Crystallography Open Database

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7134984 CIFC13 H23 Fe3 N2 O18P 1 21/n 114.2147; 8.3281; 21.3984
90; 102.558; 90
2472.6Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134985 CIFC15 H27 Fe3 N2 O18P 1 21/n 114.3325; 8.4968; 21.8494
90; 102.465; 90
2598.1Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134986 CIFC12 H23 Fe3 N2 O19R -3 c :H8.2548; 8.2548; 63.391
90; 90; 120
3740.9Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134987 CIFC15 H27 Fe3 N2 O18R -3 c :H8.4183; 8.4183; 63.025
90; 90; 120
3868.1Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134988 CIFC13 H23 Fe3 N2 O18R -3 c :H8.2967; 8.2967; 62.793
90; 90; 120
3743.3Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134989 CIFC9 H9 F O3C 1 2/c 118.7223; 11.2619; 8.6284
90; 109.598; 90
1713.9Karbalaei, Sana; Franke, Alicja; Zahl, Achim; Pokkuluri, P. Raj; Beyers, Ronald J.; Ivanović-Burmazović, Ivana; Goldsmith, Christian R.
An Fe(II) complex detects hydrogen peroxide with <sup>1</sup>H and <sup>19</sup>F magnetic resonance imaging responses.
Chemical communications (Cambridge, England), 2025, 61, 15898-15901
7134990 CIFC7 H5 F O3P -17.6681; 8.3643; 11.4816
76.068; 77.79; 64.382
639.61Karbalaei, Sana; Franke, Alicja; Zahl, Achim; Pokkuluri, P. Raj; Beyers, Ronald J.; Ivanović-Burmazović, Ivana; Goldsmith, Christian R.
An Fe(II) complex detects hydrogen peroxide with <sup>1</sup>H and <sup>19</sup>F magnetic resonance imaging responses.
Chemical communications (Cambridge, England), 2025, 61, 15898-15901
7134991 CIFC58 H34 N4 O2P 18.8479; 11.4027; 11.4991
86.241; 72.076; 68.194
1023.29Yin, Xiaojun; Chen, Xuefeng; Mo, Xuechao; Chen, Junjin; Huang, Mengyu; Ma, Jiacheng; Li, Yulan; Li, Nengquan; Yang, Chuluo
Charge-transfer modulated chiroptical azacyclooctatetraene-fused [5]helicenes with AIE features.
Chemical communications (Cambridge, England), 2025, 61, 16448-16451
7134992 CIFC28.5 H21 Br Cl O4P 19.0354; 11.1067; 13.6619
106.141; 96.303; 107.287
1229.51Zhai, Jing-Jing; Lou, Shao-Jie; Zhang, Xiao-Xiao; Lan, Qiu-Yi; Jing, Cheng-Cheng; Mao, Yang-Jie; Wang, Yi-Feng; Chu, Ming-Ming; Xu, Dan-Qian
Remote asymmetric conjugate addition of naphthoquinone methides: constructing adjacent tertiary-quaternary carbon stereocenters.
Chemical communications (Cambridge, England), 2025, 61, 16644-16647
7134993 CIFC28 H22 O4P 21 21 218.8073; 12.1366; 20.0872
90; 90; 90
2147.13Zhai, Jing-Jing; Lou, Shao-Jie; Zhang, Xiao-Xiao; Lan, Qiu-Yi; Jing, Cheng-Cheng; Mao, Yang-Jie; Wang, Yi-Feng; Chu, Ming-Ming; Xu, Dan-Qian
Remote asymmetric conjugate addition of naphthoquinone methides: constructing adjacent tertiary-quaternary carbon stereocenters.
Chemical communications (Cambridge, England), 2025, 61, 16644-16647
7134994 CIFC28 H22 O4P 1 21 111.628; 15.6621; 12.0951
90; 97.484; 90
2183.98Zhai, Jing-Jing; Lou, Shao-Jie; Zhang, Xiao-Xiao; Lan, Qiu-Yi; Jing, Cheng-Cheng; Mao, Yang-Jie; Wang, Yi-Feng; Chu, Ming-Ming; Xu, Dan-Qian
Remote asymmetric conjugate addition of naphthoquinone methides: constructing adjacent tertiary-quaternary carbon stereocenters.
Chemical communications (Cambridge, England), 2025, 61, 16644-16647
7134995 CIFC27 H22 N2 O2I 1 a 15.8439; 38.1781; 9.1909
90; 94.124; 90
2045.26Kumar, Pravin; Dash, Om Prakash; Volla, Chandra M. R.
Cobalt-catalyzed regioselective (4+2)-annulation of benzamides with allenyl carbinol acetates: access to 3-vinylisoquinolinones.
Chemical communications (Cambridge, England), 2025, 61, 16962-16965
7134996 CIFC48 H38 Ag P3 SP -110.8475; 12.0536; 15.9663
72.057; 88.8299; 81.512
1963.63Łaski, Piotr; Drapała, Jakub; Kamiński, Radosław; Durka, Krzysztof; Szarejko, Dariusz; Henning, Robert; Jarzembska, Katarzyna N.
Capturing the short-lived excited singlet state in crystals of a TADF silver(I) complex.
Chemical communications (Cambridge, England), 2025, 61, 16560-16563
7134997 CIFC48 H38 Ag P3 SP -110.8455; 12.0698; 15.9133
72.271; 88.798; 81.388
1961.13Łaski, Piotr; Drapała, Jakub; Kamiński, Radosław; Durka, Krzysztof; Szarejko, Dariusz; Henning, Robert; Jarzembska, Katarzyna N.
Capturing the short-lived excited singlet state in crystals of a TADF silver(I) complex.
Chemical communications (Cambridge, England), 2025, 61, 16560-16563
7134998 CIFC21 H21 Br N2 OP 1 21/c 112.9547; 10.2165; 16.1046
90; 113.338; 90
1957.1Kar, Subarna; Ramachandran, Arya; Rit, Arnab
Efficient synthetic approach to <i>m</i>-terphenyl derivatives <i>via</i> arylation of azolium salts.
Chemical communications (Cambridge, England), 2025, 61, 16802-16805
7134999 CIFC21 H16 N O2 PP -18.71; 10.081; 11.048
99.774; 106.774; 100.943
885.5Meng, Li-Qin; Zhu, Xinrong; Xing, Qiaoyan; Zhang, Junliang; Wang, Huamin; Lin, Ying-Wu
Concise synthesis of phosphonylated heteroarenes from nitroheteroarenes by dearomatization/elimination.
Chemical communications (Cambridge, England), 2025, 61, 16810-16813
7135000 CIFC21 H18 N O2 PP 1 21/c 111.6354; 11.6264; 13.4546
90; 91.652; 90
1819.35Meng, Li-Qin; Zhu, Xinrong; Xing, Qiaoyan; Zhang, Junliang; Wang, Huamin; Lin, Ying-Wu
Concise synthesis of phosphonylated heteroarenes from nitroheteroarenes by dearomatization/elimination.
Chemical communications (Cambridge, England), 2025, 61, 16810-16813
7135001 CIFC106 H58 N18 O17 Pd2 Zn5P 1 21/n 19.9191; 32.4889; 38.6916
90; 95.533; 90
12410.7Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135002 CIFC56 H36 N10 O9 Pd Zn2C 1 2/c 133.103; 10.1085; 43.6
90; 98.346; 90
14435Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135003 CIFC56 H36 N10 O9 Pd Zn2P 1 21/c 122.815; 9.9064; 31.625
90; 95.495; 90
7114.9Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135004 CIFC58 H33 N14 O8.5 Pd Zn3C c c a :233.8282; 10.4006; 43.8964
90; 90; 90
15444.2Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135005 CIFC32 H34 Ag Cl Fe N12 O6C 1 2/c 113.4233; 16.051; 17.725
90; 95.291; 90
3802.7Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135006 CIFC32 H34 Ag Cl Fe N12 O6.16C 1 2/c 113.2411; 15.6597; 17.3891
90; 97.325; 90
3576.2Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135007 CIFC54 H30 Ag6 Fe3 N18 S3P 6525.8631; 25.8631; 20.8337
90; 90; 120
12068.6Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135008 CIFC54 H30 Ag6 Fe3 N18 S3P 6525.546; 25.546; 20.356
90; 90; 120
11504.5Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135009 CIFC28 H27 N O6 SP 1 21/c 110.2849; 24.4179; 10.3397
90; 105.642; 90
2500.5Zheng, Jianfeng; Xiong, Dong; Ye, Yongqi; Tang, Luhao; Yang, Jiajin; Yang, Zeyu; Cai, Yunfei
Efficient syntheses of 2-amino-4<i>H</i>-pyrans <i>via</i> gold-catalyzed cyclization of diester-tethered ynamides.
Chemical communications (Cambridge, England), 2025, 61, 16858-16861
7135010 CIFC18 H15 Br I N OP -16.3543; 8.4335; 16.8759
98.77; 99.305; 90.041
881.73Chen, Chen; Wang, Zi-Yi; Zhang, Xiao-Xu; Wang, Kui; Zhu, Bolin
Pd-catalyzed electrophilic cross-coupling of pyridylphosphonium salts with arylthianthrenium salts to access C4-arylated pyridines.
Chemical communications (Cambridge, England), 2025, 61, 17185-17188
7135011 CIFC33 H51 Al N2 ZnP n m a15.9848; 20.213; 9.8381
90; 90; 90
3178.7Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135012 CIFC83 H114 Ga2 N4 O2 Zn2P -19.7057; 14.4604; 14.9677
87.7489; 72.9148; 73.06
1918.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135013 CIFC64 H94 N4 Si2P -110.9267; 11.6874; 12.7613
93.932; 104.6; 111.522
1443.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135014 CIFC62 H53 B F20 N2 Si ZnP -111.1667; 12.7101; 21.923
98.644; 101.458; 102.212
2919.8Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135015 CIFC74 H115 Ga N4 Si ZnP 1 21/n 112.1549; 32.569; 18.1556
90; 101.686; 90
7038.3Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135016 CIFC74 H113.5 Ga N4 Si ZnC 1 2/c 117.5328; 19.9362; 20.5665
90; 93.366; 90
7176.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135017 CIFC33 H51 Ga N2 ZnP 21 21 219.876; 16.0049; 20.269
90; 90; 90
3203.8Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135018 CIFC74 H120 Ga2 N4 ZnC 1 2/c 117.5441; 20.0646; 20.5353
90; 93.8778; 90
7212.2Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135019 CIFC74 H120 Al Ga N4 ZnC 1 2/c 117.6429; 20.0099; 20.5546
90; 92.706; 90
7248.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135020 CIFC74 H102 Ga N4 Si ZnC 1 2/c 116.4935; 17.0584; 24.336
90; 92.0203; 90
6842.7Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135021 CIFC78 H78 O12P -16.0018; 16.2806; 16.8345
107.589; 97.731; 95.825
1536.1Yamini, Pokhriyal; Duklan, Bhoomika; Nirmal, Mukesh; Yadagiri, Dongari
Light-induced intramolecular carbene C(sp<sup>3</sup>)-H insertion of <i>N</i>-tosylhydrazones; synthesis of functionalized coumarans and indolines.
Chemical communications (Cambridge, England), 2025, 61, 17017-17020
7135022 CIFC8 H9 N3 O2P b c a12.8099; 7.7737; 18.5183
90; 90; 90
1844.06Kumar, Prashant; Kant, Ruchir; Rastogi, Namrata
Nitrogen atom insertion into NN double bonds: straightforward access to triazenes.
Chemical communications (Cambridge, England), 2025, 61, 16632-16635
7135023 CIFC21 H17 N O2P n m a15.204; 6.943; 15.282
90; 90; 90
1613Bai, Fang; Liu, Pengpeng; Xu, Hongyan; Li, Mengjie; Liu, Binghui; Xu, Miaomiao; Gao, Qinghe
Auto-oxidation-driven vicinal C(sp<sup>3</sup>)-H desaturative cyclization of tertiary alkylamines for the synthesis of pyrido[3,2-<i>c</i>]coumarins.
Chemical communications (Cambridge, England), 2025, 61, 16818-16821
7135024 CIFC20 H20 Dy2 O20P 1 21/n 17.6415; 15.8785; 21.8456
90; 97.457; 90
2628.23Shao, Xueying; Yang, Yue; Dong, Xiaofang; Wang, Shen; Liang, Yulu; Liu, Zhongyi; Min, Hui; Wang, Yu-Xia; Cheng, Peng
Magnetic modulation and magnetocaloric effect of lanthanide porous organic frameworks with croconic acid.
Chemical communications (Cambridge, England), 2025, 61, 16862-16865
7135025 CIFC60 H50 Cl1.5 Dy8.5 O86P 4/m21.7419; 21.7419; 7.7397
90; 90; 90
3658.64Shao, Xueying; Yang, Yue; Dong, Xiaofang; Wang, Shen; Liang, Yulu; Liu, Zhongyi; Min, Hui; Wang, Yu-Xia; Cheng, Peng
Magnetic modulation and magnetocaloric effect of lanthanide porous organic frameworks with croconic acid.
Chemical communications (Cambridge, England), 2025, 61, 16862-16865
7135026 CIFC60 H52 Cl1.5 Gd8.5 O86P 4/m21.8854; 21.8854; 7.7744
90; 90; 90
3723.71Shao, Xueying; Yang, Yue; Dong, Xiaofang; Wang, Shen; Liang, Yulu; Liu, Zhongyi; Min, Hui; Wang, Yu-Xia; Cheng, Peng
Magnetic modulation and magnetocaloric effect of lanthanide porous organic frameworks with croconic acid.
Chemical communications (Cambridge, England), 2025, 61, 16862-16865
7135027 CIFC11 H11 N O2P 1 21/n 113.1083; 6.8867; 21.4225
90; 92.066; 90
1932.61Shi, Yaolian; Gong, Yuchen; Li, Ganpeng; Zhao, Xiao-Jing; He, Yonghui
Cobalt-salen complexes/organic photoredox-cocatalyzed selective oxidative formylation of enaminones.
Chemical communications (Cambridge, England), 2025, 61, 17173-17176
7135028 CIFC68 H92 N4 O P4P 1 c 19.94331; 17.65986; 18.49899
90; 99.9045; 90
3199.96Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135029 CIFC44 H51 N2 P Se2P -19.845; 10.4186; 21.0183
82.912; 80.297; 71.16
2005.68Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135030 CIFC48 H57 F6 N2 O3 P2 SP 1 21/n 112.1447; 29.8408; 13.06799
90; 94.1461; 90
4723.54Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135031 CIFC67.76 H90.76 N4 P2P -112.0999; 14.6052; 41.8681
85.433; 87.238; 68.411
6856.66Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135032 CIFC33 H41 F3 N2 O3 P2 SP 1 21/c 112.1104; 13.7238; 20.3093
90; 97.664; 90
3345.27Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135033 CIFC76 H102 N4 P4P b c a22.3323; 21.5645; 29.5421
90; 90; 90
14227Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135034 CIFC45 H51 F3 N2 O3 P2 S3P -110.4857; 13.3395; 16.2297
94.945; 99.955; 94.997
2215.54Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135035 CIFC21 H17 Cl N4 O2P 1 21/c 121.4394; 13.9197; 12.5913
90; 105.292; 90
3624.6Guo, Ting-Ting; Zhao, Qing-Sheng; Yang, Shu; Chen, Tian-Tian; Liu, Jin; Yan, Sheng-Jiao
Rh(III)-catalyzed cyclization of 5-amino-pyrazoles with maleimides to pyrazoloquinazolines.
Chemical communications (Cambridge, England), 2025, 61, 16846-16849
7135036 CIFC21 H21 Cl N4 O4P 1 21/c 19.5672; 35.984; 5.9462
90; 95.563; 90
2037.4Guo, Ting-Ting; Zhao, Qing-Sheng; Yang, Shu; Chen, Tian-Tian; Liu, Jin; Yan, Sheng-Jiao
Rh(III)-catalyzed cyclization of 5-amino-pyrazoles with maleimides to pyrazoloquinazolines.
Chemical communications (Cambridge, England), 2025, 61, 16846-16849
7135037 CIFC14 H14 N4 OP 1 21/n 110.6661; 4.919; 23.7529
90; 102.205; 90
1218.06Guo, Ting-Ting; Zhao, Qing-Sheng; Yang, Shu; Chen, Tian-Tian; Liu, Jin; Yan, Sheng-Jiao
Rh(III)-catalyzed cyclization of 5-amino-pyrazoles with maleimides to pyrazoloquinazolines.
Chemical communications (Cambridge, England), 2025, 61, 16846-16849
7135038 CIFC36 H37 N OP b c a9.7987; 20.5217; 28.652
90; 90; 90
5761.5Yu, Yue; Guan, Ning; Zhao, Chunying; Cao, Hua; Ma, Yan-Long
Mechanochemically controllable synthesis of mono- or di-alkenylated indolizines.
Chemical communications (Cambridge, England), 2025, 61, 16834-16837
7135039 CIFC57 H61 N O3P 1 21 111.4318; 11.308; 18.3289
90; 93.843; 90
2364.1Yu, Yue; Guan, Ning; Zhao, Chunying; Cao, Hua; Ma, Yan-Long
Mechanochemically controllable synthesis of mono- or di-alkenylated indolizines.
Chemical communications (Cambridge, England), 2025, 61, 16834-16837
7135040 CIFC H9 B3 F2 N4 O5P -17.2945; 7.969; 8.237
107.653; 101.435; 95.312
441.19Shen, Chunjie; Zhou, Huan; Hu, Chenhui; Yang, Zhihua; Zhang, Feng; Pan, Shilie
CN<sub>4</sub>H<sub>7</sub>B<sub>3</sub>O<sub>3</sub>F<sub>2</sub>(OH)<sub>2</sub>: short-wave UV hydroxyfluorooxyborate crystals with large birefringence.
Chemical communications (Cambridge, England), 2025, 61, 16997-17000
7135041 CIFC8 H20 Cd3 Cl7 NP -17.818; 11.1147; 13.4404
66.714; 82.325; 70.712
1012.55Chen, Hui-Ping; Wang, Zhen-Yu; Qi, Jun-Chao; Peng, Hang; Yang, Tian-En; Zhang, Xiao-Xuan; Luo, Xin-Yu; Liao, Wei-Qiang
A five- and six-coordinated two-dimensional metal halide organic-inorganic phase transition material.
Chemical communications (Cambridge, England), 2025, 61, 16636-16639
7135042 CIFC8 H20 Cd3 Cl7 NP -17.855; 11.1928; 13.5318
67.72; 81.919; 69.603
1031.81Chen, Hui-Ping; Wang, Zhen-Yu; Qi, Jun-Chao; Peng, Hang; Yang, Tian-En; Zhang, Xiao-Xuan; Luo, Xin-Yu; Liao, Wei-Qiang
A five- and six-coordinated two-dimensional metal halide organic-inorganic phase transition material.
Chemical communications (Cambridge, England), 2025, 61, 16636-16639
7135043 CIFC20 H22 N2 O3P 21 21 219.8569; 13.5366; 13.7081
90; 90; 90
1829.06Huang, Yinghong; Zheng, Renhua; Cheng, Xiaomeng; Geng, Xiao; Wang, Lei; Zhu, Bihong
Dehalogenation hydrolysis of CF<sub>2</sub>Br<sub>2</sub> enables four-component aminocarbonylation <i>via</i> photocatalytic radical-polar crossover.
Chemical communications (Cambridge, England), 2025, 61, 17033-17036
7135044 CIFC19 H14 F3 N OP 1 21/c 18.33; 17.1545; 11.1957
90; 97.513; 90
1586.1Sachin, ?; Sharma, Tamanna; Rav, Shourabh; Sharma, Upendra
Ru(II)-catalysed, inherent-directing-group-enabled site-selective C-H vinyl trifluoromethylation of isoquinolones and benzamides.
Chemical communications (Cambridge, England), 2025, 61, 17416-17419
7135045 CIFC27 H27 Dy N4 O3P 1 21/c 116.7777; 19.0804; 7.7909
90; 97.375; 90
2473.4Hasegawa, Natsuki; Yanai, Akiho; Masaki, Hinako; Kirishima, Akira; Tsunashima, Ryo; Masuya-Suzuki, Atsuko
Stepwise selective crystallization of Fe and Dy complexes from a Fe/Nd/Dy mixture: separation despite charge and solubility similarity.
Chemical communications (Cambridge, England), 2025, 61, 17384-17387
7135046 CIFC23 H17 O2 PP 1 21/c 112.0273; 5.9723; 24.2673
90; 91.698; 90
1742.37Eichhorn, Katharina; Bruhn, Clemens; Pietschnig, Rudolf
β-Carboxyphospholes <i>via</i> carboxylative desilylation: luminophores with a versatile connectivity attached.
Chemical communications (Cambridge, England), 2025, 61, 17129-17132
7135047 CIFC46 H32 O3 P2P 21 21 2111.0559; 16.5376; 18.8101
90; 90; 90
3439.2Eichhorn, Katharina; Bruhn, Clemens; Pietschnig, Rudolf
β-Carboxyphospholes <i>via</i> carboxylative desilylation: luminophores with a versatile connectivity attached.
Chemical communications (Cambridge, England), 2025, 61, 17129-17132
7135048 CIFC12 H20 O S Si2P 1 21/n 110.7711; 9.923; 15.3315
90; 110.531; 90
1534.57An, Kun; Liu, Mengqing; Wang, Jingxia; Nishiura, Masayoshi; Cong, Xuefeng; Hou, Zhaomin
Synthesis of [1,3]-thiasilolanes <i>via</i> rare-earth-catalysed intramolecular α-C(sp<sup>3</sup>)-H silylation of alkyl sulphides with hydrosilanes.
Chemical communications (Cambridge, England), 2025, 61, 17181-17184
7135049 CIFC21 H19 N O2P -17.208; 9.749; 12.523
73.203; 76.884; 78.341
811.6Maiti, Sandip; Roy, Charles Patriot; Kabir, Syed Ramizul; Dash, Jyotirmayee
Rh(II)-catalyzed synthesis of furo[2,3-<i>b</i>]indoles from 3-diazooxindoles and electron-rich arylacetylenes.
Chemical communications (Cambridge, England), 2025, 61, 18649-18652
7135050 CIFC24 H19 N O4 SP -111.3303; 14.1464; 14.8702
97.934; 108.308; 112.348
2000.8Maiti, Sandip; Roy, Charles Patriot; Kabir, Syed Ramizul; Dash, Jyotirmayee
Rh(II)-catalyzed synthesis of furo[2,3-<i>b</i>]indoles from 3-diazooxindoles and electron-rich arylacetylenes.
Chemical communications (Cambridge, England), 2025, 61, 18649-18652
7135051 CIFC25 H18 O3C 1 2/c 123.6123; 9.4715; 17.1625
90; 100.183; 90
3777.83Begum, Fathima; Bhumannagari, Haripriya; Balasubramanian, Sridhar; Nayani, Kiranmai
Divergent coupling of <i>ortho</i>-alkynylnaphthols and <i>p</i>-quinone monoketals through a Michael addition/intramolecular annulation cascade to access benzofuryl β-naphthols.
Chemical communications (Cambridge, England), 2025, 61, 15003-15006
7135052 CIFC25 H17 F O3C 1 2/c 128.2559; 13.6584; 10.0502
90; 91.917; 90
3876.5Begum, Fathima; Bhumannagari, Haripriya; Balasubramanian, Sridhar; Nayani, Kiranmai
Divergent coupling of <i>ortho</i>-alkynylnaphthols and <i>p</i>-quinone monoketals through a Michael addition/intramolecular annulation cascade to access benzofuryl β-naphthols.
Chemical communications (Cambridge, England), 2025, 61, 15003-15006
7135053 CIFC36 H22 O2P -110.2845; 16.121; 17.626
98.505; 98.503; 106.719
2711.5Begum, Fathima; Bhumannagari, Haripriya; Balasubramanian, Sridhar; Nayani, Kiranmai
Divergent coupling of <i>ortho</i>-alkynylnaphthols and <i>p</i>-quinone monoketals through a Michael addition/intramolecular annulation cascade to access benzofuryl β-naphthols.
Chemical communications (Cambridge, England), 2025, 61, 15003-15006
7135054 CIFC12 H11.5 Cl N1.5 O1.5P -19.0938; 11.5029; 12.1234
111.969; 98.763; 94.676
1149Thakur, Rekha; Luxami, Vijay; Paul, Kamaldeep
Ruthenium(II)-catalyzed C-2 alkenylation of indole with olefins <i>via</i> a quinazolin-4(3<i>H</i>)-one directing group: a platform for selective fluorescent anion sensors.
Chemical communications (Cambridge, England), 2025, 61, 14374-14377
7135055 CIFC21 H25 N3 O3P -18.5658; 10.1115; 23.1709
96.106; 98.963; 101.388
1923.78Paul, Subhankar; Chaudhuri, Debangshu
Side-chain dependent direct <i>vs.</i> indirect photoresponse in hydrazone-based supramolecular polymers.
Chemical communications (Cambridge, England), 2025, 61, 14366-14369
7135056 CIFC38 H22 F6 N4P 1 21/c 117.1; 17.498; 13.593
90; 112.31; 90
3762.8Panua, Anirban; Velmurugan, Gunasekaran; Comba, Peter; Rath, Harapriya
Targeted synthesis of a positional isomer of aromatic <i>N</i>-methyl <i>N</i>-confused corrole and its organocopper(III) complex.
Chemical communications (Cambridge, England), 2025, 61, 17436-17439
7135057 CIFC21 H25 N OP 21 21 219.4002; 10.6999; 17.6147
90; 90; 90
1771.71Ghosh, Subhadeep; Biswas, Sumit; Das, Indrajit
Electro-carbo-cyclization of alkyne-, alkene-, and nitrile-tethered α-halocarbonyls.
Chemical communications (Cambridge, England), 2025, 61, 17448-17451
7135058 CIFC46 H76 O2 P2C 1 2/c 115.876; 14.4684; 20.2954
90; 104.386; 90
4515.68Uttendorfer, Maria K.; Schneider, Lisa M.; Diener, Lukas S.; Hierlmeier, Gabriele; Balázs, Gábor; Wolf, Robert
A radical path to 1,2-diphosphacyclobutenes.
Chemical communications (Cambridge, England), 2025, 61, 17464-17467
7135059 CIFC22 H28 P2 Se2I 1 2/a 114.989; 8.3205; 18.148
90; 95.024; 90
2254.65Uttendorfer, Maria K.; Schneider, Lisa M.; Diener, Lukas S.; Hierlmeier, Gabriele; Balázs, Gábor; Wolf, Robert
A radical path to 1,2-diphosphacyclobutenes.
Chemical communications (Cambridge, England), 2025, 61, 17464-17467
7135060 CIFC14 H36 Cl6 Mn N4P 21 21 218.4441; 16.7468; 17.4329
90; 90; 90
2465.22Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135061 CIFC14 H36 Br6 Mn N4P 21 21 218.6152; 17.2628; 18.0558
90; 90; 90
2685.3Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135062 CIFC14 H36 Cl10 Mn3 N4P 1 21/n 19.5893; 8.8686; 16.9149
90; 90.355; 90
1438.48Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135063 CIFC14 H36 I6 Mn N4P 21 21 218.9096; 18.141; 18.976
90; 90; 90
3067.1Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135064 CIFC88.5 H47 Cu N12 OP -113.047; 13.52; 21.777
79.204; 73.104; 77.349
3554.7Jangra, Reena; Bulbul, Amir Sohel; Sankar, Muniappan
π-Extended Cis- and Trans-Bis(Tetracyanobutadiene) Cu-Porphyrins with Unusual Multiredox Behavior
Chemical Communications, 2025
7135065 CIFC88 H44 Cu N12P -113.329; 15.694; 21.415
78.765; 75.079; 68.029
3990Jangra, Reena; Bulbul, Amir Sohel; Sankar, Muniappan
π-Extended Cis- and Trans-Bis(Tetracyanobutadiene) Cu-Porphyrins with Unusual Multiredox Behavior
Chemical Communications, 2025
7135066 CIFC25 H31 N O2C 1 c 145.525; 7.0641; 6.6022
90; 94.133; 90
2117.7Xiao, Yao; Pan, Xue-Lan; Cao, Xiang-Jian; Qi, Xin; Qiu, Sheng-Qi; Yu, Zhen-Qiang
A room temperature nematic luminescent liquid crystal: a FRET donor for amplified circularly polarized luminescence.
Chemical communications (Cambridge, England), 2025, 61, 17922-17925
7135067 CIFC29 H29 N3 O4P 1 21/n 111.4876; 12.9087; 17.8682
90; 106.868; 90
2535.67Roper, Natalie J.; Hardy, George M.; Wootton, Jack M.; Waddell, Paul G.; Wilson, James; Armstrong, Roly J.
A multicomponent approach for the stereoselective synthesis of atropisomeric N-N peptide analogues.
Chemical communications (Cambridge, England), 2025, 61, 17388-17391
7135068 CIFC29 H29 N3 O4P 1 2/n 111.9144; 11.0129; 20.0815
90; 97.27; 90
2613.75Roper, Natalie J.; Hardy, George M.; Wootton, Jack M.; Waddell, Paul G.; Wilson, James; Armstrong, Roly J.
A multicomponent approach for the stereoselective synthesis of atropisomeric N-N peptide analogues.
Chemical communications (Cambridge, England), 2025, 61, 17388-17391
7135069 CIFC20 H25.69 Mn2 N8 O8.85P 1 21/c 113.7898; 12.1567; 17.2696
90; 103.019; 90
2820.6Howlett, Thomas; Wang, Ziqi; Tang, Wendy; Arora, Nyati; Shende, Prapti M.; Liu, Phillip; Kumari, Sneha; Joy, Monu; Wriedt, Mario; Smaldone, Ronald A.; Gassensmith, Jeremiah J.
From Spontaneous Ligand Evolution to High-Throughput Water-Based Synthesis: Scalable Access to CO2 Selective Mixed-Ligand Metal Organic Frameworks
Chemical Communications, 2025
7135070 CIFC68 H137.5 Al I Mo6 N Na3 O94.25P 1 21 114.6954; 34.3474; 25.064
90; 105.154; 90
12211.1Liu, Chun-Yan; Mu, Yun-Jing; Chen, Wu-Ji; Liu, Cheng-Shuai; Lin, Chang-Gen; Song, Yu-Fei
Size-matched supramolecular assembly between an asymmetric Anderson-type polyoxometalate hybrid and α-/γ-cyclodextrins.
Chemical communications (Cambridge, England), 2025, 61, 17886-17889
7135071 CIFC208 H400 Al2 I2 Mo12 N2 O223P 1 21/n 128.963; 17.363; 37.324
90; 109.111; 90
17735Liu, Chun-Yan; Mu, Yun-Jing; Chen, Wu-Ji; Liu, Cheng-Shuai; Lin, Chang-Gen; Song, Yu-Fei
Size-matched supramolecular assembly between an asymmetric Anderson-type polyoxometalate hybrid and α-/γ-cyclodextrins.
Chemical communications (Cambridge, England), 2025, 61, 17886-17889
7135072 CIFC30 H28P c c n16.2667; 16.4045; 18.0519
90; 90; 90
4817.1Gao, Feng; Xu, Yanning; Ding, Zeyang; Liu, Hanwen; Wang, Haoran; Alam, Parvej; Qiu, Zijie; Tang, Ben Zhong
Through-space conjugation engineering in methylated tetraphenylethene derivatives.
Chemical communications (Cambridge, England), 2025, 61, 18100-18103
7135073 CIFC30 H28P 1 2/n 113.061; 6.7745; 13.079
90; 91.233; 90
1157Gao, Feng; Xu, Yanning; Ding, Zeyang; Liu, Hanwen; Wang, Haoran; Alam, Parvej; Qiu, Zijie; Tang, Ben Zhong
Through-space conjugation engineering in methylated tetraphenylethene derivatives.
Chemical communications (Cambridge, England), 2025, 61, 18100-18103
7135074 CIFC30 H28P 1 21/c 121.3224; 5.817; 19.767
90; 109.562; 90
2310.2Gao, Feng; Xu, Yanning; Ding, Zeyang; Liu, Hanwen; Wang, Haoran; Alam, Parvej; Qiu, Zijie; Tang, Ben Zhong
Through-space conjugation engineering in methylated tetraphenylethene derivatives.
Chemical communications (Cambridge, England), 2025, 61, 18100-18103
7135075 CIFC42 H38 N2 O9P -15.9506; 11.9443; 13.0049
83.657; 78.757; 84.862
898.85Hu, Longhao; Lin, Chaohui; Zeng, Dailin; Qin, Xianjiao; Lai, Xiao-Li; Gong, Lingshan; Ye, Yingxiang; AlShahrani, Thamraa; Ma, Shengqian
Solvent-induced conformational changes in color-tunable hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 17882-17885
7135076 CIFC38 H30 N2 O8P -14.7799; 11.7694; 14.1229
94.792; 91.588; 93.494
789.83Hu, Longhao; Lin, Chaohui; Zeng, Dailin; Qin, Xianjiao; Lai, Xiao-Li; Gong, Lingshan; Ye, Yingxiang; AlShahrani, Thamraa; Ma, Shengqian
Solvent-induced conformational changes in color-tunable hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 17882-17885
7135077 CIFC13 H9 SP 1 21/n 112.122; 5.585; 14.566
90; 107.22; 90
941.9Nag, Bedabara; Kumar, Akshai
Key role of oxygen and base in catalytic thioetherification: access to sulfur bridged poly-aromatic hydrocarbons.
Chemical communications (Cambridge, England), 2025, 61, 18120-18123
7135078 CIFC26 H8 F10 S2P 1 21/c 113.016; 4.9514; 17.4745
90; 102.038; 90
1101.42Nag, Bedabara; Kumar, Akshai
Key role of oxygen and base in catalytic thioetherification: access to sulfur bridged poly-aromatic hydrocarbons.
Chemical communications (Cambridge, England), 2025, 61, 18120-18123
7135079 CIFC26 H16 Br2 S2P 1 21/n 18.9039; 5.6737; 22.1636
90; 101.035; 90
1098.96Nag, Bedabara; Kumar, Akshai
Key role of oxygen and base in catalytic thioetherification: access to sulfur bridged poly-aromatic hydrocarbons.
Chemical communications (Cambridge, England), 2025, 61, 18120-18123
7135080 CIFC28 H24 N2 O6P -19.9897; 11.2443; 12.144
108.063; 102.688; 90.502
1260.85Tang, Shou-Yang; Sang, Qian-Qian; Chen, Ze-Le; Cai, Bao-Gui; Xuan, Jun
Visible-light-promoted synthesis of imidazo[1,5-<i>a</i>]indole-3-ones <i>via</i> cascade carbene N-H insertion and oxidative cyclization.
Chemical communications (Cambridge, England), 2025, 61, 17870-17873
7135081 CIFC2.21 H2.34 N0.28 O0.62P 1 21/c 121.4354; 9.9487; 15.1153
90; 104.054; 90
3126.92Biswas, Sourabh; Srinivasu, Vinjamuri; Mallick, Manasi; Chandu, Palasetty; Sureshkumar, Devarajulu
Photoredox-driven tandem ring-opening and vinylation: a route to distal alkenyl ketones from cyclopropenes.
Chemical communications (Cambridge, England), 2025, 61, 18388-18391
7135082 CIFC16 H11 F3 O6P -19.1458; 9.3792; 10.2964
86.62; 77.558; 63.535
771.41Ni, Tongtong; Xu, Xuefeng; Li, Wenguang; Li, Shiyuan; Sheng, Heyun; Zhang, Xu
Nickel-catalyzed [4+2] cycloadditions of β-ketoesters and alkynes.
Chemical communications (Cambridge, England), 2025, 61, 17645-17648
7135083 CIFC22 H23 N O2P 21 21 218.541; 12.2915; 17.0269
90; 90; 90
1787.51Manna, Sabyasachi; Sreedhara, Rahul Halanuru; Punesh, Thanay Umesh; Prabhu, Kandikere Ramaiah
Use of tailored boronic acids both as a radical donor and acceptor in a visible light-mediated di-functionalization of maleimides: rapid access to fused benzo[<i>e</i>]isoindole-1,3-diones.
Chemical communications (Cambridge, England), 2025, 61, 17669-17672
7135084 CIFC8 H24 Cl6 Mo N2 NaP 1 21/n 19.0726; 6.8264; 15.7029
90; 90.066; 90
972.53Binwal, Devesh Chandra; Vishnoi, Pratap
One-dimensional magnetic halide double perovskites [N(CH<sub>3</sub>)<sub>4</sub>]<sub>2</sub>M<sup>I</sup>MoCl<sub>6</sub> (M<sup>I</sup> = Na, Ag) with large A-site cations.
Chemical communications (Cambridge, England), 2025, 61, 18352-18355
7135085 CIFC8 H24 Ag Cl6 Mo N2P 63/m m c9.054; 9.054; 6.7638
90; 90; 120
480.18Binwal, Devesh Chandra; Vishnoi, Pratap
One-dimensional magnetic halide double perovskites [N(CH<sub>3</sub>)<sub>4</sub>]<sub>2</sub>M<sup>I</sup>MoCl<sub>6</sub> (M<sup>I</sup> = Na, Ag) with large A-site cations.
Chemical communications (Cambridge, England), 2025, 61, 18352-18355
7135086 CIFC71 H133 Fe K N7 O11 Si4P 1 21/c 118.115; 19.364; 25.348
90; 106.419; 90
8528.9Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135087 CIFC39 H83 Fe K N5 O6 Si4P -112.6097; 13.1708; 17.6115
110.391; 93.952; 93.322
2724.6Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135088 CIFC44 H96 Fe K N5 O6 Si4P -112.6019; 13.1359; 17.7179
110.508; 93.368; 93.329
2732.63Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135089 CIFC72 H152 F4 Fe2 K2 N8 O12 S4 Si8P -111.8028; 15.389; 29.1949
103.183; 92.864; 99.764
5066.5Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135090 CIFC28.6 H22.9 Cl Cu N6.3C 1 2/c 123.24; 30.2; 7.495
90; 97.687; 90
5213.1David, A. John; Seethapathy, Logeshwari; Kumar, S. Vijay; Das, Rajorshi; Das, Anjan
Photocatalytic carboxylation of aryl halides/alkenes with a copper(I) complex bypassing the demand for dual catalysts.
Chemical communications (Cambridge, England), 2025, 61, 17677-17680
7135091 CIFC17 H16 N2 OP 1 21/n 18.8248; 13.1914; 11.6734
90; 102.126; 90
1328.6Liu, Xiang; Wu, Wen-Rong; Ma, Shaohong; Chen, Juan; Meng, Yuan-Jie; Yang, Zi-Feng; Zhang, Shang-Shi; Feng, Pengju
Base-promoted [3+2] annulation of <i>N</i>-aminoisoquinolinium derivatives with cyclic iodonium ylide/2,2-difluorovinyl tosylate.
Chemical communications (Cambridge, England), 2025, 61, 17673-17676
7135092 CIFC16 H17 N3 SP 1 21/c 17.8135; 27.8711; 13.276
90; 90.854; 90
2890.8Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135093 CIFC39 H22 B Cl2 F10 N3 SP -112.0186; 12.5059; 13.7414
95.301; 106.618; 113.936
1756.94Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135094 CIFC27 H13 B F10 N2 O SP -19.6678; 10.2025; 13.9028
104.522; 95.869; 111.606
1205.04Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135095 CIFC28 H16 B F10 N3 SP -19.8457; 10.564; 13.7846
105.553; 90.551; 113.918
1251.18Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135096 CIFC17 H19 F6 O P SiP -18.9992; 10.1647; 11.3907
99.1849; 91.1844; 112.8
944.31Kopp, Richard O.; Rigo, Massimo; Groth, Lucie J.; Coles, Nathan T.; Neale, Samuel E.; Frank, Samantha; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Dynamic activation of alcohols by an electrophilic phosphinine.
Chemical communications (Cambridge, England), 2025, 61, 18625-18628
7135097 CIFC18 H21 F6 O P SiP -110.0771; 10.5675; 11.3486
92.695; 109.345; 114.43
1014.09Kopp, Richard O.; Rigo, Massimo; Groth, Lucie J.; Coles, Nathan T.; Neale, Samuel E.; Frank, Samantha; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Dynamic activation of alcohols by an electrophilic phosphinine.
Chemical communications (Cambridge, England), 2025, 61, 18625-18628
7135098 CIFC44 H88 Cl4 Cu4 Si4P -17.4937; 13.8967; 27.206
100.646; 91.838; 91.599
2781.3Gupta, Arvind Kumar; Fayet, Océane Y O; Tian, Lei; Berger, Raphael J. F.; Lomoth, Reiner; Orthaber, Andreas
Base-mediated alkynyl-cubane to Cu<sub>8</sub>-alkynide cluster transformation.
Chemical communications (Cambridge, England), 2025, 61, 18673-18676
7135099 CIFC88 H168 Cu8 Si8P 21 21 2114.9963; 22.5357; 30.877
90; 90; 90
10434.9Gupta, Arvind Kumar; Fayet, Océane Y O; Tian, Lei; Berger, Raphael J. F.; Lomoth, Reiner; Orthaber, Andreas
Base-mediated alkynyl-cubane to Cu<sub>8</sub>-alkynide cluster transformation.
Chemical communications (Cambridge, England), 2025, 61, 18673-18676
7135100 CIFC34 H20 F4 N2 SC 1 2/c 129.3094; 14.7807; 6.9665
90; 98.9151; 90
2981.5Gnanasekaran, Premkumar; Chen, Chia-Yu; Chu, Ting-Hung; Lin, Po-Heng; Chang, Yuan Jay
Eco-friendly synthesis of highly emissive benzothiadiazole-based fluorophores <i>via</i> a solvent-free hand-grinding Horner-Wadsworth-Emmons reaction in ≤1 minute.
Chemical communications (Cambridge, England), 2025, 61, 18148-18151
7135101 CIFC22 H16 N2 SP 1 21/c 19.5987; 15.087; 11.7651
90; 101.039; 90
1672.25Gnanasekaran, Premkumar; Chen, Chia-Yu; Chu, Ting-Hung; Lin, Po-Heng; Chang, Yuan Jay
Eco-friendly synthesis of highly emissive benzothiadiazole-based fluorophores <i>via</i> a solvent-free hand-grinding Horner-Wadsworth-Emmons reaction in ≤1 minute.
Chemical communications (Cambridge, England), 2025, 61, 18148-18151
7135102 CIFC13 H9 B F2 N2 SP 1 21/c 112.1127; 9.1231; 11.7692
90; 113.578; 90
1191.98Tian, Liang; Cao, Yiman; Chen, Can; Ni, Zhigang; Fan, Cong; Mack, John; Dai, Peidi; Lu, Hua; Gai, Lizhi
Small is different: <i>N</i>,<i>N</i>-chelated organoboron complexes with seven-membered rings.
Chemical communications (Cambridge, England), 2025, 61, 18641-18644
7135103 CIFC15 H13 B F2 N2 SP 1 21/c 16.9891; 13.5514; 14.4026
90; 95.392; 90
1358.06Tian, Liang; Cao, Yiman; Chen, Can; Ni, Zhigang; Fan, Cong; Mack, John; Dai, Peidi; Lu, Hua; Gai, Lizhi
Small is different: <i>N</i>,<i>N</i>-chelated organoboron complexes with seven-membered rings.
Chemical communications (Cambridge, England), 2025, 61, 18641-18644
7135104 CIFC105 H102 Cl6 N18 Se3P 3119.6339; 19.6339; 26.1675
90; 90; 120
8735.9Liu, Chao; Du, Ziwei; Ding, Xu; Wang, Zhixuan; Cao, Lili; Zhou, Ziwen; Chen, Jia; Zhang, Ning
Precise Heteroatoms Engineering for Iodine Capture Promotion in Porous Organic Cages
Chemical Communications, 2025
7135105 CIFC27 H26 N O2 SeP 1 21 15.4585; 20.644; 21.236
90; 93.871; 90
2387.5Reddy, Chada Raji; Vinaya, Puthiya Purayil; Ajaykumar, Uprety; Nagendraprasad, Thallamapuram
Electrophilic aryl migration of <i>N</i>-benzyl propiolamides to functionalized-acrylamides.
Chemical communications (Cambridge, England), 2025, 61, 18669-18672
7135106 CIFC34 H52 B2 F2 O10 S2P -18.7369; 10.5221; 11.1567
69.401; 88.06; 71.327
905.93Wang, Shuting; Tang, Shuai; Han, Xiao-Le; Zhang, Hua
Regioselective postmodification of aryl sulfonyl fluorides <i>via</i> iridium(I)-catalysed C-H borylation.
Chemical communications (Cambridge, England), 2025, 61, 18830-18833
7135107 CIFC52 H52 Ag2 F6 N12 O8 S4P 18.38282; 13.97902; 14.3924
115.939; 100.085; 95.7768
1462.99Sawant, Diksha U.; Halat, Peter; McKay, Alasdair I.; Izgorodina, Ekaterina I.; Turner, David R.
Dependence of an anion template on amino acid binding in DMSO/H<sub>2</sub>O by a chiral Ag/urea-based tweezer.
Chemical communications (Cambridge, England), 2025, 61, 18846-18849
7135108 CIFC23 H25 Cl N2 O2P 21 21 2110.5633; 10.5879; 18.4454
90; 90; 90
2062.99Liu, Shiqi; Ma, Yao-Rui; Leitch, David; Arseniyadis, Stellios; Jean, Alexandre; Clark, Paul; Keenan, Thomas; Huang, Jingjun; Hasija, Avantika; Huang, Pei-Qiang
Palladium-Catalysed Asymmetric Allylic Alkylation of Hydantoins using Bench-Stable Chiral Palladium Precatalysts
Chemical Communications, 2025
7135109 CIFC29 H20 N2 O3 S2 Se2P 1 21/c 15.7891; 14.1638; 32.308
90; 94.605; 90
2640.6Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135110 CIFC14 H4 Cl2 N2 Se2P -17.8604; 8.7632; 11.4837
93.4629; 106.53; 112.541
687.45Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135111 CIFC36 H34 N2 O4 S2P 1 21/n 15.9391; 23.454; 23.02
90; 93.477; 90
3200.7Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135112 CIFC28 H18 N2 O4 S2P 1 21/c 111.6031; 16.6534; 12.2098
90; 96.077; 90
2346.1Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135113 CIFC28 H18 N2 O2 S4P 1 n 16.1558; 16.8897; 12.1311
90; 103.961; 90
1224Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135114 CIFC36 H34 N2 O2 S2 Se2P -15.6312; 17.0766; 17.206
86.595; 81.468; 87.677
1632.5Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135115 CIFC31.5 H26 N2 O2 S2 Se2P -16.2952; 11.3991; 20.6848
104.048; 91.718; 99.82
1414.88Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135116 CIFC32 H27 F O2 SC 1 2/c 135.9609; 12.6981; 11.4122
90; 91.584; 90
5209.2Yu, Tianxin; Shi, Tingchang; Zhang, Zhilei; Xu, Hai-Bing; He, Zikai; Jiang, Lang; Gu, Xinggui; Wang, Erjing
Boosting aggregation-induced emission of hydroxylated tetraphenylthiophene via biogenic amine entangling
Chemical Communications, 2025
7135117 CIFC31 H29 I O3P 1 21/c 120.985; 10.746; 12.2193
90; 102.749; 90
2687.57Maurya, Sundaram; Patil, Vaibhav B.; Raghu Ramudu, G.; Amrutkar, Virendra S.; Mendapara, Yash G.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
CuH-Catalyzed Stereoselective Desymmetrization of Prochiral Cyclopentane-1,3-diones via Alkoxyallylation
Chemical Communications, 2025
7135118 CIFC25 H28 O3P 1 21 18.4261; 11.7773; 11.2319
90; 107.842; 90
1061.01Maurya, Sundaram; Patil, Vaibhav B.; Raghu Ramudu, G.; Amrutkar, Virendra S.; Mendapara, Yash G.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
CuH-Catalyzed Stereoselective Desymmetrization of Prochiral Cyclopentane-1,3-diones via Alkoxyallylation
Chemical Communications, 2025
7135119 CIFC25 H18 N2 O4P -18.1541; 8.182; 15.3186
103.249; 101.047; 92.876
971.63Liu, Luyao; Xiao, Chenfa; Li, Yin; Wan, Jiaxing; Tang, Ben Zhong; Wang, Zhiming
An ultra-simple construction strategy for uncommon 3,4-diaryl-modified maleimide luminophores and their unique aggregation-induced asymmetric effect (AIAE) on conformation.
Chemical communications (Cambridge, England), 2025, 61, 18380-18383
7135120 CIFC47 H32 N4 O2P 1 21/c 114.78458; 16.90271; 14.64273
90; 108.139; 90
3477.36Liu, Luyao; Xiao, Chenfa; Li, Yin; Wan, Jiaxing; Tang, Ben Zhong; Wang, Zhiming
An ultra-simple construction strategy for uncommon 3,4-diaryl-modified maleimide luminophores and their unique aggregation-induced asymmetric effect (AIAE) on conformation.
Chemical communications (Cambridge, England), 2025, 61, 18380-18383
7135121 CIFC13 H10 N4 O7P -17.4442; 9.0095; 10.8263
88.03; 76.686; 87.558
705.721Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135122 CIFC6 H6 N2 OP 1 21/c 115.999; 8.007; 9.943
90; 105.312; 90
1228.5Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135123 CIFC19 H16 N6 O8P -18.1848; 10.8341; 12.2177
71.159; 81.7; 89.974
1013.38Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135124 CIFC14 H11 N3 O8P 1 21/n 18.4196; 13.3701; 13.4639
90; 101.402; 90
1485.7Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135125 CIFC31 H23 N7 O14C 1 2/c 117.8367; 12.2586; 13.8777
90; 90.554; 90
3034.26Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135126 CIFC19 H19 N5 O4P -17.9234; 8.7843; 13.3922
92.797; 101.022; 95.147
909.16Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135127 CIFC20 H17 N5 O9P -17.2524; 8.8044; 16.4118
93.805; 91.218; 94.787
1041.61Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135128 CIFC46 H45 Cl2 Fe2 N O6 S4P 21 21 2110.6274; 13.5606; 31.507
90; 90; 90
4540.6Li, Shiguang; Wang, Jiang; Lv, Ya; Chi, Yonggui Robin; Gan, Xiuhai; Wu, Xingxing
N-Heterocyclic Carbene-Catalyzed Asymmetric Synthesis of Bis-Ferrocene Derivatives bearing Two Stereogenic Planes
Chemical Communications, 2025
7135129 CIFC22 H18 F N O3P 1 21/n 111.0201; 7.3436; 21.6386
90; 94.376; 90
1746.05Lin, Wei; Luo, Zhenli; Zhu, Huixuan; Hu, Jinhui; Xiong, Zhuang; Wu, Jia-Qiang
Rh(III)-catalyzed C-H activation/β-F elimination/Michael addition: diastereoselective access to dihydroisoquinolinones featuring β-amino α-fluorocarbonyl motif.
Chemical communications (Cambridge, England), 2025, 61, 18709-18712
7135130 CIFC11 H9 F0.5 N0.5 O1.5P 1 21/n 17.3449; 9.4651; 25.5608
90; 93.017; 90
1774.53Lin, Wei; Luo, Zhenli; Zhu, Huixuan; Hu, Jinhui; Xiong, Zhuang; Wu, Jia-Qiang
Rh(III)-catalyzed C-H activation/β-F elimination/Michael addition: diastereoselective access to dihydroisoquinolinones featuring β-amino α-fluorocarbonyl motif.
Chemical communications (Cambridge, England), 2025, 61, 18709-18712
7135131 CIFF K1.999 Na0.501 O4 P Sc0.5P -3 m 111.2963; 11.2963; 7.1996
90; 90; 120
795.63Zhao, Huijian; Li, Conggang; Ye, Ning; Hu, Zhanggui
Tailoring UV waveplate materials <i>via</i> rational assembly of functional motifs in scandium fluoride phosphate.
Chemical communications (Cambridge, England), 2025, 61, 17145-17148
7135132 CIFC25 H19 N O5P 1 21/c 19.51124; 15.99027; 12.44468
90; 101.867; 90
1852.23Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135133 CIFC20 H16 O5P 1 21/c 110.2969; 9.8246; 14.8656
90; 93.018; 90
1501.76Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135134 CIFC20.5 H16.98 Cl O6C 1 2/c 120.9727; 8.1208; 20.9626
90; 100.685; 90
3508.34Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135135 CIFC19 H14 O5P 1 21/c 18.3627; 10.9839; 16.0035
90; 97.525; 90
1457.34Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135136 CIFC20 H18 O3P -17.8446; 8.6853; 11.0599
77.008; 83.439; 81.312
723.3Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135137 CIFC16 H11 N O3 SP 1 21/c 110.3033; 16.8149; 7.3464
90; 92.449; 90
1271.59Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135138 CIFC22 H21 I O6P -19.0209; 9.603; 13.967
73.695; 71.448; 66.6
1036.01Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135139 CIFC56 H119 Au Cl N Sb2 Si9P 1 21/n 118.0962; 23.3405; 18.1023
90; 100.648; 90
7514.29Palui, Prasenjit; Bollenbeck, Matthias; Langellotti, Vincenzo; Schnakenburg, Gregor; Gomila, Rosa Maria; Frontera, Antonio; Bismuto, Alessandro
Synthesis and reactivity of a small distibacycle featuring an Au─Sb bimetallic linkage
Chemical Communications, 2025
7135140 CIFC106 H224 Au2 Cl2 N2 O Sb4 Si18P 1 21/n 112.5283; 36.1287; 17.215
90; 109.18; 90
7359.5Palui, Prasenjit; Bollenbeck, Matthias; Langellotti, Vincenzo; Schnakenburg, Gregor; Gomila, Rosa Maria; Frontera, Antonio; Bismuto, Alessandro
Synthesis and reactivity of a small distibacycle featuring an Au─Sb bimetallic linkage
Chemical Communications, 2025
7135141 CIFC40.5 H30 Cl6 Ir N5 S2P 1 21/c 113.353; 15.201; 20.751
90; 91.064; 90
4211.3Fernández-Moreira, Vanesa; Morales-Pioz, Eva; Redrado, Marta; Benedí Visiedo, Andrea; de Aquino, Araceli; García-Orduña, Pilar; Royo-Cañas, María; Godino, Javier; Marzo, Isabel; Rodriguez, Laura; Gimeno, M. Concepción
Cyclometallated Iridium(III) Complexes: Ligand-Driven Selectivity for Chemotherapy and Photodynamic Therapy
Chemical Communications, 2025
7135142 CIFC27 H19 BP -111.7047; 11.9303; 13.8652
98.8114; 95.4596; 94.8484
1894.93Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135143 CIFC26 H16 B FP 1 21/c 13.8479; 25.12; 18.2066
90; 92.161; 90
1758.6Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135144 CIFC46 H28 B2C 1 2/c 159.4616; 9.983; 21.9645
90; 105.428; 90
12568.4Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135145 CIFC48 H38 B2P 1 21/n 127.7844; 3.9198; 32.0442
90; 103.451; 90
3394.2Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135146 CIFC38 H26 B NP 1 21/c 19.2605; 31.4635; 10.1892
90; 116.391; 90
2659.39Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135147 CIFC29 H23 BP 1 21/c 111.4924; 4.8929; 36.2021
90; 97.4308; 90
2018.59Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135148 CIFC24 H21 BP -17.4166; 12.7823; 19.1202
79.8121; 89.9142; 85.4566
1778.29Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135149 CIFC32 H26 N2 OP -18.8121; 10.1918; 13.9891
99.49; 97.145; 103.344
1188.33Ma, Qiyuan; Qin, Hao; He, Xulong; Zheng, Zexi; Ding, Yawen; Yuan, Yu; Zhang, Shuwei; Jia, Xiaodong
Design, synthesis and structural investigation of a novel class of aggregation-induced emission (AIE) molecular scaffolds
Chemical Communications, 2025
7135150 CIFC32 H26 N2 OP 21 21 2111.6092; 12.2172; 16.4574
90; 90; 90
2334.2Ma, Qiyuan; Qin, Hao; He, Xulong; Zheng, Zexi; Ding, Yawen; Yuan, Yu; Zhang, Shuwei; Jia, Xiaodong
Design, synthesis and structural investigation of a novel class of aggregation-induced emission (AIE) molecular scaffolds
Chemical Communications, 2025
7135151 CIFC59 H56 Cl6 N8 O3P -115.1639; 18.904; 20.266
89.732; 74.207; 89.827
5590Liu, Shuangbin; Xiang, Yuanke; Chen, Xinqi; Gao, Haofeng; Yang, Xiaoran; Li, Jinmei; Fan, Jianxian; Liu, Ziyuan; He, Tianwei; Qiu, Li
Molecular Engineering of Porous Organic Cages for Iodine Capture and Fluorescence Detection
Chemical Communications, 2025
7135152 CIFC73 H64 Cl12 N6 O3P -110.502; 17.367; 38.68
93.004; 90.221; 92.104
7040.2Liu, Shuangbin; Xiang, Yuanke; Chen, Xinqi; Gao, Haofeng; Yang, Xiaoran; Li, Jinmei; Fan, Jianxian; Liu, Ziyuan; He, Tianwei; Qiu, Li
Molecular Engineering of Porous Organic Cages for Iodine Capture and Fluorescence Detection
Chemical Communications, 2025
7135153 CIFC43 H40 F10 N4 O9 ZnP 1 21 110.981; 14.833; 13.238
90; 90.05; 90
2156.2Sarwa, Aleksandra; Matviyishyn, Maksym; Perdek, Jędrzej P.; Trzaskowski, Bartosz; Kulesza, Dagmara; Zych, Eugeniusz; Szyszko, Bartosz
Mechanically Interlocked Porphyrinoids: Self-Assembly of Metal-Stabilised Catenaphyrins
Chemical Communications, 2025
7135154 CIFC76 H64 N12 O8 Zn2P 31 2 123.123; 23.123; 16.184
90; 90; 120
7494Sarwa, Aleksandra; Matviyishyn, Maksym; Perdek, Jędrzej P.; Trzaskowski, Bartosz; Kulesza, Dagmara; Zych, Eugeniusz; Szyszko, Bartosz
Mechanically Interlocked Porphyrinoids: Self-Assembly of Metal-Stabilised Catenaphyrins
Chemical Communications, 2025
7135155 CIFC46 H59 Br Cl2 N2 PdP 1 21/c 113.0408; 15.0939; 21.6308
90; 95.267; 90
4239.75Tzouras, Nikolaos V.; Fleischer, Ruben; Satta, Pierpaolo; Manna, Sourav; Doppiu, Angelino; Goossen, Lukas J.
Mild cross-coupling of tertiary alkoxides with aryl chlorides enabled by a shelf-stable methylnaphthyl palladium NHC complex
Chemical Communications, 2025
7135156 CIFC20 H17 Br N4 O3P 1 21/c 120.707; 6.5276; 13.766
90; 95.222; 90
1853Shivpuje, Umesh; Ahmad, Manzoor; Roy, Naveen Joseph; Talukdar, Pinaki
Ligand-responsive ON-OFF anion transport using copper-caged acylhydrazone transporters
Chemical Communications, 2025
7135157 CIFC64 H84 O4 S4I 41/a :228.37523; 28.37523; 14.57079
90; 90; 90
11731.7Losus, Renny Maria; Bleus, Sem; Bon, Volodymyr; Kaskel, Stefan; Dehaen, Wim; Dobrzańska, Liliana
Adaptive crystals of homothiacalix[4]arene capable of molecular recognition, with preferential uptake of benzene over cyclohexane.
Chemical communications (Cambridge, England), 2025
7135158 CIFC52 H72 O4 S4P -110.7957; 11.4363; 12.1971
68.795; 86.611; 62.936
1240.07Losus, Renny Maria; Bleus, Sem; Bon, Volodymyr; Kaskel, Stefan; Dehaen, Wim; Dobrzańska, Liliana
Adaptive crystals of homothiacalix[4]arene capable of molecular recognition, with preferential uptake of benzene over cyclohexane.
Chemical communications (Cambridge, England), 2025
7135159 CIFC52 H72 O4 S4P c c n13.5017; 24.9584; 14.6029
90; 90; 90
4920.9Losus, Renny Maria; Bleus, Sem; Bon, Volodymyr; Kaskel, Stefan; Dehaen, Wim; Dobrzańska, Liliana
Adaptive crystals of homothiacalix[4]arene capable of molecular recognition, with preferential uptake of benzene over cyclohexane.
Chemical communications (Cambridge, England), 2025
7135160 CIFC257 H205 Co4 N11 O45P -122.5652; 22.5982; 30.2731
77.825; 85.366; 65.661
13748.6Ma, Li-Li; Liu, Shengjin; Yang, Feinian; Cao, Jian; Ding, Longyi; Li, Yang; Yuan, Guozan
Integration of perylene diimide into a two-dimensional cobalt-organic framework for enhanced photocatalysis
Chemical Communications, 2025
7135161 CIFC29 H27 N3 O4 S2I 1 2/a 121.6291; 8.6367; 30.4166
90; 94.806; 90
5661.97Yadav, Anup Kumar; Kumar, Vipin; Singh, Saurabh; Samai, Subhasis; Singh, Maya Shankar
Synthesis of pyrrolo[3,4-c]pyridines via metal-free cross-coupling/cyclization cascades of β-ketothioamides with 2aroylmalononitrile at room temperature
Chemical Communications, 2025
7135162 CIFC20 H20 N2 OP c a 2112.718; 6.6198; 20.0762
90; 90; 90
1690.2Hu, Qianqian; Hu, Cangzhu; Tang, Tian; Wu, Qing; Hu, Weiming; Dai, Qiang; Wang, Lei
Palladium-catalyzed aminoalkynylation/alleneamination of urea-tethered alkenes: access to imidazolidinones bearing alkynes and allenes.
Chemical communications (Cambridge, England), 2025, 61, 17898-17901
7135163 CIFC23 H26 N2 OP 1 21/n 114.5518; 7.7103; 18.9048
90; 110.142; 90
1991.4Hu, Qianqian; Hu, Cangzhu; Tang, Tian; Wu, Qing; Hu, Weiming; Dai, Qiang; Wang, Lei
Palladium-catalyzed aminoalkynylation/alleneamination of urea-tethered alkenes: access to imidazolidinones bearing alkynes and allenes.
Chemical communications (Cambridge, England), 2025, 61, 17898-17901
7135164 CIFC316 H654 N34 O236 P16 V52C 1 2/c 139.393; 29.71; 48.245
90; 103.779; 90
54839Han, Shicheng; Liu, Fangcheng; Fu, Gang; Guo, Ji; Lin, Jiaheng; Wu, Hongyu; Mu, Chengyi; Fang, Xikui
Diphosphonate Functionalization of a Polyoxometalate-Organic Cage Enhances Proton Conductivity
Chemical Communications, 2025
7135165 CIFC H N OP -19.7302; 10.877; 11.3278
108.364; 92.134; 90.464
1136.79Saikia, Anil Kumar; Arandhara, Pallav Jyoti; Chutia, Archana
Leveraging cascade annulation of 2-alkynylcyclopropanes with substituted azides to access fused N-heterocyclic scaffolds
Chemical Communications, 2025
7135166 CIFB8 F12 K4 Na8 O24 Y8P 41 21 26.674; 6.674; 19.991
90; 90; 90
890.4Zhao, Huijian; Liu, Mengru; Nan, Weina; Yang, Ning; Li, Conggang; Ye, Ning; Hu, Zhanggui
KNa<sub>2</sub>Y<sub>2</sub>B<sub>2</sub>O<sub>6</sub>F<sub>3</sub>: a beryllium free deep-UV nonlinear optical crystal with well-balanced properties.
Chemical communications (Cambridge, England), 2025, 61, 17878-17881
7135167 CIFC78 H100 Cl2 Cu2 N6 P2 Si2P b c a13.856; 18.909; 33.767
90; 90; 90
8847Kaulage, Sandeep; Shah, Brij; Sharma, Himanshu; Panday, Rishukumar; Vanka, Kumar; Khan, Shabana
Silylene-Copper(I) Catalysis: Regioselective Protoboration of Terminal Alkynes
Chemical Communications, 2025
7135168 CIFC48 H61 Cu N3 P SiP 1 21/c 111.1435; 21.864; 18.789
90; 104.38; 90
4434.4Kaulage, Sandeep; Shah, Brij; Sharma, Himanshu; Panday, Rishukumar; Vanka, Kumar; Khan, Shabana
Silylene-Copper(I) Catalysis: Regioselective Protoboration of Terminal Alkynes
Chemical Communications, 2025
7135169 CIFC42 H65 Cu N3 P SiP 1 21 110.0396; 19.1146; 11.968
90; 114.685; 90
2086.8Kaulage, Sandeep; Shah, Brij; Sharma, Himanshu; Panday, Rishukumar; Vanka, Kumar; Khan, Shabana
Silylene-Copper(I) Catalysis: Regioselective Protoboration of Terminal Alkynes
Chemical Communications, 2025
7135170 CIFC19 H13 N O2P 1 21/c 127.591; 8.5988; 12.4
90; 100.846; 90
2889.3Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135171 CIFC19 H13 N O2P 1 21/c 127.509; 8.6819; 12.636
90; 101.062; 90
2961.8Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135172 CIFC21 H19 N O3P 1 21/c 18.52527; 26.3892; 15.8287
90; 100.735; 90
3498.74Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135173 CIFC22 H21 N O3P 1 21/c 18.50169; 27.8458; 8.1178
90; 103.313; 90
1870.13Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135174 CIFC20 H17 N O3P 1 21/n 18.1669; 26.4699; 15.7893
90; 104.465; 90
3305.1Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135175 CIFC102 H63.43 Mn4 N10 O26.71P b c a22.7346; 13.7881; 26.2173
90; 90; 90
8218.3Liu, Jiang; Xu, Sha-Sha; Liang, Jia-Zheng; Yao, Su-Juan; Li, Ning; Shi, Jing-Wen; Lan, Yaqian
Microenvironment Regulation of Active Sites for Efficient Photocatalytic Reduction of Nitrobenzene
Chemical Communications, 2025
7135176 CIFC75.7 H62.42 Mn4 N7 O30.91C 1 2/c 124.6796; 13.604; 21.497
90; 91.574; 90
7214.7Liu, Jiang; Xu, Sha-Sha; Liang, Jia-Zheng; Yao, Su-Juan; Li, Ning; Shi, Jing-Wen; Lan, Yaqian
Microenvironment Regulation of Active Sites for Efficient Photocatalytic Reduction of Nitrobenzene
Chemical Communications, 2025
7135177 CIFC23 H21 N O2 SP 21 21 216.4453; 14.9945; 20.1091
90; 90; 90
1943.42Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Nandy, Abhijit; Arora, Kirti; Banerjee, Shibdas; Verma, Akhilesh K.
Vinyl benzotriazole to indole: an iodine-mediated denitrogenative transannulation approach for the synthesis of indoles.
Chemical communications (Cambridge, England), 2025
7135178 CIFC18 H18 I N3 O2 SP 1 21/c 17.6989; 13.6394; 17.7709
90; 98.755; 90
1844.35Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Nandy, Abhijit; Arora, Kirti; Banerjee, Shibdas; Verma, Akhilesh K.
Vinyl benzotriazole to indole: an iodine-mediated denitrogenative transannulation approach for the synthesis of indoles.
Chemical communications (Cambridge, England), 2025
7135179 CIFC22 H19 N O3 SP c a 2115.1706; 11.7513; 21.1278
90; 90; 90
3766.5Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Nandy, Abhijit; Arora, Kirti; Banerjee, Shibdas; Verma, Akhilesh K.
Vinyl benzotriazole to indole: an iodine-mediated denitrogenative transannulation approach for the synthesis of indoles.
Chemical communications (Cambridge, England), 2025
7135180 CIFC26 H19 Br2 N O SP -18.2318; 10.8621; 13.1254
78.435; 79.26; 79.268
1116.05Chen, Jiahong; Huang, Yuanyuan; Wang, Nan; Wang, Mengke; Huang, Weichun; Wu, Xin-Xing; Xu, Xiao-Ping; Zi, You
Regioselective Functionalization of Sulfenamides: S-Arylation with Cyclic Diaryl λ3 -Bromanes and λ3 -Chloranes
Chemical Communications, 2025
7135181 CIFC40 H60 Mo2 O4 UC 1 2/c 116.2375; 13.6368; 17.8447
90; 95.875; 90
3930.55Valerio, Leyla R.; Patra, Kamaless; Shiels, Dominic; Brennessel, William W.; Matson, Ellen M.
Synthesis and characterization of a low-valent uranium complex supported by a redox-active molybdenum oxide metalloligand.
Chemical communications (Cambridge, England), 2025
7135182 CIFC40 H60 Cl Mo2 O4 UP n m a18.2457; 16.2988; 13.5222
90; 90; 90
4021.27Valerio, Leyla R.; Patra, Kamaless; Shiels, Dominic; Brennessel, William W.; Matson, Ellen M.
Synthesis and characterization of a low-valent uranium complex supported by a redox-active molybdenum oxide metalloligand.
Chemical communications (Cambridge, England), 2025
7135183 CIFC26 H30 N2 O6 S2P b c a10.405; 10.958; 23.3754
90; 90; 90
2665.2Nemichand, ?; Waghmode, Amol G.; Awchar, Vilas M.; Baskaran, Sundarababu
Oxidative cyclization of active methylene amides: efficient synthesis of functionalized 3-azabicyclo[<i>n</i>.1.0]alkanes.
Chemical communications (Cambridge, England), 2025

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