Crystallography Open Database

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1558048 CIFC43 H121 Er3 N12 O43 Yb3R -3 :H16.7567; 16.7567; 25.0576
90; 90; 120		6093.2Gálico, Diogo A; Ovens, Jeffrey S.; Murugesu, Muralee
NIR-to-NIR emission on a water-soluble {Er<sub>6</sub>} and {Er<sub>3</sub>Yb<sub>3</sub>} nanosized molecular wheel.
Nanoscale, 2020, 12, 11435-11439
1558049 CIFC40 H86 Cl4 N12 O39 Yb6P -112.1098; 12.8247; 24.7696
97.196; 102.549; 98.363		3665.67Gálico, Diogo A; Ovens, Jeffrey S.; Murugesu, Muralee
NIR-to-NIR emission on a water-soluble {Er<sub>6</sub>} and {Er<sub>3</sub>Yb<sub>3</sub>} nanosized molecular wheel.
Nanoscale, 2020, 12, 11435-11439
1558050 CIFC15 H12 N4P 1 21/c 118.3346; 15.7546; 18.3241
90; 90.531; 90		5292.8Horiuchi, Sachio; Ishibashi, Shoji; Haruki, Rie; Kumai, Reiji; Inada, Satoshi; Aoyagi, Shigenobu
Metaelectric multiphase transitions in a highly polarizable molecular crystal.
Chemical science, 2020, 11, 6183-6192
1558051 CIFC15 H12 N4P 4318.3126; 18.3126; 15.7252
90; 90; 90		5273.5Horiuchi, Sachio; Ishibashi, Shoji; Haruki, Rie; Kumai, Reiji; Inada, Satoshi; Aoyagi, Shigenobu
Metaelectric multiphase transitions in a highly polarizable molecular crystal.
Chemical science, 2020, 11, 6183-6192
1558052 CIFC15 H12 N4P 4118.2293; 18.2293; 15.6088
90; 90; 90		5186.9Horiuchi, Sachio; Ishibashi, Shoji; Haruki, Rie; Kumai, Reiji; Inada, Satoshi; Aoyagi, Shigenobu
Metaelectric multiphase transitions in a highly polarizable molecular crystal.
Chemical science, 2020, 11, 6183-6192
1558053 CIFC31 H28 N8 OC 1 2/c 122.088; 5.586; 24.017
90; 115.257; 90		2680Horiuchi, Sachio; Ishibashi, Shoji; Haruki, Rie; Kumai, Reiji; Inada, Satoshi; Aoyagi, Shigenobu
Metaelectric multiphase transitions in a highly polarizable molecular crystal.
Chemical science, 2020, 11, 6183-6192
1558054 CIFC15 H12 N4P 1 21/c 118.3296; 15.7595; 18.3254
90; 90.612; 90		5293.3Horiuchi, Sachio; Ishibashi, Shoji; Haruki, Rie; Kumai, Reiji; Inada, Satoshi; Aoyagi, Shigenobu
Metaelectric multiphase transitions in a highly polarizable molecular crystal.
Chemical science, 2020, 11, 6183-6192
1558055 CIFC16 H12 N4P 1 21/n 17.963; 8.349; 9.742
90; 111.776; 90		601.5Deville, Claire; Folkjær, Mads; Reinholdt, Peter; Hvid, Mathias S.; Lamagni, Paolo; Borup, Kasper; Sun, Zhaozong; Lauritsen, Jeppe Vang; McKee, Vickie; Jensen, Kirsten M Ø; Lock, Nina
Cubes on a string: a series of linear coordination polymers with cubane-like nodes and dicarboxylate linkers.
Nanoscale, 2020, 12, 11601-11611
1558056 CIFC82 H65 Co4 N16 O12I 1 2 115.6211; 21.1135; 32.721
90; 93.605; 90		10770.6Deville, Claire; Folkjær, Mads; Reinholdt, Peter; Hvid, Mathias S.; Lamagni, Paolo; Borup, Kasper; Sun, Zhaozong; Lauritsen, Jeppe Vang; McKee, Vickie; Jensen, Kirsten M Ø; Lock, Nina
Cubes on a string: a series of linear coordination polymers with cubane-like nodes and dicarboxylate linkers.
Nanoscale, 2020, 12, 11601-11611
1558057 CIFC80 H64 Co4 N16 O14P 42 21 219.5696; 19.5696; 26.6481
90; 90; 90		10205.4Deville, Claire; Folkjær, Mads; Reinholdt, Peter; Hvid, Mathias S.; Lamagni, Paolo; Borup, Kasper; Sun, Zhaozong; Lauritsen, Jeppe Vang; McKee, Vickie; Jensen, Kirsten M Ø; Lock, Nina
Cubes on a string: a series of linear coordination polymers with cubane-like nodes and dicarboxylate linkers.
Nanoscale, 2020, 12, 11601-11611
1558058 CIFC38 H60 Al N3P 1 21/n 110.236; 32.92; 10.7797
90; 105.178; 90		3505.7Drescher, Regina; Lin, Shujuan; Hofmann, Alexander; Lenczyk, Carsten; Kachel, Stephanie; Krummenacher, Ivo; Lin, Zhenyang; Braunschweig, Holger
Ring expansion of alumoles with organic azides: selective formation of six-membered aluminum-nitrogen heterocycles.
Chemical science, 2020, 11, 5559-5564
1558059 CIFC32 H58 Al2P 1 21/n 18.755; 15.965; 11.067
90; 96.64; 90		1536.5Drescher, Regina; Lin, Shujuan; Hofmann, Alexander; Lenczyk, Carsten; Kachel, Stephanie; Krummenacher, Ivo; Lin, Zhenyang; Braunschweig, Holger
Ring expansion of alumoles with organic azides: selective formation of six-membered aluminum-nitrogen heterocycles.
Chemical science, 2020, 11, 5559-5564
1558060 CIFC36 H59 Al N2P 1 21/n 112.957; 16.692; 15.618
90; 96.13; 90		3359Drescher, Regina; Lin, Shujuan; Hofmann, Alexander; Lenczyk, Carsten; Kachel, Stephanie; Krummenacher, Ivo; Lin, Zhenyang; Braunschweig, Holger
Ring expansion of alumoles with organic azides: selective formation of six-membered aluminum-nitrogen heterocycles.
Chemical science, 2020, 11, 5559-5564
1558061 CIFC29 H49 AlP 1 21/n 19.335; 16.672; 17.185
90; 93.88; 90		2668Drescher, Regina; Lin, Shujuan; Hofmann, Alexander; Lenczyk, Carsten; Kachel, Stephanie; Krummenacher, Ivo; Lin, Zhenyang; Braunschweig, Holger
Ring expansion of alumoles with organic azides: selective formation of six-membered aluminum-nitrogen heterocycles.
Chemical science, 2020, 11, 5559-5564
1558062 CIFC32 H58 Al N SiP -19.601; 12.75; 13.314
97.397; 93.793; 94.404		1606.7Drescher, Regina; Lin, Shujuan; Hofmann, Alexander; Lenczyk, Carsten; Kachel, Stephanie; Krummenacher, Ivo; Lin, Zhenyang; Braunschweig, Holger
Ring expansion of alumoles with organic azides: selective formation of six-membered aluminum-nitrogen heterocycles.
Chemical science, 2020, 11, 5559-5564
1558063 CIFC47 H62 Al N3P 1 21/c 119.5714; 14.2192; 14.836
90; 96.397; 90		4103Drescher, Regina; Lin, Shujuan; Hofmann, Alexander; Lenczyk, Carsten; Kachel, Stephanie; Krummenacher, Ivo; Lin, Zhenyang; Braunschweig, Holger
Ring expansion of alumoles with organic azides: selective formation of six-membered aluminum-nitrogen heterocycles.
Chemical science, 2020, 11, 5559-5564
1558064 CIFC22 H28 I2 Ir N3 O2P 1 21/n 19.29339; 13.27724; 20.1881
90; 91.3644; 90		2490.31Zhang, Wen-Ying; Banerjee, Samya; Hughes, George M.; Bridgewater, Hannah E.; Song, Ji-Inn; Breeze, Ben G.; Clarkson, Guy J.; Coverdale, James P. C.; Sanchez-Cano, Carlos; Ponte, Fortuna; Sicilia, Emilia; Sadler, Peter J.
Ligand-centred redox activation of inert organoiridium anticancer catalysts
Chemical Science, 2020, 11, 5466-5480
1558065 CIFC26 H25.5 F3 I Ir N3 O P0.5P 1 2/c 123.165; 7.44609; 15.706
90; 107.268; 90		2587.01Zhang, Wen-Ying; Banerjee, Samya; Hughes, George M.; Bridgewater, Hannah E.; Song, Ji-Inn; Breeze, Ben G.; Clarkson, Guy J.; Coverdale, James P. C.; Sanchez-Cano, Carlos; Ponte, Fortuna; Sicilia, Emilia; Sadler, Peter J.
Ligand-centred redox activation of inert organoiridium anticancer catalysts
Chemical Science, 2020, 11, 5466-5480
1558066 CIFC22 H27 Br F6 I Ir N3 O2 PP 1 21/n 19.61097; 20.10144; 14.45419
90; 103.426; 90		2716.15Zhang, Wen-Ying; Banerjee, Samya; Hughes, George M.; Bridgewater, Hannah E.; Song, Ji-Inn; Breeze, Ben G.; Clarkson, Guy J.; Coverdale, James P. C.; Sanchez-Cano, Carlos; Ponte, Fortuna; Sicilia, Emilia; Sadler, Peter J.
Ligand-centred redox activation of inert organoiridium anticancer catalysts
Chemical Science, 2020, 11, 5466-5480
1558067 CIFC23 H27 F9 I Ir N3 O2 PP 1 21/n 19.8587; 20.2807; 15.0835
90; 105.245; 90		2909.69Zhang, Wen-Ying; Banerjee, Samya; Hughes, George M.; Bridgewater, Hannah E.; Song, Ji-Inn; Breeze, Ben G.; Clarkson, Guy J.; Coverdale, James P. C.; Sanchez-Cano, Carlos; Ponte, Fortuna; Sicilia, Emilia; Sadler, Peter J.
Ligand-centred redox activation of inert organoiridium anticancer catalysts
Chemical Science, 2020, 11, 5466-5480
1558068 CIFC26 H26 I2 Ir N3P 1 21/c 19.1942; 8.2158; 33.7933
90; 95.783; 90		2539.68Zhang, Wen-Ying; Banerjee, Samya; Hughes, George M.; Bridgewater, Hannah E.; Song, Ji-Inn; Breeze, Ben G.; Clarkson, Guy J.; Coverdale, James P. C.; Sanchez-Cano, Carlos; Ponte, Fortuna; Sicilia, Emilia; Sadler, Peter J.
Ligand-centred redox activation of inert organoiridium anticancer catalysts
Chemical Science, 2020, 11, 5466-5480
1558069 CIFC21 H24 I2 Ir N3C 1 2/c 131.7681; 8.7023; 16.6407
90; 94.935; 90		4583.36Zhang, Wen-Ying; Banerjee, Samya; Hughes, George M.; Bridgewater, Hannah E.; Song, Ji-Inn; Breeze, Ben G.; Clarkson, Guy J.; Coverdale, James P. C.; Sanchez-Cano, Carlos; Ponte, Fortuna; Sicilia, Emilia; Sadler, Peter J.
Ligand-centred redox activation of inert organoiridium anticancer catalysts
Chemical Science, 2020, 11, 5466-5480
1558070 CIFC22 H27.5 Cl1.5 Ir N3 O2P 1 21/n 18.93939; 18.6768; 13.452
90; 94.066; 90		2240.28Zhang, Wen-Ying; Banerjee, Samya; Hughes, George M.; Bridgewater, Hannah E.; Song, Ji-Inn; Breeze, Ben G.; Clarkson, Guy J.; Coverdale, James P. C.; Sanchez-Cano, Carlos; Ponte, Fortuna; Sicilia, Emilia; Sadler, Peter J.
Ligand-centred redox activation of inert organoiridium anticancer catalysts
Chemical Science, 2020, 11, 5466-5480
1558071 CIFC26 H26 Cl F6 Ir N3 O PP -18.71914; 9.9018; 15.7288
89.3248; 78.0376; 88.7062		1328.09Zhang, Wen-Ying; Banerjee, Samya; Hughes, George M.; Bridgewater, Hannah E.; Song, Ji-Inn; Breeze, Ben G.; Clarkson, Guy J.; Coverdale, James P. C.; Sanchez-Cano, Carlos; Ponte, Fortuna; Sicilia, Emilia; Sadler, Peter J.
Ligand-centred redox activation of inert organoiridium anticancer catalysts
Chemical Science, 2020, 11, 5466-5480
1558072 CIFC15 H19 N2 O4 ReP 1 21/c 114.6069; 8.871; 12.0927
90; 90.801; 90		1566.79Li, Jing; Lutz, Martin; Klein Gebbink, Robertus J. M.
N,N,O-Coordinated tricarbonylrhenium precatalysts for the aerobic deoxydehydration of diols and polyols
Catalysis Science & Technology, 2020, 10, 3782-3788
1558073 CIFC23 H35 N2 O4 ReC 1 2/c 123.927; 9.4928; 22.1646
90; 106.575; 90		4825.1Li, Jing; Lutz, Martin; Klein Gebbink, Robertus J. M.
N,N,O-Coordinated tricarbonylrhenium precatalysts for the aerobic deoxydehydration of diols and polyols
Catalysis Science & Technology, 2020, 10, 3782-3788
1558074 CIFC15 H18 N3 O6 ReP b c a8.90063; 11.9803; 31.8099
90; 90; 90		3391.96Li, Jing; Lutz, Martin; Klein Gebbink, Robertus J. M.
N,N,O-Coordinated tricarbonylrhenium precatalysts for the aerobic deoxydehydration of diols and polyols
Catalysis Science & Technology, 2020, 10, 3782-3788
1558075 CIFC21 H21 Fe N O3P 21 21 217.9439; 8.6162; 25.8718
90; 90; 90		1770.83Larin, Egor M.; Loup, Joachim; Polishchuk, Iuliia; Ross, Rachel J.; Whyte, Andrew; Lautens, Mark
Enantio- and diastereoselective conjugate borylation/Mannich cyclization
Chemical Science, 2020, 11, 5716-5723
1558076 CIFC34 H72 B4 Dy2 O2P -110.0067; 14.2962; 16.3689
99.987; 105.704; 107.788		2061He, Mian; Guo, Fu-Sheng; Tang, Jinkui; Mansikkamäki, Akseli; Layfield, Richard A.
Fulvalene as a platform for the synthesis of a dimetallic dysprosocenium single-molecule magnet.
Chemical science, 2020, 11, 5745-5752
1558077 CIFC46 H78 B2 Dy2P 1 21/n 113.3199; 18.1439; 19.6411
90; 107.366; 90		4530.39He, Mian; Guo, Fu-Sheng; Tang, Jinkui; Mansikkamäki, Akseli; Layfield, Richard A.
Fulvalene as a platform for the synthesis of a dimetallic dysprosocenium single-molecule magnet.
Chemical science, 2020, 11, 5745-5752
1558078 CIFC70 H74 B2 Dy2 F20P 1 21/n 118.1029; 20.9327; 19.4229
90; 111.812; 90		6833.2He, Mian; Guo, Fu-Sheng; Tang, Jinkui; Mansikkamäki, Akseli; Layfield, Richard A.
Fulvalene as a platform for the synthesis of a dimetallic dysprosocenium single-molecule magnet.
Chemical science, 2020, 11, 5745-5752
1558079 CIFC56 H128 Ce K N16 P4P -113.16; 13.956; 23.75
74.835; 81.559; 65.275		3820.6Rice, Natalie T.; Popov, Ivan A.; Russo, Dominic R.; Gompa, Thaige P.; Ramanathan, Arun; Bacsa, John; Batista, Enrique R.; Yang, Ping; La Pierre, Henry S.
Comparison of tetravalent cerium and terbium ions in a conserved, homoleptic imidophosphorane ligand field.
Chemical science, 2020, 11, 6149-6159
1558080 CIFC56 H128 Ce N16 P4I -413.3726; 13.3726; 21.0511
90; 90; 90		3764.5Rice, Natalie T.; Popov, Ivan A.; Russo, Dominic R.; Gompa, Thaige P.; Ramanathan, Arun; Bacsa, John; Batista, Enrique R.; Yang, Ping; La Pierre, Henry S.
Comparison of tetravalent cerium and terbium ions in a conserved, homoleptic imidophosphorane ligand field.
Chemical science, 2020, 11, 6149-6159
1558081 CIFC50 H46 Ag2 B2 F8 N10 O4P 1 21/c 111.76962; 15.5527; 14.3675
90; 100.026; 90		2589.8Wang, Shi; Bai, Dongya; Wang, Yanbo; Fu, Jiya; Zhu, Junyan; Fang, Xiaomin
Hierarchical self-assembly of helical coordination polymers and formation of a lamellar structure via the cooperativity of two-step Ag(i) coordination and π-π interactions.
Nanoscale, 2020, 12, 10972-10976
1558082 CIFC38 H50 Co N P2 SP 1 21/n 114.5788; 14.6329; 16.7346
90; 96.683; 90		3545.7Foley, Bryan J.; Palit, Chandra Mouli; Bhuvanesh, Nattamai; Zhou, Jia; Ozerov, Oleg V.
Concerted aryl-sulfur reductive elimination from PNP pincer-supported Co(iii) and subsequent Co(i)/Co(iii) comproportionation.
Chemical science, 2020, 11, 6075-6084
1558083 CIFC33 H47 Co N P2P 1 21/c 115.273; 10.83; 18.993
90; 98.062; 90		3110.5Foley, Bryan J.; Palit, Chandra Mouli; Bhuvanesh, Nattamai; Zhou, Jia; Ozerov, Oleg V.
Concerted aryl-sulfur reductive elimination from PNP pincer-supported Co(iii) and subsequent Co(i)/Co(iii) comproportionation.
Chemical science, 2020, 11, 6075-6084
1558084 CIFC34 H48 Co N O2 P2C 1 2/c 133.34; 13.858; 14.143
90; 99.023; 90		6454Foley, Bryan J.; Palit, Chandra Mouli; Bhuvanesh, Nattamai; Zhou, Jia; Ozerov, Oleg V.
Concerted aryl-sulfur reductive elimination from PNP pincer-supported Co(iii) and subsequent Co(i)/Co(iii) comproportionation.
Chemical science, 2020, 11, 6075-6084
1558085 CIFC45 H48 Cl2 Co2 N4 O12C 1 2/c 118.88; 7.915; 30.41
90; 98.22; 90		4498Chen, Xin-Ran; Zhang, Shuo-Qing; Meyer, Tjark H.; Yang, Chun-Hui; Zhang, Qin-Hao; Liu, Ji-Ren; Xu, Hua-Jian; Cao, Fa-He; Ackermann, Lutz; Hong, Xin
Carboxylate breaks the arene C‒H bond via a hydrogen-atom-transfer mechanism in electrochemical cobalt catalysis
Chemical Science, 2020, 11, 5790-5796
1558086 CIFC124 H150 Au13 P3 Pd S7P -117.1801; 17.7175; 22.9577
95.508; 90.634; 106.355		6669Fu, Xuemei; Lin, Xinzhang; Ren, Xiuqing; Wu, Ren'an; Liu, Chao; Huang, Jiahui
The synthesis and structure of the [PdAu<sub>13</sub>(PPh<sub>3</sub>)<sub>3</sub>(SR)<sub>7</sub>]<sup>+</sup> nanocluster.
Nanoscale, 2020, 12, 11825-11829
1558087 CIFC5 H8 N2 O2P 21 21 217.1989; 7.2267; 13.0042
90; 90; 90		676.53Wang, Yunzhong; Tang, Saixing; Wen, Yating; Zheng, Shuyuan; Yang, Bing; Yuan, Wang Zhang
Nonconventional luminophores with unprecedented efficiencies and color-tunable afterglows
Materials Horizons, 2020, 7, 2105-2112
1558088 CIFC3 H4 N2 O2C 1 2/c 19.3446; 12.244; 7.3458
90; 105.194; 90		811.1Wang, Yunzhong; Tang, Saixing; Wen, Yating; Zheng, Shuyuan; Yang, Bing; Yuan, Wang Zhang
Nonconventional luminophores with unprecedented efficiencies and color-tunable afterglows
Materials Horizons, 2020, 7, 2105-2112
1558089 CIFC8 H10 N4 O4P 1 21/c 15.8982; 12.4995; 14.3372
90; 114.292; 90		963.42Wang, Yunzhong; Tang, Saixing; Wen, Yating; Zheng, Shuyuan; Yang, Bing; Yuan, Wang Zhang
Nonconventional luminophores with unprecedented efficiencies and color-tunable afterglows
Materials Horizons, 2020, 7, 2105-2112
1558090 CIFC7 H8 N4 O4P 1 21/n 19.597; 17.769; 11.34
90; 114.24; 90		1763.3Wang, Yunzhong; Tang, Saixing; Wen, Yating; Zheng, Shuyuan; Yang, Bing; Yuan, Wang Zhang
Nonconventional luminophores with unprecedented efficiencies and color-tunable afterglows
Materials Horizons, 2020, 7, 2105-2112
1558091 CIF
HKL
Paper		C5 H9 Cl N2P 21 21 216.3076; 9.549; 11.3951
90; 90; 90		686.34Anderson, Grace; Mirjafari, Arsalan; Zeller, Matthias; Hillesheim, Patrick C.
2,3-Dimethyl-1<i>H</i>-imidazol-3-ium chloride
IUCrData, 2020, 5, x200660
1558092 CIFC33 H28 F6 N2 S2P 1 21 110.6734; 13.492; 10.8926
90; 106.158; 90		1506.63Yu, Zhang-Long; Cheng, Yong-Feng; Jiang, Na-Chuan; Wang, Jian; Fan, Li-Wen; Yuan, Yue; Li, Zhong-Liang; Gu, Qiang-Shuai; Liu, Xin-Yuan
Desymmetrization of unactivated bis-alkenes via chiral Brønsted acid-catalysed hydroamination
Chemical Science, 2020, 11, 5987-5993
1558093 CIFC45 H44 N2 O4P 1 21/c 127.3782; 16.4038; 8.0743
90; 96.106; 90		3605.6Samanta, Samaresh; Ray, Subir Kumar; Deolka, Shubham; Saha, Sudipta; K R, Pradeep; Bhowal, Rohit; Ghosh, Nirmalya; Chaudhuri, Debangshu
Safeguarding long-lived excitons from excimer traps in H-aggregated dye-assemblies.
Chemical science, 2020, 11, 5710-5715
1558094 CIFC92 H76 N6 O8P -111.2545; 18.0672; 20.425
114.844; 101.984; 90.435		3665.6Xu, Jianbin; Liang, Lusheng; Mai, Chi-Lun; Zhang, Zilong; Zhou, Qin; Xiong, Qiu; Zhang, Zhuangzhuang; Deng, Longhui; Gao, Peng
Lewis-base containing spiro type hole transporting materials for high-performance perovskite solar cells with efficiency approaching 20.
Nanoscale, 2020, 12, 13157-13164
1558095 CIFC24 H54 Ag6 O46 S6 Si W12P n a 2127.1669; 18.3273; 13.8912
90; 90; 90		6916.4Hu, Ting; Hu, Chunli; Li, Yuhang; Meng, Lingyi; Xie, Yiming; Liao, Mingyue; Zhong, Guiming; Lu, Can-Zhong
Synthesis and characterization of a nanocluster-based silver(i) tert-butylethynide compound with a large second-harmonic generation response.
Nanoscale, 2020, 12, 11847-11857
1558097 CIFC45 H31 N5 SP -17.8139; 9.9797; 21.6351
87.227; 84.36; 86.871		1674.87Luo, Qing; Li, Lin; Ma, Huili; Lv, Chunyan; Jiang, Xueyan; Gu, Xinggui; An, Zhongfu; Zou, Bo; Zhang, Cheng; Zhang, Yujian
Deep-red fluorescence from isolated dimers: a highly bright excimer and imaging in vivo
Chemical Science, 2020, 11, 6020-6025
1558098 CIFC76 H144 Co2 K2 N4 O15 P8P -113.7131; 15.2042; 25.3794
74.859; 78.818; 65.926		4640.57Piesch, Martin; Seidl, Michael; Scheer, Manfred
Transformations of the cyclo-P4 ligand in [Cp′′′Co(η4-P4)]
Chemical Science, 2020, 11, 6745-6751
1558099 CIFC43 H82 Co Li N2 O7 P4P b c a17.8715; 22.5218; 24.946
90; 90; 90		10040.7Piesch, Martin; Seidl, Michael; Scheer, Manfred
Transformations of the cyclo-P4 ligand in [Cp′′′Co(η4-P4)]
Chemical Science, 2020, 11, 6745-6751
1558100 CIFC53.5 H99 Co2 Li O3.25 P8P 1 21/c 131.947; 15.571; 12.6636
90; 91.67; 90		6296.8Piesch, Martin; Seidl, Michael; Scheer, Manfred
Transformations of the cyclo-P4 ligand in [Cp′′′Co(η4-P4)]
Chemical Science, 2020, 11, 6745-6751
1558101 CIFC25 H50 Co Na O5 P4P -18.8103; 10.6602; 17.7138
78.926; 89.741; 85.158		1626.75Piesch, Martin; Seidl, Michael; Scheer, Manfred
Transformations of the cyclo-P4 ligand in [Cp′′′Co(η4-P4)]
Chemical Science, 2020, 11, 6745-6751
1558102 CIFC80 H156 Co2 Li2 O17.5 P8 Si2P -114.474; 18.2968; 19.7326
87.037; 77.66; 86.306		5090.5Piesch, Martin; Seidl, Michael; Scheer, Manfred
Transformations of the cyclo-P4 ligand in [Cp′′′Co(η4-P4)]
Chemical Science, 2020, 11, 6745-6751
1558103 CIFC53 H106 Co2 Li O6 P8 SiP -114.2675; 15.0423; 18.2337
102.047; 94.044; 114.602		3424.69Piesch, Martin; Seidl, Michael; Scheer, Manfred
Transformations of the cyclo-P4 ligand in [Cp′′′Co(η4-P4)]
Chemical Science, 2020, 11, 6745-6751
1558104 CIFC29 H38 O5P 21 21 2110.047; 11.0487; 24.242
90; 90; 90		2691Li, Xin; He, Songtao; Song, Qiuling
Enantio- and diastereoselective diarylmethylation of 1,3-dicarbonyl compounds
Chemical Science, 2020, 11, 5969-5973
1558105 CIFC33 H37 N O7P 21 21 2110.4833; 14.435; 21.245
90; 90; 90		3214.9Li, Xin; He, Songtao; Song, Qiuling
Enantio- and diastereoselective diarylmethylation of 1,3-dicarbonyl compounds
Chemical Science, 2020, 11, 5969-5973
1558106 CIFC31 H39 O4 SC 1 2 123.808; 10.36; 11.8065
90; 95.046; 90		2900.8Li, Xin; He, Songtao; Song, Qiuling
Enantio- and diastereoselective diarylmethylation of 1,3-dicarbonyl compounds
Chemical Science, 2020, 11, 5969-5973
1558113 CIFC6 H20.8 Gd2 N2 O19.4 P6P -19.756; 10.186; 12.84
98.371; 106.552; 90.234		1208.7Mendes, Ricardo F.; Barbosa, Paula; Domingues, Eddy M.; Silva, Patrícia; Figueiredo, Filipe; Almeida Paz, Filipe A.
Enhanced proton conductivity in a layered coordination polymer.
Chemical science, 2020, 11, 6305-6311
1558114 CIFC35 H59 N2 P Si2 UC 1 c 120.0922; 11.4805; 18.359
90; 120.155; 90		3661.7Ward, Robert J.; Rungthanaphatsophon, Pokpong; Rosal, Iker del; Kelley, Steven P.; Maron, Laurent; Walensky, Justin R.
Divergent uranium- versus phosphorus-based reduction of Me3SiN3 with steric modification of phosphido ligands
Chemical Science, 2020, 11, 5830-5835
1558115 CIFC35 H58 N2 P Si2 UP -19.8231; 11.2078; 19.039
82.061; 76.9; 65.055		1849Ward, Robert J.; Rungthanaphatsophon, Pokpong; Rosal, Iker del; Kelley, Steven P.; Maron, Laurent; Walensky, Justin R.
Divergent uranium- versus phosphorus-based reduction of Me3SiN3 with steric modification of phosphido ligands
Chemical Science, 2020, 11, 5830-5835
1558116 CIFC33 H56 N P Si2 UP -110.6409; 16.5027; 20.4856
85.363; 89.696; 85.317		3573.6Ward, Robert J.; Rungthanaphatsophon, Pokpong; Rosal, Iker del; Kelley, Steven P.; Maron, Laurent; Walensky, Justin R.
Divergent uranium- versus phosphorus-based reduction of Me3SiN3 with steric modification of phosphido ligands
Chemical Science, 2020, 11, 5830-5835
1558117 CIFC73 H70 Cl2 Fe2 N8 O12 S12P -111.3618; 12.1577; 18.2103
98.637; 99.864; 113.651		2202.3Qiu, Ya-Ru; Cui, Long; Cai, Pei-Yu; Yu, Fei; Kurmoo, Mohamedally; Leong, Chanel F.; D'Alessandro, Deanna M; Zuo, Jing-Lin
Enhanced dielectricity coupled to spin-crossover in a one-dimensional polymer iron(ii) incorporating tetrathiafulvalene.
Chemical science, 2020, 11, 6229-6235
1558118 CIFC36 H34 Fe N4 O6 S6P -111.36; 12.085; 16.842
91.22; 109.72; 111.47		1998Qiu, Ya-Ru; Cui, Long; Cai, Pei-Yu; Yu, Fei; Kurmoo, Mohamedally; Leong, Chanel F.; D'Alessandro, Deanna M; Zuo, Jing-Lin
Enhanced dielectricity coupled to spin-crossover in a one-dimensional polymer iron(ii) incorporating tetrathiafulvalene.
Chemical science, 2020, 11, 6229-6235
1558119 CIFC28 H31 N3 O6 S6P 1 21/c 14.795; 25.807; 26.902
90; 91.827; 90		3327.3Qiu, Ya-Ru; Cui, Long; Cai, Pei-Yu; Yu, Fei; Kurmoo, Mohamedally; Leong, Chanel F.; D'Alessandro, Deanna M; Zuo, Jing-Lin
Enhanced dielectricity coupled to spin-crossover in a one-dimensional polymer iron(ii) incorporating tetrathiafulvalene.
Chemical science, 2020, 11, 6229-6235
1558120 CIFC25 H31 B F2 N2 OP -17.9871; 15.6608; 19.341
74.494; 87.66; 76.49		2266.1Clark, Ryan; Nawawi, Mohd A.; Dobre, Ana; Pugh, David; Liu, Qingshan; Ivanov, Aleksandar P.; White, Andrew J. P.; Edel, Joshua B.; Kuimova, Marina K.; McIntosh, Alastair J. S.; Welton, Tom
The effect of structural heterogeneity upon the microviscosity of ionic liquids.
Chemical science, 2020, 11, 6121-6133
1558121 CIFC24 H22 F6 N2 O4 S4P -113.7964; 14.4462; 14.8908
103.965; 99.568; 104.025		2713.5Clark, Ryan; Nawawi, Mohd A.; Dobre, Ana; Pugh, David; Liu, Qingshan; Ivanov, Aleksandar P.; White, Andrew J. P.; Edel, Joshua B.; Kuimova, Marina K.; McIntosh, Alastair J. S.; Welton, Tom
The effect of structural heterogeneity upon the microviscosity of ionic liquids.
Chemical science, 2020, 11, 6121-6133
1558122 CIFC22 H23 Cl2 I N2 S2P -17.9187; 12.1261; 13.0689
82.67; 78.619; 79.315		1203.5Clark, Ryan; Nawawi, Mohd A.; Dobre, Ana; Pugh, David; Liu, Qingshan; Ivanov, Aleksandar P.; White, Andrew J. P.; Edel, Joshua B.; Kuimova, Marina K.; McIntosh, Alastair J. S.; Welton, Tom
The effect of structural heterogeneity upon the microviscosity of ionic liquids.
Chemical science, 2020, 11, 6121-6133
1558123 CIFC21 H21 B0.43 F1.72 I0.57 N2 S2C 1 2/c 117.7575; 19.0198; 15.2682
90; 114.649; 90		4686.9Clark, Ryan; Nawawi, Mohd A.; Dobre, Ana; Pugh, David; Liu, Qingshan; Ivanov, Aleksandar P.; White, Andrew J. P.; Edel, Joshua B.; Kuimova, Marina K.; McIntosh, Alastair J. S.; Welton, Tom
The effect of structural heterogeneity upon the microviscosity of ionic liquids.
Chemical science, 2020, 11, 6121-6133
1558124 CIFC22 H21 F3 N2 O3 S3P 1 21/n 113.3057; 12.066; 14.7108
90; 108.185; 90		2243.81Clark, Ryan; Nawawi, Mohd A.; Dobre, Ana; Pugh, David; Liu, Qingshan; Ivanov, Aleksandar P.; White, Andrew J. P.; Edel, Joshua B.; Kuimova, Marina K.; McIntosh, Alastair J. S.; Welton, Tom
The effect of structural heterogeneity upon the microviscosity of ionic liquids.
Chemical science, 2020, 11, 6121-6133
1558125 CIFC23 H21 F6 N3 O4 S4I 1 2/a 114.7979; 21.9313; 18.008
90; 112.854; 90		5385.48Clark, Ryan; Nawawi, Mohd A.; Dobre, Ana; Pugh, David; Liu, Qingshan; Ivanov, Aleksandar P.; White, Andrew J. P.; Edel, Joshua B.; Kuimova, Marina K.; McIntosh, Alastair J. S.; Welton, Tom
The effect of structural heterogeneity upon the microviscosity of ionic liquids.
Chemical science, 2020, 11, 6121-6133
1558126 CIFC21 H21 F6 N2 P S2C 1 2/c 117.6864; 18.688; 15.795
90; 114.792; 90		4739.5Clark, Ryan; Nawawi, Mohd A.; Dobre, Ana; Pugh, David; Liu, Qingshan; Ivanov, Aleksandar P.; White, Andrew J. P.; Edel, Joshua B.; Kuimova, Marina K.; McIntosh, Alastair J. S.; Welton, Tom
The effect of structural heterogeneity upon the microviscosity of ionic liquids.
Chemical science, 2020, 11, 6121-6133
1558127 CIFC33 H37 N OP -110.7051; 10.9218; 12.9779
81.166; 67.584; 72.381		1335.66Shankar, Majji; Rit, Raja K.; Sau, Somratan; Mukherjee, Kallol; Gandon, Vincent; Sahoo, Akhila K.
Double annulation of ortho- and peri-C–H bonds of fused (hetero)arenes to unusual oxepino-pyridines
Chemical Science, 2020, 11, 10770-10777
1558128 CIFC28.48 H23 Cl N O2P 1 21/n 114.5781; 9.3138; 18.8307
90; 94.961; 90		2547.21Shankar, Majji; Rit, Raja K.; Sau, Somratan; Mukherjee, Kallol; Gandon, Vincent; Sahoo, Akhila K.
Double annulation of ortho- and peri-C‒H bonds of fused (hetero)arenes to unusual oxepino-pyridines
Chemical Science, 2020, 11, 10770-10777
1558129 CIFC41 H45 N OP 1 21/n 115.001; 10.5247; 22.239
90; 94.419; 90		3500.7Shankar, Majji; Rit, Raja K.; Sau, Somratan; Mukherjee, Kallol; Gandon, Vincent; Sahoo, Akhila K.
Double annulation of ortho- and peri-C–H bonds of fused (hetero)arenes to unusual oxepino-pyridines
Chemical Science, 2020, 11, 10770-10777
1558130 CIFC16 H8 O12 UC 1 2/c 117.7447; 12.5982; 9.2934
90; 114.702; 90		1887.4Halter, Dominik P.; Klein, Ryan A.; Boreen, Michael; Trump, Benjamin A.; Brown, Craig M.; Long, Jeffrey R.
Self-Adjusting Binding Pockets Enhance H2 and CH4 Adsorption in a Uranium-Based Metal‒Organic Framework
Chemical Science, 2020
1558131 CIFC28 H24 Cl N2 O5P 4/n :226.429; 26.429; 7.867
90; 90; 90		5495Duan, Wen-Di; Zhang, Yu-Fang; Hu, Youhong
NaH Promoted One-Pot Tandem Reactions of 3-(1-Alkynyl) Chromones to Form 2-Nitrogen-Substituted Xanthones
ACS Omega, 2020, 5, 13454-13461
1558132 CIFC20 H24 Cl N O4P 1 21/n 122.7581; 7.6989; 23.0256
90; 113.649; 90		3695.56Xu, Beibei; Jiang, Xunjin; Xiong, Jing; Lan, Jun; Tian, Yuan; Zhong, Linhai; Wang, Xinquan; Xu, Ning; Cao, Hanwei; Zhang, Wenqing; Zhang, Hao; Hong, Xiaoting; Zhan, Yan-Yan; Zhang, Yandong; Hu, Tianhui
Structure-Activity Relationship Study Enables the Discovery of a Novel Berberine Analogue as RXRα Activator to Inhibit Colon Cancer.
Journal of medicinal chemistry, 2020
1558133 CIFC20 H26 N0 O5 SP 1 21 16.703; 8.4049; 17.5344
90; 98.188; 90		977.78Zhao, Zhifei; Bagdi, Prasanta Ray; Yang, Shuang; Liu, Jinggong; Cotman, Andrej Emanuel; Xu, Weici; Fang, Xinqiang
Correction to Stereodivergent Access to Enantioenriched Epoxy Alcohols with Three Stereogenic Centers via Ruthenium-Catalyzed Transfer Hydrogenation
Organic Letters, 2020
1558134 CIFC13 H16 O2P 21 21 215.5579; 7.7831; 25.2947
90; 90; 90		1094.19Zhao, Zhifei; Bagdi, Prasanta Ray; Yang, Shuang; Liu, Jinggong; Cotman, Andrej Emanuel; Xu, Weici; Fang, Xinqiang
Correction to Stereodivergent Access to Enantioenriched Epoxy Alcohols with Three Stereogenic Centers via Ruthenium-Catalyzed Transfer Hydrogenation
Organic Letters, 2020
1558135 CIFC18 H32 Cl Cu N7 O4C 1 c 19.682; 18.886; 24.789
90; 99.902; 90		4465Martínez-Camarena, Álvaro; Sánchez-Murcia, Pedro A; Blasco, Salvador; González, Leticia; García-España, Enrique
Unveiling the reaction mechanism of novel copper N-alkylated tetra-azacyclophanes with outstanding superoxide dismutase activity.
Chemical communications (Cambridge, England), 2020, 56, 7511-7514
1558136 CIFC32 H38 Au F6 Fe N2 O5 SbP 1 21/n 112.4358; 18.8623; 15.7372
90; 89.999; 90		3691.4Ponduru, Tharun Teja; Wang, Guocang; Manoj, Sai; Pan, Sudip; Zhao, Lili; Frenking, Gernot; Dias, H. V. Rasika
Synthesis and characterization of heterometallic complexes involving coinage metals and isoelectronic Fe(CO)<sub>5</sub>, [Mn(CO)<sub>5</sub>]<sup>-</sup> and [Fe(CO)<sub>4</sub>CN]<sup>-</sup> ligands.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 8566-8581
1558137 CIFC27 H35 Au F6 Fe N O5 SbP 1 21/n 114.2376; 15.3986; 14.8972
90; 98.783; 90		3227.8Ponduru, Tharun Teja; Wang, Guocang; Manoj, Sai; Pan, Sudip; Zhao, Lili; Frenking, Gernot; Dias, H. V. Rasika
Synthesis and characterization of heterometallic complexes involving coinage metals and isoelectronic Fe(CO)<sub>5</sub>, [Mn(CO)<sub>5</sub>]<sup>-</sup> and [Fe(CO)<sub>4</sub>CN]<sup>-</sup> ligands.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 8566-8581
1558138 CIFC36 H46 Au Mn N2 O6P b c m8.6463; 19.4473; 21.4257
90; 90; 90		3602.7Ponduru, Tharun Teja; Wang, Guocang; Manoj, Sai; Pan, Sudip; Zhao, Lili; Frenking, Gernot; Dias, H. V. Rasika
Synthesis and characterization of heterometallic complexes involving coinage metals and isoelectronic Fe(CO)<sub>5</sub>, [Mn(CO)<sub>5</sub>]<sup>-</sup> and [Fe(CO)<sub>4</sub>CN]<sup>-</sup> ligands.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 8566-8581
1558139 CIFC32 H33 Au Mn O5 PP -110.8061; 11.9033; 13.6638
82.628; 78.028; 64.197		1546.5Ponduru, Tharun Teja; Wang, Guocang; Manoj, Sai; Pan, Sudip; Zhao, Lili; Frenking, Gernot; Dias, H. V. Rasika
Synthesis and characterization of heterometallic complexes involving coinage metals and isoelectronic Fe(CO)<sub>5</sub>, [Mn(CO)<sub>5</sub>]<sup>-</sup> and [Fe(CO)<sub>4</sub>CN]<sup>-</sup> ligands.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 8566-8581
1558140 CIFC36 H46 Ag Mn N2 O6P b c m8.6971; 19.4845; 21.3902
90; 90; 90		3624.8Ponduru, Tharun Teja; Wang, Guocang; Manoj, Sai; Pan, Sudip; Zhao, Lili; Frenking, Gernot; Dias, H. V. Rasika
Synthesis and characterization of heterometallic complexes involving coinage metals and isoelectronic Fe(CO)<sub>5</sub>, [Mn(CO)<sub>5</sub>]<sup>-</sup> and [Fe(CO)<sub>4</sub>CN]<sup>-</sup> ligands.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 8566-8581
1558141 CIFC33 H40 Cl2 Cu Fe N3 O4P 1 21/n 111.1739; 18.4203; 18.3635
90; 106.685; 90		3620.6Ponduru, Tharun Teja; Wang, Guocang; Manoj, Sai; Pan, Sudip; Zhao, Lili; Frenking, Gernot; Dias, H. V. Rasika
Synthesis and characterization of heterometallic complexes involving coinage metals and isoelectronic Fe(CO)<sub>5</sub>, [Mn(CO)<sub>5</sub>]<sup>-</sup> and [Fe(CO)<sub>4</sub>CN]<sup>-</sup> ligands.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 8566-8581
1558142 CIFC53 H75 N2 O2 UP 1 21/c 120.552; 11.9252; 21.1347
90; 112.708; 90		4778.3Boreen, Michael A.; Gould, Colin A.; Booth, Corwin H.; Hohloch, Stephan; Arnold, John
Structure and magnetism of a tetrahedral uranium(iii) β-diketiminate complex.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 7938-7944
1558143 CIFC85 H123 I2 N4 O2 U2P -112.2023; 16.5876; 22.5734
75.346; 80.632; 69.918		4137.1Boreen, Michael A.; Gould, Colin A.; Booth, Corwin H.; Hohloch, Stephan; Arnold, John
Structure and magnetism of a tetrahedral uranium(iii) β-diketiminate complex.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 7938-7944
1558144 CIFC23 H17 Cl N2 O3P 1 21/c 114.9291; 10.5173; 14.418
90; 111.081; 90		2112.31Husain, Ali; Ganesan, Asaithampi; Machacek, Miloslav; Cerveny, Lukas; Kubat, Pavel; Ghazal, Basma; Zimcik, Petr; Makhseed, Saad
Dually directional glycosylated phthalocyanines as extracellular red-emitting fluorescent probes.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 9605-9617
1558145 CIFC46 H36 N4 O6P -18.4034; 10.6002; 12.8112
65.879; 83.922; 82.056		1030Husain, Ali; Ganesan, Asaithampi; Machacek, Miloslav; Cerveny, Lukas; Kubat, Pavel; Ghazal, Basma; Zimcik, Petr; Makhseed, Saad
Dually directional glycosylated phthalocyanines as extracellular red-emitting fluorescent probes.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 9605-9617
1558146 CIFC23 H18 N2 O3P -110.4756; 11.1851; 11.4936
101.408; 107.744; 117.153		1047.2Husain, Ali; Ganesan, Asaithampi; Machacek, Miloslav; Cerveny, Lukas; Kubat, Pavel; Ghazal, Basma; Zimcik, Petr; Makhseed, Saad
Dually directional glycosylated phthalocyanines as extracellular red-emitting fluorescent probes.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 9605-9617
1558147 CIFC8 H7 N3 SP 1 21/c 111.1251; 7.5242; 11.194
90; 115.098; 90		848.55Manna, Amit Kumar; Chowdhury, Shubhamoy; Patra, Goutam K.
Combined experimental and theoretical studies on a phenyl thiadiazole-based novel turn-on fluorescent colorimetric Schiff base chemosensor for the selective and sensitive detection of Al3+
New Journal of Chemistry, 2020, 44, 10819-10832
1558148 CIFC16 H26 O3P 21 21 218.3643; 9.9485; 17.7102
90; 90; 90		1473.71Lydon, Christina A.; Mathivathanan, Logesh; Sanchez, Juanita; Dos Santos, Larissa A. H.; Sauvage, Thomas; Gunasekera, Sarath P.; Paul, Valerie J.; Berry, John P.
Eudesmacarbonate, a Eudesmane-Type Sesquiterpene from a Marine Filamentous Cyanobacterial Mat (Oscillatoriales) in the Florida Keys.
Journal of natural products, 2020
1558149 CIFC28 H24 Co N2 O10 S2C 1 2/c 120.1441; 12.2778; 11.4937
90; 92.993; 90		2838.8Yang, Chun; Cai, Wen-Jing; Yu, Bin-Bin; Qiu, Hong; Li, Meng-Li; Zhu, Lian-Wen; Yan, Zheng; Hou, Lei; Wang, Yao-Yu
Performance enhancement of oxygen evolution reaction through incorporating bimetallic electrocatalysts in two-dimensional metal‒organic frameworks
Catalysis Science & Technology, 2020, 10, 3897-3903
1558150 CIFC28 H24 Co0.79 Fe0.21 N2 O10 S2C 1 2/c 120.1868; 12.2668; 11.4817
90; 92.862; 90		2839.64Yang, Chun; Cai, Wen-Jing; Yu, Bin-Bin; Qiu, Hong; Li, Meng-Li; Zhu, Lian-Wen; Yan, Zheng; Hou, Lei; Wang, Yao-Yu
Performance enhancement of oxygen evolution reaction through incorporating bimetallic electrocatalysts in two-dimensional metal‒organic frameworks
Catalysis Science & Technology, 2020, 10, 3897-3903
1558151 CIFC28 H24 Co0.29 N2 Ni0.71 O10 S2C 1 2/c 120.1616; 12.1398; 11.4274
90; 92.792; 90		2793.63Yang, Chun; Cai, Wen-Jing; Yu, Bin-Bin; Qiu, Hong; Li, Meng-Li; Zhu, Lian-Wen; Yan, Zheng; Hou, Lei; Wang, Yao-Yu
Performance enhancement of oxygen evolution reaction through incorporating bimetallic electrocatalysts in two-dimensional metal‒organic frameworks
Catalysis Science & Technology, 2020, 10, 3897-3903
1558152 CIFC31 H34 O4P -17.8821; 12.0559; 14.7116
86.518; 74.563; 78.674		1321.25Xu, Zhengshuai; Tang, Yitian; Shen, Chaoren; Zhang, Hongru; Gan, Yuxin; Ji, Xiaolei; Tian, Xinxin; Dong, Kaiwu
Nickel-catalyzed regio- and diastereoselective hydroarylative and hydroalkenylative cyclization of 1,6-dienes.
Chemical communications (Cambridge, England), 2020, 56, 7741-7744
1558153 CIFC25 H23 N O5 SP 1 21 15.9143; 12.5172; 14.5829
90; 97.421; 90		1070.54Tao, Mengna; Tu, Youshao; Liu, Yu; Wu, Haihong; Liu, Lu; Zhang, Junliang
Pd/Xiang-Phos-catalyzed enantioselective intermolecular carboheterofunctionalization under mild conditions.
Chemical science, 2020, 11, 6283-6288
1558154 CIFC17 H17 N O3 SP 21 21 218.9043; 10.7948; 31.6319
90; 90; 90		3040.46Tao, Mengna; Tu, Youshao; Liu, Yu; Wu, Haihong; Liu, Lu; Zhang, Junliang
Pd/Xiang-Phos-catalyzed enantioselective intermolecular carboheterofunctionalization under mild conditions.
Chemical science, 2020, 11, 6283-6288
1558155 CIFC98 H129 Cl4 Mn2 N7 O12 ZnP -114.1647; 15.302; 25.9901
88.142; 84.223; 66.438		5137.23Doistau, Benjamin; Benda, Lorien; Cantin, Jean-Louis; Cador, Olivier; Pointillart, Fabrice; Wernsdorfer, Wolfgang; Chamoreau, Lise-Marie; Marvaud, Valérie; Hasenknopf, Bernold; Vives, Guillaume
Dual switchable molecular tweezers incorporating anisotropic Mn<sup>III</sup>-salphen complexes.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 8872-8882
1558156 CIFC194 H240 Cl4 Mn4 N17 O27 Zn3P -115.1358; 16.5212; 22.9401
89.629; 72.981; 73.972		5254.7Doistau, Benjamin; Benda, Lorien; Cantin, Jean-Louis; Cador, Olivier; Pointillart, Fabrice; Wernsdorfer, Wolfgang; Chamoreau, Lise-Marie; Marvaud, Valérie; Hasenknopf, Bernold; Vives, Guillaume
Dual switchable molecular tweezers incorporating anisotropic Mn<sup>III</sup>-salphen complexes.
Dalton transactions (Cambridge, England : 2003), 2020, 49, 8872-8882
1558157 CIFC22 H30 N4 O8 ZnP -110.854; 14.735; 17.464
67.045; 79.81; 77.424		2497Wen, Yuehong; Liu, Qiang; Su, Shaodong; Yang, Yuying; Li, Xiaofang; Zhu, Qi-Long; Wu, Xintao
Coordination tailoring of water-labile 3D MOFs to fabricate ultrathin 2D MOF nanosheets.
Nanoscale, 2020, 12, 12767-12772
1558158 CIFC20 H28 O2P 21 21 218.5365; 12.2999; 16.448
90; 90; 90		1727.01Seijo, Lorenzo; Ondet, Pierrick; Olivero, Sandra; Duñach, Elisabet
Heterogeneous catalysis for the tandem cyclisation of unsaturated alcohols
New Journal of Chemistry, 2020, 44, 10479-10483
1558159 CIF
HKL
Paper		C25 H18 Cl F2 N5 SP 1 21/c 116.9376; 13.144; 10.6399
90; 92.891; 90		2365.72Alanazi, Saud A.; Abdel-Wahab, Bakr F.; Hegazy, Amany S.; Kariuki, Benson M.; El-Hiti, Gamal A.
2-[3-(4-Chlorophenyl)-5-(4-fluorophenyl)-4,5-dihydro-1<i>H</i>-pyrazol-1-yl]-5-[(4-fluorophenyl)diazenyl]-4-methylthiazole
IUCrData, 2020, 5, x200700
1558160 CIF
HKL
Paper		C16 H22 N4 O3 SP 1 21/n 110.882; 8.4029; 18.9678
90; 95.44; 90		1726.61Cyr, Noah; Zeller, Matthias; Hillesheim, Patrick C.; Mirjafari, Arsalan
2,3-Dimethyl-1<i>H</i>-imidazol-3-ium benzenesulfonate–1,2-dimethyl-1<i>H</i>-imidazole co-crystal
IUCrData, 2020, 5, x200689
1558161 CIF
Paper		C12 H22 N2 O3 SP 1 n 110.2564; 6.5369; 10.9683
90; 95.067; 90		732.5Sarr, Bougar; Mbaye, Abdou; Touré, Assane; Diop, Cheikh Abdoul Khadir; Sidibé, Mamadou; Michaud, François
Dipropylammonium 4-aminobenzenesulfonate
IUCrData, 2020, 5, x200659
1558162 CIFC32 H44 O10P 21 21 218.4907; 9.263; 38.6476
90; 90; 90		3039.61Yu, Jin-Hai; Zhang, Hua; Zhou, Bin; Zimbres, Flavia M.; Dalal, Seema; Liu, Qun-Fang; Cassera, Maria B.; Yue, Jian-Min
Limonoids from <i>Cipadessa baccifera</i>.
Journal of natural products, 2020
1558163 CIFC20 H20 O8P 1 21/c 19.271; 9.6883; 19.4904
90; 92.098; 90		1749.46Lum, Kah Yean; Taki, Aya C.; Gasser, Robin B.; Tietjen, Ian; Ekins, Merrick G.; White, Jonathan M.; Addison, Russell S.; Hayes, Sasha; St John, James; Davis, Rohan A.
Comatulins A-E, Taurine-Conjugated Anthraquinones from the Australian Crinoid <i>Comatula rotalaria</i>.
Journal of natural products, 2020, 83, 1971-1979
1558164 CIFC16 H29 Cl F6 N2 O P Ru SbP 1 21/n 111.7394; 14.7656; 14.6955
90; 108.172; 90		2420.26González-Fernández, Rebeca; Álvarez, Daniel; Crochet, Pascale; Cadierno, Victorio; Menéndez, M. Isabel; López, Ramón
Catalytic hydration of cyanamides with phosphinous acid-based ruthenium(ii) and osmium(ii) complexes: scope and mechanistic insights
Catalysis Science & Technology, 2020, 10, 4084-4098
1558165 CIFC17 H31 Cl F6 N2 O P Ru SbP 1 21/n 18.3717; 21.574; 14.8558
90; 105.025; 90		2591.39González-Fernández, Rebeca; Álvarez, Daniel; Crochet, Pascale; Cadierno, Victorio; Menéndez, M. Isabel; López, Ramón
Catalytic hydration of cyanamides with phosphinous acid-based ruthenium(ii) and osmium(ii) complexes: scope and mechanistic insights
Catalysis Science & Technology, 2020, 10, 4084-4098
1558166 CIFC55 H49 Co N4 O3P -3 c 126.2516; 26.2516; 26.8975
90; 90; 120		16052.9Wu, Zhenqiang; Peng, Chi-How; Fu, Xuefeng
Tacticity control approached by visible-light induced organocobalt-mediated radical polymerization: the synthesis of crystalline poly(N,N-dimethylacrylamide) with high isotacticity
Polymer Chemistry, 2020, 11, 4387-4395
1558167 CIFC73 H57 Br2 Cl3 N2 Ni OP 1 21/c 126.3082; 13.2167; 19.661
90; 94.33; 90		6816.8Hu, Xiaoqiang; Wang, Chaoqun; Jian, Zhongbao
Comprehensive studies of the ligand electronic effect on unsymmetrical α-diimine nickel(ii) promoted ethylene (co)polymerizations
Polymer Chemistry, 2020, 11, 4005-4012
1558168 CIFC72 H52 Br2 F4 N2 Ni OP -111.6968; 14.6139; 20.2591
93.384; 95.778; 100.036		3382.3Hu, Xiaoqiang; Wang, Chaoqun; Jian, Zhongbao
Comprehensive studies of the ligand electronic effect on unsymmetrical α-diimine nickel(ii) promoted ethylene (co)polymerizations
Polymer Chemistry, 2020, 11, 4005-4012
1558171 CIFC13 H13 Bi S2P -14.0972; 10.591; 16.59
108.6; 94.491; 90.019		680Mukhopadhyay, Deb Pratim; Schleier, Domenik; Wirsing, Sara; Ramler, Jacqueline; Kaiser, Dustin; Reusch, Engelbert; Hemberger, Patrick; Preitschopf, Tobias; Krummenacher, Ivo; Engels, Bernd; Fischer, Ingo; Lichtenberg, Crispin
Methylbismuth: an Organometallic Bismuthinidene Biradical
Chemical Science, 2020
1558174 CIFC18 H18 N2 O2 SP 1 21/n 16.6095; 17.787; 14.0522
90; 103.1; 90		1609.03Pagire, Santosh K.; Kumagai, Naoya; Shibasaki, Masakatsu
Introduction of a 7-aza-6-MeO-indoline auxiliary in Lewis-acid/photoredox cooperative catalysis: highly enantioselective aminomethylation of α,β-unsaturated amides
Chemical Science, 2020, 11, 5168-5174
1558175 CIFC19 H23 N3 O2P 16.0571; 10.1647; 14.3715
103.628; 98.272; 101.112		827.01Pagire, Santosh K.; Kumagai, Naoya; Shibasaki, Masakatsu
Introduction of a 7-aza-6-MeO-indoline auxiliary in Lewis-acid/photoredox cooperative catalysis: highly enantioselective aminomethylation of α,β-unsaturated amides
Chemical Science, 2020, 11, 5168-5174
1558176 CIFC80 H87 Cu F6 N3 O5 P3P 1 21/c 121.7889; 16.4491; 24.0629
90; 106.505; 90		8269Pagire, Santosh K.; Kumagai, Naoya; Shibasaki, Masakatsu
Introduction of a 7-aza-6-MeO-indoline auxiliary in Lewis-acid/photoredox cooperative catalysis: highly enantioselective aminomethylation of α,β-unsaturated amides
Chemical Science, 2020, 11, 5168-5174
1558177 CIFC96 H74 Cl6P 1 21/n 113.9419; 18.9963; 14.6207
90; 97.9869; 90		3834.65Shudo, Hiroki; Kuwayama, Motonobu; Segawa, Yasutomo; Itami, Kenichiro
Synthesis of Cycloiptycenes from Carbon Nanobelt
Chemical Science, 2020
1558178 CIFC74 H84 O19R -3 :H31.0383; 31.0383; 11.8708
90; 90; 120		9903.9Shudo, Hiroki; Kuwayama, Motonobu; Segawa, Yasutomo; Itami, Kenichiro
Synthesis of Cycloiptycenes from Carbon Nanobelt
Chemical Science, 2020
1558179 CIFC201 H174 Cl6C 1 2/c 146.422; 7.7267; 46.356
90; 109.884; 90		15636Shudo, Hiroki; Kuwayama, Motonobu; Segawa, Yasutomo; Itami, Kenichiro
Synthesis of Cycloiptycenes from Carbon Nanobelt
Chemical Science, 2020
1558180 CIFC142.5 H106 O2P -111.0799; 15.4092; 16.833
111.731; 95.979; 99.11		2594.2Shudo, Hiroki; Kuwayama, Motonobu; Segawa, Yasutomo; Itami, Kenichiro
Synthesis of Cycloiptycenes from Carbon Nanobelt
Chemical Science, 2020
1558181 CIFC52 H83 Cl2 Cu N13 O9 SiP -18.9253; 15.5724; 25.2322
98.168; 91.134; 103.075		3376.5Peters, Anna D.; Borsley, Stefan; della Sala, Flavio; Cairns-Gibson, Dominic F.; Leonidou, Marios; Clayden, Jonathan; Whitehead, George F. S.; Vitorica-Yrzebal, Inigo; Takano, Eriko; Burthem, John; Cockroft, Scott Lee; Webb, Simon
Switchable foldamer ion channels with antibacterial activity
Chemical Science, 2020
1558182 CIFC53.81 H87.51 N13 O9.45 SiP -19.207; 15.6088; 23.6308
85.168; 79.223; 76.681		3243.35Peters, Anna D.; Borsley, Stefan; della Sala, Flavio; Cairns-Gibson, Dominic F.; Leonidou, Marios; Clayden, Jonathan; Whitehead, George F. S.; Vitorica-Yrzebal, Inigo; Takano, Eriko; Burthem, John; Cockroft, Scott Lee; Webb, Simon
Switchable foldamer ion channels with antibacterial activity
Chemical Science, 2020
1558183 CIFC53 H84 Cl Cu N13 O12 SiP 21 21 219.1099; 24.1351; 34.1137
90; 90; 90		7500.5Peters, Anna D.; Borsley, Stefan; della Sala, Flavio; Cairns-Gibson, Dominic F.; Leonidou, Marios; Clayden, Jonathan; Whitehead, George F. S.; Vitorica-Yrzebal, Inigo; Takano, Eriko; Burthem, John; Cockroft, Scott Lee; Webb, Simon
Switchable foldamer ion channels with antibacterial activity
Chemical Science, 2020
1558184 CIFC14 H14 O2P 1 21/a 112.7006; 10.0271; 20.1044
90; 106.525; 90		2454.55RESENDE, Pamela C. S.; COURI, Mara R. C.; MIGUEL, Fábio B.; CUIN, Alexandre
Analytical, Spectroscopic and Crystallographic Characterization of 3-[(2<i>E</i>)-3-Phenylprop-2-en-1-ylidene]pentane-2,4-dione
X-ray Structure Analysis Online, 2020, 36, 15-16
1558185 CIFC47 H37 Cl Cu F6 N2 O P3P 1 21/c 110.4786; 18.9864; 22.1096
90; 100.077; 90		4330.87Meyer, Marco; Brunner, Fabian; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
Chimera Diimine Ligands in Emissive [Cu(P^P)(N^N)][PF6] Complexes
Inorganics, 2020, 8, 33
1558186 CIFC50 H41 Cl Cu F6 N2 O P3P -111.4363; 14.0871; 14.803
89.133; 68.457; 88.73		2217.62Meyer, Marco; Brunner, Fabian; Prescimone, Alessandro; Constable, Edwin C.; Housecroft, Catherine E.
Chimera Diimine Ligands in Emissive [Cu(P^P)(N^N)][PF6] Complexes
Inorganics, 2020, 8, 33
1558187 CIFC29 H27 N O SnP 1 21/n 19.3351; 18.4709; 14.3598
90; 93.846; 90		2470.5Bender, Desiree N.; Lough, Alan J.; Wylie, R. Stephen; Gossage, Robert A.; Foucher, Daniel A.
Preparation and DFT Studies of κ2C,N-Hypercoordinated Oxazoline Organotins: Monomer Constructs for Stable Polystannanes
Inorganics, 2020, 8, 35
1558188 CIFC23 H22 Cl N O SnP -19.1303; 9.302; 24.2461
90.942; 91.775; 91.724		2056.99Bender, Desiree N.; Lough, Alan J.; Wylie, R. Stephen; Gossage, Robert A.; Foucher, Daniel A.
Preparation and DFT Studies of κ2C,N-Hypercoordinated Oxazoline Organotins: Monomer Constructs for Stable Polystannanes
Inorganics, 2020, 8, 35
1558189 CIFC17 H17 Br2 N O SnP 1 21/n 110.5295; 10.0336; 17.1396
90; 96.677; 90		1798.5Bender, Desiree N.; Lough, Alan J.; Wylie, R. Stephen; Gossage, Robert A.; Foucher, Daniel A.
Preparation and DFT Studies of κ2C,N-Hypercoordinated Oxazoline Organotins: Monomer Constructs for Stable Polystannanes
Inorganics, 2020, 8, 35
1558190 CIFC18 H19 Br2 N O SnP -18.453; 10.2368; 11.7987
93.059; 101.936; 108.325		940.5Bender, Desiree N.; Lough, Alan J.; Wylie, R. Stephen; Gossage, Robert A.; Foucher, Daniel A.
Preparation and DFT Studies of κ2C,N-Hypercoordinated Oxazoline Organotins: Monomer Constructs for Stable Polystannanes
Inorganics, 2020, 8, 35
1558191 CIFC30 H29 N O SnP 21 21 218.4502; 18.9557; 31.5231
90; 90; 90		5049.4Bender, Desiree N.; Lough, Alan J.; Wylie, R. Stephen; Gossage, Robert A.; Foucher, Daniel A.
Preparation and DFT Studies of κ2C,N-Hypercoordinated Oxazoline Organotins: Monomer Constructs for Stable Polystannanes
Inorganics, 2020, 8, 35
1558192 CIFC133 H101 Cl5 I3 N9 Ni12 O35P -119.422; 22.654; 25.321
115.783; 92.992; 106.118		9443Perlepe, Panagiota S.; Pantelis, Konstantinos N.; Cunha-Silva, Luís; Bekiari, Vlasoula; Escuer, Albert; Stamatatos, Theocharis C.
Rare Nuclearities in Ni(II) Cluster Chemistry: An Unprecedented {Ni12} Nanosized Cage from the Use of N-Naphthalidene-2-Amino-5-Chlorobenzoic Acid
Inorganics, 2020, 8, 32
1558193 CIFCu Ga S4 Zn2I -4 2 m5.3626; 5.3626; 10.5873
90; 90; 90		304.46Bindi, Luca; Jaszczak, John A.
Richardsite, Zn2CuGaS4, A New Gallium-Essential Member of the Stannite Group from the Gem Mines near Merelani, Tanzania
Minerals, 2020, 10, 467
1558194 CIFC23 H18 Br N O6P 1 21/n 19.4765; 9.2067; 24.1253
90; 92.1209; 90		2103.43Ryzhkova, Yuliya E.; Ryzhkov, Fedor V.; Elinson, Michail N.
3-(4-Bromophenyl)-4-{[3-hydroxy-6-(hydroxymethyl)-4-oxo-4H-pyran-2-yl](m-tolyl)methyl}isoxazol-5(2H)-one
Molbank, 2020, 2020, M1135
1558195 CIFC12 H36 Ag Br12 In N4P 1 2/c 18.4965; 7.8419; 26.1413
90; 90.318; 90		1741.73Connor, Bridget A.; Biega, Raisa-Ioana; Leppert, Linn; Karunadasa, Hemamala I.
Dimensional reduction of the small-bandgap double perovskite Cs<sub>2</sub>AgTlBr<sub>6</sub>.
Chemical science, 2020, 11, 7708-7715
1558196 CIFC10 H22 Ag Br8 N6 TlC 1 2/c 111.3098; 12.6075; 18.2063
90; 95.713; 90		2583.11Connor, Bridget A.; Biega, Raisa-Ioana; Leppert, Linn; Karunadasa, Hemamala I.
Dimensional reduction of the small-bandgap double perovskite Cs<sub>2</sub>AgTlBr<sub>6</sub>.
Chemical science, 2020, 11, 7708-7715
1558197 CIFC12 H36 Ag Br12 N4 TlP 1 2/c 18.4673; 7.8406; 26.1647
90; 90.312; 90		1737.01Connor, Bridget A.; Biega, Raisa-Ioana; Leppert, Linn; Karunadasa, Hemamala I.
Dimensional reduction of the small-bandgap double perovskite Cs<sub>2</sub>AgTlBr<sub>6</sub>.
Chemical science, 2020, 11, 7708-7715
1558198 CIFC16 H24 Ag Br7 Cs N2 TlP -17.8617; 7.8687; 23.0185
83.703; 85.727; 89.818		1411.41Connor, Bridget A.; Biega, Raisa-Ioana; Leppert, Linn; Karunadasa, Hemamala I.
Dimensional reduction of the small-bandgap double perovskite Cs<sub>2</sub>AgTlBr<sub>6</sub>.
Chemical science, 2020, 11, 7708-7715
1558199 CIFC18 H14.61 N2 O2P -18.1603; 9.806; 10.9374
92.13; 108.187; 114.618		741.61Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558200 CIFC18 H14.6 N2 O2P -18.18873; 9.82362; 10.94583
92.3016; 108.097; 114.537		746.66Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558201 CIFC18 H14.58 N2 O2P -18.20354; 9.82973; 10.95062
92.3825; 108.058; 114.49		749.11Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558202 CIFC18 H14.6 N2 O2P -18.23553; 9.85058; 10.96006
92.5489; 107.957; 114.434		754.73Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558203 CIFC18 H14.59 N2 O2P -18.17391; 9.8142; 10.94231
92.2144; 108.147; 114.571		744.1Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558204 CIFC18 H15.03 N2 O2P -18.12328; 9.8351; 10.91847
92.3839; 107.856; 114.498		741.07Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558205 CIFC18 H14.61 N2 O2P -18.21931; 9.84133; 10.95472
92.4662; 108.006; 114.464		751.94Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558206 CIFC18 H15.01 N2 O2P -18.13837; 9.845; 10.92312
92.4784; 107.824; 114.466		743.63Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558207 CIFC18 H15.02 N2 O2P -18.15433; 9.85391; 10.92795
92.5643; 107.788; 114.426		746.298Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558208 CIFC18 H15.02 N2 O2P -18.18944; 9.8706; 10.93717
92.7279; 107.74; 114.348		751.727Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558209 CIFC18 H15.02 N2 O2P -18.17154; 9.86186; 10.93238
92.6441; 107.766; 114.385		748.951Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558210 CIFC18 H15.02 N2 O2P -18.2084; 9.88002; 10.94248
92.814; 107.711; 114.311		754.705Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558211 CIFC18.01 H15.51 N2 O2P -18.09764; 9.8669; 10.89543
92.528; 107.588; 114.469		740.79Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558212 CIFC18 H15.5 N2 O2P -18.11309; 9.8742; 10.89995
92.6153; 107.553; 114.438		743.2Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558213 CIFC18.01 H15.51 N2 O2P -18.14797; 9.89332; 10.90921
92.7875; 107.497; 114.364		748.78Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558214 CIFC18.01 H15.51 N2 O2P -18.13025; 9.88487; 10.90533
92.7008; 107.519; 114.402		746.12Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558215 CIFC18.01 H15.51 N2 O2P -18.16783; 9.90151; 10.91446
92.8705; 107.486; 114.321		751.69Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558216 CIFC16.95 H14 N3.05 O2P -18.07384; 9.7536; 10.90755
92.9033; 107.326; 114.087		733.83Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558217 CIFC16.92 H14 N3.07 O2P -18.1172; 9.7795; 10.9256
93.2084; 107.177; 113.972		741.6Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558218 CIFC16.9 H14 N3.08 O2P -18.1338; 9.791; 10.934
93.322; 107.125; 113.929		744.78Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558219 CIFC16.96 H14 N3.04 O2P -18.10148; 9.7713; 10.9201
93.1101; 107.23; 114.004		738.97Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558220 CIFC16.97 H14 N3.01 O2P -18.0587; 9.7436; 10.9027
92.797; 107.379; 114.108		731.27Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558221 CIFC18.02 H15.52 N2 O2P -18.18898; 9.90985; 10.91962
92.962; 107.478; 114.277		754.69Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558222 CIFC16.53 H14 N3.47 O2P -17.9981; 9.7278; 10.8484
93.16; 106.919; 113.993		723.07Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558223 CIFC16.51 H14 N3.49 O2P -18.01758; 9.732; 10.86038
93.301; 106.87; 113.897		726.41Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558224 CIFC16.94 H14 N3.06 O2P -18.08726; 9.7628; 10.91257
93.0131; 107.272; 114.044		736.33Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558225 CIFC16.48 H14 N3.52 O2P -18.0515; 9.7483; 10.8766
93.548; 106.805; 113.77		732.23Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558226 CIFC16.49 H14 N3.51 O2P -18.0696; 9.7563; 10.8866
93.656; 106.798; 113.712		735.24Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558227 CIFC16.47 H14 N3.52 O2P -18.0903; 9.7624; 10.8911
93.754; 106.789; 113.675		737.88Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558228 CIFC16.51 H14 N3.49 O2P -18.03328; 9.7401; 10.8685
93.4267; 106.846; 113.829		729.18Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558229 CIFC17.6 H15.6 N2.4 O2P -18.0377; 9.8551; 10.8773
92.913; 107.077; 114.297		735.96Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558230 CIFC17.57 H15.57 N2.43 O2P -18.05644; 9.86768; 10.88249
92.9895; 107.093; 114.302		738.62Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558231 CIFC17.03 H15.03 N2.97 O2P -18.06741; 9.8484; 10.893
93.6858; 106.675; 113.951		741.35Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558232 CIFC17.56 H15.56 N2.44 O2P -18.09014; 9.88806; 10.89279
93.1584; 107.044; 114.243		744.09Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558233 CIFC17.54 H15.54 N2.46 O2P -18.10962; 9.89822; 10.89834
93.245; 107.036; 114.206		747.06Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558234 CIFC17.04 H15.04 N2.96 O2P -18.04836; 9.83877; 10.88786
93.5909; 106.703; 113.993		738.39Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558235 CIFC17.55 H15.55 N2.45 O2P -18.07233; 9.87774; 10.88779
93.07; 107.065; 114.273		741.29Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558236 CIFC17.08 H15.08 N2.92 O2P -17.99695; 9.8077; 10.8728
93.323; 106.818; 114.09		729.92Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558237 CIFC17.54 H15.54 N2.46 O2P -18.13099; 9.90773; 10.90319
93.353; 107.021; 114.161		750.13Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558238 CIFC17.09 H15.09 N2.91 O2P -18.03047; 9.82913; 10.88163
93.5015; 106.735; 114.029		735.48Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558239 CIFC17.07 H15.07 N2.93 O2P -18.01388; 9.81882; 10.8766
93.4063; 106.777; 114.063		732.7Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558240 CIFC17.05 H15.05 N2.95 O2P -18.0886; 9.8583; 10.9012
93.7995; 106.674; 113.898		744.61Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558241 CIFC16.46 H14.46 N3.54 O2P -17.98898; 9.77584; 10.85419
93.7189; 106.507; 113.822		727.76Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558242 CIFC17.34 H14 N2.66 O2P -18.17264; 9.78791; 10.94559
92.4657; 107.828; 114.409		744.37Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558243 CIFC17.31 H14 N2.69 O2P -18.1874; 9.79793; 10.95147
92.5603; 107.767; 114.368		747.21Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558244 CIFC17.35 H14 N2.65 O2P -18.15991; 9.7782; 10.9363
92.3422; 107.888; 114.448		741.61Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558245 CIFC17.31 H14 N2.69 O2P -18.20177; 9.80593; 10.9558
92.6345; 107.715; 114.33		749.76Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558246 CIFC16.59 H14.59 N3.41 O2P -17.9687; 9.7664; 10.8474
93.626; 106.527; 113.856		724.72Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558247 CIFC17.35 H14 N2.65 O2P -18.14555; 9.77001; 10.9352
92.273; 107.942; 114.49		739.23Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558248 CIFC17.35 H14 N2.65 O2P -18.13293; 9.7619; 10.9275
92.167; 107.99; 114.537		736.68Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558249 CIFC16.46 H14.46 N3.54 O2P -18.02672; 9.79494; 10.86753
93.9195; 106.46; 113.719		733.83Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558250 CIFC16.45 H14.45 N3.55 O2P -18.00509; 9.78356; 10.8603
93.8151; 106.48; 113.764		730.44Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558251 CIFC16.46 H14.46 N3.54 O2P -18.04776; 9.80445; 10.87711
94.0306; 106.45; 113.656		737.25Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558252 CIFC16.5 H14.5 N3.5 O2P -17.9561; 9.75452; 10.8395
93.5338; 106.566; 113.885		722.05Ding, Xiaodan; Unruh, Daniel K.; Groeneman , Ryan; Hutchins, Kristin M.
Controlling thermal expansion within mixed cocrystals by tuning molecular motion capability
Chemical Science, 2020
1558253 CIFC26 H25 B F2 N6C 1 2/c 128.78; 10.3596; 15.8174
90; 90.308; 90		4715.9Wang, Danfeng; Malmberg, Robert; Pernik, Indrek; Prasad, Shyamal K. K.; Roemer, Max; Venkatesan, Koushik; Schmidt, Timothy W.; Keaveney, Sinead T.; Messerle, Barbara A.
Development of tethered dual catalysts: synergy between photo- and transition metal catalysts for enhanced catalysis.
Chemical science, 2020, 11, 6256-6267
1558254 CIFC60.5 H61 B2 Cl2 F2 Ir N6P 1 21/c 116.4813; 27.568; 12.5577
90; 104.255; 90		5530Wang, Danfeng; Malmberg, Robert; Pernik, Indrek; Prasad, Shyamal K. K.; Roemer, Max; Venkatesan, Koushik; Schmidt, Timothy W.; Keaveney, Sinead T.; Messerle, Barbara A.
Development of tethered dual catalysts: synergy between photo- and transition metal catalysts for enhanced catalysis.
Chemical science, 2020, 11, 6256-6267
1558255 CIFC26 H25 B F2 N6C 1 2/c 126.308; 7.8235; 24.123
90; 112.783; 90		4577.6Wang, Danfeng; Malmberg, Robert; Pernik, Indrek; Prasad, Shyamal K. K.; Roemer, Max; Venkatesan, Koushik; Schmidt, Timothy W.; Keaveney, Sinead T.; Messerle, Barbara A.
Development of tethered dual catalysts: synergy between photo- and transition metal catalysts for enhanced catalysis.
Chemical science, 2020, 11, 6256-6267
1558256 CIFC61.88 H40.12 B2 F26 Ir N6 O2P -118.4114; 18.6821; 22.004
93.733; 105.248; 113.314		6582.5Wang, Danfeng; Malmberg, Robert; Pernik, Indrek; Prasad, Shyamal K. K.; Roemer, Max; Venkatesan, Koushik; Schmidt, Timothy W.; Keaveney, Sinead T.; Messerle, Barbara A.
Development of tethered dual catalysts: synergy between photo- and transition metal catalysts for enhanced catalysis.
Chemical science, 2020, 11, 6256-6267
1558257 CIFC51 H53 Cl2 P3 RuP 1 21/n 112.4966; 21.3798; 17.4791
90; 99.826; 90		4601.5Wang, Zheng; Zhao, Ziwei; Li, Yong; Zhong, Yanxia; Zhang, Qiuyue; Liu, Qingbin; Solan, Gregory; Ma, Yanping; Sun, Wen Hua
Ruthenium-catalyzed Hydrogenation of CO2 as a Route to Methyl Esters for use as Biofuels or fine Chemicals
Chemical Science, 2020
1558258 CIFC52 H55 Cl2 O5 P3 RuP 1 21/c 119.968; 12.863; 19.229
90; 105.75; 90		4753.5Wang, Zheng; Zhao, Ziwei; Li, Yong; Zhong, Yanxia; Zhang, Qiuyue; Liu, Qingbin; Solan, Gregory; Ma, Yanping; Sun, Wen Hua
Ruthenium-catalyzed Hydrogenation of CO2 as a Route to Methyl Esters for use as Biofuels or fine Chemicals
Chemical Science, 2020
1558259 CIFC34 H26 Co N4 O2P b c a15.1904; 15.2935; 23.3304
90; 90; 90		5419.99Xu, Li-Ping; Liu, Elaine E. L.-N.; Bacsa, John; MacBeth, Cora E.; Musaev, Djamaladdin G.
Mechanistic details of the cobalt-mediated dehydrogenative dimerization of aminoquinoline-directed benzamides.
Chemical science, 2020, 11, 6085-6096
1558260 CIFC34 H24 Co N4 O2P 1 21/c 111.1539; 16.6946; 14.6989
90; 99.257; 90		2701.43Xu, Li-Ping; Liu, Elaine E. L.-N.; Bacsa, John; MacBeth, Cora E.; Musaev, Djamaladdin G.
Mechanistic details of the cobalt-mediated dehydrogenative dimerization of aminoquinoline-directed benzamides.
Chemical science, 2020, 11, 6085-6096
1558261 CIFC38 H35 Co N4 O4P -114.5135; 16.2562; 17.4421
87.763; 69.624; 70.719		3627.9Xu, Li-Ping; Liu, Elaine E. L.-N.; Bacsa, John; MacBeth, Cora E.; Musaev, Djamaladdin G.
Mechanistic details of the cobalt-mediated dehydrogenative dimerization of aminoquinoline-directed benzamides.
Chemical science, 2020, 11, 6085-6096
1558262 CIFC45 H39 Co N2 O5 PP -110.53544; 12.59025; 15.1966
79.8711; 86.4335; 78.999		1947Xu, Li-Ping; Liu, Elaine E. L.-N.; Bacsa, John; MacBeth, Cora E.; Musaev, Djamaladdin G.
Mechanistic details of the cobalt-mediated dehydrogenative dimerization of aminoquinoline-directed benzamides.
Chemical science, 2020, 11, 6085-6096
1558263 CIFC55 H61 Co N2 O6 PP 1 21/n 113.10757; 22.2355; 16.9979
90; 101.054; 90		4862.18Xu, Li-Ping; Liu, Elaine E. L.-N.; Bacsa, John; MacBeth, Cora E.; Musaev, Djamaladdin G.
Mechanistic details of the cobalt-mediated dehydrogenative dimerization of aminoquinoline-directed benzamides.
Chemical science, 2020, 11, 6085-6096
1558264 CIFC53 H41 Cl4 Co N6 O3P 1 21/c 111.6863; 20.5971; 19.6222
90; 106.514; 90		4528.3Xu, Li-Ping; Liu, Elaine E. L.-N.; Bacsa, John; MacBeth, Cora E.; Musaev, Djamaladdin G.
Mechanistic details of the cobalt-mediated dehydrogenative dimerization of aminoquinoline-directed benzamides.
Chemical science, 2020, 11, 6085-6096
1558265 CIFC45 H39 Co N4 O4P -110.9148; 12.216; 14.515
77.378; 74.686; 89.375		1819.28Xu, Li-Ping; Liu, Elaine E. L.-N.; Bacsa, John; MacBeth, Cora E.; Musaev, Djamaladdin G.
Mechanistic details of the cobalt-mediated dehydrogenative dimerization of aminoquinoline-directed benzamides.
Chemical science, 2020, 11, 6085-6096
1558270 CIFC70.98 H100.97 Fe2 N4 O7.98 Ti2P 1 21/c 122.6283; 8.7736; 18.5643
90; 105.17; 90		3557.2Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558271 CIFC39 H57.63 Fe N2 O4 ZrP 1 21/c 122.8642; 9.1582; 19.4463
90; 106.447; 90		3905.3Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558272 CIFC31.51 H58.93 N2 O4 ZrP -19.0808; 9.9464; 21.5037
93.147; 91.175; 115.995		1741Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558273 CIFC30.5 H58 N2 O4 TiP 1 21/c 126.1034; 13.6068; 18.7389
90; 90.427; 90		6655.6Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558274 CIFC21 H28 B F4 N2 O2.5P 1 21 18.0721; 15.6353; 16.4422
90; 98.2832; 90		2053.52Turley, Andrew; Danos, Andrew; Prlj, Antonio; Monkman, Andrew P.; Curchod, Basile; McGonigal, Paul R.; Etherington, Marc Kenneth
Modulation of Charge Transfer by N-Alkylation to Control Photoluminescence Energy and Quantum Yield
Chemical Science, 2020
1558275 CIFC22 H30 B2 F8 N2 O2P 21 21 219.6961; 10.2407; 23.6533
90; 90; 90		2348.65Turley, Andrew; Danos, Andrew; Prlj, Antonio; Monkman, Andrew P.; Curchod, Basile; McGonigal, Paul R.; Etherington, Marc Kenneth
Modulation of Charge Transfer by N-Alkylation to Control Photoluminescence Energy and Quantum Yield
Chemical Science, 2020
1558276 CIFC14 H9 N7P b c n33.189; 10.162; 7.2434
90; 90; 90		2443Cariati, Elena; Lucenti, Elena; Forni, Alessandra; Previtali, Andrea; Marinotto, Daniele; Malpicci, Daniele; Righetto, Stefania; Giannini, Clelia; Virgili, Tersilla; Kabacinski, Piotr; Ganzer, Lucia; Giovanella, Umberto; Botta, Chiara
Unravelling the intricated photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine AIE and RTP polymorphs
Chemical Science, 2020
1558277 CIFC14 H9 N7 O1.7P 1 21/c 13.7357; 14.805; 23.784
90; 90.284; 90		1315.4Cariati, Elena; Lucenti, Elena; Forni, Alessandra; Previtali, Andrea; Marinotto, Daniele; Malpicci, Daniele; Righetto, Stefania; Giannini, Clelia; Virgili, Tersilla; Kabacinski, Piotr; Ganzer, Lucia; Giovanella, Umberto; Botta, Chiara
Unravelling the intricated photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine AIE and RTP polymorphs
Chemical Science, 2020
1558278 CIFC14 H9 N7P 1 21/c 118.0949; 8.8509; 17.3684
90; 117.796; 90		2460.69Cariati, Elena; Lucenti, Elena; Forni, Alessandra; Previtali, Andrea; Marinotto, Daniele; Malpicci, Daniele; Righetto, Stefania; Giannini, Clelia; Virgili, Tersilla; Kabacinski, Piotr; Ganzer, Lucia; Giovanella, Umberto; Botta, Chiara
Unravelling the intricated photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine AIE and RTP polymorphs
Chemical Science, 2020
1558279 CIFC198 H88 Au42 F66P -120.0369; 20.7253; 37.5767
91.916; 97.441; 118.103		13569.1Guan, Zong-Jie; Hu, Feng; Li, Jiao-Jiao; Liu, Zi-Rui; Wang, Quan-Ming
Homoleptic alkynyl-protected gold nanoclusters with unusual compositions and structures.
Nanoscale, 2020, 12, 13346-13350
1558280 CIFC208 H104 Au50 F26P 1 21/n 117.5491; 38.753; 32.9349
90; 91.332; 90		22392.3Guan, Zong-Jie; Hu, Feng; Li, Jiao-Jiao; Liu, Zi-Rui; Wang, Quan-Ming
Homoleptic alkynyl-protected gold nanoclusters with unusual compositions and structures.
Nanoscale, 2020, 12, 13346-13350
1558281 CIF
HKL
Paper		C11 H13 Br N2P b c a10.907; 18.8993; 21.6608
90; 90; 90		4465Peppel, Tim; Wulf, Christoph; Spannenberg, Anke
1-Benzyl-3-methylimidazolium bromide
IUCrData, 2020, 5, x200768
1558282 CIFC23 H21 N O5P 1 21/c 116.6707; 9.3051; 13.8903
90; 107.808; 90		2051.5Yang, Ping; Zheng, Chao; Nie, Yu-Han; You, Shuli
Palladium-Catalyzed Dearomative 1,4-Difunctionalization of Naphthalenes
Chemical Science, 2020
1558283 CIFC24 H20 N2 OP 1 21/n 112.8388; 11.4187; 13.7487
90; 113.469; 90		1848.85Yang, Ping; Zheng, Chao; Nie, Yu-Han; You, Shuli
Palladium-Catalyzed Dearomative 1,4-Difunctionalization of Naphthalenes
Chemical Science, 2020
1558284 CIFC99 H144 K4 Si8 Th2P 1 21/n 124.4252; 10.9277; 40.2845
90; 107.399; 90		10260.4Boronski, Josef; Wooles, Ashley; Liddle, Stephen
Heteroleptic Actinocenes: A Thorium(IV)-Cyclobutadienyl-Cyclooctatetraenyl-Di-Potassium-Cyclooctatetraenyl Complex
Chemical Science, 2020
1558285 CIFC46 H40 N2 O6P 1 2/n 112.5498; 9.3561; 20.332
90; 93.893; 90		2381.8Hu, Xiaofan; Mu, Hongliang; Miao, Jie; Lu, Yao; Wang, Xianwei; Meng, Xiangsheng; Wang, Zhen; Yan, Jingling
Synthesis and gas separation performance of intrinsically microporous polyimides derived from sterically hindered binaphthalenetetracarboxylic dianhydride
Polymer Chemistry, 2020, 11, 4172-4179
1558288 CIFC19 H28 O3P 21 21 219.1596; 9.9432; 17.9178
90; 90; 90		1631.9Li, Fengli; Lin, Shuang; Zhang, Sitian; Pan, Lifen; Chai, Chenwei; Su, Jun-Cheng; Yang, Beiye; Liu, Junjun; Wang, Jianping; Hu, Zhengxi; Zhang, Yonghui
Modified Fusicoccane-Type Diterpenoids from <i>Alternaria brassicicola</i>.
Journal of natural products, 2020, 83, 1931-1938
1558289 CIFC21 H28 O5P 1 21 110.9785; 7.5525; 11.4085
90; 99.327; 90		933.431Li, Fengli; Lin, Shuang; Zhang, Sitian; Pan, Lifen; Chai, Chenwei; Su, Jun-Cheng; Yang, Beiye; Liu, Junjun; Wang, Jianping; Hu, Zhengxi; Zhang, Yonghui
Modified Fusicoccane-Type Diterpenoids from <i>Alternaria brassicicola</i>.
Journal of natural products, 2020, 83, 1931-1938
1558290 CIFC27 H25 F6 N9 O6 P PrC 1 2/c 124.6944; 12.1525; 24.3587
90; 119.085; 90		6388.2Hasegawa, Miki; Sakurai, Shoya; Yamaguchi, Masafumi Andrew; Iwasawa, Daichi; Yajima, Naho; Ogata, Shuhei; Inazuka, Yudai; Ishii, Ayumi; Suzuki, Kengo
Aspects of lanthanide complexes for selectivity, intensity and sharpness in luminescence bands from twenty-four praseodymium, europium and gadolinium complexes with differently distorted-hexadentate ligands.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, 19, 1054-1062
1558291 CIFC29 H29 F6 N9 O6 P PrP -111.2569; 12.6567; 13.684
63.881; 88.073; 85.069		1744.04Hasegawa, Miki; Sakurai, Shoya; Yamaguchi, Masafumi Andrew; Iwasawa, Daichi; Yajima, Naho; Ogata, Shuhei; Inazuka, Yudai; Ishii, Ayumi; Suzuki, Kengo
Aspects of lanthanide complexes for selectivity, intensity and sharpness in luminescence bands from twenty-four praseodymium, europium and gadolinium complexes with differently distorted-hexadentate ligands.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, 19, 1054-1062
1558292 CIFC27 H25 F6 N9 O6 P PrP 1 21/n 113.2587; 11.8157; 20.586
90; 96.707; 90		3202.9Hasegawa, Miki; Sakurai, Shoya; Yamaguchi, Masafumi Andrew; Iwasawa, Daichi; Yajima, Naho; Ogata, Shuhei; Inazuka, Yudai; Ishii, Ayumi; Suzuki, Kengo
Aspects of lanthanide complexes for selectivity, intensity and sharpness in luminescence bands from twenty-four praseodymium, europium and gadolinium complexes with differently distorted-hexadentate ligands.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, 19, 1054-1062
1558293 CIFC26 H23 F6 N9 O6 P PrP -18.9374; 12.2439; 16.3426
110.156; 105.64; 92.586		1597.71Hasegawa, Miki; Sakurai, Shoya; Yamaguchi, Masafumi Andrew; Iwasawa, Daichi; Yajima, Naho; Ogata, Shuhei; Inazuka, Yudai; Ishii, Ayumi; Suzuki, Kengo
Aspects of lanthanide complexes for selectivity, intensity and sharpness in luminescence bands from twenty-four praseodymium, europium and gadolinium complexes with differently distorted-hexadentate ligands.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, 19, 1054-1062
1558294 CIFC27 H25 Eu F6 N9 O6 PP 1 21/n 113.2647; 11.7465; 20.5653
90; 96.906; 90		3181.1Hasegawa, Miki; Sakurai, Shoya; Yamaguchi, Masafumi Andrew; Iwasawa, Daichi; Yajima, Naho; Ogata, Shuhei; Inazuka, Yudai; Ishii, Ayumi; Suzuki, Kengo
Aspects of lanthanide complexes for selectivity, intensity and sharpness in luminescence bands from twenty-four praseodymium, europium and gadolinium complexes with differently distorted-hexadentate ligands.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, 19, 1054-1062
1558295 CIFC27 H26 Eu F6 N8 O6 PP b c a16.7522; 14.5415; 25.718
90; 90; 90		6265Hasegawa, Miki; Sakurai, Shoya; Yamaguchi, Masafumi Andrew; Iwasawa, Daichi; Yajima, Naho; Ogata, Shuhei; Inazuka, Yudai; Ishii, Ayumi; Suzuki, Kengo
Aspects of lanthanide complexes for selectivity, intensity and sharpness in luminescence bands from twenty-four praseodymium, europium and gadolinium complexes with differently distorted-hexadentate ligands.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, 19, 1054-1062
1558296 CIFC86 H88 N10 O7 U2C 1 2/c 116.9463; 24.3235; 17.9675
90; 98.7581; 90		7319.7Cowie, Bradley E.; Douair, Iskander; Laurent, Maron; Love, Jason; Arnold, Polly Louise
Selective Oxo Ligand Functionalisation and Substitution Reactivity in an Oxo/Catecholate-Bridged UIV/UIV Pacman Complex
Chemical Science, 2020
1558297 CIFC74 H62 Cl2 N10 O2 U2P 1 21/m 114.0058; 21.7361; 14.7736
90; 105.395; 90		4336.17Cowie, Bradley E.; Douair, Iskander; Laurent, Maron; Love, Jason; Arnold, Polly Louise
Selective Oxo Ligand Functionalisation and Substitution Reactivity in an Oxo/Catecholate-Bridged UIV/UIV Pacman Complex
Chemical Science, 2020
1558298 CIFC68 H58 Cl2 N10 O U2P -112.2163; 13.1548; 21.1659
77.753; 76.263; 72.589		3116Cowie, Bradley E.; Douair, Iskander; Laurent, Maron; Love, Jason; Arnold, Polly Louise
Selective Oxo Ligand Functionalisation and Substitution Reactivity in an Oxo/Catecholate-Bridged UIV/UIV Pacman Complex
Chemical Science, 2020
1558299 CIFC92 H96 B F N10 O11 U2P -114.6146; 16.3896; 18.1536
77.518; 78.699; 82.007		4141.91Cowie, Bradley E.; Douair, Iskander; Laurent, Maron; Love, Jason; Arnold, Polly Louise
Selective Oxo Ligand Functionalisation and Substitution Reactivity in an Oxo/Catecholate-Bridged UIV/UIV Pacman Complex
Chemical Science, 2020
1558300 CIFC81.69 H73.06 N10 O4 U2P -110.6363; 14.9997; 21.8493
90.546; 102.195; 94.113		3397.3Cowie, Bradley E.; Douair, Iskander; Laurent, Maron; Love, Jason; Arnold, Polly Louise
Selective Oxo Ligand Functionalisation and Substitution Reactivity in an Oxo/Catecholate-Bridged UIV/UIV Pacman Complex
Chemical Science, 2020
1558301 CIFC99 H88 N15 O2 S2 U2P -113.7332; 17.5327; 18.0598
77.619; 85.469; 88.925		4234.03Cowie, Bradley E.; Douair, Iskander; Laurent, Maron; Love, Jason; Arnold, Polly Louise
Selective Oxo Ligand Functionalisation and Substitution Reactivity in an Oxo/Catecholate-Bridged UIV/UIV Pacman Complex
Chemical Science, 2020
1558302 CIFC76 H66 Cl4 N10 O2 Se2 U2P 1 21/c 110.9153; 19.1212; 34.2194
90; 92.935; 90		7132.7Cowie, Bradley E.; Douair, Iskander; Laurent, Maron; Love, Jason; Arnold, Polly Louise
Selective Oxo Ligand Functionalisation and Substitution Reactivity in an Oxo/Catecholate-Bridged UIV/UIV Pacman Complex
Chemical Science, 2020
1558303 CIFC94 H82 F2 N14 O2 U2P 1 21/n 117.5381; 26.228; 17.8435
90; 91.942; 90		8203.1Cowie, Bradley E.; Douair, Iskander; Laurent, Maron; Love, Jason; Arnold, Polly Louise
Selective Oxo Ligand Functionalisation and Substitution Reactivity in an Oxo/Catecholate-Bridged UIV/UIV Pacman Complex
Chemical Science, 2020
1558304 CIFC36 H29 B F2 N2 O0.5C 1 2/c 124.325; 9.9336; 28.2901
90; 104.953; 90		6604.4Labella, Jorge; Durán-Sampedro, Gonzalo; Martínez-Díaz, M. Victoria; Torres, Tomás
Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
Chemical Science, 2020, 11, 10778-10785
1558305 CIFC34 H25 B F2 N2P 1 21/c 111.6062; 32.6033; 7.6374
90; 108.632; 90		2738.53Labella, Jorge; Durán-Sampedro, Gonzalo; Martínez-Díaz, M. Victoria; Torres, Tomás
Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
Chemical Science, 2020, 11, 10778-10785
1558306 CIFC44 H33 B F2 N2P 1 21/c 112.5426; 41.2031; 13.9741
90; 115.881; 90		6497.4Labella, Jorge; Durán-Sampedro, Gonzalo; Martínez-Díaz, M. Victoria; Torres, Tomás
Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
Chemical Science, 2020, 11, 10778-10785
1558307 CIFC48 H38 N2 O2C 1 2/c 120.361; 16.095; 23.355
90; 114.048; 90		6989Labella, Jorge; Durán-Sampedro, Gonzalo; Martínez-Díaz, M. Victoria; Torres, Tomás
Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
Chemical Science, 2020, 11, 10778-10785
1558308 CIFC36 H29 B F2 N2P -110.1937; 11.001; 14.28
105.446; 103.611; 94.765		1481.92Labella, Jorge; Durán-Sampedro, Gonzalo; Martínez-Díaz, M. Victoria; Torres, Tomás
Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
Chemical Science, 2020, 11, 10778-10785
1558309 CIFC36 H29 B F2 N2P 1 21/n 114.395; 14.038; 18.526
90; 108.639; 90		3547.3Labella, Jorge; Durán-Sampedro, Gonzalo; Martínez-Díaz, M. Victoria; Torres, Tomás
Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
Chemical Science, 2020, 11, 10778-10785
1558310 CIFC31 H25 B F2 N2P -17.916; 10.089; 15.968
79.032; 88.721; 85.253		1247.7Labella, Jorge; Durán-Sampedro, Gonzalo; Martínez-Díaz, M. Victoria; Torres, Tomás
Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
Chemical Science, 2020, 11, 10778-10785
1558311 CIFC31 H25 B F2 N2P 1 21/c 116.0345; 8.5128; 17.8694
90; 93.426; 90		2434.79Labella, Jorge; Durán-Sampedro, Gonzalo; Martínez-Díaz, M. Victoria; Torres, Tomás
Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
Chemical Science, 2020, 11, 10778-10785
1558312 CIFC46 H33 B F2 N2P n m a21.0905; 18.983; 8.7486
90; 90; 90		3502.6Labella, Jorge; Durán-Sampedro, Gonzalo; Martínez-Díaz, M. Victoria; Torres, Tomás
Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
Chemical Science, 2020, 11, 10778-10785
1558313 CIFC36 H29 B F2 N2I 41 c d17.6517; 17.6517; 36.5175
90; 90; 90		11378.2Labella, Jorge; Durán-Sampedro, Gonzalo; Martínez-Díaz, M. Victoria; Torres, Tomás
Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
Chemical Science, 2020, 11, 10778-10785
1558314 CIFC48 H37 B F2 N2 O2P -17.4833; 14.4445; 19.1563
111.599; 95.542; 94.737		1900.6Labella, Jorge; Durán-Sampedro, Gonzalo; Martínez-Díaz, M. Victoria; Torres, Tomás
Annulative π-extension of BODIPYs made easy via gold(i)-catalyzed cycloisomerization
Chemical Science, 2020, 11, 10778-10785
1558315 CIFC9 H12 N2 O5P 1 21 16.241; 5.293; 15.726
90; 101.19; 90		509.6Singh, Pijush; Misra, Souvik; Sepay, Nayim; Mondal, Sanjoy; Ray, Debes; Aswal, Vinod K.; Nanda, Jayanta
Self-assembling behaviour of a modified aromatic amino acid in competitive medium.
Soft matter, 2020, 16, 6599-6607
1558316 CIF
HKL
Paper		C18 H16 O3P 1 21/c 17.7611; 7.2894; 24.0331
90; 93.5573; 90		1357.02Encarnacion-Thomas, Elvia; Sommer, Roger D.; Mallia, Ajay; Sloop, Joseph
(<i>E</i>)-2-(3,5-Dimethoxybenzylidene)indan-1-one
IUCrData, 2020, 5, x200759
1558317 CIFC20 H20 F8 N4 O5 SP 1 21 16.12766; 20.247; 10.0261
90; 94.623; 90		1239.86Zhang, Chen; Ye, Fei; Wang, Jianmin; He, Ping; Lei, Ming; Huang, Longbin; Huang, Anbang; Tang, Pingming; Lin, Hongjun; Liao, Yuting; Liang, Yong; Ni, Jia; Yan, Pangke
Design, Synthesis, and Evaluation of a Series of Novel Super Long-Acting DPP-4 Inhibitors for the Treatment of Type 2 Diabetes.
Journal of medicinal chemistry, 2020
1558318 CIFC22 H27 N O7P 1 21 118.754; 9.0751; 26.1928
90; 102.75; 90		4347.95Stakanovs, Georgijs; Mishnev, Anatoly; Rasina, Dace; Jirgensons, Aigars
A Concise Bioinspired Semisynthesis of Rumphellaones A-C and Their C-8 Epimers from β-Caryophyllene.
Journal of natural products, 2020, 83, 2004-2009
1558319 CIFC15 H22 O3P 21 21 215.8085; 7.3835; 33.4086
90; 90; 90		1432.8Stakanovs, Georgijs; Mishnev, Anatoly; Rasina, Dace; Jirgensons, Aigars
A Concise Bioinspired Semisynthesis of Rumphellaones A-C and Their C-8 Epimers from β-Caryophyllene.
Journal of natural products, 2020, 83, 2004-2009
1558320 CIFC24 H16 Co N10 S2P 1 2/c 110.1578; 11.4859; 14.985
90; 106.365; 90		1677.5Zaworotko, Michael; Kumar, Naveen; Chang, Ze; Yu, Mei-Hui; Kumar, Amrit; O’Nolan, Daniel; Bu, Xian-He; Patyk-Kaźmierczak, Ewa; Bezrukov, Andrey A.; Mukherjee, Soumya; Wang, Shi-Qiang
Crystal engineering of a rectangular sql coordination network to enable xylenes selectivity over ethylbenzene
Chemical Science, 2020
1558321 CIFC84 H72 Co2 N28 S4P -113.6994; 20.4799; 21.1055
78.892; 73.265; 79.327		5511.1Zaworotko, Michael; Kumar, Naveen; Chang, Ze; Yu, Mei-Hui; Kumar, Amrit; O’Nolan, Daniel; Bu, Xian-He; Patyk-Kaźmierczak, Ewa; Bezrukov, Andrey A.; Mukherjee, Soumya; Wang, Shi-Qiang
Crystal engineering of a rectangular sql coordination network to enable xylenes selectivity over ethylbenzene
Chemical Science, 2020
1558322 CIFC40 H36 Co N10 S2C 1 2/c 124.756; 11.4713; 14.4235
90; 100.226; 90		4031Zaworotko, Michael; Kumar, Naveen; Chang, Ze; Yu, Mei-Hui; Kumar, Amrit; O’Nolan, Daniel; Bu, Xian-He; Patyk-Kaźmierczak, Ewa; Bezrukov, Andrey A.; Mukherjee, Soumya; Wang, Shi-Qiang
Crystal engineering of a rectangular sql coordination network to enable xylenes selectivity over ethylbenzene
Chemical Science, 2020
1558323 CIFC42 H36 Co N14 S2P 41 2 221.7573; 21.7573; 20.5483
90; 90; 90		9727.2Zaworotko, Michael; Kumar, Naveen; Chang, Ze; Yu, Mei-Hui; Kumar, Amrit; O’Nolan, Daniel; Bu, Xian-He; Patyk-Kaźmierczak, Ewa; Bezrukov, Andrey A.; Mukherjee, Soumya; Wang, Shi-Qiang
Crystal engineering of a rectangular sql coordination network to enable xylenes selectivity over ethylbenzene
Chemical Science, 2020
1558324 CIFC26 H16 Co N14 S2C m c e20.881; 14.7201; 8.7578
90; 90; 90		2691.9Zaworotko, Michael; Kumar, Naveen; Chang, Ze; Yu, Mei-Hui; Kumar, Amrit; O’Nolan, Daniel; Bu, Xian-He; Patyk-Kaźmierczak, Ewa; Bezrukov, Andrey A.; Mukherjee, Soumya; Wang, Shi-Qiang
Crystal engineering of a rectangular sql coordination network to enable xylenes selectivity over ethylbenzene
Chemical Science, 2020
1558325 CIFC40 H36 Co N10 S2C 1 2/c 124.8225; 11.4779; 14.301
90; 100.423; 90		4007.3Zaworotko, Michael; Kumar, Naveen; Chang, Ze; Yu, Mei-Hui; Kumar, Amrit; O’Nolan, Daniel; Bu, Xian-He; Patyk-Kaźmierczak, Ewa; Bezrukov, Andrey A.; Mukherjee, Soumya; Wang, Shi-Qiang
Crystal engineering of a rectangular sql coordination network to enable xylenes selectivity over ethylbenzene
Chemical Science, 2020
1558326 CIFC32 H55 Ir N2 P2P -110.1782; 10.3488; 16.3633
82.027; 74.303; 82.556		1635.59Smith, Joel; Durrant, George; Ess, Daniel H.; Gelfand, Benjamin Sidney; Piers, Warren
H/D Exchange Under Mild Conditions in Arenes and Unactivated Alkanes with C6D6 and D2O Using Rigid, Electron-rich Iridium PCP Pincer Complexes
Chemical Science, 2020
1558327 CIFC38 H55 Ir N2 P2P b c a10.1805; 22.3462; 31.76
90; 90; 90		7225.3Smith, Joel; Durrant, George; Ess, Daniel H.; Gelfand, Benjamin Sidney; Piers, Warren
H/D Exchange Under Mild Conditions in Arenes and Unactivated Alkanes with C6D6 and D2O Using Rigid, Electron-rich Iridium PCP Pincer Complexes
Chemical Science, 2020
1558328 CIFC18 H22 Cu N4 O9F d d 221.561; 35.637; 11.1216
90; 90; 90		8545Vegas, V. G.; Beobide, G.; Castillo, O.; Reyes, E.; Gómez-García, C J; Zamora, F.; Amo-Ochoa, P
A bioinspired metal-organic approach to cross-linked functional 3D nanofibrous hydro- and aero-gels with effective mixture separation of nucleobases by molecular recognition.
Nanoscale, 2020, 12, 14699-14707
1558329 CIF
HKL
Paper		C23 H34 Cl3 N O12P 15.5734; 9.2537; 14.2547
91.995; 99.103; 95.567		721.56Amaro Hernández, Aldo Guillermo; Rodríguez Tzompantzi, Tomasa; Dávila García, Álvaro; Meza-León, Rosa Luisa; Bernès, Sylvain
Ethyl (3<i>S</i>)-3-[(3a<i>R</i>,5<i>R</i>,6<i>S</i>,6a<i>R</i>)-6-hydroxy-2,2-dimethyltetrahydrofuro[4,5-<i>d</i>][1,3]dioxol-5-yl]-3-{(3<i>S</i>)-3-[(3a<i>R</i>,5<i>R</i>,6<i>S</i>,6a<i>R</i>)-6-hydroxy-2,2-dimethyltetrahydrofuro[4,5-<i>d</i>][1,3]dioxol-5-yl]-5-oxoisoxazolidin-2-yl}propanoate chloroform monosolvate
IUCrData, 2020, 5, x200788
1558330 CIF
HKL
Paper		C28 H28 O6P 1 21/c 19.9641; 10.2338; 23.541
90; 100.086; 90		2363.4Yoo, Miri; Koh, Dongsoo
(<i>E</i>)-3-{4,6-Dimethoxy-2-[(<i>E</i>)-4-methoxystyryl]-3-methylphenyl}-1-(2-hydroxy-5-methoxyphenyl)prop-2-en-1-one
IUCrData, 2020, 5, x200792
1558331 CIFC31 H48 O6P 1 21 110.90373; 9.73486; 14.2878
90; 102.003; 90		1483.44Xie, Shuangshuang; Tan, Xiaosheng; Liu, Yaping; Duan, Yulin; Chen, Gang; Feng, Hao; Sun, Lingjuan; Huang, Yingying; Guo, Yi; Shi, Zhengyi; Zhou, Yuan; Qi, Changxing; Zhang, Yonghui
Hypersonins A-D, Polycyclic Polyprenylated Acylphloroglucinols with a 1,2-<i>seco</i>-Homoadamantane Architecture from <i>Hypericum wilsonii</i>.
Journal of natural products, 2020, 83, 1804-1809
1558332 CIFC20 H16 N2 O S2P -19.7982; 9.859; 11.1142
115.511; 101.209; 106.861		861.61Sinclair, Geoffrey S.; Kukor, Andrew J.; Imperial, Kevin Karl G.; Schipper, Derek J.
Transition-Metal-Free ipso-Arylative Condensation
Macromolecules, 2020
1558333 CIFC42 H40 B N8 O3 ZnP 1 21/n 111.1116; 22.132; 16.382
90; 105.947; 90		3873.7Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558334 CIFC39 H33 B N10 O2 ZnP 1 21/c 119.2031; 17.4413; 10.8662
90; 103.602; 90		3537.3Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558335 CIFC48 H45 B N9 O2 ZnP -111.951; 12.222; 33.4
96.044; 90.661; 117.154		4307Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558336 CIFC40.5 H39 B N10 O3.5 ZnP 1 21/c 122.1038; 18.2437; 20.8443
90; 110.728; 90		7861.5Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558337 CIFC40 H40 B N9 O3 ZnP -111.652; 12.368; 13.917
92.104; 105.552; 103.261		1870.3Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558338 CIFC38 H34 B N12 O0.5 ZnC 1 2/c 121.265; 12.2666; 26.802
90; 96.968; 90		6939.6Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558339 CIFC39 H38 B N9 O3 ZnP -111.5454; 12.4466; 13.3968
87.861; 72.845; 88.996		1838.16Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558340 CIFC53 H48 B N8 O2 ZnP -111.7557; 13.389; 16.6386
67.385; 74.545; 89.452		2317.3Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558341 CIFC91 H81 B2 N24 Zn2P -114.29; 16.009; 20.236
111.296; 101.338; 94.752		4168.4Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558342 CIFC45 H41 B N8 O2 S ZnP -111.7747; 12.2627; 16.6658
88.998; 71.411; 63.502		2019.03Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558343 CIFC39 H32 B N9 O2 S ZnP -111.3437; 12.4724; 13.2663
93.307; 106.813; 102.442		1740.01Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558344 CIFC39 H37 B N8 O3 S ZnP -111.767; 13.044; 14.552
110.451; 94.891; 107.004		1957Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558345 CIFC38 H32 B N11 S ZnP -111.3854; 12.2324; 12.9278
95.296; 103.872; 100.76		1699.4Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558346 CIFC44 H38 B N11 S ZnP 1 21/n 111.4626; 24.908; 14.0421
90; 92.074; 90		4006.5Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558347 CIFC45 H41 B N8 O2 S ZnP 1 21/n 113.2942; 16.9309; 18.117
90; 90.612; 90		4077.6Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558348 CIFC38 H32 B N7 O2 S ZnP 1 21/c 125.354; 12.7294; 21.364
90; 99.223; 90		6805.9Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558349 CIFC45 H38 B N9 O2 S ZnP 1 21/n 111.5071; 24.8201; 14.2983
90; 93.957; 90		4074Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558350 CIFC39 H32 B N9 O3 ZnP -111.529; 12.532; 13.17
92.476; 108.327; 103.041		1746.3Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558351 CIFC44 H39 B N8 O2 S ZnP 1 21/c 118.2805; 24.6819; 17.9965
90; 103.043; 90		7910.5Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558352 CIFC38 H32 B N11 O ZnP -111.466; 12.2164; 12.9213
95.393; 104.423; 100.415		1705.55Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558353 CIFC38 H32 B N7 O2 S ZnP 1 21/n 111.8071; 20.2004; 14.5401
90; 95.99; 90		3449Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558354 CIFC45 H41 B N8 O3 ZnP -111.7292; 11.9654; 16.3974
100.704; 96.654; 114.105		2016.3Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558355 CIFC43.5 H41 B N7 O3 ZnP 1 21/n 115.5694; 14.5978; 17.7711
90; 106.12; 90		3880.2Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558356 CIFC50 H46 B N9 O2 ZnP -111.902; 13.512; 15.071
65.558; 87.822; 87.374		2203.7Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558357 CIFC38 H35 B N8 O4 ZnP -111.93; 13.078; 14.235
107.583; 93.055; 106.031		2012.1Dick, Benjamin L.; Patel, Ashay; Cohen, Seth M.
Effect of Heterocycle Content on Metal Binding Isostere Coordination
Chemical Science, 2020
1558358 CIFC98 H150 N12 O4 S4P -114.5133; 16.3538; 22.1946
87.79; 79.14; 67.556		4778.4Berry, Stuart N.; Qin, Lei; Lewis, William; Jolliffe, Katrina A.
Conformationally Adaptable Macrocyclic Receptors for Ditopic Anions: Analysis of Chelate Cooperativity in Aqueous Containing Media
Chemical Science, 2020
1558359 CIFC206 H324 N24 O10 S10C 1 2/c 132.333; 32.042; 22.621
90; 114.382; 90		21346Berry, Stuart N.; Qin, Lei; Lewis, William; Jolliffe, Katrina A.
Conformationally Adaptable Macrocyclic Receptors for Ditopic Anions: Analysis of Chelate Cooperativity in Aqueous Containing Media
Chemical Science, 2020
1558360 CIFC195 H307 N24 O12 S10.5P -115.483; 22.547; 30.092
100.331; 91.268; 100.461		10147Berry, Stuart N.; Qin, Lei; Lewis, William; Jolliffe, Katrina A.
Conformationally Adaptable Macrocyclic Receptors for Ditopic Anions: Analysis of Chelate Cooperativity in Aqueous Containing Media
Chemical Science, 2020
1558364 CIFC43 H52 B F10 Li N PP -112.0597; 12.1028; 16.2479
98.045; 99.315; 111.182		2130.75Watanabe, Kohei; Ueno, Atsushi; Tao, Xin; Skoch, Karel; Jie, Xiaoming; Vagin, Sergei; Rieger, Bernhard; Daniliuc, Constantin Gabriel; Letzel, Mathias C.; Kehr, Gerald; Erker, Gerhard
Reactions of an Anionic Chelate Phosphane/borata-alkene Ligand with [Rh(nbd)Cl]2, [Rh(CO)2Cl]2 and [Ir(cod)Cl]2.
Chemical Science, 2020
1558365 CIFC39 H33 B F10 P RhP 1 21/c 111.386; 24.4438; 12.1411
90; 95.579; 90		3363.1Watanabe, Kohei; Ueno, Atsushi; Tao, Xin; Skoch, Karel; Jie, Xiaoming; Vagin, Sergei; Rieger, Bernhard; Daniliuc, Constantin Gabriel; Letzel, Mathias C.; Kehr, Gerald; Erker, Gerhard
Reactions of an Anionic Chelate Phosphane/borata-alkene Ligand with [Rh(nbd)Cl]2, [Rh(CO)2Cl]2 and [Ir(cod)Cl]2.
Chemical Science, 2020
1558366 CIFC48 H52 B F10 Li N PP 1 21/n 112.4065; 20.2711; 18.1486
90; 95.676; 90		4541.88Watanabe, Kohei; Ueno, Atsushi; Tao, Xin; Skoch, Karel; Jie, Xiaoming; Vagin, Sergei; Rieger, Bernhard; Daniliuc, Constantin Gabriel; Letzel, Mathias C.; Kehr, Gerald; Erker, Gerhard
Reactions of an Anionic Chelate Phosphane/borata-alkene Ligand with [Rh(nbd)Cl]2, [Rh(CO)2Cl]2 and [Ir(cod)Cl]2.
Chemical Science, 2020
1558367 CIFC39 H37 B F10 O2 P RhP 1 21/c 111.1535; 28.4831; 12.0712
90; 100.231; 90		3773.9Watanabe, Kohei; Ueno, Atsushi; Tao, Xin; Skoch, Karel; Jie, Xiaoming; Vagin, Sergei; Rieger, Bernhard; Daniliuc, Constantin Gabriel; Letzel, Mathias C.; Kehr, Gerald; Erker, Gerhard
Reactions of an Anionic Chelate Phosphane/borata-alkene Ligand with [Rh(nbd)Cl]2, [Rh(CO)2Cl]2 and [Ir(cod)Cl]2.
Chemical Science, 2020
1558368 CIFC44 H27 B2 F20 PP -110.4373; 11.5018; 20.052
101.416; 99.845; 98.08		2286.61Watanabe, Kohei; Ueno, Atsushi; Tao, Xin; Skoch, Karel; Jie, Xiaoming; Vagin, Sergei; Rieger, Bernhard; Daniliuc, Constantin Gabriel; Letzel, Mathias C.; Kehr, Gerald; Erker, Gerhard
Reactions of an Anionic Chelate Phosphane/borata-alkene Ligand with [Rh(nbd)Cl]2, [Rh(CO)2Cl]2 and [Ir(cod)Cl]2.
Chemical Science, 2020
1558369 CIFC40 H37 B F10 Ir PP -111.0013; 13.0591; 28.8517
102.805; 92.594; 105.065		3879.7Watanabe, Kohei; Ueno, Atsushi; Tao, Xin; Skoch, Karel; Jie, Xiaoming; Vagin, Sergei; Rieger, Bernhard; Daniliuc, Constantin Gabriel; Letzel, Mathias C.; Kehr, Gerald; Erker, Gerhard
Reactions of an Anionic Chelate Phosphane/borata-alkene Ligand with [Rh(nbd)Cl]2, [Rh(CO)2Cl]2 and [Ir(cod)Cl]2.
Chemical Science, 2020
1558370 CIFC36 H28 B2 Br2 N2I 1 2/a 118.504; 17.9348; 19.6933
90; 108.694; 90		6190.7Guo, Rui; Jiang, Jingxing; Hu, Chenyang; Liu, Liu Leo; Cui, Ping; Zhao, Meihua; Ke, Zhuofeng; Tung, Chen-Ho; Kong, Lingbing
BNN-1,3-dipoles: isolation and intramolecular cycloaddition with unactivated arenes
Chemical Science, 2020
1558371 CIFC36 H60 B2 Br2 N2R -3 :H32.9585; 32.9585; 9.9663
90; 90; 120		9375.6Guo, Rui; Jiang, Jingxing; Hu, Chenyang; Liu, Liu Leo; Cui, Ping; Zhao, Meihua; Ke, Zhuofeng; Tung, Chen-Ho; Kong, Lingbing
BNN-1,3-dipoles: isolation and intramolecular cycloaddition with unactivated arenes
Chemical Science, 2020
1558372 CIFC24 H26 B Br NP 1 21/n 113.4204; 13.4075; 13.5682
90; 118.076; 90		2154.09Guo, Rui; Jiang, Jingxing; Hu, Chenyang; Liu, Liu Leo; Cui, Ping; Zhao, Meihua; Ke, Zhuofeng; Tung, Chen-Ho; Kong, Lingbing
BNN-1,3-dipoles: isolation and intramolecular cycloaddition with unactivated arenes
Chemical Science, 2020
1558373 CIFC57.5 H90 B2 N4P -111.7577; 13.9324; 18.6526
102.637; 99.834; 105.896		2779.5Guo, Rui; Jiang, Jingxing; Hu, Chenyang; Liu, Liu Leo; Cui, Ping; Zhao, Meihua; Ke, Zhuofeng; Tung, Chen-Ho; Kong, Lingbing
BNN-1,3-dipoles: isolation and intramolecular cycloaddition with unactivated arenes
Chemical Science, 2020
1558374 CIFC66 H78 B2 N4P 1 21/n 111.75034; 23.8044; 19.95734
90; 98.1553; 90		5525.81Guo, Rui; Jiang, Jingxing; Hu, Chenyang; Liu, Liu Leo; Cui, Ping; Zhao, Meihua; Ke, Zhuofeng; Tung, Chen-Ho; Kong, Lingbing
BNN-1,3-dipoles: isolation and intramolecular cycloaddition with unactivated arenes
Chemical Science, 2020
1558375 CIFC47 H46 B2 N4P 1 21/n 111.2493; 26.0979; 13.6593
90; 109.818; 90		3772.64Guo, Rui; Jiang, Jingxing; Hu, Chenyang; Liu, Liu Leo; Cui, Ping; Zhao, Meihua; Ke, Zhuofeng; Tung, Chen-Ho; Kong, Lingbing
BNN-1,3-dipoles: isolation and intramolecular cycloaddition with unactivated arenes
Chemical Science, 2020
1558376 CIFC38 H58 B2 N2 O4P -19.0716; 9.8412; 11.5149
76.803; 82.173; 68.411		929.1Guo, Rui; Jiang, Jingxing; Hu, Chenyang; Liu, Liu Leo; Cui, Ping; Zhao, Meihua; Ke, Zhuofeng; Tung, Chen-Ho; Kong, Lingbing
BNN-1,3-dipoles: isolation and intramolecular cycloaddition with unactivated arenes
Chemical Science, 2020
1558377 CIFC41 H56 O4 SiP 21 21 2111.4985; 13.7129; 24.4365
90; 90; 90		3853.1Yu, Tianzi; Sun, Ying; Tu, Canhui; Chen, Ting; Fu, Shaomin; Liu, Bo
Total Synthesis of Crotophorbolone
Chemical Science, 2020
1558378 CIFC36 H47 O3 SiP 21 21 2110.7809; 12.9537; 23.2649
90; 90; 90		3249Yu, Tianzi; Sun, Ying; Tu, Canhui; Chen, Ting; Fu, Shaomin; Liu, Bo
Total Synthesis of Crotophorbolone
Chemical Science, 2020
1558379 CIF
HKL
Paper		C48 H40 Co2 N8 O20P -17.2747; 10.4927; 16.356
97.735; 102.84; 102.607		1165.71Srinivasan, Bikshandarkoil R.; Harmalkar, Sarvesh S.; D'Souza, Luann R.; Dhuri, Sunder N.
Di-μ-aqua-bis[aqua(2,2′-bipyridine)(4-nitrobenzoato)cobalt(II)] bis(4-nitrobenzoate)
IUCrData, 2020, 5, x200796
1558383 CIFC27 H20 N2 O2 SP -112.3819; 12.8413; 14.0834
86.212; 84.496; 72.066		2119.1Jena, Satyam; Dhanalakshmi, Pandi; Bano, Gulista; Thilagar, Pakkirisamy
Delayed Fluorescence, Room Temperature Phosphorescence, and Mechanofluorochromic Naphthalimides: Differential Imaging of Normoxia and Hypoxia Live Cancer Cells.
The journal of physical chemistry. B, 2020, 124, 5393-5406
1558384 CIFC27 H20 N2 O3P b c n27.169; 7.8353; 19.215
90; 90; 90		4090.4Jena, Satyam; Dhanalakshmi, Pandi; Bano, Gulista; Thilagar, Pakkirisamy
Delayed Fluorescence, Room Temperature Phosphorescence, and Mechanofluorochromic Naphthalimides: Differential Imaging of Normoxia and Hypoxia Live Cancer Cells.
The journal of physical chemistry. B, 2020, 124, 5393-5406
1558385 CIFC27 H20 N2 O2C 1 2/c 128.102; 8.21; 19.944
90; 115.706; 90		4146Jena, Satyam; Dhanalakshmi, Pandi; Bano, Gulista; Thilagar, Pakkirisamy
Delayed Fluorescence, Room Temperature Phosphorescence, and Mechanofluorochromic Naphthalimides: Differential Imaging of Normoxia and Hypoxia Live Cancer Cells.
The journal of physical chemistry. B, 2020, 124, 5393-5406
1558386 CIFC27 H20 N2 O2C 1 c 112.063; 27.127; 8.2526
90; 129.29; 90		2090.1Jena, Satyam; Dhanalakshmi, Pandi; Bano, Gulista; Thilagar, Pakkirisamy
Delayed Fluorescence, Room Temperature Phosphorescence, and Mechanofluorochromic Naphthalimides: Differential Imaging of Normoxia and Hypoxia Live Cancer Cells.
The journal of physical chemistry. B, 2020, 124, 5393-5406
1558387 CIFC27 H22 N2 O2P -17.8985; 11.3746; 13.1673
79.62; 73.19; 70.55		1063.19Jena, Satyam; Dhanalakshmi, Pandi; Bano, Gulista; Thilagar, Pakkirisamy
Delayed Fluorescence, Room Temperature Phosphorescence, and Mechanofluorochromic Naphthalimides: Differential Imaging of Normoxia and Hypoxia Live Cancer Cells.
The journal of physical chemistry. B, 2020, 124, 5393-5406
1558388 CIFC25 H39 N2 O3 P RuP 1 21/c 19.5765; 12.9092; 21.0501
90; 100.084; 90		2562.12Zou, You-Quan; Zhou, Quan-Quan; Diskin-Posner, Yael; Ben-David, Yehoshoa; Milstein, David
Synthesis of oxalamides by acceptorless dehydrogenative coupling of ethylene glycol and amines and the reverse hydrogenation catalyzed by ruthenium
Chemical Science, 2020
1558389 CIFC17 H19 N O3P 21 21 2110.206; 11.8825; 12.7337
90; 90; 90		1544.25Thombal, Raju S.; Feoktistova, Taisiia; González-Montiel, Gisela A.; Cheong, Paul H.-Y.; Lee, Yong Rok
Palladium-catalyzed synthesis of β-hydroxy compounds via a strained 6,4-palladacycle from directed C–H activation of anilines and C–O insertion of epoxides
Chemical Science, 2020, 11, 7260-7265
1558390 CIFC60 H76 F2 S2 Si2P -19.0185; 11.1498; 13.696
84.062; 89.316; 81.541		1354.9Pace, Natalie; Rugg, Brandon K.; Chang, Christopher H.; Reid, Obadiah; Thorley, Karl J.; Parkin, Sean R.; Anthony, John E.; Johnson, Justin C.
Conversion between Triplet Pair States is Controlled by Molecular Coupling in Pentadithiophene Thin Films
Chemical Science, 2020
1558391 CIFC66 H94 S2 Si4C 1 2/c 144.36; 8.4599; 17.8448
90; 102.684; 90		6533.4Pace, Natalie; Rugg, Brandon K.; Chang, Christopher H.; Reid, Obadiah; Thorley, Karl J.; Parkin, Sean R.; Anthony, John E.; Johnson, Justin C.
Conversion between Triplet Pair States is Controlled by Molecular Coupling in Pentadithiophene Thin Films
Chemical Science, 2020
1558392 CIFC14 H12 O4P 1 21 18.1025; 6.6401; 11.7134
90; 102.405; 90		615.485Cui, Jin; Kumagai, Naoya; Watanabe, Takumi; Shibasaki, Masakatsu
Direct catalytic asymmetric and anti-selective vinylogous addition of butenolides to chromones
Chemical Science, 2020, 11, 7170-7176
1558393 CIFC14 H11 N O6P 1 21 112.4535; 6.5482; 15.9054
90; 105.099; 90		1252.28Cui, Jin; Kumagai, Naoya; Watanabe, Takumi; Shibasaki, Masakatsu
Direct catalytic asymmetric and anti-selective vinylogous addition of butenolides to chromones
Chemical Science, 2020, 11, 7170-7176
1558397 CIFC17 H10 F6 I N O3P -17.5364; 8.1598; 14.6308
74.8246; 86.9207; 83.589		862.64Ding, Wei; Wang, Chen; Tan, Jie Ren; Ho, Chang Chin; León, Felix; Garcia, Felipe; Yoshikai, Naohiko
Site-selective aromatic C–H λ3-iodanation with cyclic iodine(III) electrophile in solution and solid phases
Chemical Science, 2020
1558398 CIFC16 H19 N O3P 1 21 16.0356; 10.8751; 10.5262
90; 97.925; 90		684.32Inanaga, Kazato; Wollenburg, Marco; Bachman, Shoshana; Hafeman, Nicholas; Stoltz, Brian M.
Catalytic Enantioselective Synthesis of Carbocyclic and Heterocyclic Spiranes via a Decarboxylative Aldol Cyclization
Chemical Science, 2020
1558399 CIFF I2 O6 YP 656.8455; 6.8455; 21.807
90; 90; 120		885Peng, Guang; Yang, Yi; Yan, Tao; Zhao, Dan; Li, Bing-Xuan; Zhang, Ge; Lin, Zheshuai; Ye, Ning
Helix-constructed Polar Rare-earth Iodate Fluoride as Laser Nonlinear Optical Multifunctional Materials
Chemical Science, 2020
1558400 CIFC25 H19 N O2P 21 21 215.2753; 8.2287; 45.0822
90; 90; 90		1956.97Fernandez, Zulema; Fernández, Berta; Quiñoá, Emilio; Riguera, Ricardo; Freire, Felix
Chiral Information Harvesting in Helical Poly(acetylene) Derivatives Using Oligo(p-phenyleneethynylene)s as Spacers
Chemical Science, 2020
1558401 CIFC33 H23 N O2P 21 21 215.3349; 8.0996; 58.179
90; 90; 90		2513.95Fernandez, Zulema; Fernández, Berta; Quiñoá, Emilio; Riguera, Ricardo; Freire, Felix
Chiral Information Harvesting in Helical Poly(acetylene) Derivatives Using Oligo(p-phenyleneethynylene)s as Spacers
Chemical Science, 2020
1558402 CIFC96 H112 Cl8 I8 Mo6 Na4.5 O107P 1 21 115.8187; 32.856; 17.4013
90; 93.728; 90		9025Falaise, Clément; Ivanov, Anton A.; Molard, Yann; Amela Cortes, Maria; Shestopalov, Michael A.; Haouas, Mohamed; Cadot, Emmanuel; Cordier, Stéphane
From supramolecular to solid state chemistry: crystal engineering of luminescent materials by trapping molecular clusters in an aluminium-based host matrix
Materials Horizons, 2020, 7, 2399-2406
1558403 CIFC144 H168 Br8 Cl6 Mo6 Na4 O138I 4 2 223.715; 23.715; 56.802
90; 90; 90		31946Falaise, Clément; Ivanov, Anton A.; Molard, Yann; Amela Cortes, Maria; Shestopalov, Michael A.; Haouas, Mohamed; Cadot, Emmanuel; Cordier, Stéphane
From supramolecular to solid state chemistry: crystal engineering of luminescent materials by trapping molecular clusters in an aluminium-based host matrix
Materials Horizons, 2020, 7, 2399-2406
1558404 CIFC144 H168 Cl6 I8 Mo6 O138I 4 2 223.7708; 23.7708; 57.456
90; 90; 90		32466Falaise, Clément; Ivanov, Anton A.; Molard, Yann; Amela Cortes, Maria; Shestopalov, Michael A.; Haouas, Mohamed; Cadot, Emmanuel; Cordier, Stéphane
From supramolecular to solid state chemistry: crystal engineering of luminescent materials by trapping molecular clusters in an aluminium-based host matrix
Materials Horizons, 2020, 7, 2399-2406
1558405 CIFC96 H112 Al13 Br8 Cl10 Mo6 O120P 62 2 219.805; 19.805; 57.843
90; 90; 120		19649Falaise, Clément; Ivanov, Anton A.; Molard, Yann; Amela Cortes, Maria; Shestopalov, Michael A.; Haouas, Mohamed; Cadot, Emmanuel; Cordier, Stéphane
From supramolecular to solid state chemistry: crystal engineering of luminescent materials by trapping molecular clusters in an aluminium-based host matrix
Materials Horizons, 2020, 7, 2399-2406
1558406 CIFC96 H108 Al13 Cl8.5 I8 Mo6 O120P 62 2 219.751; 19.751; 57.616
90; 90; 120		19465Falaise, Clément; Ivanov, Anton A.; Molard, Yann; Amela Cortes, Maria; Shestopalov, Michael A.; Haouas, Mohamed; Cadot, Emmanuel; Cordier, Stéphane
From supramolecular to solid state chemistry: crystal engineering of luminescent materials by trapping molecular clusters in an aluminium-based host matrix
Materials Horizons, 2020, 7, 2399-2406
1558407 CIFC96 H112 Br8 Cl8 Mo6 Na5 O102.5P 1 21 115.8501; 32.821; 17.405
90; 93.734; 90		9035.1Falaise, Clément; Ivanov, Anton A.; Molard, Yann; Amela Cortes, Maria; Shestopalov, Michael A.; Haouas, Mohamed; Cadot, Emmanuel; Cordier, Stéphane
From supramolecular to solid state chemistry: crystal engineering of luminescent materials by trapping molecular clusters in an aluminium-based host matrix
Materials Horizons, 2020, 7, 2399-2406
1558414 CIFC48 H36 N24 O12 Zn6I -4 3 m17.2715; 17.2715; 17.2715
90; 90; 90		5152.2Mengwen, Li; Ao, Shen; Yueqi, Liang; Hao, Zhen; Xiaohui, Hao; Xueliang, Liu; Xinchao, Sun; Yunxu, Yang
The selective and sensitive detection of formaldehyde by ZIF-90-LWvia aza-Cope rearrangement
Analytical Methods, 2020, 12, 3748-3755
1558415 CIFC24 H8 F12 SnI 41/a c d :213.3697; 13.3697; 23.8975
90; 90; 90		4271.7Gini, Andrea; Paraja, Miguel; Galmés, Bartomeu; Besnard, Celine; Poblador-Bahamonde, Amalia I.; Sakai, Naomi; Frontera, Antonio; Matile, Stefan
Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations
Chemical Science, 2020
1558416 CIFC24 H8 F12 GeI 41/a c d :214.40851; 14.40851; 20.9644
90; 90; 90		4352.32Gini, Andrea; Paraja, Miguel; Galmés, Bartomeu; Besnard, Celine; Poblador-Bahamonde, Amalia I.; Sakai, Naomi; Frontera, Antonio; Matile, Stefan
Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations
Chemical Science, 2020
1558417 CIFC18 H6 F9 SbP -17.11145; 14.5572; 16.9641
98.5536; 93.9179; 102.025		1689.55Gini, Andrea; Paraja, Miguel; Galmés, Bartomeu; Besnard, Celine; Poblador-Bahamonde, Amalia I.; Sakai, Naomi; Frontera, Antonio; Matile, Stefan
Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations
Chemical Science, 2020
1558418 CIFC14 H26 O3P 1 21/n 15.84981; 15.5147; 14.8525
90; 90.681; 90		1347.89Gini, Andrea; Paraja, Miguel; Galmés, Bartomeu; Besnard, Celine; Poblador-Bahamonde, Amalia I.; Sakai, Naomi; Frontera, Antonio; Matile, Stefan
Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations
Chemical Science, 2020
1558419 CIFC18 H6 Bi F9P -17.16588; 14.61823; 17.01631
98.5736; 94.0812; 102.497		1710.92Gini, Andrea; Paraja, Miguel; Galmés, Bartomeu; Besnard, Celine; Poblador-Bahamonde, Amalia I.; Sakai, Naomi; Frontera, Antonio; Matile, Stefan
Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations
Chemical Science, 2020
1558420 CIFC25 H2 Cl6 F15 O2 SbP 1 21/n 110.37807; 18.8151; 15.5321
90; 103.434; 90		2949.88Gini, Andrea; Paraja, Miguel; Galmés, Bartomeu; Besnard, Celine; Poblador-Bahamonde, Amalia I.; Sakai, Naomi; Frontera, Antonio; Matile, Stefan
Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations
Chemical Science, 2020
1558421 CIFC18 H6 F9 SbP -14.6572; 11.8323; 15.386
102.271; 90.684; 100.761		812.73Gini, Andrea; Paraja, Miguel; Galmés, Bartomeu; Besnard, Celine; Poblador-Bahamonde, Amalia I.; Sakai, Naomi; Frontera, Antonio; Matile, Stefan
Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations
Chemical Science, 2020
1558422 CIFC18 F15 SbP 1 21/n 15.9325; 20.3604; 14.9916
90; 92.882; 90		1808.52Gini, Andrea; Paraja, Miguel; Galmés, Bartomeu; Besnard, Celine; Poblador-Bahamonde, Amalia I.; Sakai, Naomi; Frontera, Antonio; Matile, Stefan
Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations
Chemical Science, 2020
1558423 CIFC18 H6 F9 SbP n m a10.2444; 17.0576; 9.5358
90; 90; 90		1666.33Gini, Andrea; Paraja, Miguel; Galmés, Bartomeu; Besnard, Celine; Poblador-Bahamonde, Amalia I.; Sakai, Naomi; Frontera, Antonio; Matile, Stefan
Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations
Chemical Science, 2020
1558424 CIFC49 H14 Cl10 F18 O4 Sb2P -111.428; 14.4693; 17.6698
103.096; 97.1; 102.831		2727.81Gini, Andrea; Paraja, Miguel; Galmés, Bartomeu; Besnard, Celine; Poblador-Bahamonde, Amalia I.; Sakai, Naomi; Frontera, Antonio; Matile, Stefan
Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations
Chemical Science, 2020
1558425 CIFC25 H8 Cl6 F9 O2 SbP 1 21/n 19.96666; 16.7568; 17.1842
90; 102.174; 90		2805.38Gini, Andrea; Paraja, Miguel; Galmés, Bartomeu; Besnard, Celine; Poblador-Bahamonde, Amalia I.; Sakai, Naomi; Frontera, Antonio; Matile, Stefan
Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations
Chemical Science, 2020
1558426 CIFC34 H20C 1 c 111.0876; 20.5912; 19.1254
90; 96.758; 90		4336.12Zhou, Fulin; Zhou, Fujian; Su, Rongchuan; Yang, Yudong; You, Jingsong
Build-Up of Double Carbohelicenes Using Nitroarenes: Dual Role of the Nitro Functionality as Activation and Leaving Group
Chemical Science, 2020
1558427 CIFC34 H18P n m a7.8468; 23.408; 11.3681
90; 90; 90		2088.1Zhou, Fulin; Zhou, Fujian; Su, Rongchuan; Yang, Yudong; You, Jingsong
Build-Up of Double Carbohelicenes Using Nitroarenes: Dual Role of the Nitro Functionality as Activation and Leaving Group
Chemical Science, 2020
1558429 CIFC15 H11 Br F2 N4 O SP -18.0375; 9.3645; 12.0386
92.048; 106.633; 102.379		843.44Yu, Bin; Zhou, Shuang; Cao, Lixin; Hao, Zesheng; Yang, Dongyan; Guo, Xiaofeng; Zhang, Nailou; Bakulev, Vasiliy A.; Fan, Zhijin
Design, Synthesis and Evaluation of Antifungal Activity of Novel Pyrazole-thiazole Carboxamides as Succinate Dehydrogenase Inhibitors.
Journal of agricultural and food chemistry, 2020
1558430 CIFC17 H21 N O8P 21 21 215.4754; 15.6795; 20.1088
90; 90; 90		1726.37Habel, Deenamma; Nair, Divya S.; Kallingathodi, Zabeera; Mohan, Chithra; Pillai, Sarath M.; Nair, Rani R.; Thomas, Grace; Haleema, Simimole; Gopinath, Chithra; Abdul, Rinshad V.; Fritz, Matthew; Puente, Andrew R.; Johnson, Jordan L.; Polavarapu, Prasad L.; Ibnusaud, Ibrahim
Natural Product-Derived Chiral Pyrrolidine-2,5-diones, Their Molecular Structures and Conversion to Pharmacologically Important Skeletons.
Journal of natural products, 2020
1558431 CIFC16 H21 N O5C 1 2 124.693; 5.0152; 24.78
90; 101.05; 90		3011.9Habel, Deenamma; Nair, Divya S.; Kallingathodi, Zabeera; Mohan, Chithra; Pillai, Sarath M.; Nair, Rani R.; Thomas, Grace; Haleema, Simimole; Gopinath, Chithra; Abdul, Rinshad V.; Fritz, Matthew; Puente, Andrew R.; Johnson, Jordan L.; Polavarapu, Prasad L.; Ibnusaud, Ibrahim
Natural Product-Derived Chiral Pyrrolidine-2,5-diones, Their Molecular Structures and Conversion to Pharmacologically Important Skeletons.
Journal of natural products, 2020
1558432 CIFC16 H18 N2 O4P 1 21 15.666; 9.3371; 12.7013
90; 93.2; 90		670.9Habel, Deenamma; Nair, Divya S.; Kallingathodi, Zabeera; Mohan, Chithra; Pillai, Sarath M.; Nair, Rani R.; Thomas, Grace; Haleema, Simimole; Gopinath, Chithra; Abdul, Rinshad V.; Fritz, Matthew; Puente, Andrew R.; Johnson, Jordan L.; Polavarapu, Prasad L.; Ibnusaud, Ibrahim
Natural Product-Derived Chiral Pyrrolidine-2,5-diones, Their Molecular Structures and Conversion to Pharmacologically Important Skeletons.
Journal of natural products, 2020
1558433 CIFC17.5 H18 N2 O4P 1 21 116.8725; 5.1182; 17.3866
90; 92.854; 90		1499.59Habel, Deenamma; Nair, Divya S.; Kallingathodi, Zabeera; Mohan, Chithra; Pillai, Sarath M.; Nair, Rani R.; Thomas, Grace; Haleema, Simimole; Gopinath, Chithra; Abdul, Rinshad V.; Fritz, Matthew; Puente, Andrew R.; Johnson, Jordan L.; Polavarapu, Prasad L.; Ibnusaud, Ibrahim
Natural Product-Derived Chiral Pyrrolidine-2,5-diones, Their Molecular Structures and Conversion to Pharmacologically Important Skeletons.
Journal of natural products, 2020
1558434 CIFC16 H23 N O7P 21 21 215.674; 10.99; 26.414
90; 90; 90		1647.1Habel, Deenamma; Nair, Divya S.; Kallingathodi, Zabeera; Mohan, Chithra; Pillai, Sarath M.; Nair, Rani R.; Thomas, Grace; Haleema, Simimole; Gopinath, Chithra; Abdul, Rinshad V.; Fritz, Matthew; Puente, Andrew R.; Johnson, Jordan L.; Polavarapu, Prasad L.; Ibnusaud, Ibrahim
Natural Product-Derived Chiral Pyrrolidine-2,5-diones, Their Molecular Structures and Conversion to Pharmacologically Important Skeletons.
Journal of natural products, 2020
1558435 CIFC19 H22 N2 O6.5C 1 2 125.448; 6.6873; 11.1323
90; 91.972; 90		1893.4Habel, Deenamma; Nair, Divya S.; Kallingathodi, Zabeera; Mohan, Chithra; Pillai, Sarath M.; Nair, Rani R.; Thomas, Grace; Haleema, Simimole; Gopinath, Chithra; Abdul, Rinshad V.; Fritz, Matthew; Puente, Andrew R.; Johnson, Jordan L.; Polavarapu, Prasad L.; Ibnusaud, Ibrahim
Natural Product-Derived Chiral Pyrrolidine-2,5-diones, Their Molecular Structures and Conversion to Pharmacologically Important Skeletons.
Journal of natural products, 2020
1558436 CIFC16 H20 N O6P 1 21 18.811; 8.873; 10.494
90; 106.154; 90		788Habel, Deenamma; Nair, Divya S.; Kallingathodi, Zabeera; Mohan, Chithra; Pillai, Sarath M.; Nair, Rani R.; Thomas, Grace; Haleema, Simimole; Gopinath, Chithra; Abdul, Rinshad V.; Fritz, Matthew; Puente, Andrew R.; Johnson, Jordan L.; Polavarapu, Prasad L.; Ibnusaud, Ibrahim
Natural Product-Derived Chiral Pyrrolidine-2,5-diones, Their Molecular Structures and Conversion to Pharmacologically Important Skeletons.
Journal of natural products, 2020
1558437 CIF
HKL
Paper		C17 H13 N OP -15.8686; 7.4955; 15.2792
102.195; 90.649; 90.454		656.86Arunkumar, Dandavathi; Samshuddin, Seranthimata; Ansar, Mhammed; Mague, Joel T.; Ramli, Youssef
4-[(<i>E</i>)-3-(4-Methylphenyl)-3-oxoprop-1-en-1-yl]benzonitrile
IUCrData, 2020, 5, x200800
1558447 CIFC40 H56 O5P 21 21 216.9234; 12.1772; 41.1985
90; 90; 90		3473.35Raksat, Achara; Aree, Thammarat; Pudhom, Khanitha
Pterolobirins A and B, Oxygen-Bridged Cassane Diterpenoid Dimers from the Fruits of Pterolobium macropterum
Journal of Natural Products, 2020
1558448 CIFC20 H22 O6P 21 21 219.1387; 24.286; 38.773
90; 90; 90		8605.4Rivera-Chávez, José; Bustos-Brito, Celia; Aguilar-Ramírez, Enrique; Martínez-Otero, Diego; Rosales-Vázquez, Luis D.; Dorazco-González, Alejandro; Cano-Sánchez, Patricia
Hydroxy-neo-Clerodanes and 5,10-seco-neo-Clerodanes from Salvia decora
Journal of Natural Products, 2020
1558449 CIFC22.61 H25.48 O7P 1 21 112.3816; 7.604; 21.7468
90; 101.769; 90		2004.41Rivera-Chávez, José; Bustos-Brito, Celia; Aguilar-Ramírez, Enrique; Martínez-Otero, Diego; Rosales-Vázquez, Luis D.; Dorazco-González, Alejandro; Cano-Sánchez, Patricia
Hydroxy-neo-Clerodanes and 5,10-seco-neo-Clerodanes from Salvia decora
Journal of Natural Products, 2020
1558450 CIFC408 H400 N48 O64 Pd8P -122.2838; 27.0021; 29.9657
87.829; 86.244; 70.024		16907.1He, Lizhen; Cai, Li-Xuan; Li, Meng-Hua; Zhang, Guanglu; Zhou, Lipeng; Chen, Tianfeng; Lin, Mei-Jin; Sun, Qing-Fu
Designing Highly Stable Coordination-Driven Metallacycle for Imaging-Guided Photodynamic Cancer Theranostics
Chemical Science, 2020
1558451 CIFC20 H13 Au Br4 N2P -17.2134; 12.0436; 13.6068
113.303; 94.23; 100.284		1054.5Reiersolmoen, Ann Chrisitn; Battaglia, Stefano; Øien-Ødegaard, Sigurd; Gupta, Arvind Kumar Kumar; Fiksdahl, Anne; Lindh, Roland; Erdelyi, Mate
Symmetry of Three-Center, Four-Electron Bonds
Chemical Science, 2020
1558452 CIFC20.66 H13.5 Ag B Cl1.5 F4 N2P -16.987; 13.924; 21.312
85.099; 86.731; 81.161		2039Reiersolmoen, Ann Chrisitn; Battaglia, Stefano; Øien-Ødegaard, Sigurd; Gupta, Arvind Kumar Kumar; Fiksdahl, Anne; Lindh, Roland; Erdelyi, Mate
Symmetry of Three-Center, Four-Electron Bonds
Chemical Science, 2020
1558453 CIFC20.64 H13.44 Au B Cl1.44 F4 N2P -16.943; 14.1421; 21.3969
85.536; 86.97; 78.487		2050.9Reiersolmoen, Ann Chrisitn; Battaglia, Stefano; Øien-Ødegaard, Sigurd; Gupta, Arvind Kumar Kumar; Fiksdahl, Anne; Lindh, Roland; Erdelyi, Mate
Symmetry of Three-Center, Four-Electron Bonds
Chemical Science, 2020
1558454 CIFC72 H36 B F24 N4 NaP b c a18.2569; 25.817; 27.739
90; 90; 90		13074Reiersolmoen, Ann Chrisitn; Battaglia, Stefano; Øien-Ødegaard, Sigurd; Gupta, Arvind Kumar Kumar; Fiksdahl, Anne; Lindh, Roland; Erdelyi, Mate
Symmetry of Three-Center, Four-Electron Bonds
Chemical Science, 2020
1558455 CIFC41.5 H27 B2 Cl3 F8 I2 N4P -17.0108; 14.2732; 21.1647
86.903; 87.804; 77.898		2067Reiersolmoen, Ann Chrisitn; Battaglia, Stefano; Øien-Ødegaard, Sigurd; Gupta, Arvind Kumar Kumar; Fiksdahl, Anne; Lindh, Roland; Erdelyi, Mate
Symmetry of Three-Center, Four-Electron Bonds
Chemical Science, 2020
1558456 CIF
HKL
Paper		C30 H39 B I3 N2P 1 21/c 116.01; 12.5361; 16.3086
90; 90.041; 90		3273.2Schödel, Frauke; Lerner, Hans-Wolfram; Bolte, Michael
[1,3-Bis(2,6-diisopropylphenyl)-1,3-dihydro-2<i>H</i>-imidazol-2-ylidene]triiodoborane benzene hemisolvate
IUCrData, 2020, 5, x200863
1558460 CIFC11 H14.5 O3.25P 1 21 15.90591; 16.31586; 19.9754
90; 91.6764; 90		1924.01Banwell, Martin G.; Liu, Xin; Connal, Luke A.; Gardiner, Michael G.
Synthesis of Functionally and Stereochemically Diverse Polymers via Ring-Opening Metathesis Polymerization of Derivatives of the Biomass-Derived Platform Molecule Levoglucosenone Produced at Industrial Scale
Macromolecules, 2020
1558461 CIFC11 H12 O3P 21 21 216.947; 7.5101; 17.0105
90; 90; 90		887.48Banwell, Martin G.; Liu, Xin; Connal, Luke A.; Gardiner, Michael G.
Synthesis of Functionally and Stereochemically Diverse Polymers via Ring-Opening Metathesis Polymerization of Derivatives of the Biomass-Derived Platform Molecule Levoglucosenone Produced at Industrial Scale
Macromolecules, 2020
1558462 CIFC11 H14 O3P 1 21 19.9654; 9.084; 10.6678
90; 107.529; 90		920.867Banwell, Martin G.; Liu, Xin; Connal, Luke A.; Gardiner, Michael G.
Synthesis of Functionally and Stereochemically Diverse Polymers via Ring-Opening Metathesis Polymerization of Derivatives of the Biomass-Derived Platform Molecule Levoglucosenone Produced at Industrial Scale
Macromolecules, 2020
1558463 CIFC22 H27 F3 N2 O2P 1 21/n 111.3691; 13.8088; 12.4633
90; 95.417; 90		1947.92Jermaks, Janis; Quach, Phong; Seibel, Zara M.; Pomarole, Julien; Lambert, Tristan
Ring-Opening Carbonyl-Olefin Metathesis of Norbornenes
Chemical Science, 2020
1558464 CIFC16 H14 F O2P 1 21/n 15.6436; 36.318; 6.6768
90; 107.69; 90		1303.79Jin, Shengfei; Dang, Hang T.; Haug, Graham C.; Nguyen, Viet D.; Arman, Hadi; Larionov, Oleg V.
Deoxygenative α-Alkylation and α-Arylation of 1,2-Dicarbonyls
Chemical Science, 2020
1558465 CIFC28 H47 B N3 O2 PP 1 21/c 111.3547; 17.4727; 14.737
90; 99.889; 90		2880.34Jin, Shengfei; Dang, Hang T.; Haug, Graham C.; Nguyen, Viet D.; Arman, Hadi; Larionov, Oleg V.
Deoxygenative α-Alkylation and α-Arylation of 1,2-Dicarbonyls
Chemical Science, 2020
1558466 CIFC17 H17 N O2P n a 2123.0271; 5.7175; 20.879
90; 90; 90		2748.88Jin, Shengfei; Dang, Hang T.; Haug, Graham C.; Nguyen, Viet D.; Arman, Hadi; Larionov, Oleg V.
Deoxygenative α-Alkylation and α-Arylation of 1,2-Dicarbonyls
Chemical Science, 2020
1558467 CIFC16 H16 O2P 1 21 17.157; 7.4823; 11.605
90; 90.91; 90		621.38Jin, Shengfei; Dang, Hang T.; Haug, Graham C.; Nguyen, Viet D.; Arman, Hadi; Larionov, Oleg V.
Deoxygenative α-Alkylation and α-Arylation of 1,2-Dicarbonyls
Chemical Science, 2020
1558471 CIFC45 H31 Cl3 N4P -19.6121; 14.2479; 14.6368
107.63; 101.505; 97.424		1833Ishizuka, Tomoya; Sakashita, Ryuichi; Iwanaga, Osamu; Morimoto, Tatsuki; Mori, Shigeki; Ishida, Masatoshi; Toganoh, Motoki; Takegoshi, Kiyonori; Osuka, Atsuhiro; Furuta, Hiroyuki
NH Tautomerism of N-Confused Porphyrin: Solvent/Substituent Effects and Isomerization Mechanism.
The journal of physical chemistry. A, 2020
1558472 CIFC50 H44 N6 O2P -112.6211; 13.1779; 13.5455
98.691; 116.169; 92.716		1982.2Ishizuka, Tomoya; Sakashita, Ryuichi; Iwanaga, Osamu; Morimoto, Tatsuki; Mori, Shigeki; Ishida, Masatoshi; Toganoh, Motoki; Takegoshi, Kiyonori; Osuka, Atsuhiro; Furuta, Hiroyuki
NH Tautomerism of N-Confused Porphyrin: Solvent/Substituent Effects and Isomerization Mechanism.
The journal of physical chemistry. A, 2020
1558473 CIFC48 H38 N4P 1 21/c 114.3901; 8.4196; 15.7484
90; 95.333; 90		1899.8Ishizuka, Tomoya; Sakashita, Ryuichi; Iwanaga, Osamu; Morimoto, Tatsuki; Mori, Shigeki; Ishida, Masatoshi; Toganoh, Motoki; Takegoshi, Kiyonori; Osuka, Atsuhiro; Furuta, Hiroyuki
NH Tautomerism of N-Confused Porphyrin: Solvent/Substituent Effects and Isomerization Mechanism.
The journal of physical chemistry. A, 2020
1558474 CIFC44 H32 N4 OP -18.7618; 13.5724; 14.6798
74.067; 85.926; 73.962		1613.3Ishizuka, Tomoya; Sakashita, Ryuichi; Iwanaga, Osamu; Morimoto, Tatsuki; Mori, Shigeki; Ishida, Masatoshi; Toganoh, Motoki; Takegoshi, Kiyonori; Osuka, Atsuhiro; Furuta, Hiroyuki
NH Tautomerism of N-Confused Porphyrin: Solvent/Substituent Effects and Isomerization Mechanism.
The journal of physical chemistry. A, 2020
1558475 CIFC15 H13 N O3P 1 21/n 110.7032; 6.6627; 16.9382
90; 92.303; 90		1206.92Vik, Erik C.; Li, Ping; Maier, Josef M.; Madukwe, Daniel O.; Rassolov, Vitaly A.; Pellechia, Perry J.; Masson, Eric; Shimizu, Ken D.
Large Transition State Stabilization from a Weak Hydrogen Bond
Chemical Science, 2020
1558476 CIFC17 H14 N2 O3P n a 2125.6129; 7.265; 7.5367
90; 90; 90		1402.41Vik, Erik C.; Li, Ping; Maier, Josef M.; Madukwe, Daniel O.; Rassolov, Vitaly A.; Pellechia, Perry J.; Masson, Eric; Shimizu, Ken D.
Large Transition State Stabilization from a Weak Hydrogen Bond
Chemical Science, 2020
1558477 CIFC16 H14 N2 O5P -17.7842; 9.7899; 10.0423
81.677; 82.193; 67.584		697.29Vik, Erik C.; Li, Ping; Maier, Josef M.; Madukwe, Daniel O.; Rassolov, Vitaly A.; Pellechia, Perry J.; Masson, Eric; Shimizu, Ken D.
Large Transition State Stabilization from a Weak Hydrogen Bond
Chemical Science, 2020
1558478 CIFC15 H12 Cl N O3P 1 21/c 121.357; 6.819; 20.0691
90; 115.008; 90		2648.72Vik, Erik C.; Li, Ping; Maier, Josef M.; Madukwe, Daniel O.; Rassolov, Vitaly A.; Pellechia, Perry J.; Masson, Eric; Shimizu, Ken D.
Large Transition State Stabilization from a Weak Hydrogen Bond
Chemical Science, 2020
1558479 CIFC15 H12 Cl N O3I 1 2/a 117.4699; 6.8917; 22.137
90; 103.57; 90		2590.8Vik, Erik C.; Li, Ping; Maier, Josef M.; Madukwe, Daniel O.; Rassolov, Vitaly A.; Pellechia, Perry J.; Masson, Eric; Shimizu, Ken D.
Large Transition State Stabilization from a Weak Hydrogen Bond
Chemical Science, 2020
1558480 CIFC16 H14 Cl N O3P 21 21 219.8726; 10.9075; 12.7229
90; 90; 90		1370.07Vik, Erik C.; Li, Ping; Maier, Josef M.; Madukwe, Daniel O.; Rassolov, Vitaly A.; Pellechia, Perry J.; Masson, Eric; Shimizu, Ken D.
Large Transition State Stabilization from a Weak Hydrogen Bond
Chemical Science, 2020
1558481 CIFC101 H157 Cl Ir N2 Si7P -116.5707; 16.9084; 21.231
105.174; 96.576; 109.461		5278.5Poitiers, Nadine Elisabeth; Giarrana, Luisa; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Exohedral functionalization vs. core expansion of siliconoids with Group 9 metals: catalytic activity in alkene isomerization
Chemical Science, 2020
1558482 CIFC105 H154 Cl N2 O Rh Si7P -114.9387; 17.6518; 21.0713
102.165; 92.721; 108.26		5119.4Poitiers, Nadine Elisabeth; Giarrana, Luisa; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Exohedral functionalization vs. core expansion of siliconoids with Group 9 metals: catalytic activity in alkene isomerization
Chemical Science, 2020
1558483 CIFC101 H157 Cl Ir N2 Si6 SnP -115.7798; 26.095; 27.363
104.327; 106.15; 90.156		10455Poitiers, Nadine Elisabeth; Giarrana, Luisa; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Exohedral functionalization vs. core expansion of siliconoids with Group 9 metals: catalytic activity in alkene isomerization
Chemical Science, 2020
1558484 CIFC92 H138 Cl N2 O2 Rh Si7P n a 2137.608; 13.6961; 18.1426
90; 90; 90		9344.9Poitiers, Nadine Elisabeth; Giarrana, Luisa; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Exohedral functionalization vs. core expansion of siliconoids with Group 9 metals: catalytic activity in alkene isomerization
Chemical Science, 2020
1558485 CIFC104 H164 Cl Ge N2 Rh Si6P 1 21/n 129.9006; 22.525; 32.5302
90; 103.5; 90		21304.1Poitiers, Nadine Elisabeth; Giarrana, Luisa; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Exohedral functionalization vs. core expansion of siliconoids with Group 9 metals: catalytic activity in alkene isomerization
Chemical Science, 2020
1558486 CIFC101 H157 Cl Ge Ir N2 Si6P 1 21/n 115.7711; 31.3736; 21.3327
90; 106.081; 90		10142.3Poitiers, Nadine Elisabeth; Giarrana, Luisa; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Exohedral functionalization vs. core expansion of siliconoids with Group 9 metals: catalytic activity in alkene isomerization
Chemical Science, 2020
1558490 CIFC95 H104 B2 Cl2 Co2 F10 O12 P6P b c a26.2086; 27.5599; 28.9629
90; 90; 90		20920.1Papa, Veronica; Cabrero-Antonino, Jose R.; Spannenberg, Anke; Junge, Kathrin; Beller, Matthias
Homogeneous cobalt-catalyzed deoxygenative hydrogenation of amides to amines
Catalysis Science & Technology, 2020, 10, 6116-6128
1558491 CIFC19 H14 N4P n a 2116.0816; 18.5757; 5.1129
90; 90; 90		1527.36Szukalski, Adam; Haupa, Karolina A.; Janczak, Jan; Przybył, Bartosz; Sznitko, Lech; Myśliwiec, Jarosław
Lasing Properties Activation by Constitutional Isomerism of an Electron-Accepting Group
The Journal of Physical Chemistry C, 2020, 124, 13845-13857
1558492 CIFC19 H14 N4C 1 2/c 127.9461; 8.4289; 13.7881
90; 105.092; 90		3135.8Szukalski, Adam; Haupa, Karolina A.; Janczak, Jan; Przybył, Bartosz; Sznitko, Lech; Myśliwiec, Jarosław
Lasing Properties Activation by Constitutional Isomerism of an Electron-Accepting Group
The Journal of Physical Chemistry C, 2020, 124, 13845-13857
1558493 CIFF6 H12 Mn O6 SiP 1 21/c 16.473; 9.639; 8.579
90; 100.009; 90		527.1MIKURIYA, Masahiro; WATANABE, Nanami; KOYAMA, Yoshiki; YOSHIOKA, Daisuke; OGAWA, Junya; MITSUHASHI, Ryoji; HANDA, Makoto
Crystal Structure and Magnetic Property of Manganese(II) Hexafluorosilicate Hexahydrate
X-ray Structure Analysis Online, 2020, 36, 17-19
1558494 CIFC376 H392 B16 Co8 F64 N72 O33C 1 2/c 133.04569; 30.13654; 39.97965
90; 96.4337; 90		39564.3Taylor, Christopher G. P.; Train, Jennifer S.; Ward, Michael D.
Interactions of Small-Molecule Guests with Interior and Exterior Surfaces of a Coordination Cage Host
Chemistry, 2020, 2, 510-524
1558495 CIFC395.5 H411 B16 Co8 F64 N72 O35C 1 2/c 132.8649; 29.89225; 40.5389
90; 95.9164; 90		39613.5Taylor, Christopher G. P.; Train, Jennifer S.; Ward, Michael D.
Interactions of Small-Molecule Guests with Interior and Exterior Surfaces of a Coordination Cage Host
Chemistry, 2020, 2, 510-524
1558496 CIFC380.04 H422.24 B16 Co8 F64 N73.12 O38.44 S1.12C 1 2/c 132.81236; 30.21497; 40.09564
90; 96.3312; 90		39509.4Taylor, Christopher G. P.; Train, Jennifer S.; Ward, Michael D.
Interactions of Small-Molecule Guests with Interior and Exterior Surfaces of a Coordination Cage Host
Chemistry, 2020, 2, 510-524
1558497 CIFC377 H416 B16 Cl2 Co8 F64 N72 O39C 1 2/c 132.8588; 30.06718; 40.1053
90; 96.0585; 90		39401.6Taylor, Christopher G. P.; Train, Jennifer S.; Ward, Michael D.
Interactions of Small-Molecule Guests with Interior and Exterior Surfaces of a Coordination Cage Host
Chemistry, 2020, 2, 510-524
1558498 CIFC407.8 H417.66 B16 Co8 F64 N72 O31.03C 1 2/c 132.56923; 30.16165; 40.83634
90; 95.9061; 90		39902.3Taylor, Christopher G. P.; Train, Jennifer S.; Ward, Michael D.
Interactions of Small-Molecule Guests with Interior and Exterior Surfaces of a Coordination Cage Host
Chemistry, 2020, 2, 510-524
1558499 CIFCa7.97 Fe0.56 Mg9.47 O48 P12C 1 2/c 122.7973; 9.9833; 17.0522
90; 99.954; 90		3822.53Britvin, Sergey N.; Krzhizhanovskaya, Maria G.; Bocharov, Vladimir N.; Obolonskaya, Edita V.
Crystal Chemistry of Stanfieldite, Ca7M2Mg9(PO4)12 (M = Ca, Mg, Fe2+), a Structural Base of Ca3Mg3(PO4)4 Phosphors
Crystals, 2020, 10, 464
1558500 CIFC36 H20 Br3.77 Cl8 Cu2 N4P -17.8673; 11.0031; 11.7131
82.325; 89.994; 81.179		992.76Finocchio, Giada; Rizzato, Silvia; Macetti, Giovanni; Tusha, Gers; Lo Presti, Leonardo
Unravelling the Chemistry of the [Cu(4,7-Dichloroquinoline)2Br2]2 Dimeric Complex through Structural Analysis: A Borderline Ligand Field Case
Crystals, 2020, 10, 477
1558501 CIFC18 H13.5 B Cu F4 N6 O0.75C 1 c 119.6546; 17.9133; 24.0581
90; 112.816; 90		7807.6Beveridge, Stuart; McAnally, Craig A.; Nichol, Gary S.; Kennedy, Alan R.; Cussen, Edmund J.; Fletcher, Ashleigh J.
Unexpected Selective Gas Adsorption on a ‘Non-Porous’ Metal Organic Framework
Crystals, 2020, 10, 548
1558504 CIFC15 H22 O3P 21 21 219.77217; 9.81597; 13.76057
90; 90; 90		1319.96Li, Huaqiang; Zhang, Runge; Cao, Fei; Wang, Jianping; Hu, Zhengxi; Zhang, Yonghui
Proversilins A-E, Drimane-Type Sesquiterpenoids from the Endophytic <i>Aspergillus versicolor</i>.
Journal of natural products, 2020, 83, 2200-2206
1558505 CIFC11 H13 N O3P 21 21 215.42071; 12.6801; 14.9194
90; 90; 90		1025.49Li, Huaqiang; Zhang, Runge; Cao, Fei; Wang, Jianping; Hu, Zhengxi; Zhang, Yonghui
Proversilins A-E, Drimane-Type Sesquiterpenoids from the Endophytic <i>Aspergillus versicolor</i>.
Journal of natural products, 2020, 83, 2200-2206
1558506 CIFC15 H22 O4P 1 21 16.34756; 7.9249; 13.5609
90; 93.6003; 90		680.82Li, Huaqiang; Zhang, Runge; Cao, Fei; Wang, Jianping; Hu, Zhengxi; Zhang, Yonghui
Proversilins A-E, Drimane-Type Sesquiterpenoids from the Endophytic <i>Aspergillus versicolor</i>.
Journal of natural products, 2020, 83, 2200-2206
1558507 CIFC24 H26 Cl N7 OP 1 21/c 18.6917; 15.6895; 17.8706
90; 101.494; 90		2388.11Hussain, MD. Waseem; Bhardwaj, Vipin; Giri, Arkaprabha; Chande, Ajit; Patra, Abhijit
Multifunctional ionic porous frameworks for CO2 conversion and combating microbes
Chemical Science, 2020, 11, 7910-7920
1558508 CIFC15 H16 O2P 1 21/c 112.389; 12.5456; 7.5297
90; 99.928; 90		1152.8Wu, An; Qian, Hui; Zhao, Wanxiang; Sun, Jianwei
Benzannulation of Isobenzopyryliums with Electron-Rich Alkynes: A Modular Access to β-Functionalized Naphthalenes
Chemical Science, 2020
1558509 CIFC15 H15 F O2P 1 21/n 17.37471; 19.0645; 9.32895
90; 111.872; 90		1217.19Wu, An; Qian, Hui; Zhao, Wanxiang; Sun, Jianwei
Benzannulation of Isobenzopyryliums with Electron-Rich Alkynes: A Modular Access to β-Functionalized Naphthalenes
Chemical Science, 2020
1558510 CIFC22 H21 O2 PP 1 21 16.0977; 8.3134; 18.1062
90; 97.792; 90		909.38Yang, Zhiping; Gu, Xiaodong; Han, Li-Biao; Wang, Jun (Joelle)
Palladium-catalyzed asymmetric hydrophosphorylation of alkynes: facile access to P-stereogenic phosphinates
Chemical Science, 2020, 11, 7451-7455
1558511 CIFC19 H25 B F4 TeP b c a11.7351; 15.9629; 21.44
90; 90; 90		4016.3Zhou, Benyu; Gabbaï, François P.
Redox-controlled chalcogen-bonding at tellurium: Impact on Lewis acidity and chloride anion transport properties
Chemical Science, 2020
1558512 CIFC16 H14 B F9 TeP 1 21/n 112.377; 11.7628; 13.8733
90; 115.705; 90		1819.9Zhou, Benyu; Gabbaï, François P.
Redox-controlled chalcogen-bonding at tellurium: Impact on Lewis acidity and chloride anion transport properties
Chemical Science, 2020
1558513 CIFC13 H3 B F14 TeP 1 21/c 18.5716; 7.433; 25.0537
90; 97.146; 90		1583.84Zhou, Benyu; Gabbaï, François P.
Redox-controlled chalcogen-bonding at tellurium: Impact on Lewis acidity and chloride anion transport properties
Chemical Science, 2020
1558521 CIFC20 H30 O6P 21 21 217.9639; 8.3386; 28.4084
90; 90; 90		1886.54Pu, De-Bing; Zhang, Xing-Jie; Bi, De-Wen; Gao, Jun-Bo; Yang, Yan; Li, Xiao-Li; Lin, Jing; Li, Xiao-Nian; Zhang, Rui-Han; Xiao, Wei-Lie
Callicarpins, Two Classes of Rearranged <i>ent</i>-Clerodane Diterpenoids from <i>Callicarpa</i> Plants Blocking NLRP3 Inflammasome-Induced Pyroptosis.
Journal of natural products, 2020, 83, 2191-2199
1558522 CIFC21 H32 O6P 21 21 217.8764; 8.2662; 31.176
90; 90; 90		2029.8Pu, De-Bing; Zhang, Xing-Jie; Bi, De-Wen; Gao, Jun-Bo; Yang, Yan; Li, Xiao-Li; Lin, Jing; Li, Xiao-Nian; Zhang, Rui-Han; Xiao, Wei-Lie
Callicarpins, Two Classes of Rearranged <i>ent</i>-Clerodane Diterpenoids from <i>Callicarpa</i> Plants Blocking NLRP3 Inflammasome-Induced Pyroptosis.
Journal of natural products, 2020, 83, 2191-2199
1558523 CIFC19 H29 O5.5P 1 21 110.7266; 10.6192; 16.318
90; 100.492; 90		1827.67Pu, De-Bing; Zhang, Xing-Jie; Bi, De-Wen; Gao, Jun-Bo; Yang, Yan; Li, Xiao-Li; Lin, Jing; Li, Xiao-Nian; Zhang, Rui-Han; Xiao, Wei-Lie
Callicarpins, Two Classes of Rearranged <i>ent</i>-Clerodane Diterpenoids from <i>Callicarpa</i> Plants Blocking NLRP3 Inflammasome-Induced Pyroptosis.
Journal of natural products, 2020, 83, 2191-2199
1558524 CIFC21 H34 O8P 1 21 18.4232; 30.675; 8.5481
90; 101.44; 90		2164.8Pu, De-Bing; Zhang, Xing-Jie; Bi, De-Wen; Gao, Jun-Bo; Yang, Yan; Li, Xiao-Li; Lin, Jing; Li, Xiao-Nian; Zhang, Rui-Han; Xiao, Wei-Lie
Callicarpins, Two Classes of Rearranged <i>ent</i>-Clerodane Diterpenoids from <i>Callicarpa</i> Plants Blocking NLRP3 Inflammasome-Induced Pyroptosis.
Journal of natural products, 2020, 83, 2191-2199
1558525 CIFC26 H36 O9P 1 21 16.6138; 10.491; 18.5288
90; 99.538; 90		1267.86Pu, De-Bing; Zhang, Xing-Jie; Bi, De-Wen; Gao, Jun-Bo; Yang, Yan; Li, Xiao-Li; Lin, Jing; Li, Xiao-Nian; Zhang, Rui-Han; Xiao, Wei-Lie
Callicarpins, Two Classes of Rearranged <i>ent</i>-Clerodane Diterpenoids from <i>Callicarpa</i> Plants Blocking NLRP3 Inflammasome-Induced Pyroptosis.
Journal of natural products, 2020, 83, 2191-2199
1558526 CIFC19 H28 O2P 21 21 217.9409; 11.0197; 18.8393
90; 90; 90		1648.56Li, Hao; Liang, Yu-Ru; Chen, Shao-Xin; Wang, Wen-Xuan; Zou, Yike; Nuryyeva, Selbi; Houk, K. N.; Xiong, Juan; Hu, Jin-Feng
Amentotaxins C-V, Structurally Diverse Diterpenoids from the Leaves and Twigs of the Vulnerable Conifer <i>Amentotaxus argotaenia</i> and Their Cytotoxic Effects.
Journal of natural products, 2020, 83, 2129-2144
1558527 CIFC20 H33 O3.5P 21 21 217.6538; 22.4697; 44.905
90; 90; 90		7722.7Li, Hao; Liang, Yu-Ru; Chen, Shao-Xin; Wang, Wen-Xuan; Zou, Yike; Nuryyeva, Selbi; Houk, K. N.; Xiong, Juan; Hu, Jin-Feng
Amentotaxins C-V, Structurally Diverse Diterpenoids from the Leaves and Twigs of the Vulnerable Conifer <i>Amentotaxus argotaenia</i> and Their Cytotoxic Effects.
Journal of natural products, 2020, 83, 2129-2144
1558528 CIFC19.5 H28 O3.5P 21 21 216.7321; 13.4089; 37.6911
90; 90; 90		3402.4Li, Hao; Liang, Yu-Ru; Chen, Shao-Xin; Wang, Wen-Xuan; Zou, Yike; Nuryyeva, Selbi; Houk, K. N.; Xiong, Juan; Hu, Jin-Feng
Amentotaxins C-V, Structurally Diverse Diterpenoids from the Leaves and Twigs of the Vulnerable Conifer <i>Amentotaxus argotaenia</i> and Their Cytotoxic Effects.
Journal of natural products, 2020, 83, 2129-2144
1558529 CIFC144 H150 Cu4 N14 O74P -112.865; 16.2889; 20.1106
111.308; 101.254; 90.736		3834.5Leonhardt, Viktoria; Fimmel, Stefanie; Krause, Ana-Maria; Beuerle, Florian
A Covalent Organic Cage Compound Acting as a Supramolecular Shadow Mask for the Regioselective Functionalization of C60
Chemical Science, 2020
1558530 CIFC27 H34 B F2 N O2 SC 1 2/c 129.1214; 10.5552; 17.3216
90; 104.072; 90		5164.6Shen, Feng; Lv, Long; Shen, Qilong
Electrophilic Fluoroalkylthiolation Induced Diastereoselective and Stereospecific 1,2-Metalate Migration of Alkenylboronate Complexes
Chemical Science, 2020
1558531 CIFC16 H19 N O3 SP 21 21 219.726; 11.7737; 13.0343
90; 90; 90		1492.57Zhang, Lin; Yamazaki, Ken; Leitch, Jamie A.; Manzano, Ruben; Atkinson, Victoria A. M.; Hamlin, Trevor A.; Dixon, Darren J.
Dual catalytic enantioselective desymmetrization of allene-tethered cyclohexanones
Chemical Science, 2020
1558532 CIFC22 H20 O3 SP 1 21/c 119.855; 5.7928; 16.427
90; 105.359; 90		1821.9Zhang, Xueying; Zhang, Zhansong; Song, Jin-Na; Wang, Zikun
Reductive radical-initiated 1,2-C migration assisted by azidyl group
Chemical Science, 2020
1558533 CIFC20 H22 O3 SP -19.2575; 9.6845; 10.1145
79.903; 84.497; 80.659		878.8Zhang, Xueying; Zhang, Zhansong; Song, Jin-Na; Wang, Zikun
Reductive radical-initiated 1,2-C migration assisted by azidyl group
Chemical Science, 2020
1558534 CIFH76 K8 N Na9 Nd2 O165 Se4 W35P -118.6658; 21.9717; 22.0792
71.751; 67.119; 68.721		7616.1Li, Hailou; Lian, Chen; Chen, Lijuan; Zhao, Junwei; Yang, Guo-Yu
Two unusual nanosized Nd<sup>3+</sup>-substituted selenotungstate aggregates simultaneously comprising lacunary Keggin and Dawson polyoxotungstate segments.
Nanoscale, 2020, 12, 16091-16101
1558535 CIFC14 H275 N7 Na4 Nd6 O310 Se6 W58P -119.6262; 28.53; 30.005
90.355; 99.225; 94.275		16535Li, Hailou; Lian, Chen; Chen, Lijuan; Zhao, Junwei; Yang, Guo-Yu
Two unusual nanosized Nd<sup>3+</sup>-substituted selenotungstate aggregates simultaneously comprising lacunary Keggin and Dawson polyoxotungstate segments.
Nanoscale, 2020, 12, 16091-16101
1558536 CIFC18 H16 O2 TeP c a 2118.4073; 13.2209; 6.2891
90; 90; 90		1530.5Nishiyama, Hiroki; Zheng, Feng; Inagi, Shinsuke; Fueno, Hiroyuki; Tanaka, Kazuyoshi; Tomita, Ikuyoshi
Tellurophene-containing π-conjugated polymers with unique heteroatom–heteroatom interactions by post-element-transformation of an organotitanium polymer
Polymer Chemistry, 2020, 11, 4693-4698
1558537 CIFC18 H16 Br2 O2 TeP -19.6046; 10.539; 19.635
99.405; 103.196; 102.209		1843.9Nishiyama, Hiroki; Zheng, Feng; Inagi, Shinsuke; Fueno, Hiroyuki; Tanaka, Kazuyoshi; Tomita, Ikuyoshi
Tellurophene-containing π-conjugated polymers with unique heteroatom‒heteroatom interactions by post-element-transformation of an organotitanium polymer
Polymer Chemistry, 2020, 11, 4693-4698
1558539 CIFC136 H112 Au8 Fe4 P8P -116.136; 19.7871; 23.2458
76.706; 73.016; 80.103		6864.3Li, Shuo Hao; Liu, Xu; Hu, Weigang; Chen, Mingyang; Zhu, Yan
An Au<sub>8</sub> Cluster Fortified by Four Ferrocenes.
The journal of physical chemistry. A, 2020, 124, 6061-6067
1558540 CIFC19 H21 Cl2 N RuP c a 217.1672; 13.7037; 17.9697
90; 90; 90		1764.93Chatterjee, Basujit; Kalsi, Deepti; Kaithal, Akash; Bordet, Alexis; Leitner, Walter; Gunanathan, Chidambaram
One-pot dual catalysis for the hydrogenation of heteroarenes and arenes
Catalysis Science & Technology, 2020, 10, 5163-5170
1558541 CIFC33 H47 Al N2 OP 1 21/c 110.8627; 12.5842; 22.6057
90; 97.098; 90		3066.48Hooper, Thomas; Brown, Ryan; Rekhroukh, Feriel; Garçon, Martí; White, Andrew J. P.; Costa, Paulo J.; Crimmin, Mark Richard
Catalyst Control of Selectivity in the C‒O Bond Alumination of Biomass Derived Furans
Chemical Science, 2020
1558542 CIFC35 H49 Al N2 OP n a 2116.5281; 12.2177; 15.9821
90; 90; 90		3227.4Hooper, Thomas; Brown, Ryan; Rekhroukh, Feriel; Garçon, Martí; White, Andrew J. P.; Costa, Paulo J.; Crimmin, Mark Richard
Catalyst Control of Selectivity in the C‒O Bond Alumination of Biomass Derived Furans
Chemical Science, 2020
1558543 CIFC34 H47 Al N2 OP n a 2116.1355; 12.4185; 15.8598
90; 90; 90		3177.97Hooper, Thomas; Brown, Ryan; Rekhroukh, Feriel; Garçon, Martí; White, Andrew J. P.; Costa, Paulo J.; Crimmin, Mark Richard
Catalyst Control of Selectivity in the C‒O Bond Alumination of Biomass Derived Furans
Chemical Science, 2020
1558544 CIFC33 H45 Al N2 OP 1 21/c 110.9108; 12.4443; 22.7523
90; 99.2427; 90		3049.14Hooper, Thomas; Brown, Ryan; Rekhroukh, Feriel; Garçon, Martí; White, Andrew J. P.; Costa, Paulo J.; Crimmin, Mark Richard
Catalyst Control of Selectivity in the C‒O Bond Alumination of Biomass Derived Furans
Chemical Science, 2020
1558545 CIFC75 H110 Al2 N4 O4P -113.6025; 17.2522; 17.7358
108.504; 93.588; 112.988		3549.6Hooper, Thomas; Brown, Ryan; Rekhroukh, Feriel; Garçon, Martí; White, Andrew J. P.; Costa, Paulo J.; Crimmin, Mark Richard
Catalyst Control of Selectivity in the C‒O Bond Alumination of Biomass Derived Furans
Chemical Science, 2020
1558546 CIFC34 H49 Al N2 OP 1 21/c 114.319; 9.8459; 23.113
90; 98.845; 90		3219.8Hooper, Thomas; Brown, Ryan; Rekhroukh, Feriel; Garçon, Martí; White, Andrew J. P.; Costa, Paulo J.; Crimmin, Mark Richard
Catalyst Control of Selectivity in the C‒O Bond Alumination of Biomass Derived Furans
Chemical Science, 2020
1558547 CIFC34 H47 Al N2 OP 1 21/c 118.62; 8.9532; 32.557
90; 144.73; 90		3134Hooper, Thomas; Brown, Ryan; Rekhroukh, Feriel; Garçon, Martí; White, Andrew J. P.; Costa, Paulo J.; Crimmin, Mark Richard
Catalyst Control of Selectivity in the C‒O Bond Alumination of Biomass Derived Furans
Chemical Science, 2020
1558552 CIFC20 H19 N O5P 1 21 18.9401; 10.3433; 9.3915
90; 103.451; 90		844.611Luo, Weiwei; Sun, Zhicheng; Fernando, E. H. Nisala; Nesterov, Vladimir; Cundari, Thomas R.; Wang, Hong
Formal Oxo- and Aza-[3+2] Reactions of α-Enaminones and Quinones: A Double Divergent Process and the Roles of Chiral Phosphoric Acid and Molecular Sieves
Chemical Science, 2020
1558553 CIFC14 H14 O6P 21 21 217.17307; 9.46902; 36.9162
90; 90; 90		2507.42Luo, Weiwei; Sun, Zhicheng; Fernando, E. H. Nisala; Nesterov, Vladimir; Cundari, Thomas R.; Wang, Hong
Formal Oxo- and Aza-[3+2] Reactions of α-Enaminones and Quinones: A Double Divergent Process and the Roles of Chiral Phosphoric Acid and Molecular Sieves
Chemical Science, 2020
1558554 CIFC20 H17 N O4P 1 21/c 112.273; 13.8593; 19.0331
90; 103.984; 90		3141.49Luo, Weiwei; Sun, Zhicheng; Fernando, E. H. Nisala; Nesterov, Vladimir; Cundari, Thomas R.; Wang, Hong
Formal Oxo- and Aza-[3+2] Reactions of α-Enaminones and Quinones: A Double Divergent Process and the Roles of Chiral Phosphoric Acid and Molecular Sieves
Chemical Science, 2020
1558555 CIFC58 H86 O16 S2 Si2P 21 21 2117.815; 18.8153; 19.2663
90; 90; 90		6458Rose, John A.; Mahapatra, Subham; Li, Xin; Wang, Chao; Chen, Lei; Swick, Steven M.; Herzon, Seth B.
Synthesis of the bis(cyclohexenone) core of (−)-lomaiviticin A
Chemical Science, 2020
1558556 CIFC15 H14 N6 O3P 1 21/c 16.3096; 29.084; 7.5539
90; 91.45; 90		1385.8Ismail, Ismail; Chen, Zhuoyue; Sun, Lu; Ji, Xiuru; Ye, Haishun; Kang, Xueying; Huang, Haojie; Song, Haibin; Bolton, Sarah G.; Xi, Zhen; Pluth, Michael D.; Yi, Long
Highly efficient H2S scavengers via thiolysis of positively-charged NBD amines
Chemical Science, 2020, 11, 7823-7828
1558557 CIFC16 H17 I N6 O3P 1 21/c 119.9828; 12.5986; 14.2705
90; 101.853; 90		3516.1Ismail, Ismail; Chen, Zhuoyue; Sun, Lu; Ji, Xiuru; Ye, Haishun; Kang, Xueying; Huang, Haojie; Song, Haibin; Bolton, Sarah G.; Xi, Zhen; Pluth, Michael D.; Yi, Long
Highly efficient H2S scavengers via thiolysis of positively-charged NBD amines
Chemical Science, 2020, 11, 7823-7828
1558560 CIFC111 H119.5 Au2 N5 OP 1 21/m 114.4078; 24.1255; 14.433
90; 99.165; 90		4952.8Ibáñez, Susana; Poyatos, Macarena; Peris, Eduardo
N-Heterocyclic Carbenes: A Door Open to Supramolecular Organometallic Chemistry.
Accounts of chemical research, 2020
1558561 CIF
HKL		C56 H20 F20 N4 ZnC 1 2/c 134.176; 6.3699; 26.382
90; 123.428; 90		4793.2Lin, Zeyuan; Li, Jianfeng
[5,10,15,20-Tetrakis(pentafluorophenyl)porphyrinato]zinc(II) benzene disolvate
IUCrData, 2020, 5, x200877
1558562 CIF
Paper		C16 H14 F N O3P 1 21 19.74134; 9.83313; 14.91737
90; 98.2662; 90		1414.06Lee, Kathleen S.; Turner, Luke; Powell, Cynthia B.; Reinheimer, Eric W.
(<i>S</i>)-2-[(4-Fluorophenyl)formamido]-3-phenylpropanoic acid
IUCrData, 2020, 5, x200897
1558563 CIF
HKL
Paper		C29 H25 F N2 O4P 1 21/n 18.996; 15.921; 18.297
90; 102.59; 90		2557.6Jiang, Hong; Li, Yu-Long; Zhou, Jin; Sun, Hong-Shun; Zhang, Qing-Yu; Shi, Xing-Hao; Zhang, Zhi-Yuan; Ling, Tian
Diethyl 3,3'-[(3-fluorophenyl)methylene]bis(1<i>H</i>-indole-2-carboxylate)
IUCrData, 2020, 5, x200912
1558564 CIF
HKL
Paper		C12 H13 N O2P 1 21 15.7173; 7.346; 12.436
90; 93.07; 90		521.6Linkova, Elena I.; Grinev, Vyacheslav S.; Mayorova, Oksana A.; Yegorova, Alevtina Yu.
7a-Phenyltetrahydropyrrolo[2,1-<i>b</i>]oxazol-5(6<i>H</i>)-one
IUCrData, 2020, 5, x200919
1558565 CIF
HKL
Paper		C22 H15 N3 O2P 21 21 217.2994; 9.6105; 23.9296
90; 90; 90		1678.68Devika, S.; Begum, Noor Shahina; Manjappa, Kiran B.; Yang, Ding-Yah
(2-Hydroxyphenyl)(4,2':4',4''-terpyridin-6'-yl)methanone
IUCrData, 2020, 5, x200857
1558566 CIFC60 H59 Br4 Cl9 O13P 1 21 114.1567; 6.2892; 37.652
90; 95.26; 90		3338.2Pederson, Petra J.; Cai, Shengxin; Carver, Chase; Powell, Douglas R.; Risinger, April L.; Grkovic, Tanja; O'Keefe, Barry R; Mooberry, Susan L.; Cichewicz, Robert H.
Triple-Negative Breast Cancer Cells Exhibit Differential Sensitivity to Cardenolides from <i>Calotropis gigantea</i>.
Journal of natural products, 2020, 83, 2269-2280
1558567 CIFC31 H41 N O8 SP 21 21 2112.537; 12.7632; 18.2961
90; 90; 90		2927.6Pederson, Petra J.; Cai, Shengxin; Carver, Chase; Powell, Douglas R.; Risinger, April L.; Grkovic, Tanja; O'Keefe, Barry R; Mooberry, Susan L.; Cichewicz, Robert H.
Triple-Negative Breast Cancer Cells Exhibit Differential Sensitivity to Cardenolides from <i>Calotropis gigantea</i>.
Journal of natural products, 2020, 83, 2269-2280
1558568 CIFC29 H40 O10P 21 21 214.5716; 30.3441; 12.135
90; 90; 90		5365.6Pederson, Petra J.; Cai, Shengxin; Carver, Chase; Powell, Douglas R.; Risinger, April L.; Grkovic, Tanja; O'Keefe, Barry R; Mooberry, Susan L.; Cichewicz, Robert H.
Triple-Negative Breast Cancer Cells Exhibit Differential Sensitivity to Cardenolides from <i>Calotropis gigantea</i>.
Journal of natural products, 2020, 83, 2269-2280
1558569 CIFC23 H34 O4P 1 21 16.3191; 11.9806; 12.9208
90; 100.742; 90		961.05Pederson, Petra J.; Cai, Shengxin; Carver, Chase; Powell, Douglas R.; Risinger, April L.; Grkovic, Tanja; O'Keefe, Barry R; Mooberry, Susan L.; Cichewicz, Robert H.
Triple-Negative Breast Cancer Cells Exhibit Differential Sensitivity to Cardenolides from <i>Calotropis gigantea</i>.
Journal of natural products, 2020, 83, 2269-2280
1558570 CIFC23 H36 O6P 1 21 17.6298; 7.8915; 16.7699
90; 94.598; 90		1006.48Pederson, Petra J.; Cai, Shengxin; Carver, Chase; Powell, Douglas R.; Risinger, April L.; Grkovic, Tanja; O'Keefe, Barry R; Mooberry, Susan L.; Cichewicz, Robert H.
Triple-Negative Breast Cancer Cells Exhibit Differential Sensitivity to Cardenolides from <i>Calotropis gigantea</i>.
Journal of natural products, 2020, 83, 2269-2280
1558571 CIFC29 H44 O9P 21 21 216.469; 11.9665; 33.9275
90; 90; 90		2626.4Pederson, Petra J.; Cai, Shengxin; Carver, Chase; Powell, Douglas R.; Risinger, April L.; Grkovic, Tanja; O'Keefe, Barry R; Mooberry, Susan L.; Cichewicz, Robert H.
Triple-Negative Breast Cancer Cells Exhibit Differential Sensitivity to Cardenolides from <i>Calotropis gigantea</i>.
Journal of natural products, 2020, 83, 2269-2280
1558578 CIFC20 H30 O4P 21 21 217.57; 10.8882; 45.5723
90; 90; 90		3756.24Mao, Xu-Dong; Zhang, Cheng-Gang; Chen, Ting; Zhao, Sen-Miao; Chou, Gui-Xin
Cytotoxic Diterpenoids from <i>Caryopteris aureoglandulosa</i>.
Journal of natural products, 2020, 83, 2093-2101
1558579 CIFC19 H14 O6.5P 1 21 111.7598; 6.7923; 19.84
90; 94.713; 90		1579.4Mao, Xu-Dong; Zhang, Cheng-Gang; Chen, Ting; Zhao, Sen-Miao; Chou, Gui-Xin
Cytotoxic Diterpenoids from <i>Caryopteris aureoglandulosa</i>.
Journal of natural products, 2020, 83, 2093-2101
1558580 CIFC20 H18 O5C 1 c 118.522; 13.0651; 7.0412
90; 103.76; 90		1655.01Mao, Xu-Dong; Zhang, Cheng-Gang; Chen, Ting; Zhao, Sen-Miao; Chou, Gui-Xin
Cytotoxic Diterpenoids from <i>Caryopteris aureoglandulosa</i>.
Journal of natural products, 2020, 83, 2093-2101
1558581 CIFC19 H14 O7P 21 21 218.4122; 20.175; 26.6799
90; 90; 90		4528Mao, Xu-Dong; Zhang, Cheng-Gang; Chen, Ting; Zhao, Sen-Miao; Chou, Gui-Xin
Cytotoxic Diterpenoids from <i>Caryopteris aureoglandulosa</i>.
Journal of natural products, 2020, 83, 2093-2101
1558582 CIFC5 H11 Mn N O6C 1 c 114.345; 8.3232; 8.8793
90; 120.694; 90		911.6Liu, Chao; Zhai, Kun; Yu, Zhipeng; Nie, Anmin; Liu, Zhongyuan; Sun, Young
Hydrogen Bond Tuning of Magnetoelectric Coupling in Metal‒Organic Frameworks
The Journal of Physical Chemistry C, 2020
1558583 CIFC5 H11 Mn N O6R -3 c :H8.3371; 8.3371; 22.909
90; 90; 120		1379Liu, Chao; Zhai, Kun; Yu, Zhipeng; Nie, Anmin; Liu, Zhongyuan; Sun, Young
Hydrogen Bond Tuning of Magnetoelectric Coupling in Metal‒Organic Frameworks
The Journal of Physical Chemistry C, 2020
1558584 CIFC48 H30 F6 O6P 1 21/n 19.423; 40.326; 10.692
90; 107.3; 90		3879.1Miyazaki, Takuya; Shoji, Yoshiaki; Ishiwari, Fumitaka; Kajitani, Takashi; Fukushima, Takanori
Design of a molecular memory element with an alternating circular array of dipolar rotors and rotation suppressors
Chemical Science, 2020
1558585 CIFC48 H30 F6 O6P -111.3765; 13.951; 14.046
69.423; 70.729; 86.627		1966Miyazaki, Takuya; Shoji, Yoshiaki; Ishiwari, Fumitaka; Kajitani, Takashi; Fukushima, Takanori
Design of a molecular memory element with an alternating circular array of dipolar rotors and rotation suppressors
Chemical Science, 2020
1558586 CIFC53 H41.5 N4.5 O4P n m a16.087; 25.358; 21.354
90; 90; 90		8711Mirzaei, Saber; Castro, Edison; Hernández Sánchez, Raúl
Tubularenes
Chemical Science, 2020
1558587 CIFC46 H62 Al2 O6C 1 2/c 116.1738; 11.4534; 27.691
90; 96.754; 90		5094Wang, Zhe; Zhang, Xianhui; Liang, Hongwen; Xian, Mo; Wang, Xiaowu
Binuclear aluminum Lewis acid and its behavior in the polymerization of methyl methacrylate and n-butyl acrylate
Polymer Chemistry, 2020, 11, 5526-5533
1558588 CIFC30 H40 O11P 1 21 113.4072; 7.2619; 14.8167
90; 101.307; 90		1414.58Bedane, Kibrom Gebreheiwot; Brieger, Lukas; Strohmann, Carsten; Seo, Ean-Jeong; Efferth, Thomas; Spiteller, Michael
Cytotoxic Bufadienolides from the Leaves of <i>Melianthus major</i>.
Journal of natural products, 2020, 83, 2122-2128
1558589 CIFC26 H30 O7P 1 21 110.146; 10.4082; 10.8554
90; 110.004; 90		1077.19Bedane, Kibrom Gebreheiwot; Brieger, Lukas; Strohmann, Carsten; Seo, Ean-Jeong; Efferth, Thomas; Spiteller, Michael
Cytotoxic Bufadienolides from the Leaves of <i>Melianthus major</i>.
Journal of natural products, 2020, 83, 2122-2128
1558590 CIFC109 H114 F12 N10 O33 Rh4 S4P -115.7031; 15.8728; 27.7808
83.548; 76.381; 62.29		5957.9Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
Selective synthesis and structural transformation between a molecular ring-in-ring architecture and an abnormal trefoil knot
Chemical Science, 2020
1558591 CIFC131 H146 F12 N16 O34 Rh4 S4P 1 21/n 129.994; 14.8641; 33.736
90; 103.709; 90		14612.2Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
Selective synthesis and structural transformation between a molecular ring-in-ring architecture and an abnormal trefoil knot
Chemical Science, 2020
1558592 CIFC154 H182 F12 Ir4 N24 O33 S4C 2 2 2121.4001; 56.956; 13.5367
90; 90; 90		16499.4Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
Selective synthesis and structural transformation between a molecular ring-in-ring architecture and an abnormal trefoil knot
Chemical Science, 2020
1558593 CIFC156 H163 F12 N16 O34 Rh4 S4P -114.7048; 20.1231; 28.5603
105.589; 95.648; 100.981		7890.6Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
Selective synthesis and structural transformation between a molecular ring-in-ring architecture and an abnormal trefoil knot
Chemical Science, 2020
1558594 CIFC160 H184 F12 Ir4 N20 O26 S4P 1 21/n 130.1831; 15.0508; 33.4363
90; 103.152; 90		14791Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
Selective synthesis and structural transformation between a molecular ring-in-ring architecture and an abnormal trefoil knot
Chemical Science, 2020
1558595 CIFC286 H393 Ag2 F18 N31 O58 Rh6 S6P 1 21/c 136.05; 39.906; 43.383
90; 108.546; 90		59170Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
Selective synthesis and structural transformation between a molecular ring-in-ring architecture and an abnormal trefoil knot
Chemical Science, 2020
1558605 CIFC20 H24 Cr N2 O4P 1 21/n 19.8861; 7.5065; 12.9438
90; 94.152; 90		958.04Vinum, Morten Gotthold; Voigt, Laura; Hansen, Steen H.; Bell, Colby; Clark, Kensha Marie; Larsen, René Wugt; Pedersen, Kasper S.
Ligand field-actuated redox-activity of acetylacetonate
Chemical Science, 2020, 11, 8267-8272
1558606 CIFC10 H14 Cr O4P 1 21/n 110.2476; 4.7011; 11.3501
90; 92.163; 90		546.4Vinum, Morten Gotthold; Voigt, Laura; Hansen, Steen H.; Bell, Colby; Clark, Kensha Marie; Larsen, René Wugt; Pedersen, Kasper S.
Ligand field-actuated redox-activity of acetylacetonate
Chemical Science, 2020, 11, 8267-8272
1558607 CIFC24 H34 Cr N4 O4P -17.9894; 8.5405; 9.4779
103.054; 101.71; 92.188		614.49Vinum, Morten Gotthold; Voigt, Laura; Hansen, Steen H.; Bell, Colby; Clark, Kensha Marie; Larsen, René Wugt; Pedersen, Kasper S.
Ligand field-actuated redox-activity of acetylacetonate
Chemical Science, 2020, 11, 8267-8272
1558608 CIFC22 H22 Cr F6 N2 O4P 1 21/c 19.9399; 9.5252; 12.143
90; 94.29; 90		1146.47Vinum, Morten Gotthold; Voigt, Laura; Hansen, Steen H.; Bell, Colby; Clark, Kensha Marie; Larsen, René Wugt; Pedersen, Kasper S.
Ligand field-actuated redox-activity of acetylacetonate
Chemical Science, 2020, 11, 8267-8272
1558609 CIFC49 H83 La N2 O4 Si2P 1 21/c 117.0458; 16.5877; 19.5942
90; 112.851; 90		5105.5Dong, Xiang; Robinson, Jerome
The Role of Neutral Donor Ligands in the Isoselective Ring-Opening Polymerization of rac-β-Butyrolactone
Chemical Science, 2020
1558610 CIFC91 H111 La N2 O4 P2 Si2P 1 21/n 115.355; 15.378; 35.734
90; 94.563; 90		8411.1Dong, Xiang; Robinson, Jerome
The Role of Neutral Donor Ligands in the Isoselective Ring-Opening Polymerization of rac-β-Butyrolactone
Chemical Science, 2020
1558611 CIFC91 H111 N2 O4 P2 Si2 YP 1 21/n 115.221; 15.3725; 35.552
90; 93.759; 90		8300.7Dong, Xiang; Robinson, Jerome
The Role of Neutral Donor Ligands in the Isoselective Ring-Opening Polymerization of rac-β-Butyrolactone
Chemical Science, 2020
1558612 CIFC23 H21 Cl O7I 1 2/a 19.04; 16.15; 14.32
90; 101.67; 90		2047Chakraborty , Sandip; Joseph, Manu M.; Varughese, Sunil; Ghosh, Samrat; Maiti, Kaustabh; Samanta, Animesh; Ajayaghosh, Ayyappanpillai
A new pentacyclic pyrylium fluorescent probe that responds to pH imbalance during apoptosis
Chemical Science, 2020
1558613 CIFC11 H11 N O4P 1 21/c 16.29482; 13.8975; 11.1692
90; 90.663; 90		977.04Birchall, Lee T.; Shehata, Sara; McCarthy, Sean; Shepherd, Helena J.; Clark, Ewan R.; Serpell, Christopher J.; Biagini, Stefano C. G.
Supramolecular behaviour and fluorescence of rhodamine-functionalised ROMP polymers
Polymer Chemistry, 2020, 11, 5279-5285
1558614 CIFC41 H42 N4 O5P -110.4936; 12.3484; 16.1383
99.335; 102.497; 112.561		1814.32Birchall, Lee T.; Shehata, Sara; McCarthy, Sean; Shepherd, Helena J.; Clark, Ewan R.; Serpell, Christopher J.; Biagini, Stefano C. G.
Supramolecular behaviour and fluorescence of rhodamine-functionalised ROMP polymers
Polymer Chemistry, 2020, 11, 5279-5285
1558615 CIFC39 H42 N4 O4P b c a15.72214; 19.9433; 20.9335
90; 90; 90		6563.73Birchall, Lee T.; Shehata, Sara; McCarthy, Sean; Shepherd, Helena J.; Clark, Ewan R.; Serpell, Christopher J.; Biagini, Stefano C. G.
Supramolecular behaviour and fluorescence of rhodamine-functionalised ROMP polymers
Polymer Chemistry, 2020, 11, 5279-5285
1558616 CIFC21 H19 N O4P 1 21/c 120.276; 8.9776; 9.1929
90; 99.218; 90		1651.8Ling, Xia; Huang, Letao; Li, Youzhen; Wan, Qing; Wang, Zhiming; Qin, Anjun; Gao, Meng; Tang, Ben Zhong
Photoactivatable dihydroalkaloids for cancer cell imaging and chemotherapy with high spatiotemporal resolution
Materials Horizons, 2020, 7, 2696-2701
1558617 CIFC22 H22 Cl N O5P 1 21/c 113.288; 8.182; 17.804
90; 96.917; 90		1921.6Ling, Xia; Huang, Letao; Li, Youzhen; Wan, Qing; Wang, Zhiming; Qin, Anjun; Gao, Meng; Tang, Ben Zhong
Photoactivatable dihydroalkaloids for cancer cell imaging and chemotherapy with high spatiotemporal resolution
Materials Horizons, 2020, 7, 2696-2701
1558618 CIFC20 H15 N O4P -19.3078; 10.2556; 17.487
103.668; 100.331; 103.757		1525.61Ling, Xia; Huang, Letao; Li, Youzhen; Wan, Qing; Wang, Zhiming; Qin, Anjun; Gao, Meng; Tang, Ben Zhong
Photoactivatable dihydroalkaloids for cancer cell imaging and chemotherapy with high spatiotemporal resolution
Materials Horizons, 2020, 7, 2696-2701
1558619 CIF
HKL
Paper		C32 H48 N12 O8 Os3 P4P b c a18.75; 15.8889; 27.5984
90; 90; 90		8222.03Marolf, David M.; Brehm, Kristen L.; Lynch, Vincent M.; Powell, Gregory L.
1,1,2,2,2,3,3,3-Octacarbonyl-1,1,2,3-tetrakis(1,3,5-triaza-7-phosphatricyclo[3.3.1.1^3,7^]decane-κ<i>P</i>)-<i>triangulo</i>-triosmium(0)
IUCrData, 2020, 5, x200935
1558620 CIF
HKL
Paper		C17 H10 Br Cl2 N O2C 1 2/c 155.051; 3.8355; 35.979
90; 125.214; 90		6207Mayorova, Oksana A.; Grinev, Vyacheslav S.; Yegorova, Alevtina Yu.
(<i>Z</i>)-5-(4-Bromophenyl)-3-{[(3,5-dichlorophenyl)amino]methylidene}furan-2(3<i>H</i>)-one
IUCrData, 2020, 5, x200937
1558621 CIF
HKL
Paper		C93 H138 I Mo3 N3 S13P 3 1 c23.6627; 23.6627; 10.9815
90; 90; 120		5325Chen, Yueli; Wang, Bo; Fontenot, Patricia; Donahue, James P.
Tris[<i>N</i>,<i>N</i>-bis(3,5-di-<i>tert</i>-butylbenzyl)dithiocarbamato-κ^2^<i>S</i>,<i>S</i>']-μ~3~-sulfido-tris-μ~2~-disulfido-<i>triangulo</i>-trimolybdenum(IV) iodide
IUCrData, 2020, 5, x200939
1558623 CIFC20 H20 N2 O3P 21 21 217.6535; 13.7374; 31.5932
90; 90; 90		3321.7Zhang, Jian; Liu, Zhi-Wen; Li, Yong; Wei, Cui-Jie; Xie, Jing; Yuan, Meng-Fei; Zhang, Dong-Mei; Ye, Wen-Cai; Zhang, Xiao-Qi
Structurally Diverse Indole Alkaloids with Vasorelaxant Activity from Melodinus hemsleyanus
Journal of Natural Products, 2020
1558624 CIFC20 H25 N3 O9P 21 21 218.7009; 11.6468; 42.6723
90; 90; 90		4324.31Zhang, Jian; Liu, Zhi-Wen; Li, Yong; Wei, Cui-Jie; Xie, Jing; Yuan, Meng-Fei; Zhang, Dong-Mei; Ye, Wen-Cai; Zhang, Xiao-Qi
Structurally Diverse Indole Alkaloids with Vasorelaxant Activity from Melodinus hemsleyanus
Journal of Natural Products, 2020
1558626 CIFC29 H53 N O2P 1 21 14.5997; 56.635; 5.5074
90; 99.223; 90		1416.15Hall, Amy V.; Yufit, Dimitrii S.; Apperley, D. C.; Senak, Larry; Musa, Osama; Hood, David K.; Steed, Jonathan W.
The Crystal Engineering of Radiation-Sensitive Diacetylene Cocrystals and Salts
Chemical Science, 2020
1558627 CIFC31 H47 N O2P 1 21/c 15.4494; 8.9235; 57.441
90; 92.643; 90		2790.3Hall, Amy V.; Yufit, Dimitrii S.; Apperley, D. C.; Senak, Larry; Musa, Osama; Hood, David K.; Steed, Jonathan W.
The Crystal Engineering of Radiation-Sensitive Diacetylene Cocrystals and Salts
Chemical Science, 2020
1558628 CIFC30 H46 N2 O2P -15.3544; 6.8239; 39.92
87.742; 88.869; 75.291		1409.62Hall, Amy V.; Yufit, Dimitrii S.; Apperley, D. C.; Senak, Larry; Musa, Osama; Hood, David K.; Steed, Jonathan W.
The Crystal Engineering of Radiation-Sensitive Diacetylene Cocrystals and Salts
Chemical Science, 2020
1558629 CIFC54 H95 N O4P 1 2/n 19.5968; 4.6441; 57.52
90; 92.59; 90		2561Hall, Amy V.; Yufit, Dimitrii S.; Apperley, D. C.; Senak, Larry; Musa, Osama; Hood, David K.; Steed, Jonathan W.
The Crystal Engineering of Radiation-Sensitive Diacetylene Cocrystals and Salts
Chemical Science, 2020
1558630 CIFC60 H104 N2 O4P -15.577; 11.8339; 23.0041
100.67; 96.096; 103.007		1436.25Hall, Amy V.; Yufit, Dimitrii S.; Apperley, D. C.; Senak, Larry; Musa, Osama; Hood, David K.; Steed, Jonathan W.
The Crystal Engineering of Radiation-Sensitive Diacetylene Cocrystals and Salts
Chemical Science, 2020
1558631 CIFC25 H42 O2P -14.5738; 5.3909; 46.647
88.6499; 88.5073; 81.4017		1136.63Hall, Amy V.; Yufit, Dimitrii S.; Apperley, D. C.; Senak, Larry; Musa, Osama; Hood, David K.; Steed, Jonathan W.
The Crystal Engineering of Radiation-Sensitive Diacetylene Cocrystals and Salts
Chemical Science, 2020

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