-Frédérique; Wright, James; Roseveare, Thomas M.; Clark, Ewan R.; Macgregor, Stuart A.; Riddlestone, Ian M.
Contrasting reactivity of B-Cl and B-H bonds at [Ni(IMes)<sub>2</sub>] to form unsupported Ni-boryls.
Chemical communications (Cambridge, England), 2024, 60, 874-877
7132492 CIFC57 H69 B N6 Ni OP -111.4827; 15.0976; 15.7441
85.618; 84.57; 75.422		2625.77Audsley, Gabrielle; Carpentier, Ambre; Pécharman, Anne-Frédérique; Wright, James; Roseveare, Thomas M.; Clark, Ewan R.; Macgregor, Stuart A.; Riddlestone, Ian M.
Contrasting reactivity of B-Cl and B-H bonds at [Ni(IMes)<sub>2</sub>] to form unsupported Ni-boryls.
Chemical communications (Cambridge, England), 2024, 60, 874-877
7132493 CIFC54 H52 B Cl D6 N4 Ni O2P 1 21/n 110.482; 13.929; 33.577
90; 96.737; 90		4869Audsley, Gabrielle; Carpentier, Ambre; Pécharman, Anne-Frédérique; Wright, James; Roseveare, Thomas M.; Clark, Ewan R.; Macgregor, Stuart A.; Riddlestone, Ian M.
Contrasting reactivity of B-Cl and B-H bonds at [Ni(IMes)<sub>2</sub>] to form unsupported Ni-boryls.
Chemical communications (Cambridge, England), 2024, 60, 874-877
7132494 CIFC63 H65 B2 Cu2 F10 N5P -111.432; 14.578; 17.78
93.226; 107.118; 94.524		2813.2Duwe, Dario; Saha, Koushik; Endres, Lukas; Brückner, Tobias; Dewhurst, Rian D.; Dietz, Maximilian; Radacki, Krzysztof; Fantuzzi, Felipe; Braunschweig, Holger
Stepwise and selective synthesis of chelating, multimetallic and mixed-metal π-diborene complexes.
Chemical communications (Cambridge, England), 2024, 60, 1120-1123
7132495 CIFC109 H138 Au2 B4 Br2 N10P 1 21/n 112.547; 18.489; 21.362
90; 93.295; 90		4947Duwe, Dario; Saha, Koushik; Endres, Lukas; Brückner, Tobias; Dewhurst, Rian D.; Dietz, Maximilian; Radacki, Krzysztof; Fantuzzi, Felipe; Braunschweig, Holger
Stepwise and selective synthesis of chelating, multimetallic and mixed-metal π-diborene complexes.
Chemical communications (Cambridge, England), 2024, 60, 1120-1123
7132496 CIFC51 H63 B2 Cl2 Cu2 N5P 1 21/c 118.1438; 11.818; 23.6127
90; 112.15; 90		4689.46Duwe, Dario; Saha, Koushik; Endres, Lukas; Brückner, Tobias; Dewhurst, Rian D.; Dietz, Maximilian; Radacki, Krzysztof; Fantuzzi, Felipe; Braunschweig, Holger
Stepwise and selective synthesis of chelating, multimetallic and mixed-metal π-diborene complexes.
Chemical communications (Cambridge, England), 2024, 60, 1120-1123
7132497 CIFC51 H65 B2 Cl Cu N5P 1 21/c 113.704; 13.7578; 24.4253
90; 101.318; 90		4515.52Duwe, Dario; Saha, Koushik; Endres, Lukas; Brückner, Tobias; Dewhurst, Rian D.; Dietz, Maximilian; Radacki, Krzysztof; Fantuzzi, Felipe; Braunschweig, Holger
Stepwise and selective synthesis of chelating, multimetallic and mixed-metal π-diborene complexes.
Chemical communications (Cambridge, England), 2024, 60, 1120-1123
7132498 CIFC60 H74 Ag B2 Cl N5I 1 2/a 123.8864; 12.6825; 36.1057
90; 95.522; 90		10887.1Duwe, Dario; Saha, Koushik; Endres, Lukas; Brückner, Tobias; Dewhurst, Rian D.; Dietz, Maximilian; Radacki, Krzysztof; Fantuzzi, Felipe; Braunschweig, Holger
Stepwise and selective synthesis of chelating, multimetallic and mixed-metal π-diborene complexes.
Chemical communications (Cambridge, England), 2024, 60, 1120-1123
7132499 CIFC120 H148 Au2 B4 Cl4 Cu2 N10C 1 c 135.642; 11.768; 26.907
90; 101.525; 90		11058Duwe, Dario; Saha, Koushik; Endres, Lukas; Brückner, Tobias; Dewhurst, Rian D.; Dietz, Maximilian; Radacki, Krzysztof; Fantuzzi, Felipe; Braunschweig, Holger
Stepwise and selective synthesis of chelating, multimetallic and mixed-metal π-diborene complexes.
Chemical communications (Cambridge, England), 2024, 60, 1120-1123
7132500 CIFC123 H154 Au2 B4 Cl2 N10P 1 21/c 113.643; 21.105; 19.074
90; 91.484; 90		5490Duwe, Dario; Saha, Koushik; Endres, Lukas; Brückner, Tobias; Dewhurst, Rian D.; Dietz, Maximilian; Radacki, Krzysztof; Fantuzzi, Felipe; Braunschweig, Holger
Stepwise and selective synthesis of chelating, multimetallic and mixed-metal π-diborene complexes.
Chemical communications (Cambridge, England), 2024, 60, 1120-1123
7132501 CIFC51 H65 B2 Cl4 Cu4 N5P -115.0923; 17.1901; 25.434
102.384; 91.28; 90.589		6442.6Duwe, Dario; Saha, Koushik; Endres, Lukas; Brückner, Tobias; Dewhurst, Rian D.; Dietz, Maximilian; Radacki, Krzysztof; Fantuzzi, Felipe; Braunschweig, Holger
Stepwise and selective synthesis of chelating, multimetallic and mixed-metal π-diborene complexes.
Chemical communications (Cambridge, England), 2024, 60, 1120-1123
7132502 CIFC12 H13 N3 SeP -110.093; 11.029; 12.285
102.228; 113.956; 91.965		1210.2Wang, Hui-Hui; Zhu, Yang-Yun; Chen, Chuan-Li; Huang, Xiao-Bo; Liu, Miao-Chang; Zhou, Yun-Bing; Wu, Hua-Yue
Transition-metal-free four-component reaction of nitriles and disulfides/diselenides.
Chemical communications (Cambridge, England), 2024, 60, 862-865
7132503 CIFC18 H13 Br N2 OP 21 21 217.0262; 9.2338; 24.1
90; 90; 90		1563.6Ishida, Moeka; Adachi, Rina; Kobayashi, Kazuki; Yamamoto, Yukiko; Kawahara, Chinatsu; Yamada, Tsuyoshi; Aoyama, Hiroshi; Kanomata, Kyohei; Akai, Shuji; Lam, Patrick Y. S.; Sajiki, Hironao; Ikawa, Takashi
First atroposelective Chan-Lam coupling for the synthesis of C-N linked biaryls.
Chemical communications (Cambridge, England), 2024, 60, 678-681
7132504 CIFC76 H76 N4 O3 Ru2P 1 21/n 110.4746; 23.45; 23.6481
90; 91.91; 90		5805.44Himmelbauer, Daniel; Müller, Fabian; Schweinzer, Clara; Casas, Fernando; Pribanic, Bruno; Le Corre, Grégoire; Thöny, Debora; Trincado, Monica; Grützmacher, Hansjörg
Selective dehydrogenation of ammonia borane to polycondensated BN rings catalysed by ruthenium olefin complexes.
Chemical communications (Cambridge, England), 2024, 60, 885-888
7132505 CIFC24 H40 F6 N2 O6 S2C 1 2/c 122.6531; 10.6359; 13.5057
90; 112.83; 90		2999.1Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mehta, Sakshi; Krummenacher, Ivo; Mondal, Abhishake; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
Bis-[cyclic(alkyl)(amino)carbene]-derived diradicals.
Chemical communications (Cambridge, England), 2024, 60, 1739-1742
7132506 CIFC30 H48 F6 N2 O6 S2P -16.6145; 8.4668; 15.3473
88.298; 79.536; 88.611		844.68Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mehta, Sakshi; Krummenacher, Ivo; Mondal, Abhishake; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
Bis-[cyclic(alkyl)(amino)carbene]-derived diradicals.
Chemical communications (Cambridge, England), 2024, 60, 1739-1742
7132507 CIFC26 H46 N2 S2C m c e12.2275; 7.8196; 27.4908
90; 90; 90		2628.5Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mehta, Sakshi; Krummenacher, Ivo; Mondal, Abhishake; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
Bis-[cyclic(alkyl)(amino)carbene]-derived diradicals.
Chemical communications (Cambridge, England), 2024, 60, 1739-1742
7132508 CIFC16 H27 F3 Li N O4 SP 1 21/c 111.4316; 17.5255; 10.7728
90; 101.125; 90		2117.7Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mehta, Sakshi; Krummenacher, Ivo; Mondal, Abhishake; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
Bis-[cyclic(alkyl)(amino)carbene]-derived diradicals.
Chemical communications (Cambridge, England), 2024, 60, 1739-1742
7132509 CIFC22 H38 N2 S2P 1 21/c 19.2307; 7.8541; 15.9582
90; 100.261; 90		1138.45Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mehta, Sakshi; Krummenacher, Ivo; Mondal, Abhishake; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
Bis-[cyclic(alkyl)(amino)carbene]-derived diradicals.
Chemical communications (Cambridge, England), 2024, 60, 1739-1742
7132510 CIFC28 H46 N2 S2P 1 21/n 16.1244; 12.4798; 17.3975
90; 93.516; 90		1327.21Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mehta, Sakshi; Krummenacher, Ivo; Mondal, Abhishake; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
Bis-[cyclic(alkyl)(amino)carbene]-derived diradicals.
Chemical communications (Cambridge, England), 2024, 60, 1739-1742
7132511 CIFC18 H31 F3 Li N O4 SP 1 21/n 111.8035; 11.8153; 16.7982
90; 104.459; 90		2268.51Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mehta, Sakshi; Krummenacher, Ivo; Mondal, Abhishake; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
Bis-[cyclic(alkyl)(amino)carbene]-derived diradicals.
Chemical communications (Cambridge, England), 2024, 60, 1739-1742
7132512 CIFC19 H31 F3 Li N O4 SP -110.0875; 11.4427; 11.5307
94.43; 113.237; 109.486		1118.94Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mehta, Sakshi; Krummenacher, Ivo; Mondal, Abhishake; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
Bis-[cyclic(alkyl)(amino)carbene]-derived diradicals.
Chemical communications (Cambridge, England), 2024, 60, 1739-1742
7132513 CIFC50 H60 N2 O2P 1 21/c 113.0791; 12.0402; 12.4424
90; 92.773; 90		1957.07Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mehta, Sakshi; Krummenacher, Ivo; Mondal, Abhishake; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
Bis-[cyclic(alkyl)(amino)carbene]-derived diradicals.
Chemical communications (Cambridge, England), 2024, 60, 1739-1742
7132514 CIFC50 H60 F6 N2 O8 S2P 1 21/c 122.9053; 14.0233; 16.6472
90; 106.774; 90		5119.7Nayak, Mithilesh Kumar; Elvers, Benedict J.; Mehta, Sakshi; Krummenacher, Ivo; Mondal, Abhishake; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
Bis-[cyclic(alkyl)(amino)carbene]-derived diradicals.
Chemical communications (Cambridge, England), 2024, 60, 1739-1742
7132515 CIFC104 H148 K2 Mg2 N4 O2P -116.5142; 16.8828; 17.9517
90.877; 90.703; 106.972		4785.76Mondal, Rahul; Evans, Matthew J.; Nguyen, Dat T.; Rajeshkumar, Thayalan; Maron, Laurent; Jones, Cameron
Steric control of Mg-Mg bond formation <i>vs.</i> N<sub>2</sub> activation in the reduction of bulky magnesium diamide complexes.
Chemical communications (Cambridge, England), 2024, 60, 1016-1019
7132516 CIFC113 H168 K2 Mg2 N4 O2P -117.4631; 18.269; 19.28
102.56; 105.43; 92.826		5749.7Mondal, Rahul; Evans, Matthew J.; Nguyen, Dat T.; Rajeshkumar, Thayalan; Maron, Laurent; Jones, Cameron
Steric control of Mg-Mg bond formation <i>vs.</i> N<sub>2</sub> activation in the reduction of bulky magnesium diamide complexes.
Chemical communications (Cambridge, England), 2024, 60, 1016-1019
7132517 CIFC103 H144 K2 Mg2 N4 O3P 21 21 2118.1842; 22.1675; 24.5607
90; 90; 90		9900.38Mondal, Rahul; Evans, Matthew J.; Nguyen, Dat T.; Rajeshkumar, Thayalan; Maron, Laurent; Jones, Cameron
Steric control of Mg-Mg bond formation <i>vs.</i> N<sub>2</sub> activation in the reduction of bulky magnesium diamide complexes.
Chemical communications (Cambridge, England), 2024, 60, 1016-1019
7132518 CIFC130 H162 K2 Mg2 N4 O4C 1 2/c 158.863; 9.9267; 34.1523
90; 144.652; 90		11545Mondal, Rahul; Evans, Matthew J.; Nguyen, Dat T.; Rajeshkumar, Thayalan; Maron, Laurent; Jones, Cameron
Steric control of Mg-Mg bond formation <i>vs.</i> N<sub>2</sub> activation in the reduction of bulky magnesium diamide complexes.
Chemical communications (Cambridge, England), 2024, 60, 1016-1019
7132519 CIFC49 H68 N2 OP -113.0578; 13.4792; 13.9769
67.548; 70.378; 81.771		2141.24Mondal, Rahul; Evans, Matthew J.; Nguyen, Dat T.; Rajeshkumar, Thayalan; Maron, Laurent; Jones, Cameron
Steric control of Mg-Mg bond formation <i>vs.</i> N<sub>2</sub> activation in the reduction of bulky magnesium diamide complexes.
Chemical communications (Cambridge, England), 2024, 60, 1016-1019
7132520 CIFC118 H178 K2 Mg2 N4 O4P b c a19.617; 21.324; 25.718
90; 90; 90		10758Mondal, Rahul; Evans, Matthew J.; Nguyen, Dat T.; Rajeshkumar, Thayalan; Maron, Laurent; Jones, Cameron
Steric control of Mg-Mg bond formation <i>vs.</i> N<sub>2</sub> activation in the reduction of bulky magnesium diamide complexes.
Chemical communications (Cambridge, England), 2024, 60, 1016-1019
7132521 CIFC43 H45 N8 O8.5P 1 21/n 115.804; 30.856; 21.944
90; 101.44; 90		10488Muang-Non, Phonlakrit; Zhou, Carmen; Macreadie, Lauren K.; White, Nicholas G.
Hydrogen-bonded frameworks containing aliphatic 3D linkers show high-capacity water vapour sorption.
Chemical communications (Cambridge, England), 2024, 60, 746-749
7132522 CIFC49 H44 N8 O8P -4 n 223.5856; 23.5856; 7.525
90; 90; 90		4186Muang-Non, Phonlakrit; Zhou, Carmen; Macreadie, Lauren K.; White, Nicholas G.
Hydrogen-bonded frameworks containing aliphatic 3D linkers show high-capacity water vapour sorption.
Chemical communications (Cambridge, England), 2024, 60, 746-749
7132523 CIFC49 H44 N8 O8I 1 2/a 113.879; 12.595; 27.719
90; 102.35; 90		4733Muang-Non, Phonlakrit; Zhou, Carmen; Macreadie, Lauren K.; White, Nicholas G.
Hydrogen-bonded frameworks containing aliphatic 3D linkers show high-capacity water vapour sorption.
Chemical communications (Cambridge, England), 2024, 60, 746-749
7132524 CIFC49 H44 N8 O8I 1 2/a 111.6434; 16.4405; 26.1717
90; 96.002; 90		4982.4Muang-Non, Phonlakrit; Zhou, Carmen; Macreadie, Lauren K.; White, Nicholas G.
Hydrogen-bonded frameworks containing aliphatic 3D linkers show high-capacity water vapour sorption.
Chemical communications (Cambridge, England), 2024, 60, 746-749
7132525 CIFC49 H60 N8 O16P -113.6429; 15.3717; 16.0809
62.706; 89.94; 63.745		2600.16Muang-Non, Phonlakrit; Zhou, Carmen; Macreadie, Lauren K.; White, Nicholas G.
Hydrogen-bonded frameworks containing aliphatic 3D linkers show high-capacity water vapour sorption.
Chemical communications (Cambridge, England), 2024, 60, 746-749
7132526 CIFC13 H15 Br N2 O4C 1 2/c 119.5005; 7.9603; 18.992
90; 110.951; 90		2753.2Zhang, Congcong; Chen, Qinhao; Qin, Yunlong; Bu, Zhanwei; Wang, Qilin
Solvent-controlled halohydroxylation or C3-C2 coupling of pyridinium salts through an interrupted dearomative reduction.
Chemical communications (Cambridge, England), 2024, 60, 992-995
7132527 CIFC13 H13 Br N2 O3P 1 21/c 110.5757; 12.8565; 10.0965
90; 111.417; 90		1277.99Zhang, Congcong; Chen, Qinhao; Qin, Yunlong; Bu, Zhanwei; Wang, Qilin
Solvent-controlled halohydroxylation or C3-C2 coupling of pyridinium salts through an interrupted dearomative reduction.
Chemical communications (Cambridge, England), 2024, 60, 992-995
7132528 CIFC10 H15 Br N2 O3 SP 1 21/c 17.8851; 16.802; 10.6416
90; 111.647; 90		1310.4Zhang, Congcong; Chen, Qinhao; Qin, Yunlong; Bu, Zhanwei; Wang, Qilin
Solvent-controlled halohydroxylation or C3-C2 coupling of pyridinium salts through an interrupted dearomative reduction.
Chemical communications (Cambridge, England), 2024, 60, 992-995
7132529 CIFC24 H24 N4 O4P 1 21 18.7417; 13.759; 9.4773
90; 112.031; 90		1056.67Zhang, Congcong; Chen, Qinhao; Qin, Yunlong; Bu, Zhanwei; Wang, Qilin
Solvent-controlled halohydroxylation or C3-C2 coupling of pyridinium salts through an interrupted dearomative reduction.
Chemical communications (Cambridge, England), 2024, 60, 992-995
7132530 CIFC12 H10 N2 O3P 1 21/c 112.1802; 11.8247; 14.6931
90; 90.067; 90		2116.2Zhang, Congcong; Chen, Qinhao; Qin, Yunlong; Bu, Zhanwei; Wang, Qilin
Solvent-controlled halohydroxylation or C3-C2 coupling of pyridinium salts through an interrupted dearomative reduction.
Chemical communications (Cambridge, England), 2024, 60, 992-995
7132531 CIFC20 H8 N6 Se2 TeP 63/m m c21.656; 21.656; 7.6612
90; 90; 120		3111.6Eckstein, Brian J.; Martin, Hannah R.; Moghadasnia, Michael P.; Halder, Arijit; Melville, Michael J.; Buzinski, Tara N.; Balaich, Gary J.; McGuirk, C. Michael
Influence of donor point modifications on the assembly of chalcogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 758-761
7132532 CIFC20 H8 N6 Se2 TeC 1 2/c 112.505; 36.9389; 7.7404
90; 107.994; 90		3400.57Eckstein, Brian J.; Martin, Hannah R.; Moghadasnia, Michael P.; Halder, Arijit; Melville, Michael J.; Buzinski, Tara N.; Balaich, Gary J.; McGuirk, C. Michael
Influence of donor point modifications on the assembly of chalcogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 758-761
7132533 CIFC20 H8 N6 Se2 TeP 63/m m c21.529; 21.529; 7.653
90; 90; 120		3071.9Eckstein, Brian J.; Martin, Hannah R.; Moghadasnia, Michael P.; Halder, Arijit; Melville, Michael J.; Buzinski, Tara N.; Balaich, Gary J.; McGuirk, C. Michael
Influence of donor point modifications on the assembly of chalcogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 758-761
7132534 CIFC37 H31 Cl8 Ga N2 P2P c a 2142.402; 11.4012; 16.4543
90; 90; 90		7954.6Kim, Hyehwang; Lough, Alan; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Addition and NN bond cleavage of diazo-compounds by phosphino-phosphenium cations.
Chemical communications (Cambridge, England), 2024, 60, 1031-1034
7132535 CIFC76 H70 Cl8 Ga2 N10 O P4P -19.9147; 18.9028; 23.475
68.039; 85.656; 76.81		3972.5Kim, Hyehwang; Lough, Alan; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Addition and NN bond cleavage of diazo-compounds by phosphino-phosphenium cations.
Chemical communications (Cambridge, England), 2024, 60, 1031-1034
7132536 CIFC44 H51 Cl4 Ga N2 O2 P2P -111.2788; 13.1565; 16.1265
95.445; 108.409; 91.577		2256.1Kim, Hyehwang; Lough, Alan; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Addition and NN bond cleavage of diazo-compounds by phosphino-phosphenium cations.
Chemical communications (Cambridge, England), 2024, 60, 1031-1034
7132537 CIFC41 H45 Cl6 Ga N2 O4 P2P 19.792; 10.064; 12.02
96.899; 93.763; 95.349		1167.3Kim, Hyehwang; Lough, Alan; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Addition and NN bond cleavage of diazo-compounds by phosphino-phosphenium cations.
Chemical communications (Cambridge, England), 2024, 60, 1031-1034
7132538 CIFC43 H33.5 Cl4 F2 Ga N3 P2P 1 n 112.1657; 18.5693; 19.1345
90; 102.701; 90		4216.9Kim, Hyehwang; Lough, Alan; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Addition and NN bond cleavage of diazo-compounds by phosphino-phosphenium cations.
Chemical communications (Cambridge, England), 2024, 60, 1031-1034
7132539 CIFC78 H140 Al2 K2 N4 O10 Si4P 1 21 115.7613; 13.63024; 21.2238
90; 89.397; 90		4559.3O'Reilly, Andrea; Gardiner, Michael G.; McMullin, Claire L.; Fulton, J. Robin; Coles, Martyn P.
Aluminyl derived ethene functionalization with heteroallenes, leading to an intramolecular ligand rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 881-884
7132540 CIFC116 H170 Al2 K2 N8 O2 Si4P 1 21/c 113.45606; 23.22737; 19.4534
90; 108.146; 90		5777.75O'Reilly, Andrea; Gardiner, Michael G.; McMullin, Claire L.; Fulton, J. Robin; Coles, Martyn P.
Aluminyl derived ethene functionalization with heteroallenes, leading to an intramolecular ligand rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 881-884
7132541 CIFC85 H146 Al2 K2 N8 O3 Si4P 1 21/c 121.7767; 16.40993; 25.5079
90; 98.7193; 90		9010.01O'Reilly, Andrea; Gardiner, Michael G.; McMullin, Claire L.; Fulton, J. Robin; Coles, Martyn P.
Aluminyl derived ethene functionalization with heteroallenes, leading to an intramolecular ligand rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 881-884
7132542 CIFC118 H89 B2 F8 N19 Pd2P 1 21 114.567; 22.094; 18.901
90; 105.02; 90		5875Wu, Meng-Xiang; Hong, Qiong-Yan; Li, Minghui; Jiang, Wei-Ling; Huang, Bin; Lu, Shuai; Wang, Heng; Yang, Hai-Bo; Zhao, Xiao-Li; Shi, Xueliang
Self-assembly of conformation-adaptive dihydrophenazine-based coordination cages.
Chemical communications (Cambridge, England), 2024, 60, 1184-1187
7132543 CIFC36 H28 Cl4 N4P 1 21/n 113.1218; 7.9693; 15.0239
90; 98.834; 90		1552.44Wu, Meng-Xiang; Hong, Qiong-Yan; Li, Minghui; Jiang, Wei-Ling; Huang, Bin; Lu, Shuai; Wang, Heng; Yang, Hai-Bo; Zhao, Xiao-Li; Shi, Xueliang
Self-assembly of conformation-adaptive dihydrophenazine-based coordination cages.
Chemical communications (Cambridge, England), 2024, 60, 1184-1187
7132544 CIFC29.5 H24 Cl3 N4C 1 2 126.38; 7.7267; 12.814
90; 98.307; 90		2584.5Wu, Meng-Xiang; Hong, Qiong-Yan; Li, Minghui; Jiang, Wei-Ling; Huang, Bin; Lu, Shuai; Wang, Heng; Yang, Hai-Bo; Zhao, Xiao-Li; Shi, Xueliang
Self-assembly of conformation-adaptive dihydrophenazine-based coordination cages.
Chemical communications (Cambridge, England), 2024, 60, 1184-1187
7132545 CIFC204 H144 B6 F24 N24 Pd3P -116.7748; 28.6322; 29.6738
110.451; 94.927; 100.329		12965.9Wu, Meng-Xiang; Hong, Qiong-Yan; Li, Minghui; Jiang, Wei-Ling; Huang, Bin; Lu, Shuai; Wang, Heng; Yang, Hai-Bo; Zhao, Xiao-Li; Shi, Xueliang
Self-assembly of conformation-adaptive dihydrophenazine-based coordination cages.
Chemical communications (Cambridge, England), 2024, 60, 1184-1187
7132546 CIFC18 H16 Br N O2 S2P b c n18.3295; 10.5061; 18.8191
90; 90; 90		3624.02Chen, Xi; Li, Rui-Peng; Long, Peng; Tang, Yuxi; Li, Jia; Tang, Shouchu
Indium-catalyzed inter- and intramolecular dithianyl-alkyne metathesis reactions.
Chemical communications (Cambridge, England), 2024, 60, 1285-1288
7132547 CIFC61 H61 Cl0.08 F0.92 N6 ThP 1 21/c 116.63492; 11.85014; 24.83906
90; 90.9154; 90		4895.8Mangel, Daniel N.; Brewster, James T.; Juarez, Gabriel J.; Lynch, Vincent M.; Sessler, Jonathan L.
Cyclopentadienyl capped thorium(IV) porphyrinoid complex.
Chemical communications (Cambridge, England), 2024, 60, 1020-1022
7132548 CIFC78 H82 N6 O6 ThP -114.3339; 14.7275; 17.9016
92.412; 90.923; 117.468		3347.4Mangel, Daniel N.; Brewster, James T.; Juarez, Gabriel J.; Lynch, Vincent M.; Sessler, Jonathan L.
Cyclopentadienyl capped thorium(IV) porphyrinoid complex.
Chemical communications (Cambridge, England), 2024, 60, 1020-1022
7132549 CIFC19 H14 N O P SP -18.385; 10.473; 10.511
109.339; 92.044; 102.717		843.7Sun, Guangping; Li, Menghang; Cai, Lijuan; Zhu, Jinli; Tang, Yanfeng; Yao, Yong
Carbazole-based artificial light-harvesting system for photocatalytic cross-coupling dehydrogenation reaction.
Chemical communications (Cambridge, England), 2024, 60, 1412-1415
7132550 CIFC296 H122 Ag27 Au34 F68 PP -121.0215; 22.1806; 35.4832
88.101; 74.928; 87.324		15954.4Deng, Guocheng; Ki, Taeyoung; Liu, Xiaolin; Chen, Yuping; Lee, Kangjae; Yoo, Seungwoo; Tang, Qing; Bootharaju, Megalamane S.; Hyeon, Taeghwan
Tailoring the subshell and electronic structure of an atomically precise AuAg alloy nanocluster.
Chemical communications (Cambridge, England), 2024, 60, 1289-1292
7132551 CIFC62 H62 N14 O18 S2P -18.6132; 14.1366; 15.1958
103.568; 105.921; 102.22		1652.5Zhang, Xin; Mao, Lijun; He, Rongjing; Shi, Yanting; Li, Lingyi; Li, Shuo; Zhu, Chenghao; Zhang, Yanjing; Ma, Da
Tunable cyclic operation of dissipative molecular switches based on anion recognition.
Chemical communications (Cambridge, England), 2024, 60, 1180-1183
7132552 CIFC44 H68 B10 N4 S2 Si2P -113.3084; 13.6054; 16.2398
76.297; 82.378; 61.662		2513.7Liu, Rui; Mondal, Kartik Chandra; Wang, Chenfeng; Suthar, Sonam; Fang, Zijie; Zuo, Darui; Li, Yan
Synthesis of SiN/SiS-heterocycles <i>via</i> the reactions of a bis-silylene with isocyanate/isothiocyanate molecules.
Chemical communications (Cambridge, England), 2024, 60, 1148-1151
7132553 CIFC48 H64 B10 F6 N6 O3 Si2P 1 21/c 114.118; 18.777; 20.911
90; 99.975; 90		5460Liu, Rui; Mondal, Kartik Chandra; Wang, Chenfeng; Suthar, Sonam; Fang, Zijie; Zuo, Darui; Li, Yan
Synthesis of SiN/SiS-heterocycles <i>via</i> the reactions of a bis-silylene with isocyanate/isothiocyanate molecules.
Chemical communications (Cambridge, England), 2024, 60, 1148-1151
7132554 CIFC40 H63 B10 N5 O3 Si2P 1 21/n 112.922; 17.399; 21.674
90; 104.21; 90		4724Liu, Rui; Mondal, Kartik Chandra; Wang, Chenfeng; Suthar, Sonam; Fang, Zijie; Zuo, Darui; Li, Yan
Synthesis of SiN/SiS-heterocycles <i>via</i> the reactions of a bis-silylene with isocyanate/isothiocyanate molecules.
Chemical communications (Cambridge, England), 2024, 60, 1148-1151
7132555 CIFC64 H88.54 B10 N6 O2 S2 Si2P -111.741; 17.4714; 18.7329
112.618; 101.299; 100.144		3341.5Liu, Rui; Mondal, Kartik Chandra; Wang, Chenfeng; Suthar, Sonam; Fang, Zijie; Zuo, Darui; Li, Yan
Synthesis of SiN/SiS-heterocycles <i>via</i> the reactions of a bis-silylene with isocyanate/isothiocyanate molecules.
Chemical communications (Cambridge, England), 2024, 60, 1148-1151
7132556 CIFC62 H87 B10 N6 O3 Si2P 1 21/n 112.2822; 20.2269; 25.5456
90; 90.955; 90		6345.4Liu, Rui; Mondal, Kartik Chandra; Wang, Chenfeng; Suthar, Sonam; Fang, Zijie; Zuo, Darui; Li, Yan
Synthesis of SiN/SiS-heterocycles <i>via</i> the reactions of a bis-silylene with isocyanate/isothiocyanate molecules.
Chemical communications (Cambridge, England), 2024, 60, 1148-1151
7132557 CIFC14 H20 B10P 1 21/c 115.8355; 10.979; 9.9081
90; 100.451; 90		1694Yang, Han-Bo; Guo, Yan; Cao, Ke; Jiang, Qi-Jia; Teng, Chao-Chao; Zhu, Dao-Yong; Wang, Shao-Hua
Iridium-catalyzed selective arylation of B(6)-H of 3-aryl-<i>o</i>-carboranes with arylboronic acid <i>via</i> direct B-H activation.
Chemical communications (Cambridge, England), 2024, 60, 1124-1127
7132558 CIFC61 H74 O10 S4C 1 2/c 121.59; 20.575; 13.578
90; 97.516; 90		5979.7Zhao, Xueru; Hua, Bin; Shao, Li
Constructing a solid-state supramolecular polymer based on host-guest recognition between perethylated pillar[5]arene and tetrathiafulvalene.
Chemical communications (Cambridge, England), 2024, 60, 1164-1167
7132559 CIFC14 H14 Cd O2 S2P -16.8847; 8.411; 12.8724
92.96; 101.422; 105.459		699.89Nishibe, Asuka; Akiyoshi, Ryohei; Saeki, Akinori; Ogasawara, Kazuyoshi; Tsuruoka, Takaaki; Tanaka, Daisuke
Engineering of CdS-chain arrays assembled through S⋯S interactions in 1D semiconductive coordination polymers.
Chemical communications (Cambridge, England), 2024, 60, 1277-1280
7132560 CIFC14 H14 Cd O2 S2I b a 235.4228; 16.8199; 7.2761
90; 90; 90		4335.2Nishibe, Asuka; Akiyoshi, Ryohei; Saeki, Akinori; Ogasawara, Kazuyoshi; Tsuruoka, Takaaki; Tanaka, Daisuke
Engineering of CdS-chain arrays assembled through S⋯S interactions in 1D semiconductive coordination polymers.
Chemical communications (Cambridge, England), 2024, 60, 1277-1280
7132561 CIFC14 H14 Cd O2 S2P c c n28.1725; 13.9425; 7.0402
90; 90; 90		2765.36Nishibe, Asuka; Akiyoshi, Ryohei; Saeki, Akinori; Ogasawara, Kazuyoshi; Tsuruoka, Takaaki; Tanaka, Daisuke
Engineering of CdS-chain arrays assembled through S⋯S interactions in 1D semiconductive coordination polymers.
Chemical communications (Cambridge, England), 2024, 60, 1277-1280
7132562 CIFC76 Cl28C 1 2/c 117.137; 23.973; 15.008
90; 90.389; 90		6165.5Brotsman, Victor A.; Troyanov, Sergey I.
Non-classical (NC), heptagon-containing fullerenes obtained <i>via</i> chlorination-promoted cage transformations: C<sub>76</sub>(NC2a)Cl<sub>24</sub> and C<sub>76</sub>(NC2b)Cl<sub>28</sub>.
Chemical communications (Cambridge, England), 2024, 60, 893-896
7132563 CIFC83 H8 Cl24C 1 2/c 123.672; 21.259; 16.433
90; 131.763; 90		6168.5Brotsman, Victor A.; Troyanov, Sergey I.
Non-classical (NC), heptagon-containing fullerenes obtained <i>via</i> chlorination-promoted cage transformations: C<sub>76</sub>(NC2a)Cl<sub>24</sub> and C<sub>76</sub>(NC2b)Cl<sub>28</sub>.
Chemical communications (Cambridge, England), 2024, 60, 893-896
7132564 CIFC34 H21 F6 N OP c a 2127.071; 13.5223; 7.5005
90; 90; 90		2745.6Barhate, Komal Vasant; Wadawale, Amey P.; Chandrakumar, K. R. S.; Agarwal, Neeraj
Modulation of Δ<i>E</i><sub>ST</sub> and room temperature phosphorescence in carbazole derivatives.
Chemical communications (Cambridge, England), 2024, 60, 1408-1411
7132565 CIFC32 H21 F2 N OP 1 21/c 114.5446; 21.9876; 7.5051
90; 101.383; 90		2352.93Barhate, Komal Vasant; Wadawale, Amey P.; Chandrakumar, K. R. S.; Agarwal, Neeraj
Modulation of Δ<i>E</i><sub>ST</sub> and room temperature phosphorescence in carbazole derivatives.
Chemical communications (Cambridge, England), 2024, 60, 1408-1411
7132566 CIFC57 H74.5 Br2.94 Cl1.06 Mg N5.5 O4 Zn2P -113.4199; 20.874; 23.345
96.6727; 97.517; 107.576		6096.2Banks, Henry J. S.; Frese, Josef W. A.; Elsegood, Mark R. J.; Redshaw, Carl
Mixed-magnesium/zinc calix[4]arene complexes: structure, and ring opening polymerisation studies.
Chemical communications (Cambridge, England), 2024, 60, 304-307
7132567 CIFC108.92 H138.37 Br2.52 Cl0.48 Mg3 N10.46 O10 Zn3P n m a28.44051; 33.62784; 12.56775
90; 90; 90		12019.7Banks, Henry J. S.; Frese, Josef W. A.; Elsegood, Mark R. J.; Redshaw, Carl
Mixed-magnesium/zinc calix[4]arene complexes: structure, and ring opening polymerisation studies.
Chemical communications (Cambridge, England), 2024, 60, 304-307
7132568 CIFC200 H259 Mg5 N7 O20 Zn2P -117.175; 23.5379; 25.6364
89.281; 73.491; 87.287		9925.5Banks, Henry J. S.; Frese, Josef W. A.; Elsegood, Mark R. J.; Redshaw, Carl
Mixed-magnesium/zinc calix[4]arene complexes: structure, and ring opening polymerisation studies.
Chemical communications (Cambridge, England), 2024, 60, 304-307
7132569 CIFC112.37 H147.56 Br3.42 Cl0.58 Mg2 N9.19 O10 Zn4P 1 21/c 119.81378; 25.56149; 24.42596
90; 108.387; 90		11739.5Banks, Henry J. S.; Frese, Josef W. A.; Elsegood, Mark R. J.; Redshaw, Carl
Mixed-magnesium/zinc calix[4]arene complexes: structure, and ring opening polymerisation studies.
Chemical communications (Cambridge, England), 2024, 60, 304-307
7132570 CIFC36 H29 N O3 SP 1 21/c 118.5043; 8.0564; 18.619
90; 103.185; 90		2702.5Nakate, Ashwini K.; Kataria, Priyanka; Sambherao, Pooja I.; Krishna, Gamidi Rama; Kontham, Ravindar
Divergent access to polycyclic spiro- and fused-<i>N</i>,O-ketals through Bi(OTf)<sub>3</sub>-catalyzed [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines and alkynols.
Chemical communications (Cambridge, England), 2024, 60, 1144-1147
7132571 CIFC21 H23 N O3 SP 21 21 2110.2093; 12.452; 14.4031
90; 90; 90		1831.01Nakate, Ashwini K.; Kataria, Priyanka; Sambherao, Pooja I.; Krishna, Gamidi Rama; Kontham, Ravindar
Divergent access to polycyclic spiro- and fused-<i>N</i>,O-ketals through Bi(OTf)<sub>3</sub>-catalyzed [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines and alkynols.
Chemical communications (Cambridge, England), 2024, 60, 1144-1147
7132572 CIFC23 H25 N O4 SP 1 21/n 110.2361; 18.336; 10.7234
90; 98.878; 90		1988.6Nakate, Ashwini K.; Kataria, Priyanka; Sambherao, Pooja I.; Krishna, Gamidi Rama; Kontham, Ravindar
Divergent access to polycyclic spiro- and fused-<i>N</i>,O-ketals through Bi(OTf)<sub>3</sub>-catalyzed [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines and alkynols.
Chemical communications (Cambridge, England), 2024, 60, 1144-1147
7132573 CIFC25 H23 N O3 SP 1 21/n 110.9271; 16.5749; 10.9904
90; 93.352; 90		1987.1Nakate, Ashwini K.; Kataria, Priyanka; Sambherao, Pooja I.; Krishna, Gamidi Rama; Kontham, Ravindar
Divergent access to polycyclic spiro- and fused-<i>N</i>,O-ketals through Bi(OTf)<sub>3</sub>-catalyzed [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines and alkynols.
Chemical communications (Cambridge, England), 2024, 60, 1144-1147
7132574 CIFC26 H31 N O4P 21 21 217.5575; 12.6622; 25.9109
90; 90; 90		2479.5Xie, Xiang-Qi; Li, Xingguang; Liu, Pei-Nian
Enantioselective synthesis of spiro-<i>N</i>,<i>O</i>-ketals <i>via</i> iridium and Brønsted acid co-catalyzed asymmetric formal [4+2] cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 1448-1451
7132575 CIFC26 H31 N O4P 21 21 218.9352; 9.9706; 26.0378
90; 90; 90		2319.7Xie, Xiang-Qi; Li, Xingguang; Liu, Pei-Nian
Enantioselective synthesis of spiro-<i>N</i>,<i>O</i>-ketals <i>via</i> iridium and Brønsted acid co-catalyzed asymmetric formal [4+2] cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 1448-1451
7132576 CIFC50.56 H53.12 N6 O4.28P 6518.9446; 18.9446; 22.0233
90; 90; 120		6845.2Hokimoto, Yuya; Nakamura, Takashi
Synthesis of a macrocyclic oligomer of pyridylbenzoxazole utilizing dynamic covalent bonds and its unsymmetric conversion.
Chemical communications (Cambridge, England), 2024, 60, 1281-1284
7132577 CIFC48 H46 N6 O5P 21 21 2116.082; 17.555; 17.564
90; 90; 90		4959Hokimoto, Yuya; Nakamura, Takashi
Synthesis of a macrocyclic oligomer of pyridylbenzoxazole utilizing dynamic covalent bonds and its unsymmetric conversion.
Chemical communications (Cambridge, England), 2024, 60, 1281-1284
7132578 CIFC56 H64 N6 O7P -111.244; 12.917; 17.778
86.525; 87.331; 75.394		2492.7Hokimoto, Yuya; Nakamura, Takashi
Synthesis of a macrocyclic oligomer of pyridylbenzoxazole utilizing dynamic covalent bonds and its unsymmetric conversion.
Chemical communications (Cambridge, England), 2024, 60, 1281-1284
7132579 CIFC106 H110 Cl18 F6 N12 O20 S2 ZnP -116.0885; 20.1668; 21.6212
103.611; 101.577; 109.328		6129.8Hokimoto, Yuya; Nakamura, Takashi
Synthesis of a macrocyclic oligomer of pyridylbenzoxazole utilizing dynamic covalent bonds and its unsymmetric conversion.
Chemical communications (Cambridge, England), 2024, 60, 1281-1284
7132580 CIFC19 H17 N3 SP 1 21/c 17.7135; 22.94; 9.6284
90; 100.29; 90		1676.3Zhang, Xiaoxiang; Liu, Chenrui; Wei, Wanxing; Zhang, Zhuan; Liang, Taoyuan
Iodine-dependent oxidative regioselective aminochalcogenation of indolines.
Chemical communications (Cambridge, England), 2024, 60, 1152-1155
7132581 CIFC25 H26 O5P -110.1019; 10.718; 11.1905
64.873; 69.562; 83.168		1027.3Wu, Shu-Yi; Li, Yang; Shen, Peng; Yang, Xin-Han; Ran, Guang-Yao
Palladium-catalysed fragmentary esterification-induced allylic alkylation of allyl carbonates and cyclic vinylogous anhydrides.
Chemical communications (Cambridge, England), 2024, 60, 1416-1419
7132582 CIFC25 H21 Co F O4 PC 1 2/c 120.3694; 11.8516; 19.7496
90; 106.855; 90		4562.9Pietraru, Marie-Hélène; Ponsard, Louise; Lentz, Nicolas; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault
Fluorophosphoniums as Lewis acids in organometallic catalysis: application to the carbonylation of β-lactones.
Chemical communications (Cambridge, England), 2024, 60, 1043-1046
7132583 CIFC22 H33 Co F O4 PP n m a16.5748; 13.6875; 10.2341
90; 90; 90		2321.79Pietraru, Marie-Hélène; Ponsard, Louise; Lentz, Nicolas; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault
Fluorophosphoniums as Lewis acids in organometallic catalysis: application to the carbonylation of β-lactones.
Chemical communications (Cambridge, England), 2024, 60, 1043-1046
7132584 CIFC16 H27 Co F O4 PP b c a14.9882; 15.8456; 16.4634
90; 90; 90		3910Pietraru, Marie-Hélène; Ponsard, Louise; Lentz, Nicolas; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault
Fluorophosphoniums as Lewis acids in organometallic catalysis: application to the carbonylation of β-lactones.
Chemical communications (Cambridge, England), 2024, 60, 1043-1046
7132585 CIFC116 H128 N8 O24 S8P 1 21/c 115.6273; 11.1454; 21.3411
90; 104.896; 90		3592.1Ho, An T.; Vanable, Evan P.; Miguel, Chelsea San; Hull, Kami L.
Iridium-catalysed hydroamination of internal homoallylic amines.
Chemical communications (Cambridge, England), 2024, 60, 1615-1618
7132586 CIFC31 H42 N2 O7 S2P 21 21 2111.1123; 11.2096; 24.9678
90; 90; 90		3110.1Ho, An T.; Vanable, Evan P.; Miguel, Chelsea San; Hull, Kami L.
Iridium-catalysed hydroamination of internal homoallylic amines.
Chemical communications (Cambridge, England), 2024, 60, 1615-1618
7132587 CIFC25.5 H31 Cl N5C 1 2/c 129.863; 9.4396; 17.2974
90; 101.266; 90		4782.1Mohanty, Aisa; Rout, Smruti Rekha; Dandela, Rambabu; Daw, Prosenjit
Ammonia synthesis by the reductive N-N bond cleavage of hydrazine using an air-stable, phosphine-free ruthenium catalyst.
Chemical communications (Cambridge, England), 2024, 60, 416-419
7132588 CIFC14 H19 N O6P c a 2117.469; 7.599; 11.007
90; 90; 90		1461.1Zheng, Peng Xuan; Ou, Song Lin; Qu, Lei Yu; Zhang, Ying; Jiang, Shi Qing; Li, Xiang; Wan, Jun Xiong; Zhang, Min; Bao, Xin
Enriched switching in a donor-acceptor Stenhouse adduct <i>via</i> reversible covalent bonding.
Chemical communications (Cambridge, England), 2024, 60, 1333-1336
7132589 CIFC151.5 H201 Au14 Cl F3 P4.5 S9P -115.8928; 20.0176; 29.1486
75.045; 78.775; 78.621		8681.3Liu, Dong; Gao, Guiqi; Zhang, Yongyu; Li, Qinzhen; Yang, Sha; Chai, Jinsong; Yu, Haizhu; Zhu, Manzhou
[Au<sub>14</sub>(2-SAdm)<sub>9</sub>(Dppe)<sub>2</sub>]<sup>+</sup>: a gold nanocluster with a crystallization-induced emission enhancement phenomenon.
Chemical communications (Cambridge, England), 2024, 60, 1337-1340
7132590 CIFC24 H21 N3 O3 SP -18.0853; 10.9301; 13.3531
104.791; 92.638; 111.152		1051.52Tang, Yi; Zhang, Rulei; Dong, Yujie; Yu, Songcheng; Wu, Yongjun; Xiao, Yumei; Guo, Hongchao
4-Vinylbenzodioxinones as a new type of precursor for palladium-catalyzed (4+3) cycloaddition of azomethine imines.
Chemical communications (Cambridge, England), 2024, 60, 1436-1439
7132591 CIFC24 H20 Br3 N3 O3 SP -110.8989; 11.4714; 11.6523
66.814; 72.69; 71.71		1246Tang, Yi; Zhang, Rulei; Dong, Yujie; Yu, Songcheng; Wu, Yongjun; Xiao, Yumei; Guo, Hongchao
4-Vinylbenzodioxinones as a new type of precursor for palladium-catalyzed (4+3) cycloaddition of azomethine imines.
Chemical communications (Cambridge, England), 2024, 60, 1436-1439
7132592 CIFC26 H25 N3 O4 SP 21 21 2110.5361; 17.81; 26.2442
90; 90; 90		4924.67Tang, Yi; Zhang, Rulei; Dong, Yujie; Yu, Songcheng; Wu, Yongjun; Xiao, Yumei; Guo, Hongchao
4-Vinylbenzodioxinones as a new type of precursor for palladium-catalyzed (4+3) cycloaddition of azomethine imines.
Chemical communications (Cambridge, England), 2024, 60, 1436-1439
7132593 CIFC12 H9 Ag3 N6 O3F d d 245.975; 37.787; 3.754
90; 90; 90		6521.7Peng, Shuyin; Sun, Yuqian; Li, Qingqing; Jiang, Zhongwen; Rao, Yin; Wu, Yichen; Li, Qiaowei
Stepwise construction of coordinative linkages and dynamic covalent linkages for a porous metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 1488-1491
7132594 CIFC27 H30 N2 O3 SP 21 21 219.7941; 11.2385; 23.348
90; 90; 90		2569.9Cui, Chen-Chang; Lin, Feng; Wang, Lu-Yao; Liu, Yin-Ping; Tu, Shu-Jiang; Tu, Man-Su; Hao, Wen-Juan; Jiang, Bo
Olefin skeletal rearrangement enabling access to multiarylated <i>N</i>-sulfonyl amidines.
Chemical communications (Cambridge, England), 2024, 60, 1492-1495
7132595 CIFC24 H22 I2 N4 O4 SP 14.7109; 5.1887; 25.0379
84.32; 88.126; 87.821		608.31Cao, Jinlian; Weng, Peimin; Qi, Yuanwei; Lin, Kexin; Yan, Xiaosheng
Noncovalent interaction network of chalcogen, halogen and hydrogen bonds for supramolecular β-sheet organization.
Chemical communications (Cambridge, England), 2024, 60, 1484-1487
7132596 CIFC73 H55 Cl3 N6 O3P c a 2124.6915; 14.7339; 15.6091
90; 90; 90		5678.6Chen, Lihua; Li, Chenfei; Liu, Zheng-Fei; Kuboi, Yoshiaki; Fu, Enguang; Vargas, Lydia Sosa; Adachi, Chihaya; Mathevet, Fabrice; Zhang, Shaodong
A donor-acceptor cage for circularly polarized TADF emission.
Chemical communications (Cambridge, England), 2024, 60, 1758-1761
7132597 CIFC60 H82 B3 K N6 OC 1 2/c 125.1162; 13.2745; 18.3072
90; 110.891; 90		5702.5Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132598 CIFC67 H86 B3 Br N6 O2 SiP 1 21 111.4979; 20.9867; 13.7765
90; 104.384; 90		3220.1Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132599 CIFC54 H76 B3 Br N6P 1 21/c 113.321; 20.663; 19.283
90; 100.62; 90		5217Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132600 CIFC108 H152 B6 Cl6 N12 O2 Si2P 21 21 2119.4723; 23.1794; 24.8889
90; 90; 90		11233.8Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132601 CIFC61.5 H83.5 B3 Cl Ge N6 OP -116.4864; 16.4582; 44.137
95.16; 97.087; 89.93		11835.7Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132602 CIFC108 H152 B6 Br6 N12 O2 Si2P 21 21 2119.5876; 23.2994; 24.9438
90; 90; 90		11383.8Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132603 CIFC162 H228 B9 Cl3 N18 O3 Sn3P 1 21/n 130.8728; 16.2163; 33.9145
90; 106.314; 90		16295.4Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132604 CIFC23 H22 N2P 1 21/c 110.8961; 18.4187; 9.4952
90; 111.962; 90		1767.3Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132605 CIFC22 H19 F N2P 1 21/c 110.454; 20.0412; 9.0834
90; 106.374; 90		1825.9Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132606 CIFC22 H20 N2P 1 21/c 110.0309; 19.6236; 9.0074
90; 104.371; 90		1717.6Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132607 CIFC23 H20 N2 OP -17.4394; 10.1901; 13.5234
98.505; 92.733; 110.436		944.63Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132608 CIFC44 H43 Cl2 N3 O6 SP -18.7541; 15.3319; 15.5807
82.471; 85.577; 81.058		2044.53Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132609 CIFC48 H43 Cl O P2 PdC 1 2/m 119.3124; 18.4281; 12.7741
90; 103.027; 90		4429.2Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132610 CIFC49 H41 F3 O4 P2 Pd SP 1 21/m 19.2641; 18.7713; 12.8967
90; 101.38; 90		2198.6Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132611 CIFC4 H6 N8 O2P n a 216.744; 11.212; 9.487
90; 90; 90		717.3Kumar, Parasar; Kumar, Navaneet; Ghule, Vikas D.; Dharavath, Srinivas
Zwitterionic fused pyrazolo-triazole based high performing energetic materials.
Chemical communications (Cambridge, England), 2024, 60, 1646-1649
7132612 CIFC52 H50 N2 O4C 1 2/c 119.961; 14.527; 16.049
90; 118.68; 90		4082.8Gentile, Giuseppe; Bartolomei, Beatrice; Dosso, Jacopo; Demitri, Nicola; Filippini, Giacomo; Prato, Maurizio
Synthesis of a novel tetra-phenol π-extended phenazine and its application as an organo-photocatalyst.
Chemical communications (Cambridge, England), 2024, 60, 602-605
7132613 CIFC56 H95 Mo6 N7 O18P 1 21/c 112.4406; 29.2646; 18.9032
90; 92.548; 90		6875.27Jones, Claire F.; Hood, Bethany R.; de Coene, Yovan; Lopez-Poves, Ivan; Champagne, Benoît; Clays, Koen; Fielden, John
Bridge improvement work: maximising non-linear optical performance in polyoxometalate derivatives.
Chemical communications (Cambridge, England), 2024, 60, 1731-1734
7132614 CIFC30 H33 O3 PP 1 21 110.97433; 9.78846; 11.7517
90; 102.023; 90		1234.7Huang, Yu; Zhang, Yulong; Pan, Li; Wu, Qian; Li, Ning; Shi, Enxue; Xiao, Junhua
CAMDOL-enabled diastereoselective synthesis of α-substituted phosphonates.
Chemical communications (Cambridge, England), 2024, 60, 1924-1927
7132615 CIFC27 H34 N3 O3 PP 1 21 111.2201; 8.4447; 13.8792
90; 98.303; 90		1301.28Chen, Zi-Jia; Fan, Ling-Jie; Xie, Pei-Pei; Qian, Pu-Fan; Hu, Xinquan; Zhou, Tao; Shi, Bing-Feng
Pd(II)-Catalyzed enantioselective C-H olefination toward the synthesis of <i>P</i>-stereogenic phosphinamides.
Chemical communications (Cambridge, England), 2024, 60, 1623-1626
7132616 CIFC44 H54 B N3 Ni PP 1 21/c 114.5193; 29.0183; 9.5279
90; 103.894; 90		3896.89Bermejo, José; Ortega-Lepe, Isabel; Santos, Laura L.; Rendón, Nuria; López-Serrano, Joaquín; Álvarez, Eleuterio; Suárez, Andrés
Nitrous oxide activation by picoline-derived Ni-CNP hydrides.
Chemical communications (Cambridge, England), 2024, 60, 1575-1578
7132617 CIFC26 H36 N3 Ni O PP 42/n :221.355; 21.355; 11.6688
90; 90; 90		5321.4Bermejo, José; Ortega-Lepe, Isabel; Santos, Laura L.; Rendón, Nuria; López-Serrano, Joaquín; Álvarez, Eleuterio; Suárez, Andrés
Nitrous oxide activation by picoline-derived Ni-CNP hydrides.
Chemical communications (Cambridge, England), 2024, 60, 1575-1578
7132618 CIFC10 H32 Bi I9 N4C m c m11.8846; 11.8525; 23.941
90; 90; 90		3372.4Wang, Yu-Yin; Kang, Huai-Yuan; Zhang, Shao-Ya; Qu, Hao; Zhu, Lin; Zhao, Dan; Li, Xian-Feng; Lei, Xiao-Wu; Yue, Cheng-Yang
Exploring 0D lead-free metal halide with highly efficient blue light emission and high-sensitivity photodetection.
Chemical communications (Cambridge, England), 2024, 60, 2784-2787
7132619 CIFC52 H98 N4 O6 Si6P -111.9643; 16.5858; 17.5688
90.529; 98.876; 109.35		3243.16Kim, Junghwan; Kim, Chungryeol; Lee, Dongwhan
Fluoride-triggered phase transition of metallogels for on-demand <i>in situ</i> containment of fluids.
Chemical communications (Cambridge, England), 2024, 60, 1762-1765
7132620 CIFC70 H134 N4 O6 Si6P -115.9929; 16.1504; 17.3188
79.449; 65.041; 78.584		3950.26Kim, Junghwan; Kim, Chungryeol; Lee, Dongwhan
Fluoride-triggered phase transition of metallogels for on-demand <i>in situ</i> containment of fluids.
Chemical communications (Cambridge, England), 2024, 60, 1762-1765
7132621 CIFC36 H26 N8 Ni O4P b c n12.655; 15.538; 17.066
90; 90; 90		3355.7Nogita, Kohei; Sugahara, Takaya; Miki, Koji; Mu, Huiying; Kobayashi, Minoru; Harada, Hiroshi; Ohe, Kouichi
A reductively convertible nickel phthalocyanine precursor as a biological thiol-responsive turn-on photoacoustic contrast agent.
Chemical communications (Cambridge, England), 2024, 60, 1472-1475
7132622 CIFC18 H17 Cl N2 O2P c c n21.1441; 11.5844; 12.8398
90; 90; 90		3145Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132623 CIFC18 H18 N2 O3 SP 1 21/c 113.7896; 9.0412; 13.8981
90; 108.87; 90		1639.61Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132624 CIFC19 H18 N2 O2P 1 21/n 19.1979; 15.6759; 10.7636
90; 95.704; 90		1544.27Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132625 CIFC20 H17 Cl N2 O2P n a 2110.2787; 11.9147; 27.5592
90; 90; 90		3375.1Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132626 CIFC13 H9 N O3P 21 21 213.8378; 8.6367; 29.4303
90; 90; 90		975.49Chand, Tapasi; Gupta, Princi; Oza, Nehali; Kapur, Manmohan
Cobalt(II)-catalyzed <i>peri</i>-C(sp<sup>2</sup>)-H selective hydroxylation of naphthalene monoimides.
Chemical communications (Cambridge, England), 2024, 60, 1770-1773
7132627 CIFC38.49 H30.98 Cl3.98 P2 SbF d d 228.25; 31.29; 15.7735
90; 90; 90		13943Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132628 CIFC38.5 H31 Br Cl3 P2 SbF d d 227.674; 31.304; 16.183
90; 90; 90		14019Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132629 CIFC39 H32 Cl4 F6 P2 Sb2P 1 21/n 114.6987; 15.5168; 17.522
90; 93.975; 90		3986.7Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132630 CIFC40 H34 Au Bi Cl8 P2P 1 21/c 111.6409; 23.1633; 15.8194
90; 97.161; 90		4232.3Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132631 CIFC141 H87.9 B2 Br2 Cl5.9 F48.05 P4 Sb2P -112.135; 16.6073; 18.5495
107.079; 95.331; 99.299		3487.2Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132632 CIFC41 H37 Br F6 O P2 Sb2P 1 21/c 110.3202; 20.6841; 18.508
90; 92.122; 90		3948.1Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132633 CIFC40 H34 Au Cl8 P2 SbP 1 21/c 111.6084; 23.1906; 15.8524
90; 97.164; 90		4234.2Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132634 CIFC27 H21 In N6P 1 21/c 116.1797; 15.4641; 9.7077
90; 99.032; 90		2398.8Fu, Li-Zhi; He, Piao; Wang, Jia-Wei; Ma, Fan; Liu, Chao; Chen, Guo; Yi, Xiao-Yi
Mononuclear indium(III) photosensitizers for photo-dehalogenation and olefin reduction.
Chemical communications (Cambridge, England), 2024, 60, 1595-1598
7132635 CIFC33 H33 In N6P -19.9431; 10.4086; 14.78
83.547; 80.299; 74.885		1451.83Fu, Li-Zhi; He, Piao; Wang, Jia-Wei; Ma, Fan; Liu, Chao; Chen, Guo; Yi, Xiao-Yi
Mononuclear indium(III) photosensitizers for photo-dehalogenation and olefin reduction.
Chemical communications (Cambridge, England), 2024, 60, 1595-1598
7132636 CIFC54 H72 B2 N4 SiP 1 21/c 112.4737; 14.971; 26.1547
90; 92.786; 90		4878.5Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132637 CIFC52 H68 B2 N4 SiP 1 21/c 122.4231; 11.6708; 19.4398
90; 113.005; 90		4682.72Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132638 CIFC110 H142 B4 N8 Si2P -111.641; 12.3141; 17.9847
95.791; 101.108; 104.877		2414.05Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132639 CIFC54 H72 B2 N4 SiI 1 2/a 124.18452; 11.44862; 68.9173
90; 90.4985; 90		19081.1Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132640 CIFC18 H37 BrP -15.561; 7.204; 46.69
87.22; 87.14; 89.974		1865.9Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132641 CIFC35 H69 Br2 N S2P -18.7215; 9.0562; 25.5173
93.301; 91.998; 106.02		1931.3Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132642 CIFC21 H40 Br N S2P -18.6976; 9.0477; 15.3351
96.503; 101.075; 100.606		1150.16Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132643 CIFC35 H73 N O4 S3P 1 21 15.0644; 7.3853; 51.831
90; 90.179; 90		1938.58Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132644 CIFC17 H16 N2P 1 21/c 112.0756; 8.8912; 12.87
90; 92.604; 90		1380.4Zhao, Mi-Na; Yang, Zi-Mo; Li, Lian-Qing
DMF as an amine source: iron-catalyzed cyclization of 2<i>H</i>-azirines to imidazoles.
Chemical communications (Cambridge, England), 2024, 60, 1904-1907
7132645 CIFC39 H27 N3 SP -110.2867; 12.154; 12.446
79.931; 88.875; 74.591		1476.4Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132646 CIFC39 H27 N3 OP 1 21/c 114.239; 8.5693; 23.345
90; 102.743; 90		2778.4Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132647 CIFC40 H29 Cl2 N3 O SP -110.8035; 11.2186; 15.653
69.437; 83.85; 70.803		1677.4Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132648 CIFC39 H27 N3 O SP 1 21/c 117.993; 17.184; 9.741
90; 103.718; 90		2925.9Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132649 CIFC39 H27 N3 SP -110.141; 10.944; 15.802
90.812; 103.552; 114.74		1535.9Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132650 CIFC32 H41 F6 N PP -111.0504; 11.3069; 13.576
112.089; 90.039; 102.919		1525.21Inoue, Takeru; Matsuura, Yuuka; Horii, Koki; Konishi, Akihito; Nishida, Jun-Ichi; Yasuda, Makoto; Kawase, Takeshi
<i>N</i>-2,6-Di(isopropyl)phenyl-2-azaphenalenyl radical cations.
Chemical communications (Cambridge, England), 2024, 60, 1735-1738
7132651 CIFC17 H14 N3 O2P -17.1044; 10.0383; 10.7169
102.103; 109.324; 102.128		672.07Kuroda, Yusuke; Krell, Maya; Kurokawa, Kazuma; Takasu, Kiyosei
Synthesis of mesoionic triazolones <i>via</i> a formal [3+2] cycloaddition between 4-phenyl-1,2,4-triazoline-3,5-dione and alkynes.
Chemical communications (Cambridge, England), 2024, 60, 1719-1722
7132652 CIFC46 H38 N2 O3 PtP -110.8643; 11.6179; 14.5758
77.263; 82.321; 84.958		1775.15Ikeshita, Masahiro; Watanabe, Shinya; Suzuki, Seika; Tanaka, Shota; Hattori, Shingo; Shinozaki, Kazuteru; Imai, Yoshitane; Tsuno, Takashi
Circularly polarized phosphorescence with a large dissymmetry factor from a helical platinum(II) complex.
Chemical communications (Cambridge, England), 2024, 60, 2413-2416
7132653 CIFC30 H24 N2 O PtP 1 21/n 111.8288; 15.4199; 12.409
90; 98.051; 90		2241.08Ikeshita, Masahiro; Watanabe, Shinya; Suzuki, Seika; Tanaka, Shota; Hattori, Shingo; Shinozaki, Kazuteru; Imai, Yoshitane; Tsuno, Takashi
Circularly polarized phosphorescence with a large dissymmetry factor from a helical platinum(II) complex.
Chemical communications (Cambridge, England), 2024, 60, 2413-2416
7132654 CIFC20 H40 N6 ZnC 1 2/c 115.4081; 10.2686; 15.6427
90; 99.301; 90		2442.44Zhang, Xiaofeng; Li, Yinghua; Fan, Weibin; Huang, Deguang
Direct transformation of nitriles to cyanide using chloride anion as catalyst.
Chemical communications (Cambridge, England), 2024, 60, 2058-2061
7132655 CIFC57 H34 Cl Co N6 O5P -110.5787; 13.3611; 18.6693
73.222; 89.394; 84.62		2514.9Bulbul, Amir Sohel; Rathour, Vikram; Ganesan, Vellaichamy; Sankar, Muniappan
π-Extended nonplanar cobalt porphyrins immobilized on MWCNTs as efficient electrocatalysts for selective oxygen reduction reaction.
Chemical communications (Cambridge, England), 2024, 60, 3146-3149
7132656 CIFC36 H48 Cl2 Cu2 N10 O12P -111.652; 13.232; 16.02
106.82; 96.99; 110.12		2151.7De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132657 CIFC12 H20 Cu F6 N4 O8 S2P 1 21/c 110.686; 14.011; 8.0619
90; 110.87; 90		1127.8De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132658 CIFC40 H52 Cu2 F6 N10 O10 S2P n m a13.529; 20.929; 16.907
90; 90; 90		4787.2De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132659 CIFC37.12 H54.51 B2 Cl0.37 Cu2 F8 N10.38 O6.26P -111.5059; 15.193; 15.47
76.645; 73.531; 68.4		2386.8De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132660 CIFC15 H20 N4 O7P 1 21/c 111.301; 23.093; 6.9978
90; 105.89; 90		1756.5De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132661 CIFC126 H102 N6 S6I a -333.06; 33.06; 33.06
90; 90; 90		36133.4Yamamoto, Koji; Tsutsui, Kanta; Tanuma, Miho; Ito, Kaname; Wakamatsu, Kan; Yamamoto, Koji; Nakamura, Yosuke
Phenothiazine cyclic hexamers: synthesis, properties, and complexation behavior with C<sub>60</sub>.
Chemical communications (Cambridge, England), 2024, 60, 2220-2223
7132662 CIFC84 H98 N13 O24 Sc3P 1 21/n 115.847; 16.418; 34.089
90; 101.579; 90		8689Wang, Hao; Shi, Le; Xiong, Zhangyi; Ma, Si; Cao, Honghao; Cai, Shijia; Qiao, Zhiwei; Pan, Jun; Chen, Zhijie
A two-dimensional metal-organic framework assembled from scandium-based cages for the selective capture of sulfur hexafluoride.
Chemical communications (Cambridge, England), 2024, 60, 2397-2400
7132663 CIFC25 H16 F3 N3 O2P 1 21/c 111.571; 21.464; 8.872
90; 107.385; 90		2102.8Lai, Dipti; Bhattacharjee, Suvam; Mandal, Saurodeep; Ghosh, Sumit; Sahoo, Prithidipa; Sinha, Subrata; Hajra, Alakananda
Iodine(III)-promoted oxidative carbotrifluoromethylation of maleimides with imidazopyridines and Langlois' reagent.
Chemical communications (Cambridge, England), 2024, 60, 2232-2235
7132664 CIFC38 H20 Co N6I 41/a :213.6416; 13.6416; 14.5402
90; 90; 90		2705.83Mine, Kosuke; Arae, Sachie; Murakawa, Hiroshi; Tsuchiizu, Masahisa; Hanasaki, Noriaki; Matsuda, Masaki
Diamond lattice in single-component molecular crystals comprising tetrabenzoporphyrin neutral radicals.
Chemical communications (Cambridge, England), 2024, 60, 3019-3022
7132665 CIFC38 H20 Fe N6I 41/a :213.7275; 13.7275; 14.5027
90; 90; 90		2732.95Mine, Kosuke; Arae, Sachie; Murakawa, Hiroshi; Tsuchiizu, Masahisa; Hanasaki, Noriaki; Matsuda, Masaki
Diamond lattice in single-component molecular crystals comprising tetrabenzoporphyrin neutral radicals.
Chemical communications (Cambridge, England), 2024, 60, 3019-3022
7132666 CIFC36 H20 Cl2 Mn N4I 41/a :213.789; 13.789; 14.4334
90; 90; 90		2744.32Mine, Kosuke; Arae, Sachie; Murakawa, Hiroshi; Tsuchiizu, Masahisa; Hanasaki, Noriaki; Matsuda, Masaki
Diamond lattice in single-component molecular crystals comprising tetrabenzoporphyrin neutral radicals.
Chemical communications (Cambridge, England), 2024, 60, 3019-3022
7132667 CIFC360 H380 B2 Cu58 F8 O12 P4 S36I 41/a c d :250.9312; 50.9312; 64.4799
90; 90; 90		167260Zhang, Qian; Zheng, Hao; Zhou, Jie; Yang, Jia-Ji; Xu, Kai-Yue; Shen, Lian-Yun; Guan, Zong-Jie; Yang, Yang
A bowl-shaped phosphangulene-protected cubic Cu<sub>58</sub> nanocluster.
Chemical communications (Cambridge, England), 2024, 60, 2389-2392
7132668 CIFC32 H34 Cl2 N2 O4P 21 21 2110.2222; 10.4342; 27.3088
90; 90; 90		2912.77Qiu, Xujun; Seibert, Jasmin; Fuhr, Olaf; Biedermann, Frank; Bräse, Stefan
Reversing the stereoselectivity of intramolecular [2+2] photocycloaddition utilizing cucurbit[8]uril as a molecular flask.
Chemical communications (Cambridge, England), 2024, 60, 3267-3270
7132669 CIFC38 H46 N10 O8 P4P -19.9127; 12.0311; 17.7893
96.019; 99.704; 95.561		2065.42Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132670 CIFC15 H18.8 N5 O2 PP -19.0435; 10.15596; 10.73364
108.653; 99.9637; 113.648		802.4Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132671 CIFC52 H80 N20 O12 P4 Zn2P 1 21/n 117.7137; 10.1405; 18.5083
90; 92.467; 90		3321.49Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132672 CIFC46 H66 Co2 N18 O10 P4P 1 21/n 112.2983; 10.2366; 22.8341
90; 94.766; 90		2864.7Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132673 CIFC52 H80 Co2 N20 O12 P4P 1 21/n 117.5968; 10.1687; 18.3843
90; 92.14; 90		3287.3Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132674 CIFB2 F O4 SbP -14.3436; 6.3169; 7.0009
92.888; 95.126; 104.803		184.44Hu, Chenhui; Wu, Mengfan; Han, Jian; Yang, Zhihua; Han, Shujuan; Pan, Shilie
New antimony fluorooxoborates with strong birefringence and unprecedented structural characterisation.
Chemical communications (Cambridge, England), 2024, 60, 2653-2656
7132675 CIFC19 H16 F2 O2P c a 217.534; 12.716; 15.945
90; 90; 90		1527.6Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132676 CIFC27 H24 N4 OI 41/a :224.3936; 24.3936; 16.9622
90; 90; 90		10093.3Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132677 CIFC27 H24 N4 OP b c n26.264; 9.4519; 18.6059
90; 90; 90		4618.8Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132678 CIFC27 H22 Cl2 N4 OP 1 21 110.1692; 9.7507; 23.6934
90; 101.686; 90		2300.67Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132679 CIFC23 H18 Br N3 O2P 1 21/c 17.8608; 18.2829; 13.4885
90; 96.3335; 90		1926.7Aghaie, Kimia; Amiri, Kamran; Rezaei-Gohar, Mohammad; Rominger, Frank; Dar'in, Dmitry; Sapegin, Alexander; Balalaie, Saeed
Transition-metal-free intramolecular double hydrofunctionalization of alkyne to access 6/7/5-fused heterocyclic skeletons.
Chemical communications (Cambridge, England), 2024, 60, 2661-2664
7132680 CIFC23 H18 Br N3 OP 1 21/n 19.9612; 15.0034; 13.3232
90; 99.6334; 90		1963.1Aghaie, Kimia; Amiri, Kamran; Rezaei-Gohar, Mohammad; Rominger, Frank; Dar'in, Dmitry; Sapegin, Alexander; Balalaie, Saeed
Transition-metal-free intramolecular double hydrofunctionalization of alkyne to access 6/7/5-fused heterocyclic skeletons.
Chemical communications (Cambridge, England), 2024, 60, 2661-2664
7132681 CIFC26 H19 Mo O6 PP 1 21/c 19.4364; 30.672; 24.941
90; 94.189; 90		7199.5Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132682 CIFC24 H24 Br O3 PP -19.5566; 10.874; 12.1513
97.716; 112.057; 109.43		1054.03Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132683 CIFC21 H19 O PP -18.1143; 8.9827; 12.4136
94.652; 90.566; 113.742		824.6Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132684 CIFC24 H24 Br O2 PP -18.8789; 9.5863; 13.4826
84.831; 87.383; 65.062		1036.32Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132685 CIFC28 H23 Mo O6 PP -19.4957; 18.3164; 22.5419
99.296; 92.701; 95.011		3846.9Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132686 CIFC29 H26 Br O2 PP -18.9276; 10.5777; 14.307
69.469; 84.259; 72.909		1209.4Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132687 CIFC20 H15 F OP b c a16.4099; 10.0684; 18.6788
90; 90; 90		3086.1Zhang, Zhou; Li, Jin; Cai, Zhiwei; Kang, Songyao; Wang, Jian; Cui, Yue; Han, Siyuan; Sheng, Lei; Yin, Qing; Dai, Ang; Zhao, Weining; Zhao, Fangyuan
Electrochemical aerobic Wacker-type oxygenation of triaryl substituted alkenes to 1,2,2-triarylethanones.
Chemical communications (Cambridge, England), 2024, 60, 3035-3038
7132688 CIFC23 H18 N2 OP 21 21 216.2987; 7.8754; 36.641
90; 90; 90		1817.57Wang, Mingxu; Gao, Ying; Zhao, Xiao-Jing; Gao, Lu; He, Yonghui
Electrochemical multicomponent [2+2+1] cascade cyclization of enaminones and primary amines towards the synthesis of 4-acylimidazoles.
Chemical communications (Cambridge, England), 2024, 60, 2677-2680
7132689 CIFC56 H71 Cl Ga Ge N2P -111.3222; 12.2948; 20.0701
98.212; 91.794; 114.236		2508.9Bücker, Anna; Gehlhaar, Alexander; Wölper, Christoph; Schulz, Stephan
Activation of non-polar bonds by an electron-rich gallagermylene.
Chemical communications (Cambridge, England), 2024, 60, 2902-2905
7132690 CIFC53 H66 Cl Ga Ge N2 P4C 1 2/c 145.016; 10.0401; 23.339
90; 102.56; 90		10296Bücker, Anna; Gehlhaar, Alexander; Wölper, Christoph; Schulz, Stephan
Activation of non-polar bonds by an electron-rich gallagermylene.
Chemical communications (Cambridge, England), 2024, 60, 2902-2905
7132691 CIFC33 H21 F OP 21 21 218.733; 16.125; 16.631
90; 90; 90		2342Hore, Soumyadip; Singh, Abhijeet; Singh, Ravi P.
Asymmetric 1,2-diaxial synthesis of bi-(hetero)aryl benzofulvene atropisomers <i>via</i> transient directing group-assisted dehydrogenative coupling.
Chemical communications (Cambridge, England), 2024, 60, 2524-2527
7132692 CIFC44 H36 Br Cl2 N3P 1 21/c 115.5477; 14.2729; 16.1793
90; 92.941; 90		3585.6Bernt, Felix; Leonhardt, Christopher M.; Schatz, Dominic; Wegner, Hermann A.
Synthesis and investigation of a <i>meta</i>[6]cycloparaphenylene gold(I) <i>N</i>-heterocyclic carbene complex.
Chemical communications (Cambridge, England), 2024, 60, 3055-3058
7132693 CIFC57 H46 Au Br Cl8 N2P 1 21/m 110.2999; 14.4369; 17.7726
90; 98.815; 90		2611.5Bernt, Felix; Leonhardt, Christopher M.; Schatz, Dominic; Wegner, Hermann A.
Synthesis and investigation of a <i>meta</i>[6]cycloparaphenylene gold(I) <i>N</i>-heterocyclic carbene complex.
Chemical communications (Cambridge, England), 2024, 60, 3055-3058
7132694 CIFC39 H51 O P SiP -114.1352; 15.4491; 19.4502
85.75; 69.641; 64.337		3574.6Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132695 CIFC46 H32 Cl6 O2 P2 SP -114.0465; 14.1358; 14.4268
118.189; 92.506; 114.771		2185.5Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132696 CIFC29 H21 O2 PP 1 21/c 19.475; 18.8265; 12.489
90; 109.249; 90		2103.26Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132697 CIFC29 H22 N3 O PP -19.9714; 10.8463; 22.5248
77.043; 86.915; 82.273		2351.83Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132698 CIFC24 H26 O5 SP 1 21/n 110.416; 19.09; 11.659
90; 113.372; 90		2128.1Mishra, Manmath; Verma, Kshitiz; Banerjee, Sonbidya; Punniyamurthy, Tharmalingam
Iron-catalyzed cascade C-C/C-O bond formation of 2,4-dienals with donor-acceptor cyclopropanes: access to functionalized hexahydrocyclopentapyrans.
Chemical communications (Cambridge, England), 2024, 60, 2788-2791
7132699 CIFC14 H19 N O3P 1 21/c 18.4622; 17.4106; 10.0167
90; 109.344; 90		1392.47Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132700 CIFC17 H17 N O3P 1 21/n 110.8048; 10.1624; 14.3028
90; 110.088; 90		1474.95Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132701 CIFC13 H16 Cl N O3P 1 21/c 18.5014; 16.7568; 10.0698
90; 105.68; 90		1381.12Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132702 CIFC16 H14 Cl N O3P 1 21/c 110.9337; 9.852; 14.5888
90; 111.998; 90		1457.08Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132703 CIFC27 H35 Cl N2 O6P 1 21 18.5052; 16.9899; 10.0551
90; 107.507; 90		1385.69Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132704 CIFC30 H33 Cl N2 O6P 1 21 110.7599; 9.7943; 14.5273
90; 111.649; 90		1422.98Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132705 CIFC29 H30 Cl2 N2 O6P 1 21 110.7438; 9.7103; 14.4644
90; 110.923; 90		1409.5Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132706 CIFC16 H15 N O3P 1 21/c 111.2259; 9.0079; 14.0101
90; 107.097; 90		1354.12Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132707 CIFC31 H36 N2 O6P 1 21 110.6827; 9.9438; 14.441
90; 110.66; 90		1435.37Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132708 CIFC33 H31 Cl N2 O6P 1 21 110.8824; 10.0217; 14.4325
90; 111.003; 90		1469.44Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132709 CIFC13 H17 N O3P 1 21/c 110.7023; 9.0828; 13.337
90; 103.692; 90		1259.61Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132710 CIFC30 H33 Cl N2 O6P 1 21 110.7094; 9.8205; 14.5002
90; 111.286; 90		1420.97Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132711 CIFC31 H30 F6 N2 O6P 1 21 113.8243; 9.1832; 13.8585
90; 117.871; 90		1555.27Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132712 CIFC33 H29 F3 N2 O6P 1 21 112.9498; 9.6063; 13.1925
90; 117.118; 90		1460.7Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132713 CIFC29 H32 N2 O6P 1 21 110.9173; 9.1344; 14.1599
90; 108.014; 90		1342.85Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132714 CIFC30 H31 F3 N2 O6P 1 21 111.4316; 9.5763; 14.2272
90; 111.456; 90		1449.55Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132715 CIFC14 H16 F3 N O3P 1 21/c 18.966; 17.0296; 10.0714
90; 107.371; 90		1467.64Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132716 CIFC20 H38 K16 N2 Na10.5 O218 P7 W39 Zr3P 31 2 122.6518; 22.6518; 75.9558
90; 90; 120		33751.8Yang, Dongsheng; Liu, Lihua; Zhang, Yunfan; Zhang, Miao; Ma, Pengtao; Wang, Jingping; Niu, Jingyang
A wheel-shaped Zr-substituted phosphotungstate [{Zr(C<sub>2</sub>O<sub>4</sub>)<sub>2</sub>}<sub>3</sub> (PO<sub>4</sub>)(P<sub>6</sub>W<sub>39</sub>O<sub>150</sub>)]<sup>39-</sup> with tunable proton conduction properties.
Chemical communications (Cambridge, England), 2024, 60, 3043-3046
7132717 CIFC20 H48 N10 P2 UP 1 21/n 19.909; 10.674; 14.833
90; 104.484; 90		1519Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132718 CIFC40 H98 N10 P4 U2P -110.769; 13.579; 20.817
82.853; 79.684; 69.571		2800.2Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132719 CIFC40 H96 N20 P4 U2P 21 21 210.5753; 27.797; 10.3786
90; 90; 90		3050.9Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132720 CIFC40 H96 N20 P4 U2C 1 2/c 125.24; 10.392; 25.465
90; 110.915; 90		6239Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132721 CIFC40 H96 N20 P4 U2C 1 2/c 125.206; 10.392; 25.457
90; 110.647; 90		6240Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132722 CIFC20 H48 N10 P2 UC 1 2/c 125.309; 10.4218; 25.538
90; 110.799; 90		6297.1Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132723 CIFC40 H96 N20 P4 U2C 1 2/c 125.279; 10.4213; 25.477
90; 110.786; 90		6274.8Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132724 CIFC40 H96 N20 P4 U2P 21 21 210.5761; 27.7942; 10.3688
90; 90; 90		3048Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132725 CIFC80 H192 N40 P8 U4P 1 2/n 124.9458; 10.2858; 25.3172
90; 111.158; 90		6058.2Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132726 CIFC20 H48 N10 P2 UP 1 21/n 110.1931; 10.6719; 14.9477
90; 102.736; 90		1586Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132727 CIFC20 H48 N10 P2 UP 1 21/n 19.8845; 10.6539; 14.7678
90; 104.838; 90		1503.32Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132728 CIFC40 H96 N20 P4 U2P 21 21 210.5757; 27.8005; 10.3708
90; 90; 90		3049.1Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132729 CIFC20 H48 N10 P2 UP 1 2/n 124.9421; 10.2665; 25.3542
90; 111.169; 90		6054.3Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132730 CIFC16 H14 Cl2 N2 O2 SnC 1 c 110.7059; 14.2716; 10.8582
90; 101.977; 90		1622.91Žáková, Andrea; Saha, Pritha; Paparakis, Alexandros; Zábranský, Martin; Gastelu, Gabriela; Kukla, Jaroslav; Uranga, Jorge G.; Hulla, Martin
Hexacoordinated tin complexes catalyse imine hydrogenation with H<sub>2</sub>.
Chemical communications (Cambridge, England), 2024, 60, 3287-3290
7132731 CIFC51 H40 B Cl4 N OP -19.2148; 13.8751; 16.7722
74.99; 87.948; 80.579		2043.28Huang, Yong; Jia, Mengjiao; Li, Chuan; Yang, Yang; He, Yuling; Luo, Yanju; Huang, Yan; Zhou, Liang; Lu, Zhiyun
A spiroacridine-based thermally activated delayed fluorescence emitter for high-efficiency and narrow-band deep-blue OLEDs.
Chemical communications (Cambridge, England), 2024, 60, 3194-3197
7132732 CIFC194 H142 Ag14 Cl4 F36 P8 Pd S6P 1 21/c 117.46; 36.131; 18.471
90; 110.07; 90		10945Ma, Along; Ren, Yonggang; Zuo, Yang; Wang, Jiawei; Huang, Shutong; Ma, Xiaoshuang; Wang, Shuxin
Ligand-controlled exposure of active sites on the Pd<sub>1</sub>Ag<sub>14</sub> nanocluster surface to boost electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 3162-3165
7132733 CIFC183 H171 Ag14 O21 P7 Pd S6P -119.457; 20.805; 27.84
82.006; 74.854; 84.149		10747Ma, Along; Ren, Yonggang; Zuo, Yang; Wang, Jiawei; Huang, Shutong; Ma, Xiaoshuang; Wang, Shuxin
Ligand-controlled exposure of active sites on the Pd<sub>1</sub>Ag<sub>14</sub> nanocluster surface to boost electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 3162-3165
7132734 CIFC18 H15 Br O3P 1 21 17.2004; 6.8661; 16.0022
90; 100.88; 90		776.91Sarkar, Rahul; Korell, Alexander; Schneider, Christoph
Organocatalytic enantioselective oxa-Piancatelli rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 3063-3066
7132735 CIFC66 H58 Hg O P4 S2C 1 2/c 124.571; 14.09; 20.038
90; 122.893; 90		5825Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132736 CIFC31 H26 P2 SP 1 21/n 19.72967; 15.22975; 16.93649
90; 91.2641; 90		2509.05Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132737 CIFC58 H63 Cl P2 S UP -112.0774; 14.1627; 14.3748
94.016; 90.702; 93.297		2448.4Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132738 CIFC43 H49 K O6 P2 SP -19.4692; 10.8945; 21.4146
77.036; 83.374; 73.667		2062.75Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132739 CIFC58 H63 Cl P2 S ThP -112.1389; 14.1799; 14.3984
94.193; 90.436; 93.016		2468.15Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132740 CIFC19 H20 N2 OP 1 21/c 18.637; 13.293; 29.631
90; 96.679; 90		3378.9Zhang, Min; Zheng, Yongpeng; Jin, Yangbin; Jiang, Huanfeng; Wu, Wanqing
Palladium-catalyzed ligand-regulated divergent synthesis of pyrrole[2,3-<i>b</i>]indoles and ureas from 2-ethynylanilines and isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2950-2953
7132741 CIFC26 H28 N4C 1 2/c 115.2301; 10.2357; 28.4109
90; 95.828; 90		4406.1Zhang, Min; Zheng, Yongpeng; Jin, Yangbin; Jiang, Huanfeng; Wu, Wanqing
Palladium-catalyzed ligand-regulated divergent synthesis of pyrrole[2,3-<i>b</i>]indoles and ureas from 2-ethynylanilines and isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2950-2953
7132742 CIFC17 H14 B F3 N2P -18.4898; 11.7179; 16.2792
90.732; 99.945; 95.106		1588.18McDonald, Peter W.; Ritchie, Chris
A multi-chromic boron trifluoride-pyridyl Lewis adduct.
Chemical communications (Cambridge, England), 2024, 60, 3051-3054
7132743 CIFC17 H15 B F4 N2P 1 21 110.3062; 7.7018; 10.3247
90; 101.056; 90		804.326McDonald, Peter W.; Ritchie, Chris
A multi-chromic boron trifluoride-pyridyl Lewis adduct.
Chemical communications (Cambridge, England), 2024, 60, 3051-3054
7132744 CIFC17 H14 B F3 N2P -18.359; 11.6452; 16.1214
90.762; 100.271; 94.709		1538.31McDonald, Peter W.; Ritchie, Chris
A multi-chromic boron trifluoride-pyridyl Lewis adduct.
Chemical communications (Cambridge, England), 2024, 60, 3051-3054
7132745 CIFC5 H8 Er N3 O8P c c a8.2526; 6.5427; 19.313
90; 90; 90		1042.8Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132746 CIFC5 H8 Er N3 O8P c c a8.1956; 6.534; 19.322
90; 90; 90		1034.7Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132747 CIFC5 H8 Er N3 O8P c c a8.4551; 6.584; 19.2134
90; 90; 90		1069.58Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132748 CIFC5 H8 Er N3 O8P c c a7.8462; 6.5142; 19.58
90; 90; 90		1000.8Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132749 CIFC5 H8 Er N3 O8P c c a8.3154; 6.549; 19.234
90; 90; 90		1047.44Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132750 CIFC5 H8 Er N3 O8P c c a8.3583; 6.5585; 19.218
90; 90; 90		1053.49Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132751 CIFC5 H8 Er N3 O8P c c a7.801; 6.5107; 19.64
90; 90; 90		997.5Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132752 CIFC5 H8 Er N3 O8P c c a8.4958; 6.5946; 19.201
90; 90; 90		1075.76Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132753 CIFC5 H8 Er N3 O8P c c a7.736; 6.479; 19.71
90; 90; 90		988Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132754 CIFC5 H8 Er N3 O8P c c a8.4154; 6.5724; 19.21
90; 90; 90		1062.49Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132755 CIFC6 H10 Er N O8P 1 2/n 19.1183; 8.948; 13.1042
90; 96.446; 90		1062.4Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132756 CIFC6 H10 Er N O8P 1 2/n 19.1326; 8.974; 13.1405
90; 96.41; 90		1070.2Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132757 CIFC6 H10 Er N O8P 1 2/n 19.1263; 8.963; 13.1305
90; 96.44; 90		1067.3Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132758 CIFC6 H10 Er N O8P 1 2/a 19.0759; 8.863; 6.4822
90; 96.228; 90		518.3Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132759 CIFC6 H10 Er N O8P 1 2/a 19.0907; 8.903; 6.5091
90; 96.38; 90		523.5Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132760 CIFC6 H10 Er N O8P 1 2/n 19.1539; 8.9987; 13.1797
90; 96.604; 90		1078.5Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132761 CIFC6 H10 Er N O8P 1 2/a 19.0471; 8.792; 6.4339
90; 96.131; 90		508.8Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132762 CIFC6 H10 Er N O8P 1 2/n 19.1533; 8.9945; 13.1812
90; 96.747; 90		1077.68Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132763 CIFC6 H10 Er N O8P 1 2/a 19.1025; 8.913; 6.5273
90; 96.442; 90		526.2Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132764 CIFC141 H123 Ag4 Cd6 N7 O2 S16I 1 2/m 115.6408; 26.8262; 40.7797
90; 90.156; 90		17110.4Li, Yan-Ling; Liu, Yu-Dong; Li, Wei-Li; Li, Fu-An; Feng, Yun-Xiao; Luo, Xiao-Qiang; Han, Yong-Jun
Ligand engineering to achieve synergistic properties in a 2D bilayer supertetrahedral chalcogenide cluster-based assembled material.
Chemical communications (Cambridge, England), 2024, 60, 3279-3282
7132765 CIFC35 H36 N2 O9P -110.6256; 14.683; 20.9217
110.478; 90.035; 90.542		3057.7Emenike, Bright U.; Shinn, David W.; Spinelle, Ronald A.; Yoo, Barney; Rosario, Ambar M.
Quantifying macrocyclization-induced strain utilizing <i>N</i>-phenylimides as conformational reporters.
Chemical communications (Cambridge, England), 2024, 60, 4040-4043
7132766 CIFC71 H73 Cl3 N4 O16 S2P -110.084; 15.1221; 22.373
100.593; 94.039; 95.97		3321.3Emenike, Bright U.; Shinn, David W.; Spinelle, Ronald A.; Yoo, Barney; Rosario, Ambar M.
Quantifying macrocyclization-induced strain utilizing <i>N</i>-phenylimides as conformational reporters.
Chemical communications (Cambridge, England), 2024, 60, 4040-4043
7132767 CIFC124 H120 N8 O24P 1 21/n 117.0682; 11.8271; 27.346
90; 106.721; 90		5286.9Emenike, Bright U.; Shinn, David W.; Spinelle, Ronald A.; Yoo, Barney; Rosario, Ambar M.
Quantifying macrocyclization-induced strain utilizing <i>N</i>-phenylimides as conformational reporters.
Chemical communications (Cambridge, England), 2024, 60, 4040-4043
7132768 CIFC23 H18 Cl3 N O2P 21 21 215.5787; 13.2751; 27.4431
90; 90; 90		2032.4Wei, Jian; Du, Zhongjian; Wang, Xu; Ji, Chenlei; Li, Longji; You, Yang'en
Palladium-catalyzed enantioselective arylation of trichloro- or tri-/difluoroacetaldimine precursors.
Chemical communications (Cambridge, England), 2024, 60, 3303-3306
7132769 CIFC29 H31 N3 O6 SP -18.2702; 12.562; 13.769
89.503; 79.822; 87.707		1406.8Samantaray, Swati; Maharana, Prabhat Kumar; Kar, Subhradeep; Saha, Sharajit; Punniyamurthy, Tharmalingam
Redox-neutral zinc-catalyzed cascade [1,4]-H shift/annulation of diaziridines with donor-acceptor aziridines.
Chemical communications (Cambridge, England), 2024, 60, 3441-3444
7132770 CIFC13 H14 Cl N O4 SP 1 21 15.5934; 10.4137; 12.5612
90; 97.969; 90		724.6Wan, Chuan; Yang, Dongyan; Guo, Xiaochun; Zhang, Tuanjie; Ruan, Zhijun; Dai, Chuan; Xing, Yun; Yin, Feng; Wang, Rui; Li, Zigang
β-Carbonyl sulfonium enables cysteine-specific bioconjugation for activity-based protein profiling in live cells.
Chemical communications (Cambridge, England), 2024, 60, 3725-3728
7132771 CIFC26.68 H32.49 N6 O1.56R -3 :H37.3204; 37.3204; 9.7227
90; 90; 120		11727.6Kang, Xiang; Zhang, Mingtao; Tang, Weiwei; Gong, Junbo
Growth "self-inhibition" of irbesartan desmotrope: surface intra-annular tautomer inter-conversion is the culprit.
Chemical communications (Cambridge, England), 2024, 60, 3511-3514
7132772 CIFC12 H14 Cl4 N2 O4 Pb S2P 1 21/c 14.3263; 18.5138; 12.3948
90; 97.504; 90		984.27Wang, Jing; Yang, Jin-Hai; Chen, Jie; Wang, Shuai-Hua; Chen, Yong-Jun; Xu, Gang
1D Pb halide perovskite-like materials for high performance X-ray detection.
Chemical communications (Cambridge, England), 2024, 60, 3311-3314
7132773 CIFC12 H12 Br4 N2 O4 Pb S2P 1 21/c 14.4621; 19.0334; 12.5804
90; 98.489; 90		1056.73Wang, Jing; Yang, Jin-Hai; Chen, Jie; Wang, Shuai-Hua; Chen, Yong-Jun; Xu, Gang
1D Pb halide perovskite-like materials for high performance X-ray detection.
Chemical communications (Cambridge, England), 2024, 60, 3311-3314
7132774 CIFC12 H12 I4 N2 O4 Pb S2P 1 21/c 14.6903; 19.9065; 12.82
90; 99.393; 90		1180.92Wang, Jing; Yang, Jin-Hai; Chen, Jie; Wang, Shuai-Hua; Chen, Yong-Jun; Xu, Gang
1D Pb halide perovskite-like materials for high performance X-ray detection.
Chemical communications (Cambridge, England), 2024, 60, 3311-3314
7132775 CIFC62 H66 N10 O14 S4C 1 2/c 137.954; 10.748; 24.5839
90; 93.542; 90		10009.3Huang, Ming-Feng; Cao, Li-Hui; Zhou, Bin
A solvent-controlled photoresponsive ionic hydrogen-bonded organic framework for encryption applications.
Chemical communications (Cambridge, England), 2024, 60, 3437-3440
7132776 CIFC42 H48 N8 O16 S4P 1 21/c 112.9205; 27.6064; 15.3072
90; 113.718; 90		4998.72Huang, Ming-Feng; Cao, Li-Hui; Zhou, Bin
A solvent-controlled photoresponsive ionic hydrogen-bonded organic framework for encryption applications.
Chemical communications (Cambridge, England), 2024, 60, 3437-3440
7132777 CIFC41 H33 N O7 SP 1 21 19.1592; 17.6405; 10.2784
90; 94.192; 90		1656.27Barik, Shilpa; Sankar, Ganga; Biju, Akkattu T.
Enantioselective synthesis of tricyclic oxoquinolines <i>via</i> NHC-catalyzed Michael-aldol-lactamization-dehydration cascade.
Chemical communications (Cambridge, England), 2024, 60, 4290-4293
7132778 CIFC18 H14 Ca F9 N3 O8P 1 21/n 124.1213; 8.1633; 24.2668
90; 98.981; 90		4719.8Baudet, Judith; Lesur, Emilie; Ribéraud, Maxime; Chevalier, Arnaud; D'Anfray, Timothée; Thuéry, Pierre; Audisio, Davide; Taran, Frédéric
Synthesis of sydnonimines from sydnones and their use for bioorthogonal release of isocyanates in cells.
Chemical communications (Cambridge, England), 2024, 60, 3657-3660
7132779 CIFC36 H92 I2 K O10 Si8 UP -113.4213; 15.8641; 16.3965
104.442; 102.934; 96.066		3246.4Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132780 CIFC36 H98 I2 K O11 Si8 UP 1 2/c 114.8717; 15.8095; 28.9025
90; 103.785; 90		6599.7Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132781 CIFC40 H98 I2 K O10 Si8 UC 1 2/c 149.049; 13.108; 21.124
90; 90.054; 90		13581Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132782 CIFC27 H15 B F N5P -18.0536; 8.9238; 15.0934
79.306; 85.035; 65.599		970.63Kage, Yuto; Jiang, Yuchuan; Minakuchi, Namiki; Mori, Shigeki; Shimizu, Soji
One-pot synthesis of azabora[6]helicene by a Schiff base forming reaction.
Chemical communications (Cambridge, England), 2024, 60, 3543-3546
7132783 CIFC34 H22 B Cl2 N5P -19.3419; 10.0645; 14.7904
91.141; 105.751; 90.019		1338.11Kage, Yuto; Jiang, Yuchuan; Minakuchi, Namiki; Mori, Shigeki; Shimizu, Soji
One-pot synthesis of azabora[6]helicene by a Schiff base forming reaction.
Chemical communications (Cambridge, England), 2024, 60, 3543-3546
7132784 CIFC16 H13 F2 N OP 1 21/n 110.169; 10.856; 12.0502
90; 102.79; 90		1297.27Wang, Xuan; Li, Jianlong; Du, Haifang; Liang, Weihong; Luo, Cheng; Wu, Yunshan; Liu, Bo
Synthesis of 1,4-epoxy-2-aryltetrahydro-1-benzazepines <i>via</i> rhodium(III)-catalyzed C-H allylation/intramolecular 1,3-dipolar cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 2401-2404
7132785 CIFC16 H13 F2 N OP -19.7065; 11.7198; 12.029
77.71; 89.322; 71.433		1265.13Wang, Xuan; Li, Jianlong; Du, Haifang; Liang, Weihong; Luo, Cheng; Wu, Yunshan; Liu, Bo
Synthesis of 1,4-epoxy-2-aryltetrahydro-1-benzazepines <i>via</i> rhodium(III)-catalyzed C-H allylation/intramolecular 1,3-dipolar cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 2401-2404
7132786 CIFC210 H228 Ag3 B F4 N36 O24R 3 2 :H38.1751; 38.1751; 37.5163
90; 90; 120		47349Bajpayee, Nikhil; Pophali, Salil; Vijayakanth, Thangavel; Nandi, Shyamapada; Desai, Aamod V.; Kumar, Vinod; Jain, Rahul; Bera, Santu; Shimon, Linda J. W.; Misra, Rajkumar
Metal-driven folding and assembly of a minimal β-sheet into a 3D-porous honeycomb framework.
Chemical communications (Cambridge, England), 2024, 60, 2621-2624
7132787 CIFC76 H65 Cu2 N20 O16.5P 4319.7601; 19.7601; 19.9303
90; 90; 90		7782Qiu, Zhao-Feng; Wang, Peng; Zhang, Xiao-Yu; Chen, Jia-Qi; Zhang, Kai-Yang; Lu, Xiang-Yu; Zhao, Yue; Sun, Wei-Yin
Supramolecular assemblies of Cu(II) with a tetraphenylethene-imidazole ligand for tuning photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 2204-2207
7132788 CIFC40 H33 Cl4 Cu2 N9 OP 1 21/n 115.805; 9.323; 27.137
90; 99.835; 90		3939.9Qiu, Zhao-Feng; Wang, Peng; Zhang, Xiao-Yu; Chen, Jia-Qi; Zhang, Kai-Yang; Lu, Xiang-Yu; Zhao, Yue; Sun, Wei-Yin
Supramolecular assemblies of Cu(II) with a tetraphenylethene-imidazole ligand for tuning photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 2204-2207
7132789 CIFC41.5 H45.5 N6.5 O18 Tb TiP m -3 n25.9298; 25.9298; 25.9298
90; 90; 90		17434Yao, Qingxia; Pan, Xuze; Si, Xuezhen; Wang, Xin; Zhang, Xiaoying; Hou, Jinle; Su, Jie; Qiu, Yi; Li, Jun
A porous and photoactive Ti-MOF based on a novel tetranuclear [Ti<sub>2</sub>Tb<sub>2</sub>] cluster.
Chemical communications (Cambridge, England), 2024, 60, 2188-2191
7132790 CIFC29 H32 N2 O5P -111.4759; 11.5363; 19.7187
85.779; 79.152; 85.444		2551.2Lai, Jingxiong; Huang, You
A highly diastereoselective (5+1) annulation of allenoates and pyrazolones catalyzed by CH<sub>3</sub>OK.
Chemical communications (Cambridge, England), 2024, 60, 2066-2069
7132791 CIFC10 H19 N O3P 1 21 15.4153; 11.2753; 9.4479
90; 98.633; 90		570.34Zhang, Qiuxin; Zhang, Heng; Geng, Senbai; Zhao, Xian; Liu, Shucheng; Hong, Kun; Pan, Jianming; Yan, Xingchen
Green transformation of CO<sub>2</sub> into γ-amino alcohols with continuous stereocenters.
Chemical communications (Cambridge, England), 2024, 60, 2062-2065
7132792 CIFC52 H52 B2 Hg N14 O4 Se2 W2P -113.7335; 21.8752; 22.673
117.984; 91.487; 103.84		5764.1Onn, Chee S.; Hill, Anthony F.; Ward, Jas S.
Spodium bonding in bis(alkynyl)mecurials.
Chemical communications (Cambridge, England), 2024, 60, 2552-2555
7132793 CIFC20 H23 B N6 O2 Se WP 1 21/c 17.9715; 18.2689; 19.7379
90; 101.415; 90		2817.58Onn, Chee S.; Hill, Anthony F.; Ward, Jas S.
Spodium bonding in bis(alkynyl)mecurials.
Chemical communications (Cambridge, England), 2024, 60, 2552-2555
7132794 CIFC29 H43 B N6 O2 Si Te WP -110.6281; 11.0432; 15.1354
84.687; 87.521; 75.938		1715.38Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132795 CIFC21 H30 Au B Cl6 N6 O2 S Te WP -111.1523; 11.161; 14.3505
89.093; 89.186; 77.275		1742.02Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132796 CIFC64 H100 B2 Cl4 Cu4 N12 O4 Si2 Te2 W2P 1 21/n 110.9539; 18.7716; 20.4333
90; 102.63; 90		4099.87Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132797 CIFC24 H27 B N8 O2 Te WP 1 21 17.9095; 18.2594; 9.7522
90; 99.742; 90		1388.13Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132798 CIFC23 H31 Au B Cl N6 O2 S Si WP 1 21/m 112.3181; 24.9472; 16.5061
90; 108.592; 90		4807.6Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132799 CIFC26 H27 B N6 O2 Te WP 1 21/n 120.5319; 14.2779; 21.6073
90; 117.804; 90		5602.9Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132800 CIFC33 H28 F3 N3 O2P 21 21 218.2405; 13.6044; 25.8384
90; 90; 90		2896.67Wang, Lan; Lu, Mengxi; Li, Kuan; Yang, Sen; Wang, Lei; Guo, Hongchao
Palladium-catalyzed enantioselective umpolung allylation of amido-tethered allylic carbonates with isatin-derived ketimines.
Chemical communications (Cambridge, England), 2024, 60, 3729-3732
7132801 CIFC22 H17 F N2P 1 21/c 16.2418; 18.1094; 15.2988
90; 96.701; 90		1717.49Qin, Jiaze; Jiang, Shixuan; Luo, Xiaofeng; Wang, Tianqiang; Liu, Peihua; Yuan, Bingxiang; Yan, Rulong
I<sub>2</sub>-catalyzed synthesis of 3-aminopyrrole with homopropargylic amines and nitrosoarenes.
Chemical communications (Cambridge, England), 2024, 60, 3701-3704
7132802 CIFC38 H28 N8P 1 21/n 111.5521; 9.4107; 32.526
90; 95.722; 90		3518.39Zhang, Li; Luo, Yu-Ting; Xiao, Sai-Jin; Fan, Jia-Qi; Tan, Quan-Gen; Sun, Chen; Song, An-Min; Liang, Ru-Ping; Qiu, Jian-Ding
The construction of a stable hydrogen-bonded organic framework for the photocatalytic reduction and removal of uranium.
Chemical communications (Cambridge, England), 2024, 60, 3583-3586
7132803 CIFC19 H17 Br O2P 21 21 217.1586; 11.9651; 18.845
90; 90; 90		1614.1Li, Zheyao; Zhang, Huiwen; Zhao, Lin; Ma, Yueyue; Wu, Qiufang; Ren, Haosong; Lin, Zhongren; Zheng, Jun; Yu, Xinhong
Metal-free β,γ-C(sp<sup>3</sup>)-H difunctionalization of propanols: DMP-initiated asymmetric spirocyclopropanation.
Chemical communications (Cambridge, England), 2024, 60, 3579-3582
7132804 CIFC29 H19 N O5P -19.9434; 11.2111; 11.3362
100.833; 92.317; 115.863		1106.1Wang, Kai-Kai; Li, Yan-Li; Li, Ya-Fei; Yao, Wei-Wei; Li, Lan-Xin; He, Xiao-Long; Chen, Rongxiang
Substrate-controlled [4+1] and [3+2] annulations of ninhydrin-derived Morita-Baylis-Hillman carbonates to access polysubstituted furans and cyclopentenes.
Chemical communications (Cambridge, England), 2024, 60, 3717-3720
7132805 CIFC29 H18 O6P 1 21/c 18.5559; 26.5; 9.988
90; 99.097; 90		2236.1Wang, Kai-Kai; Li, Yan-Li; Li, Ya-Fei; Yao, Wei-Wei; Li, Lan-Xin; He, Xiao-Long; Chen, Rongxiang
Substrate-controlled [4+1] and [3+2] annulations of ninhydrin-derived Morita-Baylis-Hillman carbonates to access polysubstituted furans and cyclopentenes.
Chemical communications (Cambridge, England), 2024, 60, 3717-3720
7132806 CIFC27 H23 NP 1 21/n 19.4988; 11.9651; 17.3667
90; 97.139; 90		1958.49Shinde, Jivan; Suresh, Sundaram; Kavala, Veerababurao; Yao, Ching-Fa
Pd(II)-catalyzed hydroarylations/hydroalkenylations of terminal alkynes: regioselective synthesis of allylic, homoallylic, and 1,3-diene systems.
Chemical communications (Cambridge, England), 2024, 60, 3790-3793
7132807 CIFC16 H14 O2P n a 2116.5657; 5.4295; 14.0697
90; 90; 90		1265.48Shinde, Jivan; Suresh, Sundaram; Kavala, Veerababurao; Yao, Ching-Fa
Pd(II)-catalyzed hydroarylations/hydroalkenylations of terminal alkynes: regioselective synthesis of allylic, homoallylic, and 1,3-diene systems.
Chemical communications (Cambridge, England), 2024, 60, 3790-3793
7132808 CIFC26 H23.62 Cl0.38 N2 O3 SP 1 21/n 110.908; 15.648; 14.141
90; 112.321; 90		2232.8Wang, Bi; Liang, Ren-Xiao; Shen, Zhen-Lu; Jia, Yi-Xia
Copper-catalyzed intramolecular dearomative aza-Wacker reaction of indole.
Chemical communications (Cambridge, England), 2024, 60, 3858-3861
7132809 CIFC20 H22 O2P 1 21 18.546; 6.518; 15.6
90; 105.428; 90		837.7Magham, Lakshmi Revati; Samad, Abdus; Thopate, Satish B.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
Organocatalytic enantioselective desymmetrization of enal-tethered cyclohexane-1,3-diones.
Chemical communications (Cambridge, England), 2024, 60, 3834-3837
7132810 CIFC18 H20 Cl N O2P -18.3513; 13.4596; 15.583
77.965; 76.1; 77.207		1635.64Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132811 CIFC18 H17 Cl F3 N OP 1 21/c 16.2156; 11.1571; 24.7517
90; 92.551; 90		1714.78Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132812 CIFC17 H24 Cl N OP 1 21/n 19.2235; 7.0079; 25.1221
90; 94.528; 90		1618.76Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132813 CIFC14 H18 Cl N OI 1 2/a 118.5653; 6.3699; 23.6434
90; 108.817; 90		2646.61Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132814 CIFC19 H22 Cl N OP 1 21/n 116.7373; 6.1891; 18.0916
90; 110.509; 90		1755.3Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132815 CIFC15 H20 Cl N OC 1 2/c 117.0047; 6.656; 24.757
90; 92.075; 90		2800.24Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132816 CIFC16 H22 Cl N OP 1 21/c 112.6132; 6.8258; 17.3255
90; 93.319; 90		1489.14Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132817 CIFC17 H18 Cl N OP 21 21 217.6345; 9.6295; 20.4737
90; 90; 90		1505.15Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132818 CIFC13 H18 Cl N OP -16.66649; 9.4285; 10.2117
93.58; 96.362; 93.083		635.47Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132819 CIFC26 H44 B N2 SiP -110.212; 11.708; 12.522
106.885; 100.518; 90.377		1405.7Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132820 CIFC35 H62 B N3 O SiP 1 21/n 110.2572; 18.663; 19.5822
90; 99.642; 90		3695.67Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132821 CIFC66 H96 B2 N4 O2 Si2C 1 2/c 116.1834; 30.376; 17.5363
90; 113.974; 90		7876.9Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132822 CIFC20 H15 Cl3 O2P 1 21/c 110.8147; 9.8903; 16.969
90; 104.319; 90		1758.6Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132823 CIFC24 H16 O2P 1 21/c 112.2366; 17.3994; 8.2782
90; 102.186; 90		1722.8Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132824 CIFC19 H15 Cl OP -19.6677; 12.9019; 13.3368
73.28; 88.509; 71.049		1502.7Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132825 CIFC12 H11 Br2 N3 ZnP -17.8069; 7.8757; 11.9902
77.783; 85.879; 77.735		703.79Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132826 CIFC14 H17 Br2 N3 S ZnP -17.852; 10.8828; 11.3769
75.796; 74.568; 76.283		892.99Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132827 CIFC15 H19 Br2 N3 O S ZnP -17.5172; 10.647; 13.487
105.076; 92.008; 109.849		971.3Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132828 CIFC15 H17 Br2 N3 O S ZnP 1 21/c 17.3412; 19.033; 13.475
90; 98.398; 90		1862.6Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132829 CIFC26 H26 Cl N3 O5P -18.2719; 10.9748; 14.3779
91.073; 98.225; 110.945		1203Li, Ming-Jun; Lu, Ming-Ming; Xu, Peng; Chen, Si-Qi; Wu, Luan-Ting; Zhang, Ze; Xu, Hui
Chemodivergent mechanosynthesis of cyclopentenyl and pyrrolinyl spirobarbiturates from unsaturated barbiturates and enamino esters.
Chemical communications (Cambridge, England), 2024, 60, 3958-3961
7132830 CIFC28.01 H30.01 Br N3 O5P -111.0881; 11.9277; 12.1514
115.124; 105.133; 100.196		1326.22Li, Ming-Jun; Lu, Ming-Ming; Xu, Peng; Chen, Si-Qi; Wu, Luan-Ting; Zhang, Ze; Xu, Hui
Chemodivergent mechanosynthesis of cyclopentenyl and pyrrolinyl spirobarbiturates from unsaturated barbiturates and enamino esters.
Chemical communications (Cambridge, England), 2024, 60, 3958-3961
7132831 CIFC98 H72 Cl4 Cu2 F20 N8P 1 21/c 117.46; 22.68; 14.222
90; 95.69; 90		5604Dong, Yuting; Qian, Long; Chen, Feng; Wang, Yue; Zhang, Tao; Qiu, Fengxian; Teranishi, Toshiharu; Xue, Songlin
Benzene-fused porphyrin(2.1.2.1) array: synthesis, structure, and electrocatalytic hydrogen evolution.
Chemical communications (Cambridge, England), 2024, 60, 3986-3989
7132832 CIFC19 H17 F3 N2 O4 SP b c a19.2019; 13.9245; 28.2926
90; 90; 90		7564.8Lou, Mingliang; Liu, Xiaolei; Han, Shoule; Bai, Songlin; Qi, Xiangbing
Total synthesis of (±)-3-demethoxyerythratidinone <i>via</i> Tf<sub>2</sub>O-promoted cascade reaction of enaminone.
Chemical communications (Cambridge, England), 2024, 60, 3842-3845
7132833 CIFC18 H17 F3 N2 O4 SP b c a19.421; 13.8099; 27.8614
90; 90; 90		7472.49Lou, Mingliang; Liu, Xiaolei; Han, Shoule; Bai, Songlin; Qi, Xiangbing
Total synthesis of (±)-3-demethoxyerythratidinone <i>via</i> Tf<sub>2</sub>O-promoted cascade reaction of enaminone.
Chemical communications (Cambridge, England), 2024, 60, 3842-3845
7132834 CIFC20 H18 N2 O4.5 VP 1 21/c 115.3045; 8.8087; 13.3399
90; 98.687; 90		1777.76Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132835 CIFC55.66 H21.3 Cl3.31 F10 N8 Pd SP 1 21 113.3831; 7.1785; 26.0801
90; 93.166; 90		2501.71Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132836 CIFC45 H29 B Cl3 F4 N3 Pd SP -19.276; 14.42; 15.664
112.75; 91.73; 91.28		1930Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132837 CIFC74 H42 B F20 N3 Pd SP 1 21/n 113.546; 27.1678; 16.8019
90; 99.633; 90		6096.17Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132838 CIFC46 H32 Cl4 F6 N3 P Pd SP 1 21/c 113.77; 16.0819; 19.035
90; 90.479; 90		4215.1Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132839 CIFC55 H29 Cl3 N8 Pd SP -114.7468; 17.6065; 20.521
69.671; 82.618; 65.328		4539.2Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132840 CIFC47 H20.5 Cl0.5 F16 N3 P Pd SP n a 2128.14; 14.513; 20.554
90; 90; 90		8394Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132841 CIFC20 H26 O4I 1 2/a 110.1083; 14.7871; 22.9034
90; 91.199; 90		3422.68Koyama, Ryosei; Anada, Masahiro; Sueki, Shunsuke; Makino, Kosho; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Divergent synthesis of multi-substituted phenanthrenes <i>via</i> an internal redox reaction/ring expansion sequence.
Chemical communications (Cambridge, England), 2024, 60, 3822-3825
7132842 CIFC18 H24 O2P -19.864; 9.8656; 16.5931
105.165; 97.065; 105.295		1471Koyama, Ryosei; Anada, Masahiro; Sueki, Shunsuke; Makino, Kosho; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Divergent synthesis of multi-substituted phenanthrenes <i>via</i> an internal redox reaction/ring expansion sequence.
Chemical communications (Cambridge, England), 2024, 60, 3822-3825
7132843 CIFC27 H15 Br O2P 1 21/c 117.7637; 15.582; 7.0233
90; 95.518; 90		1935Nishimoto, Mikey; Uetake, Yuta; Yakiyama, Yumi; Sakurai, Hidehiro
Strain-induced carbon-carbon bond cleavage of bowl-shaped sumanenone.
Chemical communications (Cambridge, England), 2024, 60, 3982-3985
7132844 CIFC14 H11 N3 O2P 21 21 218.1213; 11.1938; 13.6325
90; 90; 90		1239.31Bhattacharjee, Suvam; Hajra, Alakananda
Site-selective direct nitration of 2<i>H</i>-indazoles: easy access to 7-nitroindazoles.
Chemical communications (Cambridge, England), 2024, 60, 4076-4079
7132845 CIFC38 H61 N4 P2 Sc SiP 1 21/c 115.5452; 15.3097; 17.8477
90; 97.496; 90		4211.3Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132846 CIFC73 H110 N10 Ni2 P4 Sc2P -112.49; 12.54; 13.517
65.861; 73.439; 76.945		1837.3Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132847 CIFC46 H59 N6 Ni P2 ScP -110.9882; 11.7463; 18.988
74.157; 89.563; 72.84		2245.6Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132848 CIFC43 H57 N4 Ni P2 ScP -111.122; 11.696; 16.447
101.88; 96.172; 90.996		2079.8Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132849 CIFC48 H68 N5 Ni O1.5 P2 ScP -110.142; 10.213; 23.78
77.96; 79.02; 81.49		2350Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132850 CIFC118 H142 N10 Ni2 O2 P4 Sc2C 1 2/c 128.918; 11.542; 36.001
90; 109.45; 90		11330Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132851 CIFC43 H58 N5 Ni P2 ScP -112.237; 13.83; 15.21
68.64; 72.04; 64.89		2134Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132852 CIFC21 H19 N O2P 1 21/c 110.0187; 15.8815; 10.6953
90; 99.728; 90		1677.28Karjee, Pallab; Debnath, Bijoy; Mandal, Santu; Saha, Sharajit; Punniyamurthy, Tharmalingam
One-pot C-N/C-C bond formation and oxidation of donor-acceptor cyclopropanes with tetrahydroisoquinolines: access to benzo-fused indolizines.
Chemical communications (Cambridge, England), 2024, 60, 4068-4071
7132853 CIFC22 H20 O5P 1 21/n 19.08906; 9.90544; 20.1477
90; 92.251; 90		1812.52Nambu, Hisanori; Onuki, Yuta; Aso, Kana; Kanamori, Momoka; Tomohara, Keisuke; Tsuge, Kiyoshi; Yakura, Takayuki
Ring expansion of spirocyclopropanes with stabilized sulfonium ylides: highly diastereoselective synthesis of cyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 4537-4540
7132854 CIFC21 H14 O2P 1 21/c 18.1483; 18.778; 9.9744
90; 98.77; 90		1508.3Gopalakrishnan, Dinesh Kumar; Bhardwaj, Srashti; Kumar, Sandeep; Karmakar, Tarak; Vaitla, Janakiram
Carbene-mediated stereoselective olefination of vinyl sulfoxonium ylides with diazo compounds and acetals.
Chemical communications (Cambridge, England), 2024, 60, 3846-3849
7132855 CIFC21 H18 O4P -18.487; 10.1115; 10.5324
91.975; 93.296; 108.179		856.01Gopalakrishnan, Dinesh Kumar; Bhardwaj, Srashti; Kumar, Sandeep; Karmakar, Tarak; Vaitla, Janakiram
Carbene-mediated stereoselective olefination of vinyl sulfoxonium ylides with diazo compounds and acetals.
Chemical communications (Cambridge, England), 2024, 60, 3846-3849
7132856 CIFC27 H50 Mn3 N6 O53 P W9P 3 1 c18.9481; 18.9481; 29.4882
90; 90; 120		9168.8Liu, Fangcheng; Han, Shicheng; Dong, Liwei; Fang, Xikui
Functionalized polyoxometalates enable fast ion transport in solid-state batteries at room temperature.
Chemical communications (Cambridge, England), 2024, 60, 4198-4201
7132857 CIFC17 H18 OP 1 21 111.5667; 5.2499; 12.1291
90; 117.369; 90		654.08Wang, Kun; Niu, Saisai; Tang, Weijun; Xue, Dong; Xiao, Jianliang; Li, Hongfeng; Wang, Chao
Ru-catalyzed asymmetric hydrogenation of α,β-unsaturated ketones <i>via</i> a hydrogenation/isomerization cascade.
Chemical communications (Cambridge, England), 2024, 60, 4338-4341
7132858 CIFC30 H45 F5 O2P 1 21 112.4586; 9.2797; 13.4386
90; 105.661; 90		1495.99Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132859 CIFC31 H45 F7 O2P 1 21 112.9607; 8.8159; 13.5926
90; 106.421; 90		1489.74Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132860 CIFC32 H45 F9 O2P 1 21 112.299; 9.2607; 14.5611
90; 94.027; 90		1654.38Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132861 CIFC31 H45 F7 O2P 1 21 112.7803; 9.3254; 13.7005
90; 104.745; 90		1579.07Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132862 CIFC33 H45 F11 O2P 21 21 219.236; 12.542; 29.3792
90; 90; 90		3403.2Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132863 CIFC34 H45 F13 O2P 1 21 113.3455; 8.8735; 14.404
90; 90.499; 90		1705.68Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132864 CIFC44 H53 Ca I N2 O2P 1 21/c 111.1453; 21.6411; 16.4519
90; 99.62; 90		3912.34Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132865 CIFC44 H53 I N2 O2 SrP 1 21/c 111.1365; 21.9592; 16.4408
90; 99.267; 90		3968.1Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132866 CIFC40 H57 N3 O Si2 SrC 1 2/c 122.9542; 9.945; 37.2321
90; 105.936; 90		8172.69Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132867 CIFC35.99 H48.98 Ca N3 Si2C 1 2/c 121.9451; 9.6032; 35.7576
90; 105.893; 90		7247.62Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132868 CIFC88 H64 N16 Pt2C 1 2/m 114.2019; 21.4417; 19.1515
90; 98.888; 90		5761.9van Hilst, Quinn V. C.; Pearcy, Aston C.; Preston, Dan; Wright, L. James; Hartinger, Christian G.; Brooks, Heather J. L.; Crowley, James D.
A dynamic covalent approach to [Pt<sub><i>n</i></sub>L<sub>2<i>n</i></sub>]<sup>2<i>n</i>+</sup> cages.
Chemical communications (Cambridge, England), 2024, 60, 4302-4305
7132869 CIFC100 H80 B4 F16 N16 Pt2P -111.1598; 14.8934; 17.8869
87.192; 75.514; 86.266		2870.67van Hilst, Quinn V. C.; Pearcy, Aston C.; Preston, Dan; Wright, L. James; Hartinger, Christian G.; Brooks, Heather J. L.; Crowley, James D.
A dynamic covalent approach to [Pt<sub><i>n</i></sub>L<sub>2<i>n</i></sub>]<sup>2<i>n</i>+</sup> cages.
Chemical communications (Cambridge, England), 2024, 60, 4302-4305
7132870 CIFC19 H17 Cl N2 O4P -19.6699; 9.6753; 10.4512
76.908; 71.347; 71.318		869.2Porashar, Bikoshita; Behera, Bipin Kumar; Phukon, Hunmoina; Saikia, Anil K.
Synthesis of tetrahydroquinazolines from 2-aminobenzonitriles and alkylidene malonates <i>via</i> 1,4-conjugate addition and an unprecedented rearrangement reaction.
Chemical communications (Cambridge, England), 2024, 60, 4358-4361
7132871 CIFC52 H34.66 Au3 Lu N20 O9.33P b c a19.9815; 23.8662; 23.8919
90; 90; 90		11393.6Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132872 CIFC52 H34.34 Au3 N20 O9.17 TbP b c a20.0668; 23.8472; 23.9197
90; 90; 90		11446.5Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132873 CIFC52 H34.51 Au3 Eu N20 O9.25P b c a20.1041; 23.8591; 23.936
90; 90; 90		11481.3Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132874 CIFC52 H34.4 Au3 Ce N20 O9.2P b c a20.2203; 23.8559; 23.9799
90; 90; 90		11567.3Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132875 CIFC19 H16 O4P 1 21/c 110.9362; 17.792; 8.2146
90; 108.127; 90		1519.04Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333
7132876 CIFC20 H22 O5 SC 1 2/c 121.549; 10.8252; 17.856
90; 113.929; 90		3807.3Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333
7132877 CIFC25 H22 O4P 1 21/c 110.2833; 10.038; 20.688
90; 98.406; 90		2112.6Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333
7132878 CIFC16 H19 N O4P 1 21/n 113.824; 7.5535; 14.7562
90; 100.354; 90		1515.75Feng, Shishen; Liu, Hong; Li, Yan; Fang, Yewen
Photoredox-catalyzed radical-radical cross coupling of ketyl radicals with unstabilized primary alkyl radicals.
Chemical communications (Cambridge, England), 2024, 60, 4431-4434
7132879 CIFC57 H43 Au Br Cl18 Fe N6 OC m m m20.0212; 28.7967; 16.6677
90; 90; 90		9609.7Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132880 CIFC57 H43 Au Br Cl18 Fe N6 OP m m m10.4824; 14.6177; 17.0399
90; 90; 90		2611Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132881 CIFC88 H140 Co Fe N17 O19P m m m10.218; 14.6762; 17.0726
90; 90; 90		2560.2Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132882 CIFC83 H118 Fe2 N16 O15C m m m19.818; 29.05; 16.4847
90; 90; 90		9490.5Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132883 CIFC83 H118 Fe2 N16 O15C m m m20.623; 29.23; 17.01
90; 90; 90		10253.8Lyu, Bang-Heng; Xie, Kai-Ping; Cui, Wen; Chen, Yan-Cong; Chen, Guan-Xi; Wu, Si-Guo; Tong, Ming-Liang
Cyanometallic charge engineering in spin crossover metal-organic frameworks.
Chemical communications (Cambridge, England), 2024, 60, 4318-4321
7132884 CIFC18 H13 N O3P b c a11.248; 11.9893; 21.1722
90; 90; 90		2855.19Liao, Zhi-Yu; Gao, Fan; Ye, Yu-Hang; Yu, Qian-Hui; Yang, Cui; Luo, Qing-Yu; Du, Fei; Pan, Bin; Zhong, Wen-Wu; Liang, Wu
Construction of cyclobutane-fused tetracyclic skeletons <i>via</i> substrate-dependent EnT-enabled dearomative [2+2] cycloaddition of benzofurans (benzothiophenes)/maleimides.
Chemical communications (Cambridge, England), 2024, 60, 4455-4458
7132885 CIFC21 H23 N O3 SP 1 21 110.5669; 8.0829; 11.7127
90; 113; 90		920.87Li, Hongye; Zhou, Yuqiao; Tan, Zheng; Wang, Xiangyu; Zhang, Yuxin; Wang, Fei; Feng, Xiaoming; Liu, Xiaohua
Enantioselective sulfonylation to construct 3-sulfonylated oxindoles.
Chemical communications (Cambridge, England), 2024, 60, 4354-4357
7132886 CIFC20 H16 Br N OP 1 21/c 110.887; 13.619; 11.857
90; 110.116; 90		1650.8Solanke, Pooja R.; Kumar, Prakash; Mainkar, Prathama S.; Nayani, Kiranmai; Chandrasekhar, Srivari
Synthesis of <i>cis</i>-fused cyclopentenone-pyrrolidine scaffolds <i>via</i> sequential aza-Piancatelli and Conia-ene type reactions in one pot.
Chemical communications (Cambridge, England), 2024, 60, 4234-4237
7132887 CIFC26 H21 N OP 1 n 18.577; 16.525; 29.33
90; 98.477; 90		4112Solanke, Pooja R.; Kumar, Prakash; Mainkar, Prathama S.; Nayani, Kiranmai; Chandrasekhar, Srivari
Synthesis of <i>cis</i>-fused cyclopentenone-pyrrolidine scaffolds <i>via</i> sequential aza-Piancatelli and Conia-ene type reactions in one pot.
Chemical communications (Cambridge, England), 2024, 60, 4234-4237
7132888 CIFC58 H46 O10I 1 2/a 17.6531; 20.7577; 37.5707
90; 92.335; 90		5963.6Zhang, Qiaoyu; Luo, Guiwen; Hu, Rui; Yang, Guoqiang; Chen, Jinping; Yu, Tianjun; Zeng, Yi; Li, Yi
Crystalline hydrogen-bonded organic framework for air-tolerant triplet-triplet annihilation upconversion.
Chemical communications (Cambridge, England), 2024, 60, 4475-4478
7132889 CIFC16 H21 N O2C 1 2/c 121.9697; 6.3504; 23.532
90; 114.886; 90		2978.3Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132890 CIFC24 H41 N O4P 21 21 216.372; 21.111; 17.2221
90; 90; 90		2316.7Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132891 CIFC32 H42 N2 O4P -15.6228; 11.5801; 22.772
88.886; 84.246; 83.434		1465.5Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132892 CIFC24 H39 N O3P 21 21 2110.4856; 14.332; 14.635
90; 90; 90		2199.3Liu, Ruzhang; Wang, Juan; Wu, Hao; Quan, Xianfeng; Wang, Shilin; Guo, Jiandong; Wang, Yang; Li, Heting
Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.
Chemical communications (Cambridge, England), 2024, 60, 4362-4365
7132893 CIFC35 H41 Cl4 O P RuP 1 21 110.0658; 15.252; 11.7038
90; 110.346; 90		1684.71Boym, Mikhail A.; Pototskiy, Roman A.; Podyacheva, Evgeniya S.; Chusov, Denis A.; Nelyubina, Yulia V.; Perekalin, Dmitry S.
Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C-H activation.
Chemical communications (Cambridge, England), 2024, 60, 4491-4494
7132894 CIFC15 H19 Br N2 O2P 1 21 17.049; 11.48; 19.45
90; 98.623; 90		1556.2Boym, Mikhail A.; Pototskiy, Roman A.; Podyacheva, Evgeniya S.; Chusov, Denis A.; Nelyubina, Yulia V.; Perekalin, Dmitry S.
Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C-H activation.
Chemical communications (Cambridge, England), 2024, 60, 4491-4494
7132895 CIFC28 H40 Cl4 Ru2P 1 21/c 112.2863; 18.7694; 12.3374
90; 93.047; 90		2841.06Boym, Mikhail A.; Pototskiy, Roman A.; Podyacheva, Evgeniya S.; Chusov, Denis A.; Nelyubina, Yulia V.; Perekalin, Dmitry S.
Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C-H activation.
Chemical communications (Cambridge, England), 2024, 60, 4491-4494
7132896 CIFC46 H55 Cl2 N2 O2 SbC 1 c 120.0826; 14.1346; 15.2463
90; 100.815; 90		4250.9Agou, Tomohiro; Kuroiwa, Shunsuke; Fukumoto, Hiroki; Nabeshima, Tatsuya
Synthesis and optical properties of antimony(V) complexes of a trianionic N<sub>2</sub>O<sub>2</sub>-type tetradentate dipyrrin ligand.
Chemical communications (Cambridge, England), 2024, 60, 4557-4560
7132897 CIFC49 H62 Cl N2 O4 SbP 1 21/c 124.3993; 16.832; 11.663
90; 100.297; 90		4712.7Agou, Tomohiro; Kuroiwa, Shunsuke; Fukumoto, Hiroki; Nabeshima, Tatsuya
Synthesis and optical properties of antimony(V) complexes of a trianionic N<sub>2</sub>O<sub>2</sub>-type tetradentate dipyrrin ligand.
Chemical communications (Cambridge, England), 2024, 60, 4557-4560
7132898 CIFC46 H57 N2 O4 SbP b c a28.4574; 27.9101; 32.3437
90; 90; 90		25688.9Agou, Tomohiro; Kuroiwa, Shunsuke; Fukumoto, Hiroki; Nabeshima, Tatsuya
Synthesis and optical properties of antimony(V) complexes of a trianionic N<sub>2</sub>O<sub>2</sub>-type tetradentate dipyrrin ligand.
Chemical communications (Cambridge, England), 2024, 60, 4557-4560
7132899 CIFC31 H37 N O3 S SiP -19.462; 9.6433; 17.6776
75.612; 75.789; 87.111		1514.5Zhang, Zhen; Lu, Lichao; Li, Guiling; Sheng, Xiaoyu; Zhang, Yijia; Yang, Lin; Zhao, Jiaqi; Xie, Lei; Li, Jiazhu; Sun, Kai
Radical cascade silylation/cyclization of 1,7-dienes to access silyl-substituted benzo[<i>b</i>]azepin-2-ones.
Chemical communications (Cambridge, England), 2024, 60, 4206-4209
7132900 CIFC17 H10 N2P 21 21 214.5044; 12.6636; 19.6473
90; 90; 90		1120.72Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132901 CIFC24 H14 N2 OP -17.6716; 9.16801; 12.73071
106.171; 91.1629; 109.967		801.64Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132902 CIFC25 H14 N2P 21 21 215.7818; 12.8402; 21.6872
90; 90; 90		1610.05Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132903 CIFC17 H12 N2 OC 1 2/c 116.3278; 7.4345; 21.1425
90; 99.071; 90		2534.37Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132904 CIFC23 H16 N2 OP 1 21/c 112.43235; 12.20419; 11.52302
90; 102.48; 90		1707.04Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132905 CIFC17 H9 N3 OP 1 21/c 13.77916; 16.2226; 19.1757
90; 93.565; 90		1173.35Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132906 CIFC23 H16 N2 OP -18.22512; 10.0169; 12.1195
104.088; 101.613; 109.165		870.66Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132907 CIFC19 H12 N2P 1 21/n 117.6032; 3.8528; 18.9019
90; 99.58; 90		1264.08Sadaphal, Vikas Ashokrao; Wu, Tien-Lin; Liu, Rai-Shung
Synthesis of two nitrogen-containing polyaromatic compounds through gold catalysis/DBU-promoted cyclizations.
Chemical communications (Cambridge, England), 2024, 60, 4294-4297
7132908 CIFC18 H21 N O6P 1 21/c 111.5445; 11.4051; 12.9631
90; 93.189; 90		1704.16Wen, Yongshun; Jin, Hong-Xian; Qiu, Yan-Hua; Zong, Yingtong; Luo, Wenjun; Chen, Zhengwang; Yu, Daohong
Photo-induced tungsten-catalyzed cascade synthesis of pyrrolo[2,1-<i>a</i>]isoquinoline-1,3-dicarboxylate and its reaction mechanism.
Chemical communications (Cambridge, England), 2024, 60, 4573-4576
7132909 CIFC44 H44 O10P -115.186; 15.823; 16.474
69.815; 88.884; 81.886		3676.4Soliman, Luc; Ramassamy, Elsa; Dujarric, Katia; Naulet, Guillaume; Dechambenoit, Pierre; Bock, Harald; Durola, Fabien
Coronenes with push-pull geometries from macrocycle-forming Perkin condensations.
Chemical communications (Cambridge, England), 2024, 60, 4439-4442
7132910 CIFC36 H28 O8P -16.9314; 13.781; 16.068
86.662; 82.997; 76.021		1477.62Soliman, Luc; Ramassamy, Elsa; Dujarric, Katia; Naulet, Guillaume; Dechambenoit, Pierre; Bock, Harald; Durola, Fabien
Coronenes with push-pull geometries from macrocycle-forming Perkin condensations.
Chemical communications (Cambridge, England), 2024, 60, 4439-4442
7132911 CIFC38 H38 B Cl4 F6 N S SbP c c n8.895; 16.5456; 27.257
90; 90; 90		4011.5Cosby, Taylor P. L.; Bhattacharjee, Avik; Henneberry, Samantha K.; LeBlanc, Jesse; Caputo, Christopher B.
Unlocking Lewis acidity <i>via</i> the redox non-innocence of a phenothiazine-substituted borane.
Chemical communications (Cambridge, England), 2024, 60, 5391-5394
7132912 CIFC20 H14 N2 O6 WC 1 2/c 116.6532; 10.7273; 11.4809
90; 103.498; 90		1994.3Song, Heng; Xiao, Yuting; Wei, Jingjing; Liu, Yuzan; Yang, Liqing; Bai, Pengtao; Yang, Fu; Yu, Kai; Xu, Chen; Cai, Xingwei
Low-valent-tungsten catalysis enables hydroboration of esters and nitriles.
Chemical communications (Cambridge, England), 2024, 60, 5026-5029
7132913 CIFC10 H14 Br4 F N2 ZnP 1 21/c 18.0955; 20.9526; 9.8012
90; 102.25; 90		1624.64Wang, Yu-Yin; Kang, Huai-Yuan; Zhang, Shao-Ya; Qu, Hao; Zhu, Lin; Zhao, Dan; Li, Xian-Feng; Lei, Xiao-Wu; Yue, Cheng-Yang
Exploring 0D lead-free metal halide with highly efficient blue light emission and high-sensitivity photodetection.
Chemical communications (Cambridge, England), 2024, 60, 2784-2787
7132914 CIFC21 H28 Cl2 Co N3P 1 21/n 110.4791; 15.9525; 12.9626
90; 99.6049; 90		2136.55Boity, Biswaranjan; Sidiqque, Misba; Rit, Arnab
Amine-functionalized bifunctional Co<sup>III</sup>-NHC complexes: highly effective phosphine-free catalysts for the α-alkylation of nitriles.
Chemical communications (Cambridge, England), 2024, 60, 3142-3145
7132915 CIFC16 H11 N3 OP 21 21 213.741; 17.187; 18.371
90; 90; 90		1181.19Sarkar, Souradip; Bhunya, Sourav; Pan, Subarna; Datta, Arnadeep; Roy, Lisa; Samanta, Rajarshi
Rh(II)-catalysed <i>N</i><sup>2</sup>-selective arylation of benzotriazoles and indazoles using quinoid carbenes <i>via</i> 1,5-H shift.
Chemical communications (Cambridge, England), 2024, 60, 4727-4730
7132916 CIFC17 H12 N2 OP b c a11.511; 10.247; 21.356
90; 90; 90		2519Sarkar, Souradip; Bhunya, Sourav; Pan, Subarna; Datta, Arnadeep; Roy, Lisa; Samanta, Rajarshi
Rh(II)-catalysed <i>N</i><sup>2</sup>-selective arylation of benzotriazoles and indazoles using quinoid carbenes <i>via</i> 1,5-H shift.
Chemical communications (Cambridge, England), 2024, 60, 4727-4730
7132917 CIFC31 H29 N O5P -110.8447; 11.198; 12.0881
101.529; 90.637; 113.153		1315.93Pramanik, Sourav; Hazra, Subhadeep; Chatterjee, Ayan; Saha, Jaideep
Hydrogen bonding-promoted tunable approach for access to aza-bicyclo-[3.3.0]octanes and cyclopenta[<i>b</i>] pyrroles.
Chemical communications (Cambridge, England), 2024, 60, 4922-4925
7132918 CIFC56 H40 As4 Cl4 Cu4 Mo8 O16 Sb4P -115.055; 15.1827; 17.1422
89.358; 89.116; 69.16		3661.4Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132919 CIFC15 H12 As Cl2 Cu I Mo2 O4 SbP 1 21/n 110.4347; 15.6404; 13.4725
90; 92.374; 90		2196.86Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132920 CIFC56 H40 As4 Br4 Cu4 Mo8 O16 Sb4P -114.9733; 15.0851; 17.339
89.022; 88.933; 70.588		3692.9Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132921 CIFC67 H25 Al As2 Cl2 Cu F46 Mo4 N O11 Sb2P 1 21/c 120.9582; 33.303; 12.1289
90; 105.237; 90		8168.03Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132922 CIFC129 H42 Ag2 Al2 As4 Cl2 F92 Mo8 O22 Sb4P 1 21/n 111.4664; 40.5323; 33.5837
90; 91.704; 90		15601.4Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132923 CIFC108.8 H34.6 Al2 As2 Cl5.6 Cu2 F92 Mo4 N3 O14 Sb2P 1 21/n 123.6343; 19.0078; 31.4538
90; 98.5123; 90		13974.5Elsayed Moussa, Mehdi; Shelyganov, Pavel A.; Seidl, Michael; Zimmermann, Lisa; Scheer, Manfred
Supramolecular compounds assembled from the heteroleptic tetrahedral complex [{CpMo(CO)<sub>2</sub>}<sub>2</sub>(μ,η<sup>2</sup>-AsSb)] and metal salts.
Chemical communications (Cambridge, England), 2024, 60, 4703-4706
7132924 CIFC30 H30 Si3P 1 21/c 19.9325; 18.2411; 15.0008
90; 102.356; 90		2654.89Wakefield, 4th, Herbert; Melvin, Sophia J.; Jiang, Jennifer; Kevlishvili, Ilia; Siegler, Maxime A.; Craig, Stephen L.; Kulik, Heather J.; Klausen, Rebekka S.
Angle-strained sila-cycloalkynes.
Chemical communications (Cambridge, England), 2024, 60, 4842-4845
7132925 CIFC37 H37 N3 Si3P 1 21/c 112.98096; 26.6317; 10.50266
90; 91.5598; 90		3629.48Wakefield, 4th, Herbert; Melvin, Sophia J.; Jiang, Jennifer; Kevlishvili, Ilia; Siegler, Maxime A.; Craig, Stephen L.; Kulik, Heather J.; Klausen, Rebekka S.
Angle-strained sila-cycloalkynes.
Chemical communications (Cambridge, England), 2024, 60, 4842-4845
7132926 CIFC32 H36 Si4P 1 21/c 124.3501; 11.0409; 25.4353
90; 115.708; 90		6161.3Wakefield, 4th, Herbert; Melvin, Sophia J.; Jiang, Jennifer; Kevlishvili, Ilia; Siegler, Maxime A.; Craig, Stephen L.; Kulik, Heather J.; Klausen, Rebekka S.
Angle-strained sila-cycloalkynes.
Chemical communications (Cambridge, England), 2024, 60, 4842-4845
7132927 CIFC35 H25 N O2 SP -18.8511; 10.7751; 14.2389
81.33; 88.876; 74.316		1292.16Malik, Nirmal; De, Ritobrata; Pal, Santanu Kumar; Ramasastry, S. S. V.
A one-pot telescopic synthesis of benzo[<i>b</i>]carbazoles and exploration of their liquid crystalline properties.
Chemical communications (Cambridge, England), 2024, 60, 4797-4800
7132928 CIFC90 H80 B2 N6 Ni2 O4C 1 2/c 132.431; 24.9205; 24.931
90; 123.299; 90		16841Patra, Suman; Atta, Sayan; Ghosh, Soumili; Majumdar, Amit; Dey, Abhishek
Kinetic isotope effect offers selectivity in CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 4826-4829
7132929 CIFC19 H22 Cl N3 Ni O7P 1 21/c 19.1074; 16.575; 14.4535
90; 107.064; 90		2085.8Patra, Suman; Atta, Sayan; Ghosh, Soumili; Majumdar, Amit; Dey, Abhishek
Kinetic isotope effect offers selectivity in CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 4826-4829
7132930 CIFC62 H66 N6 O17 P4 U2C 1 2/c 131.0258; 12.8733; 16.8307
90; 114.157; 90		6133.6Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132931 CIFC28 H26 N2 O2 P2P 1 21/c 110.1143; 28.2649; 8.4249
90; 98.202; 90		2383.87Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132932 CIFC56 H52 N10 O28 P4 U3P 1 21/c 119.1125; 10.6852; 17.9947
90; 107.716; 90		3500.6Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132933 CIFC28 H26 N2 O2 P2P -18.231; 11.7984; 13.6524
73.829; 85.363; 76.865		1239.83Yang, Xiaofan; Fang, Dong; Wang, Shihui; Tian, Zhenjiang; Xu, Lei; Liu, Jiyong; Zhang, Anyun; Xiao, Chengliang
Epimerization effects on coordination behaviours of phenanthroline-based phosphine-oxide ligands with uranyl ions.
Chemical communications (Cambridge, England), 2024, 60, 5042-5045
7132934 CIFC72 H98 S2 TmP -113.2573; 14.2636; 18.3627
104.34; 93.693; 98.57		3307.9Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132935 CIFC72 H98 I Nd S2P -113.3492; 14.1047; 18.6556
102.433; 94.721; 99.287		3360.2Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132936 CIFC72 H98 Nd S2P -113.2169; 14.2162; 18.5245
104.917; 93.8221; 97.9184		3312.3Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132937 CIFC72 H98 I La S2P -113.2786; 14.2335; 18.678
102.71; 94.255; 99.004		3379.5Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132938 CIFC72 H98 I0.13 La S2P -113.209; 14.2623; 18.5499
104.544; 93.628; 98.433		3327.73Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132939 CIFC84 H108 N2 S2 SmP b c n16.0032; 18.7417; 24.3011
90; 90; 90		7288.6Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132940 CIFC84 H108 N2 Nd S2P b c n15.9566; 18.7918; 24.254
90; 90; 90		7272.6Gilbert-Bass, Kito; Stennett, Cary R.; Grotjahn, Robin; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Exploring sulfur donor atom coordination chemistry with La(II), Nd(II), and Tm(II) using a terphenylthiolate ligand.
Chemical communications (Cambridge, England), 2024, 60, 4601-4604
7132941 CIFC17 H22 N2 O2 SP 1 21 110.9048; 14.2184; 11.9956
90; 110.377; 90		1743.51Wei, Tao; Xie, Ming-Sheng; Guo, Hai-Ming
Construction of thioglycoside bonds <i>via</i> an asymmetric organocatalyzed sulfa-Michael/aldol reaction: access to 4'-thionucleosides.
Chemical communications (Cambridge, England), 2024, 60, 5018-5021
7132942 CIFC23 H18 N2 O SP 1 21/n 18.252; 14.7387; 15.4992
90; 96.548; 90		1872.8Wang, Xinxin; Wang, Jie; Ji, Meishan; Wu, Xinxin; Zhu, Chen
<i>Z</i>-selective radical difunctionalization of aromatic alkynes: synthesis of multi-substituted triarylethenes.
Chemical communications (Cambridge, England), 2024, 60, 4894-4897
7132943 CIFC23 H16 F N O SC 1 2/c 112.5347; 15.7748; 19.3093
90; 98.0108; 90		3780.8Wang, Xinxin; Wang, Jie; Ji, Meishan; Wu, Xinxin; Zhu, Chen
<i>Z</i>-selective radical difunctionalization of aromatic alkynes: synthesis of multi-substituted triarylethenes.
Chemical communications (Cambridge, England), 2024, 60, 4894-4897
7132944 CIFC100 H86 N2 O32 P4 W10P -113.5793; 15.3135; 15.4699
117.216; 113.848; 92.658		2508.49Gu, Chen; Yatabe, Takafumi; Yamaguchi, Kazuya; Suzuki, Kosuke
Photocatalytic aerobic α-oxygenation of amides to imides using a highly durable decatungstate tetraphenylphosphonium salt.
Chemical communications (Cambridge, England), 2024, 60, 4906-4909
7132945 CIFC41.5 H21.5 Cl0.25 N5 O5.5P 1 21/m 112.7611; 18.5038; 14.1018
90; 100.643; 90		3272.56Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132946 CIFC81.46 H39.92 Cl0.92 N9 O6I 1 2/a 130.8326; 13.5754; 31.1005
90; 106.96; 90		12451.4Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132947 CIFC153 H47 Cl4 N9 O6P 1 21/n 113.0791; 32.0488; 27.0224
90; 94.916; 90		11285.3Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132948 CIFC163 H47 Cl4 N9 O6P 1 21/n 126.5926; 32.943; 30.1206
90; 113.007; 90		24288Zhang, Fan; Du, Xu-Sheng; Song, Kui-Zhu; Han, Ying; Lu, Hai-Yan; Chen, Chuan-Feng
A calix[3]carbazole-based cavitand: synthesis, structure and its complexation with fullerenes.
Chemical communications (Cambridge, England), 2024, 60, 4962-4965
7132949 CIFC20 H6 Cl8 NP 1 21/c 114.0305; 8.0731; 18.9296
90; 94.608; 90		2137.2Lv, Kuo; Zhang, Minzhe; Xia, Xin; Liu, Wenjing; Wan, Keke; Zhang, Ming; Li, Feng
Cyano modified triphenylmethyl radical skeletons: higher stability and efficiency.
Chemical communications (Cambridge, England), 2024, 60, 4846-4849
7132950 CIFC21 H6 Cl7 N2P -18.2197; 11.2036; 13.6336
67.189; 84.761; 73.004		1106.4Lv, Kuo; Zhang, Minzhe; Xia, Xin; Liu, Wenjing; Wan, Keke; Zhang, Ming; Li, Feng
Cyano modified triphenylmethyl radical skeletons: higher stability and efficiency.
Chemical communications (Cambridge, England), 2024, 60, 4846-4849
7132951 CIFC26 H22 Cl N O2P -17.7575; 11.8553; 12.4714
68.379; 88.015; 75.886		1032.14Sui, Jia-Li; Zhong, Long-Jin; Xiong, Bi-Quan; Tang, Ke-Wen; Liu, Yu
Regioselective synthesis of N-containing polycyclic compounds <i>via</i> radical annulation cyclization of 1,7-dienes with aldehydes.
Chemical communications (Cambridge, England), 2024, 60, 4834-4837
7132952 CIFC16 H19 N O2P 1 21/c 116.3685; 10.1416; 33.0222
90; 92.147; 90		5477.93Liu, Zhaosheng; Ji, Xiaochen; Duan, Lilan; Deng, Guo-Jun; Huang, Huawen
Accessing pyrrolo[1,2-<i>a</i>]indole derivatives <i>via</i> visible-light-induced dearomatizative cyclization of indoles.
Chemical communications (Cambridge, England), 2024, 60, 4902-4905
7132953 CIFC13 H15 N O2P 1 21/c 119.4445; 8.085; 15.4094
90; 111.936; 90		2247.1Liu, Zhaosheng; Ji, Xiaochen; Duan, Lilan; Deng, Guo-Jun; Huang, Huawen
Accessing pyrrolo[1,2-<i>a</i>]indole derivatives <i>via</i> visible-light-induced dearomatizative cyclization of indoles.
Chemical communications (Cambridge, England), 2024, 60, 4902-4905
7132954 CIFC40 H36 N2 O2P -112.0197; 12.0255; 13.0084
87.125; 64.484; 67.794		1556.7Ishikawa, Shuhei; Sakamaki, Daisuke; Gon, Masayuki; Tanaka, Kazuo; Fujiwara, Hideki
Solvent-free synthesis and chiroptical properties of a C-N axially chiral cruciform dimer of benzo[<i>b</i>]phenoxazine.
Chemical communications (Cambridge, England), 2024, 60, 4946-4949
7132955 CIFC43 H43 N2 O2P 112.3589; 12.8347; 22.1604
79.4229; 87.2486; 87.6565		3449.59Ishikawa, Shuhei; Sakamaki, Daisuke; Gon, Masayuki; Tanaka, Kazuo; Fujiwara, Hideki
Solvent-free synthesis and chiroptical properties of a C-N axially chiral cruciform dimer of benzo[<i>b</i>]phenoxazine.
Chemical communications (Cambridge, England), 2024, 60, 4946-4949
7132956 CIFC43 H43 N2 O2P 112.3589; 12.8455; 22.1587
79.4344; 87.2227; 87.6319		3452.24Ishikawa, Shuhei; Sakamaki, Daisuke; Gon, Masayuki; Tanaka, Kazuo; Fujiwara, Hideki
Solvent-free synthesis and chiroptical properties of a C-N axially chiral cruciform dimer of benzo[<i>b</i>]phenoxazine.
Chemical communications (Cambridge, England), 2024, 60, 4946-4949
7132957 CIFC18 H17 N O2P 1 21/c 16.3783; 7.1006; 31.5404
90; 93.88; 90		1425.18Gao, Ying; Wang, Mingxu; Sun, Jingxian; Zhao, Xiao-Jing; He, Yonghui
Electrochemical-induced solvent-tuned selective C(sp<sup>3</sup>)-H bond activation towards the synthesis of C3-functionalized chromone derivatives.
Chemical communications (Cambridge, England), 2024, 60, 5050-5053
7132958 CIFC50 H45 B2 F4 N5 O2P -112.912; 16.473; 22.588
71.34; 83.507; 79.792		4471.7Wang, Long; Cheng, Cheng; Yu, Changjiang; Wu, Qinghua; Kang, Zhengxin; Wang, Hua; Jiao, Lijuan; Hao, Erhong
NIR-absorbing and emitting α,α-nitrogen-bridged BODIPY dimers with strong excitonic coupling.
Chemical communications (Cambridge, England), 2024, 60, 5054-5057
7132959 CIFC17 H14 F N OP n a 2112.4495; 20.4914; 5.0901
90; 90; 90		1298.52Liu, Hongxin; Tang, Tingyu; Li, Bin; Wang, Baiquan
Manganese(I)-catalyzed nucleophilic addition of C(sp<sup>3</sup>)-H bonds to aldehydes.
Chemical communications (Cambridge, England), 2024, 60, 5066-5069
7132960 CIFC14 H8 Mn N O4P 1 21/n 17.631; 8.00772; 20.9823
90; 98.411; 90		1268.37Liu, Hongxin; Tang, Tingyu; Li, Bin; Wang, Baiquan
Manganese(I)-catalyzed nucleophilic addition of C(sp<sup>3</sup>)-H bonds to aldehydes.
Chemical communications (Cambridge, England), 2024, 60, 5066-5069
7132961 CIFC34 H34 S2R -3 :H37.256; 37.256; 5.1212
90; 90; 120		6155.9Su, Yangzhe; Wang, Min; Xu, Jianping; Chen, Weinan; Zhou, Gang
C-H arylation of thiopyran derivatives with aryl halides.
Chemical communications (Cambridge, England), 2024, 60, 5193-5196
7132962 CIFC30 H22 SP 1 21/c 114.9168; 5.1215; 80.8465
90; 92.323; 90		6171.3Su, Yangzhe; Wang, Min; Xu, Jianping; Chen, Weinan; Zhou, Gang
C-H arylation of thiopyran derivatives with aryl halides.
Chemical communications (Cambridge, England), 2024, 60, 5193-5196
7132963 CIFC27 H24 SP -112.0192; 13.1986; 13.5978
91.326; 92.661; 113.371		1975.96Su, Yangzhe; Wang, Min; Xu, Jianping; Chen, Weinan; Zhou, Gang
C-H arylation of thiopyran derivatives with aryl halides.
Chemical communications (Cambridge, England), 2024, 60, 5193-5196
7132964 CIFC19 H19 F3 N2P 1 21/c 110.34; 15.24; 11.008
90; 94.938; 90		1728.2Yang, Ming; Meng, Yu-Xuan; Mehfooz, Haroon; Zhao, Yu-Long
Visible light-promoted [3+2] cyclization reaction of vinyl azides with perfluoroalkyl-substituted-imidoyl sulfoxonium ylides.
Chemical communications (Cambridge, England), 2024, 60, 5407-5410
7132965 CIFC34 H33 N O2P 1 21/c 121.901; 11.9356; 10.1958
90; 95.864; 90		2651.3Pramanik, Shyamal; Samanta, Apurba; Maity, Soumitra
A two carbon homologation of Friedel-Crafts alkylation enabled by photochemical alkene stitching: modular assembly of cyclolignans.
Chemical communications (Cambridge, England), 2024, 60, 5282-5285
7132966 CIFC22 H26 O6P 1 21/c 113.0879; 11.0775; 14.0938
90; 102.597; 90		1994.1Pramanik, Shyamal; Samanta, Apurba; Maity, Soumitra
A two carbon homologation of Friedel-Crafts alkylation enabled by photochemical alkene stitching: modular assembly of cyclolignans.
Chemical communications (Cambridge, England), 2024, 60, 5282-5285
7132967 CIFC18 H16 N12 O8 S Zn3P 1 21/c 114.143; 9.9829; 25.111
90; 96.777; 90		3520.6Deng, Yu-Xin; Yang, Guo-Ping; Wang, Yao-Yu
Pure separation of acetylene based on a sulfonic acid and amino group functionalized Zn-MOF.
Chemical communications (Cambridge, England), 2024, 60, 5046-5049
7132968 CIFC18 H14 N12 O7 S Zn3P 1 21/c 114.0795; 9.851; 25.9541
90; 95.909; 90		3580.6Deng, Yu-Xin; Yang, Guo-Ping; Wang, Yao-Yu
Pure separation of acetylene based on a sulfonic acid and amino group functionalized Zn-MOF.
Chemical communications (Cambridge, England), 2024, 60, 5046-5049
7132969 CIFC32 H28 Cl2 O8P -19.951; 10.5842; 14.9945
96.395; 99.389; 117.914		1344.5Kelsey, Shaun R.; Griaznov, Georgii; Spaeth, Andrew D.; Janzen, Daron E.; Douglas, Justin T.; Thompson, Ward H.; Barybin, Mikhail V.
Tuning the redox profile of the 6,6'-biazulenic platform through functionalization along its molecular axis.
Chemical communications (Cambridge, England), 2024, 60, 5213-5216
7132970 CIFFe Nb Te2P 1 21/c 17.28; 6.305; 7.992
90; 92.33; 90		366.5Stepanova, Anna V.; Mironov, Andrei V.; Bogach, Alexey V.; Azarevich, Andrey N.; Presniakov, Igor A.; Sobolev, Alexey V.; Pankratov, Denis A.; Zayakhanov, Vladimir A.; Starchikov, Sergey S.; Verchenko, Valeriy Yu; Shevelkov, Andrei V.
Bulk ferromagnetism in cleavable van der Waals telluride NbFeTe<sub>2</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5518-5521
7132971 CIFC52 H46 F3 Fe N3 P2P -111.711; 12.5996; 16.8271
96.344; 100.608; 116.094		2139.53Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132972 CIFC48 H50 Fe N4 P2P -110.7765; 13.6127; 14.6156
90.015; 96.865; 100.703		2091.1Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132973 CIFC60 H52 F6 Fe N2 O P2P -113.4659; 13.8415; 14.7796
93.409; 105.088; 106.332		2526.2Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132974 CIFC78 H64 F4 Fe N2 P2C 1 2/c 129.4666; 13.8824; 16.5411
90; 114.212; 90		6171.2Stevens, Jeremiah E.; Miller, Justin D.; Fitzsimmons, Matthew C.; Moore, Curtis E.; Thomas, Christine M.
<i>Z</i>-selective dimerization of terminal alkynes by a (PNNP)Fe<sup>II</sup> complex.
Chemical communications (Cambridge, England), 2024, 60, 5169-5172
7132975 CIFC26 H20 N2 O3I 1 2/a 115.6096; 16.4461; 16.1674
90; 96.743; 90		4121.74Zhao, Shuang; Chen, Mengxiao; Zhou, Wenlu; Ni, Dan; Li, Zhenghua; Nie, Shenyou; He, Yi
Green synthesis for diverse bioactive benzo-fused spiroindolines through DBU-catalysed post-Ugi double cyclization.
Chemical communications (Cambridge, England), 2024, 60, 5455-5458
7132976 CIFC28 H18 N2 O4P -110.0719; 10.5354; 10.8948
92.2576; 111.172; 93.0417		1074.38Akbari, Alireza; Khosravi, Hormoz; Bauer, Felix; Rominger, Frank; Breit, Bernhard; Balalaie, Saeed
Metal- and solvent-free domino reaction of 2-isocyanophenol esters to benzoxazines: long-range 1,5-acyl migration on 1,4-diazabutatriene.
Chemical communications (Cambridge, England), 2024, 60, 5451-5454
7132977 CIFC16 H13 N O3P -16.7066; 8.7863; 12.6844
100.298; 96.3058; 111.389		672.14Akbari, Alireza; Khosravi, Hormoz; Bauer, Felix; Rominger, Frank; Breit, Bernhard; Balalaie, Saeed
Metal- and solvent-free domino reaction of 2-isocyanophenol esters to benzoxazines: long-range 1,5-acyl migration on 1,4-diazabutatriene.
Chemical communications (Cambridge, England), 2024, 60, 5451-5454
7132978 CIFC97 H203 Ag45 Nb6 O47 S23P b c a28.7435; 28.3372; 48.7703
90; 90; 90		39723.9Zhao, Zichen; Zhao, Mengyun; Deng, Lan; Li, Qing; Zhang, Jing; Su, Haifeng; Lv, Hongjin; Yang, Guo-Yu
Two structurally new Lindqvist hexaniobate-templated silver thiolate clusters.
Chemical communications (Cambridge, England), 2024, 60, 5415-5418
7132979 CIFC82 H210 Ag41 K Nb6 O42.5 S26.5P 42 21 232.1512; 32.1512; 17.6732
90; 90; 90		18268.8Zhao, Zichen; Zhao, Mengyun; Deng, Lan; Li, Qing; Zhang, Jing; Su, Haifeng; Lv, Hongjin; Yang, Guo-Yu
Two structurally new Lindqvist hexaniobate-templated silver thiolate clusters.
Chemical communications (Cambridge, England), 2024, 60, 5415-5418
7132980 CIFC32 H72 Cu2 I4 P2P -112.4248; 12.9746; 16.828
86.253; 75.221; 64.491		2364.3Delafoulhouze, Jérémy; Cordier, Marie; Mevellec, Jean-Yves; Massuyeau, Florian; Hernandez, Olivier; Latouche, Camille; Perruchas, Sandrine
Mechanoresponsive luminescence triggered by phase transition of a supercooled copper(I) complex.
Chemical communications (Cambridge, England), 2024, 60, 5278-5281
7132981 CIFC8 H3 O5 TiI 41 2 215.1203; 15.1203; 11.9863
90; 90; 90		2740.35Zeng, Xiangdi; Li, Jiangnan; He, Meng; Lu, Wanpeng; Crawshaw, Danielle; Guo, Lixia; Ma, Yujie; Kippax-Jones, Meredydd; Cheng, Yongqiang; Manuel, Pascal; Rudić, Svemir; Frogley, Mark D.; Schröder, Martin; Yang, Sihai
High adsorption of ammonia in a titanium-based metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 5912-5915
7132982 CIFC8 H3 D1.25 N0.42 O5 TiI 41 2 215.0507; 15.0507; 12.0595
90; 90; 90		2731.8Zeng, Xiangdi; Li, Jiangnan; He, Meng; Lu, Wanpeng; Crawshaw, Danielle; Guo, Lixia; Ma, Yujie; Kippax-Jones, Meredydd; Cheng, Yongqiang; Manuel, Pascal; Rudić, Svemir; Frogley, Mark D.; Schröder, Martin; Yang, Sihai
High adsorption of ammonia in a titanium-based metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 5912-5915
7132983 CIFC8 H3 D3.82 N1.27 O5 TiI 41 2 214.92; 14.92; 12.1536
90; 90; 90		2705.47Zeng, Xiangdi; Li, Jiangnan; He, Meng; Lu, Wanpeng; Crawshaw, Danielle; Guo, Lixia; Ma, Yujie; Kippax-Jones, Meredydd; Cheng, Yongqiang; Manuel, Pascal; Rudić, Svemir; Frogley, Mark D.; Schröder, Martin; Yang, Sihai
High adsorption of ammonia in a titanium-based metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 5912-5915
7132984 CIFC36 H32 N2 O11 Pb2P 1 21/n 116.46; 11.3441; 19.5207
90; 94.325; 90		3634.6Luo, Qi; Li, Yuxia; Huang, Xin; Zheng, Yi; Gu, Qi; Wang, Shuaihua; Wu, Shaofan
Tetraphenylene-based semiconductive metal-organic framework crystals for direct X-ray detection and imaging.
Chemical communications (Cambridge, England), 2024, 60, 5510-5513
7132985 CIFC19 H15 Cl2 N O3P 1 21/c 116.1234; 11.9822; 8.9939
90; 94.945; 90		1731.1Harsha, ?; Kumar, Rohit; Jain, Nidhi
<sup>1</sup>O<sub>2</sub> mediated synthesis of carbonyl substituted quinoline-2,4(1<i>H</i>,3<i>H</i>)-diones in visible light: 4CzIPN as a reusable photocatalyst.
Chemical communications (Cambridge, England), 2024, 60, 5646-5649
7132986 CIFC148 H188 F12 Fe2 N18 O28 S4P 1 21/m 116.4651; 23.3184; 17.2067
90; 97.467; 90		6550.3Mobili, Riccardo; Preda, Giovanni; Dondi, Daniele; Monzani, Enrico; Vadivel, Dhanalakshmi; Massera, Chiara; Pasini, Dario; Amendola, Valeria
Triptycene-based diiron(II) mesocates: spin-crossover in solution.
Chemical communications (Cambridge, England), 2024, 60, 5522-5525
7132987 CIFC246 H340 F12 N34 O33 P2P -121.5297; 24.7451; 29.6954
109.868; 104.145; 101.331		13733.1Huang, Song; Wang, Zhenwen; Wu, Jinyang; Mai, Xinyan; Qin, Song; Zhou, Yuqiao; Yuan, Daqiang; Li, Xiaowei; Feng, Wen; Yuan, Lihua
A molecular sheaf: doubly threaded [6]rotaxane.
Chemical communications (Cambridge, England), 2024, 60, 5622-5625
7132988 CIFC16 H24 Au B3 F12 N8C 1 2/c 115.3073; 15.711; 22.0225
90; 99.885; 90		5217.63Barwise, Lachlan; Moon, Lachlan J.; Dhakal, Bibidh; Hogan, Conor F.; White, Keith F.; Dutton, Jason L.
An extremely electron poor Au(III) trication bearing acetonitrile ligands.
Chemical communications (Cambridge, England), 2024, 60, 5586-5589
7132989 CIFC21 H29 Au B2 F8 N6P 1 21 19.4083; 19.422; 15.7483
90; 103.473; 90		2798.46Barwise, Lachlan; Moon, Lachlan J.; Dhakal, Bibidh; Hogan, Conor F.; White, Keith F.; Dutton, Jason L.
An extremely electron poor Au(III) trication bearing acetonitrile ligands.
Chemical communications (Cambridge, England), 2024, 60, 5586-5589
7132990 CIFC198 H251 N6 O46P 1 21/n 122.4005; 26.9673; 32.2242
90; 90.916; 90		19463.5Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132991 CIFC152.46 H189.38 N6 O23.23 S13.23P -121.1953; 26.1285; 31.3285
73.564; 72.242; 68.045		15042Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132992 CIFC190 H208 N6 O58C 1 2/c 139.4383; 27.5839; 35.2015
90; 109.998; 90		35985.4Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132993 CIFC174 H256 N6 O34 S24P 63 2 219.9064; 19.9064; 33.451
90; 90; 120		11479.6Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132994 CIFC138 H148 N6 O16 S6P -121.6989; 27.1612; 27.6258
94.1928; 111.564; 109.903		13867Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132995 CIFC342 H393 N12 O80.01P -121.4803; 27.0745; 29.3858
94.133; 108.263; 112.968		14568.6Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132996 CIFC154.5 H176.5 N15.5 O19.5P -121.6013; 27.1502; 28.3933
93.864; 111.256; 110.441		14178.7Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132997 CIFC132 H130 N6 O13 S3I 1 2 151.7627; 21.7575; 57.0058
90; 90.443; 90		64199.5Shields, C. E.; Fellowes, T.; Slater, A. G.; Cooper, A. I.; Andrews, K. G.; Szczypiński, F T
Exploration of the polymorphic solid-state landscape of an amide-linked organic cage using computation and automation.
Chemical communications (Cambridge, England), 2024, 60, 6023-6026
7132998 CIFC17 H10 F5 N3P 1 21/c 114.4065; 6.1767; 17.7705
90; 109.917; 90		1486.72Das, Animesh; Maji, Biplab
Substrate-controlled divergent remote C-H and N-H polyfluoroarylation of 2-aminopyrimidines with polyfluoroarenes <i>via</i> Pd(II)/Pd(0) catalysis.
Chemical communications (Cambridge, England), 2024, 60, 5630-5633
7132999 CIFC15 H14 F5 N3P 1 21/c 112.4951; 7.6806; 16.1712
90; 108.511; 90		1471.65Das, Animesh; Maji, Biplab
Substrate-controlled divergent remote C-H and N-H polyfluoroarylation of 2-aminopyrimidines with polyfluoroarenes <i>via</i> Pd(II)/Pd(0) catalysis.
Chemical communications (Cambridge, England), 2024, 60, 5630-5633
7133000 CIFC20 H20 Cl4 N4 NpC 1 2/c 119.2449; 9.5303; 15.6081
90; 127.522; 90		2270.4Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133001 CIFC8 H12 Cl4 N4 NpC 1 2/c 114.6308; 8.4327; 13.7095
90; 91.687; 90		1690.71Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133002 CIFC36 H30 Cl4 Np O2 P2P 1 21 19.9552; 15.3552; 11.9194
90; 98.955; 90		1799.84Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133003 CIFC45.76 H67.53 Cl4 N4 Np O2.44P 1 21/n 116.6555; 11.535; 25.751
90; 94.5345; 90		4931.8Lopez, Lauren M.; Uible, Madeleine C.; Zeller, Matthias; Bart, Suzanne C.
Lewis base adducts of NpCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2024, 60, 5956-5959
7133004 CIFC18 H20 O3C 1 2/c 133.38; 5.972; 18.656
90; 119.978; 90		3221Kumar, Rakesh; Dutt, Shiv; Banerjee, Prabal
Electrochemical oxidative C-C bond cleavage of methylenecyclopropanes with alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4246-4249
7133005 CIFC23 H22 N2 OP c a 2110.0123; 18.3467; 10.107
90; 90; 90		1856.58Kumar, Dharmendra; Unnikrishnan, Urmila; Kuram, Malleswara Rao
Facile access to <i>C</i>-substituted piperazin-2-ones and mianserin derivative enabled by chemoselective carbene insertion and cyclization cascade.
Chemical communications (Cambridge, England), 2024, 60, 5691-5694
7133006 CIFC9 H19 F3 N2 O4 S2P 1 21/c 19.52; 8.588; 18.645
90; 99.465; 90		1503.6Nakazono, Yosuke; Inoue, Ryota; Sumitani, Ryo; Mochida, Tomoyuki
Solvent-free transformation of protic ionic liquids into zwitterions.
Chemical communications (Cambridge, England), 2024, 60, 5711-5714
7133007 CIFC9 H17 F3 N2 O4 S2P 1 21/c 18.664; 9.443; 17.044
90; 95.637; 90		1387.7Nakazono, Yosuke; Inoue, Ryota; Sumitani, Ryo; Mochida, Tomoyuki
Solvent-free transformation of protic ionic liquids into zwitterions.
Chemical communications (Cambridge, England), 2024, 60, 5711-5714
7133008 CIFC10 H16 F3 N3 O4 S2P -19.869; 17.149; 18.682
93.615; 92.206; 94.036		3145Nakazono, Yosuke; Inoue, Ryota; Sumitani, Ryo; Mochida, Tomoyuki
Solvent-free transformation of protic ionic liquids into zwitterions.
Chemical communications (Cambridge, England), 2024, 60, 5711-5714
7133009 CIFC45 H36 O9P b c m16.1779; 7.77835; 27.1947
90; 90; 90		3422.11Han, Ying; Guo, Wei-Chen; Du, Xu-Sheng; Chen, Chuan-Feng
Synthesis and properties of an <i>O</i>-doped aromatic belt.
Chemical communications (Cambridge, England), 2024, 60, 5719-5722
7133010 CIFC39 H18 O3P 1 21/n 111.4275; 15.9886; 16.0325
90; 97.391; 90		2904.96Han, Ying; Guo, Wei-Chen; Du, Xu-Sheng; Chen, Chuan-Feng
Synthesis and properties of an <i>O</i>-doped aromatic belt.
Chemical communications (Cambridge, England), 2024, 60, 5719-5722
7133011 CIFC58 H41 N3P 21 21 2112.7061; 14.0855; 23.6488
90; 90; 90		4232.5Sharma, Priyank Kumar; Jana, Palash; Bandyopadhyay, Subhajit; Das, Soumyajit
Cyano disubstituted tetrabenzoindeno[2,1-<i>a</i>]fluorene: open-shell or closed-shell?
Chemical communications (Cambridge, England), 2024, 60, 7319-7322
7133012 CIFC27 H42 N4 O5 SiP 1 21/c 112.838; 15.169; 15.0877
90; 102.909; 90		2863.91Jeanmard, Laksamee; Lodovici, Giacomo; George, Ian; Bray, Joshua T. W.; Whitwood, Adrian C.; Thomas, Gavin H.; Fairlamb, Ian J. S.; Unsworth, William P.; Clarke, Paul A.
Stereoselective synthesis of an advanced <i>trans</i>-decalin intermediate towards the total synthesis of anthracimycin.
Chemical communications (Cambridge, England), 2024, 60, 5699-5702
7133013 CIFC17 H22 O5P 21 21 217.18006; 12.9367; 17.2317
90; 90; 90		1600.59Jeanmard, Laksamee; Lodovici, Giacomo; George, Ian; Bray, Joshua T. W.; Whitwood, Adrian C.; Thomas, Gavin H.; Fairlamb, Ian J. S.; Unsworth, William P.; Clarke, Paul A.
Stereoselective synthesis of an advanced <i>trans</i>-decalin intermediate towards the total synthesis of anthracimycin.
Chemical communications (Cambridge, England), 2024, 60, 5699-5702
7133014 CIFC94 H150 Mg N4 Ni2 O8P -110.3314; 12.155; 20.115
85.509; 76.039; 68.417		2279.4Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133015 CIFC67 H100 Mg N4 Ni O4P -111.7869; 13.1585; 21.6061
95.572; 101.159; 101.843		3184.9Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133016 CIFC86 H133 Ca N5 Ni2 O12P -113.1189; 18.636; 19.149
81.507; 86.676; 74.077		4451.9Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133017 CIFC96 H158 Mg N4 Ni2 O8P 1 21/c 128.041; 14.697; 24.348
90; 104.01; 90		9736Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133018 CIFC92 H150 Ca N4 Ni2 O12P 1 n 116.7438; 14.268; 20.0197
90; 97.276; 90		4744.2Wolff, Siad; Ponsonby, Annabelle; Dallmann, André; Herwig, Christian; Beckmann, Fabian; Cula, Beatrice; Limberg, Christian
Appropriation of group II metals: synthesis and characterisation of the first alkaline earth metal supported transition metal carbonite complexes.
Chemical communications (Cambridge, England), 2024, 60, 5816-5819
7133019 CIFC18 H14 Cl N OP 1 21/c 17.8569; 16.8285; 11.212
90; 104.254; 90		1436.81Sachin, ?; Sharma, Tamanna; Chandra, Devesh; Sumit, ?; Sharma, Upendra
Inherent directing group-enabled Co(III)-catalyzed C-H allylation/vinylation of isoquinolones.
Chemical communications (Cambridge, England), 2024, 60, 5626-5629
7133020 CIFC62 H47 Cl3 N6 O10 P2 Ru2P 1 21/c 119.7908; 15.1911; 23.1446
90; 107.604; 90		6632.4Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133021 CIFC24 H12 Br4 N6I 1 2/a 111.9288; 6.8445; 27.4989
90; 90.376; 90		2245.15Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133022 CIFC56 H41 Br3 Cl4 N4 O6 P2 RuP 1 21/c 118.3915; 14.4654; 20.9301
90; 100.804; 90		5469.55Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133023 CIFC58 H49 Cl N4 O6 P2 RuP -115.601; 21.105; 22.1703
110.152; 101.134; 99.661		6502.66Arya, Yogita; Ansari, Toufik; Bera, Sudip Kumar; Panda, Sanjib; Indra, Arindam; Lahiri, Goutam Kumar
Superior electrocatalytic hydrogen evolution activity of a triply bridged diruthenium(II) complex on a carbon cloth support.
Chemical communications (Cambridge, England), 2024, 60, 6011-6014
7133024 CIFC40 H46 Cd N0.5 O17.5 S4P 1 21/n 110.722; 39.433; 14.317
90; 97; 90		6008Su, Jian; Han, Xiao; Ke, Si-Wen; Zhou, Xiao-Cheng; Yuan, Shuai; Ding, Mengning; Zuo, Jing-Lin
Construction of a stable radical hydrogen-bonded metal-organic framework with functionalized tetrathiafulvalene linkers.
Chemical communications (Cambridge, England), 2024, 60, 5812-5815
7133025 CIFC43 H59 B N4 SiP -19.474; 13.9943; 16.2737
90.635; 90.829; 106.097		2072.54Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133026 CIFC57 H67 B N4 O2 SiP 1 21/n 112.9587; 24.1745; 16.8361
90; 103.559; 90		5127.2Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133027 CIFC69 H75 B N4 O2 SiC 1 c 111.765; 23.8074; 23.7692
90; 97.721; 90		6597.3Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133028 CIFC43 H59 B Ge N4P -19.5039; 14.0108; 16.3294
90.542; 90.684; 106.025		2089.55Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133029 CIFC86 H118 B2 N8 O2 Si2P 1 21/n 113.5861; 20.8352; 14.9701
90; 100.035; 90		4172.7Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133030 CIFC48 H59 B F5 N5 SiP 1 21/c 119.2831; 10.4515; 24.172
90; 103.424; 90		4738.5Chen, Wenhao; Hu, Haisheng; Feng, Jie; Zhu, Lei; Wu, Di
Synthetic, structural and reactivity studies of a boryl-ethynyl Silylene.
Chemical communications (Cambridge, England), 2024, 60, 5828-5831
7133031 CIFCs6 Na3 Nd O54 W10P -111.3552; 15.4905; 16.9027
101.371; 104.424; 91.701		2813.17Colliard, Ian; Deblonde, Gauthier J.-P.
Characterization of the first Peacock-Weakley polyoxometalate containing a transplutonium element: curium bis-pentatungstate [Cm(W<sub>5</sub>O<sub>18</sub>)<sub>2</sub>]<sup>9</sup>.
Chemical communications (Cambridge, England), 2024, 60, 5999-6002
7133032 CIFCm Cs8 Na O50 W10P -111.46121; 14.46007; 17.5536
101.11; 99.4298; 103.293		2711.36Colliard, Ian; Deblonde, Gauthier J.-P.
Characterization of the first Peacock-Weakley polyoxometalate containing a transplutonium element: curium bis-pentatungstate [Cm(W<sub>5</sub>O<sub>18</sub>)<sub>2</sub>]<sup>9</sup>.
Chemical communications (Cambridge, England), 2024, 60, 5999-6002
7133033 CIFC33 H26 N4 O6P 1 21/c 112.5972; 10.0613; 21.8687
90; 90.553; 90		2771.6Zhu, Shugao; Huang, Wenliang; Liu, Shihan; Yu, Rongjing; Ma, Yufeng; Wang, Hong; Zhang, Rui; Liu, Bin; Lan, Yu; Shen, Ruwei
Synthesis of benzooxepane-fused cyclobutene derivatives <i>via</i> Pd-catalyzed cascade reactions of haloarenes and diynylic ethers.
Chemical communications (Cambridge, England), 2024, 60, 5707-5710
7133034 CIFC21 H34 O4P 1 21 16.1621; 11.6465; 13.7206
90; 102.517; 90		961.28Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step synthesis of (-)-larikaempferic acid methyl ester enabled by skeletal rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7164-7167
7133035 CIFC21 H34 O4P 21 21 216.9015; 11.1195; 24.8315
90; 90; 90		1905.6Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step synthesis of (-)-larikaempferic acid methyl ester enabled by skeletal rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7164-7167
7133036 CIFC21 H34 O4I 1 2 120.0209; 6.9482; 29.3036
90; 107.026; 90		3897.74Rivera, Mario E.; Li, Lei; Kolisetti, Aditya; Chi, Nina; Dai, Mingji
9-Step synthesis of (-)-larikaempferic acid methyl ester enabled by skeletal rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7164-7167
7133037 CIFC23 H28 F3 N O8 SP 1 21 112.4612; 10.5196; 20.4828
90; 107.749; 90		2557.22Moore, Jonathan C.; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen P.; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective <i>de novo</i> synthesis of 14-hydroxy-6-oxomorphinans.
Chemical communications (Cambridge, England), 2024, 60, 6007-6010
7133038 CIFC23 H28 F3 N O8 SP 1 21 111.0308; 11.6724; 11.0847
90; 116.773; 90		1274.22Moore, Jonathan C.; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen P.; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective <i>de novo</i> synthesis of 14-hydroxy-6-oxomorphinans.
Chemical communications (Cambridge, England), 2024, 60, 6007-6010
7133039 CIFC19 H23 N O3P 1 21 110.163; 13.6943; 11.4184
90; 92.889; 90		1587.14Moore, Jonathan C.; Modell, Louis; Glenn, Jacqueline R.; Jones, Kieran D.; Argent, Stephen P.; Lane, J. Robert; Canals, Meritxell; Lam, Hon Wai
Enantioselective <i>de novo</i> synthesis of 14-hydroxy-6-oxomorphinans.
Chemical communications (Cambridge, England), 2024, 60, 6007-6010
7133040 CIFC19 H24 O2 SP 1 21/n 111.562; 5.6279; 26.4527
90; 92.458; 90		1719.7Suryawanshi, Sharad M.; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and <i>β</i>-dicarbonyls.
Chemical communications (Cambridge, England), 2024, 60, 5836-5839
7133041 CIFC16 H24 O2P c a 2110.399; 13.561; 9.888
90; 90; 90		1394.4Suryawanshi, Sharad M.; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and <i>β</i>-dicarbonyls.
Chemical communications (Cambridge, England), 2024, 60, 5836-5839
7133042 CIFC17 H18 O2P 1 21/c 111.0571; 10.1834; 11.8525
90; 102.1; 90		1304.93Suryawanshi, Sharad M.; Sahoo, Suman; Shaligram, Parth S.; Manna, Narugopal; Samanta, Ramesh C.
Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and <i>β</i>-dicarbonyls.
Chemical communications (Cambridge, England), 2024, 60, 5836-5839
7133043 CIFC12 H14 O4P 1 21/n 15.8827; 24.9167; 8.1339
90; 110.149; 90		1119.28Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133044 CIFC18 H18 O4P 1 21/n 15.845; 17.181; 7.9441
90; 107.273; 90		761.8Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133045 CIFC15 H16 O4P 1 21/c 110.828; 7.9485; 15.2171
90; 95.439; 90		1303.8Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133046 CIFC17 H18 O5P -15.8137; 8.5017; 16.6639
99.886; 92.872; 108.302		765.58Tao, Li; Wang, He; Liu, Xiao-Fei; Ren, Wei-Min; Lu, Xiao-Bing; Zhang, Wen-Zhen
Electrochemical ring-opening carboxylation of cyclic carbonate with carbon dioxide.
Chemical communications (Cambridge, England), 2024, 60, 5735-5738
7133047 CIFC35 H15 B F15 N OP 1 21/n 110.78652; 21.7974; 17.9089
90; 105.265; 90		4062.15Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133048 CIFC29 H8 B F15 N2I 1 2/a 113.6313; 19.4305; 24.194
90; 99.003; 90		6329.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133049 CIFC35 H12 B F15 N4 O2P 1 21/c 112.0468; 16.3233; 15.715
90; 95.2169; 90		3077.45Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133050 CIFC30 H11 B Cl3 F15 N2C 1 2/c 134.981; 9.9268; 19.229
90; 109.205; 90		6305.7Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133051 CIFC27 H7 B F15 NP -111.505; 12.536; 17.074
77.759; 87.576; 77.117		2345.9Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133052 CIFC33 H11 B F15 NP -19.3635; 12.334; 13.652
108.894; 103.287; 96.811		1419.5Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133053 CIFC33 H11 B F15 NP -110.152; 10.204; 14.905
100.952; 99.276; 103.819		1437.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133054 CIFC38 H21 B F15 N3P 1 21/c 112.1553; 18.4902; 15.9842
90; 111.521; 90		3342.1Liang, Pei; Wei, Junhui; Wei, Yongliang; Wang, Xue; Liu, Fei; Wang, Tongdao
Hetero Diels-Alder reactions of isolable <i>N</i>-borylenamines.
Chemical communications (Cambridge, England), 2024, 60, 5964-5967
7133055 CIFC58.06 H70.12 Cl4.12 F4 I2 N6 O9 SeI 1 2/a 121.6338; 28.0204; 21.9354
90; 98.596; 90		13147.6Liu, Chuan-Zhi; Zhang, Chi; Li, Zhong-Yi; Chen, Jiale; Wang, Tonglu; Zhang, Xiang-Kun; Yan, Meng; Zhai, Bin
Multiple non-covalent-interaction-directed supramolecular double helices: the orthogonality of hydrogen, halogen and chalcogen bonding.
Chemical communications (Cambridge, England), 2024, 60, 6063-6066
7133056 CIFC32 H34 F3 I N4 O5 SeP -19.5768; 10.0412; 18.3416
96.6; 101.321; 98.752		1690.13Liu, Chuan-Zhi; Zhang, Chi; Li, Zhong-Yi; Chen, Jiale; Wang, Tonglu; Zhang, Xiang-Kun; Yan, Meng; Zhai, Bin
Multiple non-covalent-interaction-directed supramolecular double helices: the orthogonality of hydrogen, halogen and chalcogen bonding.
Chemical communications (Cambridge, England), 2024, 60, 6063-6066
7133057 CIFC56 H46 Cd2 N6 O10P 21 21 219.6443; 17.67; 36.653
90; 90; 90		6246.2Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133058 CIFC55 H42 Cd2 N6 O10P 21 21 219.6554; 17.7129; 36.6589
90; 90; 90		6269.6Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133059 CIFC45 H39 N4 O13 Zn4P 21 21 2113.6565; 29.6834; 14.1762
90; 90; 90		5746.6Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133060 CIFC45 H34 N4 O13 Zn4P 21 21 2113.6827; 14.1989; 29.77
90; 90; 90		5783.7Fu, Hong-Ru; Ren, Dan-Dan; Zhang, Kun; Wang, Shuang; Yang, Xu-Jing; Ding, Qing-Rong; Wu, Ya-Pan
Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.
Chemical communications (Cambridge, England), 2024, 60, 6182-6185
7133061 CIFC4 H6 Na O14 Re U2C 1 2/m 115.2417; 8.1267; 15.0583
90; 113.798; 90		1706.6Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133062 CIFC8 H12 Na2 O30 Tc2 U4C 1 2/m 115.2356; 8.1216; 15.0053
90; 114.061; 90		1695.39Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133063 CIFC4 H18 O32 Re2 U5P -17.7354; 8.4717; 12.782
94.029; 99.086; 109.92		770.66Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133064 CIFC4 H6 O32 Tc2 U5P -17.7451; 8.4501; 12.7565
93.982; 99.211; 109.708		768.96Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133065 CIFC8 H20 O25.75 Tc U4P b c n14.371; 13.8231; 14.8033
90; 90; 90		2940.7Shohel, Mohammad; Nyman, May
Uranyl-Tc(VII)/Tc(V) hybrid clusters.
Chemical communications (Cambridge, England), 2024, 60, 5820-5823
7133066 CIFC13 H8 Br N SP 1 21/c 111.7154; 14.3463; 7.0036
90; 102.82; 90		1147.77Maeda, Bumpei; Akiyoshi, Ryohei; Tanaka, Daisuke; Sato, Kohei; Murakami, Kei
Synthesis of <i>N</i>-β-brominated alkenyl isothiocyanates <i>via</i> dehydrogenation of alkyl isothiocyanates.
Chemical communications (Cambridge, England), 2024, 60, 6015-6018
7133067 CIFC15 H10 Br N SP b c a7.4897; 18.6819; 19.2474
90; 90; 90		2693.13Maeda, Bumpei; Akiyoshi, Ryohei; Tanaka, Daisuke; Sato, Kohei; Murakami, Kei
Synthesis of <i>N</i>-β-brominated alkenyl isothiocyanates <i>via</i> dehydrogenation of alkyl isothiocyanates.
Chemical communications (Cambridge, England), 2024, 60, 6015-6018
7133068 CIFC36 H44 N4 O13 S3P 1 21 117.0638; 4.9924; 23.7104
90; 101.092; 90		1982.14Zhao, Chenyang; Li, Zujian; Ji, Lukang; Wang, Hanxiao; Ouyang, Guanghui; Liu, Minghua
Aggregate-state-dependent photochromism and circularly polarized luminescence of a chiral biquinoline amphiphile.
Chemical communications (Cambridge, England), 2024, 60, 6047-6050
7133069 CIFC26 H32 Br2.31 I1.69 N6 O2 ZnP -18.6011; 12.1473; 17.1881
71.236; 80.474; 79.466		1660.7Manna, Subarna; Sahoo, Sangita; Rit, Arnab
Synthesis of quinazolinone scaffolds <i>via</i> a zinc(II)-stabilized amidyl radical-promoted deaminative approach.
Chemical communications (Cambridge, England), 2024, 60, 7097-7100
7133070 CIFC107 H97 Cl3 O4P -110.8817; 15.6992; 25.2074
92.731; 92.591; 108.886		4061.44Hirano, Junichiro; Miyoshi, Sayaka; Yashima, Eiji; Ikai, Tomoyuki; Shinokubo, Hiroshi; Fukui, Norihito
Synthesis of sterically congested double helicene by alkyne cycloisomerization.
Chemical communications (Cambridge, England), 2024, 60, 6035-6038
7133071 CIFC11 H17 N O S2P 1 21/c 115.8974; 7.835; 9.4791
90; 100.682; 90		1160.2Cheng, Yuhe; Hyodo, Tadashi; Yamaguchi, Kentaro; Ohwada, Tomohiko; Otani, Yuko
Complete amide <i>cis</i>-<i>trans</i> switching synchronized with disulfide bond formation and cleavage in a proline-mimicking system.
Chemical communications (Cambridge, England), 2024, 60, 6158-6161
7133072 CIFC19 H20 N2 O4P -18.1324; 11.0134; 20.24
77.534; 79.396; 80.934		1726.67Liu, Zi; Greaney, Michael F.
Aminoarylation of alkynes using diarylanilines.
Chemical communications (Cambridge, England), 2024, 60, 6296-6299
7133073 CIFC15 H11 N SP -19.2993; 9.8997; 13.2708
82.308; 83.479; 77.987		1179.57George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133074 CIFC15 H11 N SP -19.2758; 9.9051; 13.2567
82.254; 83.462; 77.957		1175.69George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133075 CIFC15 H11 N SP -19.2177; 9.9216; 13.2043
82.062; 83.369; 77.928		1164.89George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133076 CIFC15 H11 N SP -19.1868; 9.9277; 13.1688
81.952; 83.305; 77.93		1158.19George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133077 CIFC15 H11 N SP -19.2356; 9.9171; 13.2232
82.118; 83.407; 77.923		1168.48George, 3rd, Gary C; Kruse, Samantha J.; Forbes, Tori Z.; Hutchins, Kristin M.
Off-the-shelf thermosalience of anthracene-9-thiocarboxamide.
Chemical communications (Cambridge, England), 2024, 60, 7697-7700
7133078 CIFC14 H11 N O S2P -19.6697; 10.5598; 13.8151
93.577; 100.035; 113.048		1264.85Wakabayashi, Ryota; Wang, Shuo; Kurogi, Takashi; Yorimitsu, Hideki
Arylation of benzazoles at the 4 positions by activation of their 2-methylsulfinyl groups.
Chemical communications (Cambridge, England), 2024, 60, 6166-6169
7133079 CIFC21 H16 N4 O5 Ru SP b c a10.1221; 16.1027; 25.1176
90; 90; 90		4094Yang, Jing; Zhan, Shaoqi; Wang, Linqin; Yang, Hao; Duan, Lele; Fan, Xiaolei; Liu, Tianqi; Sun, Licheng
Adaptive water oxidation catalysis on a carboxylate-sulfonate ligand with low onset potential.
Chemical communications (Cambridge, England), 2024, 60, 6162-6165
7133080 CIFC54 H58 B2 N6 O2 S2P 1 21/c 120.704; 6.2953; 18.9378
90; 108.615; 90		2339.2Fukami, Shuhei; Mori, Shigeki; Harada, Takunori; Shimizu, Soji
Far-red fluorescence and chiroptical properties of pyrrolopyrrole aza-BODIPYs induced by the <i>B</i>,<i>O</i>-chelation.
Chemical communications (Cambridge, England), 2024, 60, 6170-6173
7133081 CIFC38 H46 B2 F4 N6 S4P -17.7011; 11.6851; 11.8911
75.307; 71.596; 76.096		967.05Fukami, Shuhei; Mori, Shigeki; Harada, Takunori; Shimizu, Soji
Far-red fluorescence and chiroptical properties of pyrrolopyrrole aza-BODIPYs induced by the <i>B</i>,<i>O</i>-chelation.
Chemical communications (Cambridge, England), 2024, 60, 6170-6173
7133082 CIFC25 H22 Br N3 OP 1 21/c 15.946; 22.981; 16.1913
90; 96.653; 90		2197.56Fall, Arona; Magdei, Mihaela; Savchuk, Mariia; Oudeyer, Sylvain; Beucher, Hélène; Brière, Jean-François
Iron-catalyzed decarboxylative radical addition to chiral azomethine imines upon visible light.
Chemical communications (Cambridge, England), 2024, 60, 6316-6319
7133083 CIFC26 H25 N3 O2P 1 21/c 116.9362; 10.0156; 27.6433
90; 106.283; 90		4500.94Fall, Arona; Magdei, Mihaela; Savchuk, Mariia; Oudeyer, Sylvain; Beucher, Hélène; Brière, Jean-François
Iron-catalyzed decarboxylative radical addition to chiral azomethine imines upon visible light.
Chemical communications (Cambridge, England), 2024, 60, 6316-6319
7133084 CIFAl B3 Cl Cs O6P -3 c 17.0716; 7.0716; 18.0458
90; 90; 120		781.52Liu, Haoran; Jiao, Jiahao; Tudi, Abudukadi; Liu, Qingyu; Yang, Zhihua; Pan, Shilie; Zhang, Min
CsAlB<sub>3</sub>O<sub>6</sub>Cl: the rational construction of a KBBF-type structure with aligned <sup>2</sup><sub>∞</sub>[AlB<sub>3</sub>O<sub>6</sub>Cl] layers <i>via</i> introducing unprecedented [AlO<sub>3</sub>Cl] tetrahedra.
Chemical communications (Cambridge, England), 2024, 60, 6516-6519
7133085 CIFC6 I3 N PbP n m a7.8521; 11.3081; 15.9901
90; 90; 90		1419.8Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133086 CIFC5 H12 I NI 4/m7.3846; 7.3846; 7.2299
90; 90; 90		394.263Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133087 CIFC5 H12 I3 N PbP 63/m16.745; 16.745; 8.387
90; 90; 120		2036.6Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133088 CIFC5 H12 I3 N PbP 63/m16.4064; 16.4064; 8.3883
90; 90; 120		1955.38Möbs, Jakob; Tomori, Ajna; Heine, Johanna
Formation of iminium ions during the processing of metal halide perovskites.
Chemical communications (Cambridge, England), 2024, 60, 6488-6491
7133089 CIFC84 H62 N2 O12 S8C 1 c 127.458; 23.377; 11.615
90; 90.454; 90		7455Du, Zhenglin; Xie, Jialin; Liu, Yandie; Tang, Yisong; Chen, Qing; Li, Xia; Zhu, Kelong
A π-extended molecular belt with selective binding capability for fullerene C<sub>70</sub>.
Chemical communications (Cambridge, England), 2024, 60, 6387-6390
7133090 CIFC142 H52 O8 S8P 1 21/n 117.1449; 33.6954; 21.4769
90; 92.559; 90		12394.9Du, Zhenglin; Xie, Jialin; Liu, Yandie; Tang, Yisong; Chen, Qing; Li, Xia; Zhu, Kelong
A π-extended molecular belt with selective binding capability for fullerene C<sub>70</sub>.
Chemical communications (Cambridge, England), 2024, 60, 6387-6390
7133091 CIFC30 H32 N2 O6P -110.405; 10.991; 12.216
109.33; 91.872; 104.146		1268.4Songsermsawad, Sarita; Shemchuk, Oleksii; Robeyns, Koen; Collard, Laurent; E Flood, Adrian; Leyssens, Tom
Simultaneously resolving BINOL and proline using a stoichiometric cocrystal switch.
Chemical communications (Cambridge, England), 2024, 60, 6607-6610
7133092 CIFC45 H37 N O6P 21 21 219.12901; 13.7793; 27.6456
90; 90; 90		3477.58Songsermsawad, Sarita; Shemchuk, Oleksii; Robeyns, Koen; Collard, Laurent; E Flood, Adrian; Leyssens, Tom
Simultaneously resolving BINOL and proline using a stoichiometric cocrystal switch.
Chemical communications (Cambridge, England), 2024, 60, 6607-6610
7133093 CIFC10 H20 Cu2 N5I b a m14.9083; 8.1008; 12.162
90; 90; 90		1468.79Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133094 CIFC10 H20 Cu2 N5I b a m14.8851; 8.1225; 12.2203
90; 90; 90		1477.49Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133095 CIFC10 H20 Cu2 N5I b a m14.7778; 8.2376; 12.5337
90; 90; 90		1525.77Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133096 CIFC10 H20 Cu2 N5I b a m14.8065; 8.2051; 12.4448
90; 90; 90		1511.9Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133097 CIFC10 H20 Cu2 N5I b a m14.8624; 8.1463; 12.2872
90; 90; 90		1487.66Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133098 CIFC10 H20 Cu2 N5I b a m14.8279; 8.1752; 12.366
90; 90; 90		1499.02Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133099 CIFC10 H20 Cu2 N5I b a m14.7531; 8.2731; 12.6466
90; 90; 90		1543.57Iwai, Yuudai; Nakaya, Manabu; Tsuji, Yuta; Le Ouay, Benjamin; Ohba, Masaaki; Ohtani, Ryo
Giant anisotropic thermal expansion of copper-cyanido flat layers with flexible copper nodes.
Chemical communications (Cambridge, England), 2024, 60, 6512-6515
7133100 CIFC27 H17 N O3P b c a7.3843; 20.0427; 24.5666
90; 90; 90		3635.89Tanioka, Masaru; Mori, Minori; Harada, Mei; Matsuya, Yuji; Kamino, Shinichiro
Nonpolar selective emission (NPSE) of carbonyl-bridged rhodols.
Chemical communications (Cambridge, England), 2024, 60, 6407-6410
7133101 CIFC28 H16 F3 N O3P -110.994; 11.0404; 17.6631
83.512; 80.77; 72.972		2018.43Tanioka, Masaru; Mori, Minori; Harada, Mei; Matsuya, Yuji; Kamino, Shinichiro
Nonpolar selective emission (NPSE) of carbonyl-bridged rhodols.
Chemical communications (Cambridge, England), 2024, 60, 6407-6410
7133102 CIFC32 H19 N O3P b c a7.75825; 18.8157; 31.7145
90; 90; 90		4629.58Tanioka, Masaru; Mori, Minori; Harada, Mei; Matsuya, Yuji; Kamino, Shinichiro
Nonpolar selective emission (NPSE) of carbonyl-bridged rhodols.
Chemical communications (Cambridge, England), 2024, 60, 6407-6410
7133103 CIFC44 H32 Fe N10P -19.8316; 10.568; 17.2201
81.653; 83.058; 85.688		1754.2Sung, Yu-Shien; Tomat, Elisa
Quinoline-based tetrazolium prochelators: formazan release, iron sequestration, and antiproliferative efficacy in cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 6150-6153
7133104 CIFC26 H25 N O5P 21 21 215.0705; 19.7168; 21.861
90; 90; 90		2185.53Yang, Yang; Yang, Chenchen; Zhu, Xuefeng; Zhang, Li; Liu, Minghua
Interfacial self-assembly of a chiral pyrene exciplex into a superhelix with enhanced circularly polarized luminescence.
Chemical communications (Cambridge, England), 2024, 60, 6631-6634
7133105 CIFC68 H58 Cu2 N6 O16C 1 2/c 132.307; 14.1238; 16.6531
90; 97.426; 90		7535Saura-Sanmartin, Adrian; Cutillas-Font, Guillermo; Martinez-Cuezva, Alberto; Alajarin, Mateo; Esteban-Betegón, Fátima; Pena-Sánchez, Pilar; Gándara, Felipe; Berna, Jose
Mechanical bonding of rigid MORFs using a tetratopic rotaxane.
Chemical communications (Cambridge, England), 2024, 60, 6431-6434
7133106 CIFC68 H60 Co2 N6 O19P n m a16.795; 33.97; 13.8988
90; 90; 90		7929.6Saura-Sanmartin, Adrian; Cutillas-Font, Guillermo; Martinez-Cuezva, Alberto; Alajarin, Mateo; Esteban-Betegón, Fátima; Pena-Sánchez, Pilar; Gándara, Felipe; Berna, Jose
Mechanical bonding of rigid MORFs using a tetratopic rotaxane.
Chemical communications (Cambridge, England), 2024, 60, 6431-6434
7133107 CIFC33 H25 N OP -15.82; 9.093; 23.432
79.032; 87.963; 78.447		1192.7Yao, Yu-Xiang; Zhang, Jing; Min, Xuehong; Qin, Lan; Wei, Yi; Gao, Yang; Hu, Xiao-Qiang
Expedient access to polysubstituted acrylamides <i>via</i> strain-release-driven dual phosphine and palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6532-6535
7133108 CIFC35 H27 Cl2 N O2P 1 21/c 112.4215; 27.311; 9.588
90; 112.62; 90		3002.5Yao, Yu-Xiang; Zhang, Jing; Min, Xuehong; Qin, Lan; Wei, Yi; Gao, Yang; Hu, Xiao-Qiang
Expedient access to polysubstituted acrylamides <i>via</i> strain-release-driven dual phosphine and palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6532-6535
7133109 CIFC29 H23 N O3P 1 21/c 111.302; 22.17; 9.91
90; 107.88; 90		2363Yao, Yu-Xiang; Zhang, Jing; Min, Xuehong; Qin, Lan; Wei, Yi; Gao, Yang; Hu, Xiao-Qiang
Expedient access to polysubstituted acrylamides <i>via</i> strain-release-driven dual phosphine and palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6532-6535
7133110 CIFC27 H25 F3 O5 SP n a 2130.2694; 7.47312; 21.66
90; 90; 90		4899.64Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133111 CIFC25 H19 F3 O4 SC 1 c 17.3296; 14.8403; 19.798
90; 99.989; 90		2120.85Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133112 CIFC24 H19 B F4 OP 1 21/n 16.8567; 19.3806; 14.5799
90; 93.309; 90		1934.25Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133113 CIFC26 H19 F6 N O5 S2P -17.7877; 13.5269; 14.2246
115.433; 102.323; 95.02		1294.53Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133114 CIFC26 H19 F6 N O5 S2P -114.2426; 14.5647; 15.1706
117.808; 98.1608; 104.991		2558.64Shimajiri, Takuya; Tsue, Taiga; Koakutsu, Shumpei; Ishigaki, Yusuke; Suzuki, Takanori
Crystallographic and spectroscopic studies on persistent triarylpropargyl cations.
Chemical communications (Cambridge, England), 2024, 60, 7152-7155
7133115 CIFC17 H11 F3 N2 O4P -19.7758; 10.513; 11.2193
90.001; 112.552; 105.12		1021.51Wang, Manqing; Xu, Yuanshuang; Hou, Huihang; Zhang, Xinying; Fan, Xuesen
Divergent synthesis of pyrrolizine derivatives through C-H bond functionalization of pyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6536-6539
7133116 CIFC17 H15 F3 N2 O3P 1 21/c 110.9356; 17.2071; 9.5578
90; 113.916; 90		1644.07Wang, Manqing; Xu, Yuanshuang; Hou, Huihang; Zhang, Xinying; Fan, Xuesen
Divergent synthesis of pyrrolizine derivatives through C-H bond functionalization of pyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6536-6539
7133117 CIFC39 H50 N PP -110.7562; 13.4826; 14.1323
115.435; 107.508; 96.665		1692Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133118 CIFC33 H36 Br NP 1 21/c 110.4197; 14.0561; 18.9616
90; 100.363; 90		2731.82Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133119 CIFC109 H143 La2 N2 O P5P -115.498; 16.566; 22.288
76.309; 70.924; 69.957		5030.1Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133120 CIFC47 H69 K N O2 PP 1 21/n 111.463; 16.2623; 24.992
90; 97.374; 90		4620.3Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133121 CIFC164 H216 Cl10 K2 La4 N4 O2 P4P -112.833; 16.681; 21.1112
98.117; 100.137; 108.631		4120Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133122 CIFC85.6 H117 Cl La N2 O1.9 P2P 1 21/c 120.5986; 24.7411; 32.569
90; 95.767; 90		16514.2Wittwer, B.; Heim, F.; Wurst, K.; Hohloch, S.
A bridging bis-phosphanido-phosphinidene complex of lanthanum supported by a sterically encumbering PN ligand.
Chemical communications (Cambridge, England), 2024, 60, 7299-7302
7133123 CIFC11 H11 N9 OP 1 21/c 16.4786; 15.6097; 13.6164
90; 100.478; 90		1354.05Liu, Ziwei; Jiang, Clancy Zhijian; Bond, Andrew D.; Tosca, Nicholas J.; Sutherland, John D.
Manganese(II) promotes prebiotically plausible non-enzymatic RNA ligation reactions.
Chemical communications (Cambridge, England), 2024, 60, 6528-6531
7133124 CIFC46 H48 Br2 N2 O6 S4P -113.3806; 13.864; 15.8118
114.886; 90.41; 117.953		2272.67Li, Jia; Li, Liang; Mao, Mingming; Li, Rui-Peng; Huo, Xing; Tang, Shouchu
Site-selective synthesis of indanyl-substituted indole derivatives <i>via</i> 1,3-dithiane induced Nazarov cyclization.
Chemical communications (Cambridge, England), 2024, 60, 6540-6543
7133125 CIFC165 H129 Ce4 N39 O27P -122.747; 25.744; 26.168
82.095; 83.235; 63.886		13601Zhao, Lehua; Zhang, Yu; Wang, Huali; Wang, Jing; He, Cheng; Zhao, Liang; Duan, Chunying
Isolation of a copper photocatalyst on a metal-organic cage for the sulfonylation of aryl halides resulting from visible-light-mediated C(sp<sup>2</sup>)-S cross-coupling.
Chemical communications (Cambridge, England), 2024, 60, 6805-6808
7133126 CIFC27 H23 F Ge OP -19.8789; 11.0575; 11.8202
106.201; 104.242; 105.035		1124.69Lu, Xiao-Yu; Qian, Yu-Jun; Sun, Hai-Lun; Su, Meng-Xue; Wang, Zi-Zhen; Jiang, Fan; Zhou, Xin-Yue; Sun, Yan-Xi; Shi, Wan-Li; Wan, Ji-Ru
Photoinduced decarboxylative germylation of α-fluoroacrylic acids: access to germylated monofluoroalkenes.
Chemical communications (Cambridge, England), 2024, 60, 6556-6559
7133127 CIFC14 H16 N4 O5P 1 21/n 113.8775; 7.5913; 15.0147
90; 116.937; 90		1410.2Al Rahal, Okba; Ferguson, Michael; Lennox, Cameron B.; Male, Louise; Friščić, Tomislav
Structure of the caffeine-pyrogallol complex: revisiting a pioneering structural analysis of a model pharmaceutical cocrystal.
Chemical communications (Cambridge, England), 2024, 60, 7431-7434
7133128 CIFC14 H24 N4 O9P 42/n :223.1123; 23.1123; 6.8449
90; 90; 90		3656.4Al Rahal, Okba; Ferguson, Michael; Lennox, Cameron B.; Male, Louise; Friščić, Tomislav
Structure of the caffeine-pyrogallol complex: revisiting a pioneering structural analysis of a model pharmaceutical cocrystal.
Chemical communications (Cambridge, England), 2024, 60, 7431-7434
7133129 CIFC13 H16 Br2 N4 O3 WP 1 21/n 110.5949; 14.4051; 11.7972
90; 91.105; 90		1800.16Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133130 CIFC11 H12 Br2 Cl3 N3 O3 WP -19.2942; 10.3885; 11.1039
63.402; 75.498; 79.694		925.34Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133131 CIFC22 H30 Br Cl3 N6 O4 W2P 21 21 27.857; 15.9287; 12.3215
90; 90; 90		1542.06Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133132 CIFC15 H21 Br2 N5 O WP 1 21/c 111.3229; 8.0358; 21.4613
90; 95.852; 90		1942.56Steiner, Lorenz; Ćorović, Miljan Z; Dupé, Antoine; Mösch-Zanetti, Nadia C
Vinyl-pyrazole as a biomimetic acetaldehyde surrogate.
Chemical communications (Cambridge, England), 2024, 60, 6873-6876
7133133 CIFC15 H20 O5P -110.7822; 10.9047; 12.0558
88.037; 83.186; 89.353		1406.6Liu, Hongjian; Jiang, Huanfeng; Qi, Chaorong
Macrocyclization of carbon dioxide with 3-triflyloxybenzynes and tetrahydrofuran: straightforward access to 14-membered macrolactones.
Chemical communications (Cambridge, England), 2024, 60, 6639-6642
7133134 CIFC18 H23 F3 O7 SP 21 21 218.8302; 11.4492; 20.293
90; 90; 90		2051.6Liu, Hongjian; Jiang, Huanfeng; Qi, Chaorong
Macrocyclization of carbon dioxide with 3-triflyloxybenzynes and tetrahydrofuran: straightforward access to 14-membered macrolactones.
Chemical communications (Cambridge, England), 2024, 60, 6639-6642
7133135 CIFC24 H27 F3 O7 SP -113.4729; 13.6729; 14.874
65.885; 84.653; 77.547		2442Liu, Hongjian; Jiang, Huanfeng; Qi, Chaorong
Macrocyclization of carbon dioxide with 3-triflyloxybenzynes and tetrahydrofuran: straightforward access to 14-membered macrolactones.
Chemical communications (Cambridge, England), 2024, 60, 6639-6642
7133136 CIFC20 H30 OP -16.0028; 11.2789; 13.1074
64.982; 80.954; 87.69		793.83Dethe, Dattatraya H.; Sharma, Nitin; Juyal, Sakshi; Singh, Prabhakar; Siddiqui, Salman A.
Enantioselective total synthesis of atisane diterpenoids: (+)-sapinsigin H, (+)-agallochaol C, and (+)-16α, 17-dihydroxy-atisan-3-one.
Chemical communications (Cambridge, England), 2024, 60, 7866-7869
7133137 CIFC61 H92 Cr Li N4 O5P -112.3655; 14.1523; 19.2237
69.523; 76.232; 65.51		2850.94D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133138 CIFC62 H95 Cr Li N4 O5P -111.7699; 16.1506; 17.7227
97.669; 105.27; 108.783		2987.77D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133139 CIFC61 H90 Cr K N4 O8P -111.7863; 14.0237; 19.3145
85.096; 78.035; 75.843		3026.2D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133140 CIFC102 H140 Cr2 K2 N8 O5R -3 :H41.8744; 41.8744; 15.4776
90; 90; 120		23503.4D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133141 CIFC140 H202 Cr2 K2 N8 O17P -112.1161; 19.5547; 29.7051
82.767; 81.408; 78.704		6790.16D'Arpino, Alexander A; Wolczanski, Peter T.; MacMillan, Samantha N.; Cundari, Thomas R.; Krumov, Mihail R.
Reduction of (pddi)Cr reveals redox noninnocence <i>via</i> C-C bond formation amidst competing electrophilicity: [(cpta)CrMe<sub><i>n</i></sub>]<sup>-</sup> (<i>n</i> = 0, 1) and [(pta)Cr]<sup/>.
Chemical communications (Cambridge, England), 2024, 60, 6785-6788
7133142 CIFC70 H63 B Cl3 F24 N2 O3 PP -112.6492; 13.6605; 21.8343
81.4; 78.136; 78.97		3600.1Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133143 CIFC149 H136 B2 F48 N4 O6 P2P -113.6399; 16.8477; 19.2953
115.857; 102.316; 98.273		3754.1Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133144 CIFC45 H60 Cl7 Ga2 N2 O3 PC 1 c 120.964; 12.2176; 20.1457
90; 93.743; 90		5148.9Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133145 CIFC86 H85 B F24 N5 O3 PP -112.1449; 18.623; 20.405
70.624; 73.911; 75.97		4125.1Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133146 CIFC91 H88 B F24 N2 O3 PP 1 21/n 113.9705; 31.6393; 19.2626
90; 93.898; 90		8494.7Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133147 CIFC89.36 H97.27 B F24 N2 O3 P SiP -113.1456; 17.6698; 20.0734
95.272; 103.875; 91.26		4502.8Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133148 CIFC79 H74 B F24 N2 O3 PP -113.9743; 16.814; 19.335
115.292; 106.112; 94.371		3845.7Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133149 CIFC79 H64 B F24 N2 O3 PP 1 21/c 112.366; 20.9073; 29.743
90; 97.228; 90		7628.6Karnbrock, Simon B. H.; Golz, Christopher; Alcarazo, Manuel
P(V)-bis(amidophenolate) ligand cooperation: stoichiometric CO-bond cleavage in aldehydes and ketones.
Chemical communications (Cambridge, England), 2024, 60, 6745-6748
7133150 CIFC28 H30 N2 O4C 1 c 114.4111; 20.2712; 10.3678
90; 129.444; 90		2338.94Sakai, Dan; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Stereoselective synthesis of 6/7/6-fused heterocycles with multiple stereocenters <i>via</i> an internal redox reaction/inverse electron-demand hetero-Diels-Alder reaction sequence.
Chemical communications (Cambridge, England), 2024, 60, 6797-6800
7133151 CIFC29 H32 Cl2 N2 O4P -19.9028; 11.7064; 11.8877
89.667; 74.086; 77.512		1291.8Sakai, Dan; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Stereoselective synthesis of 6/7/6-fused heterocycles with multiple stereocenters <i>via</i> an internal redox reaction/inverse electron-demand hetero-Diels-Alder reaction sequence.
Chemical communications (Cambridge, England), 2024, 60, 6797-6800
7133152 CIFC31 H46 F N S Si2P 1 21 18.1462; 13.1951; 15.8775
90; 96.946; 90		1694.15Zhou, Pengfei; Liang, Xinyao; Xu, Zekun; Chen, Honggu; Wei, Zongwu; Liang, Taoyuan; Jiang, Jun; Zhang, Zhuan
Regiodivergent C-H alkynylation of 2-arylthiazoles switched by Ru<sup>II</sup> and Pd<sup>II</sup> catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6679-6682
7133153 CIFC22 H29 N O S SiP -18.798; 12.4654; 21.0908
104.49; 90.974; 91.921		2237.4Zhou, Pengfei; Liang, Xinyao; Xu, Zekun; Chen, Honggu; Wei, Zongwu; Liang, Taoyuan; Jiang, Jun; Zhang, Zhuan
Regiodivergent C-H alkynylation of 2-arylthiazoles switched by Ru<sup>II</sup> and Pd<sup>II</sup> catalysis.
Chemical communications (Cambridge, England), 2024, 60, 6679-6682
7133154 CIFC38 H39 N O8P 21 21 217.7775; 19.6476; 22.0751
90; 90; 90		3373.28Sun, Chunzhao; Inokuma, Tsubasa; Tsuji, Daisuke; Yamaoka, Yousuke; Akagi, Reiko; Yamada, Ken-Ichi
Total synthesis of 1,4a-di-<i>epi-ent</i>-pancratistatin, exemplifying a stereodivergent approach to pancratistatin isomers.
Chemical communications (Cambridge, England), 2024, 60, 6757-6760
7133155 CIFC51 H39 Cl2 N O13P 1 21 110.8258; 13.1828; 15.3126
90; 79.363; 90		2147.78Sun, Chunzhao; Inokuma, Tsubasa; Tsuji, Daisuke; Yamaoka, Yousuke; Akagi, Reiko; Yamada, Ken-Ichi
Total synthesis of 1,4a-di-<i>epi-ent</i>-pancratistatin, exemplifying a stereodivergent approach to pancratistatin isomers.
Chemical communications (Cambridge, England), 2024, 60, 6757-6760
7133156 CIFC6 H22 Br5 In N2 O2P n m a20.264; 7.9353; 11.0226
90; 90; 90		1772.4Biswas, Shuva; Mandal, Arnab; Swain, Diptikanta; Biswas, Kanishka
Synthesis and soft crystal structure-induced broad emission of (NH<sub>3</sub>C<sub>6</sub>H<sub>12</sub>NH<sub>3</sub>)InBr<sub>5</sub>·2H<sub>2</sub>O.
Chemical communications (Cambridge, England), 2024, 60, 7757-7760
7133157 CIFC6 H22 Br5 In N2 O2P 1 21/n 17.8333; 20.223; 10.9317
90; 91.232; 90		1731.3Biswas, Shuva; Mandal, Arnab; Swain, Diptikanta; Biswas, Kanishka
Synthesis and soft crystal structure-induced broad emission of (NH<sub>3</sub>C<sub>6</sub>H<sub>12</sub>NH<sub>3</sub>)InBr<sub>5</sub>·2H<sub>2</sub>O.
Chemical communications (Cambridge, England), 2024, 60, 7757-7760
7133158 CIFC18 H14 O2P 1 21/c 111.2312; 14.7726; 8.2671
90; 109.062; 90		1296.42Zhang, Xu; Chang, Mengfan; Xu, Xuefeng; Zhao, Qiang
Direct access to furan and cyclopropane derivatives <i>via</i> palladium-catalyzed C-H activation/alkene insertion/annulation.
Chemical communications (Cambridge, England), 2024, 60, 6769-6772
7133159 CIFC19 H19 N O4 SP 1 21/c 18.301; 11.0651; 18.7113
90; 93.468; 90		1715.51Li, Shuhui; Xu, Dan; Yao, Hui; Tan, Mengting; Li, Xiaoxuan; Liu, Mingguo; Wang, Long; Huang, Nianyu; Wang, Nengzhong
Facile synthesis of 2-vinylindolines <i>via</i> a phosphine-mediated α-umpolung/Wittig olefination/cyclization cascade process.
Chemical communications (Cambridge, England), 2024, 60, 6773-6776
7133160 CIFC27 H29 N O4 S2P 1 21/n 19.2418; 19.5215; 14.0366
90; 99.178; 90		2499.98Li, Shuhui; Xu, Dan; Yao, Hui; Tan, Mengting; Li, Xiaoxuan; Liu, Mingguo; Wang, Long; Huang, Nianyu; Wang, Nengzhong
Facile synthesis of 2-vinylindolines <i>via</i> a phosphine-mediated α-umpolung/Wittig olefination/cyclization cascade process.
Chemical communications (Cambridge, England), 2024, 60, 6773-6776
7133161 CIFC20 H21 N O5 SP -18.0093; 9.9303; 13.0524
92.274; 107.728; 106.033		941.63Li, Shuhui; Xu, Dan; Yao, Hui; Tan, Mengting; Li, Xiaoxuan; Liu, Mingguo; Wang, Long; Huang, Nianyu; Wang, Nengzhong
Facile synthesis of 2-vinylindolines <i>via</i> a phosphine-mediated α-umpolung/Wittig olefination/cyclization cascade process.
Chemical communications (Cambridge, England), 2024, 60, 6773-6776
7133162 CIFC12 H18 N2 O4C 1 2/c 123.2511; 6.0802; 18.4786
90; 97.79; 90		2588.2Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133163 CIFC18 H22 N2 O4P -19.5021; 9.6751; 10.0293
77.914; 71.586; 89.936		853.33Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133164 CIFC22 H29 N3 O5P -19.6012; 10.4718; 11.4984
86.861; 70.637; 79.609		1072.78Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133165 CIFC19 H22 N O4P 1 21/c 115.1005; 9.909; 11.5159
90; 93.934; 90		1719.1Shi, Lin; Liu, Lidong; Lei, Xingyu; Wang, Yihan; Fang, Yeguang; Jiao, Peng
Dearomative pyrrole (3+2) reaction with geminal bromonitroalkane: synthesis of 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6953-6956
7133166 CIFC32 H52 Bi2 F12 N4 Sb2C 1 2/c 136.971; 11.0199; 21.471
90; 101.205; 90		8581Sen, Nilanjana; Sarkar, Pallavi; Meena, Yadram; Tothadi, Srinu; Pati, Swapan K.; Khan, Shabana
Synthesis and catalytic application of a donor-free bismuthenium cation.
Chemical communications (Cambridge, England), 2024, 60, 6877-6880
7133167 CIFC93 H88 Ce4 N4P 1 21/c 18.0983; 17.5589; 27.1102
90; 90.172; 90		3854.98Gupta, Himanshu; Vincenzini, Brett D.; Bacon, Alexandra M.; Schelter, Eric J.
Assembly of a trapped valent Ce<sup>III/IV</sup>-TCNQ complex through metal-ligand redox cooperativity.
Chemical communications (Cambridge, England), 2024, 60, 6909-6912
7133168 CIFC7 H6 O2P 1 21/n 15.502; 5.137; 21.927
90; 97.045; 90		615.1Sun, Hainan; Li, Lili; Chen, Yahui; Kim, Yong Beom; Kim, Hyunseung; Fei, Liangshuang; Shao, Zongping; Jung, WooChul
Crystal structure optimization of copper oxides for the benzyl alcohol oxidation reaction.
Chemical communications (Cambridge, England), 2024, 60, 7224-7227
7133169 CIFC54 H53 N3P -110.502; 11.537; 19.141
96.877; 98.17; 99.193		2241.9Naniyil, Athira; Koroth Valappil, Naveen; Andrews, Alex P.; Gokulnath, Sabapathi
Carbazole-embedded <i>p</i>-benziporphyrinoid: synthesis, structure and a reversible chemodosimeter for mercury(II) ions.
Chemical communications (Cambridge, England), 2024, 60, 6957-6960
7133170 CIFC56 H54 Cl7 Hg N3R -3 :H43.456; 43.456; 14.847
90; 90; 120		24281Naniyil, Athira; Koroth Valappil, Naveen; Andrews, Alex P.; Gokulnath, Sabapathi
Carbazole-embedded <i>p</i>-benziporphyrinoid: synthesis, structure and a reversible chemodosimeter for mercury(II) ions.
Chemical communications (Cambridge, England), 2024, 60, 6957-6960
7133171 CIFC38 H53 Au N4 SiP -113.0228; 16.875; 18.996
76.362; 79.196; 70.713		3801.7Bakhoda, Abolghasem 'Gus'
Gold(I)-catalyzed homologation of aryl aldehydes with trimethylsilyldiazomethane.
Chemical communications (Cambridge, England), 2024, 60, 6937-6940
7133172 CIFC116.94 H127.44 Cl8.84 N12P -114.354; 18.2341; 23.2636
110.586; 101.322; 93.081		5538.9Heim, Gavin P.; Hirahara, Masanari; Dev, Vidhya M.; Agapie, Theodor
Synthesis and electronic properties of nitrogen-rich nanographene.
Chemical communications (Cambridge, England), 2024, 60, 7343-7346
7133173 CIFC25 H47 Ir P2P b c a10.0014; 17.1635; 28.5541
90; 90; 90		4901.6Demchuk, Mitchell J.; Zurakowski, Joseph A.; Drover, Marcus W.
Tridentate κ<sup>3</sup>-<i>P</i>,<i>P</i>,<i>C</i> iridium complexes: influence of ligand saturation on intramolecular C-H bond activation.
Chemical communications (Cambridge, England), 2024, 60, 7566-7569
7133174 CIFC25 H47 Ir P2P 1 21/c 110.405; 18.494; 13.748
90; 109.51; 90		2494Demchuk, Mitchell J.; Zurakowski, Joseph A.; Drover, Marcus W.
Tridentate κ<sup>3</sup>-<i>P</i>,<i>P</i>,<i>C</i> iridium complexes: influence of ligand saturation on intramolecular C-H bond activation.
Chemical communications (Cambridge, England), 2024, 60, 7566-7569
7133175 CIFC25 H49 Ir P2P b c a17.8681; 14.8775; 38.003
90; 90; 90		10102.4Demchuk, Mitchell J.; Zurakowski, Joseph A.; Drover, Marcus W.
Tridentate κ<sup>3</sup>-<i>P</i>,<i>P</i>,<i>C</i> iridium complexes: influence of ligand saturation on intramolecular C-H bond activation.
Chemical communications (Cambridge, England), 2024, 60, 7566-7569
7133176 CIFC5 H8 Cl F2 NP n m a10.0074; 7.0673; 9.5009
90; 90; 90		671.95Charlesworth, Natalie G.; Arunprasath, Dhanarajan; Graham, Mark A.; Argent, Stephen P.; Datsenko, Oleksandr P.; Mykhailiuk, Pavel K.; Denton, Ross M.
Modular synthesis of cyclic β-difluoroamines.
Chemical communications (Cambridge, England), 2024, 60, 7701-7704
7133177 CIFC29 H28 N0 O4C 1 2/c 119.9766; 15.8235; 15.6346
90; 93.935; 90		4930.4Ren, Yue; Shi, Wangyu; Tang, Yi; Guo, Hongchao
Phosphine-catalyzed (3+3) annulation of cinnamaldehyde-derived Morita-Baylis-Hillman carbonates with dinucleophiles.
Chemical communications (Cambridge, England), 2024, 60, 6897-6900
7133178 CIFC23 H18 N2 O5P 1 21/c 111.6492; 7.4491; 22.0277
90; 97.248; 90		1896.2He, Yongjun; He, Tian-Juan; Cheng, Xiufang; Wei, Yibo; Wang, Huamin; Lin, Ying-Wu
Phosphine-catalyzed dearomative [3+2] cycloaddition of 4-nitroisoxazoles with allenoates or Morita-Baylis-Hillman carbonates.
Chemical communications (Cambridge, England), 2024, 60, 6961-6964
7133179 CIFC15 H12 N4 O5 SP 1 21/c 113.0981; 11.5834; 10.0872
90; 100.284; 90		1505.85He, Yongjun; He, Tian-Juan; Cheng, Xiufang; Wei, Yibo; Wang, Huamin; Lin, Ying-Wu
Phosphine-catalyzed dearomative [3+2] cycloaddition of 4-nitroisoxazoles with allenoates or Morita-Baylis-Hillman carbonates.
Chemical communications (Cambridge, England), 2024, 60, 6961-6964
7133180 CIFC37 H39 B O2 SiC 1 2/c 116.206; 14.988; 26.246
90; 99.955; 90		6279Fujii, Ikuya; Hirata, Haruka; Moniwa, Hirokazu; Shintani, Ryo
Synthesis of (1-silyl)allylboronates by KO<i>t</i>Bu-catalyzed ring-opening <i>gem</i>-silylborylation of cyclopropenes.
Chemical communications (Cambridge, England), 2024, 60, 6921-6924
7133181 CIFC29 H46 Cr O2 P2P -110.4305; 10.4775; 14.5388
78.486; 83.946; 71.492		1474.9Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martín A; Arulsamy, Navamoney; Mock, Michael T.
Dinitrogen activation at chromium by photochemically induced Cr<sup>II</sup>-C bond homolysis.
Chemical communications (Cambridge, England), 2024, 60, 7029-7032
7133182 CIFC29 H46 Cr O2 P2P 1 21 18.2502; 15.8605; 11.8231
90; 106.188; 90		1485.74Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martín A; Arulsamy, Navamoney; Mock, Michael T.
Dinitrogen activation at chromium by photochemically induced Cr<sup>II</sup>-C bond homolysis.
Chemical communications (Cambridge, England), 2024, 60, 7029-7032
7133183 CIFC46 H83 Cr2 N2 O4.5 P4P 1 21/n 115.7583; 14.4111; 24.856
90; 107.974; 90		5369.2Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martín A; Arulsamy, Navamoney; Mock, Michael T.
Dinitrogen activation at chromium by photochemically induced Cr<sup>II</sup>-C bond homolysis.
Chemical communications (Cambridge, England), 2024, 60, 7029-7032
7133184 CIFC26 H21 N O4P 1 21 16.9055; 21.4299; 27.6189
90; 92.031; 90		4084.6Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4<i>H</i>-benzo[<i>d</i>][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6933-6936
7133185 CIFC24 H21 Cl N2 O3P -19.6896; 10.1998; 10.8323
89.99; 71.675; 84.875		1011.78Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4<i>H</i>-benzo[<i>d</i>][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6933-6936
7133186 CIFC34 H30 N2 O3P 1 21/c 111.847; 18.1061; 13.0266
90; 95.964; 90		2779.1Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4<i>H</i>-benzo[<i>d</i>][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles.
Chemical communications (Cambridge, England), 2024, 60, 6933-6936
7133187 CIFC10 H11 N O3P 1 21/c 19.9227; 5.672; 16.1656
90; 99.498; 90		897.35Winter, Johannes; Lühr, Susan; Hochadel, Kyra; Gálvez-Vázquez, María de Jesús; Prenzel, Tobias; Schollmeyer, Dieter; Waldvogel, Siegfried R.
Simple electrochemical synthesis of cyclic hydroxamic acids by reduction of nitroarenes.
Chemical communications (Cambridge, England), 2024, 60, 7065-7068
7133188 CIFC81 H106 N2 O18P 1 21/c 112.3241; 33.684; 20.229
90; 96.013; 90		8351Li, Bin; Wang, Yun; Wang, Yuan; Liu, Yue; Wang, Lu; Zhang, Zhi-Yuan; Li, Chunju
Vapochromic separation of toluene and pyridine azeotropes using adaptive macrocycle co-crystals.
Chemical communications (Cambridge, England), 2024, 60, 6889-6892
7133189 CIFC93 H110 N6 O14P -112.08; 12.4509; 29.1324
94.272; 92.465; 106.74		4174.8Li, Bin; Wang, Yun; Wang, Yuan; Liu, Yue; Wang, Lu; Zhang, Zhi-Yuan; Li, Chunju
Vapochromic separation of toluene and pyridine azeotropes using adaptive macrocycle co-crystals.
Chemical communications (Cambridge, England), 2024, 60, 6889-6892
7133190 CIFC52 H76 Fe N2 O2P -19.5346; 13.1604; 18.8315
91.84; 90.463; 91.367		2361Kulathungage, Lakshani W.; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient carbene transfer reactivity mediated by Fe(II) complexes supported by bulky alkoxides.
Chemical communications (Cambridge, England), 2024, 60, 7033-7036
7133191 CIFC37 H28 O8P 1 21/c 110.323; 19.0774; 8.7024
90; 114.576; 90		1558.56Kulathungage, Lakshani W.; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient carbene transfer reactivity mediated by Fe(II) complexes supported by bulky alkoxides.
Chemical communications (Cambridge, England), 2024, 60, 7033-7036
7133192 CIFC5 H6 O4P -15.006; 7.2628; 8.6451
106.71; 102.405; 92.116		292.37Kulathungage, Lakshani W.; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient carbene transfer reactivity mediated by Fe(II) complexes supported by bulky alkoxides.
Chemical communications (Cambridge, England), 2024, 60, 7033-7036
7133193 CIFC26.9 H40.71 Cl6.1 Ga2 N4 O P PtP -18.30726; 15.0654; 15.9963
70.9877; 84.8936; 79.8892		1862.28Govindarajan, R.; Vardhanapu, Pavan K.; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from Pt<sup>II</sup> to gallium and indium.
Chemical communications (Cambridge, England), 2024, 60, 7216-7219
7133194 CIFC27 H41 Cl6 In2 N4 O P PtP 1 21/n 18.88651; 12.2296; 35.1991
90; 93.5845; 90		3817.9Govindarajan, R.; Vardhanapu, Pavan K.; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from Pt<sup>II</sup> to gallium and indium.
Chemical communications (Cambridge, England), 2024, 60, 7216-7219
7133195 CIFC28.77 H41.3 Cl6.23 In2 N4 O P PtP -18.71612; 14.4778; 17.6581
65.9038; 81.2608; 73.8299		1951.78Govindarajan, R.; Vardhanapu, Pavan K.; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from Pt<sup>II</sup> to gallium and indium.
Chemical communications (Cambridge, England), 2024, 60, 7216-7219
7133196 CIFC28 H22 N O2 PP -19.2305; 9.3886; 15.0613
83.016; 81.79; 62.191		1140.4Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: access to 2-phosphinoyl indoles/indol-3-ols.
Chemical communications (Cambridge, England), 2024, 60, 7196-7199
7133197 CIFC29 H24 N O3 PP -110.1021; 10.6285; 12.0861
95.272; 112.661; 92.657		1187.71Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: access to 2-phosphinoyl indoles/indol-3-ols.
Chemical communications (Cambridge, England), 2024, 60, 7196-7199
7133198 CIFC29.6 H25.2 Cl1.2 N O3 PP -19.9338; 11.4115; 13.4261
91.104; 99.247; 107.898		1425.68Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: access to 2-phosphinoyl indoles/indol-3-ols.
Chemical communications (Cambridge, England), 2024, 60, 7196-7199
7133199 CIFC46 H41 N2 O8 S2P -110.581; 10.781; 20.524
88.303; 85.635; 63.604		2091.1Bhati, Kuldeep Singh; Sharma, Siddharth
Electrochemically-driven difunctionalization of the isocyanide and Mumm rearrangement cascade: expeditious synthesis of <i>N</i>-acyl-<i>N</i>-alkyl <i>S</i>-thiocarbamates.
Chemical communications (Cambridge, England), 2024, 60, 7355-7358
7133200 CIFC26 H19 Cl F6 N2 O4P b c n16.652; 14.997; 21.13
90; 90; 90		5276.8Tang, Yong-Xing; Zhou, You; Wu, Hao-Xuan; Wang, Li-Sheng; Wu, Chun-Yan; Zhuang, Shi-Yi; Wu, An-Xin
<i>N</i>-Benzylhydroxylamine as a novel synthetic block in "C1N1" embedding reaction <i>via</i> α-C(sp<sup>3</sup>)-H activation strategy.
Chemical communications (Cambridge, England), 2024, 60, 7180-7183
7133201 CIFC15 H13 N O2C 1 2/c 112.719; 13.852; 14.156
90; 97.096; 90		2475Tang, Yong-Xing; Zhou, You; Wu, Hao-Xuan; Wang, Li-Sheng; Wu, Chun-Yan; Zhuang, Shi-Yi; Wu, An-Xin
<i>N</i>-Benzylhydroxylamine as a novel synthetic block in "C1N1" embedding reaction <i>via</i> α-C(sp<sup>3</sup>)-H activation strategy.
Chemical communications (Cambridge, England), 2024, 60, 7180-7183
7133202 CIFC38 H28 O3 P2P b c a16.51047; 16.41081; 23.08005
90; 90; 90		6253.54Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133203 CIFC19 H13 P SC 1 2/c 114.248; 13.5359; 15.8127
90; 90.772; 90		3049.35Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133204 CIFC24 H22 N O PP n a 2117.3159; 9.40206; 12.4887
90; 90; 90		2033.22Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133205 CIFC19 H13 P SeC 1 2/c 114.1963; 13.7375; 15.8281
90; 90.897; 90		3086.4Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133206 CIFC26 H20 N O2 P SP 1 21/c 18.19512; 13.942; 19.4641
90; 99.7093; 90		2192.04Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133207 CIFC34 H36 N O2 P SP 21 21 219.31097; 12.97197; 24.0692
90; 90; 90		2907.12Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133208 CIFC44 H33 B F4 N PP c a 2112.867; 13.069; 21.505
90; 90; 90		3616.3Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133209 CIFC25.5 H19 B Cl F3 N PP 1 21/c 19.5904; 16.0488; 14.2154
90; 101.406; 90		2144.74Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133210 CIFC31 H23 N O3 P2P 1 21/c 111.81181; 19.91502; 11.98573
90; 118.939; 90		2467.38Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133211 CIFC38 H28 O3 P2P b c a16.3712; 16.281; 22.9501
90; 90; 90		6117.11Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133212 CIFC19 H14 O2 PC 1 2/c 120.3958; 13.4454; 12.1945
90; 117.604; 90		2963.44Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133213 CIFC19 H13 P SeC 1 2/c 114.0369; 13.6803; 15.7202
90; 90.789; 90		3018.45Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133214 CIFC19 H13 O PP -17.2774; 8.0944; 13.1388
81.7506; 79.8049; 70.6319		715.63Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133215 CIFC25 H18 N PP 21 21 218.9413; 13.6176; 15.5673
90; 90; 90		1895.46Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133216 CIFC44 H20 B Cl2 F15 N PP -111.2365; 12.2624; 14.8185
83.39; 78.06; 74.601		1921.98Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133217 CIFC31 H30 N PP 1 21/n 19.0484; 18.306; 14.4219
90; 90.4144; 90		2388.78Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133218 CIFC27 H19 F6 N2 O4 P S2P -18.3718; 17.3368; 20.1621
113.925; 91.4063; 93.9353		2664.18Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133219 CIFC19 H13 P SC 1 2/c 114.0811; 13.4388; 15.6879
90; 90.464; 90		2968.57Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024, 60, 7073-7076
7133220 CIFC27 H38 N2 O5 S SiP 1 21 18.956; 12.4093; 12.9018
90; 95.349; 90		1427.63Mroczyńska, Karina; Dobrzańska, Liliana; Rafiński, Zbigniew
Enantioselective synthesis of C3-functionalized 2,1-benzothiazine 2,2-dioxides by N-heterocyclic carbene catalysis.
Chemical communications (Cambridge, England), 2024, 60, 7176-7179
7133221 CIFC41 H35 Cl3 N0.5 O5 PP -111.7184; 12.545; 14.696
101.781; 98.985; 114.481		1853.15Zhou, Xiaocong; Wang, Jian; Ma, Dumei; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical synthesis of phosphorylated azaspiro[4.5]di/trienones through dearomative spirocyclization.
Chemical communications (Cambridge, England), 2024, 60, 7351-7354
7133222 CIFC58 H51.67 N2 O8 P2P b c a21.3419; 21.1766; 21.9827
90; 90; 90		9935.1Zhou, Xiaocong; Wang, Jian; Ma, Dumei; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical synthesis of phosphorylated azaspiro[4.5]di/trienones through dearomative spirocyclization.
Chemical communications (Cambridge, England), 2024, 60, 7351-7354
7133223 CIFC29 H24 Cl4 F N O2 PP -110.835; 12.7978; 20.779
81.75; 80.192; 89.486		2809.45Zhou, Xiaocong; Wang, Jian; Ma, Dumei; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical synthesis of phosphorylated azaspiro[4.5]di/trienones through dearomative spirocyclization.
Chemical communications (Cambridge, England), 2024, 60, 7351-7354
7133224 CIFC18 H13 N3 O2P -16.902; 13.8797; 16.3061
66.241; 89.878; 76.826		1385Chatterjee, Sarat; Khatun, Rousunara; Ali, Mahammad; Chowdhury, Chinmay
A solvent controlled regioselective synthesis of 2- and 4-substituted α-carbolines under palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 7427-7430
7133225 CIFC19 H16 N2P 1 21/n 113.4739; 7.1393; 14.6043
90; 101.576; 90		1376.27Chatterjee, Sarat; Khatun, Rousunara; Ali, Mahammad; Chowdhury, Chinmay
A solvent controlled regioselective synthesis of 2- and 4-substituted α-carbolines under palladium catalysis.
Chemical communications (Cambridge, England), 2024, 60, 7427-7430
7133226 CIFC56 H92 Mg2 N4 O2 Si4P 1 21/n 115.637; 11.51056; 17.4414
90; 108.662; 90		2974.23O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133227 CIFC42 H68 K Mg N2 O3 Si2P 1 21/n 114.3212; 20.5716; 15.38509
90; 94.3942; 90		4519.28O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133228 CIFC66 H112 K2 Mg2 N4 O6 Si4P -110.9645; 15.9181; 23.3852
70.892; 89.038; 72.072		3653.33O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133229 CIFC138 H224 K4 Mg4 N12 O4 Si8P -116.3939; 21.2191; 21.8811
81.3508; 89.9089; 88.1901		7521.29O'Reilly, Andrea; Haynes, Matthew D.; Turner, Zoë R; McMullin, Claire L.; Harder, Sjoerd; O'Hare, Dermot; Fulton, J. Robin; Coles, Martyn P.
Mixing and matching <i>N</i>,<i>N</i>- and <i>N</i>,<i>O</i>-chelates in anionic Mg(I) compounds: synthesis and reactivity with RNCNR and CO.
Chemical communications (Cambridge, England), 2024, 60, 7204-7207
7133230 CIFC24 H18 O5P -18.3038; 11.289; 11.546
63.736; 87.201; 78.91		951.7Singh, Sanjay; Sharma, Pragya; Dutta, Sayantan; Vishwakarma, Rahul; Hazra, Chinmoy K.
An organocatalytic domino annulation approach <i>via</i> C(sp<sup>2</sup>)-OMe cleavage to unlock the synthesis of pyranochromenones enabled by HFIP.
Chemical communications (Cambridge, England), 2024, 60, 7200-7203
7133231 CIFC24 H17 Cl O5P -17.3859; 10.8372; 12.379
101.327; 97.246; 92.314		961.6Singh, Sanjay; Sharma, Pragya; Dutta, Sayantan; Vishwakarma, Rahul; Hazra, Chinmoy K.
An organocatalytic domino annulation approach <i>via</i> C(sp<sup>2</sup>)-OMe cleavage to unlock the synthesis of pyranochromenones enabled by HFIP.
Chemical communications (Cambridge, England), 2024, 60, 7200-7203
7133232 CIFC6 H36 Ho2 O30R -3 :H30.5; 30.5; 7.127
90; 90; 120		5742El Alouani Dahmouni, Nadia; Orts-Arroyo, Marta; Sanchis-Perucho, Adrián; Moliner, Nicolás; Mayans, Júlia; Pacheco, Mario; Castro, Isabel; De Munno, Giovanni; Marino, Nadia; Ruiz-García, Rafael; Martínez-Lillo, José
Magnetocaloric efficiency tuning through solvent-triggered 3D to 2D interconversion in holmium(III)-based dynamic MOFs.
Chemical communications (Cambridge, England), 2024, 60, 7451-7454
7133233 CIFC6 H20 Ho2 O22P 1 21/c 110.9347; 9.604; 9.9542
90; 114.143; 90		953.92El Alouani Dahmouni, Nadia; Orts-Arroyo, Marta; Sanchis-Perucho, Adrián; Moliner, Nicolás; Mayans, Júlia; Pacheco, Mario; Castro, Isabel; De Munno, Giovanni; Marino, Nadia; Ruiz-García, Rafael; Martínez-Lillo, José
Magnetocaloric efficiency tuning through solvent-triggered 3D to 2D interconversion in holmium(III)-based dynamic MOFs.
Chemical communications (Cambridge, England), 2024, 60, 7451-7454
7133234 CIFC21 H20 O4P 21 21 218.5423; 12.3659; 16.7686
90; 90; 90		1771.32Zeng, Hongkun; Wen, Gang; Lin, Lili; Feng, Xiaoming
Asymmetric dearomatization of benzyl 1-naphthyl ethers <i>via</i> [1,3] O-to-C rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7507-7510
7133235 CIFC55 H88 B2 Co F8 N4 O7P 1 21 112.6042; 16.7477; 13.9724
90; 90.008; 90		2949.45Zeng, Hongkun; Wen, Gang; Lin, Lili; Feng, Xiaoming
Asymmetric dearomatization of benzyl 1-naphthyl ethers <i>via</i> [1,3] O-to-C rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 7507-7510
7133236 CIFC48 H96 Al4 Eu4 N8 O32I 1 2/a 127.7753; 10.2408; 29.891
90; 117.95; 90		7510.5Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133237 CIFC216 H440 Al16 Er16 N40 O136I 1 2/a 128.9871; 10.1594; 27.5988
90; 99.049; 90		8026.5Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133238 CIFC48 H96 Al4 N8 O32 Sm4I 1 2/a 127.9072; 10.2096; 29.8833
90; 118.087; 90		7511.7Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133239 CIFC47.99 H95.97 Al4 Gd4 N8 O32I 1 2/a 127.5463; 10.2945; 29.7052
90; 117.751; 90		7454.8Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133240 CIFC51 H103 Al4 Dy4 N9 O33I 1 2/a 129.1901; 10.2991; 27.6382
90; 98.946; 90		8207.8Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133241 CIFC51 H101 Al4 Ho4 N9 O33I 1 2/a 128.9677; 10.1285; 27.67
90; 99.14; 90		8015.3Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133242 CIFC48 H96 Al4 N8 O32 Tm4I 1 2/a 127.599; 10.1083; 28.8433
90; 99.182; 90		7943.6Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133243 CIFC54 H110 Al4 N10 O34 Tb4I 1 2/a 127.9239; 10.1329; 28.9993
90; 99.256; 90		8098.5Sun, Qian-Ru; Luo, Dan; Lv, Yaokang; Fang, Wei-Hui; Zhang, Jian
Synthesis and photoluminescence properties of polymer chains based on pre-designed heterometallic Al<sub>4</sub>Ln<sub>4</sub> molecular rings.
Chemical communications (Cambridge, England), 2024, 60, 7574-7577
7133244 CIFC106 H92.03 N6 O18P -114.4561; 21.9459; 22.0092
60.305; 83.03; 74.276		5837.8Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133245 CIFC102 H90 N6 O18P -114.3348; 21.7619; 21.9674
114.642; 97.609; 108.079		5642.86Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133246 CIFC107 H98.1 N6 O18P -114.4122; 21.9201; 22.0159
60.357; 83.564; 74.23		5815.3Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133247 CIFC144 H135 N9 O27C 1 2/c 138.116; 21.9306; 42.5599
90; 103.44; 90		34601.8Samanta, Krishanu; Mi, Jiashan; Chen, Albert D.; Li, Fangzhou; Staples, Richard J.; Rossini, Aaron J.; Ke, Chenfeng
Porous organic crystals crosslinked by free-radical reactions.
Chemical communications (Cambridge, England), 2024, 60, 7311-7314
7133248 CIFC12 H36 Ag Br11.74 Cl0.26 N4 SbP 1 c 18.6321; 7.8942; 25.961
90; 90.123; 90		1769.1Rajput, Shubham Ajaykumar; Antharjanam, Sudhadevi; Chandiran, Aravind Kumar
An above-room-temperature ferroelectric two-dimensional halide double perovskite with direction dependent properties.
Chemical communications (Cambridge, England), 2024, 60, 7898-7901
7133249 CIFC144 H290 Cu48 N16 O189 P16 S20C 1 2 132.3485; 19.7547; 32.5262
90; 112.66; 90		19180.9Teng, Qian; Gao, Ran; Bao, Song-Song; Zheng, Li-Min
Cu<sub>12</sub>-cluster-based metal-organic framework as a metastable intermediate in the formation of a layered copper phosphonate.
Chemical communications (Cambridge, England), 2024, 60, 7765-7768
7133250 CIFC9.5 H19 Cu2 N O10 P SP 21 21 217.0932; 7.3733; 31.2935
90; 90; 90		1636.66Teng, Qian; Gao, Ran; Bao, Song-Song; Zheng, Li-Min
Cu<sub>12</sub>-cluster-based metal-organic framework as a metastable intermediate in the formation of a layered copper phosphonate.
Chemical communications (Cambridge, England), 2024, 60, 7765-7768
7133251 CIFC34 H35 N3 O4 SP 1 21/c 114.791; 11.623; 18.6337
90; 109.354; 90		3022.4Sun, Zetian; Zhang, Jianting; Du, Xiaohua; Liu, Lulu; Gao, Shuo; Qi, Chenchen; Li, Xiaoqing; Xu, Xiangsheng
Photoinduced EnT-mediated sulfonamidylimination of alkenes and (hetero)arenes with iminophenylacetic acid oxime esters.
Chemical communications (Cambridge, England), 2024, 60, 7934-7937
7133252 CIFC61 H68 Cl2 O13R 3 c :H13.5991; 13.5991; 52.4778
90; 90; 120		8404.8Liu, Rui; Li, Ming; Liu, Zhongwen; Hua, Bin
Separation of cyclohexanol from cyclohexanol/cyclohexene mixtures by crystals of pillar[6]arene containing three benzoquinone units.
Chemical communications (Cambridge, England), 2024, 60, 7626-7629
7133253 CIFC39 H45 N3 O12P 1 21/c 116.1387; 28.3321; 8.3321
90; 95.419; 90		3792.8Wu, Simei; Tao, Wei; Wang, Tao; Xu, Jieqiong; Wei, Peifa
A crown ether embedded responsive π-gelator for transition from a one-component gel to a two-component gel.
Chemical communications (Cambridge, England), 2024, 60, 8232-8235
7133254 CIFC37 H41 N2 O12P 1 21/c 131.3061; 4.701; 26.9834
90; 93.029; 90		3965.6Wu, Simei; Tao, Wei; Wang, Tao; Xu, Jieqiong; Wei, Peifa
A crown ether embedded responsive π-gelator for transition from a one-component gel to a two-component gel.
Chemical communications (Cambridge, England), 2024, 60, 8232-8235
7133255 CIFC50 H36 O2P 1 21/n 117.155; 10.5253; 19.426
90; 91.508; 90		3506.4Sheokand, Sonu; Sharma, Sunita; Mohite, Manali A.; Rajaraman, Gopalan; Balakrishna, Maravanji S.
ZnCl<sub>2</sub>-catalysed transfer hydrogenation of carbonyls and chemoselective reduction of the CC bond in α,β-unsaturated ketones.
Chemical communications (Cambridge, England), 2024, 60, 7733-7736
7133256 CIFC48 H36 N2 O6 ZnP 1 21/c 17.9091; 23.3932; 20.4994
90; 90.281; 90		3792.74Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133257 CIFC48 H36 N2 O6 ZnP 1 21/c 17.9164; 23.6249; 20.5918
90; 91.802; 90		3849.3Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133258 CIFC48 H36 N2 O6 ZnP 1 21/c 17.8927; 23.5873; 20.5265
90; 91.988; 90		3819.1Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133259 CIFC48 H36 N2 O6 ZnP 1 21/c 17.8858; 23.506; 20.4093
90; 91.544; 90		3781.8Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133260 CIFC48 H36 N2 O6 ZnP 1 21/c 17.8902; 23.5724; 20.3308
90; 92.206; 90		3778.54Pham-Tran, Victoria N P; Moffat, James G. D.; Marczenko, Katherine M.
Polymorph driven diversification of photosalient responses in a zinc(II) coordination complex.
Chemical communications (Cambridge, England), 2024, 60, 7890-7893
7133261 CIFC144 H212 K2 N2 O26 Ti2P -113.452; 22.8729; 23.7434
101.621; 94.411; 90.086		7133.5Ishida, Yutaka; Nakanishi, Yusuke; Hiratsuka, Takuma; Kawaguchi, Hiroyuki
Hydrazido complexes prepared by methylation of an anionic end-on bridging dinitrogen dititanium complex.
Chemical communications (Cambridge, England), 2024, 60, 7459-7462
7133262 CIFC108 H158 K2 N2 O10 Ti2C 1 c 113.92; 25.4342; 30.2821
90; 103.153; 90		10439.9Ishida, Yutaka; Nakanishi, Yusuke; Hiratsuka, Takuma; Kawaguchi, Hiroyuki
Hydrazido complexes prepared by methylation of an anionic end-on bridging dinitrogen dititanium complex.
Chemical communications (Cambridge, England), 2024, 60, 7459-7462
7133263 CIFC64 H64 N4P 1 21/n 112.6774; 23.2733; 17.2556
90; 92.162; 90		5087.6Jiang, Zhiyan; Kuninobu, Yoichiro
Synthesis of a novel twisted π-conjugated macrocycle <i>via</i> double Friedel-Crafts reaction and its physical properties.
Chemical communications (Cambridge, England), 2024, 60, 7642-7645
7133264 CIFC77 H61 Li8 N7 O19P -19.8956; 13.8451; 14.417
95.736; 94.844; 102.727		1905.5Li, Shu-Fan; Meng, Ya-Ru; Xu, Min-Jie; Zhang, Gen; Su, Jian
Construction of a redox-active metal-organic framework with an octanuclear lithium one-dimensional building block.
Chemical communications (Cambridge, England), 2024, 60, 8047-8050
7133265 CIFC136 H204 Ca4 N8 Zn4P -115.2503; 16.0371; 16.0776
69.051; 69.699; 71.172		3354.3Pearce, Kyle G.; Neale, Samuel E.; McMullin, Claire L.; Mahon, Mary F.; Hill, Michael S.
Pathway to a molecular calcium methyl.
Chemical communications (Cambridge, England), 2024, 60, 7882-7885
7133266 CIFC72 H116 Ca2 N4P 1 21/n 113.5951; 19.1092; 14.1535
90; 108.43; 90		3488.37Pearce, Kyle G.; Neale, Samuel E.; McMullin, Claire L.; Mahon, Mary F.; Hill, Michael S.
Pathway to a molecular calcium methyl.
Chemical communications (Cambridge, England), 2024, 60, 7882-7885
7133267 CIFC48 H31 Cl2 NP -110.6735; 11.3393; 15.9814
96.998; 104.429; 106.09		1761.56Wang, Ru-Jia; Zheng, Fan; Liu, Xiao-Long; Wu, Yu-Lan; Jin, Jia-Ming; Li, Ze-Yan; Chen, Wen-Cheng; Huo, Yanping
A through-space charge transfer pyrene-based fluorophore with anti-quenching behavior for deep-blue organic light-emitting devices.
Chemical communications (Cambridge, England), 2024, 60, 7946-7949
7133268 CIFC20 H18 O4P 21 21 216.3415; 8.4205; 30.8465
90; 90; 90		1647.16Tan, Zheng; Yihuo, Aying; Wu, Zhao; Wang, Fei; Dong, Shunxi; Feng, Xiaoming
Concise synthesis of chiral γ-butenolides <i>via</i> an allylation/lactonization cascade reaction.
Chemical communications (Cambridge, England), 2024, 60, 7926-7929
7133269 CIFC79 H69.5 Cd F12 N8.5 O8 P2P 1 21/n 112.4369; 24.8732; 25.4913
90; 101.228; 90		7734.7Wang, Shih-Yu; Lin, Lin-Ting; Rani, Alisha; Lee, Guan-Sian; Chan, Yi-Tsu
Stepwise construction of a metallocatenane based on non-labile bis(terpyridine)-Cd<sup>II</sup> complexes.
Chemical communications (Cambridge, England), 2024, 60, 7914-7917
7133270 CIFC26 H28 B N3P 1 21/c 18.4111; 15.3474; 17.0335
90; 96.326; 90		2185.4Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133271 CIFC32 H33 B2 N3P -18.9434; 12.002; 13.5298
105.413; 90.951; 109.556		1310.34Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133272 CIFC34 H43 B2 N3P 1 21/n 111.6929; 17.5821; 14.6284
90; 104.319; 90		2914Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133273 CIFC26 H28 B2 F3 N3P c a 2113.4867; 12.7379; 13.3863
90; 90; 90		2299.7Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133274 CIFC32 H33 B2 Cl2 N3P -18.2484; 8.6731; 22.3744
81.768; 85.754; 62.036		1399.1Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133275 CIFC26 H28 B2 Cl3 N3P 1 21/c 115.6649; 11.3864; 15.8645
90; 115.787; 90		2547.9Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133276 CIFC27 H31 B I N3P 1 21/c 18.0398; 28.378; 11.9315
90; 108.797; 90		2577Pattathil, Vignesh; Pranckevicius, Conor
Aromaticity transfer in an annulated 1,4,2-diazaborole: facile access to <i>C</i><sub>s</sub> symmetric 1,4,2,5-diazadiborinines.
Chemical communications (Cambridge, England), 2024, 60, 7705-7708
7133277 CIFC94 H162 Be2 Cl2 Li2 N4 O14 Si4P 1 21/c 121.4089; 22.319; 22.5227
90; 102.668; 90		10499.9Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133278 CIFC48 H86 Be Cl K N2 O9 Si2P 1 21/n 110.5322; 21.8852; 24.244
90; 92.113; 90		5584.43Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133279 CIFC50 H90 Be Cl N2 Na O10 Si2P 1 21/c 115.1421; 20.7692; 18.2654
90; 91.531; 90		5742.2Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133280 CIFC52.5 H86 Be Cl N2 O6 Rb Si2P 1 21/n 116.7051; 21.103; 17.1977
90; 103.361; 90		5898.57Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133281 CIFC58 H94 Be Cl N2 Na O8 Si2P 1 21/n 112.1829; 17.5093; 29.91
90; 96.725; 90		6336.33Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133282 CIFC46 H82 Be Cl K N2 O8 Si2P 1 21 114.9011; 19.7649; 18.0278
90; 93.633; 90		5298.86Pearce, Kyle G.; Neale, Samuel E.; Mahon, Mary F.; McMullin, Claire L.; Hill, Michael S.
Alkali metal reduction of crown ether encapsulated alkali metal cations.
Chemical communications (Cambridge, England), 2024, 60, 8391-8394
7133283 CIFC24 H21 N O6 SP 21 21 219.792; 10.139; 21.399
90; 90; 90		2124.5Yang, Ji Seon; Kim, Sung-Gon
Catalytic enantioselective [3+2] and [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines with γ- or δ-hydroxy-α,β-unsaturated ketones.
Chemical communications (Cambridge, England), 2024, 60, 7954-7957
7133284 CIFC21 H21 N O6 SP 41 21 28.4145; 8.4145; 56.119
90; 90; 90		3973.4Yang, Ji Seon; Kim, Sung-Gon
Catalytic enantioselective [3+2] and [4+2]-annulation of cyclic <i>N</i>-sulfonyl ketimines with γ- or δ-hydroxy-α,β-unsaturated ketones.
Chemical communications (Cambridge, England), 2024, 60, 7954-7957
7133285 CIFC25 H51 Os TaC 1 2/c 117.7258; 16.513; 19.8168
90; 104.405; 90		5618.14Lachguar, Abdelhak; Ye, Christopher Z.; Kelly, Sheridon N.; Jeanneau, Erwann; Del Rosal, Iker; Maron, Laurent; Veyre, Laurent; Thieuleux, Chloé; Arnold, John; Camp, Clément
CO<sub>2</sub> cleavage by tantalum/M (M = iridium, osmium) heterobimetallic complexes.
Chemical communications (Cambridge, England), 2024, 60, 7878-7881
7133286 CIFC11 H18 O OsP 1 21/n 18.149; 11.0276; 13.2481
90; 101.769; 90		1165.5Lachguar, Abdelhak; Ye, Christopher Z.; Kelly, Sheridon N.; Jeanneau, Erwann; Del Rosal, Iker; Maron, Laurent; Veyre, Laurent; Thieuleux, Chloé; Arnold, John; Camp, Clément
CO<sub>2</sub> cleavage by tantalum/M (M = iridium, osmium) heterobimetallic complexes.
Chemical communications (Cambridge, England), 2024, 60, 7878-7881
7133287 CIFC30 H22 Co N12 O6 S4P -17.7485; 10.1105; 12.1657
103.064; 92.24; 112.226		851.18Shekhawat, Bhawana; Gahlaut, Puneet Singh; Gautam, Deepak; Jana, Barun
<i>N</i>-Alkylation of amines with primary/secondary alcohols using a novel cobalt(II) inverse triazolyl-pyridine complex.
Chemical communications (Cambridge, England), 2024, 60, 8581-8584
7133288 CIFC25 H27 N O5 SP -110.6593; 11.0723; 11.354
90.428; 111.448; 105.959		1190.4Li, Meng-Ru; Zheng, Meng-Yao; Wang, Dong-Chao; Guo, Hai-Ming
Pd-catalyzed 5-<i>exo-dig</i> cyclization/etherification cascade of <i>N</i>-propargyl arylamines for the synthesis of polysubstituted furans.
Chemical communications (Cambridge, England), 2024, 60, 7721-7724
7133289 CIFC28 H33 Br4 Cl2 N6 O0.5 Pd2C 1 2/c 129.2; 8.5804; 28.6903
90; 93.068; 90		7178Kumar, Shashi; Singh, Dushyant; Rit, Arnab
Cooperativity between metal centers in homobimetallic Pd<sup>II</sup>-NHC complexes: catalytic potential towards hydrodefluorination.
Chemical communications (Cambridge, England), 2024, 60, 7761-7764
7133290 CIFC41 H59 B N4P -19.959; 10.779; 18.206
81.921; 74.267; 88.188		1862.4Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133291 CIFC36 H56 B N5 OP -110.1623; 10.4669; 17.7919
80.944; 74.936; 71.058		1722.96Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133292 CIFC35 H54 B N5P 1 21/n 113.3291; 13.6009; 18.6157
90; 92.442; 90		3371.73Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133293 CIFC35 H52 B Cl2 N5P 1 21/c 123.6475; 15.5802; 18.9468
90; 93.614; 90		6966.74Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133294 CIFC35 H54 B N5P -110.802; 12.3555; 13.8232
76.108; 79.11; 68.167		1652.28Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133295 CIFC36 H56 B N5 OP 1 21/n 19.6634; 19.2539; 18.6478
90; 103.619; 90		3372.02Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133296 CIFC44 H65 B N4P 1 21/n 110.5315; 16.4623; 23.1574
90; 96.209; 90		3991.31Witte, Robert; Kar, Sourav; Radacki, Krzysztof; Härterich, Marcel; Rang, Maximilian; Michel, Maximilian; Mihm, Cornelius; Czernetzki, Corinna; Brückner, Tobias; Beck, Eva; Lutz, Sarah; Dewhurst, Rian D.; Braunschweig, Holger
Transition-metal-like coordination chemistry of dicoordinate borylenes with organic azides.
Chemical communications (Cambridge, England), 2024, 60, 8629-8632
7133297 CIFC240 H152 Au28 Cl48 Cu12 P4 S24P -122.0728; 27.5087; 27.5493
86.596; 78.05; 88.55		16334.9Tang, Shisi; Song, Tongxin; Cai, Xiao; Ding, Weiping; Zhu, Yan
Nitrate electroreduction to ammonia catalysed by atomically precise Au<sub>28</sub>Cu<sub>12</sub> clusters.
Chemical communications (Cambridge, England), 2024, 60, 7785-7788
7133298 CIFC162 H243 Cu28 P3 S18P 1 21/n 119.622; 39.5629; 26.1094
90; 91.255; 90		20263.9Tang, Shisi; Song, Tongxin; Cai, Xiao; Ding, Weiping; Zhu, Yan
Nitrate electroreduction to ammonia catalysed by atomically precise Au<sub>28</sub>Cu<sub>12</sub> clusters.
Chemical communications (Cambridge, England), 2024, 60, 7785-7788
7133299 CIFC40 H41 Cl2 F9 N6 Ni2 O10 S3P 1 21/n 111.118; 20.6674; 21.7121
90; 98.029; 90		4940.1Lillo, Hayley L.; Buss, Joshua A.
A dinuclear nickel peroxycarbonate complex: CO<sub>2</sub> addition promotes H<sub>2</sub>O<sub>2</sub> release.
Chemical communications (Cambridge, England), 2024, 60, 8549-8552
7133300 CIFC38 H57 F3 N6 Ni2 O17 SP -110.2519; 11.2496; 21.492
77.624; 79.248; 80.429		2357.88Lillo, Hayley L.; Buss, Joshua A.
A dinuclear nickel peroxycarbonate complex: CO<sub>2</sub> addition promotes H<sub>2</sub>O<sub>2</sub> release.
Chemical communications (Cambridge, England), 2024, 60, 8549-8552
7133301 CIFC74 H82 F6 N12 Ni4 O12 S2P 21 21 2113.7338; 18.9753; 33.797
90; 90; 90		8807.6Lillo, Hayley L.; Buss, Joshua A.
A dinuclear nickel peroxycarbonate complex: CO<sub>2</sub> addition promotes H<sub>2</sub>O<sub>2</sub> release.
Chemical communications (Cambridge, England), 2024, 60, 8549-8552
7133302 CIFC76 H82 F6 N12 Ni4 O16 S2P 1 21/c 116.1401; 32.5762; 17.5728
90; 111.887; 90		8573.5Lillo, Hayley L.; Buss, Joshua A.
A dinuclear nickel peroxycarbonate complex: CO<sub>2</sub> addition promotes H<sub>2</sub>O<sub>2</sub> release.
Chemical communications (Cambridge, England), 2024, 60, 8549-8552
7133303 CIFC29 H23 N2 O2 PP 1 21/c 114.8254; 13.4214; 11.2282
90; 93.113; 90		2230.86Huang, Jun; Ban, Caijin; Qin, Jiangping; Xu, Jiali; Gu, Yunqiong; Wei, Liang; Yuan, Jing-Mei; Huang, Guobao
Visible-light promoted radical cascade cyclization of 3-allyl-2-arylquinazolinones for the synthesis of phosphorylated dihydroisoquinolino[1,2-<i>b</i>]quinazolinones.
Chemical communications (Cambridge, England), 2024, 60, 8119-8122
7133304 CIFC39 H51 Cl2 N2 P2P -110.894; 11.6371; 17.3041
86.498; 73.235; 66.584		1923.91Haberstroh, Jan; Taube, Clemens; Fidelius, Jannis; Schulz, Stephen; Israel, Noel; Dmitrieva, Evgenia; Gomila, Rosa M.; Frontera, Antonio; Wolf, Robert; Schwedtmann, Kai; Weigand, Jan J.
A neutral diphosphene radical: synthesis, electronic structure and white phosphorus activation.
Chemical communications (Cambridge, England), 2024, 60, 8537-8540
7133305 CIFC88 H126 Cl4 N4 O2 P4C 1 2/c 114.6385; 34.7552; 18.1897
90; 109.167; 90		8741.26Haberstroh, Jan; Taube, Clemens; Fidelius, Jannis; Schulz, Stephen; Israel, Noel; Dmitrieva, Evgenia; Gomila, Rosa M.; Frontera, Antonio; Wolf, Robert; Schwedtmann, Kai; Weigand, Jan J.
A neutral diphosphene radical: synthesis, electronic structure and white phosphorus activation.
Chemical communications (Cambridge, England), 2024, 60, 8537-8540
7133306 CIFC84 H107 Cl4 F N4 P8P 1 21/c 122.3963; 24.8472; 15.6004
90; 96.933; 90		8617.92Haberstroh, Jan; Taube, Clemens; Fidelius, Jannis; Schulz, Stephen; Israel, Noel; Dmitrieva, Evgenia; Gomila, Rosa M.; Frontera, Antonio; Wolf, Robert; Schwedtmann, Kai; Weigand, Jan J.
A neutral diphosphene radical: synthesis, electronic structure and white phosphorus activation.
Chemical communications (Cambridge, England), 2024, 60, 8537-8540
7133307 CIFC16 H8 N4 O9 ZnP -18.0263; 8.9753; 13.924
95.081; 93.392; 92.034		996.5Dinda, Susanta; Deb, Sourav; Mahato, Bidyadhar; Baitalik, Sujoy; Ghoshal, Debajyoti
Visual detection and efficient capture of hydrogen chloride and ammonia vapours by a sustainable dual emissive metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 8466-8469
7133308 CIFC53.67 H34.45 Cd2 Cl2 N18 O22.05P -111.8103; 12.5965; 13.3862
80.395; 84.225; 78.443		1919.06Jiang, Qiao; Suzuki, Hiroaki; Wada, Yuki; Wang, Xiaohan; Murakami, Yoichi; Matsumoto, Takaya; Usov, Pavel M.; Kawano, Masaki
Magnetic and thermodynamic control of coordination network crystallization using a hexaazaphenalene-based ligand.
Chemical communications (Cambridge, England), 2024, 60, 8236-8239
7133309 CIFC49.22 H31.49 Cd N18 O16.9P c a 2130.3621; 7.9636; 28.193
90; 90; 90		6816.83Jiang, Qiao; Suzuki, Hiroaki; Wada, Yuki; Wang, Xiaohan; Murakami, Yoichi; Matsumoto, Takaya; Usov, Pavel M.; Kawano, Masaki
Magnetic and thermodynamic control of coordination network crystallization using a hexaazaphenalene-based ligand.
Chemical communications (Cambridge, England), 2024, 60, 8236-8239
7133310 CIFC29 H62 N3 Si3P -111.5884; 17.221; 18.536
69.558; 80.011; 82.655		3404.5Kiefer, Fiona J.; Kostenko, Arseni; Holzner, Richard; Inoue, Shigeyoshi
A neutral crystalline imino-substituted silyl radical.
Chemical communications (Cambridge, England), 2024, 60, 8577-8580
7133311 CIFC23 H18 N2 O3P 21 21 216.84; 11.12; 24.67
90; 90; 90		1876Purkait, Anisha; Pal, Surya Veer Singh; Soni, Kaushik; Bhattacharyya, Kalishankar; Jana, Chandan K.
Nitroso-azomethine(ene) reaction enabled annulations of nitrosoarenes, azomethines and alkenes.
Chemical communications (Cambridge, England), 2024, 60, 8541-8544
7133312 CIFC28 H37 P S2 Si3P 1 21/n 117.3438; 7.4997; 23.1443
90; 91.611; 90		3009.27Ishida, Shintaro; Yoshida, Yusuke; Iwamoto, Takeaki
Metal-catalyzed valence isomerization of a methylene(thioxo)phosphorane to a thiaphosphirane.
Chemical communications (Cambridge, England), 2024, 60, 8288-8291
7133313 CIFC36 H48 Cl P Si4P 1 21/n 116.1335; 13.1016; 16.7859
90; 91.24; 90		3547.28Ishida, Shintaro; Yoshida, Yusuke; Iwamoto, Takeaki
Metal-catalyzed valence isomerization of a methylene(thioxo)phosphorane to a thiaphosphirane.
Chemical communications (Cambridge, England), 2024, 60, 8288-8291
7133314 CIFC28 H37 P S Si3P 1 21/c 113.1508; 9.7019; 22.7273
90; 101.809; 90		2838.35Ishida, Shintaro; Yoshida, Yusuke; Iwamoto, Takeaki
Metal-catalyzed valence isomerization of a methylene(thioxo)phosphorane to a thiaphosphirane.
Chemical communications (Cambridge, England), 2024, 60, 8288-8291
7133315 CIFC28 H37 P S Si3P 1 21/c 113.2702; 12.96; 17.3599
90; 107.126; 90		2853.2Ishida, Shintaro; Yoshida, Yusuke; Iwamoto, Takeaki
Metal-catalyzed valence isomerization of a methylene(thioxo)phosphorane to a thiaphosphirane.
Chemical communications (Cambridge, England), 2024, 60, 8288-8291
7133316 CIFC34 H37 Au F5 P S Si3P -113.8756; 20.1815; 25.941
88.525; 87.728; 75.68		7032.08Ishida, Shintaro; Yoshida, Yusuke; Iwamoto, Takeaki
Metal-catalyzed valence isomerization of a methylene(thioxo)phosphorane to a thiaphosphirane.
Chemical communications (Cambridge, England), 2024, 60, 8288-8291
7133317 CIFC53 H28 Cl2 N2 O4P 1 21 18.1505; 11.3913; 20.8223
90; 92.329; 90		1931.6Wang, Yuxiang; Liao, Qi; Feng, Yabin; Wang, Yiran; Li, Yunzhi; Meng, Qi
Synthesis and resolution of multi-chiral carbonyl-N embedded hetero[7]helicenes for efficient circularly polarized luminescence.
Chemical communications (Cambridge, England), 2024, 60, 8292-8295
7133318 CIFC64 H54 N2 O4P 6113.1642; 13.1642; 48.25
90; 90; 120		7241.3Wang, Yuxiang; Liao, Qi; Feng, Yabin; Wang, Yiran; Li, Yunzhi; Meng, Qi
Synthesis and resolution of multi-chiral carbonyl-N embedded hetero[7]helicenes for efficient circularly polarized luminescence.
Chemical communications (Cambridge, England), 2024, 60, 8292-8295
7133319 CIFC35 H30 N2 O5P -111.1034; 11.1882; 12.5867
70.9583; 87.9029; 71.6281		1398.89Yadav, Suresh Kumar; Jeganmohan, Masilamani
Co(III)-catalyzed regioselective benzannulation of substituted pyridones with 1,6-diynes <i>via</i> dual C-H bond activation.
Chemical communications (Cambridge, England), 2024, 60, 8296-8299
7133320 CIFC40 H42 Li2 O4P 1 21/c 110.8476; 10.0967; 15.5113
90; 94.807; 90		1692.9Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133321 CIFC48 H62 K2 O8P 1 21/c 111.1442; 13.0688; 16.746
90; 106.828; 90		2334.47Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133322 CIFC48 H62 Na2 O8P 1 21/c 111.0913; 13.2818; 15.8392
90; 105.146; 90		2252.26Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133323 CIFC83.7 H83.7 Ce K O4.7P -110.2856; 13.0071; 25.713
80.814; 88.212; 78.113		3323.09Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133324 CIFC80 H84 Ce K O8P 1 2/n 115.8469; 10.1787; 21.4308
90; 94.056; 90		3448.15Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133325 CIFC80 H84 K O8 TbP 1 2/n 115.6241; 10.2214; 21.5624
90; 94.643; 90		3432.22Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133326 CIFC76 H74 Li O6 YP 1 21/c 110.33655; 25.4845; 23.3833
90; 96.3298; 90		6122.12Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133327 CIFC100 H116 Cl6 Mg2 O9 Y2P b c m14.8775; 21.4215; 37.4724
90; 90; 90		11942.4Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133328 CIFC53.33 H56 K0.67 La0.67 O5.33P 1 2/n 115.9186; 10.1537; 21.3582
90; 93.633; 90		3445.25Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133329 CIFC176 H184 Mg O12 Y2P 1 21/n 117.52153; 19.2375; 21.05544
90; 92.9279; 90		7087.9Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133330 CIFC96 H108 Na O8 YbP 1 2/n 120.1809; 15.78844; 25.03591
90; 90.51; 90		7976.75Katzer, Nicholas J.; Kaur, Mandeep; Sen, Asmita; Nimaiyar, Rupal; Autschbach, Jochen; Arnold, Polly L.; Hintermair, Ulrich
Tetraphenylpentalenide organolanthanide complexes.
Chemical communications (Cambridge, England), 2024, 60, 9749-9752
7133331 CIFC19 H23 NP n m a11.2368; 7.0029; 19.2578
90; 90; 90		1515.4Yang, Fang; Li, Heyang; Li, Huijie; He, Xiaoming
Manipulation of 1D and 2D self-assembly <i>via</i> geometry modulation of adamantane isocyanide Pt(II) complexes.
Chemical communications (Cambridge, England), 2024, 60, 8605-8608
7133332 CIFC28 H30 N2P 1 21/c 16.7908; 19.6373; 16.4833
90; 90.029; 90		2198.1Yang, Fang; Li, Heyang; Li, Huijie; He, Xiaoming
Manipulation of 1D and 2D self-assembly <i>via</i> geometry modulation of adamantane isocyanide Pt(II) complexes.
Chemical communications (Cambridge, England), 2024, 60, 8605-8608
7133333 CIFC26 H24 B Cr2 N4 Na O13P c a 2123.3656; 9.1918; 31.7925
90; 90; 90		6828.14Luff, Martin S.; Bertermann, Rüdiger; Finze, Maik; Radius, Udo
The tetracyanoborate anion as a building block for the heterocubane cluster cage [Cr<sub>4</sub>{B(CN)<sub>4</sub>}<sub>4</sub>]<sup>4</sup>.
Chemical communications (Cambridge, England), 2024, 60, 8621-8624
7133334 CIFC24 H32 B Cr N4 Na O8P -19.8572; 12.1418; 12.9109
100.325; 96.817; 95.944		1497.09Luff, Martin S.; Bertermann, Rüdiger; Finze, Maik; Radius, Udo
The tetracyanoborate anion as a building block for the heterocubane cluster cage [Cr<sub>4</sub>{B(CN)<sub>4</sub>}<sub>4</sub>]<sup>4</sup>.
Chemical communications (Cambridge, England), 2024, 60, 8621-8624
7133335 CIFC308 H280 B8 Cr8 N32 O39 P8P -116.6054; 18.2464; 27.5141
93.222; 99.544; 113.692		7458.23Luff, Martin S.; Bertermann, Rüdiger; Finze, Maik; Radius, Udo
The tetracyanoborate anion as a building block for the heterocubane cluster cage [Cr<sub>4</sub>{B(CN)<sub>4</sub>}<sub>4</sub>]<sup>4</sup>.
Chemical communications (Cambridge, England), 2024, 60, 8621-8624
7133336 CIFC104 H152 B4 Cr4 N16 Na4 O31P 1 21/n 117.5473; 20.8549; 35.3881
90; 102.2; 90		12657.7Luff, Martin S.; Bertermann, Rüdiger; Finze, Maik; Radius, Udo
The tetracyanoborate anion as a building block for the heterocubane cluster cage [Cr<sub>4</sub>{B(CN)<sub>4</sub>}<sub>4</sub>]<sup>4</sup>.
Chemical communications (Cambridge, England), 2024, 60, 8621-8624
7133337 CIFC37 H28 N4 O2P -19.5486; 9.8277; 16.757
103.234; 103.776; 97.299		1459Balasubramani, Alagesan; Sudarshana, K. A.; Kushwaha, Roli; Chakravarty, Sumana; Pabbaraja, Srihari; Mehta, Goverdhan
One flask cascade approach to a complex pyrano[2,3-<i>c</i>]pyrazole-pyrazolone hybrid heterocyclic system and its initiatory neurobiological profiling.
Chemical communications (Cambridge, England), 2024, 60, 8443-8446
7133338 CIFC41 H32 N4 O2P -19.341; 11.471; 15.177
88.237; 77.033; 83.309		1574Balasubramani, Alagesan; Sudarshana, K. A.; Kushwaha, Roli; Chakravarty, Sumana; Pabbaraja, Srihari; Mehta, Goverdhan
One flask cascade approach to a complex pyrano[2,3-<i>c</i>]pyrazole-pyrazolone hybrid heterocyclic system and its initiatory neurobiological profiling.
Chemical communications (Cambridge, England), 2024, 60, 8443-8446
7133339 CIFC37 H26 Cl2 N4 O2P -19.724; 12.297; 13.872
103.225; 106.099; 98.327		1512.5Balasubramani, Alagesan; Sudarshana, K. A.; Kushwaha, Roli; Chakravarty, Sumana; Pabbaraja, Srihari; Mehta, Goverdhan
One flask cascade approach to a complex pyrano[2,3-<i>c</i>]pyrazole-pyrazolone hybrid heterocyclic system and its initiatory neurobiological profiling.
Chemical communications (Cambridge, England), 2024, 60, 8443-8446
7133340 CIFC47 H82 N4 Si4 YbP b c a17.9657; 22.4892; 28.4392
90; 90; 90		11490.4Xu, Cheng; Zhao, Sixuan; Zhang, Heng; Peng, Qian; Chen, Yaofeng
Yb/Si frustrated Lewis pairs with a labile naphthalenyl bridge.
Chemical communications (Cambridge, England), 2024, 60, 8411-8414
7133341 CIFC50 H88 N4 Si4 YbP 1 21/c 114.1534; 17.7808; 22.4677
90; 100.898; 90		5552.2Xu, Cheng; Zhao, Sixuan; Zhang, Heng; Peng, Qian; Chen, Yaofeng
Yb/Si frustrated Lewis pairs with a labile naphthalenyl bridge.
Chemical communications (Cambridge, England), 2024, 60, 8411-8414
7133342 CIFC46 H83 N5 Si4 YbP 1 21/n 113.2397; 22.4875; 18.0354
90; 105.208; 90		5181.6Xu, Cheng; Zhao, Sixuan; Zhang, Heng; Peng, Qian; Chen, Yaofeng
Yb/Si frustrated Lewis pairs with a labile naphthalenyl bridge.
Chemical communications (Cambridge, England), 2024, 60, 8411-8414
7133343 CIFC50 H90 N4 Si4 YbP b c a18.0881; 22.6537; 26.9902
90; 90; 90		11059.6Xu, Cheng; Zhao, Sixuan; Zhang, Heng; Peng, Qian; Chen, Yaofeng
Yb/Si frustrated Lewis pairs with a labile naphthalenyl bridge.
Chemical communications (Cambridge, England), 2024, 60, 8411-8414
7133344 CIFC34.06 H68.23 N4 O0.06 S2 Si4 YbP -115.4962; 17.7037; 19.308
78.382; 69.436; 69.691		4632.04Xu, Cheng; Zhao, Sixuan; Zhang, Heng; Peng, Qian; Chen, Yaofeng
Yb/Si frustrated Lewis pairs with a labile naphthalenyl bridge.
Chemical communications (Cambridge, England), 2024, 60, 8411-8414
7133345 CIFC37 H39 N3 TiP b c a16.6089; 14.6227; 24.9167
90; 90; 90		6051.44Fritsche, Paul; Geyer, Lucia; Czernetzki, Corinna; Hierlmeier, Gabriele
Coordination-induced reductive elimination from a titanium(IV) complex.
Chemical communications (Cambridge, England), 2024, 60, 9030-9033
7133346 CIFC30 H31 N3 TiP 1 21/c 111.5575; 17.8865; 11.9883
90; 103.609; 90		2408.68Fritsche, Paul; Geyer, Lucia; Czernetzki, Corinna; Hierlmeier, Gabriele
Coordination-induced reductive elimination from a titanium(IV) complex.
Chemical communications (Cambridge, England), 2024, 60, 9030-9033
7133347 CIFC45 H55 N3 TiP -110.1395; 12.8171; 16.6592
71.421; 85.313; 66.806		1883.94Fritsche, Paul; Geyer, Lucia; Czernetzki, Corinna; Hierlmeier, Gabriele
Coordination-induced reductive elimination from a titanium(IV) complex.
Chemical communications (Cambridge, England), 2024, 60, 9030-9033
7133348 CIFC39 H53 N3 TiP -111.0602; 12.062; 14.3315
77.339; 77.207; 70.619		1736.62Fritsche, Paul; Geyer, Lucia; Czernetzki, Corinna; Hierlmeier, Gabriele
Coordination-induced reductive elimination from a titanium(IV) complex.
Chemical communications (Cambridge, England), 2024, 60, 9030-9033
7133349 CIFC17 H22 B Br N2 O4P 21 21 218.2775; 8.4391; 27.6673
90; 90; 90		1932.69Ankudinov, Nikita M.; Komarova, Alina A.; Podyacheva, Evgeniya S.; Chusov, Denis A.; Danshina, Anastasia A.; Perekalin, Dmitry S.
Synthesis of chiral boranes <i>via</i> asymmetric insertion of carbenes into B-H bonds catalyzed by the rhodium(I) diene complex.
Chemical communications (Cambridge, England), 2024, 60, 8601-8604
7133350 CIFC139 H103 Cd6 N13 O33P -112.2239; 12.3893; 30.5039
80.911; 84.233; 61.359		4001.9Chang, Manman; Li, Nan; Guo, Lingxiao; Zhang, Yijia; Liu, Xiao-Ting; Lu, Chao
Manipulating AIE ligands into layers of pillar-layered MOFs for enhanced emission.
Chemical communications (Cambridge, England), 2024, 60, 8696-8699
7133351 CIFC29 H23 Cd N4 O5P -19.8998; 10.3818; 13.7847
85.545; 75.783; 70.838		1297.27Chang, Manman; Li, Nan; Guo, Lingxiao; Zhang, Yijia; Liu, Xiao-Ting; Lu, Chao
Manipulating AIE ligands into layers of pillar-layered MOFs for enhanced emission.
Chemical communications (Cambridge, England), 2024, 60, 8696-8699
7133352 CIFC108 H92 Cd4 N12 O24C 1 2/c 126.0598; 8.2468; 22.9568
90; 93.487; 90		4924.5Chang, Manman; Li, Nan; Guo, Lingxiao; Zhang, Yijia; Liu, Xiao-Ting; Lu, Chao
Manipulating AIE ligands into layers of pillar-layered MOFs for enhanced emission.
Chemical communications (Cambridge, England), 2024, 60, 8696-8699
7133353 CIFC100 H92 Cd4 N12 O24C 1 2/c 126.241; 7.6898; 23.0522
90; 91.71; 90		4649.6Chang, Manman; Li, Nan; Guo, Lingxiao; Zhang, Yijia; Liu, Xiao-Ting; Lu, Chao
Manipulating AIE ligands into layers of pillar-layered MOFs for enhanced emission.
Chemical communications (Cambridge, England), 2024, 60, 8696-8699
7133354 CIFC41 H32 Cd N4 O10P -19.0027; 12.5556; 16.1594
82.397; 84.317; 87.262		1800.5Chang, Manman; Li, Nan; Guo, Lingxiao; Zhang, Yijia; Liu, Xiao-Ting; Lu, Chao
Manipulating AIE ligands into layers of pillar-layered MOFs for enhanced emission.
Chemical communications (Cambridge, England), 2024, 60, 8696-8699

Left arrow Left arrow First | Left arrow Previous 1000 | of 2 | Next 1000 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!
Top of the page
All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.