Crystallography Open Database

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1547705 CIFC39 H23 Cl8 Dy N5 Na O5P 1 21/c 19.9819; 19.8256; 20.6783
90; 91.212; 90
4091.26Miralles, Sara G.; Bedoya-Pinto, Amilcar; Baldoví, José J; Cañon-Mancisidor, Walter; Prado, Yoann; Prima-Garcia, Helena; Gaita-Ariño, Alejandro; Mínguez Espallargas, Guillermo; Hueso, Luis E.; Coronado, Eugenio
Sublimable chloroquinolinate lanthanoid single-ion magnets deposited on ferromagnetic electrodes.
Chemical science, 2018, 9, 199-208
1547706 CIFC84 H58 Cl16 Dy2 K N11 O8P -115.8989; 16.0286; 19.542
98.384; 91.201; 118.115
4322.5Miralles, Sara G.; Bedoya-Pinto, Amilcar; Baldoví, José J; Cañon-Mancisidor, Walter; Prado, Yoann; Prima-Garcia, Helena; Gaita-Ariño, Alejandro; Mínguez Espallargas, Guillermo; Hueso, Luis E.; Coronado, Eugenio
Sublimable chloroquinolinate lanthanoid single-ion magnets deposited on ferromagnetic electrodes.
Chemical science, 2018, 9, 199-208
1547707 CIFC44 H36 Cl8 Dy N5 O4C 1 2/c 136.1061; 11.5705; 22.7831
90; 109.429; 90
8976Miralles, Sara G.; Bedoya-Pinto, Amilcar; Baldoví, José J; Cañon-Mancisidor, Walter; Prado, Yoann; Prima-Garcia, Helena; Gaita-Ariño, Alejandro; Mínguez Espallargas, Guillermo; Hueso, Luis E.; Coronado, Eugenio
Sublimable chloroquinolinate lanthanoid single-ion magnets deposited on ferromagnetic electrodes.
Chemical science, 2018, 9, 199-208
1547767 CIFC36 Al F30 N3P -110.86; 12.7006; 14.3671
73.501; 72.779; 89.315
1809.2Kögel, J F; Sorokin, D. A.; Khvorost, A.; Scott, M.; Harms, K.; Himmel, D.; Krossing, I.; Sundermeyer, J.
The Lewis superacid Al[N(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sub>3</sub> and its higher homolog Ga[N(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sub>3</sub> - structural features, theoretical investigation and reactions of a metal amide with higher fluoride ion affinity than SbF<sub>5</sub>.
Chemical science, 2018, 9, 245-253
1547768 CIFC105 H31 Al2 F62 Li N6P -114.4989; 18.051; 21.909
84.427; 73.249; 67.033
5054.7Kögel, J F; Sorokin, D. A.; Khvorost, A.; Scott, M.; Harms, K.; Himmel, D.; Krossing, I.; Sundermeyer, J.
The Lewis superacid Al[N(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sub>3</sub> and its higher homolog Ga[N(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sub>3</sub> - structural features, theoretical investigation and reactions of a metal amide with higher fluoride ion affinity than SbF<sub>5</sub>.
Chemical science, 2018, 9, 245-253
1547769 CIFC36 F30 Ga N3P 1 21/c 17.9908; 20.611; 22.8236
90; 108.292; 90
3569.1Kögel, J F; Sorokin, D. A.; Khvorost, A.; Scott, M.; Harms, K.; Himmel, D.; Krossing, I.; Sundermeyer, J.
The Lewis superacid Al[N(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sub>3</sub> and its higher homolog Ga[N(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sub>3</sub> - structural features, theoretical investigation and reactions of a metal amide with higher fluoride ion affinity than SbF<sub>5</sub>.
Chemical science, 2018, 9, 245-253
1547770 CIFC57 H24 Al Cs F31 N3P 1 21/c 113.0294; 26.0373; 16.8481
90; 92.421; 90
5710.6Kögel, J F; Sorokin, D. A.; Khvorost, A.; Scott, M.; Harms, K.; Himmel, D.; Krossing, I.; Sundermeyer, J.
The Lewis superacid Al[N(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sub>3</sub> and its higher homolog Ga[N(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sub>3</sub> - structural features, theoretical investigation and reactions of a metal amide with higher fluoride ion affinity than SbF<sub>5</sub>.
Chemical science, 2018, 9, 245-253
1547771 CIFC125 H52 As2 Cl2 F60 Ga2 N6P -111.2887; 13.9044; 20.9274
98.126; 103.279; 111.821
2873Kögel, J F; Sorokin, D. A.; Khvorost, A.; Scott, M.; Harms, K.; Himmel, D.; Krossing, I.; Sundermeyer, J.
The Lewis superacid Al[N(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sub>3</sub> and its higher homolog Ga[N(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>]<sub>3</sub> - structural features, theoretical investigation and reactions of a metal amide with higher fluoride ion affinity than SbF<sub>5</sub>.
Chemical science, 2018, 9, 245-253
1547772 CIFC13 H19 N OP 1 21/c 119.555; 6.165; 10.117
90; 98.628; 90
1205.9Gao, Bao; Zhang, Guoying; Zhou, Xibing; Huang, Hanmin
Palladium-catalyzed regiodivergent hydroaminocarbonylation of alkenes to primary amides with ammonium chloride.
Chemical science, 2018, 9, 380-386
1547773 CIFC9 H10 Cl N OC 1 2/c 127.159; 7.49; 9.539
90; 106.51; 90
1860.4Gao, Bao; Zhang, Guoying; Zhou, Xibing; Huang, Hanmin
Palladium-catalyzed regiodivergent hydroaminocarbonylation of alkenes to primary amides with ammonium chloride.
Chemical science, 2018, 9, 380-386
1547774 CIFC21 H36 Cl O P PdP -18.6745; 9.6624; 13.8499
86.795; 81.245; 81.324
1133.55Gao, Bao; Zhang, Guoying; Zhou, Xibing; Huang, Hanmin
Palladium-catalyzed regiodivergent hydroaminocarbonylation of alkenes to primary amides with ammonium chloride.
Chemical science, 2018, 9, 380-386
1547775 CIFC15 H15 N OP 1 21/c 112.295; 5.569; 18.014
90; 101.033; 90
1210.6Gao, Bao; Zhang, Guoying; Zhou, Xibing; Huang, Hanmin
Palladium-catalyzed regiodivergent hydroaminocarbonylation of alkenes to primary amides with ammonium chloride.
Chemical science, 2018, 9, 380-386
1547805 CIFC21 H19.5 N3 O0.5C 1 2/c 135.5176; 4.6594; 23.3989
90; 116.089; 90
3477.76Li, Wanfang; Boon, Jie Kang; Zhao, Yu
Nickel-catalyzed difunctionalization of allyl moieties using organoboronic acids and halides with divergent regioselectivities.
Chemical science, 2018, 9, 600-607
1547835 CIFC19 H20 O3P 21 21 218.3146; 11.1767; 16.4216
90; 90; 90
1526.06Joyce, Leo A.; Nawrat, Christopher C.; Sherer, Edward C.; Biba, Mirlinda; Brunskill, Andrew; Martin, Gary E.; Cohen, Ryan D.; Davies, Ian W.
Beyond optical rotation: what's left is not always right in total synthesis.
Chemical science, 2018, 9, 415-424
1547836 CIFC50 H34 Co Fe2 N14 O2C 1 2/c 127.352; 15.144; 13.336
90; 116.222; 90
4956Jiang, Wenjing; Jiao, Chengqi; Meng, Yinshan; Zhao, Liang; Liu, Qiang; Liu, Tao
Switching single chain magnet behavior <i>via</i> photoinduced bidirectional metal-to-metal charge transfer.
Chemical science, 2018, 9, 617-622
1547843 CIFC26 H22 F2 N2 O2P 1 21/c 18.3521; 12.418; 20.681
90; 97.923; 90
2124.5Lv, Zhuang; Wei, Huanjie; Li, Qing; Su, Xianlong; Liu, Shujuan; Zhang, Kenneth Yin; Lv, Wen; Zhao, Qiang; Li, Xianghong; Huang, Wei
Achieving efficient photodynamic therapy under both normoxia and hypoxia using cyclometalated Ru(ii) photosensitizer through type I photochemical process.
Chemical science, 2018, 9, 502-512
1547871 CIFC19 H24 N4 O SP 1 21/n 15.9414; 15.879; 19.207
90; 94.096; 90
1807.4Wei, Peng; Yuan, Wei; Xue, Fengfeng; Zhou, Wei; Li, Ruohan; Zhang, Datong; Yi, Tao
Deformylation reaction-based probe for <i>in vivo</i> imaging of HOCl.
Chemical science, 2018, 9, 495-501
1547872 CIFC17 H19 N3 O SP 1 21/c 116.166; 8.073; 12.176
90; 99.741; 90
1566.2Wei, Peng; Yuan, Wei; Xue, Fengfeng; Zhou, Wei; Li, Ruohan; Zhang, Datong; Yi, Tao
Deformylation reaction-based probe for <i>in vivo</i> imaging of HOCl.
Chemical science, 2018, 9, 495-501
1547877 CIFC30 H26 Eu F9 O9 S3P 1 21/c 111.81; 16.5659; 18.388
90; 92.9627; 90
3592.68Babel, Lucille; Guénée, Laure; Besnard, Céline; Eliseeva, Svetlana V.; Petoud, Stéphane; Piguet, Claude
Cooperative loading of multisite receptors with lanthanide containers: an approach for organized luminescent metallopolymers.
Chemical science, 2018, 9, 325-335
1547878 CIFC30 H26 F9 O9 S3 YP 1 21/c 110.5124; 18.3614; 18.9788
90; 98.264; 90
3625.29Babel, Lucille; Guénée, Laure; Besnard, Céline; Eliseeva, Svetlana V.; Petoud, Stéphane; Piguet, Claude
Cooperative loading of multisite receptors with lanthanide containers: an approach for organized luminescent metallopolymers.
Chemical science, 2018, 9, 325-335
1547879 CIFC72 H46 Cl2 Eu F24 N5 O6P 1 21/n 113.7492; 20.1925; 25.829
90; 90.402; 90
7170.7Babel, Lucille; Guénée, Laure; Besnard, Céline; Eliseeva, Svetlana V.; Petoud, Stéphane; Piguet, Claude
Cooperative loading of multisite receptors with lanthanide containers: an approach for organized luminescent metallopolymers.
Chemical science, 2018, 9, 325-335
1547880 CIFC36 H17 Eu F24 O9P 1 21/c 18.38538; 27.3868; 18.8875
90; 102.271; 90
4238.4Babel, Lucille; Guénée, Laure; Besnard, Céline; Eliseeva, Svetlana V.; Petoud, Stéphane; Piguet, Claude
Cooperative loading of multisite receptors with lanthanide containers: an approach for organized luminescent metallopolymers.
Chemical science, 2018, 9, 325-335
1547881 CIFC19 H19 Br N2 NiP 1 21/c 18.4028; 11.9498; 17.1489
90; 94.163; 90
1717.4Jia, Xue-Gong; Guo, Peng; Duan, Jicheng; Shu, Xing-Zhong
Dual nickel and Lewis acid catalysis for cross-electrophile coupling: the allylation of aryl halides with allylic alcohols.
Chemical science, 2018, 9, 640-645
1547882 CIFC22 H23 N O4P -18.7005; 10.2416; 11.4433
76.304; 83.414; 75.816
958.74Liu, Kai; Xu, Guangyang; Sun, Jiangtao
Gold-catalyzed stereoselective dearomatization/metal-free aerobic oxidation: access to 3-substituted indolines/oxindoles.
Chemical science, 2018, 9, 634-639
1547883 CIFC20 H23 N O6P 1 21/c 15.9171; 24.525; 13.126
90; 95.432; 90
1896.3Liu, Kai; Xu, Guangyang; Sun, Jiangtao
Gold-catalyzed stereoselective dearomatization/metal-free aerobic oxidation: access to 3-substituted indolines/oxindoles.
Chemical science, 2018, 9, 634-639
1547884 CIFC25 H23 N O4P 1 21/c 110.5469; 20.177; 10.7298
90; 114.01; 90
2085.8Liu, Kai; Xu, Guangyang; Sun, Jiangtao
Gold-catalyzed stereoselective dearomatization/metal-free aerobic oxidation: access to 3-substituted indolines/oxindoles.
Chemical science, 2018, 9, 634-639
1547885 CIFC24 H21 N O4C 1 2/c 123.476; 10.1603; 18.561
90; 118.836; 90
3878.3Liu, Kai; Xu, Guangyang; Sun, Jiangtao
Gold-catalyzed stereoselective dearomatization/metal-free aerobic oxidation: access to 3-substituted indolines/oxindoles.
Chemical science, 2018, 9, 634-639
1547942 CIFC24 H23 N O6P 1 21 110.5132; 9.6837; 10.8056
90; 93.347; 90
1098.21Kuang, Yulong; Shen, Bin; Dai, Li; Yao, Qian; Liu, Xiaohua; Lin, Lili; Feng, Xiaoming
Diastereodivergent asymmetric Michael-alkylation reactions using chiral <i>N</i>,<i>N</i>'-dioxide/metal complexes.
Chemical science, 2018, 9, 688-692
1547943 CIFC24 H23 N O6P 1 21 16.6941; 8.926; 18.2322
90; 92.895; 90
1088.01Kuang, Yulong; Shen, Bin; Dai, Li; Yao, Qian; Liu, Xiaohua; Lin, Lili; Feng, Xiaoming
Diastereodivergent asymmetric Michael-alkylation reactions using chiral <i>N</i>,<i>N</i>'-dioxide/metal complexes.
Chemical science, 2018, 9, 688-692
1547944 CIFC19 H16 Cl N O4P 1 21/n 112.3416; 17.221; 16.8272
90; 95.88; 90
3557.55Kuang, Yulong; Shen, Bin; Dai, Li; Yao, Qian; Liu, Xiaohua; Lin, Lili; Feng, Xiaoming
Diastereodivergent asymmetric Michael-alkylation reactions using chiral <i>N</i>,<i>N</i>'-dioxide/metal complexes.
Chemical science, 2018, 9, 688-692
1548021 CIFC60 H76 Co3 N36 O8 W2P -111.91; 12.221; 15.587
69.947; 81.802; 66.513
1954.6Zhang, Yuan-Zhu; Dolinar, Brian S.; Liu, Shihao; Brown, Andrew J.; Zhang, Xuan; Wang, Zhao-Xi; Dunbar, Kim R.
Enforcing Ising-like magnetic anisotropy <i>via</i> trigonal distortion in the design of a W(v)-Co(ii) cyanide single-chain magnet.
Chemical science, 2018, 9, 119-124
1548053 CIFC26 H17 NP b c a8.2997; 33.2041; 12.4646
90; 90; 90
3435Suzuki, Tsuyoshi; Okada, Hiroshi; Nakagawa, Takafumi; Komatsu, Kazuki; Fujimoto, Chikako; Kagi, Hiroyuki; Matsuo, Yutaka
A fluorenylidene-acridane that becomes dark in color upon grinding - ground state mechanochromism by conformational change.
Chemical science, 2018, 9, 475-482
1548054 CIFC27 H19 NP 1 21/a 17.379; 22.716; 9.381
90; 111.14; 90
1466.6Suzuki, Tsuyoshi; Okada, Hiroshi; Nakagawa, Takafumi; Komatsu, Kazuki; Fujimoto, Chikako; Kagi, Hiroyuki; Matsuo, Yutaka
A fluorenylidene-acridane that becomes dark in color upon grinding - ground state mechanochromism by conformational change.
Chemical science, 2018, 9, 475-482
1548055 CIFC27 H19 NP 1 21/a 18.5137; 21.963; 9.8776
90; 104.406; 90
1788.9Suzuki, Tsuyoshi; Okada, Hiroshi; Nakagawa, Takafumi; Komatsu, Kazuki; Fujimoto, Chikako; Kagi, Hiroyuki; Matsuo, Yutaka
A fluorenylidene-acridane that becomes dark in color upon grinding - ground state mechanochromism by conformational change.
Chemical science, 2018, 9, 475-482
1548056 CIFC27 H19 NP 1 21 17.3384; 18.5774; 13.3299
90; 90.1024; 90
1817.24Suzuki, Tsuyoshi; Okada, Hiroshi; Nakagawa, Takafumi; Komatsu, Kazuki; Fujimoto, Chikako; Kagi, Hiroyuki; Matsuo, Yutaka
A fluorenylidene-acridane that becomes dark in color upon grinding - ground state mechanochromism by conformational change.
Chemical science, 2018, 9, 475-482
1548064 CIFC27 H24 Fe O3P 1 21/n 111.0994; 8.5265; 21.7146
90; 97.392; 90
2037.97Wang, Yong; Dansette, Patrick M.; Pigeon, Pascal; Top, Siden; McGlinchey, Michael J.; Mansuy, Daniel; Jaouen, Gérard
A new generation of ferrociphenols leads to a great diversity of reactive metabolites, and exhibits remarkable antiproliferative properties.
Chemical science, 2018, 9, 70-78
1548110 CIFC14 H15 N O SP 1 21/c 117.7719; 8.1203; 19.0328
90; 110.633; 90
2570.5Šiaučiulis, Mindaugas; Sapmaz, Selma; Pulis, Alexander P.; Procter, David J.
Dual vicinal functionalisation of heterocycles <i>via</i> an interrupted Pummerer coupling/[3,3]-sigmatropic rearrangement cascade.
Chemical science, 2018, 9, 754-759
1548111 CIFC15 H17 N O SP -18.2973; 9.132; 9.7066
104.937; 100.291; 100.461
678.86Šiaučiulis, Mindaugas; Sapmaz, Selma; Pulis, Alexander P.; Procter, David J.
Dual vicinal functionalisation of heterocycles <i>via</i> an interrupted Pummerer coupling/[3,3]-sigmatropic rearrangement cascade.
Chemical science, 2018, 9, 754-759
1548134 CIFC88 H60 F12 N12 O12 Pd2 S8P -112.284; 15.243; 17.55
100.641; 102.198; 98.202
3099.8Wang, Chen; Tian, Li; Zhu, Wei; Wang, Shiqiang; Gao, Ning; Zhou, Kang; Yin, Xianpeng; Zhang, Wanlin; Zhao, Liang; Li, Guangtao
Molecular cage-bridged plasmonic structures with well-defined nanogaps as well as the capability of reversible and selective guest trapping.
Chemical science, 2018, 9, 889-895
1548141 CIFC16 H56 Br10 N8 SnP -110.207; 10.6944; 18.5996
94.043; 102.847; 97.904
1949.89Zhou, Chenkun; Lin, Haoran; Tian, Yu; Yuan, Zhao; Clark, Ronald; Chen, Banghao; van de Burgt, Lambertus J.; Wang, Jamie C.; Zhou, Yan; Hanson, Kenneth; Meisner, Quinton J.; Neu, Jennifer; Besara, Tiglet; Siegrist, Theo; Lambers, Eric; Djurovich, Peter; Ma, Biwu
Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency.
Chemical science, 2018, 9, 586-593
1548142 CIFC18 H40 Cl5 N2 SbP 1 21/n 18.75618; 27.2439; 10.64297
90; 97.3536; 90
2518.02Zhou, Chenkun; Lin, Haoran; Tian, Yu; Yuan, Zhao; Clark, Ronald; Chen, Banghao; van de Burgt, Lambertus J.; Wang, Jamie C.; Zhou, Yan; Hanson, Kenneth; Meisner, Quinton J.; Neu, Jennifer; Besara, Tiglet; Siegrist, Theo; Lambers, Eric; Djurovich, Peter; Ma, Biwu
Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency.
Chemical science, 2018, 9, 586-593
1548143 CIFC16 H56 I10 N8 SnP -110.7464; 10.8924; 11.1796
64.2658; 80.1825; 72.8331
1124.94Zhou, Chenkun; Lin, Haoran; Tian, Yu; Yuan, Zhao; Clark, Ronald; Chen, Banghao; van de Burgt, Lambertus J.; Wang, Jamie C.; Zhou, Yan; Hanson, Kenneth; Meisner, Quinton J.; Neu, Jennifer; Besara, Tiglet; Siegrist, Theo; Lambers, Eric; Djurovich, Peter; Ma, Biwu
Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency.
Chemical science, 2018, 9, 586-593
1548144 CIFC247.73 H123.18 N2P 1 21/c 113.1579; 37.8588; 30.9277
90; 96.192; 90
15316.5Yokoi, Hiroki; Hiroto, Satoru; Sakamaki, Daisuke; Seki, Shu; Shinokubo, Hiroshi
Supramolecular assemblies of a nitrogen-embedded buckybowl dimer with C<sub>60</sub>.
Chemical science, 2018, 9, 819-824
1548145 CIFC160 H94 N2P 1 21 117.0175; 28.9186; 22.7929
90; 100.484; 90
11029.6Yokoi, Hiroki; Hiroto, Satoru; Sakamaki, Daisuke; Seki, Shu; Shinokubo, Hiroshi
Supramolecular assemblies of a nitrogen-embedded buckybowl dimer with C<sub>60</sub>.
Chemical science, 2018, 9, 819-824
1548236 CIFC39 H53 Cl3 O9P -112.7541; 13.5008; 13.6961
94.892; 105.455; 113.791
2029.61Cheng, Min-Jing; Cao, Jia-Qing; Yang, Xin-Yi; Zhong, Li-Ping; Hu, Li-Jun; Lu, Xi; Hou, Bao-Long; Hu, Ya-Jian; Wang, Ying; You, Xue-Fu; Wang, Lei; Ye, Wen-Cai; Li, Chuang-Chuang
Catalytic asymmetric total syntheses of myrtucommuacetalone, myrtucommuacetalone B, and callistrilones A, C, D and E.
Chemical science, 2018, 9, 1488-1495
1548237 CIFC39 H54 O9P -110.6706; 13.8828; 14.1078
70.567; 84.605; 69.424
1844.5Cheng, Min-Jing; Cao, Jia-Qing; Yang, Xin-Yi; Zhong, Li-Ping; Hu, Li-Jun; Lu, Xi; Hou, Bao-Long; Hu, Ya-Jian; Wang, Ying; You, Xue-Fu; Wang, Lei; Ye, Wen-Cai; Li, Chuang-Chuang
Catalytic asymmetric total syntheses of myrtucommuacetalone, myrtucommuacetalone B, and callistrilones A, C, D and E.
Chemical science, 2018, 9, 1488-1495
1548238 CIFC34 H44 O6P 1 21 111.541; 16.4653; 32.9338
90; 95.72; 90
6227.12Cheng, Min-Jing; Cao, Jia-Qing; Yang, Xin-Yi; Zhong, Li-Ping; Hu, Li-Jun; Lu, Xi; Hou, Bao-Long; Hu, Ya-Jian; Wang, Ying; You, Xue-Fu; Wang, Lei; Ye, Wen-Cai; Li, Chuang-Chuang
Catalytic asymmetric total syntheses of myrtucommuacetalone, myrtucommuacetalone B, and callistrilones A, C, D and E.
Chemical science, 2018, 9, 1488-1495
1548239 CIFC34 H45 O7P 21 21 216.3828; 14.8993; 32.605
90; 90; 90
3100.71Cheng, Min-Jing; Cao, Jia-Qing; Yang, Xin-Yi; Zhong, Li-Ping; Hu, Li-Jun; Lu, Xi; Hou, Bao-Long; Hu, Ya-Jian; Wang, Ying; You, Xue-Fu; Wang, Lei; Ye, Wen-Cai; Li, Chuang-Chuang
Catalytic asymmetric total syntheses of myrtucommuacetalone, myrtucommuacetalone B, and callistrilones A, C, D and E.
Chemical science, 2018, 9, 1488-1495
1548240 CIFC34 H46 O7P 21 21 2112.4836; 12.5791; 20.1204
90; 90; 90
3159.56Cheng, Min-Jing; Cao, Jia-Qing; Yang, Xin-Yi; Zhong, Li-Ping; Hu, Li-Jun; Lu, Xi; Hou, Bao-Long; Hu, Ya-Jian; Wang, Ying; You, Xue-Fu; Wang, Lei; Ye, Wen-Cai; Li, Chuang-Chuang
Catalytic asymmetric total syntheses of myrtucommuacetalone, myrtucommuacetalone B, and callistrilones A, C, D and E.
Chemical science, 2018, 9, 1488-1495
1548241 CIFC16 H23 N2 O2P 21 21 216.8237; 9.6779; 23.209
90; 90; 90
1532.7Kim, Yechan; Kim, Seoung-Tae; Kang, Dahye; Sohn, Te-Ik; Jang, Eunyoung; Baik, Mu-Hyun; Hong, Sungwoo
Stereoselective construction of sterically hindered oxaspirocycles <i>via</i> chiral bidentate directing group-mediated C(sp<sup>3</sup>)-O bond formation.
Chemical science, 2018, 9, 1473-1480
1548292 CIFC164.05 H143.07 Cu2 F36 N29.98 O2.48 P6 Ru2P -112.383; 18.49; 19.983
69.381; 79.742; 88.826
4209Hayes, Dugan; Kohler, Lars; Hadt, Ryan G.; Zhang, Xiaoyi; Liu, Cunming; Mulfort, Karen L.; Chen, Lin X.
Excited state electron and energy relays in supramolecular dinuclear complexes revealed by ultrafast optical and X-ray transient absorption spectroscopy.
Chemical science, 2018, 9, 860-875
1548293 CIFC53 H45 B3 F20 N4 O2P 1 21/c 18.281; 27.653; 23.173
90; 91.817; 90
5304Zheng, Junhao; Li, Zhen Hua; Wang, Huadong
Addition of dihydrogen to a borylborenium center.
Chemical science, 2018, 9, 1433-1438
1548345 CIFC39 H38 N2 O3 SP 1 21/c 116.5942; 8.7199; 21.4742
90; 93.516; 90
3101.5Yamamoto, Y.; Murayama, T.; Jiang, J.; Yasui, T.; Shibuya, M.
The vinylogous Catellani reaction: a combined computational and experimental study.
Chemical science, 2018, 9, 1191-1199
1548346 CIFC204 H158 B8 F32 N40 O7 Zn4C 1 2/c 147.6161; 31.7486; 56.289
90; 111.305; 90
79279Yang, Linlin; Jing, Xu; An, Bowen; He, Cheng; Yang, Yang; Duan, Chunying
Binding of anions in triply interlocked coordination catenanes and dynamic allostery for dehalogenation reactions.
Chemical science, 2018, 9, 1050-1057
1548347 CIFC206 H163 B3.5 F14 I4.5 N41 O8 Zn4C 1 2/c 147.061; 32.0425; 55.568
90; 110.406; 90
78535Yang, Linlin; Jing, Xu; An, Bowen; He, Cheng; Yang, Yang; Duan, Chunying
Binding of anions in triply interlocked coordination catenanes and dynamic allostery for dehalogenation reactions.
Chemical science, 2018, 9, 1050-1057
1548380 CIFC58 H48 Ag5 F6 N17 O6 S2C m c m12.842; 21.083; 25.145
90; 90; 90
6808He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang
Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization.
Chemical science, 2018, 9, 1481-1487
1548381 CIFC59 H55 Ag5 F6 N17 O6 S2P -114.3867; 15.4794; 18.9913
101.197; 93.2; 94.368
4125.97He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang
Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization.
Chemical science, 2018, 9, 1481-1487
1548382 CIFC64 H58 Ag4 F9 N17 O10 S2C 1 2/c 132.1129; 12.1233; 24.0913
90; 130.309; 90
7152.2He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang
Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization.
Chemical science, 2018, 9, 1481-1487
1548383 CIFC73.5 H68 Ag5 F9 N18 O12.5 S3P -114.8347; 15.7643; 18.6915
96.459; 93.928; 95.369
4310.55He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang
Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization.
Chemical science, 2018, 9, 1481-1487
1548384 CIFC63 H55 Ag5 Cl4.5 F12 N17 O13.25 S4P -113.189; 13.561; 28.427
103.51; 90.23; 118.57
4302He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang
Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization.
Chemical science, 2018, 9, 1481-1487
1548385 CIFC67 H57 Ag5 F9 N17 O9 S3P 1 21/c 114.3943; 31.0527; 22.6971
90; 125.685; 90
8240.3He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang
Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization.
Chemical science, 2018, 9, 1481-1487
1548386 CIFC58 H53 Ag5 F6 N17 O6 S2P 112.278; 25.145; 12.408
90; 117.31; 90
3403.7He, Xin; Xue, Yang; Li, Cui-Cui; Wang, Yuechao; Jiang, Hong; Zhao, Liang
Synthesis of stable polymetalated aromatic complexes through metal-macrocycle capsule-triggered cyclization.
Chemical science, 2018, 9, 1481-1487
1548387 CIFC92 H118 As4 Co3 N16 O24P 4 21 220.6668; 20.6668; 16.8568
90; 90; 90
7199.8Srinivasan, Anandi; Cortijo, Miguel; Bulicanu, Vladimir; Naim, Ahmad; Clérac, Rodolphe; Sainctavit, Philippe; Rogalev, Andrei; Wilhelm, Fabrice; Rosa, Patrick; Hillard, Elizabeth A.
Enantiomeric resolution and X-ray optical activity of a tricobalt extended metal atom chain.
Chemical science, 2018, 9, 1136-1143
1548388 CIFC56 H48 As2 Co3 N16 O12C 1 2/c 117.794; 19.121; 19.042
90; 116.941; 90
5776Srinivasan, Anandi; Cortijo, Miguel; Bulicanu, Vladimir; Naim, Ahmad; Clérac, Rodolphe; Sainctavit, Philippe; Rogalev, Andrei; Wilhelm, Fabrice; Rosa, Patrick; Hillard, Elizabeth A.
Enantiomeric resolution and X-ray optical activity of a tricobalt extended metal atom chain.
Chemical science, 2018, 9, 1136-1143
1548389 CIFC50 H51 Co3 F12 N15 O P2P 1 21 111.7226; 21.8073; 12.0149
90; 112.115; 90
2845.5Srinivasan, Anandi; Cortijo, Miguel; Bulicanu, Vladimir; Naim, Ahmad; Clérac, Rodolphe; Sainctavit, Philippe; Rogalev, Andrei; Wilhelm, Fabrice; Rosa, Patrick; Hillard, Elizabeth A.
Enantiomeric resolution and X-ray optical activity of a tricobalt extended metal atom chain.
Chemical science, 2018, 9, 1136-1143
1548390 CIFC92 H118 As4 Co3 N16 O24P 4 21 220.6481; 20.6481; 16.8896
90; 90; 90
7200.8Srinivasan, Anandi; Cortijo, Miguel; Bulicanu, Vladimir; Naim, Ahmad; Clérac, Rodolphe; Sainctavit, Philippe; Rogalev, Andrei; Wilhelm, Fabrice; Rosa, Patrick; Hillard, Elizabeth A.
Enantiomeric resolution and X-ray optical activity of a tricobalt extended metal atom chain.
Chemical science, 2018, 9, 1136-1143
1548396 CIFC28 H30 N4 Ni2 O15 SI a -339.7584; 39.7584; 39.7584
90; 90; 90
62847.3Feng, Rui; Jia, Yan-Yuan; Li, Zhao-Yang; Chang, Ze; Bu, Xian-He
Enhancing the stability and porosity of penetrated metal-organic frameworks through the insertion of coordination sites.
Chemical science, 2018, 9, 950-955
1548397 CIFC36 H20 Co2 N6 O15F d -3 m :246.6983; 46.6983; 46.6983
90; 90; 90
101836Feng, Rui; Jia, Yan-Yuan; Li, Zhao-Yang; Chang, Ze; Bu, Xian-He
Enhancing the stability and porosity of penetrated metal-organic frameworks through the insertion of coordination sites.
Chemical science, 2018, 9, 950-955
1548407 CIFC44 H44 B4 Cl6 Dy2 N24 O4P 1 21/n 113.932; 15.014; 14.827
90; 107.69; 90
2954.8Zhang, Peng; Perfetti, Mauro; Kern, Michal; Hallmen, Philipp P.; Ungur, Liviu; Lenz, Samuel; Ringenberg, Mark R.; Frey, Wolfgang; Stoll, Hermann; Rauhut, Guntram; van Slageren, Joris
Exchange coupling and single molecule magnetism in redox-active tetraoxolene-bridged dilanthanide complexes.
Chemical science, 2018, 9, 1221-1230
1548408 CIFC44 H44 B4 Cl6 N24 O4 Y2P 1 21/n 113.937; 15.046; 14.786
90; 107.46; 90
2957.7Zhang, Peng; Perfetti, Mauro; Kern, Michal; Hallmen, Philipp P.; Ungur, Liviu; Lenz, Samuel; Ringenberg, Mark R.; Frey, Wolfgang; Stoll, Hermann; Rauhut, Guntram; van Slageren, Joris
Exchange coupling and single molecule magnetism in redox-active tetraoxolene-bridged dilanthanide complexes.
Chemical science, 2018, 9, 1221-1230
1548409 CIFC44 H44 B4 Cl6 Gd2 N24 O4P 1 21/n 114.15; 15.225; 14.969
90; 107.75; 90
3071.3Zhang, Peng; Perfetti, Mauro; Kern, Michal; Hallmen, Philipp P.; Ungur, Liviu; Lenz, Samuel; Ringenberg, Mark R.; Frey, Wolfgang; Stoll, Hermann; Rauhut, Guntram; van Slageren, Joris
Exchange coupling and single molecule magnetism in redox-active tetraoxolene-bridged dilanthanide complexes.
Chemical science, 2018, 9, 1221-1230
1548410 CIFC44 H44 B4 Cl6 N24 O4 Tb2P 1 21/n 114.003; 15.079; 14.825
90; 107.59; 90
2984Zhang, Peng; Perfetti, Mauro; Kern, Michal; Hallmen, Philipp P.; Ungur, Liviu; Lenz, Samuel; Ringenberg, Mark R.; Frey, Wolfgang; Stoll, Hermann; Rauhut, Guntram; van Slageren, Joris
Exchange coupling and single molecule magnetism in redox-active tetraoxolene-bridged dilanthanide complexes.
Chemical science, 2018, 9, 1221-1230
1548427 CIFC38 H48 B2 N2 O2P 1 21/a 117.6; 19.466; 20.232
90; 96.305; 90
6889.6Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548428 CIFC48 H56 B2 F3 N3 O2P 1 21/c 111.335; 10.991; 35.202
90; 95.263; 90
4367Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548429 CIFC29 H39 B2 N O2P 1 21/n 18.723; 23.773; 13.264
90; 99.499; 90
2712.9Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548430 CIFC28 H38 B2 N2 O2P 1 21/n 110.134; 18.98; 13.58
90; 96.976; 90
2592.7Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548431 CIFC40 H50 B2 N2 O4P -18.4242; 15.698; 28.081
89.956; 87.717; 89.896
3710.6Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548432 CIFC49 H59 B2 N3 O4P -110.951; 14.21; 16.118
104.201; 92.6541; 111.94
2228.7Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548433 CIFC54 H69 B2 N3 O2P 1 21/c 110.6242; 20.635; 22.708
90; 100.578; 90
4893.7Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548434 CIFC37 H47 B2 N3 O2P 1 21/n 110.981; 10.43; 28.55
90; 94.578; 90
3259.5Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548435 CIFC37 H47 B2 N3 O2P 1 21/a 115.319; 13.7912; 17.481
90; 112.051; 90
3423Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548436 CIFC38 H48 B2 N2 O2P 1 21/n 18.565; 33.036; 11.991
90; 90.444; 90
3393Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548437 CIFC48 H56 B2 F3 N3 O2P 1 21/n 114.692; 11.21; 27.115
90; 105.567; 90
4302Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548438 CIFC45 H62 B2 N2 O4P -111.4491; 12.8149; 15.929
74.652; 86.76; 65.452
2046.2Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548439 CIFC49 H59 B2 N3 O4P -18.034; 10.856; 26.173
97.069; 97.132; 102.212
2187.4Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548440 CIFC53 H63 B2 N3 O2P -111.821; 12.93; 16.755
101.05; 95.8819; 111.862
2289.8Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548441 CIFC39 H37 B2 F3 N2 O2P 21 21 2116.004; 21.403; 32.93
90; 90; 90
11280Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548442 CIFC39 H47 B2 F3 N2 O2P 1 21/c 114.252; 17.527; 14.877
90; 93.855; 90
3707.8Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548443 CIFC89 H112 B4 N4 O4P -19.894; 12.714; 16.323
101.384; 91.511; 100.757
1973.3Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548444 CIFC38 H47 B2 Cl N2 O2P 1 21/c 110.777; 8.468; 38.298
90; 95.088; 90
3481Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548445 CIFC45 H64 B2 N2 O3P n a 2119.208; 13.253; 16.091
90; 90; 90
4096.2Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto
Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives.
Chemical science, 2018, 9, 1301-1310
1548455 CIFC22 H25 N O4P 21 21 2110.3192; 11.0867; 17.4057
90; 90; 90
1991.31Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain
Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench.
Chemical science, 2018, 9, 1352-1357
1548456 CIFC20 H23 N O2P 21 21 216.1094; 14.2823; 19.8409
90; 90; 90
1731.24Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain
Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench.
Chemical science, 2018, 9, 1352-1357
1548457 CIFC27 H21 N O2P -17.9717; 9.2791; 14.2492
95.3798; 105.336; 98.2795
996.24Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain
Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench.
Chemical science, 2018, 9, 1352-1357
1548458 CIFC23 H27 N O4P 1 21 19.495; 8.8357; 12.0617
90; 90.258; 90
1011.91Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain
Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench.
Chemical science, 2018, 9, 1352-1357
1548459 CIFC106 H66 B4 F40 O2 P2P n a 2123.2043; 30.9754; 14.803
90; 90; 90
10639.8Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs.
Chemical science, 2018, 9, 1544-1550
1548460 CIFC88 H62 B4 F40 O2 P2P -111.163; 16.2067; 24.8378
76.432; 87.505; 76.034
4238.6Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs.
Chemical science, 2018, 9, 1544-1550
1548461 CIFC31 H32 B F10 PP 1 21/n 117.6792; 8.532; 19.5972
90; 99.052; 90
2919.2Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs.
Chemical science, 2018, 9, 1544-1550
1548462 CIFC40 H34 B F10 PP 1 21/n 113.2212; 16.1944; 19.5088
90; 94.223; 90
4165.7Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs.
Chemical science, 2018, 9, 1544-1550
1548463 CIFC34 H38 B F10 PP -113.2091; 14.4202; 17.4143
102.465; 96.491; 91.561
3213.5Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs.
Chemical science, 2018, 9, 1544-1550
1548464 CIFC141 H111 B6 F60 O3 P3P 1 21/n 112.2916; 38.2278; 34.996
90; 90.268; 90
16443.8Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard
Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs.
Chemical science, 2018, 9, 1544-1550
1548465 CIFC144 H72 Mn3 N12 O70 Zr12I m -3 m38.4015; 38.4015; 38.4015
90; 90; 90
56630Gallagher, Audrey T.; Lee, Jung Yoon; Kathiresan, Venkatesan; Anderson, John S.; Hoffman, Brian M.; Harris, T. David
A structurally-characterized peroxomanganese(iv) porphyrin from reversible O<sub>2</sub> binding within a metal-organic framework.
Chemical science, 2018, 9, 1596-1603
1548466 CIFC144 H72 Mn3 N12 O52 Zr12I m -3 m38.672; 38.672; 38.672
90; 90; 90
57835Gallagher, Audrey T.; Lee, Jung Yoon; Kathiresan, Venkatesan; Anderson, John S.; Hoffman, Brian M.; Harris, T. David
A structurally-characterized peroxomanganese(iv) porphyrin from reversible O<sub>2</sub> binding within a metal-organic framework.
Chemical science, 2018, 9, 1596-1603
1548488 CIFC14 H30 Cl4 N4 Ni O4P c a 2112.5175; 13.082; 13.0989
90; 90; 90
2145Craig, Gavin A.; Sarkar, Arup; Woodall, Christopher H.; Hay, Moya A.; Marriott, Katie E. R.; Kamenev, Konstantin V.; Moggach, Stephen A.; Brechin, Euan K.; Parsons, Simon; Rajaraman, Gopalan; Murrie, Mark
Probing the origin of the giant magnetic anisotropy in trigonal bipyramidal Ni(ii) under high pressure.
Chemical science, 2018, 9, 1551-1559
1548489 CIFC14 H30 Cl4 N4 Ni O4P c a 2111.9968; 12.5527; 12.8642
90; 90; 90
1937.2Craig, Gavin A.; Sarkar, Arup; Woodall, Christopher H.; Hay, Moya A.; Marriott, Katie E. R.; Kamenev, Konstantin V.; Moggach, Stephen A.; Brechin, Euan K.; Parsons, Simon; Rajaraman, Gopalan; Murrie, Mark
Probing the origin of the giant magnetic anisotropy in trigonal bipyramidal Ni(ii) under high pressure.
Chemical science, 2018, 9, 1551-1559
1548490 CIFC14 H30 Cl4 N4 Ni O4P c a 2111.9924; 12.5546; 12.8611
90; 90; 90
1936.4Craig, Gavin A.; Sarkar, Arup; Woodall, Christopher H.; Hay, Moya A.; Marriott, Katie E. R.; Kamenev, Konstantin V.; Moggach, Stephen A.; Brechin, Euan K.; Parsons, Simon; Rajaraman, Gopalan; Murrie, Mark
Probing the origin of the giant magnetic anisotropy in trigonal bipyramidal Ni(ii) under high pressure.
Chemical science, 2018, 9, 1551-1559
1548491 CIFC14 H30 Cl4 N4 Ni O4P c a 2112.3181; 12.8429; 13.038
90; 90; 90
2062.61Craig, Gavin A.; Sarkar, Arup; Woodall, Christopher H.; Hay, Moya A.; Marriott, Katie E. R.; Kamenev, Konstantin V.; Moggach, Stephen A.; Brechin, Euan K.; Parsons, Simon; Rajaraman, Gopalan; Murrie, Mark
Probing the origin of the giant magnetic anisotropy in trigonal bipyramidal Ni(ii) under high pressure.
Chemical science, 2018, 9, 1551-1559
1548492 CIFC14 H30 Cl4 N4 Ni O4P c a 2112.2089; 12.7469; 12.9686
90; 90; 90
2018.2Craig, Gavin A.; Sarkar, Arup; Woodall, Christopher H.; Hay, Moya A.; Marriott, Katie E. R.; Kamenev, Konstantin V.; Moggach, Stephen A.; Brechin, Euan K.; Parsons, Simon; Rajaraman, Gopalan; Murrie, Mark
Probing the origin of the giant magnetic anisotropy in trigonal bipyramidal Ni(ii) under high pressure.
Chemical science, 2018, 9, 1551-1559
1548493 CIFC3 H4 Br Cl0 O2 PbP 41 21 29.0035; 9.0035; 14.39
90; 90; 90
1166.5Peng, Chengdong; Zhuang, Zewen; Yang, Huimin; Zhang, Guiyang; Fei, Honghan
Ultrastable, cationic three-dimensional lead bromide frameworks that intrinsically emit broadband white-light.
Chemical science, 2018, 9, 1627-1633
1548494 CIFC4 H4 Br4 O4 Pb3P b c n8.2193; 14.718; 10.7344
90; 90; 90
1298.56Peng, Chengdong; Zhuang, Zewen; Yang, Huimin; Zhang, Guiyang; Fei, Honghan
Ultrastable, cationic three-dimensional lead bromide frameworks that intrinsically emit broadband white-light.
Chemical science, 2018, 9, 1627-1633
1548495 CIFC3 H4 Br O2 PbP 41 21 28.9917; 8.9917; 14.354
90; 90; 90
1160.5Peng, Chengdong; Zhuang, Zewen; Yang, Huimin; Zhang, Guiyang; Fei, Honghan
Ultrastable, cationic three-dimensional lead bromide frameworks that intrinsically emit broadband white-light.
Chemical science, 2018, 9, 1627-1633
1548531 CIFC19 H46 Cl4 Eu N8 O ZnP b c a16.9858; 18.4496; 18.8816
90; 90; 90
5917.1Jenks, Tyler C.; Bailey, Matthew D.; Hovey, Jessica L.; Fernando, Shanilke; Basnayake, Gihan; Cross, Michael E.; Li, Wen; Allen, Matthew J.
First use of a divalent lanthanide for visible-light-promoted photoredox catalysis.
Chemical science, 2018, 9, 1273-1278
1548532 CIFC15 H12 N2C 1 2/c 122.851; 5.7145; 16.97
90; 98.174; 90
2193.5Joost, Maximilian; Transue, Wesley J.; Cummins, Christopher C.
Diazomethane umpolung atop anthracene: an electrophilic methylene transfer reagent.
Chemical science, 2018, 9, 1540-1543
1548533 CIFC27 H41 O2 W0.5P 21 21 215.0937; 17.6924; 9.6626
90; 90; 90
2580.3Joost, Maximilian; Transue, Wesley J.; Cummins, Christopher C.
Diazomethane umpolung atop anthracene: an electrophilic methylene transfer reagent.
Chemical science, 2018, 9, 1540-1543
1548534 CIFC68 H87 O4 P WP -113.4644; 13.7709; 18.7517
106.468; 110.976; 96.554
3021.7Joost, Maximilian; Transue, Wesley J.; Cummins, Christopher C.
Diazomethane umpolung atop anthracene: an electrophilic methylene transfer reagent.
Chemical science, 2018, 9, 1540-1543
1548543 CIFC14 H18 N2 O4P -16.746; 7.246; 7.434
77.801; 83.65; 88.409
353Zeng, Qingying; Mukherjee, Arijit; Müller, Peter; Rogers, Robin D.; Myerson, Allan S.
Exploring the role of ionic liquids to tune the polymorphic outcome of organic compounds.
Chemical science, 2018, 9, 1510-1520
1548565 CIFC37 H51.88 Br4 Co N3 O ZnP 21 21 2112.6608; 17.559; 18.5345
90; 90; 90
4120.4Werth, Jacob; Uyeda, Christopher
Regioselective Simmons-Smith-type cyclopropanations of polyalkenes enabled by transition metal catalysis.
Chemical science, 2018, 9, 1604-1609
1548566 CIFC19 H14 B F6 N OP -19.0343; 10.2063; 11.0348
66.3381; 70.1856; 78.1262
873.89Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548567 CIFC27 H26 B Cl2 N O2P 1 21/n 114.1158; 8.9604; 18.8756
90; 90.0788; 90
2387.44Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548568 CIFC29 H24 B F6 N O2P -110.014; 11.7859; 23.0748
103.818; 98.0649; 96.9376
2584.47Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548569 CIFC18 H6 B3 F9 O3C 1 2/c 112.8358; 12.6583; 12.8851
90; 119.06; 90
1830Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548570 CIFC28 H22 B2 I2 O5P -110.635; 11.4814; 12.2457
83.1389; 87.0947; 64.1817
1336.36Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548571 CIFC29 H28 B Cl2 N O2P -19.2006; 11.4729; 13.1121
101.57; 99.773; 98.085
1314.22Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548572 CIFC26 H18 B F6 N O2P 1 21/n 110.1019; 11.7656; 19.567
90; 103.69; 90
2259.56Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548573 CIFC14.5 H13 B Cl1.5 D0.5 F6 N2 OP 1 c 111.75; 11.0269; 13.1973
90; 97.3307; 90
1695.95Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548574 CIFC25 H15 B3 F9 N O3P -110.372; 11.1795; 12.3123
106.545; 111.492; 96.8493
1232.74Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548575 CIFC18 H6 B3 F9 O3P b c n17.083; 13.093; 7.99
90; 90; 90
1787.1Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548576 CIFC46 H51 B3 N4 O3P 1 21/c 121.212; 11.2705; 18.8494
90; 114.886; 90
4087.9Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548577 CIFC28 H22 B2 Cl2 O5P -110.4296; 11.147; 11.7996
84.748; 87.958; 67.5356
1262.39Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548578 CIFC32 H33 B3 N2 O3P -111.2396; 15.2054; 17.9361
89.7333; 72.0196; 84.3291
2900.27Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548579 CIFC18 H6 B3 F9 O3C 1 2/c 112.8086; 12.6262; 12.8625
90; 119.598; 90
1808.74Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548590 CIFC39 H42 B N OC 1 2/c 138.4003; 9.7146; 18.3058
90; 114.338; 90
6222Shi, Yong-Gang; Wang, Jun-Wei; Li, Haijun; Hu, Guo-Fei; Li, Xue; Mellerup, Soren K.; Wang, Nan; Peng, Tai; Wang, Suning
A simple multi-responsive system based on aldehyde functionalized amino-boranes.
Chemical science, 2018, 9, 1902-1911
1548591 CIFC25 H27 B OP -18.488; 10.8609; 12.4693
97.707; 98.593; 105.796
1075.07Shi, Yong-Gang; Wang, Jun-Wei; Li, Haijun; Hu, Guo-Fei; Li, Xue; Mellerup, Soren K.; Wang, Nan; Peng, Tai; Wang, Suning
A simple multi-responsive system based on aldehyde functionalized amino-boranes.
Chemical science, 2018, 9, 1902-1911
1548592 CIFC27 H32 B N OP 1 21/n 112.3452; 9.0371; 20.4924
90; 91.199; 90
2285.7Shi, Yong-Gang; Wang, Jun-Wei; Li, Haijun; Hu, Guo-Fei; Li, Xue; Mellerup, Soren K.; Wang, Nan; Peng, Tai; Wang, Suning
A simple multi-responsive system based on aldehyde functionalized amino-boranes.
Chemical science, 2018, 9, 1902-1911
1548593 CIFC28 H34 B N OP 1 21/c 110.146; 16.684; 16.55
90; 103.602; 90
2722.9Shi, Yong-Gang; Wang, Jun-Wei; Li, Haijun; Hu, Guo-Fei; Li, Xue; Mellerup, Soren K.; Wang, Nan; Peng, Tai; Wang, Suning
A simple multi-responsive system based on aldehyde functionalized amino-boranes.
Chemical science, 2018, 9, 1902-1911
1548594 CIFC23 H37 B N2 Se2P 1 21/c 117.551; 15.552; 17.729
90; 93.183; 90
4832Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548595 CIFC49 H70 B2 N4 SP 1 21/c 118.966; 13.037; 18.816
90; 97.143; 90
4616.3Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548596 CIFC50 H78 B2 N4 O2 Se3C 1 2/c 116.059; 17.563; 17.928
90; 103.042; 90
4926.1Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548597 CIFC50 H78 B2 N4 O2 S3C 1 2/c 115.945; 17.53; 17.924
90; 102.905; 90
4883.5Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548598 CIFC37 H49 B N2 O Se2P 1 21/n 110.784; 16.852; 19.026
90; 91.03; 90
3457Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548599 CIFC48 H68 B2 N4 S2P -18.8508; 8.8654; 14.6186
75.639; 86.11; 80.401
1095.24Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548600 CIFC42 H62 B2 N4 SeP b c a17.8352; 16.7797; 28.365
90; 90; 90
8488.8Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548601 CIFC54 H86 B2 N4 O3 S4P b c a16.39; 17.61; 38.28
90; 90; 90
11049Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548602 CIFC37 H49 B N2 O S2P 1 21/n 110.672; 16.818; 18.902
90; 91.75; 90
3391Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548603 CIFC24 H34 B N2 SeP -18.8289; 8.8405; 14.667
85.939; 75.916; 79.987
1093Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548613 CIFC17 H14 Br N OP 21 21 216.1624; 7.7041; 30.136
90; 90; 90
1430.7Luo, Hongwen; Yang, Zheng; Lin, Weilong; Zheng, Yangguangyan; Ma, Shengming
A catalytic highly enantioselective allene approach to oxazolines.
Chemical science, 2018, 9, 1964-1969
1548614 CIFC33 H37.5 B I2 N OP 1 21/n 113.751; 16.557; 28.155
90; 93.121; 90
6401Qi, Yanyu; Xu, Wenjun; Kang, Rui; Ding, Nannan; Wang, Yelei; He, Gang; Fang, Yu
Discrimination of saturated alkanes and relevant volatile compounds <i>via</i> the utilization of a conceptual fluorescent sensor array based on organoboron-containing polymers.
Chemical science, 2018, 9, 1892-1901
1548615 CIFC35.5 H61 Li Ni O8.25P -111.4664; 24.2697; 28.3765
67.455; 88.576; 85.754
7273.2Iwasaki, Takanori; Fukuoka, Asuka; Yokoyama, Wataru; Min, Xin; Hisaki, Ichiro; Yang, Tao; Ehara, Masahiro; Kuniyasu, Hitoshi; Kambe, Nobuaki
Nickel-catalyzed coupling reaction of alkyl halides with aryl Grignard reagents in the presence of 1,3-butadiene: mechanistic studies of four-component coupling and competing cross-coupling reactions.
Chemical science, 2018, 9, 2195-2211
1548634 CIFC19 H27 N O SP b c a13.4779; 8.1983; 31.894
90; 90; 90
3524.2Shen, Xianwang; Gong, Honghong; Zhou, Yang; Zhao, Yucheng; Lin, Jun; Chen, Mao
Unsymmetrical difunctionalization of cyclooctadiene under continuous flow conditions: expanding the scope of ring opening metathesis polymerization.
Chemical science, 2018, 9, 1846-1853
1548635 CIFC23 H24 O2P 21 21 219.7798; 10.6568; 17.5257
90; 90; 90
1826.55Zheng, Xinxin; Guo, Rui; Zhang, Guozhu; Zhang, Dayong
Rhodium(i)-catalyzed asymmetric [4 + 2] cycloaddition reactions of 2-alkylenecyclobutanols with cyclic enones through C-C bond cleavage: efficient access to <i>trans</i>-bicyclic compounds.
Chemical science, 2018, 9, 1873-1877
1548636 CIFC8 H14 Ag N O4P 21 21 217.786; 8.024; 16.081
90; 90; 90
1004.7Fang, Yinzhi; Zhang, Han; Huang, Zhen; Scinto, Samuel L.; Yang, Jeffrey C.; Am Ende, Christopher W.; Dmitrenko, Olga; Johnson, Douglas S.; Fox, Joseph M.
Photochemical syntheses, transformations, and bioorthogonal chemistry of <i>trans</i>-cycloheptene and sila <i>trans</i>-cycloheptene Ag(i) complexes.
Chemical science, 2018, 9, 1953-1963
1548637 CIFC18 H20 Ag N O3 SiP 1 21/c 116.509; 8.4282; 13.9655
90; 114.69; 90
1765.53Fang, Yinzhi; Zhang, Han; Huang, Zhen; Scinto, Samuel L.; Yang, Jeffrey C.; Am Ende, Christopher W.; Dmitrenko, Olga; Johnson, Douglas S.; Fox, Joseph M.
Photochemical syntheses, transformations, and bioorthogonal chemistry of <i>trans</i>-cycloheptene and sila <i>trans</i>-cycloheptene Ag(i) complexes.
Chemical science, 2018, 9, 1953-1963
1548638 CIFC30.71 H44.57 Br1.14 Fe N2 O2.86I 1 a 115.186; 13.4178; 17.1643
90; 112.449; 90
3232.4Fleischauer, Valerie E.; Muñoz Iii, Salvador B; Neate, Peter G. N.; Brennessel, William W.; Neidig, Michael L.
NHC and nucleophile chelation effects on reactive iron(ii) species in alkyl-alkyl cross-coupling.
Chemical science, 2018, 9, 1878-1891
1548639 CIFC39 H60 Fe N2 O4P -110.0953; 10.9483; 17.657
88.7501; 75.1691; 88.9205
1885.9Fleischauer, Valerie E.; Muñoz Iii, Salvador B; Neate, Peter G. N.; Brennessel, William W.; Neidig, Michael L.
NHC and nucleophile chelation effects on reactive iron(ii) species in alkyl-alkyl cross-coupling.
Chemical science, 2018, 9, 1878-1891
1548640 CIFC33 H46 Fe N2 O4C 1 c 111.2603; 22.9235; 16.1864
90; 103.878; 90
4056.2Fleischauer, Valerie E.; Muñoz Iii, Salvador B; Neate, Peter G. N.; Brennessel, William W.; Neidig, Michael L.
NHC and nucleophile chelation effects on reactive iron(ii) species in alkyl-alkyl cross-coupling.
Chemical science, 2018, 9, 1878-1891
1548651 CIFC250.5 H168.5 B5 Co6 F41 N47 O21.25 S7P -121.2508; 21.6182; 39.5929
93.208; 101.624; 118.521
15407.3Rizzuto, Felix J.; Kieffer, Marion; Nitschke, Jonathan R.
Quantified structural speciation in self-sorted CoII6L<sub>4</sub> cage systems.
Chemical science, 2018, 9, 1925-1930
1548652 CIFC273 H263.5 B60.5 Co6 F19.5 N62.5 O20.5 S6.5P -125.0303; 26.7592; 34.5514
68.113; 88.8092; 66.5154
19472.1Rizzuto, Felix J.; Kieffer, Marion; Nitschke, Jonathan R.
Quantified structural speciation in self-sorted CoII6L<sub>4</sub> cage systems.
Chemical science, 2018, 9, 1925-1930
1548653 CIFC92 H130 Cl2 N4 Ni2 O5P 1 21/n 115.5829; 39.582; 16.2027
90; 110.448; 90
9364.1Clarke, Ryan M.; Jeen, Tiffany; Rigo, Serena; Thompson, John R.; Kaake, Loren G.; Thomas, Fabrice; Storr, Tim
Exploiting exciton coupling of ligand radical intervalence charge transfer transitions to tune NIR absorption.
Chemical science, 2018, 9, 1610-1620
1548654 CIFC72 H96 N6 Ni2 O4P -111.4567; 13.1358; 25.5529
82.482; 89.48; 67.19
3510.7Clarke, Ryan M.; Jeen, Tiffany; Rigo, Serena; Thompson, John R.; Kaake, Loren G.; Thomas, Fabrice; Storr, Tim
Exploiting exciton coupling of ligand radical intervalence charge transfer transitions to tune NIR absorption.
Chemical science, 2018, 9, 1610-1620
1548655 CIFC89 H139 N4 Ni2 O4P b c a29.9305; 12.1234; 47.9429
90; 90; 90
17396.5Clarke, Ryan M.; Jeen, Tiffany; Rigo, Serena; Thompson, John R.; Kaake, Loren G.; Thomas, Fabrice; Storr, Tim
Exploiting exciton coupling of ligand radical intervalence charge transfer transitions to tune NIR absorption.
Chemical science, 2018, 9, 1610-1620
1548656 CIFC192 H133 Ca2 O29 P4P 21 21 2113.7157; 21.388; 65.483
90; 90; 90
19209.5Uno, Brice E.; Dicken, Rachel D.; Redfern, Louis R.; Stern, Charlotte M.; Krzywicki, Greg G.; Scheidt, Karl A.
Calcium(ii)-catalyzed enantioselective conjugate additions of amines.
Chemical science, 2018, 9, 1634-1639
1548657 CIFC18 H17 Br N2 O2P 14.681; 6.1091; 14.2048
100.603; 92.652; 94.55
397.25Uno, Brice E.; Dicken, Rachel D.; Redfern, Louis R.; Stern, Charlotte M.; Krzywicki, Greg G.; Scheidt, Karl A.
Calcium(ii)-catalyzed enantioselective conjugate additions of amines.
Chemical science, 2018, 9, 1634-1639
1548659 CIFC78 H78 B2 Fe2 N8 O2 P2 Zn2P 1 2/c 113.855; 9.378; 30.742
90; 101.648; 90
3912.1Abubekerov, Mark; Wei, Junnian; Swartz, Kevin R.; Xie, Zhixin; Pei, Qibing; Diaconescu, Paula L.
Preparation of multiblock copolymers <i>via</i> step-wise addition of l-lactide and trimethylene carbonate.
Chemical science, 2018, 9, 2168-2178
1548660 CIFC27 H35 B9 Hf2P 1 21/c 117.2181; 12.9003; 14.6113
90; 110.082; 90
3048.1De, Anangsha; Zhang, Qian-Fan; Mondal, Bijan; Cheung, Ling Fung; Kar, Sourav; Saha, Koushik; Varghese, Babu; Wang, Lai-Sheng; Ghosh, Sundargopal
[(Cp<sub>2</sub>M)<sub>2</sub>B<sub>9</sub>H<sub>11</sub>] (M = Zr or Hf): early transition metal 'guarded' heptaborane with strong covalent and electrostatic bonding.
Chemical science, 2018, 9, 1976-1981
1548661 CIFC27 H39 B9 Zr2P 1 21/c 117.2544; 12.8796; 14.6295
90; 109.855; 90
3057.85De, Anangsha; Zhang, Qian-Fan; Mondal, Bijan; Cheung, Ling Fung; Kar, Sourav; Saha, Koushik; Varghese, Babu; Wang, Lai-Sheng; Ghosh, Sundargopal
[(Cp<sub>2</sub>M)<sub>2</sub>B<sub>9</sub>H<sub>11</sub>] (M = Zr or Hf): early transition metal 'guarded' heptaborane with strong covalent and electrostatic bonding.
Chemical science, 2018, 9, 1976-1981
1548662 CIFC20 H24 B5 Hf2P 1 c 19.3061; 7.8838; 14.9171
90; 100.72; 90
1075.33De, Anangsha; Zhang, Qian-Fan; Mondal, Bijan; Cheung, Ling Fung; Kar, Sourav; Saha, Koushik; Varghese, Babu; Wang, Lai-Sheng; Ghosh, Sundargopal
[(Cp<sub>2</sub>M)<sub>2</sub>B<sub>9</sub>H<sub>11</sub>] (M = Zr or Hf): early transition metal 'guarded' heptaborane with strong covalent and electrostatic bonding.
Chemical science, 2018, 9, 1976-1981
1548696 CIFC12 H20 B10P 1 21/n 110.039; 14.627; 11.432
90; 96.919; 90
1666.5Chan, Tek Long; Xie, Zuowei
Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles.
Chemical science, 2018, 9, 2284-2289
1548697 CIFC5 H14 B10 SP 1 21/n 111.7439; 8.5035; 12.5486
90; 108.228; 90
1190.27Chan, Tek Long; Xie, Zuowei
Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles.
Chemical science, 2018, 9, 2284-2289
1548698 CIFC5 H16 B10 O2P 21 21 216.955; 10.8072; 16.754
90; 90; 90
1259.3Chan, Tek Long; Xie, Zuowei
Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles.
Chemical science, 2018, 9, 2284-2289
1548699 CIFC6 H17 B10 NP 1 21/n 111.9424; 8.5259; 13.3359
90; 108.729; 90
1286Chan, Tek Long; Xie, Zuowei
Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles.
Chemical science, 2018, 9, 2284-2289
1548700 CIFC14 H19 B10 NP -18.9977; 9.8055; 11.2475
87.61; 66.4692; 73.9029
871.46Chan, Tek Long; Xie, Zuowei
Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles.
Chemical science, 2018, 9, 2284-2289
1548701 CIFC36 H67 B10 Li O10P -111.9668; 12.4954; 14.9348
87.27; 75.356; 88.638
2158Chan, Tek Long; Xie, Zuowei
Synthesis, structure and aromaticity of carborane-fused carbo- and heterocycles.
Chemical science, 2018, 9, 2284-2289
1548702 CIFC29 H25 N O3 SP 1 21 19.769; 13.123; 10.039
90; 114.345; 90
1172.5Zhou, Leijie; Yuan, Chunhao; Zeng, Yuan; Liu, Honglei; Wang, Chang; Gao, Xing; Wang, Qijun; Zhang, Cheng; Guo, Hongchao
Phosphine-catalyzed [5+1] annulation of δ-sulfonamido-substituted enones with <i>N</i>-sulfonylimines: a facile synthesis of tetrahydropyridines.
Chemical science, 2018, 9, 1831-1835
1548722 CIFC12 H15 O PP 21 21 218.6681; 10.3977; 11.4123
90; 90; 90
1028.57Zhang, Kui; Cai, Lingchao; Yang, Zhongyue; Houk, K. N.; Kwon, Ohyun
Bridged [2.2.1] bicyclic phosphine oxide facilitates catalytic γ-umpolung addition-Wittig olefination.
Chemical science, 2018, 9, 1867-1872
1548738 CIFCl Co H15 N7 O5P n m a14.6048; 7.4486; 9.5237
90; 90; 90
1036.04Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548739 CIFCl Co H15 N7 O5P n m a14.7295; 7.3639; 9.5828
90; 90; 90
1039.41Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548740 CIFCl Co H15 N7 O5P n m a14.7688; 7.3395; 9.5973
90; 90; 90
1040.31Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548741 CIFCl Co H15 N7 O5P n m a14.5868; 7.4684; 9.513
90; 90; 90
1036.35Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548742 CIFCl Co H15 N7 O5P n m a14.471; 7.5428; 9.4556
90; 90; 90
1032.1Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548743 CIFCl Co H15 N7 O5P n m a14.7589; 7.348; 9.5909
90; 90; 90
1040.12Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548744 CIFCl Co H15 N7 O5P n m a14.5467; 7.4933; 9.4931
90; 90; 90
1034.77Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548745 CIFCl Co H15 N7 O5P n m a14.6615; 7.4138; 9.5536
90; 90; 90
1038.45Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548746 CIFCl Co H15 N7 O5P n m a14.7005; 7.3877; 9.5676
90; 90; 90
1039.07Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548747 CIFCl Co H15 N7 O5P n m a14.6166; 7.4465; 9.5286
90; 90; 90
1037.12Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548748 CIFCl Co H15 N7 O5P n m a14.4836; 7.5409; 9.4574
90; 90; 90
1032.93Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548749 CIFCl Co H15 N7 O5P n m a14.8308; 7.2957; 9.6188
90; 90; 90
1040.76Chizhik, Stanislav; Sidelnikov, Anatoly; Zakharov, Boris; Naumov, Panče; Boldyreva, Elena
Quantification of photoinduced bending of dynamic molecular crystals: from macroscopic strain to kinetic constants and activation energies.
Chemical science, 2018, 9, 2319-2335
1548752 CIFC34 H33 F4 Mg N3P c a 2124.8934; 13.45834; 18.5282
90; 90; 90
6207.39Bakewell, Clare; Ward, Bryan J.; White, Andrew J. P.; Crimmin, Mark R.
A combined experimental and computational study on the reaction of fluoroarenes with Mg-Mg, Mg-Zn, Mg-Al and Al-Zn bonds.
Chemical science, 2018, 9, 2348-2356
1548753 CIFC58.5 H81 Mg N4 ZnP -111.7887; 12.0703; 21.6822
80.152; 74.593; 66.945
2729Bakewell, Clare; Ward, Bryan J.; White, Andrew J. P.; Crimmin, Mark R.
A combined experimental and computational study on the reaction of fluoroarenes with Mg-Mg, Mg-Zn, Mg-Al and Al-Zn bonds.
Chemical science, 2018, 9, 2348-2356
1548754 CIFC81 H115 F3 Mg3 N6P -114.5708; 14.6964; 18.2421
91.379; 93.348; 91.651
3896.7Bakewell, Clare; Ward, Bryan J.; White, Andrew J. P.; Crimmin, Mark R.
A combined experimental and computational study on the reaction of fluoroarenes with Mg-Mg, Mg-Zn, Mg-Al and Al-Zn bonds.
Chemical science, 2018, 9, 2348-2356
1548755 CIFC35.5 H36.5 F4 Mg N3P -111.8799; 16.0457; 17.2413
83.738; 85.661; 88.935
3257.4Bakewell, Clare; Ward, Bryan J.; White, Andrew J. P.; Crimmin, Mark R.
A combined experimental and computational study on the reaction of fluoroarenes with Mg-Mg, Mg-Zn, Mg-Al and Al-Zn bonds.
Chemical science, 2018, 9, 2348-2356
1548756 CIFC59 H84 Mg N6 ZnC 1 2/c 110.18598; 24.1833; 23.1663
90; 99.0832; 90
5635.01Bakewell, Clare; Ward, Bryan J.; White, Andrew J. P.; Crimmin, Mark R.
A combined experimental and computational study on the reaction of fluoroarenes with Mg-Mg, Mg-Zn, Mg-Al and Al-Zn bonds.
Chemical science, 2018, 9, 2348-2356
1548757 CIFC46 H58 Mg N4 ZnP 1 2/n 113.4443; 8.2978; 19.6313
90; 102.544; 90
2137.75Bakewell, Clare; Ward, Bryan J.; White, Andrew J. P.; Crimmin, Mark R.
A combined experimental and computational study on the reaction of fluoroarenes with Mg-Mg, Mg-Zn, Mg-Al and Al-Zn bonds.
Chemical science, 2018, 9, 2348-2356
1548758 CIFC46.5 H56 F4 N3 ZnI 1 2/a 115.6052; 24.2499; 23.5838
90; 102.23; 90
8722.1Bakewell, Clare; Ward, Bryan J.; White, Andrew J. P.; Crimmin, Mark R.
A combined experimental and computational study on the reaction of fluoroarenes with Mg-Mg, Mg-Zn, Mg-Al and Al-Zn bonds.
Chemical science, 2018, 9, 2348-2356
1548759 CIFC56 H78 Mg N4 O ZnP 1 21/n 112.3877; 22.4084; 19.0461
90; 90.149; 90
5287Bakewell, Clare; Ward, Bryan J.; White, Andrew J. P.; Crimmin, Mark R.
A combined experimental and computational study on the reaction of fluoroarenes with Mg-Mg, Mg-Zn, Mg-Al and Al-Zn bonds.
Chemical science, 2018, 9, 2348-2356
1548760 CIFC65 H99 Al Mg N4I 1 2/a 121.9257; 15.7003; 37.0659
90; 97.8995; 90
12638.5Bakewell, Clare; Ward, Bryan J.; White, Andrew J. P.; Crimmin, Mark R.
A combined experimental and computational study on the reaction of fluoroarenes with Mg-Mg, Mg-Zn, Mg-Al and Al-Zn bonds.
Chemical science, 2018, 9, 2348-2356
1548761 CIFC58 H82 N4 Zn3P 1 21/n 112.7429; 17.3446; 13.026
90; 101.313; 90
2823.07Bakewell, Clare; Ward, Bryan J.; White, Andrew J. P.; Crimmin, Mark R.
A combined experimental and computational study on the reaction of fluoroarenes with Mg-Mg, Mg-Zn, Mg-Al and Al-Zn bonds.
Chemical science, 2018, 9, 2348-2356
1548762 CIFC54 H75 Al N4 ZnP 21 21 2113.75991; 13.8927; 26.733
90; 90; 90
5110.34Bakewell, Clare; Ward, Bryan J.; White, Andrew J. P.; Crimmin, Mark R.
A combined experimental and computational study on the reaction of fluoroarenes with Mg-Mg, Mg-Zn, Mg-Al and Al-Zn bonds.
Chemical science, 2018, 9, 2348-2356
1548769 CIFC17 H19 Cl O4P 21 21 216.9832; 8.5007; 26.483
90; 90; 90
1572.1Ngamnithiporn, Aurapat; Jette, Carina I.; Bachman, Shoshana; Virgil, Scott C.; Stoltz, Brian M.
Nickel-catalyzed enantioselective allylic alkylation of lactones and lactams with unactivated allylic alcohols.
Chemical science, 2018, 9, 2547-2551
1548770 CIFC17 H6 Cl7 N2P 1 21/n 18.7015; 14.84; 14.86
90; 105.517; 90
1848.9Kimura, Shun; Tanushi, Akira; Kusamoto, Tetsuro; Kochi, Shuntaro; Sato, Tohru; Nishihara, Hiroshi
A luminescent organic radical with two pyridyl groups: high photostability and dual stimuli-responsive properties, with theoretical analyses of photophysical processes.
Chemical science, 2018, 9, 1996-2007
1548829 CIFC260 H338 Au42 S26P -124.328; 24.845; 32.217
67.732; 76.94; 84.496
17553Zhuang, Shengli; Liao, Lingwen; Zhao, Yan; Yuan, Jinyun; Yao, Chuanhao; Liu, Xu; Li, Jin; Deng, Haiteng; Yang, Jinlong; Wu, Zhikun
Is the kernel-staples match a key-lock match?
Chemical science, 2018, 9, 2437-2442
1548838 CIFC18 H26 N4 O6 SP 17.4225; 16.5812; 21.1102
82.789; 85.375; 84.403
2559.1Lee, Jisun; Joullié, Madeleine M
Total synthesis of the reported structure of ceanothine D <i>via</i> a novel macrocyclization strategy.
Chemical science, 2018, 9, 2432-2436
1548839 CIFC21 H23 Ni0.5 O4P 1 21/n 19.6006; 15.4568; 11.7534
90; 93.542; 90
1740.8Vijaykumar, Gonela; Pariyar, Anand; Ahmed, Jasimuddin; Shaw, Bikash Kumar; Adhikari, Debashis; Mandal, Swadhin K.
Tuning the redox non-innocence of a phenalenyl ligand toward efficient nickel-assisted catalytic hydrosilylation.
Chemical science, 2018, 9, 2817-2825
1548853 CIFC23 H26 N2 O2 S2P -17.4148; 10.3516; 14.6348
82.054; 79.877; 73.007
1053.02Suzuki, Naoya; Suda, Kayo; Yokogawa, Daisuke; Kitoh-Nishioka, Hirotaka; Irle, Stephan; Ando, Akihiro; Abegão, Luis M G; Kamada, Kenji; Fukazawa, Aiko; Yamaguchi, Shigehiro
Near infrared two-photon-excited and -emissive dyes based on a strapped excited-state intramolecular proton-transfer (ESIPT) scaffold.
Chemical science, 2018, 9, 2666-2673
1548854 CIFC25 H30 N2 O2 S2P 1 21/a 110.7685; 14.2394; 16.386
90; 108.759; 90
2379.1Suzuki, Naoya; Suda, Kayo; Yokogawa, Daisuke; Kitoh-Nishioka, Hirotaka; Irle, Stephan; Ando, Akihiro; Abegão, Luis M G; Kamada, Kenji; Fukazawa, Aiko; Yamaguchi, Shigehiro
Near infrared two-photon-excited and -emissive dyes based on a strapped excited-state intramolecular proton-transfer (ESIPT) scaffold.
Chemical science, 2018, 9, 2666-2673
1548856 CIFC44 H36 N2P 1 21/c 18.6947; 17.563; 10.737
90; 97.361; 90
1626.1Sun, Xianglang; Xue, Qifan; Zhu, Zonglong; Xiao, Qi; Jiang, Kui; Yip, Hin-Lap; Yan, He; Li, Zhong'an
Fluoranthene-based dopant-free hole transporting materials for efficient perovskite solar cells.
Chemical science, 2018, 9, 2698-2704
1548857 CIFC46 H34 N4 O4P 1 21/c 114.1565; 17.917; 14.4208
90; 99.826; 90
3604.1Sun, Xianglang; Xue, Qifan; Zhu, Zonglong; Xiao, Qi; Jiang, Kui; Yip, Hin-Lap; Yan, He; Li, Zhong'an
Fluoranthene-based dopant-free hole transporting materials for efficient perovskite solar cells.
Chemical science, 2018, 9, 2698-2704
1548858 CIFC46 H34 N4P -111.856; 12.147; 13.446
102.687; 111.422; 93.005
1739.8Sun, Xianglang; Xue, Qifan; Zhu, Zonglong; Xiao, Qi; Jiang, Kui; Yip, Hin-Lap; Yan, He; Li, Zhong'an
Fluoranthene-based dopant-free hole transporting materials for efficient perovskite solar cells.
Chemical science, 2018, 9, 2698-2704
1548860 CIFC42 H36.34 N O2.17 PP 21 21 2113.9558; 15.4622; 30.6296
90; 90; 90
6609.5Ardkhean, Ruchuta; Mortimore, Mike; Paton, Robert S.; Fletcher, Stephen P.
Formation of quaternary centres by copper catalysed asymmetric conjugate addition to β-substituted cyclopentenones with the aid of a quantitative structure-selectivity relationship.
Chemical science, 2018, 9, 2628-2632
1548861 CIFC22 H20 Cl F6 NP 1 21 111.4023; 8.446; 12.168
90; 117.387; 90
1040.49Ardkhean, Ruchuta; Mortimore, Mike; Paton, Robert S.; Fletcher, Stephen P.
Formation of quaternary centres by copper catalysed asymmetric conjugate addition to β-substituted cyclopentenones with the aid of a quantitative structure-selectivity relationship.
Chemical science, 2018, 9, 2628-2632
1548862 CIFC24 H30 Cl NP 21 21 218.332; 11.3877; 22.1875
90; 90; 90
2105.2Ardkhean, Ruchuta; Mortimore, Mike; Paton, Robert S.; Fletcher, Stephen P.
Formation of quaternary centres by copper catalysed asymmetric conjugate addition to β-substituted cyclopentenones with the aid of a quantitative structure-selectivity relationship.
Chemical science, 2018, 9, 2628-2632
1548863 CIFC46.5 H39 Cl N O2 PP 1 21 113.9275; 18.6673; 15.2746
90; 110.757; 90
3713.47Ardkhean, Ruchuta; Mortimore, Mike; Paton, Robert S.; Fletcher, Stephen P.
Formation of quaternary centres by copper catalysed asymmetric conjugate addition to β-substituted cyclopentenones with the aid of a quantitative structure-selectivity relationship.
Chemical science, 2018, 9, 2628-2632
1548864 CIFC42.45 H36.9 Cl0.9 N O2 PP 21 21 224.2085; 16.0031; 8.8283
90; 90; 90
3420.18Ardkhean, Ruchuta; Mortimore, Mike; Paton, Robert S.; Fletcher, Stephen P.
Formation of quaternary centres by copper catalysed asymmetric conjugate addition to β-substituted cyclopentenones with the aid of a quantitative structure-selectivity relationship.
Chemical science, 2018, 9, 2628-2632
1548865 CIFC50 H82 B Cl N6 Ni O2 Si2C 1 2/c 127.8322; 21.4898; 26.4066
90; 116.468; 90
14138.5Hadlington, T. J.; Szilvási, T; Driess, M.
Striking transformations of the hydroborylene ligand in a HB:\ρightarrow Ni<sup>II</sup> complex with isocyanides and CO.
Chemical science, 2018, 9, 2595-2600
1548866 CIFC44 H71 B Cl N5 Ni O3 Si2P 1 21/c 110.8782; 25.2119; 17.866
90; 91.948; 90
4897.1Hadlington, T. J.; Szilvási, T; Driess, M.
Striking transformations of the hydroborylene ligand in a HB:\ρightarrow Ni<sup>II</sup> complex with isocyanides and CO.
Chemical science, 2018, 9, 2595-2600
1548867 CIFC38 H63 B Cl N5 O2P -19.8905; 12.6054; 16.945
69.66; 89.159; 78.594
1938.4Hadlington, T. J.; Szilvási, T; Driess, M.
Striking transformations of the hydroborylene ligand in a HB:\ρightarrow Ni<sup>II</sup> complex with isocyanides and CO.
Chemical science, 2018, 9, 2595-2600
1548868 CIFC66 H105 B Cl N6 Ni O6 Si2P -111.0148; 14.6131; 22.793
84.552; 83.601; 70.398
3428.1Hadlington, T. J.; Szilvási, T; Driess, M.
Striking transformations of the hydroborylene ligand in a HB:\ρightarrow Ni<sup>II</sup> complex with isocyanides and CO.
Chemical science, 2018, 9, 2595-2600
1548869 CIFC27 H49 B Cl N5P 1 21/n 113.7173; 15.3059; 15.7157
90; 110.275; 90
3095.16Hadlington, T. J.; Szilvási, T; Driess, M.
Striking transformations of the hydroborylene ligand in a HB:\ρightarrow Ni<sup>II</sup> complex with isocyanides and CO.
Chemical science, 2018, 9, 2595-2600
1548870 CIFC33 H59 B Cl N5 OP b c a15.6878; 12.3457; 36.8495
90; 90; 90
7136.9Hadlington, T. J.; Szilvási, T; Driess, M.
Striking transformations of the hydroborylene ligand in a HB:\ρightarrow Ni<sup>II</sup> complex with isocyanides and CO.
Chemical science, 2018, 9, 2595-2600
1548871 CIFC51 H78 B Cl N6 Ni O2 Si2P 1 21/c 114.0633; 26.4632; 18.1718
90; 100.801; 90
6643Hadlington, T. J.; Szilvási, T; Driess, M.
Striking transformations of the hydroborylene ligand in a HB:\ρightarrow Ni<sup>II</sup> complex with isocyanides and CO.
Chemical science, 2018, 9, 2595-2600
1548872 CIFC15 H12 F6 N O PP 1 21 110.17707; 8.43885; 18.8541
90; 101.724; 90
1585.46Sun, Y.; Cramer, N.
Tailored trisubstituted chiral Cp <sup> <i>x</i> </sup> Rh<sup>III</sup> catalysts for kinetic resolutions of phosphinic amides.
Chemical science, 2018, 9, 2981-2985
1548873 CIFC65 H60 Cl6 O4 Rh2P 21 21 219.524; 17.1108; 36.4272
90; 90; 90
5936.3Sun, Y.; Cramer, N.
Tailored trisubstituted chiral Cp <sup> <i>x</i> </sup> Rh<sup>III</sup> catalysts for kinetic resolutions of phosphinic amides.
Chemical science, 2018, 9, 2981-2985
1548874 CIFC32 H72 B20 Cl2 Cu2 O8 P4 Ru2P 1 21/n 110.4786; 16.101; 16.7081
90; 92.821; 90
2815.5Eleazer, Bennett J.; Smith, Mark D.; Popov, Alexey A.; Peryshkov, Dmitry V.
Expansion of the (BB) 〉metallacycle with coinage metal cations: formation of B-M-Ru-B (M = Cu, Ag, Au) dimetalacyclodiboryls.
Chemical science, 2018, 9, 2601-2608
1548875 CIFC18 H39 Ag B10 N2 O7 P2 RuP 1 n 110.6009; 13.8331; 11.0738
90; 103.867; 90
1576.57Eleazer, Bennett J.; Smith, Mark D.; Popov, Alexey A.; Peryshkov, Dmitry V.
Expansion of the (BB) 〉metallacycle with coinage metal cations: formation of B-M-Ru-B (M = Cu, Ag, Au) dimetalacyclodiboryls.
Chemical science, 2018, 9, 2601-2608
1548876 CIFC32 H72 Au2 B20 Cl2 O8 P4 Ru2P 1 21/c 112.421; 12.596; 19.0782
90; 101.457; 90
2925.4Eleazer, Bennett J.; Smith, Mark D.; Popov, Alexey A.; Peryshkov, Dmitry V.
Expansion of the (BB) 〉metallacycle with coinage metal cations: formation of B-M-Ru-B (M = Cu, Ag, Au) dimetalacyclodiboryls.
Chemical science, 2018, 9, 2601-2608
1548877 CIFC60 H36 Fe N14 S2P -17.945; 8.8188; 17.5482
77.665; 82.466; 81.092
1180.51Wang, Jun-Li; Liu, Qiang; Meng, Yin-Shan; Liu, Xin; Zheng, Hui; Shi, Quan; Duan, Chun-Ying; Liu, Tao
Fluorescence modulation <i>via</i> photoinduced spin crossover switched energy transfer from fluorophores to Fe<sup>II</sup> ions.
Chemical science, 2018, 9, 2892-2897
1548878 CIFC60 H36 Fe N14 S2P -18.002; 9.1057; 17.7358
76.787; 82.257; 80.099
1233.2Wang, Jun-Li; Liu, Qiang; Meng, Yin-Shan; Liu, Xin; Zheng, Hui; Shi, Quan; Duan, Chun-Ying; Liu, Tao
Fluorescence modulation <i>via</i> photoinduced spin crossover switched energy transfer from fluorophores to Fe<sup>II</sup> ions.
Chemical science, 2018, 9, 2892-2897
1548879 CIFC20 H36 B2 Co F8 N6 O2P 1 2/n 18.3869; 7.9947; 19.4819
90; 90.1405; 90
1306.27Khosrowabadi Kotyk, Juliet F.; Hanna, Caitlin M.; Combs, Rebecca L.; Ziller, Joseph W.; Yang, Jenny Y.
Intramolecular hydrogen-bonding in a cobalt aqua complex and electrochemical water oxidation activity.
Chemical science, 2018, 9, 2750-2755
1548880 CIFC22 H37 B2 Co F8 N7 OC 1 2/c 128.1807; 13.2001; 20.3454
90; 129.871; 90
5808.5Khosrowabadi Kotyk, Juliet F.; Hanna, Caitlin M.; Combs, Rebecca L.; Ziller, Joseph W.; Yang, Jenny Y.
Intramolecular hydrogen-bonding in a cobalt aqua complex and electrochemical water oxidation activity.
Chemical science, 2018, 9, 2750-2755
1548881 CIFC20 H28 B2 Co F8 N6P 21 21 219.8793; 14.9748; 17.3244
90; 90; 90
2563Khosrowabadi Kotyk, Juliet F.; Hanna, Caitlin M.; Combs, Rebecca L.; Ziller, Joseph W.; Yang, Jenny Y.
Intramolecular hydrogen-bonding in a cobalt aqua complex and electrochemical water oxidation activity.
Chemical science, 2018, 9, 2750-2755
1548882 CIFC24 H38 B2 Co F8 N8C 1 2/c 130.4582; 20.3058; 17.0511
90; 120.178; 90
9116.5Khosrowabadi Kotyk, Juliet F.; Hanna, Caitlin M.; Combs, Rebecca L.; Ziller, Joseph W.; Yang, Jenny Y.
Intramolecular hydrogen-bonding in a cobalt aqua complex and electrochemical water oxidation activity.
Chemical science, 2018, 9, 2750-2755
1548883 CIFC52 H54 Ba2 F12 Fe2 N6 O24 S4P -110.8491; 11.7518; 14.5176
75.9118; 86.5298; 71.8096
1705.3Chantarojsiri, Teera; Ziller, Joseph W.; Yang, Jenny Y.
Incorporation of redox-inactive cations promotes iron catalyzed aerobic C-H oxidation at mild potentials.
Chemical science, 2018, 9, 2567-2574
1548884 CIFC46 H48 F6 Fe2 K2 N4 O19 S2C 1 2/c 132.941; 8.2524; 21.7664
90; 108.302; 90
5617.7Chantarojsiri, Teera; Ziller, Joseph W.; Yang, Jenny Y.
Incorporation of redox-inactive cations promotes iron catalyzed aerobic C-H oxidation at mild potentials.
Chemical science, 2018, 9, 2567-2574
1548885 CIFC26 H27 Ba Cl F6 Fe N3 O12 S2P -19.7023; 12.7853; 15.6368
106.971; 104.413; 98.178
1747.82Chantarojsiri, Teera; Ziller, Joseph W.; Yang, Jenny Y.
Incorporation of redox-inactive cations promotes iron catalyzed aerobic C-H oxidation at mild potentials.
Chemical science, 2018, 9, 2567-2574
1548886 CIFC23 H24 Cl F3 Fe K N2 O9 SP 1 21/n 111.253; 17.652; 13.5982
90; 90.075; 90
2701.1Chantarojsiri, Teera; Ziller, Joseph W.; Yang, Jenny Y.
Incorporation of redox-inactive cations promotes iron catalyzed aerobic C-H oxidation at mild potentials.
Chemical science, 2018, 9, 2567-2574
1548887 CIFC26 H27 Ba F6 Fe N3 O12.5 S2P b c m9.5075; 27.3543; 28.8412
90; 90; 90
7500.8Chantarojsiri, Teera; Ziller, Joseph W.; Yang, Jenny Y.
Incorporation of redox-inactive cations promotes iron catalyzed aerobic C-H oxidation at mild potentials.
Chemical science, 2018, 9, 2567-2574
1548897 CIFC16 H23 Cl Co F6 N4 O6 S2P 1 21/n 18.8511; 24.5258; 11.1501
90; 97.066; 90
2402.1Call, Arnau; Franco, Federico; Kandoth, Noufal; Fernández, Sergio; González-Béjar, María; Pérez-Prieto, Julia; Luis, Josep M.; Lloret-Fillol, Julio
Understanding light-driven H<sub>2</sub> evolution through the electronic tuning of aminopyridine cobalt complexes.
Chemical science, 2018, 9, 2609-2619
1548898 CIFC19 H28 Co F6 N4 O8 S2C 1 c 112.8115; 24.0973; 8.7902
90; 96.927; 90
2693.9Call, Arnau; Franco, Federico; Kandoth, Noufal; Fernández, Sergio; González-Béjar, María; Pérez-Prieto, Julia; Luis, Josep M.; Lloret-Fillol, Julio
Understanding light-driven H<sub>2</sub> evolution through the electronic tuning of aminopyridine cobalt complexes.
Chemical science, 2018, 9, 2609-2619
1548899 CIFC21 H29 Co F6 N7 O6 S2P 1 21/n 114.2091; 13.4658; 15.184
90; 93.295; 90
2900.46Call, Arnau; Franco, Federico; Kandoth, Noufal; Fernández, Sergio; González-Béjar, María; Pérez-Prieto, Julia; Luis, Josep M.; Lloret-Fillol, Julio
Understanding light-driven H<sub>2</sub> evolution through the electronic tuning of aminopyridine cobalt complexes.
Chemical science, 2018, 9, 2609-2619
1548900 CIFC16 H24 Co F6 N4 O6 S2P b c a9.312; 16.956; 29.498
90; 90; 90
4657.6Call, Arnau; Franco, Federico; Kandoth, Noufal; Fernández, Sergio; González-Béjar, María; Pérez-Prieto, Julia; Luis, Josep M.; Lloret-Fillol, Julio
Understanding light-driven H<sub>2</sub> evolution through the electronic tuning of aminopyridine cobalt complexes.
Chemical science, 2018, 9, 2609-2619
1548901 CIFC18 H29 Co F6 N5 O6 S2P 1 21/n 18.802; 24.936; 12.694
90; 94.038; 90
2779.2Call, Arnau; Franco, Federico; Kandoth, Noufal; Fernández, Sergio; González-Béjar, María; Pérez-Prieto, Julia; Luis, Josep M.; Lloret-Fillol, Julio
Understanding light-driven H<sub>2</sub> evolution through the electronic tuning of aminopyridine cobalt complexes.
Chemical science, 2018, 9, 2609-2619
1548902 CIFC19 H30 Co F6 N4 O7 S2P 1 21/c 111.9921; 15.4423; 15.8756
90; 108.403; 90
2789.6Call, Arnau; Franco, Federico; Kandoth, Noufal; Fernández, Sergio; González-Béjar, María; Pérez-Prieto, Julia; Luis, Josep M.; Lloret-Fillol, Julio
Understanding light-driven H<sub>2</sub> evolution through the electronic tuning of aminopyridine cobalt complexes.
Chemical science, 2018, 9, 2609-2619
1548904 CIFC27 H32 B2 N Na O5P b c m14.245; 17.905; 11.3809
90; 90; 90
2902.8Zhang, Li; Jiao, Lei
Super electron donors derived from diboron.
Chemical science, 2018, 9, 2711-2722
1548905 CIFC32 H38 B K N2 O4P 1 21 112.3892; 40.276; 12.9956
90; 90.798; 90
6484Zhang, Li; Jiao, Lei
Super electron donors derived from diboron.
Chemical science, 2018, 9, 2711-2722
1548906 CIFC52 H57 N O2 P2 S2 TiP 1 21/c 114.314; 12.233; 27.034
90; 102.751; 90
4617Kurogi, Takashi; Won, Joonghee; Park, Bohyun; Trofymchuk, Oleksandra S.; Carroll, Patrick J.; Baik, Mu-Hyun; Mindiola, Daniel J.
Room temperature olefination of methane with titanium-carbon multiple bonds.
Chemical science, 2018, 9, 3376-3385
1548907 CIFC56 H65 N7 P2 TiP 1 21/n 111.835; 19.146; 22.47
90; 102.101; 90
4978.4Kurogi, Takashi; Won, Joonghee; Park, Bohyun; Trofymchuk, Oleksandra S.; Carroll, Patrick J.; Baik, Mu-Hyun; Mindiola, Daniel J.
Room temperature olefination of methane with titanium-carbon multiple bonds.
Chemical science, 2018, 9, 3376-3385
1548910 CIFC20 H28 Cl3 N4 O4 RuP 1 21/c 111.0085; 13.2457; 15.8552
90; 92.636; 90
2309.5Tse, Chun-Wai; Liu, Yungen; Wai-Shan Chow, Toby; Ma, Chaoqun; Yip, Wing-Ping; Chang, Xiao-Yong; Low, Kam-Hung; Huang, Jie-Sheng; Che, Chi-Ming
<i>cis</i>-Oxoruthenium complexes supported by chiral tetradentate amine (N<sub>4</sub>) ligands for hydrocarbon oxidations.
Chemical science, 2018, 9, 2803-2816
1548911 CIFC22 H29 Cl3 N5 O4 RuP 21 21 218.6233; 12.5838; 23.552
90; 90; 90
2555.7Tse, Chun-Wai; Liu, Yungen; Wai-Shan Chow, Toby; Ma, Chaoqun; Yip, Wing-Ping; Chang, Xiao-Yong; Low, Kam-Hung; Huang, Jie-Sheng; Che, Chi-Ming
<i>cis</i>-Oxoruthenium complexes supported by chiral tetradentate amine (N<sub>4</sub>) ligands for hydrocarbon oxidations.
Chemical science, 2018, 9, 2803-2816
1548912 CIFC22 H32 Cl3 N4 O4 RuP 1 2 110.505; 10.579; 11.649
90; 101.09; 90
1270.4Tse, Chun-Wai; Liu, Yungen; Wai-Shan Chow, Toby; Ma, Chaoqun; Yip, Wing-Ping; Chang, Xiao-Yong; Low, Kam-Hung; Huang, Jie-Sheng; Che, Chi-Ming
<i>cis</i>-Oxoruthenium complexes supported by chiral tetradentate amine (N<sub>4</sub>) ligands for hydrocarbon oxidations.
Chemical science, 2018, 9, 2803-2816
1548913 CIFC32 H38 Cl2 N6 O8 RuP 1 21 18.1503; 16.4241; 12.805
90; 99.016; 90
1692.9Tse, Chun-Wai; Liu, Yungen; Wai-Shan Chow, Toby; Ma, Chaoqun; Yip, Wing-Ping; Chang, Xiao-Yong; Low, Kam-Hung; Huang, Jie-Sheng; Che, Chi-Ming
<i>cis</i>-Oxoruthenium complexes supported by chiral tetradentate amine (N<sub>4</sub>) ligands for hydrocarbon oxidations.
Chemical science, 2018, 9, 2803-2816
1548914 CIFC31.65 H36.48 Cl2 N6.83 O8 RuP -19.912; 17.5103; 21.2883
81.245; 80.941; 83.022
3588.2Tse, Chun-Wai; Liu, Yungen; Wai-Shan Chow, Toby; Ma, Chaoqun; Yip, Wing-Ping; Chang, Xiao-Yong; Low, Kam-Hung; Huang, Jie-Sheng; Che, Chi-Ming
<i>cis</i>-Oxoruthenium complexes supported by chiral tetradentate amine (N<sub>4</sub>) ligands for hydrocarbon oxidations.
Chemical science, 2018, 9, 2803-2816
1548915 CIFC78 H58 Mn3.5 N4 O24 S10P -114.38; 15.3958; 21.7726
74.25; 71.751; 82.351
4399.85Yamamoto, S.; Pirillo, J.; Hijikata, Y.; Zhang, Z.; Awaga, K.
Nanopore-induced host-guest charge transfer phenomena in a metal-organic framework.
Chemical science, 2018, 9, 3282-3289
1548916 CIFC100 H17.5 Mn3.5 N10 O24P -114.639; 16.743; 20.551
100.913; 106.78; 100.119
4591.03Yamamoto, S.; Pirillo, J.; Hijikata, Y.; Zhang, Z.; Awaga, K.
Nanopore-induced host-guest charge transfer phenomena in a metal-organic framework.
Chemical science, 2018, 9, 3282-3289
1548917 CIFC32 H68 N8 ThP -110.383; 11.3585; 17.4827
89.777; 89.404; 63.76
1849.26Settineri, Nicholas S.; Arnold, John
Insertion, protonolysis and photolysis reactivity of a thorium monoalkyl amidinate complex.
Chemical science, 2018, 9, 2831-2841
1548918 CIFC35 H69 N9 Si ThP 1 21/c 116.9023; 11.4723; 21.7432
90; 95.127; 90
4199.3Settineri, Nicholas S.; Arnold, John
Insertion, protonolysis and photolysis reactivity of a thorium monoalkyl amidinate complex.
Chemical science, 2018, 9, 2831-2841
1548919 CIFC30 H62 N6 O2 Si ThP -19.4981; 11.95; 16.888
90.32; 99.06; 102.29
1848Settineri, Nicholas S.; Arnold, John
Insertion, protonolysis and photolysis reactivity of a thorium monoalkyl amidinate complex.
Chemical science, 2018, 9, 2831-2841
1548920 CIFC29 H62 N6 O Si ThP -112.986; 16.992; 17.337
103.843; 97.592; 93.871
3662.3Settineri, Nicholas S.; Arnold, John
Insertion, protonolysis and photolysis reactivity of a thorium monoalkyl amidinate complex.
Chemical science, 2018, 9, 2831-2841
1548921 CIFC13.75 H25 N3 Th0.5P -111.5082; 12.3194; 12.8462
61.8432; 79.157; 86.2752
1576.47Settineri, Nicholas S.; Arnold, John
Insertion, protonolysis and photolysis reactivity of a thorium monoalkyl amidinate complex.
Chemical science, 2018, 9, 2831-2841
1548922 CIFC37 H71 N7 Si ThP 1 21/n 110.9839; 20.99; 18.246
90; 93.46; 90
4199Settineri, Nicholas S.; Arnold, John
Insertion, protonolysis and photolysis reactivity of a thorium monoalkyl amidinate complex.
Chemical science, 2018, 9, 2831-2841
1548923 CIFC34 H67 N7 Si ThP 1 21/n 112.6373; 17.8743; 17.1544
90; 90.033; 90
3874.9Settineri, Nicholas S.; Arnold, John
Insertion, protonolysis and photolysis reactivity of a thorium monoalkyl amidinate complex.
Chemical science, 2018, 9, 2831-2841
1548924 CIFC56 H87 B N6 O2 ThP 1 21/c 118.6971; 15.8036; 18.9111
90; 103.688; 90
5429.2Settineri, Nicholas S.; Arnold, John
Insertion, protonolysis and photolysis reactivity of a thorium monoalkyl amidinate complex.
Chemical science, 2018, 9, 2831-2841
1548925 CIFC32 H67 B N6 ThP 1 21/n 112.1573; 18.4711; 16.3766
90; 90.215; 90
3677.5Settineri, Nicholas S.; Arnold, John
Insertion, protonolysis and photolysis reactivity of a thorium monoalkyl amidinate complex.
Chemical science, 2018, 9, 2831-2841
1548926 CIFC33 H58 N6 ThP 1 21/c 119.0249; 10.3942; 19.133
90; 110.105; 90
3553Settineri, Nicholas S.; Arnold, John
Insertion, protonolysis and photolysis reactivity of a thorium monoalkyl amidinate complex.
Chemical science, 2018, 9, 2831-2841
1548927 CIFC33 H63 N6 P ThP 1 21/n 122.5782; 13.2908; 25.4828
90; 100.332; 90
7522.9Settineri, Nicholas S.; Arnold, John
Insertion, protonolysis and photolysis reactivity of a thorium monoalkyl amidinate complex.
Chemical science, 2018, 9, 2831-2841
1548939 CIFC22 H23 N O2 SiP 1 21 110.4794; 7.0464; 13.4791
90; 100.094; 90
979.92Rodriguez, Kevin X.; Pilato, Tara C.; Ashfeld, Brandon L.
An unusual stereoretentive 1,3-quaternary carbon shift resulting in an enantioselective Rh<sup>II</sup>-catalyzed formal [4+1]-cycloaddition between diazo compounds and vinyl ketenes.
Chemical science, 2018, 9, 3221-3226
1548940 CIFC22 H23 N O2 SiP 21 21 219.4164; 11.6775; 17.207
90; 90; 90
1892.08Rodriguez, Kevin X.; Pilato, Tara C.; Ashfeld, Brandon L.
An unusual stereoretentive 1,3-quaternary carbon shift resulting in an enantioselective Rh<sup>II</sup>-catalyzed formal [4+1]-cycloaddition between diazo compounds and vinyl ketenes.
Chemical science, 2018, 9, 3221-3226
1548941 CIFC69.17 H38.35 B Cl2.35 F28 I N Na0 O P2 RhP -112.9788; 15.9249; 18.4205
77.6077; 73.186; 88.345
3557.34Carreras, Lucas; Serrano-Torné, Marta; van Leeuwen, Piet W. N. M.; Vidal-Ferran, Anton
<b>XBphos-Rh</b>: a halogen-bond assembled supramolecular catalyst.
Chemical science, 2018, 9, 3644-3648
1548942 CIFC70.5 H46 B F24 I N O P2 RhP -112.9235; 15.961; 18.3296
79.049; 71.52; 88.475
3518.3Carreras, Lucas; Serrano-Torné, Marta; van Leeuwen, Piet W. N. M.; Vidal-Ferran, Anton
<b>XBphos-Rh</b>: a halogen-bond assembled supramolecular catalyst.
Chemical science, 2018, 9, 3644-3648
1548943 CIFC18 H22 N2 O3 SP 1 21/c 117.417; 7.3299; 13.5997
90; 95.37; 90
1728.58Giri, Sovan Sundar; Liu, Rai-Shung
Gold-catalyzed [4+3]- and [4+2]-annulations of 3-en-1-ynamides with isoxazoles <i>via</i> novel 6π-electrocyclizations of 3-azahepta trienyl cations.
Chemical science, 2018, 9, 2991-2995
1548944 CIFC28 H26 N2 O3 SP 1 21/c 113.9904; 8.4064; 21.36
90; 104.491; 90
2432.21Giri, Sovan Sundar; Liu, Rai-Shung
Gold-catalyzed [4+3]- and [4+2]-annulations of 3-en-1-ynamides with isoxazoles <i>via</i> novel 6π-electrocyclizations of 3-azahepta trienyl cations.
Chemical science, 2018, 9, 2991-2995
1548945 CIFC18 H22 N2 O3 SP 1 21/c 112.3308; 16.1714; 8.8646
90; 94.241; 90
1762.8Giri, Sovan Sundar; Liu, Rai-Shung
Gold-catalyzed [4+3]- and [4+2]-annulations of 3-en-1-ynamides with isoxazoles <i>via</i> novel 6π-electrocyclizations of 3-azahepta trienyl cations.
Chemical science, 2018, 9, 2991-2995
1548946 CIFC21 H26 N2 O3 SP 1 21/n 19.0836; 21.4854; 9.9912
90; 92.112; 90
1948.61Giri, Sovan Sundar; Liu, Rai-Shung
Gold-catalyzed [4+3]- and [4+2]-annulations of 3-en-1-ynamides with isoxazoles <i>via</i> novel 6π-electrocyclizations of 3-azahepta trienyl cations.
Chemical science, 2018, 9, 2991-2995
1548947 CIFC24 H26 N2 O3 SP 1 21/c 19.8261; 13.6201; 16.2063
90; 96.868; 90
2153.37Giri, Sovan Sundar; Liu, Rai-Shung
Gold-catalyzed [4+3]- and [4+2]-annulations of 3-en-1-ynamides with isoxazoles <i>via</i> novel 6π-electrocyclizations of 3-azahepta trienyl cations.
Chemical science, 2018, 9, 2991-2995
1548948 CIFC16 H18 N2 O3 SC 1 2/c 110.99; 9.6096; 29.66
90; 94.047; 90
3124.6Giri, Sovan Sundar; Liu, Rai-Shung
Gold-catalyzed [4+3]- and [4+2]-annulations of 3-en-1-ynamides with isoxazoles <i>via</i> novel 6π-electrocyclizations of 3-azahepta trienyl cations.
Chemical science, 2018, 9, 2991-2995
1548949 CIFC12 H12 F4 OP 21 21 216.0422; 11.778; 15.448
90; 90; 90
1099.4Rodil, Andrea; Bosisio, Stefano; Ayoup, Mohammed Salah; Quinn, Laura; Cordes, David B.; Slawin, Alexandra M. Z.; Murphy, Cormac D.; Michel, Julien; O'Hagan, David
Metabolism and hydrophilicity of the polarised 'Janus face' all-<i>cis</i> tetrafluorocyclohexyl ring, a candidate motif for drug discovery.
Chemical science, 2018, 9, 3023-3028
1548950 CIFC12 H14 F2 OP 21 21 215.25889; 9.75241; 20.4698
90; 90; 90
1049.83Rodil, Andrea; Bosisio, Stefano; Ayoup, Mohammed Salah; Quinn, Laura; Cordes, David B.; Slawin, Alexandra M. Z.; Murphy, Cormac D.; Michel, Julien; O'Hagan, David
Metabolism and hydrophilicity of the polarised 'Janus face' all-<i>cis</i> tetrafluorocyclohexyl ring, a candidate motif for drug discovery.
Chemical science, 2018, 9, 3023-3028
1548951 CIFC12 H14 F2 OP 1 21/a 113.5173; 5.57303; 27.4909
90; 90.469; 90
2070.88Rodil, Andrea; Bosisio, Stefano; Ayoup, Mohammed Salah; Quinn, Laura; Cordes, David B.; Slawin, Alexandra M. Z.; Murphy, Cormac D.; Michel, Julien; O'Hagan, David
Metabolism and hydrophilicity of the polarised 'Janus face' all-<i>cis</i> tetrafluorocyclohexyl ring, a candidate motif for drug discovery.
Chemical science, 2018, 9, 3023-3028
1548952 CIFC12 H14 F2 OP 1 21/c 110.536; 19.983; 10.272
90; 107.972; 90
2057.2Rodil, Andrea; Bosisio, Stefano; Ayoup, Mohammed Salah; Quinn, Laura; Cordes, David B.; Slawin, Alexandra M. Z.; Murphy, Cormac D.; Michel, Julien; O'Hagan, David
Metabolism and hydrophilicity of the polarised 'Janus face' all-<i>cis</i> tetrafluorocyclohexyl ring, a candidate motif for drug discovery.
Chemical science, 2018, 9, 3023-3028
1548953 CIFC12 H15 F OP 21 21 215.33024; 9.6528; 20.0332
90; 90; 90
1030.74Rodil, Andrea; Bosisio, Stefano; Ayoup, Mohammed Salah; Quinn, Laura; Cordes, David B.; Slawin, Alexandra M. Z.; Murphy, Cormac D.; Michel, Julien; O'Hagan, David
Metabolism and hydrophilicity of the polarised 'Janus face' all-<i>cis</i> tetrafluorocyclohexyl ring, a candidate motif for drug discovery.
Chemical science, 2018, 9, 3023-3028
1548954 CIFC31 H34 O4 SP 6121.247; 21.247; 11.2694
90; 90; 120
4405.8Zhao, Jian; Jonker, Sybrand J. T.; Meyer, Denise N.; Schulz, Göran; Tran, C. Duc; Eriksson, Lars; Szabó, Kálmán J
Copper-catalyzed synthesis of allenylboronic acids. Access to sterically encumbered homopropargylic alcohols and amines by propargylboration.
Chemical science, 2018, 9, 3305-3312
1548969 CIFC31 H27 N3 O3P -17.6914; 8.8535; 18.0798
91.235; 97.803; 92.431
1218.2Xiong, Yaoyao; Vargas Jentzsch, Andreas; Osterrieth, Johannes W. M.; Sezgin, Erdinc; Sazanovich, Igor V.; Reglinski, Katharina; Galiani, Silvia; Parker, Anthony W.; Eggeling, Christian; Anderson, Harry L.
Spironaphthoxazine switchable dyes for biological imaging.
Chemical science, 2018, 9, 3029-3040
1548970 CIFC308 H374 N23 O12 P3P -121.138; 21.616; 21.948
118.123; 106.659; 99.169
7942Fatila, Elisabeth M.; Pink, Maren; Twum, Eric B.; Karty, Jonathan A.; Flood, Amar H.
Phosphate-phosphate oligomerization drives higher order co-assemblies with stacks of cyanostar macrocycles.
Chemical science, 2018, 9, 2863-2872
1548971 CIFC365.84 H508.52 Cl14.16 N26 O29.28 P7P -119.692; 22.3708; 25.201
97.908; 108.437; 113.456
9208.2Fatila, Elisabeth M.; Pink, Maren; Twum, Eric B.; Karty, Jonathan A.; Flood, Amar H.
Phosphate-phosphate oligomerization drives higher order co-assemblies with stacks of cyanostar macrocycles.
Chemical science, 2018, 9, 2863-2872
1548975 CIFC26 H15 N6 O11 Zn2I 427.458; 27.458; 18.225
90; 90; 90
13741Zhao, He; Ni, Jun; Zhang, Jian-Jun; Liu, Shu-Qin; Sun, Ying-Ji; Zhou, Huajun; Li, Yan-Qin; Duan, Chun-Ying
A trichromatic MOF composite for multidimensional ratiometric luminescent sensing.
Chemical science, 2018, 9, 2918-2926
1548976 CIFC58.5 H43.5 F6 N6.5 O2.5 ZnP 1 21/n 110.7604; 51.619; 18.6745
90; 98.394; 90
10261.5Nichols, Eva M.; Derrick, Jeffrey S.; Nistanaki, Sepand K.; Smith, Peter T.; Chang, Christopher J.
Positional effects of second-sphere amide pendants on electrochemical CO<sub>2</sub> reduction catalyzed by iron porphyrins.
Chemical science, 2018, 9, 2952-2960
1548977 CIFC9.4 H4 D5.61 O5 VI 41 2 215.1723; 15.1723; 12.0747
90; 90; 90
2779.58Lu, Zhenzhong; Godfrey, Harry G. W.; da Silva, Ivan; Cheng, Yongqiang; Savage, Mathew; Manuel, Pascal; Rudić, Svemir; Ramirez-Cuesta, Anibal J; Yang, Sihai; Schröder, Martin
Direct observation of supramolecular binding of light hydrocarbons in vanadium(iii) and (iv) metal-organic framework materials.
Chemical science, 2018, 9, 3401-3408
1548978 CIFC10.63 H4 D8.95 O5 VI 41 2 215.1668; 15.1668; 12.0716
90; 90; 90
2776.85Lu, Zhenzhong; Godfrey, Harry G. W.; da Silva, Ivan; Cheng, Yongqiang; Savage, Mathew; Manuel, Pascal; Rudić, Svemir; Ramirez-Cuesta, Anibal J; Yang, Sihai; Schröder, Martin
Direct observation of supramolecular binding of light hydrocarbons in vanadium(iii) and (iv) metal-organic framework materials.
Chemical science, 2018, 9, 3401-3408
1548979 CIFC9.01 H4 D4.06 O5 VI 41 2 215.16316; 15.16316; 12.0746
90; 90; 90
2776.21Lu, Zhenzhong; Godfrey, Harry G. W.; da Silva, Ivan; Cheng, Yongqiang; Savage, Mathew; Manuel, Pascal; Rudić, Svemir; Ramirez-Cuesta, Anibal J; Yang, Sihai; Schröder, Martin
Direct observation of supramolecular binding of light hydrocarbons in vanadium(iii) and (iv) metal-organic framework materials.
Chemical science, 2018, 9, 3401-3408
1548980 CIFC10 H4 D2 O5 VI 41 2 215.1613; 15.1613; 12.0687
90; 90; 90
2774.17Lu, Zhenzhong; Godfrey, Harry G. W.; da Silva, Ivan; Cheng, Yongqiang; Savage, Mathew; Manuel, Pascal; Rudić, Svemir; Ramirez-Cuesta, Anibal J; Yang, Sihai; Schröder, Martin
Direct observation of supramolecular binding of light hydrocarbons in vanadium(iii) and (iv) metal-organic framework materials.
Chemical science, 2018, 9, 3401-3408
1548981 CIFC10.14 H4 D4.28 O5 VI 41 2 215.1594; 15.1594; 12.071
90; 90; 90
2774.01Lu, Zhenzhong; Godfrey, Harry G. W.; da Silva, Ivan; Cheng, Yongqiang; Savage, Mathew; Manuel, Pascal; Rudić, Svemir; Ramirez-Cuesta, Anibal J; Yang, Sihai; Schröder, Martin
Direct observation of supramolecular binding of light hydrocarbons in vanadium(iii) and (iv) metal-organic framework materials.
Chemical science, 2018, 9, 3401-3408
1548982 CIFC10.07 H4 D6.2 O5 VI 41 2 215.1661; 15.1661; 12.0725
90; 90; 90
2776.8Lu, Zhenzhong; Godfrey, Harry G. W.; da Silva, Ivan; Cheng, Yongqiang; Savage, Mathew; Manuel, Pascal; Rudić, Svemir; Ramirez-Cuesta, Anibal J; Yang, Sihai; Schröder, Martin
Direct observation of supramolecular binding of light hydrocarbons in vanadium(iii) and (iv) metal-organic framework materials.
Chemical science, 2018, 9, 3401-3408
1548983 CIFC11.56 H4 D3.56 O5 VI 41 2 215.1457; 15.1457; 12.0519
90; 90; 90
2764.61Lu, Zhenzhong; Godfrey, Harry G. W.; da Silva, Ivan; Cheng, Yongqiang; Savage, Mathew; Manuel, Pascal; Rudić, Svemir; Ramirez-Cuesta, Anibal J; Yang, Sihai; Schröder, Martin
Direct observation of supramolecular binding of light hydrocarbons in vanadium(iii) and (iv) metal-organic framework materials.
Chemical science, 2018, 9, 3401-3408
1548984 CIFC15 H10 B5 F30 K5P -110.9621; 12.9672; 13.9252
111.325; 99.442; 105.532
1699.54Phelan, James P.; Wiles, Rebecca J.; Lang, Simon B.; Kelly, Christopher B.; Molander, Gary A.
Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategies.
Chemical science, 2018, 9, 3215-3220
1548989 CIFC21 H15 F6 N2 O PC 1 2/c 16.861; 10.695; 23.818
90; 96.101; 90
1737.8Rosenberg, M.; Rostgaard, K. R.; Liao, Z.; Madsen, A Ø; Martinez, K. L.; Vosch, T.; Laursen, B. W.
Design, synthesis, and time-gated cell imaging of carbon-bridged triangulenium dyes with long fluorescence lifetime and red emission.
Chemical science, 2018, 9, 3122-3130
1548990 CIFC22 H15 F6 O2 PP -18.4805; 8.5013; 14.7698
74.017; 89.013; 64.503
917.65Rosenberg, M.; Rostgaard, K. R.; Liao, Z.; Madsen, A Ø; Martinez, K. L.; Vosch, T.; Laursen, B. W.
Design, synthesis, and time-gated cell imaging of carbon-bridged triangulenium dyes with long fluorescence lifetime and red emission.
Chemical science, 2018, 9, 3122-3130
1548991 CIFC23 H18 F6 N O PP -114.162; 15.264; 20.039
87.939; 85.555; 62.365
3826.1Rosenberg, M.; Rostgaard, K. R.; Liao, Z.; Madsen, A Ø; Martinez, K. L.; Vosch, T.; Laursen, B. W.
Design, synthesis, and time-gated cell imaging of carbon-bridged triangulenium dyes with long fluorescence lifetime and red emission.
Chemical science, 2018, 9, 3122-3130
1548992 CIFC24 H21 F6 N2 PP c c n14.5591; 21.6499; 13.0273
90; 90; 90
4106.2Rosenberg, M.; Rostgaard, K. R.; Liao, Z.; Madsen, A Ø; Martinez, K. L.; Vosch, T.; Laursen, B. W.
Design, synthesis, and time-gated cell imaging of carbon-bridged triangulenium dyes with long fluorescence lifetime and red emission.
Chemical science, 2018, 9, 3122-3130
1548993 CIFC35 H35 Cl2 F3 N8 Ni O3 SP -110.0222; 12.1506; 16.0254
69.063; 75.075; 81.389
1757.6Grübel, Michael; Bosque, Irene; Altmann, Philipp J.; Bach, Thorsten; Hess, Corinna R.
Redox and photocatalytic properties of a Ni<sup>II</sup> complex with a macrocyclic biquinazoline (Mabiq) ligand.
Chemical science, 2018, 9, 3313-3317
1548994 CIFC22 H35 NP 1 21/c 117.6983; 6.2954; 17.442
90; 102.677; 90
1896Grübel, Michael; Bosque, Irene; Altmann, Philipp J.; Bach, Thorsten; Hess, Corinna R.
Redox and photocatalytic properties of a Ni<sup>II</sup> complex with a macrocyclic biquinazoline (Mabiq) ligand.
Chemical science, 2018, 9, 3313-3317
1548995 CIFC33 H33 N8 NiP 21 21 2110.1802; 20.4136; 26.689
90; 90; 90
5546.4Grübel, Michael; Bosque, Irene; Altmann, Philipp J.; Bach, Thorsten; Hess, Corinna R.
Redox and photocatalytic properties of a Ni<sup>II</sup> complex with a macrocyclic biquinazoline (Mabiq) ligand.
Chemical science, 2018, 9, 3313-3317
1548996 CIFC16 H12 F3 N O4 SP -18.4561; 8.5762; 12.4229
110.047; 111.941; 90.1156
776.24Das, Pulakesh; Gondo, Satoshi; Nagender, Punna; Uno, Hiroto; Tokunaga, Etsuko; Shibata, Norio
Access to benzo-fused nine-membered heterocyclic alkenes with a trifluoromethyl carbinol moiety <i>via</i> a double decarboxylative formal ring-expansion process under palladium catalysis.
Chemical science, 2018, 9, 3276-3281
1548997 CIFC25 H22 F3 N O3 SP b c a16.8152; 15.0512; 17.5637
90; 90; 90
4445.18Das, Pulakesh; Gondo, Satoshi; Nagender, Punna; Uno, Hiroto; Tokunaga, Etsuko; Shibata, Norio
Access to benzo-fused nine-membered heterocyclic alkenes with a trifluoromethyl carbinol moiety <i>via</i> a double decarboxylative formal ring-expansion process under palladium catalysis.
Chemical science, 2018, 9, 3276-3281
1548998 CIFC25 H22 F3 N O4 SP 1 21/c 116.8716; 7.8975; 16.7075
90; 90.3044; 90
2226.13Das, Pulakesh; Gondo, Satoshi; Nagender, Punna; Uno, Hiroto; Tokunaga, Etsuko; Shibata, Norio
Access to benzo-fused nine-membered heterocyclic alkenes with a trifluoromethyl carbinol moiety <i>via</i> a double decarboxylative formal ring-expansion process under palladium catalysis.
Chemical science, 2018, 9, 3276-3281
1548999 CIFC23 H20 F3 N O4 SP 1 21/n 114.6966; 9.1174; 17.3812
90; 116.062; 90
2092.17Das, Pulakesh; Gondo, Satoshi; Nagender, Punna; Uno, Hiroto; Tokunaga, Etsuko; Shibata, Norio
Access to benzo-fused nine-membered heterocyclic alkenes with a trifluoromethyl carbinol moiety <i>via</i> a double decarboxylative formal ring-expansion process under palladium catalysis.
Chemical science, 2018, 9, 3276-3281
1549003 CIFC28 H44 Li2 N6P 1 21/n 19.746; 25.413; 11.319
90; 105.55; 90
2700.8Engelhardt, Felix; Maaß, Christian; Andrada, Diego M.; Herbst-Irmer, Regine; Stalke, Dietmar
Benchmarking lithium amide <i>versus</i> amine bonding by charge density and energy decomposition analysis arguments.
Chemical science, 2018, 9, 3111-3121
1549004 CIFC20 H36 Li2 N6P 1 21/c 112.7937; 9.7101; 18.6728
90; 94.3121; 90
2313.12Engelhardt, Felix; Maaß, Christian; Andrada, Diego M.; Herbst-Irmer, Regine; Stalke, Dietmar
Benchmarking lithium amide <i>versus</i> amine bonding by charge density and energy decomposition analysis arguments.
Chemical science, 2018, 9, 3111-3121
1549005 CIFC40 H68 Li2 N6P 1 21/c 113.864; 30.46; 9.851
90; 105.18; 90
4014.9Engelhardt, Felix; Maaß, Christian; Andrada, Diego M.; Herbst-Irmer, Regine; Stalke, Dietmar
Benchmarking lithium amide <i>versus</i> amine bonding by charge density and energy decomposition analysis arguments.
Chemical science, 2018, 9, 3111-3121
1549011 CIFC27 H29 Cl F6 N2 P RhP 1 21/n 115.9555; 11.5878; 17.1391
90; 116.061; 90
2846.6Banerjee, Samya; Soldevila-Barreda, Joan J; Wolny, Juliusz A.; Wootton, Christopher A.; Habtemariam, Abraha; Romero-Canelón, Isolda; Chen, Feng; Clarkson, Guy J.; Prokes, Ivan; Song, Lijiang; O'Connor, Peter B; Schünemann, Volker; Sadler, Peter J.
New activation mechanism for half-sandwich organometallic anticancer complexes.
Chemical science, 2018, 9, 3177-3185
1549012 CIFC20 H23 Cl F6 N2 P RhP m n 2112.9507; 8.31; 10.5094
90; 90; 90
1131.02Banerjee, Samya; Soldevila-Barreda, Joan J; Wolny, Juliusz A.; Wootton, Christopher A.; Habtemariam, Abraha; Romero-Canelón, Isolda; Chen, Feng; Clarkson, Guy J.; Prokes, Ivan; Song, Lijiang; O'Connor, Peter B; Schünemann, Volker; Sadler, Peter J.
New activation mechanism for half-sandwich organometallic anticancer complexes.
Chemical science, 2018, 9, 3177-3185
1549013 CIFC31 H37 Cl F6 N2 O2 P RhP -18.51582; 13.5384; 14.2569
94.5969; 92.9146; 92.6758
1634.15Banerjee, Samya; Soldevila-Barreda, Joan J; Wolny, Juliusz A.; Wootton, Christopher A.; Habtemariam, Abraha; Romero-Canelón, Isolda; Chen, Feng; Clarkson, Guy J.; Prokes, Ivan; Song, Lijiang; O'Connor, Peter B; Schünemann, Volker; Sadler, Peter J.
New activation mechanism for half-sandwich organometallic anticancer complexes.
Chemical science, 2018, 9, 3177-3185
1549014 CIFC36 H35 Cl F6 N2 O P RhP -18.7508; 14.4955; 14.5101
84.91; 74.415; 82.382
1754.53Banerjee, Samya; Soldevila-Barreda, Joan J; Wolny, Juliusz A.; Wootton, Christopher A.; Habtemariam, Abraha; Romero-Canelón, Isolda; Chen, Feng; Clarkson, Guy J.; Prokes, Ivan; Song, Lijiang; O'Connor, Peter B; Schünemann, Volker; Sadler, Peter J.
New activation mechanism for half-sandwich organometallic anticancer complexes.
Chemical science, 2018, 9, 3177-3185
1549015 CIFC25 H28 F12 N3 O0.5 P2 RhP -19.84864; 10.1712; 16.1627
101.363; 90.9323; 109.801
1487.41Banerjee, Samya; Soldevila-Barreda, Joan J; Wolny, Juliusz A.; Wootton, Christopher A.; Habtemariam, Abraha; Romero-Canelón, Isolda; Chen, Feng; Clarkson, Guy J.; Prokes, Ivan; Song, Lijiang; O'Connor, Peter B; Schünemann, Volker; Sadler, Peter J.
New activation mechanism for half-sandwich organometallic anticancer complexes.
Chemical science, 2018, 9, 3177-3185
1549016 CIFC36 H39 Cl F6 N2 O P RhP 1 21/n 18.0233; 28.1842; 16.1096
90; 94.393; 90
3632.2Banerjee, Samya; Soldevila-Barreda, Joan J; Wolny, Juliusz A.; Wootton, Christopher A.; Habtemariam, Abraha; Romero-Canelón, Isolda; Chen, Feng; Clarkson, Guy J.; Prokes, Ivan; Song, Lijiang; O'Connor, Peter B; Schünemann, Volker; Sadler, Peter J.
New activation mechanism for half-sandwich organometallic anticancer complexes.
Chemical science, 2018, 9, 3177-3185
1549017 CIFC34 H35 Cl F6 N2 O P RhP -18.40215; 12.9603; 15.392
80; 86.442; 86.175
1644.79Banerjee, Samya; Soldevila-Barreda, Joan J; Wolny, Juliusz A.; Wootton, Christopher A.; Habtemariam, Abraha; Romero-Canelón, Isolda; Chen, Feng; Clarkson, Guy J.; Prokes, Ivan; Song, Lijiang; O'Connor, Peter B; Schünemann, Volker; Sadler, Peter J.
New activation mechanism for half-sandwich organometallic anticancer complexes.
Chemical science, 2018, 9, 3177-3185
1549018 CIFC28 H29 Cl F6 N2 O P RhP -18.20707; 10.08952; 17.2032
82.3397; 81.4575; 84.0175
1390.95Banerjee, Samya; Soldevila-Barreda, Joan J; Wolny, Juliusz A.; Wootton, Christopher A.; Habtemariam, Abraha; Romero-Canelón, Isolda; Chen, Feng; Clarkson, Guy J.; Prokes, Ivan; Song, Lijiang; O'Connor, Peter B; Schünemann, Volker; Sadler, Peter J.
New activation mechanism for half-sandwich organometallic anticancer complexes.
Chemical science, 2018, 9, 3177-3185
1549020 CIFC27 H20 N2 O3 SP 1 21/c 112.6727; 15.398; 11.9061
90; 110.633; 90
2174.3Roy, Bibhisan; Reddy, Mallu Chenna; Hazra, Partha
Developing the structure-property relationship to design solid state multi-stimuli responsive materials and their potential applications in different fields.
Chemical science, 2018, 9, 3592-3606
1549021 CIFC15 H11 N O3 SP -17.089; 7.256; 13.569
85.46; 77.9; 70.37
642.8Roy, Bibhisan; Reddy, Mallu Chenna; Hazra, Partha
Developing the structure-property relationship to design solid state multi-stimuli responsive materials and their potential applications in different fields.
Chemical science, 2018, 9, 3592-3606
1549022 CIFC27 H18 N2 O3 SC 1 2 125.719; 7.5368; 11.759
90; 116.39; 90
2041.8Roy, Bibhisan; Reddy, Mallu Chenna; Hazra, Partha
Developing the structure-property relationship to design solid state multi-stimuli responsive materials and their potential applications in different fields.
Chemical science, 2018, 9, 3592-3606
1549023 CIFC17 H16 N2 O3 SP 1 21/n 18.172; 9.666; 20.305
90; 99.512; 90
1581.9Roy, Bibhisan; Reddy, Mallu Chenna; Hazra, Partha
Developing the structure-property relationship to design solid state multi-stimuli responsive materials and their potential applications in different fields.
Chemical science, 2018, 9, 3592-3606
1549029 CIFC86 H162 Co Cr7 F8 N O33I 419.9066; 19.9066; 16.1991
90; 90; 90
6419.3Garlatti, Elena; Guidi, Tatiana; Chiesa, Alessandro; Ansbro, Simon; Baker, Michael L.; Ollivier, Jacques; Mutka, Hannu; Timco, Grigore A.; Vitorica-Yrezabal, Inigo; Pavarini, Eva; Santini, Paolo; Amoretti, Giuseppe; Winpenny, Richard E. P.; Carretta, Stefano
Anisotropy of Co<sup>II</sup> transferred to the Cr<sub>7</sub>Co polymetallic cluster <i>via</i> strong exchange interactions.
Chemical science, 2018, 9, 3555-3562
1549035 CIFC3 H6 N3 O10 PP 1 21/c 112.37; 8.1257; 9.943
90; 97.638; 90
990.6Manner, Virginia W.; Cawkwell, Marc J.; Kober, Edward M.; Myers, Thomas W.; Brown, Geoff W.; Tian, Hongzhao; Snyder, Christopher J.; Perriot, Romain; Preston, Daniel N.
Examining the chemical and structural properties that influence the sensitivity of energetic nitrate esters.
Chemical science, 2018, 9, 3649-3663
1549036 CIFC4 H7 N3 O9P -17.6451; 7.8238; 8.9723
100.557; 96.753; 114.76
467.59Manner, Virginia W.; Cawkwell, Marc J.; Kober, Edward M.; Myers, Thomas W.; Brown, Geoff W.; Tian, Hongzhao; Snyder, Christopher J.; Perriot, Romain; Preston, Daniel N.
Examining the chemical and structural properties that influence the sensitivity of energetic nitrate esters.
Chemical science, 2018, 9, 3649-3663
1549042 CIFC17 H19 B F4 N2 OP 1 21/c 119.5805; 9.7595; 8.9644
90; 103.158; 90
1668.08Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549043 CIFC31 H35 B N2 OP 21 21 219.49835; 11.89113; 22.8675
90; 90; 90
2582.8Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549044 CIFC10 H16 I N OP 1 21 15.40542; 6.94898; 16.0701
90; 95.864; 90
600.47Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549045 CIFC40 H66 Cl2 N10 O16I 1 2/a 115.1489; 13.2904; 24.594
90; 97.293; 90
4911.6Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549046 CIFC17 H19 Cl N2 OP 1 21/c 118.7661; 8.8339; 9.6084
90; 100.318; 90
1567.1Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549047 CIFC19 H26 Cl N5 O3P 1 21/c 17.10113; 13.625; 20.6821
90; 91.5054; 90
2000.36Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549048 CIFC22 H32 N2 O6C 1 2 113.5545; 5.84781; 14.1657
90; 110.071; 90
1054.64Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549049 CIFC14 H18 F18 K N3 P2 SP 1 21/c 124.3732; 10.4084; 9.9932
90; 93.1701; 90
2531.26Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549050 CIFC34 H42 N4 O8 SP 1 21 18.6454; 9.463; 20.0392
90; 96.753; 90
1628.06Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549051 CIFC17 H21 N2 O5 PP 1 21/c 120.7561; 9.5134; 8.5352
90; 96.5078; 90
1674.51Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549052 CIFC14 H18 Br F6 N3 SP 1 21/c 110.9874; 14.2737; 23.2106
90; 90.2783; 90
3640.1Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549053 CIFC38 H48.7 N4 O11.35P 1 21 18.81; 9.7133; 21.7147
90; 100.169; 90
1829.03Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549054 CIFC18 H19 N3 O SP 1 21/c 119.8981; 8.0213; 10.8806
90; 100.435; 90
1707.92Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549055 CIFC17 H19 I N2 OP 1 21/c 119.6674; 8.1224; 10.8447
90; 105.289; 90
1671.09Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549056 CIFC10 H16 I N OP 21 21 217.32726; 18.9411; 25.6662
90; 90; 90
3562.12Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549057 CIFC10 H16 Cl N OP 1 21 17.2565; 6.1232; 12.557
90; 102.256; 90
545.23Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549058 CIFC11 H16 N2 O SP 21 21 216.09862; 7.52704; 27.3811
90; 90; 90
1256.92Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549059 CIFC42 H46 N4 O16 Sb2C 1 2 122.3684; 8.4156; 15.6852
90; 130.585; 90
2242.36Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549060 CIFC31 H35 B N2 OP 1 21/n 110.1433; 18.6189; 14.0467
90; 99.569; 90
2615.91Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549061 CIFC10 H16 Br N OP 1 21 17.4467; 6.20961; 12.5863
90; 101.176; 90
570.97Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549062 CIFC36 H38 N4 O8P 1 21 19.0081; 9.3218; 19.4957
90; 95.351; 90
1629.95Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549063 CIFC19 H23 Cl I N5 OP 1 21/c 112.9279; 12.5457; 13.139
90; 109.843; 90
2004.48Nievergelt, Philipp P.; Babor, Martin; Čejka, Jan; Spingler, Bernhard
A high throughput screening method for the nano-crystallization of salts of organic cations.
Chemical science, 2018, 9, 3716-3722
1549068 CIFC140.5 H113.5 Cl5.5 O1.5P -115.3025; 16.0955; 22.2445
94.998; 108.991; 92.221
5147.8Cruz, Carlos M.; Márquez, Irene R; Mariz, Inês F A; Blanco, Victor; Sánchez-Sánchez, Carlos; Sobrado, Jesús M; Martín-Gago, José A; Cuerva, Juan M.; Maçôas, Ermelinda; Campaña, Araceli G
Enantiopure distorted ribbon-shaped nanographene combining two-photon absorption-based upconversion and circularly polarized luminescence.
Chemical science, 2018, 9, 3917-3924
1549069 CIFC116 H103 F3 O4 SP -114.3675; 17.3718; 18.9206
67.525; 86.143; 89.598
4352.9Cruz, Carlos M.; Márquez, Irene R; Mariz, Inês F A; Blanco, Victor; Sánchez-Sánchez, Carlos; Sobrado, Jesús M; Martín-Gago, José A; Cuerva, Juan M.; Maçôas, Ermelinda; Campaña, Araceli G
Enantiopure distorted ribbon-shaped nanographene combining two-photon absorption-based upconversion and circularly polarized luminescence.
Chemical science, 2018, 9, 3917-3924
1549080 CIFC25 H15 N O2P 1 21/n 115.4892; 7.8471; 15.5804
90; 114.831; 90
1718.65Mu, Yingxiao; Yang, Zhiyong; Chen, Junru; Yang, Zhan; Li, Wenlang; Tan, Xianbao; Mao, Zhu; Yu, Tao; Zhao, Juan; Zheng, Shizhao; Liu, Siwei; Zhang, Yi; Chi, Zhenguo; Xu, Jiarui; Aldred, Matthew P.
Mechano-induced persistent room-temperature phosphorescence from purely organic molecules.
Chemical science, 2018, 9, 3782-3787
1549081 CIFC57 H83 B2 Li O4P c c n21.5605; 26.1802; 19.2608
90; 90; 90
10871.9Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549082 CIFC56 H85 B2 Li O4P 1 21/n 110.7242; 21.4641; 24.027
90; 97.208; 90
5487Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549083 CIFC44 H56 B2P -15.974; 14.639; 21.461
82.273; 89.91; 86.79
1856.8Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549084 CIFC66 H98 B2 Li2 O7P 1 21/c 112.9451; 18.3459; 27.0962
90; 101.393; 90
6308.3Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549085 CIFC53 H75 B2 Li O3P 1 21 114.775; 19.9973; 17.9098
90; 109.105; 90
5000.2Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549086 CIFC61 H90 B2 Cl Li O8F d d 212.2698; 43.946; 21.961
90; 90; 90
11841.6Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549087 CIFC63 H87 B2 Li O4P 1 21/c 119.497; 24.7864; 23.972
90; 92.463; 90
11574Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549088 CIFC43 H54 B2P c a 2141.344; 14.272; 6.1349
90; 90; 90
3620Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549089 CIFC70 H84 B2 OP -110.4041; 11.5484; 25.736
79.323; 85.313; 81.22
2998.51Kaese, Thomas; Trageser, Timo; Budy, Hendrik; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A redox-active diborane platform performs C(sp<sup>3</sup>)-H activation and nucleophilic substitution reactions.
Chemical science, 2018, 9, 3881-3891
1549094 CIFC26 H32 O2 S2I 1 2/a 17.7604; 5.9132; 49.45
90; 95.879; 90
2257.3van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549095 CIFC26 H32 O2 S2I 1 2/a 17.856; 5.8413; 49.561
90; 95.46; 90
2264van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549096 CIFC26 H32 O2 S2I 1 2/a 18.0891; 5.7282; 49.849
90; 94.255; 90
2303.4van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549097 CIFC26 H32 O2 S2I 1 2/a 17.9306; 5.8288; 49.645
90; 95.171; 90
2285.5van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549098 CIFC26 H32 O2 S2I 1 2/a 17.9631; 5.8073; 49.723
90; 94.85; 90
2291.2van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549099 CIFC26 H32 O2 S2I 1 2/a 18.3546; 5.6236; 50.168
90; 93.146; 90
2353.5van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549100 CIFC26 H32 O2 S2I 1 2/a 18.0248; 5.7688; 49.827
90; 94.591; 90
2299.3van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549101 CIFC26 H32 O2 S2I 1 2/a 18.446; 5.58942; 50.2534
90; 92.829; 90
2369.48van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549102 CIFC26 H32 O2 S2I 1 2/a 17.8186; 5.8811; 49.458
90; 95.762; 90
2262.7van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549103 CIFC26 H32 O2 S2I 1 2/a 18.1615; 5.6918; 49.87
90; 93.819; 90
2311.5van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549104 CIFC26 H32 O2 S2I 1 2/a 18.2606; 5.6541; 49.944
90; 93.621; 90
2328van der Lee, Arie; Roche, Gilles H.; Wantz, Guillaume; Moreau, Joël J E; Dautel, Olivier J.; Filhol, Jean-Sébastien
Experimental and theoretical evidence of a supercritical-like transition in an organic semiconductor presenting colossal uniaxial negative thermal expansion.
Chemical science, 2018, 9, 3948-3956
1549107 CIFC30 H60 Br2 F4 Ni2 P4P -111.059; 12.1681; 15.1847
75.96; 89.526; 89.997
1982.25Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549108 CIFC18 H30 F5 I Ni P2I 1 2 18.0074; 11.3665; 12.9665
90; 94.616; 90
1176.33Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549109 CIFC18 H30 F5 I Ni P2I 1 2 17.8675; 11.3291; 12.9347
90; 94.392; 90
1149.51Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549110 CIFC18 H30 F4 Ni P2P 43 21 28.13398; 8.13398; 31.6136
90; 90; 90
2091.61Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549111 CIFC18 H30 F4 I2 Ni P2C m c 2112.6196; 14.8011; 13.2994
90; 90; 90
2484.11Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549112 CIFC18 H30 F4 I2 Ni P2P b c a14.0519; 14.4485; 24.3473
90; 90; 90
4943.2Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549113 CIFC18 H30 F4 I2 Ni P2P 1 21/c 19.9032; 16.1922; 15.2884
90; 93.913; 90
2445.85Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549114 CIFC18 H30 F5 I Ni P2P 1 21 19.4116; 12.701; 9.727
90; 95.377; 90
1157.62Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549115 CIFC18 H30 F5 I Ni P2I 1 2 17.892; 11.3325; 12.9439
90; 94.434; 90
1154.19Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549116 CIFC18 H30 Cl F4 I Ni P2P 1 21/c 19.95341; 16.0611; 15.04577
90; 97.0034; 90
2387.31Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549117 CIFC18 H30 Br F4 I Ni P2P 1 21/c 19.95422; 16.0712; 15.0877
90; 95.7803; 90
2401.4Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549118 CIFC18 H30 F5 I Ni P2C 1 c 117.1652; 8.5185; 16.935
90; 96.803; 90
2458.8Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549119 CIFC18 H30 Cl F4 I Ni P2P 1 21 19.2736; 13.2118; 9.817
90; 95.22; 90
1197.8Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549120 CIFC26 H30 F4 I2 Ni P2P -17.8141; 12.9211; 14.7784
76.749; 79.7; 76.748
1401.12Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549121 CIFC18 H30 F4 I2 Ni P2P 1 21/c 112.19004; 28.0191; 14.2344
90; 91.6129; 90
4859.89Thangavadivale, Vargini; Aguiar, Pedro M.; Jasim, Naseralla A.; Pike, Sarah J.; Smith, Dan A.; Whitwood, Adrian C.; Brammer, Lee; Perutz, Robin N.
Self-complementary nickel halides enable multifaceted comparisons of intermolecular halogen bonds: fluoride ligands <i>vs.</i> other halides.
Chemical science, 2018, 9, 3767-3781
1549122 CIFC69 H54 Fe N6 O4 P2P 1 21/c 117.9956; 14.2843; 23.6299
90; 111.37; 90
5656.57Lim, Jia Hui; Engelmann, Xenia; Corby, Sacha; Ganguly, Rakesh; Ray, Kallol; Soo, Han Sen
C-H activation and nucleophilic substitution in a photochemically generated high valent iron complex.
Chemical science, 2018, 9, 3992-4002
1549123 CIFC62 H34 F12 Fe N6 P2F d d 227.5449; 55.4159; 10.2412
90; 90; 90
15632Brandl, Thomas; Hoffmann, Viktor; Pannwitz, Andrea; Häussinger, Daniel; Neuburger, Markus; Fuhr, Olaf; Bernhard, Stefan; Wenger, Oliver S.; Mayor, Marcel
Chiral macrocyclic terpyridine complexes.
Chemical science, 2018, 9, 3837-3843
1549124 CIFC66 H44 F12 N6 O P2 RuP -4 21 c16.392; 16.392; 21.9038
90; 90; 90
5885.5Brandl, Thomas; Hoffmann, Viktor; Pannwitz, Andrea; Häussinger, Daniel; Neuburger, Markus; Fuhr, Olaf; Bernhard, Stefan; Wenger, Oliver S.; Mayor, Marcel
Chiral macrocyclic terpyridine complexes.
Chemical science, 2018, 9, 3837-3843
1549133 CIFC23 H23 Au F6 N O SbP 21 21 216.6287; 16.4246; 21.5858
90; 90; 90
2350.1Serra, Jordi; Font, Pau; Sosa Carrizo, E. Daiann; Mallet-Ladeira, Sonia; Massou, Stéphane; Parella, Teodor; Miqueu, Karinne; Amgoune, Abderrahmane; Ribas, Xavi; Bourissou, Didier
Cyclometalated gold(iii) complexes: noticeable differences between (N,C) and (P,C) ligands in migratory insertion.
Chemical science, 2018, 9, 3932-3940
1549134 CIFC24 H22 Au Cl4 NP -17.4651; 9.8244; 16.963
98.935; 91.454; 106.868
1172.83Serra, Jordi; Font, Pau; Sosa Carrizo, E. Daiann; Mallet-Ladeira, Sonia; Massou, Stéphane; Parella, Teodor; Miqueu, Karinne; Amgoune, Abderrahmane; Ribas, Xavi; Bourissou, Didier
Cyclometalated gold(iii) complexes: noticeable differences between (N,C) and (P,C) ligands in migratory insertion.
Chemical science, 2018, 9, 3932-3940
1549135 CIFC55 H62 N2 P2P 1 21/n 110.9502; 20.9614; 20.7528
90; 97.766; 90
4719.7Dhara, Debabrata; Kalita, Pankaj; Mondal, Subhadip; Narayanan, Ramakirushnan Suriya; Mote, Kaustubh R.; Huch, Volker; Zimmer, Michael; Yildiz, Cem B.; Scheschkewitz, David; Chandrasekhar, Vadapalli; Jana, Anukul
Reactivity enhancement of a diphosphene by reversible N-heterocyclic carbene coordination.
Chemical science, 2018, 9, 4235-4243
1549136 CIFC48 H52 P2P 1 21/c 18.3846; 21.347; 11.6195
90; 111.081; 90
1940.5Dhara, Debabrata; Kalita, Pankaj; Mondal, Subhadip; Narayanan, Ramakirushnan Suriya; Mote, Kaustubh R.; Huch, Volker; Zimmer, Michael; Yildiz, Cem B.; Scheschkewitz, David; Chandrasekhar, Vadapalli; Jana, Anukul
Reactivity enhancement of a diphosphene by reversible N-heterocyclic carbene coordination.
Chemical science, 2018, 9, 4235-4243
1549137 CIFC31 H37 N2 PP 1 21/c 18.304; 23.286; 13.9
90; 90.34; 90
2687.8Dhara, Debabrata; Kalita, Pankaj; Mondal, Subhadip; Narayanan, Ramakirushnan Suriya; Mote, Kaustubh R.; Huch, Volker; Zimmer, Michael; Yildiz, Cem B.; Scheschkewitz, David; Chandrasekhar, Vadapalli; Jana, Anukul
Reactivity enhancement of a diphosphene by reversible N-heterocyclic carbene coordination.
Chemical science, 2018, 9, 4235-4243
1549138 CIFC48 H52 O P2P b c a16.9466; 20.6986; 23.0289
90; 90; 90
8077.9Dhara, Debabrata; Kalita, Pankaj; Mondal, Subhadip; Narayanan, Ramakirushnan Suriya; Mote, Kaustubh R.; Huch, Volker; Zimmer, Michael; Yildiz, Cem B.; Scheschkewitz, David; Chandrasekhar, Vadapalli; Jana, Anukul
Reactivity enhancement of a diphosphene by reversible N-heterocyclic carbene coordination.
Chemical science, 2018, 9, 4235-4243
1549139 CIFC55 H64 N2 O P2P 1 21/n 116.228; 16.3739; 17.6769
90; 93.71; 90
4687.2Dhara, Debabrata; Kalita, Pankaj; Mondal, Subhadip; Narayanan, Ramakirushnan Suriya; Mote, Kaustubh R.; Huch, Volker; Zimmer, Michael; Yildiz, Cem B.; Scheschkewitz, David; Chandrasekhar, Vadapalli; Jana, Anukul
Reactivity enhancement of a diphosphene by reversible N-heterocyclic carbene coordination.
Chemical science, 2018, 9, 4235-4243
1549140 CIFC65 H42 F6 N4 O11P -110.6269; 14.921; 17.4851
108.065; 102.085; 91.766
2563.72Shaw, John S.; Vaiyapuri, Rajendran; Parker, Matthew P.; Murray, Claire A.; Lim, Kate J. C.; Pan, Cong; Knappert, Marcus; Cardin, Christine J.; Greenland, Barnaby W.; Grau-Crespo, Ricardo; Colquhoun, Howard M.
Elements of fractal geometry in the <sup>1</sup>H NMR spectrum of a copolymer intercalation-complex: identification of the underlying Cantor set.
Chemical science, 2018, 9, 4052-4061
1549141 CIFC34 H37 B N2P 1 21/c 122.653; 8.3251; 15.2916
90; 107.682; 90
2747.6Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549142 CIFC32 H36 B N SP 1 21/c 17.925; 21.8524; 16.0075
90; 98.766; 90
2739.8Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549143 CIFC34 H39 B N2P -110.294; 11.896; 13.128
66.239; 88.621; 75.243
1417.2Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549144 CIFC34 H39 B N2P 1 21/n 18.41; 34.22; 10.14
90; 97.87; 90
2891Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549145 CIFC32 H36 B N SP 1 21/c 17.9779; 21.8456; 15.7662
90; 98.411; 90
2718.2Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549146 CIFC35 H40 B N OP 1 21/c 17.2959; 22.3592; 17.984
90; 92.626; 90
2930.7Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549147 CIFC39 H43 B N2P -18.1029; 11.3778; 18.5298
87.821; 85.222; 71.032
1609.84Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549148 CIFC32 H34 B N SP n a 2132.54; 9.129; 9.286
90; 90; 90
2758Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549149 CIFC34 H38 B NP -17.868; 12.043; 16.695
69.575; 77.359; 76.219
1423.7Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549150 CIFC45 H49 B N2P -111.4473; 11.8684; 15.9919
94.282; 106.166; 114.679
1850.2Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549151 CIFC33 H35 B N2P 1 21/c 122.112; 8.318; 15.429
90; 110.321; 90
2661.2Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549152 CIFC31 H32 B NP 1 21/c 111.8634; 11.878; 18.2134
90; 92.179; 90
2564.7Shi, Yong-Gang; Mellerup, Soren K.; Yuan, Kang; Hu, Guo-Fei; Sauriol, Francoise; Peng, Tai; Wang, Nan; Chen, Pangkuan; Wang, Suning
Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.
Chemical science, 2018, 9, 3844-3855
1549153 CIFC9 H19 B10 NP -17.3461; 7.8073; 12.765
81.469; 78.051; 86.599
708Zhang, Xiaolei; Yan, Hong
Pd(ii)-catalyzed synthesis of bifunctionalized carboranes <i>via</i> cage B-H activation of 1-CH<sub>2</sub>NH<sub>2</sub>-<i>o</i>-carboranes.
Chemical science, 2018, 9, 3964-3969
1549154 CIFC21 H21 B10 Br2 NP 1 21/n 112.4232; 14.9794; 13.9157
90; 109.509; 90
2440.93Zhang, Xiaolei; Yan, Hong
Pd(ii)-catalyzed synthesis of bifunctionalized carboranes <i>via</i> cage B-H activation of 1-CH<sub>2</sub>NH<sub>2</sub>-<i>o</i>-carboranes.
Chemical science, 2018, 9, 3964-3969
1549155 CIFC23 H26 B10 F3 N OP 1 21/n 118.1161; 8.1173; 18.6508
90; 113.681; 90
2511.7Zhang, Xiaolei; Yan, Hong
Pd(ii)-catalyzed synthesis of bifunctionalized carboranes <i>via</i> cage B-H activation of 1-CH<sub>2</sub>NH<sub>2</sub>-<i>o</i>-carboranes.
Chemical science, 2018, 9, 3964-3969
1549156 CIFC25 H35 B10 NP 21 21 218.0494; 15.8108; 20.486
90; 90; 90
2607.2Zhang, Xiaolei; Yan, Hong
Pd(ii)-catalyzed synthesis of bifunctionalized carboranes <i>via</i> cage B-H activation of 1-CH<sub>2</sub>NH<sub>2</sub>-<i>o</i>-carboranes.
Chemical science, 2018, 9, 3964-3969
1549157 CIFC21 H28 B10 N2 O2 SP -17.7385; 10.4142; 15.9824
92.169; 102.976; 99.951
1232.3Zhang, Xiaolei; Yan, Hong
Pd(ii)-catalyzed synthesis of bifunctionalized carboranes <i>via</i> cage B-H activation of 1-CH<sub>2</sub>NH<sub>2</sub>-<i>o</i>-carboranes.
Chemical science, 2018, 9, 3964-3969
1549158 CIFC34 H35 B10 N O P PdP 1 21/c 110.5093; 22.2105; 15.7027
90; 105.021; 90
3540Zhang, Xiaolei; Yan, Hong
Pd(ii)-catalyzed synthesis of bifunctionalized carboranes <i>via</i> cage B-H activation of 1-CH<sub>2</sub>NH<sub>2</sub>-<i>o</i>-carboranes.
Chemical science, 2018, 9, 3964-3969
1549159 CIFC25 H40 B20 N2 O PdP 1 21/c 114.4456; 13.2757; 19.9354
90; 90.292; 90
3823.1Zhang, Xiaolei; Yan, Hong
Pd(ii)-catalyzed synthesis of bifunctionalized carboranes <i>via</i> cage B-H activation of 1-CH<sub>2</sub>NH<sub>2</sub>-<i>o</i>-carboranes.
Chemical science, 2018, 9, 3964-3969
1549160 CIFC19 H31 B10 NC 1 2/c 117.6118; 12.1001; 20.3538
90; 94.094; 90
4326.4Zhang, Xiaolei; Yan, Hong
Pd(ii)-catalyzed synthesis of bifunctionalized carboranes <i>via</i> cage B-H activation of 1-CH<sub>2</sub>NH<sub>2</sub>-<i>o</i>-carboranes.
Chemical science, 2018, 9, 3964-3969
1549222 CIFC24 H37 N2 O2 PC 1 2/c 119.931; 12.616; 21.565
90; 109.346; 90
5116Lin, Yi-Chun; Gilhula, James C.; Radosevich, Alexander T.
Nontrigonal constraint enhances 1,2-addition reactivity of phosphazenes.
Chemical science, 2018, 9, 4338-4347
1549223 CIFC24 H41 N4 PP 1 21/c 18.3589; 16.491; 18.049
90; 93.77; 90
2482.6Lin, Yi-Chun; Gilhula, James C.; Radosevich, Alexander T.
Nontrigonal constraint enhances 1,2-addition reactivity of phosphazenes.
Chemical science, 2018, 9, 4338-4347
1549224 CIFC26 H33 N2 O2 PP 1 21/n 18.587; 17.687; 16.43
90; 99.539; 90
2460.9Lin, Yi-Chun; Gilhula, James C.; Radosevich, Alexander T.
Nontrigonal constraint enhances 1,2-addition reactivity of phosphazenes.
Chemical science, 2018, 9, 4338-4347
1549225 CIFC26 H31 N4 PP 1 21/n 112.8565; 9.4531; 19.152
90; 96.382; 90
2313.2Lin, Yi-Chun; Gilhula, James C.; Radosevich, Alexander T.
Nontrigonal constraint enhances 1,2-addition reactivity of phosphazenes.
Chemical science, 2018, 9, 4338-4347
1549226 CIFC48 H74 N4 O4 P2C 1 2/c 127.535; 11.39; 20.157
90; 129.45; 90
4881Lin, Yi-Chun; Gilhula, James C.; Radosevich, Alexander T.
Nontrigonal constraint enhances 1,2-addition reactivity of phosphazenes.
Chemical science, 2018, 9, 4338-4347
1549227 CIFC38 H54 N4 O4 P2P 1 21/n 19.2449; 21.052; 20.977
90; 94.271; 90
4071.3Lin, Yi-Chun; Gilhula, James C.; Radosevich, Alexander T.
Nontrigonal constraint enhances 1,2-addition reactivity of phosphazenes.
Chemical science, 2018, 9, 4338-4347
1549228 CIFC34 H50 B N2 O5 PP b c a19.707; 17.611; 20.439
90; 90; 90
7094Lin, Yi-Chun; Gilhula, James C.; Radosevich, Alexander T.
Nontrigonal constraint enhances 1,2-addition reactivity of phosphazenes.
Chemical science, 2018, 9, 4338-4347
1549236 CIFC27 H22 B Br2 NP 1 21 111.269; 7.3358; 14.2605
90; 101.418; 90
1155.54Zhang, Weidong; Li, Guoping; Xu, Letian; Zhuo, Yue; Wan, Wenming; Yan, Ni; He, Gang
9,10-Azaboraphenanthrene-containing small molecules and conjugated polymers: synthesis and their application in chemodosimeters for the ratiometric detection of fluoride ions.
Chemical science, 2018, 9, 4444-4450
1549237 CIFC22 H30 Cl N O4 SP 1 21/n 112.0663; 10.1526; 18.2867
90; 103.196; 90
2181.05Maryasin, Boris; Kaldre, Dainis; Galaverna, Renan; Klose, Immo; Ruider, Stefan; Drescher, Martina; Kählig, Hanspeter; González, Leticia; Eberlin, Marcos N.; Jurberg, Igor D.; Maulide, Nuno
Unusual mechanisms in Claisen rearrangements: an ionic fragmentation leading to a <i>meta</i>-selective rearrangement.
Chemical science, 2018, 9, 4124-4131
1549238 CIFC23 H19 N O3 SF d d 222.362; 58.28; 5.779
90; 90; 90
7532Maryasin, Boris; Kaldre, Dainis; Galaverna, Renan; Klose, Immo; Ruider, Stefan; Drescher, Martina; Kählig, Hanspeter; González, Leticia; Eberlin, Marcos N.; Jurberg, Igor D.; Maulide, Nuno
Unusual mechanisms in Claisen rearrangements: an ionic fragmentation leading to a <i>meta</i>-selective rearrangement.
Chemical science, 2018, 9, 4124-4131
1549239 CIFC20 H25 N O5 SP c a 2111.7592; 10.1198; 32.161
90; 90; 90
3827.2Maryasin, Boris; Kaldre, Dainis; Galaverna, Renan; Klose, Immo; Ruider, Stefan; Drescher, Martina; Kählig, Hanspeter; González, Leticia; Eberlin, Marcos N.; Jurberg, Igor D.; Maulide, Nuno
Unusual mechanisms in Claisen rearrangements: an ionic fragmentation leading to a <i>meta</i>-selective rearrangement.
Chemical science, 2018, 9, 4124-4131
1549244 CIFC36 H56 Cu F6 N3 Sb Si3P 1 21/n 114.617; 14.759; 21.243
90; 107.874; 90
4362Parvin, Nasrina; Pal, Shiv; Echeverría, Jorge; Alvarez, Santiago; Khan, Shabana
Taming a monomeric [Cu(η<sup>6</sup>-C<sub>6</sub>H<sub>6</sub>)]<sup>+</sup> complex with silylene.
Chemical science, 2018, 9, 4333-4337
1549245 CIFC33 H42 Cu F6 N2 SbP 1 21/c 113.3555; 13.9173; 18.181
90; 102.245; 90
3302.5Parvin, Nasrina; Pal, Shiv; Echeverría, Jorge; Alvarez, Santiago; Khan, Shabana
Taming a monomeric [Cu(η<sup>6</sup>-C<sub>6</sub>H<sub>6</sub>)]<sup>+</sup> complex with silylene.
Chemical science, 2018, 9, 4333-4337
1549246 CIFC40 H56 Cl2 Cu F6 N2 SbP 1 21/n 110.506; 20.813; 20.435
90; 104.638; 90
4323Parvin, Nasrina; Pal, Shiv; Echeverría, Jorge; Alvarez, Santiago; Khan, Shabana
Taming a monomeric [Cu(η<sup>6</sup>-C<sub>6</sub>H<sub>6</sub>)]<sup>+</sup> complex with silylene.
Chemical science, 2018, 9, 4333-4337
1549247 CIFC33 H59 Cu F6 N3 Sb Si3P 1 21/c 113.605; 14.057; 21.79
90; 107.833; 90
3967Parvin, Nasrina; Pal, Shiv; Echeverría, Jorge; Alvarez, Santiago; Khan, Shabana
Taming a monomeric [Cu(η<sup>6</sup>-C<sub>6</sub>H<sub>6</sub>)]<sup>+</sup> complex with silylene.
Chemical science, 2018, 9, 4333-4337
1549253 CIFC26 H49 F3 Ir N2 O2 P2P b c a14.6519; 15.5746; 27.2406
90; 90; 90
6216.2Kinauer, Markus; Diefenbach, Martin; Bamberger, Heiko; Demeshko, Serhiy; Reijerse, Edward J.; Volkmann, Christian; Würtele, Christian; van Slageren, Joris; de Bruin, Bas; Holthausen, Max C.; Schneider, Sven
An iridium(iii/iv/v) redox series featuring a terminal imido complex with triplet ground state.
Chemical science, 2018, 9, 4325-4332
1549254 CIFC31 H55 Ir N2 O2 P2P 1 21/c 111.2846; 14.9634; 19.8058
90; 92.013; 90
3342.3Kinauer, Markus; Diefenbach, Martin; Bamberger, Heiko; Demeshko, Serhiy; Reijerse, Edward J.; Volkmann, Christian; Würtele, Christian; van Slageren, Joris; de Bruin, Bas; Holthausen, Max C.; Schneider, Sven
An iridium(iii/iv/v) redox series featuring a terminal imido complex with triplet ground state.
Chemical science, 2018, 9, 4325-4332
1549255 CIFC24 H49 Ir N2 P2P 1 21/c 111.0958; 15.4511; 16.0856
90; 100.56; 90
2711Kinauer, Markus; Diefenbach, Martin; Bamberger, Heiko; Demeshko, Serhiy; Reijerse, Edward J.; Volkmann, Christian; Würtele, Christian; van Slageren, Joris; de Bruin, Bas; Holthausen, Max C.; Schneider, Sven
An iridium(iii/iv/v) redox series featuring a terminal imido complex with triplet ground state.
Chemical science, 2018, 9, 4325-4332
1549256 CIFC25 H49 Ir N2 O2 P2P 1 21/m 17.9728; 21.7175; 8.7383
90; 113.559; 90
1386.92Kinauer, Markus; Diefenbach, Martin; Bamberger, Heiko; Demeshko, Serhiy; Reijerse, Edward J.; Volkmann, Christian; Würtele, Christian; van Slageren, Joris; de Bruin, Bas; Holthausen, Max C.; Schneider, Sven
An iridium(iii/iv/v) redox series featuring a terminal imido complex with triplet ground state.
Chemical science, 2018, 9, 4325-4332
1549269 CIFC28 H33 Br N2 O3P 1 21 15.4738; 16.81; 14.183
90; 95.627; 90
1298.8Hu, Qiupeng; Kondoh, Azusa; Terada, Masahiro
Enantioselective direct Mannich-type reactions of 2-benzylpyridine N-oxides catalyzed by chiral bis(guanidino)iminophosphorane organosuperbase.
Chemical science, 2018, 9, 4348-4351
1549270 CIFC32 H33 N O3P 31 2 112.0961; 12.0961; 30.6664
90; 90; 120
3885.8Volpe, Rohan; Lepage, Romain J.; White, Jonathan M.; Krenske, Elizabeth H.; Flynn, Bernard L.
Asymmetric synthesis of multiple quaternary stereocentre-containing cyclopentyls by oxazolidinone-promoted Nazarov cyclizations.
Chemical science, 2018, 9, 4644-4649
1549271 CIFC32 H33 N O3P 1 21 110.2041; 12.0967; 10.8841
90; 109.609; 90
1265.57Volpe, Rohan; Lepage, Romain J.; White, Jonathan M.; Krenske, Elizabeth H.; Flynn, Bernard L.
Asymmetric synthesis of multiple quaternary stereocentre-containing cyclopentyls by oxazolidinone-promoted Nazarov cyclizations.
Chemical science, 2018, 9, 4644-4649
1549273 CIFC45 H58 Cl4 Cu2 O4 P4P 21 21 2110.5101; 20.6596; 22.4637
90; 90; 90
4877.6Zatolochnaya, Olga V.; Rodríguez, Sonia; Zhang, Yongda; Lao, Kendricks S.; Tcyrulnikov, Sergei; Li, Guisheng; Wang, Xiao-Jun; Qu, Bo; Biswas, Soumik; Mangunuru, Hari P. R.; Rivalti, Daniel; Sieber, Joshua D.; Desrosiers, Jean-Nicolas; Leung, Joyce C.; Grinberg, Nelu; Lee, Heewon; Haddad, Nizar; Yee, Nathan K.; Song, Jinhua J.; Kozlowski, Marisa C.; Senanayake, Chris H.
Copper-catalyzed asymmetric hydrogenation of 2-substituted ketones <i>via</i> dynamic kinetic resolution.
Chemical science, 2018, 9, 4505-4510
1549274 CIFC64 H92 Cl2 Cu2 N4 O4 P4P 21 21 2113.69; 16.8264; 30.4315
90; 90; 90
7010Zatolochnaya, Olga V.; Rodríguez, Sonia; Zhang, Yongda; Lao, Kendricks S.; Tcyrulnikov, Sergei; Li, Guisheng; Wang, Xiao-Jun; Qu, Bo; Biswas, Soumik; Mangunuru, Hari P. R.; Rivalti, Daniel; Sieber, Joshua D.; Desrosiers, Jean-Nicolas; Leung, Joyce C.; Grinberg, Nelu; Lee, Heewon; Haddad, Nizar; Yee, Nathan K.; Song, Jinhua J.; Kozlowski, Marisa C.; Senanayake, Chris H.
Copper-catalyzed asymmetric hydrogenation of 2-substituted ketones <i>via</i> dynamic kinetic resolution.
Chemical science, 2018, 9, 4505-4510
1549275 CIFC36 H35 B F15 PC 1 2/c 128.898; 11.2532; 21.7565
90; 105.318; 90
6823.8Wang, Long; Kehr, Gerald; Daniliuc, Constantin G.; Brinkkötter, Melanie; Wiegand, Thomas; Wübker, Anna-Lena; Eckert, Hellmut; Liu, Lei; Brandenburg, Jan Gerit; Grimme, Stefan; Erker, Gerhard
Solid state frustrated Lewis pair chemistry.
Chemical science, 2018, 9, 4859-4865
1549276 CIFC36 H33 B F15 O2 P SP -110.9369; 12.602; 15.7611
90.384; 97.992; 111.759
1993.92Wang, Long; Kehr, Gerald; Daniliuc, Constantin G.; Brinkkötter, Melanie; Wiegand, Thomas; Wübker, Anna-Lena; Eckert, Hellmut; Liu, Lei; Brandenburg, Jan Gerit; Grimme, Stefan; Erker, Gerhard
Solid state frustrated Lewis pair chemistry.
Chemical science, 2018, 9, 4859-4865
1549277 CIFC38 H37 B Cl4 F15 PP b c a20.8497; 16.0333; 23.8954
90; 90; 90
7988Wang, Long; Kehr, Gerald; Daniliuc, Constantin G.; Brinkkötter, Melanie; Wiegand, Thomas; Wübker, Anna-Lena; Eckert, Hellmut; Liu, Lei; Brandenburg, Jan Gerit; Grimme, Stefan; Erker, Gerhard
Solid state frustrated Lewis pair chemistry.
Chemical science, 2018, 9, 4859-4865
1549278 CIFC20 H19 N OP 1 21/c 19.5578; 20.653; 8.4644
90; 108.514; 90
1584.4Mokar, Bhanudas Dattatray; Jadhav, Prakash D.; Pandit, Y. B.; Liu, Rai-Shung
Gold-catalyzed (4 + 2)-annulations between α-alkyl alkenylgold carbenes and benzisoxazoles with reactive alkyl groups.
Chemical science, 2018, 9, 4488-4492
1549279 CIFC18 H20 Br N OP -17.6388; 11.2206; 11.3511
116.079; 109.218; 91.505
808.23Mokar, Bhanudas Dattatray; Jadhav, Prakash D.; Pandit, Y. B.; Liu, Rai-Shung
Gold-catalyzed (4 + 2)-annulations between α-alkyl alkenylgold carbenes and benzisoxazoles with reactive alkyl groups.
Chemical science, 2018, 9, 4488-4492
1549280 CIFC21.5 H19.5 Cl1.5 N O3P -111.282; 11.457; 14.934
84.071; 88.539; 84.074
1910Mokar, Bhanudas Dattatray; Jadhav, Prakash D.; Pandit, Y. B.; Liu, Rai-Shung
Gold-catalyzed (4 + 2)-annulations between α-alkyl alkenylgold carbenes and benzisoxazoles with reactive alkyl groups.
Chemical science, 2018, 9, 4488-4492
1549281 CIFC22 H21 N O5P 1 21/c 111.8837; 10.0611; 19.6889
90; 107.518; 90
2244.9Mokar, Bhanudas Dattatray; Jadhav, Prakash D.; Pandit, Y. B.; Liu, Rai-Shung
Gold-catalyzed (4 + 2)-annulations between α-alkyl alkenylgold carbenes and benzisoxazoles with reactive alkyl groups.
Chemical science, 2018, 9, 4488-4492
1549282 CIFC43 H58 B Co F3 N6 O3 SP -111.3925; 16.9868; 21.7195
94.871; 98.674; 92.305
4134.1Hill, Ethan A.; Kelty, Margaret L.; Filatov, Alexander S.; Anderson, John S.
Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C-H activation reactivity.
Chemical science, 2018, 9, 4493-4499
1549283 CIFC63 H59 B2 Co F24 I N6 O3 SP 110.4248; 12.9027; 15.4799
101.302; 105.089; 113.446
1735.7Hill, Ethan A.; Kelty, Margaret L.; Filatov, Alexander S.; Anderson, John S.
Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C-H activation reactivity.
Chemical science, 2018, 9, 4493-4499
1549284 CIFC26 H44 B Co F3 N6 O4 SP 1 21/n 110.4361; 20.2414; 15.3862
90; 91.209; 90
3249.5Hill, Ethan A.; Kelty, Margaret L.; Filatov, Alexander S.; Anderson, John S.
Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C-H activation reactivity.
Chemical science, 2018, 9, 4493-4499
1549285 CIFC84.5 H84 B2 Cl Co F24 I N6 O3 SP -114.2995; 16.0821; 38.551
95.079; 97.357; 97.863
8658.9Hill, Ethan A.; Kelty, Margaret L.; Filatov, Alexander S.; Anderson, John S.
Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C-H activation reactivity.
Chemical science, 2018, 9, 4493-4499
1549286 CIFC71 H77 B2 Co F24 I N6 O6 SP -113.018; 17.299; 19.933
69.338; 77.588; 78.279
4062Hill, Ethan A.; Kelty, Margaret L.; Filatov, Alexander S.; Anderson, John S.
Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C-H activation reactivity.
Chemical science, 2018, 9, 4493-4499
1549287 CIFC93 H100 B2 Co F27 N8 O4 SP b c a21.493; 22.3378; 38.715
90; 90; 90
18587Hill, Ethan A.; Kelty, Margaret L.; Filatov, Alexander S.; Anderson, John S.
Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C-H activation reactivity.
Chemical science, 2018, 9, 4493-4499
1549288 CIFC28 H20P 21 21 218.3475; 10.314; 21.0732
90; 90; 90
1814.32Cai, Yuanjing; Du, Lili; Samedov, Kerim; Gu, Xinggui; Qi, Fei; Sung, Herman H. Y.; Patrick, Brian O.; Yan, Zhiping; Jiang, Xiaofang; Zhang, Haoke; Lam, Jacky W. Y.; Williams, Ian D.; Lee Phillips, David; Qin, Anjun; Tang, Ben Zhong
Deciphering the working mechanism of aggregation-induced emission of tetraphenylethylene derivatives by ultrafast spectroscopy.
Chemical science, 2018, 9, 4662-4670
1549289 CIFC30 H28P 1 21/c 118.1203; 6.99093; 19.2375
90; 112.45; 90
2252.27Cai, Yuanjing; Du, Lili; Samedov, Kerim; Gu, Xinggui; Qi, Fei; Sung, Herman H. Y.; Patrick, Brian O.; Yan, Zhiping; Jiang, Xiaofang; Zhang, Haoke; Lam, Jacky W. Y.; Williams, Ian D.; Lee Phillips, David; Qin, Anjun; Tang, Ben Zhong
Deciphering the working mechanism of aggregation-induced emission of tetraphenylethylene derivatives by ultrafast spectroscopy.
Chemical science, 2018, 9, 4662-4670
1549290 CIFC30 H24P 1 21/c 111.90924; 17.5617; 9.90343
90; 101.393; 90
2030.45Cai, Yuanjing; Du, Lili; Samedov, Kerim; Gu, Xinggui; Qi, Fei; Sung, Herman H. Y.; Patrick, Brian O.; Yan, Zhiping; Jiang, Xiaofang; Zhang, Haoke; Lam, Jacky W. Y.; Williams, Ian D.; Lee Phillips, David; Qin, Anjun; Tang, Ben Zhong
Deciphering the working mechanism of aggregation-induced emission of tetraphenylethylene derivatives by ultrafast spectroscopy.
Chemical science, 2018, 9, 4662-4670
1549291 CIFC30 H28P 1 21/n 114.1772; 10.8633; 14.2137
90; 95.1137; 90
2180.36Cai, Yuanjing; Du, Lili; Samedov, Kerim; Gu, Xinggui; Qi, Fei; Sung, Herman H. Y.; Patrick, Brian O.; Yan, Zhiping; Jiang, Xiaofang; Zhang, Haoke; Lam, Jacky W. Y.; Williams, Ian D.; Lee Phillips, David; Qin, Anjun; Tang, Ben Zhong
Deciphering the working mechanism of aggregation-induced emission of tetraphenylethylene derivatives by ultrafast spectroscopy.
Chemical science, 2018, 9, 4662-4670
1549292 CIFC30 H26P 1 21/c 117.4337; 6.9903; 17.935
90; 103.64; 90
2124Cai, Yuanjing; Du, Lili; Samedov, Kerim; Gu, Xinggui; Qi, Fei; Sung, Herman H. Y.; Patrick, Brian O.; Yan, Zhiping; Jiang, Xiaofang; Zhang, Haoke; Lam, Jacky W. Y.; Williams, Ian D.; Lee Phillips, David; Qin, Anjun; Tang, Ben Zhong
Deciphering the working mechanism of aggregation-induced emission of tetraphenylethylene derivatives by ultrafast spectroscopy.
Chemical science, 2018, 9, 4662-4670
1549293 CIFC30 H22C 1 2/c 118.2724; 19.5178; 18.301
90; 113.791; 90
5972.2Cai, Yuanjing; Du, Lili; Samedov, Kerim; Gu, Xinggui; Qi, Fei; Sung, Herman H. Y.; Patrick, Brian O.; Yan, Zhiping; Jiang, Xiaofang; Zhang, Haoke; Lam, Jacky W. Y.; Williams, Ian D.; Lee Phillips, David; Qin, Anjun; Tang, Ben Zhong
Deciphering the working mechanism of aggregation-induced emission of tetraphenylethylene derivatives by ultrafast spectroscopy.
Chemical science, 2018, 9, 4662-4670
1549294 CIFC29 H24P 1 21/c 17.396; 30.1314; 18.311
90; 91.801; 90
4078.6Cai, Yuanjing; Du, Lili; Samedov, Kerim; Gu, Xinggui; Qi, Fei; Sung, Herman H. Y.; Patrick, Brian O.; Yan, Zhiping; Jiang, Xiaofang; Zhang, Haoke; Lam, Jacky W. Y.; Williams, Ian D.; Lee Phillips, David; Qin, Anjun; Tang, Ben Zhong
Deciphering the working mechanism of aggregation-induced emission of tetraphenylethylene derivatives by ultrafast spectroscopy.
Chemical science, 2018, 9, 4662-4670
1549295 CIFC28 H22P -111.9827; 13.0612; 14.0684
117.413; 92.608; 90.268
1951.7Cai, Yuanjing; Du, Lili; Samedov, Kerim; Gu, Xinggui; Qi, Fei; Sung, Herman H. Y.; Patrick, Brian O.; Yan, Zhiping; Jiang, Xiaofang; Zhang, Haoke; Lam, Jacky W. Y.; Williams, Ian D.; Lee Phillips, David; Qin, Anjun; Tang, Ben Zhong
Deciphering the working mechanism of aggregation-induced emission of tetraphenylethylene derivatives by ultrafast spectroscopy.
Chemical science, 2018, 9, 4662-4670
1549296 CIFC36 H72 Al Cl Si3 ThP 1 21/n 114.6013; 16.3421; 18.0401
90; 93.323; 90
4297.4Altman, Alison B.; Brown, Alexandra C.; Rao, Guodong; Lohrey, Trevor D.; Britt, R. David; Maron, Laurent; Minasian, Stefan G.; Shuh, David K.; Arnold, John
Chemical structure and bonding in a thorium(iii)-aluminum heterobimetallic complex.
Chemical science, 2018, 9, 4317-4324
1549297 CIFC36 H72 Al Si3 UP -110.4534; 12.854; 17.8476
72.09; 79.893; 66.898
2094.82Altman, Alison B.; Brown, Alexandra C.; Rao, Guodong; Lohrey, Trevor D.; Britt, R. David; Maron, Laurent; Minasian, Stefan G.; Shuh, David K.; Arnold, John
Chemical structure and bonding in a thorium(iii)-aluminum heterobimetallic complex.
Chemical science, 2018, 9, 4317-4324
1549298 CIFC36 H73 Al Si3 ThP 1 21/c 118.541; 12.528; 18.971
90; 105.644; 90
4243Altman, Alison B.; Brown, Alexandra C.; Rao, Guodong; Lohrey, Trevor D.; Britt, R. David; Maron, Laurent; Minasian, Stefan G.; Shuh, David K.; Arnold, John
Chemical structure and bonding in a thorium(iii)-aluminum heterobimetallic complex.
Chemical science, 2018, 9, 4317-4324
1549299 CIFC36 H72 Al Si3 ThP 1 21/m 112.933; 12.816; 13.179
90; 94.46; 90
2178Altman, Alison B.; Brown, Alexandra C.; Rao, Guodong; Lohrey, Trevor D.; Britt, R. David; Maron, Laurent; Minasian, Stefan G.; Shuh, David K.; Arnold, John
Chemical structure and bonding in a thorium(iii)-aluminum heterobimetallic complex.
Chemical science, 2018, 9, 4317-4324
1549300 CIFC62 H88 I2 N4 O2P 1 21/n 114.01776; 11.68842; 18.61137
90; 97.6225; 90
3022.44Rottschäfer, Dennis; Neumann, Beate; Stammler, Hans-Georg; Andrada, Diego M.; Ghadwal, Rajendra S.
Kekulé diradicaloids derived from a classical N-heterocyclic carbene.
Chemical science, 2018, 9, 4970-4976
1549301 CIFC60 H80 N4P -110.4185; 10.5244; 25.1966
97.968; 90.283; 110.092
2565.5Rottschäfer, Dennis; Neumann, Beate; Stammler, Hans-Georg; Andrada, Diego M.; Ghadwal, Rajendra S.
Kekulé diradicaloids derived from a classical N-heterocyclic carbene.
Chemical science, 2018, 9, 4970-4976
1549302 CIFC70 H92 N4 OP -19.397; 11.5574; 15.1108
70.87; 84.424; 76.36
1506.4Rottschäfer, Dennis; Neumann, Beate; Stammler, Hans-Georg; Andrada, Diego M.; Ghadwal, Rajendra S.
Kekulé diradicaloids derived from a classical N-heterocyclic carbene.
Chemical science, 2018, 9, 4970-4976
1549303 CIFC69.21 H96.87 Br2 N4 O3.22P 1 21/n 19.3343; 17.7848; 20.1423
90; 95.674; 90
3327.41Rottschäfer, Dennis; Neumann, Beate; Stammler, Hans-Georg; Andrada, Diego M.; Ghadwal, Rajendra S.
Kekulé diradicaloids derived from a classical N-heterocyclic carbene.
Chemical science, 2018, 9, 4970-4976
1549304 CIFC28 H18 N2 OP 1 21/c 17.463; 23.83; 11.556
90; 101.301; 90
2015.3Zang, Qiguang; Yu, Jiayi; Yu, Wenbin; Qian, Jun; Hu, Rongrong; Tang, Ben Zhong
Red-emissive azabenzanthrone derivatives for photodynamic therapy irradiated with ultralow light power density and two-photon imaging.
Chemical science, 2018, 9, 5165-5171
1549305 CIFC28 H18 N2 OP -17.1516; 8.5555; 16.6112
100.052; 95.016; 90.498
996.63Zang, Qiguang; Yu, Jiayi; Yu, Wenbin; Qian, Jun; Hu, Rongrong; Tang, Ben Zhong
Red-emissive azabenzanthrone derivatives for photodynamic therapy irradiated with ultralow light power density and two-photon imaging.
Chemical science, 2018, 9, 5165-5171
1549306 CIFC366 H508 Cd24 N24 O178 Tb8P 4/n :230.0936; 30.0936; 39.3554
90; 90; 90
35641.2Yang, Xiaoping; Wang, Shiqing; Zhang, Yali; Liang, Guang; Zhu, Ting; Zhang, Lijie; Huang, Shaoming; Schipper, Desmond; Jones, Richard A.
A self-assembling luminescent lanthanide molecular nanoparticle with potential for live cell imaging.
Chemical science, 2018, 9, 4630-4637
1549307 CIFC386 H560 Cd24 N24 O190 Tb8F d d d :254.777; 61.944; 79.935
90; 90; 90
271228Yang, Xiaoping; Wang, Shiqing; Zhang, Yali; Liang, Guang; Zhu, Ting; Zhang, Lijie; Huang, Shaoming; Schipper, Desmond; Jones, Richard A.
A self-assembling luminescent lanthanide molecular nanoparticle with potential for live cell imaging.
Chemical science, 2018, 9, 4630-4637
1549308 CIFC1714.04 H2526.4 Cd96 N96 O683.24 Tb32F d d d :254.621; 61.479; 100.21
90; 90; 90
336510Yang, Xiaoping; Wang, Shiqing; Zhang, Yali; Liang, Guang; Zhu, Ting; Zhang, Lijie; Huang, Shaoming; Schipper, Desmond; Jones, Richard A.
A self-assembling luminescent lanthanide molecular nanoparticle with potential for live cell imaging.
Chemical science, 2018, 9, 4630-4637
1549309 CIFC386 H500 Cd24 N24 O177 Tb8P -4 n 242.806; 42.806; 37.886
90; 90; 90
69421Yang, Xiaoping; Wang, Shiqing; Zhang, Yali; Liang, Guang; Zhu, Ting; Zhang, Lijie; Huang, Shaoming; Schipper, Desmond; Jones, Richard A.
A self-assembling luminescent lanthanide molecular nanoparticle with potential for live cell imaging.
Chemical science, 2018, 9, 4630-4637
1549310 CIFC50 H103 K Mn O14P -111.5253; 16.1662; 16.7311
81.943; 88.463; 69.635
2892.8Halbach, Robert L.; Gygi, David; Bloch, Eric D.; Anderson, Bryce L.; Nocera, Daniel G.
Structurally characterized terminal manganese(iv) oxo tris(alkoxide) complex.
Chemical science, 2018, 9, 4524-4528
1549311 CIFC50 H103 K Mn O13P 1 21/n 111.3584; 17.2479; 29.111
90; 91.552; 90
5701Halbach, Robert L.; Gygi, David; Bloch, Eric D.; Anderson, Bryce L.; Nocera, Daniel G.
Structurally characterized terminal manganese(iv) oxo tris(alkoxide) complex.
Chemical science, 2018, 9, 4524-4528
1549312 CIFC38 H79 K Mn O5C 1 2/c 118.3234; 15.9361; 16.771
90; 122.093; 90
4148.8Halbach, Robert L.; Gygi, David; Bloch, Eric D.; Anderson, Bryce L.; Nocera, Daniel G.
Structurally characterized terminal manganese(iv) oxo tris(alkoxide) complex.
Chemical science, 2018, 9, 4524-4528
1549313 CIFC62 H46 B F24 Na O9P -114.295; 14.544; 17.347
100.67; 107.46; 105.51
3174Löw, Henrik; Mena-Osteritz, Elena; von Delius, Max
Self-assembled orthoester cryptands: orthoester scope, post-functionalization, kinetic locking and tunable degradation kinetics.
Chemical science, 2018, 9, 4785-4793
1549314 CIFC58 H46 B F24 Na O9P b c a19.142; 24.665; 26.029
90; 90; 90
12289Löw, Henrik; Mena-Osteritz, Elena; von Delius, Max
Self-assembled orthoester cryptands: orthoester scope, post-functionalization, kinetic locking and tunable degradation kinetics.
Chemical science, 2018, 9, 4785-4793
1549315 CIFC62 H52 B F30 Na O9P 1 21/n 120.158; 17.085; 20.698
90; 101.158; 90
6994Löw, Henrik; Mena-Osteritz, Elena; von Delius, Max
Self-assembled orthoester cryptands: orthoester scope, post-functionalization, kinetic locking and tunable degradation kinetics.
Chemical science, 2018, 9, 4785-4793
1549316 CIFC65 H75 B F24 Na O9 Si2P -113.9002; 14.0497; 21.1609
101.417; 103.6; 101.486
3804.07Löw, Henrik; Mena-Osteritz, Elena; von Delius, Max
Self-assembled orthoester cryptands: orthoester scope, post-functionalization, kinetic locking and tunable degradation kinetics.
Chemical science, 2018, 9, 4785-4793
1549317 CIFC46 H38 B F24 Li O9P 21 21 2112.8768; 17.6754; 22.1097
90; 90; 90
5032.2Löw, Henrik; Mena-Osteritz, Elena; von Delius, Max
Self-assembled orthoester cryptands: orthoester scope, post-functionalization, kinetic locking and tunable degradation kinetics.
Chemical science, 2018, 9, 4785-4793
1549318 CIFC102 H78 B2 Cl6 F48 Na2 O18P -116.654; 18.497; 20.536
70.108; 83.341; 89.951
5903Löw, Henrik; Mena-Osteritz, Elena; von Delius, Max
Self-assembled orthoester cryptands: orthoester scope, post-functionalization, kinetic locking and tunable degradation kinetics.
Chemical science, 2018, 9, 4785-4793
1549319 CIFC50 H41.87 B Cl8 F24 Na O9P 1 21/c 113.0127; 19.6275; 25.4722
90; 96.246; 90
6467.2Löw, Henrik; Mena-Osteritz, Elena; von Delius, Max
Self-assembled orthoester cryptands: orthoester scope, post-functionalization, kinetic locking and tunable degradation kinetics.
Chemical science, 2018, 9, 4785-4793
1549320 CIFC54 H54 B F24 Na O9P -112.434; 12.984; 20.025
93.798; 107.54; 104.457
2949.7Löw, Henrik; Mena-Osteritz, Elena; von Delius, Max
Self-assembled orthoester cryptands: orthoester scope, post-functionalization, kinetic locking and tunable degradation kinetics.
Chemical science, 2018, 9, 4785-4793
1549332 CIFC8 H12 Br2 Cl3 N OC 1 2/c 118.3209; 12.3996; 12.1068
90; 98.766; 90
2718.2Wappes, Ethan A.; Vanitcha, Avassaya; Nagib, David A.
β C-H di-halogenation <i>via</i> iterative hydrogen atom transfer.
Chemical science, 2018, 9, 4500-4504
1549333 CIFC48 H57 B N2 OP -112.799; 13.808; 13.844
64.938; 70.414; 66.334
1989.3Böhnke, Julian; Brückner, Tobias; Hermann, Alexander; González-Belman, Oscar F; Arrowsmith, Merle; Jiménez-Halla, J Oscar C; Braunschweig, Holger
Single and double activation of acetone by isolobal B[triple bond, length as m-dash]N and B[triple bond, length as m-dash]B triple bonds.
Chemical science, 2018, 9, 5354-5359
1549334 CIFC43 H68 B2 N2 OP 1 21/n 19.499; 22.755; 19.041
90; 91.58; 90
4114Böhnke, Julian; Brückner, Tobias; Hermann, Alexander; González-Belman, Oscar F; Arrowsmith, Merle; Jiménez-Halla, J Oscar C; Braunschweig, Holger
Single and double activation of acetone by isolobal B[triple bond, length as m-dash]N and B[triple bond, length as m-dash]B triple bonds.
Chemical science, 2018, 9, 5354-5359
1549335 CIFC45 H52 B Cl N2C 1 2/c 126.74; 9.4128; 30.763
90; 100.73; 90
7608Böhnke, Julian; Brückner, Tobias; Hermann, Alexander; González-Belman, Oscar F; Arrowsmith, Merle; Jiménez-Halla, J Oscar C; Braunschweig, Holger
Single and double activation of acetone by isolobal B[triple bond, length as m-dash]N and B[triple bond, length as m-dash]B triple bonds.
Chemical science, 2018, 9, 5354-5359
1549336 CIFC51.5 H72 B2 N4 OP -110.756; 12.715; 18.183
81.15; 87.75; 68.37
2284Böhnke, Julian; Brückner, Tobias; Hermann, Alexander; González-Belman, Oscar F; Arrowsmith, Merle; Jiménez-Halla, J Oscar C; Braunschweig, Holger
Single and double activation of acetone by isolobal B[triple bond, length as m-dash]N and B[triple bond, length as m-dash]B triple bonds.
Chemical science, 2018, 9, 5354-5359
1549337 CIFC45 H51 B N2P 1 21/c 112.303; 12.532; 24.192
90; 100.95; 90
3662Böhnke, Julian; Brückner, Tobias; Hermann, Alexander; González-Belman, Oscar F; Arrowsmith, Merle; Jiménez-Halla, J Oscar C; Braunschweig, Holger
Single and double activation of acetone by isolobal B[triple bond, length as m-dash]N and B[triple bond, length as m-dash]B triple bonds.
Chemical science, 2018, 9, 5354-5359
1549338 CIFC19 H21 O2 SP 1 21 16.612; 7.8997; 15.4119
90; 92.455; 90
804.27Cheng, Fengchang; Lu, Wenxin; Huang, Wei; Wen, Lu; Li, Mingfeng; Meng, Fanke
Cu-catalyzed enantioselective synthesis of tertiary benzylic copper complexes and their <i>in situ</i> addition to carbonyl compounds.
Chemical science, 2018, 9, 4992-4998
1549339 CIFC24 H27 B O4P 1 21 112.5495; 6.3424; 13.2506
90; 92.671; 90
1053.52Cheng, Fengchang; Lu, Wenxin; Huang, Wei; Wen, Lu; Li, Mingfeng; Meng, Fanke
Cu-catalyzed enantioselective synthesis of tertiary benzylic copper complexes and their <i>in situ</i> addition to carbonyl compounds.
Chemical science, 2018, 9, 4992-4998
1549367 CIFC54 H42 Co N4 O4P 1 21/c 114.361; 9.517; 15.449
90; 99.257; 90
2084Wang, Zikuan; Yao, Zhengmin; Lyu, Zeyu; Xiong, Qinsi; Wang, Bingwu; Fu, Xuefeng
Thermodynamic and reactivity studies of a tin corrole-cobalt porphyrin heterobimetallic complex.
Chemical science, 2018, 9, 4999-5007
1549368 CIFC62 H48 Co F N4 O4P c a 2121.495; 13.598; 16.434
90; 90; 90
4803.5Wang, Zikuan; Yao, Zhengmin; Lyu, Zeyu; Xiong, Qinsi; Wang, Bingwu; Fu, Xuefeng
Thermodynamic and reactivity studies of a tin corrole-cobalt porphyrin heterobimetallic complex.
Chemical science, 2018, 9, 4999-5007
1549369 CIFC85 H44 Co F15 N8 O4 SnP 1 21/c 117.25; 13.082; 32.044
90; 96.735; 90
7181Wang, Zikuan; Yao, Zhengmin; Lyu, Zeyu; Xiong, Qinsi; Wang, Bingwu; Fu, Xuefeng
Thermodynamic and reactivity studies of a tin corrole-cobalt porphyrin heterobimetallic complex.
Chemical science, 2018, 9, 4999-5007
1549370 CIFC74 H16 F30 N8 O Sn2P -112.8962; 15.333; 21.248
101.533; 90.07; 106.286
3944.2Wang, Zikuan; Yao, Zhengmin; Lyu, Zeyu; Xiong, Qinsi; Wang, Bingwu; Fu, Xuefeng
Thermodynamic and reactivity studies of a tin corrole-cobalt porphyrin heterobimetallic complex.
Chemical science, 2018, 9, 4999-5007
1549371 CIFC94 H52 Co F15 N8 O5 SnP -115.523; 16.499; 20.024
93.436; 111.524; 102.953
4591.9Wang, Zikuan; Yao, Zhengmin; Lyu, Zeyu; Xiong, Qinsi; Wang, Bingwu; Fu, Xuefeng
Thermodynamic and reactivity studies of a tin corrole-cobalt porphyrin heterobimetallic complex.
Chemical science, 2018, 9, 4999-5007
1549373 CIFC22 H17 N O9P c a 217.0231; 17.534; 14.6817
90; 90; 90
1807.9Panter, Fabian; Krug, Daniel; Baumann, Sascha; Müller, Rolf
Self-resistance guided genome mining uncovers new topoisomerase inhibitors from myxobacteria.
Chemical science, 2018, 9, 4898-4908
1549374 CIFC22 H17 N O9P -17.0902; 7.9097; 17.33
89.561; 84.797; 74.655
933.2Panter, Fabian; Krug, Daniel; Baumann, Sascha; Müller, Rolf
Self-resistance guided genome mining uncovers new topoisomerase inhibitors from myxobacteria.
Chemical science, 2018, 9, 4898-4908
1549375 CIFC54 H33 Cl Ir N6 S2P 1 21/n 114.6864; 15.1284; 29.6362
90; 99.037; 90
6502.9Guan, Ruilin; Chen, Yu; Zeng, Leli; Rees, Thomas W.; Jin, Chengzhi; Huang, Juanjuan; Chen, Zhe-Sheng; Ji, Liangnian; Chao, Hui
Oncosis-inducing cyclometalated iridium(iii) complexes.
Chemical science, 2018, 9, 5183-5190
1549376 CIFC19 H13 Br F3 N O3 SP 6116.963; 16.963; 11.4256
90; 90; 120
2847.2Greenhalgh, Mark D.; Qu, Shen; Slawin, Alexandra M. Z.; Smith, Andrew D.
Multiple roles of aryloxide leaving groups in enantioselective annulations employing α,β-unsaturated acyl ammonium catalysis.
Chemical science, 2018, 9, 4909-4918
1549382 CIFC21 H29 N O3 S SiP 1 21/n 111.6959; 16.06; 11.9522
90; 91.981; 90
2243.71Jayaraman, Arumugam; Misal Castro, Luis C.; Desrosiers, Vincent; Fontaine, Frédéric-Georges
Metal-free borylative dearomatization of indoles: exploring the divergent reactivity of aminoborane C-H borylation catalysts.
Chemical science, 2018, 9, 5057-5063

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