Crystallography Open Database

Result: there are 13462 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format

We are unable to provide that many records as a single archive.
You can instead download the entire COD archive as a single .zip, .tgz or .txz archive.

Searching year of publication is 2021

Left arrow Left arrow First | Left arrow Previous 500 | of 27 | Next 500 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1557244 CIFC90 H126 Mn3 N12 O27P 1 21/m 112.323; 32.145; 12.931
90; 93.58; 90
5112Peralta, Ricardo A.; Huxley, Michael T.; Young, Rosemary J.; Linder-Patton, Oliver M; Evans, Jack D.; Doonan, Christian J.; Sumby, Christopher J.
MOF matrix isolation: cooperative conformational mobility enables reliable single crystal transformations.
Faraday discussions, 2021, 225, 84-99
1557245 CIFC84 H84 Cl18 Mn3 N12 O12P 1 21/m 112.313; 31.877; 12.954
90; 92.93; 90
5078Peralta, Ricardo A.; Huxley, Michael T.; Young, Rosemary J.; Linder-Patton, Oliver M; Evans, Jack D.; Doonan, Christian J.; Sumby, Christopher J.
MOF matrix isolation: cooperative conformational mobility enables reliable single crystal transformations.
Faraday discussions, 2021, 225, 84-99
1557246 CIFC105 H103.5 Mn3 N12 O12P -112.276; 12.869; 31.586
93.98; 97.43; 92.02
4931Peralta, Ricardo A.; Huxley, Michael T.; Young, Rosemary J.; Linder-Patton, Oliver M; Evans, Jack D.; Doonan, Christian J.; Sumby, Christopher J.
MOF matrix isolation: cooperative conformational mobility enables reliable single crystal transformations.
Faraday discussions, 2021, 225, 84-99
1557247 CIFC111 H138 Mn3 N12 O21P -112.457; 13.242; 33.037
86.69; 86.08; 85.22
5411Peralta, Ricardo A.; Huxley, Michael T.; Young, Rosemary J.; Linder-Patton, Oliver M; Evans, Jack D.; Doonan, Christian J.; Sumby, Christopher J.
MOF matrix isolation: cooperative conformational mobility enables reliable single crystal transformations.
Faraday discussions, 2021, 225, 84-99
1557248 CIFC97 H126 Mn3 N12 O18P -112.364; 12.947; 30.366
99.4; 97.35; 91.57
4750.4Peralta, Ricardo A.; Huxley, Michael T.; Young, Rosemary J.; Linder-Patton, Oliver M; Evans, Jack D.; Doonan, Christian J.; Sumby, Christopher J.
MOF matrix isolation: cooperative conformational mobility enables reliable single crystal transformations.
Faraday discussions, 2021, 225, 84-99
1557249 CIFC93 H120 Mn3 N12 O21P 1 21/m 112.274; 32.826; 12.93
90; 95.51; 90
5186Peralta, Ricardo A.; Huxley, Michael T.; Young, Rosemary J.; Linder-Patton, Oliver M; Evans, Jack D.; Doonan, Christian J.; Sumby, Christopher J.
MOF matrix isolation: cooperative conformational mobility enables reliable single crystal transformations.
Faraday discussions, 2021, 225, 84-99
1557250 CIFC97.5 H111 Mn3 N12 O19.5P 1 21/m 112.307; 31.637; 13.006
90; 92.1; 90
5061Peralta, Ricardo A.; Huxley, Michael T.; Young, Rosemary J.; Linder-Patton, Oliver M; Evans, Jack D.; Doonan, Christian J.; Sumby, Christopher J.
MOF matrix isolation: cooperative conformational mobility enables reliable single crystal transformations.
Faraday discussions, 2021, 225, 84-99
1557251 CIFC111 H106 Cl2 Mn3 N12 O16 Rh2P 1 21/c 112.339; 33.798; 25.762
90; 96.1; 90
10683Peralta, Ricardo A.; Huxley, Michael T.; Young, Rosemary J.; Linder-Patton, Oliver M; Evans, Jack D.; Doonan, Christian J.; Sumby, Christopher J.
MOF matrix isolation: cooperative conformational mobility enables reliable single crystal transformations.
Faraday discussions, 2021, 225, 84-99
1557599 CIFC9 H10 N4 O3 Zn2P b a 210.51; 12.234; 4.666
90; 90; 90
599.95Huang, Zhehao; Ge, Meng; Carraro, Francesco; Doonan, Christian; Falcaro, Paolo; Zou, Xiaodong
Can 3D electron diffraction provide accurate atomic structures of metal-organic frameworks?
Faraday discussions, 2021, 225, 118-132
1557771 CIFC94 H100 Cl12 N12 O3 Pd6P 1 21 114.2257; 50.2552; 19.5481
90; 91.9145; 90
13967.4Tashiro, Shohei; Umeki, Tsutomu; Kubota, Ryou; Shionoya, Mitsuhiko
Face-selective adsorption of a prochiral compound on the chiral pore-surface of a metal-macrocycle framework (MMF) directed towards stereoselective reactions.
Faraday discussions, 2021, 225, 197-209
1557772 CIFC95.93 H98.19 Cl12 N15 O2.74 Pd6P 1 21/c 119.5269; 51.758; 14.2813
90; 91.0232; 90
14431Tashiro, Shohei; Umeki, Tsutomu; Kubota, Ryou; Shionoya, Mitsuhiko
Face-selective adsorption of a prochiral compound on the chiral pore-surface of a metal-macrocycle framework (MMF) directed towards stereoselective reactions.
Faraday discussions, 2021, 225, 197-209
1557773 CIFC86.9 H86.8 Cl12 N12 O10.13 Pd6P 1 21 114.1814; 52.5455; 19.8435
90; 91.1321; 90
14783.9Tashiro, Shohei; Umeki, Tsutomu; Kubota, Ryou; Shionoya, Mitsuhiko
Face-selective adsorption of a prochiral compound on the chiral pore-surface of a metal-macrocycle framework (MMF) directed towards stereoselective reactions.
Faraday discussions, 2021, 225, 197-209
1557774 CIFC98.4 H97.66 Cl12.55 N14.25 O2.95 Pd6P 1 21 114.338; 52.953; 19.7623
90; 90.789; 90
15002.9Tashiro, Shohei; Umeki, Tsutomu; Kubota, Ryou; Shionoya, Mitsuhiko
Face-selective adsorption of a prochiral compound on the chiral pore-surface of a metal-macrocycle framework (MMF) directed towards stereoselective reactions.
Faraday discussions, 2021, 225, 197-209
1557791 CIFC20 H16 Cl2 N4 O PtP 1 21/c 15.3046; 21.6781; 15.9776
90; 94.542; 90
1831.55Kobayashi, Atsushi; Imada, Shin-Ichiro; Wang, Dongjin; Nagao, Yuki; Yoshida, Masaki; Kato, Masako
Cooperative phenomenon of vapochromism and proton conduction of luminescent Pt(ii) complexes for the visualisation of proton conductivity.
Faraday discussions, 2021, 225, 184-196
1557792 CIFC21 H18 Cl2 N4 O PtP -18.0185; 10.5928; 13.0124
69.402; 86.254; 72.413
985.2Kobayashi, Atsushi; Imada, Shin-Ichiro; Wang, Dongjin; Nagao, Yuki; Yoshida, Masaki; Kato, Masako
Cooperative phenomenon of vapochromism and proton conduction of luminescent Pt(ii) complexes for the visualisation of proton conductivity.
Faraday discussions, 2021, 225, 184-196
1557793 CIFC40 H34 Cl6.5 N8 O6 Pt2P -113.5911; 14.4864; 14.6981
99.605; 101.408; 117.546
2401.45Kobayashi, Atsushi; Imada, Shin-Ichiro; Wang, Dongjin; Nagao, Yuki; Yoshida, Masaki; Kato, Masako
Cooperative phenomenon of vapochromism and proton conduction of luminescent Pt(ii) complexes for the visualisation of proton conductivity.
Faraday discussions, 2021, 225, 184-196
1558875 CIFC44.2 H35.32 N2.6 O16.6 Zn3C 1 2/c 132.7998; 9.7204; 18.3042
90; 96.453; 90
5798.9Cadman, Laura K.; Mahon, Mary F.; Burrows, Andrew D.
Inclusion of viologen cations leads to switchable metal-organic frameworks.
Faraday discussions, 2021, 225, 414-430
1558876 CIFC49.2 H46.78 N3.4 O18.7 Zn3C 1 2/c 132.6406; 9.63384; 18.4404
90; 102.534; 90
5660.47Cadman, Laura K.; Mahon, Mary F.; Burrows, Andrew D.
Inclusion of viologen cations leads to switchable metal-organic frameworks.
Faraday discussions, 2021, 225, 414-430
1558877 CIFC212 H260 N20 O76 Zn8P c a 2136.4926; 14.6058; 45.4204
90; 90; 90
24209.2Cadman, Laura K.; Mahon, Mary F.; Burrows, Andrew D.
Inclusion of viologen cations leads to switchable metal-organic frameworks.
Faraday discussions, 2021, 225, 414-430
1558878 CIFC36 H34 N4 O14 Zn2P 1 21/n 19.6981; 16.1078; 11.5458
90; 90.923; 90
1803.39Cadman, Laura K.; Mahon, Mary F.; Burrows, Andrew D.
Inclusion of viologen cations leads to switchable metal-organic frameworks.
Faraday discussions, 2021, 225, 414-430
1559556 CIFC68 H156 O28 Si14 Zr2P -113.346; 17.309; 23.753
86.026; 89.28; 76.624
5325.4Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559557 CIFC96 H184 O28 Si14 Zr2P b c a20.0054; 24.0516; 27.5739
90; 90; 90
13267.5Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559558 CIFC68 H156 Hf2 O28 Si14P b c a18.563; 22.017; 26.445
90; 90; 90
10808Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559559 CIFC96 H184 Hf2 O28 Si14P b c a20.061; 24.064; 27.568
90; 90; 90
13308Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559560 CIFC86 H109 N9 Na2 O11 V2P -113.4214; 14.2596; 25.2549
85.709; 78.946; 69.251
4435.9Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559561 CIFC104 H120 N8 O8 V2P -112.0966; 12.3373; 17.8971
90.8728; 107.997; 99.2458
2501.28Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559562 CIFC80 H90 Cl2 N2 O8 V2P 1 21/n 119.7039; 20.0862; 20.6921
90; 113.114; 90
7532Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559563 CIFC178 H213 N11 O20 V4P -114.0354; 17.3396; 20.1906
71.168; 84.459; 66.456
4260.59Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559564 CIFC86 H114 N6 O16 V4P -112.4983; 13.6976; 14.1554
68.166; 79.128; 75.546
2165.92Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559565 CIFC82 H90 F6 N2 O8 V2P 1 21/c 120.0005; 19.9315; 22.023
90; 116.08; 90
7885.4Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559566 CIFC355 H421 Cl2 N21 O32 V8P -119.7899; 20.6775; 22.7696
69.271; 76.567; 78.627
8407.9Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559567 CIFC49 H38 Cl2 Co F5 N3P -111.8773; 12.8721; 14.5308
97.115; 92.063; 98.641
2176.04Zhang, Qiuyue; Li, Zilong; Han, Mingyang; Xiang, Junfeng; Solan, Gregory A.; Ma, Yanping; Liang, Tongling; Sun, Wen-Hua
Fluorinated cobalt catalysts and their use in forming narrowly dispersed polyethylene waxes of high linearity and incorporating vinyl functionality
Catalysis Science & Technology, 2021, 11, 656-670
1559568 CIFC260 H220 Cl10 Co5 F25 N15P -120.2887; 22.5854; 30.0093
94.052; 105.348; 102.898
12802.4Zhang, Qiuyue; Li, Zilong; Han, Mingyang; Xiang, Junfeng; Solan, Gregory A.; Ma, Yanping; Liang, Tongling; Sun, Wen-Hua
Fluorinated cobalt catalysts and their use in forming narrowly dispersed polyethylene waxes of high linearity and incorporating vinyl functionality
Catalysis Science & Technology, 2021, 11, 656-670
1559569 CIFC75 H60 B Cl2 F24 N3 PdP -112.4888; 16.9952; 19.3546
69.171; 75.05; 81.715
3703.33Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559570 CIFC41 H45 Br2 Cl N2 PdP 1 21/n 112.8172; 18.0795; 16.7528
90; 96.977; 90
3853.36Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559571 CIFC44 H53 Cl3 N2 O2 PdP 1 21/n 111.7251; 18.4561; 19.821
90; 101.805; 90
4198.5Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559572 CIFC41 H45 Cl3 N2 PdP -111.0716; 16.373; 21.6279
89.42; 76.403; 88.652
3809.6Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559573 CIFC78 H67 B F24 I2 N3 PdP -113.006; 16.863; 19.2164
98.154; 96.07; 99.498
4078.6Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559574 CIFC77.25 H66.5 B Cl0.5 F24 N3 O2 PdP -114.4315; 16.2211; 18.6665
109.704; 107.844; 95.369
3820.3Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559575 CIFC41 H45 Cl I2 N2 PdP 1 21/c 110.0308; 19.7307; 20.2309
90; 101.055; 90
3929.69Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559614 CIFC67.55 H47.1 Cl3.09 N6 S4P -113.8855; 17.9904; 19.186
77.172; 78.221; 69.1
4324.4Rotter, Julian M.; Guntermann, Roman; Auth, Michael; Mähringer, Andre; Sperlich, Andreas; Dyakonov, Vladimir; Medina, Dana D.; Bein, Thomas
Highly conducting Wurster-type twisted covalent organic frameworks
Chemical Science, 2021
1559658 CIFC41 H28 N4P 1 21 117.049; 14.1638; 25.7784
90; 103.896; 90
6042.76Ni, Fan; Huang, Chih-Wei; Tang, Yukun; Chen, Zhanxiang; Wu, Yaxun; Xia, Shengpeng; Cao, Xiaosong; Hsu, Jung-Hsien; Lee, Wei-Kai; Zheng, Kailu; Huang, Zhongyan; Wu, Chung-Chih; Yang, Chuluo
Integrating molecular rigidity and chirality into thermally activated delayed fluorescence emitters for highly efficient sky-blue and orange circularly polarized electroluminescence
Materials Horizons, 2021, 8, 547-555
1559676 CIFC20 H22 Cd N4 O12P 31 2 113.7702; 13.7702; 13.2048
90; 90; 120
2168.42Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559677 CIFC20 H22 Cd N4 O12P 31 2 113.9775; 13.9775; 13.0994
90; 90; 120
2216.4Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559678 CIFC20 H22 Cd N4 O12P 32 2 114.8922; 14.8922; 12.7663
90; 90; 120
2452Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559679 CIFC16 H6 Cd N2 O12P 31 2 114.9689; 14.9689; 12.6934
90; 90; 120
2463.14Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559680 CIFC20 H22 Cd N4 O12P 32 2 115.0465; 15.0465; 12.6619
90; 90; 120
2482.56Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559681 CIFC20 H22 Cd N4 O12P 31 2 114.0982; 14.0982; 13.0538
90; 90; 120
2247Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559682 CIFC20 H22 Cd N4 O12P 31 2 113.6191; 13.6191; 13.2288
90; 90; 120
2124.9Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559683 CIFC20 H22 Cd N4 O12P 31 2 114.366; 14.366; 12.8607
90; 90; 120
2298.6Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559684 CIFC20 H22 Cd N4 O12P 31 2 114.218; 14.218; 13.0014
90; 90; 120
2276.1Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559685 CIFC16 H6 Cd N2 O12P 31 2 114.515; 14.515; 12.8247
90; 90; 120
2340Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559686 CIFC20 H22 Cd N4 O12P 31 2 113.9484; 13.9484; 13.1157
90; 90; 120
2209.89Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559687 CIFC16 H6 Cd N2 O12P 31 2 114.8744; 14.8744; 12.7248
90; 90; 120
2438.2Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559688 CIFC16 H6 Cd N2 O12P 31 2 114.921; 14.921; 12.7118
90; 90; 120
2450.94Watkins, Daniel; Roseveare, Thomas M.; Warren, Mark R.; Thompson, Stephen P.; Fletcher, Ashleigh J.; Brammer, Lee
Multi-stimulus linear negative expansion of a breathing M(O<sub>2</sub>CR)<sub>4</sub>-node MOF.
Faraday discussions, 2021, 225, 133-151
1559737 CIFC20 H60 Fe4 N8 O30 S6P 1 21/c 111.767; 18.7367; 12.0965
90; 117.762; 90
2359.98Hu, Lei; Wang, Qiushi; Zhu, Xiandong; Meng, Tao; Huang, Binbin; Yang, Jindong; Lin, Xiaoming; Tong, Yexiang
Novel Fe<sub>4</sub>-based metal-organic cluster-derived iron oxides/S,N dual-doped carbon hybrids for high-performance lithium storage.
Nanoscale, 2021, 13, 716-723
1559739 CIFC96.25 H87.5 Cl0 F0.25 N8.75 O8.75 P0.25P c a 2118.079; 30.1771; 14.9963
90; 90; 90
8181.6Wang, Xiaoxuan; Qi, Chunxuan; Fu, Zhiyuan; Zhang, Haoke; Wang, Jianguo; Feng, Hai-Tao; Wang, Kai; Zou, Bo; Lam, Jacky W. Y.; Tang, Ben Zhong
A synergy between the push‒pull electronic effect and twisted conformation for high-contrast mechanochromic AIEgens
Materials Horizons, 2021, 8, 630-638
1559740 CIFC38 H40 F12 N2 O4 P2P n n a15.95929; 28.8471; 8.98775
90; 90; 90
4137.77Wang, Xiaoxuan; Qi, Chunxuan; Fu, Zhiyuan; Zhang, Haoke; Wang, Jianguo; Feng, Hai-Tao; Wang, Kai; Zou, Bo; Lam, Jacky W. Y.; Tang, Ben Zhong
A synergy between the push‒pull electronic effect and twisted conformation for high-contrast mechanochromic AIEgens
Materials Horizons, 2021, 8, 630-638
1559741 CIFC38 H32 F12 N2 P2C 1 2/c 137.188; 9.2614; 10.1379
90; 94.648; 90
3480.1Wang, Xiaoxuan; Qi, Chunxuan; Fu, Zhiyuan; Zhang, Haoke; Wang, Jianguo; Feng, Hai-Tao; Wang, Kai; Zou, Bo; Lam, Jacky W. Y.; Tang, Ben Zhong
A synergy between the push‒pull electronic effect and twisted conformation for high-contrast mechanochromic AIEgens
Materials Horizons, 2021, 8, 630-638
1559799 CIFC36 H50 Ca N6 O P Si2P -19.9377; 13.2229; 17.1785
71.337; 73.927; 77.882
2036.7Liu, Na; Liu, Doudou; Liu, Bo; Zhang, Hao; Cui, Dongmei
Stereoselective polymerization of rac-lactide catalyzed by zwitterionic calcium complexes
Polymer Chemistry, 2021, 12, 1518-1525
1559800 CIFC47 H55 Ca N6 O3 P Si2P -111.2638; 12.9788; 17.8234
93.419; 100.831; 95.152
2541Liu, Na; Liu, Doudou; Liu, Bo; Zhang, Hao; Cui, Dongmei
Stereoselective polymerization of rac-lactide catalyzed by zwitterionic calcium complexes
Polymer Chemistry, 2021, 12, 1518-1525
1559801 CIFAl0.17 Ca0.18 F0.08 Fe5.4 H1.92 Mg1.25 O23.92 Si8C 1 2/m 19.54396; 18.2455; 5.3266
90; 101.883; 90
907.67Giacobbe, Carlotta; Di Giuseppe, Dario; Zoboli, Alessandro; Lassinantti Gualtieri, Magdalena; Bonasoni, Paola; Moliterni, Anna; Corriero, Nicola; Altomare, Angela; Wright, Jonathan; Gualtieri, Alessandro F.
Crystal structure determination of a lifelong biopersistent asbestos fibre using single-crystal synchrotron X-ray micro-diffraction
IUCrJ, 2021, 8, 76-86
1559802 CIFAl0.22 Ca0.17 Fe5.3 H2 Mg1.31 O24 Si8C 1 2/m 19.5343; 18.221; 5.3202
90; 101.846; 90
904.57Giacobbe, Carlotta; Di Giuseppe, Dario; Zoboli, Alessandro; Lassinantti Gualtieri, Magdalena; Bonasoni, Paola; Moliterni, Anna; Corriero, Nicola; Altomare, Angela; Wright, Jonathan; Gualtieri, Alessandro F.
Crystal structure determination of a lifelong biopersistent asbestos fibre using single-crystal synchrotron X-ray micro-diffraction
IUCrJ, 2021, 8, 76-86
1559807 CIFAs3 Fe H16 O17P 1 21/n 115.4357; 20.01; 4.7994
90; 91.728; 90
1481.71Steciuk, Gwladys; Majzlan, Juraj; Plášil, Jakub
Hydrogen disorder in kaatialaite Fe[AsO~2~(OH)~2~]5H~2~O from Jáchymov, Czech Republic: determination from low-temperature 3D electron diffraction
IUCrJ, 2021, 8, 116-123
1559811 CIFC17 H19 F6 N2 O PP 1 21/c 125.6008; 7.0486; 21.7397
90; 114.951; 90
3556.8Whitaker, Daniel J.; Huang, Zehuan; Longbottom, Brooke W.; Sala, Renata L.; Wu, Guanglu; Scherman, Oren A.
Supramolecular hydrogels prepared from fluorescent alkyl pyridinium acrylamide monomers and CB[8]
Polymer Chemistry, 2021, 12, 519-525
1559833 CIFB4 K3 O12 Tm3P 1 21/c 110.49; 17.3785; 13.7941
90; 110.495; 90
2355.5Chen, Pengyun; Murshed, M. Mangir; Gesing, Thorsten M.
Synthesis and crystal structures of novel alkali rare-earth orthoborates K3RE3(BO3)4 (RE = Pr, Nd, Sm‒Lu)
Journal of Materials Science, 2021, 56, 3639-3652
1559834 CIFB4 Er3 K3 O12P 1 21/c 110.5189; 17.4322; 13.8305
90; 110.521; 90
2375.14Chen, Pengyun; Murshed, M. Mangir; Gesing, Thorsten M.
Synthesis and crystal structures of novel alkali rare-earth orthoborates K3RE3(BO3)4 (RE = Pr, Nd, Sm‒Lu)
Journal of Materials Science, 2021, 56, 3639-3652
1559835 CIFB4 K3 O12 Pr3P -110.8167; 9.0776; 14.1014
90.051; 110.257; 89.901
1299Chen, Pengyun; Murshed, M. Mangir; Gesing, Thorsten M.
Synthesis and crystal structures of novel alkali rare-earth orthoborates K3RE3(BO3)4 (RE = Pr, Nd, Sm‒Lu)
Journal of Materials Science, 2021, 56, 3639-3652
1559863 CIFC32 H30 N2 S4 Si2P -110.1836; 16.2598; 23.1451
86.414; 81.109; 77.472
3694.6Tian, Yu; Wang, Chenglong; Wang, Guangxia; Xu, Li; Wang, Hua
Ag-Induced metallogel based on cyclooctatetrathiophene: structural characterization and stimuli-responsive properties.
Soft matter, 2021, 17, 341-345
1559864 CIFC32 H30 N2 S4 Si2R -3 :H38.5368; 38.5368; 13.3783
90; 90; 120
17206.1Tian, Yu; Wang, Chenglong; Wang, Guangxia; Xu, Li; Wang, Hua
Ag-Induced metallogel based on cyclooctatetrathiophene: structural characterization and stimuli-responsive properties.
Soft matter, 2021, 17, 341-345
1559888 CIFC7 H4 D6 O6P n a 2112.1157; 6.1134; 9.97
90; 90; 90
738.46Joffrin, Amélie M.; Saunders, Alex M.; Barneda, David; Flemington, Vikki; Thompson, Amber L.; Sanganee, Hitesh J.; Conway, Stuart J.
Development of isotope-enriched phosphatidylinositol-4- and 5-phosphate cellular mass spectrometry probes
Chemical Science, 2021, 12, 2549-2557
1559889 CIFC14 H18 O8P 1 21 110.4164; 6.6513; 11.2592
90; 96.9535; 90
774.33Joffrin, Amélie M.; Saunders, Alex M.; Barneda, David; Flemington, Vikki; Thompson, Amber L.; Sanganee, Hitesh J.; Conway, Stuart J.
Development of isotope-enriched phosphatidylinositol-4- and 5-phosphate cellular mass spectrometry probes
Chemical Science, 2021, 12, 2549-2557
1559893 CIFC12 H14 Br2 OP 1 21/c 115.797; 10.6695; 7.533
90; 91.679; 90
1269.11Roemer, Max; Gonçales, Vinicius R.; Keaveney, Sinead T.; Pernik, Indrek; Lian, Jiaxin; Downes, James; Gooding, J. Justin; Messerle, Barbara A.
Carbon supported hybrid catalysts for controlled product selectivity in the hydrosilylation of alkynes
Catalysis Science & Technology, 2021, 11, 1888-1898
1559894 CIFC18 H22 N6 OP 1 21/c 114.654; 7.0476; 17.0806
90; 91.653; 90
1763.3Roemer, Max; Gonçales, Vinicius R.; Keaveney, Sinead T.; Pernik, Indrek; Lian, Jiaxin; Downes, James; Gooding, J. Justin; Messerle, Barbara A.
Carbon supported hybrid catalysts for controlled product selectivity in the hydrosilylation of alkynes
Catalysis Science & Technology, 2021, 11, 1888-1898
1559895 CIFC23 H32 N6 OP 1 21/n 15.4266; 52.494; 8.032
90; 107.835; 90
2178.1Roemer, Max; Gonçales, Vinicius R.; Keaveney, Sinead T.; Pernik, Indrek; Lian, Jiaxin; Downes, James; Gooding, J. Justin; Messerle, Barbara A.
Carbon supported hybrid catalysts for controlled product selectivity in the hydrosilylation of alkynes
Catalysis Science & Technology, 2021, 11, 1888-1898
1559907 CIFC12 H22 B Fe NP 1 21/c 112.5601; 7.39591; 14.8102
90; 98.207; 90
1361.68Zhai, Xiaofang; Pang, Maofu; Feng, Lei; Jia, Jiong; Tung, Chen-Ho; Wang, Wenguang
Dehydrogenation of iron amido-borane and resaturation of the imino-borane complex
Chemical Science, 2021, 12, 2885-2889
1559908 CIFC68 H60 B2 F24 Fe N O2 PP -112.9415; 14.6375; 19.3031
103.817; 92.601; 92.604
3541.17Zhai, Xiaofang; Pang, Maofu; Feng, Lei; Jia, Jiong; Tung, Chen-Ho; Wang, Wenguang
Dehydrogenation of iron amido-borane and resaturation of the imino-borane complex
Chemical Science, 2021, 12, 2885-2889
1559909 CIFC81 H67 B2 F24 Fe N P2P 1 21/c 113.1206; 16.6063; 36.1078
90; 93.609; 90
7851.73Zhai, Xiaofang; Pang, Maofu; Feng, Lei; Jia, Jiong; Tung, Chen-Ho; Wang, Wenguang
Dehydrogenation of iron amido-borane and resaturation of the imino-borane complex
Chemical Science, 2021, 12, 2885-2889
1559910 CIFC28 H31 B Fe N PP 1 21/c 115.3228; 26.7339; 35.8973
90; 99.93; 90
14484.6Zhai, Xiaofang; Pang, Maofu; Feng, Lei; Jia, Jiong; Tung, Chen-Ho; Wang, Wenguang
Dehydrogenation of iron amido-borane and resaturation of the imino-borane complex
Chemical Science, 2021, 12, 2885-2889
1559911 CIFC28 H33 B Fe N PP 1 21/n 110.668; 10.792; 21.922
90; 92.119; 90
2522.1Zhai, Xiaofang; Pang, Maofu; Feng, Lei; Jia, Jiong; Tung, Chen-Ho; Wang, Wenguang
Dehydrogenation of iron amido-borane and resaturation of the imino-borane complex
Chemical Science, 2021, 12, 2885-2889
1559914 CIFC6 H18 Cl4 N2 PdP -17.2281; 8.1281; 11.7212
70.892; 87.545; 89.101
650.09Zierkiewicz, Wiktor; Michalczyk, Mariusz; Maris, Thierry; Wysokinski, Rafal; Scheiner, Steve
Experimental and Theoretical Evidence of Attractive Interactions between Dianions: [PdCl4]2-...[PdCl4]2-
Chemical Communications, 2021
1559931 CIFO384 Si192 Zn35.75F d -3 m :224.7443; 24.7443; 24.7443
90; 90; 90
15150.4Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559932 CIFO394.64 Si192 Zn38.54F d -3 m :224.7012; 24.7012; 24.7012
90; 90; 90
15071.4Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559933 CIFO384 Si192 Zn37.08F d -3 m :224.7342; 24.7342; 24.7342
90; 90; 90
15131.9Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559934 CIFO384 Si192 Zn36.44F d -3 m :224.7409; 24.7409; 24.7409
90; 90; 90
15144.2Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559935 CIFO384 Si192 Zn37F d -3 m :224.7367; 24.7367; 24.7367
90; 90; 90
15136.5Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559936 CIFO384 Si192 Zn35.93F d -3 m :224.7334; 24.7334; 24.7334
90; 90; 90
15130.4Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559937 CIFO393.88 Si192 Zn37.67F d -3 m :224.706; 24.706; 24.706
90; 90; 90
15080.2Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559938 CIFO384 Si192 Zn35.51F d -3 m :224.7496; 24.7496; 24.7496
90; 90; 90
15160.2Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559939 CIFO389.23 Si192 Zn36.1F d -3 m :224.731; 24.731; 24.731
90; 90; 90
15126Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559940 CIFO389.95 Si192 Zn35.28F d -3 m :224.7323; 24.7323; 24.7323
90; 90; 90
15128.4Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559941 CIFO384 Si192 Zn36.19F d -3 m :224.7508; 24.7508; 24.7508
90; 90; 90
15162.4Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559942 CIFO393.73 Si192 Zn37.59F d -3 m :224.7029; 24.7029; 24.7029
90; 90; 90
15074.5Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559943 CIFO384 Si192 Zn35.75F d -3 m :224.7557; 24.7557; 24.7557
90; 90; 90
15171.4Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559944 CIFO384 Si192 Zn36.82F d -3 m :224.743; 24.743; 24.743
90; 90; 90
15148.1Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559945 CIFO389.83 Si192 Zn35.41F d -3 m :224.7327; 24.7327; 24.7327
90; 90; 90
15129.2Moon, Dae Jun; Lim, Woo Taik; Peterson, Brian K.; Seff, Karl
Using Crystallography and NMR to Count the Number of Three-Aluminum Six-Rings in Fully Zn2±Exchanged Zeolite Y. These Six-Rings Concentrate at Single Six-Ring Positions
The Journal of Physical Chemistry C, 2021, 125, 583-592
1559946 CIFC30 H14 Cd N4 O8 SP b a m12.8322; 19.9878; 20.044
90; 90; 90
5141.03Ding, Bowen; Chan, Bun; Proschogo, Nicholas; Solomon, Marcello B.; Kepert, Cameron J.; D'Alessandro, Deanna M.
A cofacial metal‒organic framework based photocathode for carbon dioxide reduction
Chemical Science, 2021, 12, 3608-3614
1559947 CIFC30 H14 Cd N4 O8 SP b a m12.9936; 19.8725; 20.0366
90; 90; 90
5173.76Ding, Bowen; Chan, Bun; Proschogo, Nicholas; Solomon, Marcello B.; Kepert, Cameron J.; D'Alessandro, Deanna M.
A cofacial metal‒organic framework based photocathode for carbon dioxide reduction
Chemical Science, 2021, 12, 3608-3614
1559948 CIFC10 H34 I12 N4 Pb3C 1 2/m 18.909; 9.012; 27.896
90; 92.832; 90
2237Li, Dong; Wu, Wentao; Han, Shiguo; Liu, Xitao; Peng, Yu; Li, Xiaoqi; Li, Lina; Hong, Maochun; Luo, Junhua
A reduced-dimensional polar hybrid perovskite for self-powered broad-spectrum photodetection
Chemical Science, 2021, 12, 3050-3054
1559949 CIFC10 H34 I12 N4 Pb3P 1 c 127.3848; 9.0015; 8.8216
90; 95.999; 90
2162.65Li, Dong; Wu, Wentao; Han, Shiguo; Liu, Xitao; Peng, Yu; Li, Xiaoqi; Li, Lina; Hong, Maochun; Luo, Junhua
A reduced-dimensional polar hybrid perovskite for self-powered broad-spectrum photodetection
Chemical Science, 2021, 12, 3050-3054
1559953 CIFC15 H19 F3 N2 O5 Pt SP 1 21/n 111.3867; 13.3132; 12.4183
90; 92.717; 90
1880.42Pal, Shrinwantu; Nozaki, Kyoko; Vedernikov, Andrei N.; Love, Jennifer A.
Reversible PtII‒CH3 deuteration without methane loss: metal‒ligand cooperation vs. ligand-assisted PtII-protonation
Chemical Science, 2021, 12, 2960-2969
1559954 CIFC10 H13 F2 N O4 S2P 1 21 16.9704; 8.0097; 11.9695
90; 100.105; 90
657.9Rossi, Maria-Agustina; Martinez, Veronica; Hinchliffe, Philip; Mojica, Maria F.; Castillo, Valerie; Moreno, Diego M.; Smith, Ryan; Spellberg, Brad; Drusano, George L.; Banchio, Claudia; Bonomo, Robert A.; Spencer, James; Vila, Alejandro J.; Mahler, Graciela
2-Mercaptomethyl-thiazolidines use conserved aromatic‒S interactions to achieve broad-range inhibition of metallo-β-lactamases
Chemical Science, 2021, 12, 2898-2908
1559955 CIFC224 H252 Au44 S28R -3 c :H45.692; 45.692; 77.435
90; 90; 120
140007Liu, Xu; Yao, Guo; Cheng, Xinglian; Xu, Jiayu; Cai, Xiao; Hu, Weigang; Xu, Wen Wu; Zhang, Chunfeng; Zhu, Yan
Cd-driven surface reconstruction and photodynamics in gold nanoclusters
Chemical Science, 2021, 12, 3290-3294
1559956 CIFC240 H270 Au38 Cd4 S30P -135.243; 36.193; 46.321
78.898; 74.68; 79.183
55332Liu, Xu; Yao, Guo; Cheng, Xinglian; Xu, Jiayu; Cai, Xiao; Hu, Weigang; Xu, Wen Wu; Zhang, Chunfeng; Zhu, Yan
Cd-driven surface reconstruction and photodynamics in gold nanoclusters
Chemical Science, 2021, 12, 3290-3294
1559957 CIFC7 H4 N Na O4.875 SC 1 2/n 118.7488; 7.1526; 29.1812
90; 93.7725; 90
3904.8Rekis, Toms; Schaller, Achim M.; Kotla, Surya Rohith; Schönleber, Andreas; Noohinejad, Leila; Tolkiehn, Martin; Paulmann, Carsten; van Smaalen, Sander
Single-crystal-to-single-crystal phase transitions of commensurately modulated sodium saccharinate 1.875-hydrate
IUCrJ, 2021, 8, 139-147
1559958 CIFC7 H4 N Na O4.875 SC 1 2/n 118.747; 7.1519; 29.1807
90; 93.7723; 90
3903.97Rekis, Toms; Schaller, Achim M.; Kotla, Surya Rohith; Schönleber, Andreas; Noohinejad, Leila; Tolkiehn, Martin; Paulmann, Carsten; van Smaalen, Sander
Single-crystal-to-single-crystal phase transitions of commensurately modulated sodium saccharinate 1.875-hydrate
IUCrJ, 2021, 8, 139-147
1559959 CIFC7 H4 N Na O4.875 SC 1 2/n 118.6705; 7.123; 29.1292
90; 93.6645; 90
3865.97Rekis, Toms; Schaller, Achim M.; Kotla, Surya Rohith; Schönleber, Andreas; Noohinejad, Leila; Tolkiehn, Martin; Paulmann, Carsten; van Smaalen, Sander
Single-crystal-to-single-crystal phase transitions of commensurately modulated sodium saccharinate 1.875-hydrate
IUCrJ, 2021, 8, 139-147
1559960 CIFC7 H4 N Na O4.875 SC 1 2/n 118.5979; 7.0922; 29.0731
90; 93.5819; 90
3827.25Rekis, Toms; Schaller, Achim M.; Kotla, Surya Rohith; Schönleber, Andreas; Noohinejad, Leila; Tolkiehn, Martin; Paulmann, Carsten; van Smaalen, Sander
Single-crystal-to-single-crystal phase transitions of commensurately modulated sodium saccharinate 1.875-hydrate
IUCrJ, 2021, 8, 139-147
1559961 CIFC7 H4 N Na O4.875 SC -118.5729; 7.0819; 29.0233
89.9808; 93.511; 89.9763
3810.31Rekis, Toms; Schaller, Achim M.; Kotla, Surya Rohith; Schönleber, Andreas; Noohinejad, Leila; Tolkiehn, Martin; Paulmann, Carsten; van Smaalen, Sander
Single-crystal-to-single-crystal phase transitions of commensurately modulated sodium saccharinate 1.875-hydrate
IUCrJ, 2021, 8, 139-147
1559963 CIFBa O3 TiP m -3 m4.03542; 4.03542; 4.03542
90; 90; 90
65.715Aimi, A.; Horiuchi, K.; Yamaguchi, Y.; Ito, S.; Fujimoto, K.
Disordered off-center direction of Ti4+ in pseudo-cubic type BaTiO3 prepared by mixed hydroxide process
Journal of the Ceramic Society of Japan, 2021, 129, 73-78
1559964 CIFBa O3 TiP 4 m m3.99048; 3.99048; 4.02303
90; 90; 90
64.062Aimi, A.; Horiuchi, K.; Yamaguchi, Y.; Ito, S.; Fujimoto, K.
Disordered off-center direction of Ti4+ in pseudo-cubic type BaTiO3 prepared by mixed hydroxide process
Journal of the Ceramic Society of Japan, 2021, 129, 73-78
1559965 CIFO7 Ti2 Y2F d -3 m :210.0975; 10.0975; 10.0975
90; 90; 90
1029.54Takano, M.; Matsudaira, T.; Kawai, E.; Kawashima, N.; Matsumoto, U.; Ogawa, T.; Takeuchi, M.; Kitaoka, S.
Effect of chemical composition on mass transfer in Y2Ti2O7 under oxygen potential gradient at high temperatures
Journal of the Ceramic Society of Japan, 2021, 129, 22-31
1559971 CIFC20 H30 Fe N2 O4 Si2P 1 21/n 18.4055; 18.3319; 15.0466
90; 92.57; 90
2316.2Cingolani, Andrea; Gualandi, Isacco; Scavetta, Erika; Cesari, Cristiana; Zacchini, Stefano; Tonelli, Domenica; Zanotti, Valerio; Franchi, Paola; Lucarini, Marco; Sicilia, Emilia; Mazzone, Gloria; Nanni, Daniele; Mazzoni, Rita
Cyclopentadienone‒NHC iron(0) complexes as low valent electrocatalysts for water oxidation
Catalysis Science & Technology, 2021, 11, 1407-1418
1559978 CIFC30 H36 N2 S2P -17.0096; 11.6756; 17.1032
96.573; 98.931; 99.536
1349.48Sinclair, Geoffrey S.; Claridge, Robert C. M.; Kukor, Andrew J.; Hopkins, W. Scott; Schipper, Derek J.
N-Oxide S‒O chalcogen bonding in conjugated materials
Chemical Science, 2021, 12, 2304-2312
1559979 CIFC30 H36 N2 O S2P -16.7333; 7.2344; 14.884
85.396; 80.658; 74.043
687.4Sinclair, Geoffrey S.; Claridge, Robert C. M.; Kukor, Andrew J.; Hopkins, W. Scott; Schipper, Derek J.
N-Oxide S‒O chalcogen bonding in conjugated materials
Chemical Science, 2021, 12, 2304-2312
1559980 CIFC18 H15 N O3P 1 21/c 15.974; 16.697; 14.741
90; 91.617; 90
1469.8Cheng, Yaohang; Yu, Shijie; He, Yuhang; An, Guanghui; Li, Guangming; Yang, Zhenyu
C4-arylation and domino C4-arylation/3,2-carbonyl migration of indoles by tuning Pd catalytic modes: Pd(i)‒Pd(ii) catalysis vs. Pd(ii) catalysis
Chemical Science, 2021, 12, 3216-3225
1559981 CIFC18 H15 N O3P -18.1516; 8.1871; 11.8093
96.901; 107.557; 92.751
743.01Cheng, Yaohang; Yu, Shijie; He, Yuhang; An, Guanghui; Li, Guangming; Yang, Zhenyu
C4-arylation and domino C4-arylation/3,2-carbonyl migration of indoles by tuning Pd catalytic modes: Pd(i)–Pd(ii) catalysis vs. Pd(ii) catalysis
Chemical Science, 2021, 12, 3216-3225
1559982 CIFC285 H325 Ag21 Au B2 Cl2 Fe3 O2 P6 S12P -121.3948; 27.211; 29.938
80.347; 70.094; 67.283
15103Zou, Xuejuan; He, Shuping; Kang, Xi; Chen, Shuang; Yu, Haizhu; Jin, Shan; Astruc, Didier; Zhu, Manzhou
New atomically precise M1Ag21 (M = Au/Ag) nanoclusters as excellent oxygen reduction reaction catalysts
Chemical Science, 2021, 12, 3660-3667
1559983 CIFC298 H333 Ag22 B2 Fe3 P6 S12P -121.412; 27.2727; 29.7612
79.123; 70.493; 66.956
15040.9Zou, Xuejuan; He, Shuping; Kang, Xi; Chen, Shuang; Yu, Haizhu; Jin, Shan; Astruc, Didier; Zhu, Manzhou
New atomically precise M1Ag21 (M = Au/Ag) nanoclusters as excellent oxygen reduction reaction catalysts
Chemical Science, 2021, 12, 3660-3667
1559992 CIFC29 H21 N3 O PtP 1 21/n 110.309; 13.9097; 15.4326
90; 101.658; 90
2167.31Maisuls, Iván; Wang, Cui; Gutierrez Suburu, Matias E.; Wilde, Sebastian; Daniliuc, Constantin-Gabriel; Brünink, Dana; Doltsinis, Nikos L.; Ostendorp, Stefan; Wilde, Gerhard; Kösters, Jutta; Resch-Genger, Ute; Strassert, Cristian A.
Ligand-controlled and nanoconfinement-boosted luminescence employing Pt(ii) and Pd(ii) complexes: from color-tunable aggregation-enhanced dual emitters towards self-referenced oxygen reporters
Chemical Science, 2021, 12, 3270-3281
1559993 CIFC29 H17 F4 N3 O PdP -111.8675; 12.4514; 17.2457
94.655; 96.279; 113.088
2308.6Maisuls, Iván; Wang, Cui; Gutierrez Suburu, Matias E.; Wilde, Sebastian; Daniliuc, Constantin-Gabriel; Brünink, Dana; Doltsinis, Nikos L.; Ostendorp, Stefan; Wilde, Gerhard; Kösters, Jutta; Resch-Genger, Ute; Strassert, Cristian A.
Ligand-controlled and nanoconfinement-boosted luminescence employing Pt(ii) and Pd(ii) complexes: from color-tunable aggregation-enhanced dual emitters towards self-referenced oxygen reporters
Chemical Science, 2021, 12, 3270-3281
1559994 CIFC29 H19 F2 N3 O PtP -19.3869; 11.7589; 11.9012
117.792; 105.826; 94.593
1084.42Maisuls, Iván; Wang, Cui; Gutierrez Suburu, Matias E.; Wilde, Sebastian; Daniliuc, Constantin-Gabriel; Brünink, Dana; Doltsinis, Nikos L.; Ostendorp, Stefan; Wilde, Gerhard; Kösters, Jutta; Resch-Genger, Ute; Strassert, Cristian A.
Ligand-controlled and nanoconfinement-boosted luminescence employing Pt(ii) and Pd(ii) complexes: from color-tunable aggregation-enhanced dual emitters towards self-referenced oxygen reporters
Chemical Science, 2021, 12, 3270-3281
1559995 CIFC29 H17 F4 N3 O PtP 1 2/c 122.8339; 9.8626; 22.7576
90; 117.704; 90
4537.52Maisuls, Iván; Wang, Cui; Gutierrez Suburu, Matias E.; Wilde, Sebastian; Daniliuc, Constantin-Gabriel; Brünink, Dana; Doltsinis, Nikos L.; Ostendorp, Stefan; Wilde, Gerhard; Kösters, Jutta; Resch-Genger, Ute; Strassert, Cristian A.
Ligand-controlled and nanoconfinement-boosted luminescence employing Pt(ii) and Pd(ii) complexes: from color-tunable aggregation-enhanced dual emitters towards self-referenced oxygen reporters
Chemical Science, 2021, 12, 3270-3281
1559996 CIFC29 H17 F4 N3 O PtP -19.6007; 11.7181; 12.0959
118.283; 95.325; 104.556
1123.48Maisuls, Iván; Wang, Cui; Gutierrez Suburu, Matias E.; Wilde, Sebastian; Daniliuc, Constantin-Gabriel; Brünink, Dana; Doltsinis, Nikos L.; Ostendorp, Stefan; Wilde, Gerhard; Kösters, Jutta; Resch-Genger, Ute; Strassert, Cristian A.
Ligand-controlled and nanoconfinement-boosted luminescence employing Pt(ii) and Pd(ii) complexes: from color-tunable aggregation-enhanced dual emitters towards self-referenced oxygen reporters
Chemical Science, 2021, 12, 3270-3281
1560013 CIFC26 H30 N2 O4P 1 21/c 15.2406; 6.5334; 31.137
90; 91.691; 90
1065.6Goudappagouda, ?; Nidhankar, Aakash D.; Nayak, Rashmi A.; Santhosh Babu, Sukumaran
Aggregation-induced phosphorescence of an anthraquinone based emitter.
Organic & biomolecular chemistry, 2021, 19, 1004-1008
1560014 CIF
HKL
Paper
C17 H12 N2 OP 1 21/n 17.4548; 22.976; 8.3149
90; 115.866; 90
1281.5Chen, Lin; Hu, Jin; Sun, Hong-Shun
7,8-Dimethyl-11<i>H</i>-indeno[1,2-<i>b</i>]quinoxalin-11-one
IUCrData, 2021, 6, x210018
1560015 CIFC18 H24 O2P -18.3649; 10.0504; 10.2831
73.682; 70.348; 86.635
780.74Kleinmans, Roman; Will, Leon E.; Schwarz, J. Luca; Glorius, Frank
Photoredox-enabled 1,2-dialkylation of α-substituted acrylates via Ireland‒Claisen rearrangement
Chemical Science, 2021, 12, 2816-2822
1560016 CIFC12 H21 N O2 SP -16.3005; 10.5228; 10.9791
65.837; 82.374; 88.124
658.07Kleinmans, Roman; Will, Leon E.; Schwarz, J. Luca; Glorius, Frank
Photoredox-enabled 1,2-dialkylation of α-substituted acrylates via Ireland‒Claisen rearrangement
Chemical Science, 2021, 12, 2816-2822
1560017 CIFC22 H26 O2P 1 21/n 110.5885; 8.3629; 20.6387
90; 99.927; 90
1800.21Kleinmans, Roman; Will, Leon E.; Schwarz, J. Luca; Glorius, Frank
Photoredox-enabled 1,2-dialkylation of α-substituted acrylates via Ireland‒Claisen rearrangement
Chemical Science, 2021, 12, 2816-2822
1560018 CIFC35 H35 N2 O PP -18.9009; 10.4501; 17.0815
104.343; 91.133; 112.507
1410.37Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560019 CIFC33 H30 N O PP -18.2229; 12.4346; 13.1943
108.632; 96.25; 93.485
1264.24Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560020 CIFC32 H22 F3 O4 P SP 1 21/c 17.4114; 15.707; 22.5898
90; 92.536; 90
2627.1Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560021 CIFC33 H25 F3 N O3 P SP n a 218.0035; 27.389; 12.6664
90; 90; 90
2776.6Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560022 CIFC34 H29 F3 N O3 P SP 1 21/c 18.9602; 11.4072; 28.9126
90; 93.074; 90
2950.9Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560023 CIFC33 H25 F3 N O3 P SP 1 21/c 116.162; 12.9217; 14.4246
90; 107.362; 90
2875.2Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560024 CIFC36 H34 F3 N2 O3 P SP 1 21/c 111.0775; 19.2817; 15.3042
90; 104; 90
3171.8Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560025 CIFC33 H29 Au B Cl F4 N PP 1 21 18.2171; 20.0635; 9.9302
90; 111.472; 90
1523.51Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560026 CIFC36 H33 Au B2 F8 N P SP 1 21/c 116.5012; 15.8634; 13.7254
90; 92.673; 90
3588.9Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560027 CIFC37 H37 Au B2 F8 N P SP 1 21 18.2911; 15.0763; 14.2431
90; 97.96; 90
1763.2Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560028 CIFC39 H42 Au B2 F8 N2 P SP 1 21/n 110.2268; 8.5127; 45.347
90; 94.336; 90
3936.5Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560029 CIFC35 H34 Au B Cl F4 N2 PP 1 21/c 120.6017; 8.5026; 20.569
90; 118.012; 90
3180.9Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560030 CIFC36 H32 Au B2 Cl2 F8 O P SP -18.0106; 12.2124; 19.0728
99.359; 93.578; 101.894
1792.6Litle, Elishua D.; Wilkins, Lewis C.; Gabbaï, François P.
Ligand-enforced intimacy between a gold cation and a carbenium ion: impact on stability and reactivity
Chemical Science, 2021, 12, 3929-3936
1560031 CIFC52 H96 O Si8 U2P 21 21 2110.5444; 18.4631; 31.5083
90; 90; 90
6134.1Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560032 CIFC26 H50 O Si4 UP 1 21/n 117.5935; 9.977; 18.6747
90; 110.001; 90
3080.27Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560033 CIFC58.34 H113.47 O Si9 U2P -420.3708; 20.3708; 16.6734
90; 90; 90
6918.95Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560034 CIFC84 H168 Si12 U2P 1 21/c 126.7057; 15.99077; 26.5612
90; 117.35; 90
10074.9Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560035 CIFC24 H44 Si4 UI 41/a :231.8409; 31.8409; 11.0234
90; 90; 90
11176Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560036 CIFC28 H52 O Si4 UP 21 21 2111.40224; 16.98119; 17.03377
90; 90; 90
3298.14Tsoureas, Nikolaos; Mansikkamäki, Akseli; Layfield, Richard A.
Synthesis, bonding properties and ether activation reactivity of cyclobutadienyl-ligated hybrid uranocenes
Chemical Science, 2021, 12, 2948-2954
1560037 CIFC34 H48 N4 P2P -17.5552; 9.5169; 11.8279
76.651; 84.11; 72.543
788.85Lücke, Marcel-Philip; Yao, Shenglai; Driess, Matthias
Boosting homogeneous chemoselective hydrogenation of olefins mediated by a bis(silylenyl)terphenyl-nickel(0) pre-catalyst
Chemical Science, 2021, 12, 2909-2915
1560038 CIFC48 H58 N4 Si2C 1 2/c 125.072; 9.1667; 19.7603
90; 99.889; 90
4474Lücke, Marcel-Philip; Yao, Shenglai; Driess, Matthias
Boosting homogeneous chemoselective hydrogenation of olefins mediated by a bis(silylenyl)terphenyl-nickel(0) pre-catalyst
Chemical Science, 2021, 12, 2909-2915
1560039 CIFC34 H48 N4 Ni P2P -110.1955; 10.3773; 16.0898
76.412; 80.446; 88.451
1631.6Lücke, Marcel-Philip; Yao, Shenglai; Driess, Matthias
Boosting homogeneous chemoselective hydrogenation of olefins mediated by a bis(silylenyl)terphenyl-nickel(0) pre-catalyst
Chemical Science, 2021, 12, 2909-2915
1560040 CIFC55 H66 N4 Ni Si2P 1 21/m 19.1662; 26.4418; 9.8935
90; 90.567; 90
2397.8Lücke, Marcel-Philip; Yao, Shenglai; Driess, Matthias
Boosting homogeneous chemoselective hydrogenation of olefins mediated by a bis(silylenyl)terphenyl-nickel(0) pre-catalyst
Chemical Science, 2021, 12, 2909-2915
1560041 CIF
Paper
C20 H22 N4 O8P 17.7162; 8.9727; 16.9089
86.559; 78.838; 66.314
1051.59Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560042 CIFC18 H23 N4 O4P -17.658; 9.277; 15.152
79.304; 82.008; 65.214
958Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560043 CIFC32 H23 N3 O3.99P -19.2447; 14.4694; 19.3202
93.232; 102.634; 97.795
2488.6Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560044 CIFC12 H13 N3 O4C 1 2/c 18.7482; 14.926; 10.2464
90; 110.165; 90
1255.9Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560045 CIFC19 H15 N3 O4P -17.7638; 8.5897; 12.723
105.585; 102.978; 95.062
786.4Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560046 CIFC26 H21 N5 O4P -17.3217; 11.6513; 13.9987
105.915; 102.665; 91.242
1116.2Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560047 CIFC42 H34 N8 O8P -17.4323; 9.1138; 14.562
106.397; 103.133; 90.486
918.7Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560048 CIFC18 H17 N3 O4P 1 21/c 117.802; 7.5355; 12.5671
90; 91.187; 90
1685.5Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560049 CIFC18 H15 N3 O4P 1 21/c 117.9122; 7.4259; 12.1765
90; 92.337; 90
1618.3Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560050 CIFC16 H13 N5 O4P 1 21/c 118.213; 7.2967; 11.94
90; 92.967; 90
1584.6Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560051 CIFC20 H25 N5 O4P -17.7563; 8.1082; 16.24
97.387; 95.164; 95.007
1003.7Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560052 CIFC13 H15 N3 O4P 1 21/n 110.1301; 12.6967; 10.3338
90; 99.17; 90
1312.1Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560053 CIFC29 H26 N3 O4P 1 21 17.7925; 12.885; 12.398
90; 104.054; 90
1207.6Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560054 CIFC58 H50 N6 O8P -113.337; 13.504; 16.069
75.831; 66.422; 67.934
2442.9Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560055 CIFC40 H46 N8 O8P -17.5319; 8.6425; 15.3925
78.729; 75.782; 89.099
951.99Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560056 CIFC38 H42 N8 O8P -17.4104; 8.8964; 15.7722
95.531; 101.446; 111.676
930.47Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560057 CIFC22 H23 N3 O4 S2P -17.6512; 8.9495; 18.121
87.883; 78.725; 65.728
1108Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560058 CIFC62 H50 N6 O8P -17.684; 9.266; 18.043
96.343; 94.419; 107.054
1212.5Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560059 CIFC50 H52 N8 O8P -17.7634; 8.9486; 16.368
83.021; 82.842; 88.111
1119.7Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560060 CIFC42 H42 N8 O8P -17.5543; 8.914; 14.713
85.797; 88.497; 89.487
987.7Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560061 CIFC42 H40 N8 O8P -17.504; 9.428; 14.102
94.052; 91.192; 90.498
994.9Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560062 CIFC40 H40 N6 O8 S2P -17.489; 9.107; 14.187
97.784; 93.611; 90.872
956.5Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560063 CIFC40 H38 N6 O8 S2P -17.514; 9.272; 13.852
83.832; 89.887; 88.173
959Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560064 CIFC41 H41 N7 O8 SP -17.4741; 9.2215; 14.295
96.245; 92.609; 92.314
977.4Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560065 CIFC41 H39 N7 O8 SP -17.4078; 9.3192; 13.815
94.239; 91.445; 90.299
950.8Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560066 CIFC14 H16 Cl2 N2 O2P 1 21/n 19.302; 9.394; 17.66
90; 104.075; 90
1496.9Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560067 CIFC72 H48 Cl4 N10 O4P -110.807; 12.145; 12.466
108.22; 104.061; 101.072
1442.4Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560068 CIFC12 H12 Cl2 N2 O2P 1 21/c 18.188; 15.73; 11.247
90; 110.491; 90
1357Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560069 CIFC44 H42 Cl4 N4 O4C 1 2/c 142.727; 8.899; 22.92
90; 114.062; 90
7958Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560070 CIFC84 H54 Cl4 N4 O4C 1 2/c 133.873; 10.374; 18.332
90; 91.186; 90
6440Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560071 CIFC28 H22 Cl2 N2 O2P -18.8453; 10.4891; 12.694
94.129; 94.866; 98.239
1157.1Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560072 CIFC80 H66 Cl8 N8 O8P 1 21 117.219; 22.693; 18.331
90; 91.312; 90
7161Rajkumar, Madhu; Desiraju, Gautam R.
Quaternary and quinary molecular solids based on structural inequivalence and combinatorial approaches: 2-nitroresorcinol and 4,6-dichlororesorcinol
IUCrJ, 2021, 8, 178-185
1560073 CIFC18 H18 O3P 1 21 15.656; 8.202; 16.2422
90; 92.949; 90
752.49Mu, Yu; Zhang, Tao; Cheng, Yaping; Fu, Wenzhen; Wei, Zuting; Chen, Wanjun; Liu, Guodu
Efficient synthesis of tetrahydrofurans with chiral tertiary allylic alcohols catalyzed by Ni/P-chiral ligand DI-BIDIME
Catalysis Science & Technology, 2021, 11, 2306-2315
1560074 CIFC18 H18 O2P 21 21 216.5109; 8.5749; 26.234
90; 90; 90
1464.7Mu, Yu; Zhang, Tao; Cheng, Yaping; Fu, Wenzhen; Wei, Zuting; Chen, Wanjun; Liu, Guodu
Efficient synthesis of tetrahydrofurans with chiral tertiary allylic alcohols catalyzed by Ni/P-chiral ligand DI-BIDIME
Catalysis Science & Technology, 2021, 11, 2306-2315
1560075 CIFC23 H27 Al N2 O6P 1 21/c 18.9958; 12.8818; 19.2304
90; 96.615; 90
2213.62Diment, Wilfred T.; Stößer, Tim; Kerr, Ryan W. F.; Phanopoulos, Andreas; Durr, Christopher B.; Williams, Charlotte K.
Ortho-vanillin derived Al(iii) and Co(iii) catalyst systems for switchable catalysis using ε-decalactone, phthalic anhydride and cyclohexene oxide
Catalysis Science & Technology, 2021, 11, 1737-1745
1560076 CIFC23 H27 Co N2 O6P 1 21/c 18.9996; 12.8364; 19.0472
90; 96.745; 90
2185.15Diment, Wilfred T.; Stößer, Tim; Kerr, Ryan W. F.; Phanopoulos, Andreas; Durr, Christopher B.; Williams, Charlotte K.
Ortho-vanillin derived Al(iii) and Co(iii) catalyst systems for switchable catalysis using ε-decalactone, phthalic anhydride and cyclohexene oxide
Catalysis Science & Technology, 2021, 11, 1737-1745
1560077 CIFC23 H29 Al N2 O4P 21 21 217.869; 15.7511; 17.6113
90; 90; 90
2182.84Diment, Wilfred T.; Stößer, Tim; Kerr, Ryan W. F.; Phanopoulos, Andreas; Durr, Christopher B.; Williams, Charlotte K.
Ortho-vanillin derived Al(iii) and Co(iii) catalyst systems for switchable catalysis using ε-decalactone, phthalic anhydride and cyclohexene oxide
Catalysis Science & Technology, 2021, 11, 1737-1745
1560078 CIFC19 H13 N OP 21 21 2117.214; 14.4042; 5.5668
90; 90; 90
1380.3Li, Hui; Li, Huanhuan; Gu, Jie; He, Fei; Peng, Hao; Tao, Ye; Tian, Dan; Yang, Qingqing; Li, Ping; Zheng, Chao; Huang, Wei; Chen, Runfeng
Fluorine-induced aggregate-interlocking for color-tunable organic afterglow with a simultaneously improved efficiency and lifetime
Chemical Science, 2021, 12, 3580-3586
1560079 CIFC19 H12 F N OP b c a11.8585; 10.3783; 22.8559
90; 90; 90
2812.9Li, Hui; Li, Huanhuan; Gu, Jie; He, Fei; Peng, Hao; Tao, Ye; Tian, Dan; Yang, Qingqing; Li, Ping; Zheng, Chao; Huang, Wei; Chen, Runfeng
Fluorine-induced aggregate-interlocking for color-tunable organic afterglow with a simultaneously improved efficiency and lifetime
Chemical Science, 2021, 12, 3580-3586
1560080 CIFC19 H12 F N OP 1 21/n 114.608; 5.4287; 18.371
90; 107.996; 90
1385.6Li, Hui; Li, Huanhuan; Gu, Jie; He, Fei; Peng, Hao; Tao, Ye; Tian, Dan; Yang, Qingqing; Li, Ping; Zheng, Chao; Huang, Wei; Chen, Runfeng
Fluorine-induced aggregate-interlocking for color-tunable organic afterglow with a simultaneously improved efficiency and lifetime
Chemical Science, 2021, 12, 3580-3586
1560081 CIFC19 H12 F N OP 1 21/c 18.9406; 22.597; 7.0302
90; 91.313; 90
1419.9Li, Hui; Li, Huanhuan; Gu, Jie; He, Fei; Peng, Hao; Tao, Ye; Tian, Dan; Yang, Qingqing; Li, Ping; Zheng, Chao; Huang, Wei; Chen, Runfeng
Fluorine-induced aggregate-interlocking for color-tunable organic afterglow with a simultaneously improved efficiency and lifetime
Chemical Science, 2021, 12, 3580-3586
1560082 CIFC56 H63 N5 O4P 1 21/c 114.7734; 17.4936; 18.6427
90; 90.2338; 90
4817.98Villarón, David; Siegler, Maxime A.; Wezenberg, Sander J.
A photoswitchable strapped calix[4]pyrrole receptor: highly effective chloride binding and release
Chemical Science, 2021, 12, 3188-3193
1560083 CIFC108 H98 Mn4 Mo9 N3 O43 P5P -116.1432; 18.3888; 24.571
94.772; 109.004; 106.661
6480.2Li, Chifeng; Jimbo, Atsuhiro; Yamaguchi, Kazuya; Suzuki, Kosuke
A protecting group strategy to access stable lacunary polyoxomolybdates for introducing multinuclear metal clusters
Chemical Science, 2021, 12, 1240-1244
1560084 CIFC174 H174 Cl20 Mn6 Mo18 O74 P8P -117.3006; 19.39; 20.7716
95.31; 112.975; 99.33
6236.6Li, Chifeng; Jimbo, Atsuhiro; Yamaguchi, Kazuya; Suzuki, Kosuke
A protecting group strategy to access stable lacunary polyoxomolybdates for introducing multinuclear metal clusters
Chemical Science, 2021, 12, 1240-1244
1560085 CIFC22 H33 IrP 1 21/n 18.01647; 16.3246; 15.049
90; 92.985; 90
1966.73Tian, Yancong; Jakoobi, Martin; Boulatov, Roman; Sergeev, Alexey G.
Selective cleavage of unactivated arene ring C‒C bonds by iridium: key roles of benzylic C‒H activation and metal‒metal cooperativity
Chemical Science, 2021, 12, 3568-3579
1560086 CIFC20 H23 IrC 1 c 122.2884; 22.2818; 26.1267
90; 97.5244; 90
12863.5Tian, Yancong; Jakoobi, Martin; Boulatov, Roman; Sergeev, Alexey G.
Selective cleavage of unactivated arene ring C–C bonds by iridium: key roles of benzylic C–H activation and metal–metal cooperativity
Chemical Science, 2021, 12, 3568-3579
1560087 CIFC83 H116 N4 O4 Zn2P -19.5822; 13.6635; 15.4413
98.426; 105.508; 99.504
1882.26Payne, Jack; McKeown, Paul; Driscoll, Oliver; Kociok-Köhn, Gabriele; Emanuelsson, Emma A. C.; Jones, Matthew D.
Make or break: Mg(ii)- and Zn(ii)-catalen complexes for PLA production and recycling of commodity polyesters
Polymer Chemistry, 2021, 12, 1086-1096
1560088 CIFC30 H36 Cl2 Mg N2 O2P 1 21/c 19.9229; 14.2743; 20.5348
90; 95.319; 90
2896.08Payne, Jack; McKeown, Paul; Driscoll, Oliver; Kociok-Köhn, Gabriele; Emanuelsson, Emma A. C.; Jones, Matthew D.
Make or break: Mg(ii)- and Zn(ii)-catalen complexes for PLA production and recycling of commodity polyesters
Polymer Chemistry, 2021, 12, 1086-1096
1560089 CIFC84 H118 Mg2 N4 O4C 1 2/c 19.7766; 31.3712; 25.4191
90; 96.789; 90
7741.5Payne, Jack; McKeown, Paul; Driscoll, Oliver; Kociok-Köhn, Gabriele; Emanuelsson, Emma A. C.; Jones, Matthew D.
Make or break: Mg(ii)- and Zn(ii)-catalen complexes for PLA production and recycling of commodity polyesters
Polymer Chemistry, 2021, 12, 1086-1096
1560090 CIFC30 H36 Br2 N2 O2 ZnP 1 21/c 110.0556; 14.2825; 20.688
90; 95.646; 90
2956.78Payne, Jack; McKeown, Paul; Driscoll, Oliver; Kociok-Köhn, Gabriele; Emanuelsson, Emma A. C.; Jones, Matthew D.
Make or break: Mg(ii)- and Zn(ii)-catalen complexes for PLA production and recycling of commodity polyesters
Polymer Chemistry, 2021, 12, 1086-1096
1560091 CIFC30 H36 Br2 Mg N2 O2P 1 21/c 110.0761; 14.3226; 20.665
90; 96.011; 90
2965.9Payne, Jack; McKeown, Paul; Driscoll, Oliver; Kociok-Köhn, Gabriele; Emanuelsson, Emma A. C.; Jones, Matthew D.
Make or break: Mg(ii)- and Zn(ii)-catalen complexes for PLA production and recycling of commodity polyesters
Polymer Chemistry, 2021, 12, 1086-1096
1560092 CIFC27 H36 Cl2 Mg2 N2 O2P -110.872; 11.0298; 13.0224
112.876; 100.644; 93.112
1400.2Payne, Jack; McKeown, Paul; Driscoll, Oliver; Kociok-Köhn, Gabriele; Emanuelsson, Emma A. C.; Jones, Matthew D.
Make or break: Mg(ii)- and Zn(ii)-catalen complexes for PLA production and recycling of commodity polyesters
Polymer Chemistry, 2021, 12, 1086-1096
1560093 CIFC30 H36 Cl2 N2 O2 ZnP 1 21/c 19.8683; 14.2238; 20.5519
90; 94.567; 90
2875.6Payne, Jack; McKeown, Paul; Driscoll, Oliver; Kociok-Köhn, Gabriele; Emanuelsson, Emma A. C.; Jones, Matthew D.
Make or break: Mg(ii)- and Zn(ii)-catalen complexes for PLA production and recycling of commodity polyesters
Polymer Chemistry, 2021, 12, 1086-1096
1560094 CIFC51 H48 O6 SP 21 21 218.0941; 17.5936; 32.602
90; 90; 90
4642.7Bartelmann, Thomas; Gnannt, Frederik; Zitzmann, Max; Mayer, Peter; Dube, Henry
Sulfoxide hemithioindigo tweezers ‒ visible light addressable capture and release
Chemical Science, 2021, 12, 3651-3659
1560095 CIFC36 H53 B N6 O3 P2 Pd WP 1 21/c 116.8853; 15.2569; 15.7122
90; 91.701; 90
4046Osipova, Elena S.; Gulyaeva, Ekaterina S.; Gutsul, Evgenii I.; Kirkina, Vladislava A.; Pavlov, Alexander A.; Nelyubina, Yulia V.; Rossin, Andrea; Peruzzini, Maurizio; Epstein, Lina M.; Belkova, Natalia V.; Filippov, Oleg A.; Shubina, Elena S.
Bifunctional activation of amine-boranes by the W/Pd bimetallic analogs of “frustrated Lewis pairs”
Chemical Science, 2021, 12, 3682-3692
1560096 CIFC32 H48 O3 P2 Pd WP 1 21/c 18.2012; 37.372; 10.9355
90; 103.388; 90
3260.59Osipova, Elena S.; Gulyaeva, Ekaterina S.; Gutsul, Evgenii I.; Kirkina, Vladislava A.; Pavlov, Alexander A.; Nelyubina, Yulia V.; Rossin, Andrea; Peruzzini, Maurizio; Epstein, Lina M.; Belkova, Natalia V.; Filippov, Oleg A.; Shubina, Elena S.
Bifunctional activation of amine-boranes by the W/Pd bimetallic analogs of “frustrated Lewis pairs”
Chemical Science, 2021, 12, 3682-3692
1560097 CIFC21 H30 B F2 N O5P 1 21/c 114.1856; 17.0247; 9.5406
90; 94.364; 90
2297.4Wang, Yandong; Bai, Jingyi; Yang, Youqing; Zhao, Wenxuan; Liang, Yong; Wang, Di; Zhao, Yue; Shi, Zhuangzhi
Rhodium-catalysed selective C‒C bond activation and borylation of cyclopropanes
Chemical Science, 2021, 12, 3599-3607
1560098 CIFC22 H34 Cl2 N2 O6 Rh2P 1 21/n 19.2163; 11.7129; 13.3216
90; 108.006; 90
1367.63Wang, Yandong; Bai, Jingyi; Yang, Youqing; Zhao, Wenxuan; Liang, Yong; Wang, Di; Zhao, Yue; Shi, Zhuangzhi
Rhodium-catalysed selective C‒C bond activation and borylation of cyclopropanes
Chemical Science, 2021, 12, 3599-3607
1560099 CIFC14 H19 N OP 21 21 219.9241; 11.0168; 24.6334
90; 90; 90
2693.21Wang, Yandong; Bai, Jingyi; Yang, Youqing; Zhao, Wenxuan; Liang, Yong; Wang, Di; Zhao, Yue; Shi, Zhuangzhi
Rhodium-catalysed selective C‒C bond activation and borylation of cyclopropanes
Chemical Science, 2021, 12, 3599-3607
1560100 CIFC23 H16 OP 1 21/n 19.3347; 10.0778; 16.957
90; 101.582; 90
1562.7Uraguchi, Daisuke; Kato, Kohsuke; Ooi, Takashi
o-Quinone methide with overcrowded olefin component as a dehydridation catalyst under aerobic photoirradiation conditions
Chemical Science, 2021, 12, 2778-2783
1560101 CIFC26 H20 OP 1 21/c 110.294; 16.632; 11.319
90; 112.274; 90
1793.3Uraguchi, Daisuke; Kato, Kohsuke; Ooi, Takashi
o-Quinone methide with overcrowded olefin component as a dehydridation catalyst under aerobic photoirradiation conditions
Chemical Science, 2021, 12, 2778-2783
1560102 CIFC26 H21 B F4 OP 1 21/n 17.4982; 19.0172; 14.6488
90; 99.675; 90
2059.13Uraguchi, Daisuke; Kato, Kohsuke; Ooi, Takashi
o-Quinone methide with overcrowded olefin component as a dehydridation catalyst under aerobic photoirradiation conditions
Chemical Science, 2021, 12, 2778-2783
1560103 CIFC4 H2.67 Bi0.67 N4.67 Ni0.67 S4P -18.441; 8.6899; 11.8177
97.574; 92.137; 91.817
858.1Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560104 CIFC4 H2.67 Bi0.67 N4.67 Ni0.67 S4P -18.4472; 8.7119; 11.9671
97.041; 90.364; 91.558
873.67Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560105 CIFC2 H6 N4 SP -16.9352; 7.0096; 12.3675
90.894; 104.311; 101.787
568.89Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560106 CIFC7 Bi N7 Ni S6P 1 2/n 112.216; 36.8375; 24.5263
90; 90.224; 90
11036.9Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560107 CIFC6 H4 Bi N7 Ni S6P -18.4699; 8.6913; 11.9058
97.187; 91.149; 91.61
868.96Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560108 CIFC6 Bi K N6 Ni S6P -18.5073; 8.5686; 11.9651
97.573; 89.781; 90.997
864.46Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560109 CIFC0.92 Bi0.15 N1.25 Ni0.17 S0.86P n -3 :212.12528; 12.12528; 12.12528
90; 90; 90
1782.69Lee, Jie Yie; Ling, Sanliang; Argent, Stephen P.; Senn, Mark S.; Cañadillas-Delgado, Laura; Cliffe, Matthew J.
Controlling multiple orderings in metal thiocyanate molecular perovskites Ax{Ni[Bi(SCN)6]}
Chemical Science, 2021, 12, 3516-3525
1560111 CIFC74 H86 Li4 O2 P2 Si4P -111.4716; 12.6646; 12.7092
85.944; 86.346; 68.446
1711.6Brand, Alexander; Schulz, Stephen; Hepp, Alexander; Weigand, Jan J.; Uhl, Werner
Sterically constrained tricyclic phosphine: redox behaviour, reductive and oxidative cleavage of P‒C bonds, generation of a dilithium phosphaindole as a promising synthon in phosphine chemistry
Chemical Science, 2021, 12, 3460-3474
1560112 CIFC37 H32 O5 P2 Si2 WP 1 21/c 110.6448; 12.9069; 26.22
90; 92.664; 90
3598.5Brand, Alexander; Schulz, Stephen; Hepp, Alexander; Weigand, Jan J.; Uhl, Werner
Sterically constrained tricyclic phosphine: redox behaviour, reductive and oxidative cleavage of P‒C bonds, generation of a dilithium phosphaindole as a promising synthon in phosphine chemistry
Chemical Science, 2021, 12, 3460-3474
1560113 CIFC32 H32 P2 Si2P 1 21/c 112.2157; 10.4934; 22.6538
90; 99.262; 90
2866Brand, Alexander; Schulz, Stephen; Hepp, Alexander; Weigand, Jan J.; Uhl, Werner
Sterically constrained tricyclic phosphine: redox behaviour, reductive and oxidative cleavage of P‒C bonds, generation of a dilithium phosphaindole as a promising synthon in phosphine chemistry
Chemical Science, 2021, 12, 3460-3474
1560114 CIFC53 H60 Cl2 O4 P2 Si4P 1 21/n 110.1186; 18.8541; 27.477
90; 91.367; 90
5240.5Brand, Alexander; Schulz, Stephen; Hepp, Alexander; Weigand, Jan J.; Uhl, Werner
Sterically constrained tricyclic phosphine: redox behaviour, reductive and oxidative cleavage of P‒C bonds, generation of a dilithium phosphaindole as a promising synthon in phosphine chemistry
Chemical Science, 2021, 12, 3460-3474
1560115 CIFC6 H8 Mo N4 O4C m c 2118.363; 3.83; 14.745
90; 90; 90
1037Amarante, Tatiana R.; Neves, Patrícia; Almeida Paz, Filipe A.; Gomes, Ana C.; Pillinger, Martyn; Valente, Anabela A.; Gonçalves, Isabel S.
Heterogeneous catalysis with an organic‒inorganic hybrid based on MoO3 chains decorated with 2,2′-biimidazole ligands
Catalysis Science & Technology, 2021, 11, 2214-2228
1560116 CIFC12 H32 Cl5 N4 Ti2P n a 2119.796; 8.413; 13.102
90; 90; 90
2182.1Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560117 CIFC14 H36 Cl10 N4 Ti2P 1 21/c 113.348; 13.855; 17.166
90; 112.468; 90
2933.6Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560118 CIFC10 H24 Cl3 N2 O TiP 1 21/n 110.972; 12.308; 12.075
90; 101.587; 90
1597.4Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560119 CIFC13 H34 Cl4 N4 Ti2C 1 2/c 123.348; 8.843; 12.648
90; 121.198; 90
2233.7Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560120 CIFC6 H16 Cl I N2 ZnC 1 2/c 123.149; 7.256; 15.032
90; 111.169; 90
2354.5Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560121 CIFC13 H34 I2 N4 Zn2P 21 21 2111.494; 13.09; 14.921
90; 90; 90
2245Kurogi, Takashi; Kuroki, Kaito; Moritani, Shunsuke; Takai, Kazuhiko
Structural elucidation of a methylenation reagent of esters: synthesis and reactivity of a dinuclear titanium(iii) methylene complex
Chemical Science, 2021, 12, 3509-3515
1560122 CIFC24 H28 N2 O6P 1 21 118.5604; 7.5949; 8.0212
90; 96.383; 90
1123.69Arhangelskis, Mihails; Bučar, Dejan-Krešimir; Bordignon, Simone; Chierotti, Michele R.; Stratford, Samuel A.; Voinovich, Dario; Jones, William; Hasa, Dritan
Mechanochemical reactivity inhibited, prohibited and reversed by liquid additives: examples from crystal-form screens
Chemical Science, 2021, 12, 3264-3269
1560123 CIFC24 H28 N2 O6C 1 2 117.9007; 6.3022; 20.9554
90; 105.356; 90
2279.66Arhangelskis, Mihails; Bučar, Dejan-Krešimir; Bordignon, Simone; Chierotti, Michele R.; Stratford, Samuel A.; Voinovich, Dario; Jones, William; Hasa, Dritan
Mechanochemical reactivity inhibited, prohibited and reversed by liquid additives: examples from crystal-form screens
Chemical Science, 2021, 12, 3264-3269
1560124 CIFC24.63 H29.26 N2 O6.32C 1 2 117.8855; 6.3218; 21.0313
90; 105.346; 90
2293.19Arhangelskis, Mihails; Bučar, Dejan-Krešimir; Bordignon, Simone; Chierotti, Michele R.; Stratford, Samuel A.; Voinovich, Dario; Jones, William; Hasa, Dritan
Mechanochemical reactivity inhibited, prohibited and reversed by liquid additives: examples from crystal-form screens
Chemical Science, 2021, 12, 3264-3269
1560125 CIFC24 H20 O4P 21 21 218.9924; 19.5139; 23.2425
90; 90; 90
4078.52Yang, Chi; Wu, Tian-Rui; Li, Yan; Wu, Bing-Bing; Jin, Ruo-Xing; Hu, Duo-Duo; Li, Yuan-Bo; Bian, Kang-Jie; Wang, Xi-Sheng
Facile synthesis of axially chiral styrene-type carboxylic acids via palladium-catalyzed asymmetric C‒H activation
Chemical Science, 2021, 12, 3726-3732
1560126 CIFC25 H18 O2P 18.6935; 11.1218; 12.2142
87.376; 70.785; 81.619
1103.26Yang, Chi; Wu, Tian-Rui; Li, Yan; Wu, Bing-Bing; Jin, Ruo-Xing; Hu, Duo-Duo; Li, Yuan-Bo; Bian, Kang-Jie; Wang, Xi-Sheng
Facile synthesis of axially chiral styrene-type carboxylic acids via palladium-catalyzed asymmetric C‒H activation
Chemical Science, 2021, 12, 3726-3732
1560127 CIFC33 H20.5 Cl0.5 O S2P -111.127; 15.964; 16.195
73.91; 72.41; 73.02
2565.8Wei, Lai; Huang, Hongfeng; Gao, Chunmei; Liu, Danqing; Wang, Lei
Novel butterfly-shaped organic semiconductor and single-walled carbon nanotube composites for high performance thermoelectric generators
Materials Horizons, 2021, 8, 1207-1215
1560128 CIFC34 H18 O S4P -110.5404; 10.8365; 13.1815
92.262; 108.487; 97.789
1409.28Wei, Lai; Huang, Hongfeng; Gao, Chunmei; Liu, Danqing; Wang, Lei
Novel butterfly-shaped organic semiconductor and single-walled carbon nanotube composites for high performance thermoelectric generators
Materials Horizons, 2021, 8, 1207-1215
1560129 CIFC22 H19 N O3 S SeP 1 21 17.2473; 12.2693; 10.9251
90; 90.353; 90
971.43Hua, Jiawei; Bian, Mixue; Ma, Tao; Yang, Man; He, Wei; Yang, Zhao; Liu, ChengKou; Fang, Zheng; Guo, Kai
The sunlight-promoted aerobic selective cyclization of olefinic amides and diselenides
Catalysis Science & Technology, 2021, 11, 2299-2305
1560130 CIFC22 H19 N O3 S SeP 1 21/n 15.8297; 16.2078; 20.9813
90; 93.402; 90
1979Hua, Jiawei; Bian, Mixue; Ma, Tao; Yang, Man; He, Wei; Yang, Zhao; Liu, ChengKou; Fang, Zheng; Guo, Kai
The sunlight-promoted aerobic selective cyclization of olefinic amides and diselenides
Catalysis Science & Technology, 2021, 11, 2299-2305
1560131 CIFC23 H20 N4 O10P 1 21/n 119.932; 4.461; 24.275
90; 97.73; 90
2138.8Xia, Yanming; Wei, Yuanfeng; Chen, Hui; Qian, Shuai; Zhang, Jianjun; Gao, Yuan
Competitive cocrystallization and its application in the separation of flavonoids
IUCrJ, 2021, 8, 195-207
1560132 CIFC20 H30 O3P 1 21 111.7561; 21.9863; 14.0957
90; 101.427; 90
3571.1Kim, Jun Gu; Lee, Jin Woo; Le, Thi Phuong Linh; Han, Jae Sang; Kwon, Haeun; Lee, Dongho; Hong, Jin Tae; Kim, Youngsoo; Lee, Mi Kyeong; Hwang, Bang Yeon
Diterpenoids and Diacetylenes from the Roots of <i>Aralia cordata</i> with Inhibitory Effects on Nitric Oxide Production.
Journal of natural products, 2021
1560135 CIFC167 H154 Cl3 F4 N34 O30P 1 21/n 122.99; 45.82; 40.8
90; 90.92; 90
42973Mateus, Pedro; Jacquet, Antoine; Méndez-Ardoy, Alejandro; Boulloy, Alice; Kauffmann, Brice; Pecastaings, Gilles; Buffeteau, Thierry; Ferrand, Yann; Bassani, Dario M.; Huc, Ivan
Sensing a binding event through charge transport variations using an aromatic oligoamide capsule
Chemical Science, 2021, 12, 3743-3750
1560139 CIFC27 H43 N O3P 1 21/c 18.2116; 14.8475; 20.2921
90; 96.28; 90
2459.2Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560140 CIFC116 H190.67 K4 N4 O12I -4 3 d32.4579; 32.4579; 32.4579
90; 90; 90
34194.9Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560141 CIFC58 H94 Li2 N2 O7C 1 2/c 116.8366; 13.6239; 24.398
90; 91.454; 90
5594.6Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560142 CIFC144 H224 N6 Na12 O12P 1 21/n 116.206; 29.7416; 30.0188
90; 102.473; 90
14127.3Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560143 CIFC108 H172 N4 Na4 O12I -4 3 d32.0084; 32.0084; 32.0084
90; 90; 90
32793.8Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560144 CIFC115 H175 K10 N5 O10P 1 21/c 125.5103; 27.8549; 16.3237
90; 90.336; 90
11599.2Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560145 CIFC77 H121 Li6 N3 O8P 1 21 114.2409; 14.1749; 20.804
90; 104.449; 90
4066.7Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560146 CIFC138 H210 Li12 N6 O12P -115.9758; 16.9105; 29.646
84.635; 79.342; 87.435
7833.4Freeman, Lucas A.; Obi, Akachukwu D.; Machost, Haleigh R.; Molino, Andrew; Nichols, Asa W.; Dickie, Diane A.; Wilson, David J. D.; Machan, Charles W.; Gilliard, Robert J.
Soluble, crystalline, and thermally stable alkali CO2− and carbonite (CO22−) clusters supported by cyclic(alkyl)(amino) carbenes
Chemical Science, 2021, 12, 3544-3550
1560151 CIFC20 H20 N O2 S2P 1 21/n 112.3021; 7.9076; 18.7346
90; 97.095; 90
1808.5Hu, Jiefeng; Yang, Xianyu; Shi, Shasha; Cheng, Bo; Luo, Xiaoling; Lan, Yu; Loh, Teck-Peng
Metal-free C(sp3)‒H functionalization of sulfonamides via strain-release rearrangement
Chemical Science, 2021, 12, 4034-4040
1560152 CIFC47 H62 F6 Fe N O10 PP -111.2754; 11.2786; 19.1955
81.762; 83.501; 76.134
2337.6Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560153 CIFC47 H62 F6 Fe N O10 PP -111.3327; 11.4193; 19.3877
82.951; 80.729; 77.436
2406.89Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560154 CIFC47 H62 F6 Fe N O10 PP -111.2781; 11.2893; 19.213
83.432; 81.586; 76.335
2343.29Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560155 CIFC47 H62 F6 Fe N O10 PP -111.2958; 11.3414; 19.2872
83.238; 81.374; 76.703
2368.53Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560156 CIFC47 H62 F6 Fe N O10 PP -111.3259; 11.3917; 19.3628
83.024; 80.932; 77.121
2395.24Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560157 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.2236; 25.2061; 13.5364
90; 110.914; 90
3258.5Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560158 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.2753; 25.224; 13.5486
90; 111.171; 90
3274.6Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560159 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.3328; 25.4063; 13.6255
90; 111.122; 90
3336.6Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560160 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.361; 25.435; 13.645
90; 111.064; 90
3356Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560161 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.28; 25.269; 13.5675
90; 111.092; 90
3288.2Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560162 CIFC47 H62 F6 Fe N O10 PP -111.2892; 11.3208; 19.2519
83.33; 81.46; 76.478
2357.22Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560163 CIFC47 H62 F6 Fe N O10 PP -111.3088; 11.3689; 19.3307
83.1; 81.166; 76.913
2382.63Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560164 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.844; 11.6767; 16.7383
94.74; 95.623; 104.722
1840.28Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560165 CIFC47 H62 F6 Fe N O10 PP -111.3611; 11.5447; 19.4228
82.91; 80.543; 77.861
2446.24Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560166 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.8233; 11.6256; 16.7174
94.917; 95.464; 104.784
1825.52Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560167 CIFC47 H62 F6 Fe N O10 PP -111.3456; 11.4668; 19.414
82.907; 80.58; 77.69
2424.07Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560168 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.7522; 11.4459; 16.6761
95.5; 95.052; 104.805
1779.06Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560169 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.3108; 25.3315; 13.5949
90; 111.123; 90
3312.2Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560170 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.7269; 11.4193; 16.6601
95.565; 95.014; 104.744
1769.03Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560171 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.3821; 25.543; 13.668
90; 111.172; 90
3380Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560172 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.8091; 11.5747; 16.7136
95.109; 95.249; 104.806
1814.42Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560173 CIFC32 H40 F6 Fe N O6 PP 1 21/n 110.354; 25.443; 13.638
90; 111.061; 90
3352.7Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560174 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.8649; 11.7188; 16.7606
94.613; 95.802; 104.684
1853.36Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560175 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.691; 11.3787; 16.6251
95.673; 94.963; 104.636
1753.22Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560176 CIFC47 H62 F6 Fe N O10 PP -111.3733; 11.6068; 19.427
83.003; 80.579; 77.986
2464.26Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560177 CIFC33 H42 Cl2 F6 Fe N O6 PP -19.7922; 11.5185; 16.7041
95.266; 95.19; 104.874
1800.49Wang, Chi-Hsien; Chen, Kai-Jen; Wu, Tsung-Huan; Chang, Hung-Kai; Tsuchido, Yoshitaka; Sei, Yoshihisa; Chen, Pei-Lin; Horie, Masaki
Ring rotation of ferrocene in interlocked molecules in single crystals
Chemical Science, 2021, 12, 3871-3875
1560186 CIFC8 H8 N2 O2P -16.931; 7.59; 7.735
60.94; 82.44; 75.12
343.75Nicks, Joshua; Boer, Stephanie A.; White, Nicholas G.; Foster, Jonathan A.
Monolayer nanosheets formed by liquid exfoliation of charge-assisted hydrogen-bonded frameworks
Chemical Science, 2021, 12, 3322-3327
1560187 CIFC8 H8 N2 O2P -17.0348; 7.8512; 7.8827
61.268; 74.309; 82.32
367.54Nicks, Joshua; Boer, Stephanie A.; White, Nicholas G.; Foster, Jonathan A.
Monolayer nanosheets formed by liquid exfoliation of charge-assisted hydrogen-bonded frameworks
Chemical Science, 2021, 12, 3322-3327
1560188 CIFC8 H8 N2 O2P -15.5557; 7.8957; 9.0549
71.386; 83.555; 74.217
362.09Nicks, Joshua; Boer, Stephanie A.; White, Nicholas G.; Foster, Jonathan A.
Monolayer nanosheets formed by liquid exfoliation of charge-assisted hydrogen-bonded frameworks
Chemical Science, 2021, 12, 3322-3327
1560197 CIFC33 H17 NP 1 21/c 19.5983; 7.4141; 28.155
90; 97.017; 90
1988.6Ghosh, Animesh; Csókás, Dániel; Budanović, Maja; Webster, Richard D.; Pápai, Imre; Stuparu, Mihaiela C.
Synthesis of azahelicenes through Mallory reaction of imine precursors: corannulene substrates provide an exception to the rule in oxidative photocyclizations of diarylethenes
Chemical Science, 2021, 12, 3977-3983
1560198 CIFAs B F H4 N O4C 1 c 14.4453; 8.1098; 12.7463
90; 90; 90
459.51Bai, Zhiyong; Liu, Lehui; Wang, Dongmei; Hu, Chun-Li; Lin, Zhoubin
To improve the key properties of nonlinear optical crystals assembled with tetrahedral functional building units
Chemical Science, 2021, 12, 4014-4020
1560199 CIFC65 H65 Cu F3 N4 O4 P3 SP -110.6937; 10.7364; 25.1952
88.365; 83.658; 83.887
2858.25Weberg, Alexander B.; McCollom, Samuel P.; Thierer, Laura M.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Using internal electrostatic fields to manipulate the valence manifolds of copper complexes
Chemical Science, 2021, 12, 4395-4404
1560200 CIFC43 H49 B Cl Cu F20 N4 O P3P 1 21/c 116.4423; 20.739; 15.7833
90; 104.388; 90
5213.2Weberg, Alexander B.; McCollom, Samuel P.; Thierer, Laura M.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Using internal electrostatic fields to manipulate the valence manifolds of copper complexes
Chemical Science, 2021, 12, 4395-4404
1560201 CIFC15 H39 Cl2 Cu N4 P3P b c a16.2129; 16.8046; 17.8201
90; 90; 90
4855.1Weberg, Alexander B.; McCollom, Samuel P.; Thierer, Laura M.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Using internal electrostatic fields to manipulate the valence manifolds of copper complexes
Chemical Science, 2021, 12, 4395-4404
1560202 CIFC54 H45 B Cu F20 N4 P3P 1 21/n 112.8794; 28.2479; 15.6613
90; 110.76; 90
5327.9Weberg, Alexander B.; McCollom, Samuel P.; Thierer, Laura M.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Using internal electrostatic fields to manipulate the valence manifolds of copper complexes
Chemical Science, 2021, 12, 4395-4404
1560203 CIFC39 H39 B Cu F20 N4 P3P -113.443; 14.253; 14.599
93.503; 105.397; 107.916
2534.8Weberg, Alexander B.; McCollom, Samuel P.; Thierer, Laura M.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Using internal electrostatic fields to manipulate the valence manifolds of copper complexes
Chemical Science, 2021, 12, 4395-4404
1560204 CIFC19 H18 N2 O2 S2P 1 21 19.6009; 10.3983; 9.9867
90; 115.222; 90
901.95Zhong, Xia; Zhong, Ziwei; Wu, Zhikun; Ye, Zhen; Feng, Yuxiang; Dong, Shunxi; Liu, Xiaohua; Peng, Qian; Feng, Xiaoming
Chiral Lewis acid-bonded picolinaldehyde enables enantiodivergent carbonyl catalysis in the Mannich/condensation reaction of glycine ester
Chemical Science, 2021, 12, 4353-4360
1560205 CIFC38 H56 F9 N4 O16 S3 YbP 21 21 223.069; 24.5839; 9.5501
90; 90; 90
5416.1Zhong, Xia; Zhong, Ziwei; Wu, Zhikun; Ye, Zhen; Feng, Yuxiang; Dong, Shunxi; Liu, Xiaohua; Peng, Qian; Feng, Xiaoming
Chiral Lewis acid-bonded picolinaldehyde enables enantiodivergent carbonyl catalysis in the Mannich/condensation reaction of glycine ester
Chemical Science, 2021, 12, 4353-4360
1560206 CIFC49 H78 F9 N4 O17 S3 YbP 1 21 111.9789; 20.7474; 12.9099
90; 106.293; 90
3079.7Zhong, Xia; Zhong, Ziwei; Wu, Zhikun; Ye, Zhen; Feng, Yuxiang; Dong, Shunxi; Liu, Xiaohua; Peng, Qian; Feng, Xiaoming
Chiral Lewis acid-bonded picolinaldehyde enables enantiodivergent carbonyl catalysis in the Mannich/condensation reaction of glycine ester
Chemical Science, 2021, 12, 4353-4360
1560207 CIFC122 H112 O4 S2P -18.9363; 15.5536; 17.3731
106.709; 97.475; 95.961
2267.6Lu, Xuefeng; An, Dongyue; Han, Yi; Zou, Ya; Qiao, Yanjun; Zhang, Ning; Chang, Dongdong; Wu, Jishan; Liu, Yunqi
A cyclopenta-fused dibenzo[b,d]thiophene-co-phenanthrene macrocyclic tetraradicaloid
Chemical Science, 2021, 12, 3952-3957
1560208 CIFC63 H66 Cu3 N9P -19.7333; 27.941; 42.675
75.096; 83.457; 84.935
11121.3Xie, Mo; Chen, Xiao-Ru; Wu, Kun; Lu, Zhou; Wang, Kai; Li, Nan; Wei, Rong-Jia; Zhan, Shun-Ze; Ning, Guo-Hong; Zou, Bo; Li, Dan
Pressure-induced phosphorescence enhancement and piezochromism of a carbazole-based cyclic trinuclear Cu(i) complex
Chemical Science, 2021, 12, 4425-4431
1560209 CIFC63 H66 Cu3 N9P 1 c 111.4093; 28.8937; 17.7109
90; 104.338; 90
5656.66Xie, Mo; Chen, Xiao-Ru; Wu, Kun; Lu, Zhou; Wang, Kai; Li, Nan; Wei, Rong-Jia; Zhan, Shun-Ze; Ning, Guo-Hong; Zou, Bo; Li, Dan
Pressure-induced phosphorescence enhancement and piezochromism of a carbazole-based cyclic trinuclear Cu(i) complex
Chemical Science, 2021, 12, 4425-4431
1560210 CIFC63 H66 Cu3 N9P 1 21/c 111.52641; 29.1085; 17.85854
90; 103.99; 90
5814.11Xie, Mo; Chen, Xiao-Ru; Wu, Kun; Lu, Zhou; Wang, Kai; Li, Nan; Wei, Rong-Jia; Zhan, Shun-Ze; Ning, Guo-Hong; Zou, Bo; Li, Dan
Pressure-induced phosphorescence enhancement and piezochromism of a carbazole-based cyclic trinuclear Cu(i) complex
Chemical Science, 2021, 12, 4425-4431
1560211 CIFC22 H45 Fe N4 O7P 1 21/c 113.571; 11.046; 19.406
90; 102.992; 90
2834.6Keshari, Kritika; Bera, Moumita; Velasco, Lucía; Munshi, Sandip; Gupta, Geetika; Moonshiram, Dooshaye; Paria, Sayantan
Characterization and reactivity study of non-heme high-valent iron‒hydroxo complexes
Chemical Science, 2021, 12, 4418-4424
1560212 CIFC30 H16 O2P 1 21/c 18.1656; 15.1358; 15.7979
90; 102.468; 90
1906.5Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560213 CIFC30 H18 N2P 1 21/c 115.9958; 15.9492; 7.8148
90; 91.516; 90
1993.02Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560214 CIFC15 H8 O2 SC 1 2/c 117.7976; 10.4721; 11.7388
90; 99.158; 90
2159.97Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560215 CIFC57 H34 Cl2P 21 21 218.57192; 20.53361; 22.43166
90; 90; 90
3948.25Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560216 CIFC30 H16 S2P 1 21/n 19.338; 13.622; 16.299
90; 102.204; 90
2026.4Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560217 CIFC28.5 H16.5 Cl1.5 OP 41 2 29.0201; 9.0201; 49.382
90; 90; 90
4017.8Yanagi, Tomoyuki; Tanaka, Takayuki; Yorimitsu, Hideki
Asymmetric systematic synthesis, structures, and (chir)optical properties of a series of dihetero[8]helicenes
Chemical Science, 2021, 12, 2784-2793
1560218 CIFC70 H86 B P2 YP 1 21/c 119.84621; 15.33735; 19.6362
90; 91.1824; 90
5975.76Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560219 CIFC39 H57 Cl2 F6 P2 Ru SbP 1 21/n 114.68263; 10.27641; 28.8561
90; 94.9221; 90
4337.89Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560220 CIFC26 H36 Cl4 Hf P2P 1 21/c 113.847; 11.756; 17.937
90; 95.395; 90
2907Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560221 CIFC33 H43 Cl5 N P2 TaP b c a20.20265; 16.84883; 20.7566
90; 90; 90
7065.36Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560222 CIFC30.5 H39 Br Cl3 Mn O3 P2P 1 21/c 112.12; 18.798; 15.683
90; 111.303; 90
3329Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560223 CIFC30 H36 Cr O4 P2P 1 21/n 111.87864; 15.68278; 15.58857
90; 102.773; 90
2832.13Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560224 CIFC45 H60 Cl N O2 P2 PtP 1 21/c 118.1766; 11.59885; 21.4296
90; 114.947; 90
4096.41Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560225 CIFC38 H55 Cl5 F6 P2 Rh SbP 1 21/c 18.68119; 24.5831; 20.7842
90; 96.7728; 90
4404.61Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560226 CIFC33 H42 N2 O3 P2 WP 1 21/n 110.771; 18.02; 16.983
90; 97.989; 90
3264Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560227 CIFC29 H36 O3 P2 WP b c a15.652; 16.072; 22.3038
90; 90; 90
5610.7Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560228 CIFC33 H42 Mo N2 O3 P2P 1 21/n 110.771; 18.08; 16.992
90; 97.838; 90
3278Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560229 CIFC38 H52 Mo O6 P2P 1 21/c 110.8424; 15.9246; 22.3877
90; 101.63; 90
3786.12Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560230 CIFC35 H48 Mo O4.5 P2C 1 2/c 132.514; 11.57882; 39.5477
90; 113.917; 90
13610.2Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560231 CIFC86 H100 Au B F2 O P2P 1 21/c 111.28458; 13.79053; 47.7699
90; 90.5291; 90
7433.65Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560232 CIFC29 H36 Mo O3 P2P b c a15.65317; 16.11165; 22.26048
90; 90; 90
5614.06Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560233 CIFC56 H82 O3 P2 S2 ZnP 1 21/c 120.688; 26.218; 40.07
90; 95.99; 90
21615Wagner, Hannah K.; Wadepohl, Hubert; Ballmann, Joachim
A 2,2′-diphosphinotolane as a versatile precursor for the synthesis of P-ylidic mesoionic carbenes via reversible C‒P bond formation
Chemical Science, 2021, 12, 3693-3701
1560234 CIFC55 H38 Cl2P 1 21/c 16.2639; 22.294; 30.28
90; 95.509; 90
4209Zhao, Chong; Liu, Fupin; Feng, Lai; Nie, Mingzhe; Lu, Yuxi; Zhang, Jie; Wang, Chunru; Wang, Taishan
Construction of a double-walled carbon nanoring.
Nanoscale, 2021, 13, 4880-4886
1560235 CIF
HKL
Paper
C20 H22 N2 O4P -18.7181; 10.723; 11.2096
113.035; 91.4395; 107.402
908.09Yoo, Miri; Koh, Dongsoo
1-[5-(3,5-Dimethoxyphenyl)-3-(2-methoxyphenyl)-4,5-dihydro-1<i>H</i>-pyrazol-1-yl]ethanone
IUCrData, 2021, 6, x210096
1560236 CIFC32 H43 Ba N6 O11 S2P c a 2117.6827; 10.4422; 22.5408
90; 90; 90
4162.08Abou, Diane S.; Thiele, Nikki A.; Gutsche, Nicholas T.; Villmer, Alexandria; Zhang, Hanwen; Woods, Joshua J.; Baidoo, Kwamena E.; Escorcia, Freddy E.; Wilson, Justin J.; Thorek, Daniel L. J.
Towards the stable chelation of radium for biomedical applications with an 18-membered macrocyclic ligand
Chemical Science, 2021, 12, 3733-3742
1560237 CIFC59 H76 Cl Ir N2P 21 21 2116.297; 17.0451; 17.8125
90; 90; 90
4948.03Foster, Daven; Gao, Pengchao; Zhang, Ziyun; Sipos, Gellért; Sobolev, Alexandre N.; Nealon, Gareth; Falivene, Laura; Cavallo, Luigi; Dorta, Reto
Design, scope and mechanism of highly active and selective chiral NHC‒iridium catalysts for the intramolecular hydroamination of a variety of unactivated aminoalkenes
Chemical Science, 2021, 12, 3751-3767
1560238 CIFC55 H64 Br2 N4 O13P -19.3936; 16.783; 17.8687
75.171; 83.247; 84.427
2697.7Wilson, Benjamin H.; Abdulla, Louae M.; Schurko, Robert W.; Loeb, Stephen J.
Translational dynamics of a non-degenerate molecular shuttle imbedded in a zirconium metal‒organic framework
Chemical Science, 2021, 12, 3944-3951
1560239 CIFC50 H52 Br2 N4 O12P 1 21/n 119.889; 18.209; 33.691
90; 105.93; 90
11733Wilson, Benjamin H.; Abdulla, Louae M.; Schurko, Robert W.; Loeb, Stephen J.
Translational dynamics of a non-degenerate molecular shuttle imbedded in a zirconium metal‒organic framework
Chemical Science, 2021, 12, 3944-3951
1560240 CIFC57 H67.5 B Br2 F4 N4.5 O12.5P 1 21/c 128.49; 10.505; 43.418
90; 106.34; 90
12470Wilson, Benjamin H.; Abdulla, Louae M.; Schurko, Robert W.; Loeb, Stephen J.
Translational dynamics of a non-degenerate molecular shuttle imbedded in a zirconium metal‒organic framework
Chemical Science, 2021, 12, 3944-3951
1560241 CIFC38 H41 F3 P2P 1 21/c 19.60831; 33.8371; 10.09764
90; 99.1105; 90
3241.5Handelmann, Jens; Babu, Chatla Naga; Steinert, Henning; Schwarz, Christopher; Scherpf, Thorsten; Kroll, Alexander; Gessner, Viktoria H.
Towards the rational design of ylide-substituted phosphines for gold(i)-catalysis: from inactive to ppm-level catalysis
Chemical Science, 2021, 12, 4329-4337
1560242 CIFC41.79 H50.79 Cl0.41 N0.79 P2P -110.9245; 12.9655; 14.1731
63.574; 81.1475; 75.1466
1735.83Handelmann, Jens; Babu, Chatla Naga; Steinert, Henning; Schwarz, Christopher; Scherpf, Thorsten; Kroll, Alexander; Gessner, Viktoria H.
Towards the rational design of ylide-substituted phosphines for gold(i)-catalysis: from inactive to ppm-level catalysis
Chemical Science, 2021, 12, 4329-4337
1560243 CIFC38 H44 Au Cl O P2C 1 2/c 141.898; 15.2834; 11.6875
90; 93.097; 90
7473.1Handelmann, Jens; Babu, Chatla Naga; Steinert, Henning; Schwarz, Christopher; Scherpf, Thorsten; Kroll, Alexander; Gessner, Viktoria H.
Towards the rational design of ylide-substituted phosphines for gold(i)-catalysis: from inactive to ppm-level catalysis
Chemical Science, 2021, 12, 4329-4337
1560244 CIFC41 H50 Au Cl O P2P -19.3045; 10.502; 18.6397
97.739; 91.819; 94.738
1796.94Handelmann, Jens; Babu, Chatla Naga; Steinert, Henning; Schwarz, Christopher; Scherpf, Thorsten; Kroll, Alexander; Gessner, Viktoria H.
Towards the rational design of ylide-substituted phosphines for gold(i)-catalysis: from inactive to ppm-level catalysis
Chemical Science, 2021, 12, 4329-4337
1560245 CIFC38 H44 P2P 1 21/n 110.29027; 10.5467; 29.0177
90; 96.2428; 90
3130.57Handelmann, Jens; Babu, Chatla Naga; Steinert, Henning; Schwarz, Christopher; Scherpf, Thorsten; Kroll, Alexander; Gessner, Viktoria H.
Towards the rational design of ylide-substituted phosphines for gold(i)-catalysis: from inactive to ppm-level catalysis
Chemical Science, 2021, 12, 4329-4337
1560246 CIFC45 H52 Au Cl P2P 1 21/c 111.24594; 18.3601; 18.9125
90; 95.9476; 90
3883.97Handelmann, Jens; Babu, Chatla Naga; Steinert, Henning; Schwarz, Christopher; Scherpf, Thorsten; Kroll, Alexander; Gessner, Viktoria H.
Towards the rational design of ylide-substituted phosphines for gold(i)-catalysis: from inactive to ppm-level catalysis
Chemical Science, 2021, 12, 4329-4337
1560247 CIFC40 H48 Au Cl P2P 1 21/n 112.0432; 16.7764; 17.8978
90; 106.65; 90
3464.49Handelmann, Jens; Babu, Chatla Naga; Steinert, Henning; Schwarz, Christopher; Scherpf, Thorsten; Kroll, Alexander; Gessner, Viktoria H.
Towards the rational design of ylide-substituted phosphines for gold(i)-catalysis: from inactive to ppm-level catalysis
Chemical Science, 2021, 12, 4329-4337
1560248 CIFC38 H41 Au Cl F3 P2P -111.01072; 17.1399; 18.8182
80.1354; 77.3539; 89.9789
3411.48Handelmann, Jens; Babu, Chatla Naga; Steinert, Henning; Schwarz, Christopher; Scherpf, Thorsten; Kroll, Alexander; Gessner, Viktoria H.
Towards the rational design of ylide-substituted phosphines for gold(i)-catalysis: from inactive to ppm-level catalysis
Chemical Science, 2021, 12, 4329-4337
1560249 CIFC38 H44 O P2P c a 2111.3956; 15.6766; 18.1208
90; 90; 90
3237.18Handelmann, Jens; Babu, Chatla Naga; Steinert, Henning; Schwarz, Christopher; Scherpf, Thorsten; Kroll, Alexander; Gessner, Viktoria H.
Towards the rational design of ylide-substituted phosphines for gold(i)-catalysis: from inactive to ppm-level catalysis
Chemical Science, 2021, 12, 4329-4337
1560250 CIFC44 H50 P2P -19.3576; 13.3096; 14.9346
93.442; 93.343; 107.914
1760.89Handelmann, Jens; Babu, Chatla Naga; Steinert, Henning; Schwarz, Christopher; Scherpf, Thorsten; Kroll, Alexander; Gessner, Viktoria H.
Towards the rational design of ylide-substituted phosphines for gold(i)-catalysis: from inactive to ppm-level catalysis
Chemical Science, 2021, 12, 4329-4337
1560251 CIF
HKL
Paper
C13 H13 N3 O6P 1 21/c 18.639; 20.045; 8.116
90; 101.326; 90
1378.1Huang, Houshi; Wu, Zhichao
2-(2,4-Dinitrophenyl)-1-(pyridin-4-yl)ethanol monohydrate
IUCrData, 2021, 6, x201640
1560262 CIFC57 H73 Cl2 N2 O3.5 P2 RuP 116.268; 17.763; 23.082
87.715; 81.35; 66.621
6051.3León, Félix; Comas-Vives, Aleix; Álvarez, Eleuterio; Pizzano, Antonio
A combined experimental and computational study to decipher complexity in the asymmetric hydrogenation of imines with Ru catalysts bearing atropisomerizable ligands
Catalysis Science & Technology, 2021, 11, 2497-2511
1560263 CIFC55 H68 Cl2 N2 O3 P2 RuP 41 21 214.0362; 14.0362; 55.098
90; 90; 90
10855León, Félix; Comas-Vives, Aleix; Álvarez, Eleuterio; Pizzano, Antonio
A combined experimental and computational study to decipher complexity in the asymmetric hydrogenation of imines with Ru catalysts bearing atropisomerizable ligands
Catalysis Science & Technology, 2021, 11, 2497-2511
1560264 CIFC55 H68 Cl2 N2 O3 P2 RuP 1 21 114.485; 13.276; 16.008
90; 104.344; 90
2982.4León, Félix; Comas-Vives, Aleix; Álvarez, Eleuterio; Pizzano, Antonio
A combined experimental and computational study to decipher complexity in the asymmetric hydrogenation of imines with Ru catalysts bearing atropisomerizable ligands
Catalysis Science & Technology, 2021, 11, 2497-2511
1560265 CIFC50 H58 Cl4 N2 O5 P2 RuC 1 2 129.604; 12.869; 29.396
90; 114.68; 90
10176León, Félix; Comas-Vives, Aleix; Álvarez, Eleuterio; Pizzano, Antonio
A combined experimental and computational study to decipher complexity in the asymmetric hydrogenation of imines with Ru catalysts bearing atropisomerizable ligands
Catalysis Science & Technology, 2021, 11, 2497-2511
1560266 CIFC123 H142 Cl10 F4 N4 O6 P4 Ru2P 113.3642; 15.0349; 18.4697
89.212; 76.738; 66.771
3307.09León, Félix; Comas-Vives, Aleix; Álvarez, Eleuterio; Pizzano, Antonio
A combined experimental and computational study to decipher complexity in the asymmetric hydrogenation of imines with Ru catalysts bearing atropisomerizable ligands
Catalysis Science & Technology, 2021, 11, 2497-2511
1560267 CIFC180 H138 Ag14 Cl6 F6 P8 Pt S6C 1 2/c 148.002; 35.012; 30.277
90; 127.84; 90
40185Lin, Xinzhang; Sun, Keju; Fu, Xuemei; Ren, Xiuqing; Yang, Yang; Liu, Chao; Huang, Jiahui
Correlating Kernel‒Shell Structures with Optical Properties of Pt1Ag24 and Pt1Ag14 Nanoclusters
The Journal of Physical Chemistry C, 2021, 125, 2194-2201
1560268 CIFC180 H138 Ag14 Cl6 F6 P8 Pt S6C 1 2/c 147.8113; 34.9302; 30.1732
90; 127.995; 90
39711Lin, Xinzhang; Sun, Keju; Fu, Xuemei; Ren, Xiuqing; Yang, Yang; Liu, Chao; Huang, Jiahui
Correlating Kernel‒Shell Structures with Optical Properties of Pt1Ag24 and Pt1Ag14 Nanoclusters
The Journal of Physical Chemistry C, 2021, 125, 2194-2201
1560269 CIFC216 H140 Ag24 Cl20 F20 P4 Pt S20P -118.9452; 19.2539; 20.0639
89.647; 67.76; 71.704
6378.7Lin, Xinzhang; Sun, Keju; Fu, Xuemei; Ren, Xiuqing; Yang, Yang; Liu, Chao; Huang, Jiahui
Correlating Kernel‒Shell Structures with Optical Properties of Pt1Ag24 and Pt1Ag14 Nanoclusters
The Journal of Physical Chemistry C, 2021, 125, 2194-2201
1560270 CIFC30 H30 Cl N O2P -19.9157; 10.1069; 13.5253
78.6034; 69.679; 89.5945
1243.24MARFO-OWUSU, Emmanuel; THOMPSON, Amber L.
Crystal Structure of a Benzyltrimethylammonium Chloride Complex with <i>rac</i>-1,1′-Bi-2-naphthol: The Generation of Weak Interactions by the Influence of a Benzyl Group
X-ray Structure Analysis Online, 2021, 37, 1-2
1560271 CIFC41 H56 Cl2 Mn2 N8 O12P n m a15.052; 20.449; 14.7
90; 90; 90
4524.6MIKURIYA, Masahiro; ONO, Sayuri; KOYAMA, Yoshiki; MITSUHASHI, Ryoji; TSUBOI, Motohiro
Crystal Structure of a μ-Phenolato-μ-oxido-bridged Dinuclear Manganese(III) Complex with Dinucleating Schiff-base Ligand Having Three Phenolate Groups
X-ray Structure Analysis Online, 2021, 37, 3-5
1560272 CIFC10 H8 Cl6 N8 O2 Ru2P 1 21/c 17.1611; 10.7203; 11.6662
90; 90.805; 90
895.52Orts-Arroyo, Marta; Castro, Isabel; Martínez-Lillo, José
Detection of Hypoxanthine from Inosine and Unusual Hydrolysis of Immunosuppressive Drug Azathioprine through the Formation of a Diruthenium(III) System.
Biosensors, 2021, 11, 19
1560273 CIFC10 H12 Cl6 N8 O4 Ru2P 1 21/c 18.7139; 11.8652; 10.2858
90; 112.318; 90
983.81Orts-Arroyo, Marta; Castro, Isabel; Martínez-Lillo, José
Detection of Hypoxanthine from Inosine and Unusual Hydrolysis of Immunosuppressive Drug Azathioprine through the Formation of a Diruthenium(III) System.
Biosensors, 2021, 11, 19
1560274 CIFC32 H40 K N O6P 1 21 19.4575; 13.1739; 12.1272
90; 101.138; 90
1482.49Panetti, Grace B.; Carroll, Patrick J.; Gau, Michael R.; Manor, Brian C.; Schelter, Eric J.; Walsh, Patrick J.
Synthesis of an elusive, stable 2-azaallyl radical guided by electrochemical and reactivity studies of 2-azaallyl anions
Chemical Science, 2021, 12, 4405-4410
1560275 CIFC38 H50 N Na O6P 1 21/c 117.7615; 11.8703; 34.9201
90; 100.04; 90
7249.6Panetti, Grace B.; Carroll, Patrick J.; Gau, Michael R.; Manor, Brian C.; Schelter, Eric J.; Walsh, Patrick J.
Synthesis of an elusive, stable 2-azaallyl radical guided by electrochemical and reactivity studies of 2-azaallyl anions
Chemical Science, 2021, 12, 4405-4410
1560276 CIFC32 H46 N Na O6P -111.6153; 11.6198; 12.645
104.751; 95.937; 99.774
1607.08Panetti, Grace B.; Carroll, Patrick J.; Gau, Michael R.; Manor, Brian C.; Schelter, Eric J.; Walsh, Patrick J.
Synthesis of an elusive, stable 2-azaallyl radical guided by electrochemical and reactivity studies of 2-azaallyl anions
Chemical Science, 2021, 12, 4405-4410
1560277 CIFC26 H20 NP 1 21 19.8522; 7.7653; 12.2084
90; 95.841; 90
929.16Panetti, Grace B.; Carroll, Patrick J.; Gau, Michael R.; Manor, Brian C.; Schelter, Eric J.; Walsh, Patrick J.
Synthesis of an elusive, stable 2-azaallyl radical guided by electrochemical and reactivity studies of 2-azaallyl anions
Chemical Science, 2021, 12, 4405-4410
1560278 CIFC64 H92 Li2 N2 O12P 1 21/c 111.6347; 18.1467; 31.5962
90; 95.756; 90
6637.3Panetti, Grace B.; Carroll, Patrick J.; Gau, Michael R.; Manor, Brian C.; Schelter, Eric J.; Walsh, Patrick J.
Synthesis of an elusive, stable 2-azaallyl radical guided by electrochemical and reactivity studies of 2-azaallyl anions
Chemical Science, 2021, 12, 4405-4410
1560279 CIFC17.24 H19.73 N3 O4.75P -17.2814; 10.1224; 12.178
92.523; 106.963; 100.062
841.02Brownsey, Duncan K.; Rowley, Ben C.; Gorobets, Evgueni; Gelfand, Benjamin S.; Derksen, Darren J.
Rapid synthesis of pomalidomide-conjugates for the development of protein degrader libraries
Chemical Science, 2021, 12, 4519-4525
1560280 CIFC11 H16 O7P 21 21 214.8832; 7.5868; 35.478
90; 90; 90
1314.4Aitken, R.; Haslett, Oliver; Slawin, Alexandra
(S)-1-(Ethoxycarbonyl)ethyl(2R,5S)-2,5-dimethyl-1,3-dioxolan-4-one-2-carboxylate
Molbank, 2021, 2021, M1178
1560281 CIFC21 H27 B F2 I N3 O5P -18.6034; 9.0805; 16.4248
99.579; 94.035; 108.412
1190.09Kuno, Atsuko; Maeda, Hiromitsu
Nitro-Substituted Dipyrrolyldiketone BF<sub>2</sub> Complexes as Electronic-State-Adjustable Anion-Responsive π-Electronic Systems.
Molecules (Basel, Switzerland), 2021, 26, 595
1560282 CIFC19 H23 B F2 I N3 O4P 1 21/c 111.2903; 22.2353; 16.8402
90; 98.74; 90
4178.53Kuno, Atsuko; Maeda, Hiromitsu
Nitro-Substituted Dipyrrolyldiketone BF<sub>2</sub> Complexes as Electronic-State-Adjustable Anion-Responsive π-Electronic Systems.
Molecules (Basel, Switzerland), 2021, 26, 595
1560283 CIFC19 H24 O6P 21 21 215.20899; 13.1379; 24.88894
90; 90; 90
1703.28Gao, Ying; Duan, Fang-Fang; Liu, Lin; Peng, Xiao-Gang; Meng, Xiang-Gao; Ruan, Han-Li
Hypothemycin-Type Resorcylic Acid Lactones with Immunosuppressive Activities from a <i>Podospora</i> sp.
Journal of natural products, 2021, 84, 483-494
1560284 CIFC17 H26 O6P 1 21 18.61617; 16.0717; 12.1358
90; 90.6233; 90
1680.42Gao, Ying; Duan, Fang-Fang; Liu, Lin; Peng, Xiao-Gang; Meng, Xiang-Gao; Ruan, Han-Li
Hypothemycin-Type Resorcylic Acid Lactones with Immunosuppressive Activities from a <i>Podospora</i> sp.
Journal of natural products, 2021, 84, 483-494
1560285 CIFC19 H26 O7C 1 2 135.002; 5.4539; 23.7081
90; 126.11; 90
3656.3Gao, Ying; Duan, Fang-Fang; Liu, Lin; Peng, Xiao-Gang; Meng, Xiang-Gao; Ruan, Han-Li
Hypothemycin-Type Resorcylic Acid Lactones with Immunosuppressive Activities from a <i>Podospora</i> sp.
Journal of natural products, 2021, 84, 483-494
1560286 CIFC19 H26 O6P 21 21 215.5123; 16.2923; 39.6735
90; 90; 90
3563Gao, Ying; Duan, Fang-Fang; Liu, Lin; Peng, Xiao-Gang; Meng, Xiang-Gao; Ruan, Han-Li
Hypothemycin-Type Resorcylic Acid Lactones with Immunosuppressive Activities from a <i>Podospora</i> sp.
Journal of natural products, 2021, 84, 483-494
1560287 CIFC22 H28 O7P 1 21 15.59493; 16.1943; 11.21004
90; 97.6959; 90
1006.55Gao, Ying; Duan, Fang-Fang; Liu, Lin; Peng, Xiao-Gang; Meng, Xiang-Gao; Ruan, Han-Li
Hypothemycin-Type Resorcylic Acid Lactones with Immunosuppressive Activities from a <i>Podospora</i> sp.
Journal of natural products, 2021, 84, 483-494
1560288 CIFC18 H24 O6P 21 21 215.46419; 15.26209; 20.85735
90; 90; 90
1739.4Gao, Ying; Duan, Fang-Fang; Liu, Lin; Peng, Xiao-Gang; Meng, Xiang-Gao; Ruan, Han-Li
Hypothemycin-Type Resorcylic Acid Lactones with Immunosuppressive Activities from a <i>Podospora</i> sp.
Journal of natural products, 2021, 84, 483-494
1560289 CIFC18 H22 O6P 21 21 215.41732; 15.13174; 20.13674
90; 90; 90
1650.68Gao, Ying; Duan, Fang-Fang; Liu, Lin; Peng, Xiao-Gang; Meng, Xiang-Gao; Ruan, Han-Li
Hypothemycin-Type Resorcylic Acid Lactones with Immunosuppressive Activities from a <i>Podospora</i> sp.
Journal of natural products, 2021, 84, 483-494
1560290 CIFC19 H24 O6P 21 21 216.92375; 15.28917; 17.20264
90; 90; 90
1821.04Gao, Ying; Duan, Fang-Fang; Liu, Lin; Peng, Xiao-Gang; Meng, Xiang-Gao; Ruan, Han-Li
Hypothemycin-Type Resorcylic Acid Lactones with Immunosuppressive Activities from a <i>Podospora</i> sp.
Journal of natural products, 2021, 84, 483-494
1560291 CIFC20 H28 O9P 21 21 215.7391; 10.8943; 32.111
90; 90; 90
2007.7Gao, Ying; Duan, Fang-Fang; Liu, Lin; Peng, Xiao-Gang; Meng, Xiang-Gao; Ruan, Han-Li
Hypothemycin-Type Resorcylic Acid Lactones with Immunosuppressive Activities from a <i>Podospora</i> sp.
Journal of natural products, 2021, 84, 483-494
1560292 CIFC59.5 H70 N10 Ni2 O10.5P 1 21/n 118.9647; 12.1455; 26.148
90; 107.084; 90
5757.1Liu, Guan-Lin; Wu, Hsin-Wei; Lin, Zheng-Ian; Liao, Min-Gan; Su, Yu-Chia; Chen, Chih-Kuang; Ko, Bao-Tsan
Synthesis of functional CO2-based polycarbonates via dinuclear nickel nitrophenolate-based catalysis for degradable surfactant and drug-loaded nanoparticle applications
Polymer Chemistry, 2021, 12, 1244-1259
1560293 CIFC60 H70 Cl2 N12 Ni2 O14P -112.9818; 14.4796; 17.1256
104.692; 96.273; 90.903
3092.1Liu, Guan-Lin; Wu, Hsin-Wei; Lin, Zheng-Ian; Liao, Min-Gan; Su, Yu-Chia; Chen, Chih-Kuang; Ko, Bao-Tsan
Synthesis of functional CO2-based polycarbonates via dinuclear nickel nitrophenolate-based catalysis for degradable surfactant and drug-loaded nanoparticle applications
Polymer Chemistry, 2021, 12, 1244-1259
1560294 CIFC67 H88 N12 Ni2 O16P -114.843; 16.799; 17.052
111.232; 106.501; 104.907
3477.9Liu, Guan-Lin; Wu, Hsin-Wei; Lin, Zheng-Ian; Liao, Min-Gan; Su, Yu-Chia; Chen, Chih-Kuang; Ko, Bao-Tsan
Synthesis of functional CO2-based polycarbonates via dinuclear nickel nitrophenolate-based catalysis for degradable surfactant and drug-loaded nanoparticle applications
Polymer Chemistry, 2021, 12, 1244-1259
1560295 CIF
HKL
Paper
C13 H19 I N2 OP 21 21 218.9944; 11.325; 14.4042
90; 90; 90
1467.23Pham, Duyen N. K.; Chadeayne, Andrew R.; Golen, James A.; Manke, David R.
Bufotenidinium iodide
IUCrData, 2021, 6, x210123
1560298 CIFC22 H21 B F2 N2 O2P c a 2112.6493; 9.244; 18.0005
90; 90; 90
2104.8Meazza, Marta; Cruz, Carlos M.; Ortuño, Ana M.; Cuerva, Juan M.; Crovetto, Luis; Rios, Ramon
Studying the reactivity of alkyl substituted BODIPYs: first enantioselective addition of BODIPY to MBH carbonates
Chemical Science, 2021, 12, 4503-4508
1560301 CIFC144 H124 N2 P8 Ru2 SP n a 2125.3115; 44.5483; 10.235
90; 90; 90
11540.8Tanaka, Yuya; Kato, Yuya; Sugimoto, Kaho; Kawano, Reo; Tada, Tomofumi; Fujii, Shintaro; Kiguchi, Manabu; Akita, Munetaka
Single-molecule junctions of multinuclear organometallic wires: long-range carrier transport brought about by metal‒metal interaction
Chemical Science, 2021, 12, 4338-4344
1560302 CIFC198 H178 P12 Ru3 S2 Si2P -112.3659; 17.9279; 20.5933
108.974; 100.29; 100.6
4101.7Tanaka, Yuya; Kato, Yuya; Sugimoto, Kaho; Kawano, Reo; Tada, Tomofumi; Fujii, Shintaro; Kiguchi, Manabu; Akita, Munetaka
Single-molecule junctions of multinuclear organometallic wires: long-range carrier transport brought about by metal‒metal interaction
Chemical Science, 2021, 12, 4338-4344
1560303 CIFC126 H116 P8 Ru2 S Si2P -110.107; 15.3835; 37.02
83.51; 89.395; 86.371
5707.5Tanaka, Yuya; Kato, Yuya; Sugimoto, Kaho; Kawano, Reo; Tada, Tomofumi; Fujii, Shintaro; Kiguchi, Manabu; Akita, Munetaka
Single-molecule junctions of multinuclear organometallic wires: long-range carrier transport brought about by metal‒metal interaction
Chemical Science, 2021, 12, 4338-4344
1560304 CIFC25 H14 O3 SP 1 21/m 17.5851; 43.318; 8.593
90; 100.325; 90
2777.7Shaikh, Aslam C.; Veleta, José M.; Moutet, Jules; Gianetti, Thomas L.
Trioxatriangulenium (TOTA+) as a robust carbon-based Lewis acid in frustrated Lewis pair chemistry
Chemical Science, 2021, 12, 4841-4849
1560305 CIFC62 H41 B F24 N2 O3P -113.4502; 15.5304; 16.0826
106.612; 101.513; 105.375
2962.9Shaikh, Aslam C.; Veleta, José M.; Moutet, Jules; Gianetti, Thomas L.
Trioxatriangulenium (TOTA+) as a robust carbon-based Lewis acid in frustrated Lewis pair chemistry
Chemical Science, 2021, 12, 4841-4849
1560306 CIFC70.5 H56 B Cl F24 N3 O3 PP -113.1828; 17.102; 17.4082
114.902; 105.306; 96.778
3313.7Shaikh, Aslam C.; Veleta, José M.; Moutet, Jules; Gianetti, Thomas L.
Trioxatriangulenium (TOTA+) as a robust carbon-based Lewis acid in frustrated Lewis pair chemistry
Chemical Science, 2021, 12, 4841-4849
1560307 CIFC64 H50 B F24 O4 PP 1 21/c 119.596; 18.3533; 18.172
90; 108.476; 90
6198.7Shaikh, Aslam C.; Veleta, José M.; Moutet, Jules; Gianetti, Thomas L.
Trioxatriangulenium (TOTA+) as a robust carbon-based Lewis acid in frustrated Lewis pair chemistry
Chemical Science, 2021, 12, 4841-4849
1560308 CIFC23 H20 B Cl2 F4 O3 PP 1 21/c 110.071; 18.5524; 13.0354
90; 111.106; 90
2272.16Shaikh, Aslam C.; Veleta, José M.; Moutet, Jules; Gianetti, Thomas L.
Trioxatriangulenium (TOTA+) as a robust carbon-based Lewis acid in frustrated Lewis pair chemistry
Chemical Science, 2021, 12, 4841-4849
1560309 CIFC12 H8 N2 OP 1 21/c 114.2681; 3.9182; 17.1782
90; 109.954; 90
902.7Mayer, Robert J.; Allihn, Patrick W. A.; Hampel, Nathalie; Mayer, Peter; Sieber, Stephan A.; Ofial, Armin R.
Electrophilic reactivities of cyclic enones and α,β-unsaturated lactones
Chemical Science, 2021, 12, 4850-4865
1560310 CIFC13 H11 N O2P 1 21/c 110.6358; 9.5636; 10.4269
90; 100.187; 90
1043.87Mayer, Robert J.; Allihn, Patrick W. A.; Hampel, Nathalie; Mayer, Peter; Sieber, Stephan A.; Ofial, Armin R.
Electrophilic reactivities of cyclic enones and α,β-unsaturated lactones
Chemical Science, 2021, 12, 4850-4865
1560311 CIFC13 H11 N OP 1 21/c 110.8844; 9.9707; 9.168
90; 91.835; 90
994.45Mayer, Robert J.; Allihn, Patrick W. A.; Hampel, Nathalie; Mayer, Peter; Sieber, Stephan A.; Ofial, Armin R.
Electrophilic reactivities of cyclic enones and α,β-unsaturated lactones
Chemical Science, 2021, 12, 4850-4865
1560312 CIFC14 H13 N O2P 1 21/c 111.6656; 9.4061; 10.7626
90; 97.797; 90
1170.04Mayer, Robert J.; Allihn, Patrick W. A.; Hampel, Nathalie; Mayer, Peter; Sieber, Stephan A.; Ofial, Armin R.
Electrophilic reactivities of cyclic enones and α,β-unsaturated lactones
Chemical Science, 2021, 12, 4850-4865
1560313 CIFC23 H25 N O3C 1 2 121.9099; 6.5137; 14.4743
90; 115.663; 90
1861.93Mayer, Robert J.; Allihn, Patrick W. A.; Hampel, Nathalie; Mayer, Peter; Sieber, Stephan A.; Ofial, Armin R.
Electrophilic reactivities of cyclic enones and α,β-unsaturated lactones
Chemical Science, 2021, 12, 4850-4865
1560314 CIFC10 H11 N SP -17.3211; 7.9973; 8.7918
69.178; 74.117; 83.714
462.72Mayer, Robert J.; Allihn, Patrick W. A.; Hampel, Nathalie; Mayer, Peter; Sieber, Stephan A.; Ofial, Armin R.
Electrophilic reactivities of cyclic enones and α,β-unsaturated lactones
Chemical Science, 2021, 12, 4850-4865
1560315 CIFC13 H11 N O2P 1 21/n 112.1957; 7.1469; 12.4085
90; 105.197; 90
1043.72Mayer, Robert J.; Allihn, Patrick W. A.; Hampel, Nathalie; Mayer, Peter; Sieber, Stephan A.; Ofial, Armin R.
Electrophilic reactivities of cyclic enones and α,β-unsaturated lactones
Chemical Science, 2021, 12, 4850-4865
1560316 CIFC144 H123 Au11 Cl6 Cu N3 P7 S3P 1 21/c 117.0278; 37.9099; 26.2407
90; 99.317; 90
16715.5Wu, Haiming; Fang, Ye-Guang; Anumula, Rajini; Andrew, Gaya N.; Cui, Ganglong; Fang, Weihai; Luo, Zhixun; Yao, Jiannian
A mono-copper doped undeca-gold cluster with up-converted and anti-stokes emissions of fluorescence and phosphorescence.
Nanoscale, 2021, 13, 5300-5306
1560318 CIFC28 H29 I N OC 1 2/c 119.3573; 11.0456; 24.549
90; 101.158; 90
5149.68Tian, Minggang; Sun, Jie; Dong, Baoli; Ma, Yanyan; Lin, Weiying
Dual-Emissive Probe for Reversible Visualization of ΔΨ<sub>m</sub> Revealing Voltage Heterogeneity in a Single Mitochondrion.
Analytical chemistry, 2021, 93, 3493-3501
1560319 CIFC256 H477 N60 O72.5P 19.61; 17.037; 49.01
83.751; 88.217; 74.756
7696Lee, Jin Woo; Collins, Jennifer E.; Wendt, Karen L.; Chakrabarti, Debopam; Cichewicz, Robert H.
Leveraging Peptaibol Biosynthetic Promiscuity for Next-Generation Antiplasmodial Therapeutics.
Journal of natural products, 2021, 84, 503-517
1560320 CIFC46 H47 Br2 N2 Ni O6P 1 21/n 18.8225; 23.3225; 20.1979
90; 90; 90
4156Ma, Xin; Zhang, Yixin; Jian, Zhongbao
Tunable branching and living character in ethylene polymerization using “polyethylene glycol sandwich” α-diimine nickel catalysts
Polymer Chemistry, 2021, 12, 1236-1243
1560321 CIFC43 H43 Cl N2 O4 PdP 1 21/c 111.7634; 19.4057; 19.6256
90; 97.145; 90
4445.3Ma, Xin; Zhang, Yixin; Jian, Zhongbao
Tunable branching and living character in ethylene polymerization using “polyethylene glycol sandwich” α-diimine nickel catalysts
Polymer Chemistry, 2021, 12, 1236-1243
1560322 CIFC50 H55.5 Br2 N2 Ni O2P 1 21/c 124.6463; 40.129; 8.8579
90; 97.615; 90
8683.5Ma, Xin; Zhang, Yixin; Jian, Zhongbao
Tunable branching and living character in ethylene polymerization using “polyethylene glycol sandwich” α-diimine nickel catalysts
Polymer Chemistry, 2021, 12, 1236-1243
1560347 CIFC3.5 H4.5 Br0.5 N0.25 O0.25P 1 21/c 112.0433; 9.2013; 14.945
90; 101.24; 90
1624.4Ruan, Yang; Li, Qian-Hui; Shu, Lijin; Wan, Jun-Hua
A shape-persistent arylene ethynylene macrocycle with a multiple acetamide modified cavity: synthesis and gelation.
Soft matter, 2021, 17, 3242-3249
1560366 CIF
HKL
Paper
C20 H22 B N O2P -18.204; 9.7; 11.33
80.975; 81.242; 78.726
866.4Kanagawa, Mayu; Akagi, Kazuto; Okuno, Tsunehisa
9-[(<i>Z</i>)-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)ethenyl]-9<i>H</i>-carbazole
IUCrData, 2021, 6, x210142
1560367 CIFC35 H51 K Mn N3 O12P 1 21/c 19.4091; 15.768; 25.766
90; 94.907; 90
3808.7Yang, Yong; Ertem, Mehmed Z.; Duan, Lele
An amide-based second coordination sphere promotes the dimer pathway of Mn-catalyzed CO2-to-CO reduction at low overpotential
Chemical Science, 2021, 12, 4779-4788
1560368 CIFC16 H13 Br Mn N3 O4P 1 21/n 110.5955; 10.5011; 15.0027
90; 94.048; 90
1665.1Yang, Yong; Ertem, Mehmed Z.; Duan, Lele
An amide-based second coordination sphere promotes the dimer pathway of Mn-catalyzed CO2-to-CO reduction at low overpotential
Chemical Science, 2021, 12, 4779-4788
1560369 CIFC15 H11 Br Mn N3 O4P 1 21/c 110.65; 9.121; 16.456
90; 100.266; 90
1572.9Yang, Yong; Ertem, Mehmed Z.; Duan, Lele
An amide-based second coordination sphere promotes the dimer pathway of Mn-catalyzed CO2-to-CO reduction at low overpotential
Chemical Science, 2021, 12, 4779-4788
1560370 CIFC22 H20 N2 O9P 1 21 16.8601; 20.5081; 7.345
90; 92.708; 90
1032.2Yang, Jinghui; Xia, Yan
Mechanochemical generation of acid-degradable poly(enol ether)s
Chemical Science, 2021, 12, 4389-4394
1560371 CIFC9 H15 B F4 N6I 1 2/m 110.535; 6.4885; 18.7172
90; 92.323; 90
1278.39Stubbe, Jessica; Suhr, Simon; Beerhues, Julia; Nößler, Maite; Sarkar, Biprajit
The transformations of a methylene-bridged bis-triazolium salt: a mesoionic carbene based metallocage and analogues of TCNE and NacNac
Chemical Science, 2021, 12, 3170-3178
1560372 CIFC9 H16 B2 F8 N6P -17.1669; 9.7427; 11.6885
90.304; 91.835; 105.407
786.33Stubbe, Jessica; Suhr, Simon; Beerhues, Julia; Nößler, Maite; Sarkar, Biprajit
The transformations of a methylene-bridged bis-triazolium salt: a mesoionic carbene based metallocage and analogues of TCNE and NacNac
Chemical Science, 2021, 12, 3170-3178
1560373 CIFC22 H34 B4 F16 N14P -110.15; 11.83; 15.93
97.92; 92.65; 102.91
1841Stubbe, Jessica; Suhr, Simon; Beerhues, Julia; Nößler, Maite; Sarkar, Biprajit
The transformations of a methylene-bridged bis-triazolium salt: a mesoionic carbene based metallocage and analogues of TCNE and NacNac
Chemical Science, 2021, 12, 3170-3178
1560374 CIFC42 H57 Ag4 B4 F15.987 N27P -111.052; 14.637; 21.244
85.032; 81.796; 77.855
3319.6Stubbe, Jessica; Suhr, Simon; Beerhues, Julia; Nößler, Maite; Sarkar, Biprajit
The transformations of a methylene-bridged bis-triazolium salt: a mesoionic carbene based metallocage and analogues of TCNE and NacNac
Chemical Science, 2021, 12, 3170-3178
1560436 CIF
HKL
Paper
C13 H10 O2P 437.4781; 7.4781; 33.0219
90; 90; 90
1846.65Kotha, Sambasivarao; Fatma, Ambareen; Ansari, Saima
2,3-Dihydro-1<i>H</i>-cyclopenta[<i>b</i>]naphthalene-4,9-dione
IUCrData, 2021, 6, x210167
1560437 CIF
HKL
Paper
C28 H40 Cd2 Cl4 N6 OP 1 21/c 111.9747; 15.6483; 17.8804
90; 95.292; 90
3336.2Al-Sudani, Abdul-Razak H.; Abdulridha, Myasim Qasim; Kariuki, Benson M.
Di-μ-chlorido-bis(chlorido{8-[2-(dimethylamino)ethylamino]quinoline}cadmium) ethanol monosolvate
IUCrData, 2021, 6, x210150
1560480 CIFC25 H24 O6 SnP b c a11.9618; 16.8603; 23.0411
90; 90; 90
4646.9Wolzak, Lukas A.; Hermans, Joen J.; de Vries, Folkert; van den Berg, Keimpe J.; Reek, Joost N. H.; Tromp, Moniek; Korstanje, Ties J.
Mechanistic elucidation of monoalkyltin(iv)-catalyzed esterification
Catalysis Science & Technology, 2021, 11, 3326-3332
1560481 CIFC43 H34 Cl2 N2 O2P 1 21/c 18.09943; 31.2756; 13.9351
90; 98.024; 90
3495.4Huang, Quan; Guo, Qiang; Lan, Jingbo; Su, Rongchuan; Ran, You; Yang, Yudong; Bin, Zhengyang; You, Jingsong
Mechanically induced single-molecule white-light emission of excited-state intramolecular proton transfer (ESIPT) materials
Materials Horizons, 2021, 8, 1499-1508
1560482 CIFC42 H32 N2 O2P -110.5918; 11.6746; 13.726
103.723; 94.505; 107.201
1554.74Huang, Quan; Guo, Qiang; Lan, Jingbo; Su, Rongchuan; Ran, You; Yang, Yudong; Bin, Zhengyang; You, Jingsong
Mechanically induced single-molecule white-light emission of excited-state intramolecular proton transfer (ESIPT) materials
Materials Horizons, 2021, 8, 1499-1508
1560486 CIFC26 H16 F4 N2 O2P c a 2123.488; 13.488; 6.8185
90; 90; 90
2160.1Hamatani, Shota; Kitagawa, Daichi; Kobatake, Seiya
Fast T-Type Photochromic Crystals of Diarylbenzene
The Journal of Physical Chemistry C, 2021
1560487 CIFC26 H16 F4 N2 S2P 21 21 217.5367; 12.1564; 24.9857
90; 90; 90
2289.2Hamatani, Shota; Kitagawa, Daichi; Kobatake, Seiya
Fast T-Type Photochromic Crystals of Diarylbenzene
The Journal of Physical Chemistry C, 2021
1560488 CIFC26 H18 F2 N2 S2P 1 21/c 112.6491; 25.0889; 6.7996
90; 90.0296; 90
2157.87Hamatani, Shota; Kitagawa, Daichi; Kobatake, Seiya
Fast T-Type Photochromic Crystals of Diarylbenzene
The Journal of Physical Chemistry C, 2021
1560489 CIFC54.6 H59.2 Cl5.2 I2 O22 Si2 Zn6P -112.153; 12.359; 14.189
112.1; 108.14; 93.93
1834.3Petrus, Rafał; Utko, Józef; Gniłka, Radosław; Fleszar, Mariusz G.; Lis, Tadeusz; Sobota, Piotr
Solvothermal Alcoholysis Method for Recycling High-Consistency Silicone Rubber Waste
Macromolecules, 2021, 54, 2449-2465
1560490 CIFC42 H54 Mg2 O15P 1 21/c 115.325; 15.605; 36.005
90; 91.41; 90
8608Petrus, Rafał; Utko, Józef; Gniłka, Radosław; Fleszar, Mariusz G.; Lis, Tadeusz; Sobota, Piotr
Solvothermal Alcoholysis Method for Recycling High-Consistency Silicone Rubber Waste
Macromolecules, 2021, 54, 2449-2465
1560491 CIFC56 H58 Li2 Mg2 O20P -111.256; 11.97; 12.208
74.86; 64.78; 63.45
1326Petrus, Rafał; Utko, Józef; Gniłka, Radosław; Fleszar, Mariusz G.; Lis, Tadeusz; Sobota, Piotr
Solvothermal Alcoholysis Method for Recycling High-Consistency Silicone Rubber Waste
Macromolecules, 2021, 54, 2449-2465
1560492 CIFC64 H74 Mg2 Na2 O22P -112.842; 14.112; 19.578
83.06; 85.31; 64.38
3174Petrus, Rafał; Utko, Józef; Gniłka, Radosław; Fleszar, Mariusz G.; Lis, Tadeusz; Sobota, Piotr
Solvothermal Alcoholysis Method for Recycling High-Consistency Silicone Rubber Waste
Macromolecules, 2021, 54, 2449-2465
1560493 CIFC64 H74 K2 Mg2 O22P 42/n :217.645; 17.645; 20.477
90; 90; 90
6375.4Petrus, Rafał; Utko, Józef; Gniłka, Radosław; Fleszar, Mariusz G.; Lis, Tadeusz; Sobota, Piotr
Solvothermal Alcoholysis Method for Recycling High-Consistency Silicone Rubber Waste
Macromolecules, 2021, 54, 2449-2465
1560494 CIFC50 H46 Cl4 Li2 O18 Zn2P -111.011; 11.886; 12.07
74.65; 66.16; 63.99
1291.2Petrus, Rafał; Utko, Józef; Gniłka, Radosław; Fleszar, Mariusz G.; Lis, Tadeusz; Sobota, Piotr
Solvothermal Alcoholysis Method for Recycling High-Consistency Silicone Rubber Waste
Macromolecules, 2021, 54, 2449-2465
1560495 CIFC56 H58 Na2 O20 Zn2P -111.298; 11.637; 12.267
109.29; 104.32; 99.73
1418.5Petrus, Rafał; Utko, Józef; Gniłka, Radosław; Fleszar, Mariusz G.; Lis, Tadeusz; Sobota, Piotr
Solvothermal Alcoholysis Method for Recycling High-Consistency Silicone Rubber Waste
Macromolecules, 2021, 54, 2449-2465
1560496 CIFC34 H32 Cl4 Na2 O12 ZnP 1 21/n 116.603; 17.941; 25.607
90; 90.3; 90
7628Petrus, Rafał; Utko, Józef; Gniłka, Radosław; Fleszar, Mariusz G.; Lis, Tadeusz; Sobota, Piotr
Solvothermal Alcoholysis Method for Recycling High-Consistency Silicone Rubber Waste
Macromolecules, 2021, 54, 2449-2465
1560497 CIFC18 H23 Cl Ir N O2P 21 21 218.2268; 14.3426; 14.7546
90; 90; 90
1740.95Gatto, Giordano; De Palo, Alice; Carrasco, Ana C.; Pizarro, Ana M.; Zacchini, Stefano; Pampaloni, Guido; Marchetti, Fabio; Macchioni, Alceo
Modulating the water oxidation catalytic activity of iridium complexes by functionalizing the Cp*-ancillary ligand: hints on the nature of the active species
Catalysis Science & Technology, 2021, 11, 2885-2895
1560498 CIFC30 H32 Cl4 F2 Ir2P -18.7487; 17.713; 20.308
73.261; 89.913; 83.794
2994.6Gatto, Giordano; De Palo, Alice; Carrasco, Ana C.; Pizarro, Ana M.; Zacchini, Stefano; Pampaloni, Guido; Marchetti, Fabio; Macchioni, Alceo
Modulating the water oxidation catalytic activity of iridium complexes by functionalizing the Cp*-ancillary ligand: hints on the nature of the active species
Catalysis Science & Technology, 2021, 11, 2885-2895
1560499 CIFC57 H43 Cl3 N6 NiP 1 21/c 19.4132; 16.3463; 31.8
90; 91.407; 90
4891.6Abid, Seifallah; Gisbert, Yohan; Kojima, Mitsuru; Saffon-Merceron, Nathalie; Cuny, Jérôme; Kammerer, Claire; Rapenne, Gwénaël
Desymmetrised pentaporphyrinic gears mounted on metallo-organic anchors
Chemical Science, 2021, 12, 4709-4721
1560500 CIFC127 H101 B Br4 N12 Ni Ru S3P -116.1291; 19.1492; 24.8626
75.72; 89.677; 66.509
6787.8Abid, Seifallah; Gisbert, Yohan; Kojima, Mitsuru; Saffon-Merceron, Nathalie; Cuny, Jérôme; Kammerer, Claire; Rapenne, Gwénaël
Desymmetrised pentaporphyrinic gears mounted on metallo-organic anchors
Chemical Science, 2021, 12, 4709-4721
1560501 CIFC28 H36 Br O3 PP 21 21 219.15691; 16.71291; 17.53844
90; 90; 90
2684.06Huang, Qiu-Hong; Zhou, Qian-Yi; Yang, Chen; Chen, Li; Cheng, Jin-Pei; Li, Xin
Access to P-stereogenic compounds via desymmetrizing enantioselective bromination
Chemical Science, 2021, 12, 4582-4587
1560502 CIFC22 H20 O4P 21 21 218.9798; 11.0389; 17.2809
90; 90; 90
1713.01Lu, Xiao-Long; Qiu, Yuanyou; Yang, Baochao; He, Haibing; Gao, Shuanhu
Asymmetric total synthesis of (+)-xestoquinone and (+)-adociaquinones A and B
Chemical Science, 2021, 12, 4747-4752
1560503 CIFC22 H20 O4P 21 21 219.1038; 11.1728; 17.3015
90; 90; 90
1759.82Lu, Xiao-Long; Qiu, Yuanyou; Yang, Baochao; He, Haibing; Gao, Shuanhu
Asymmetric total synthesis of (+)-xestoquinone and (+)-adociaquinones A and B
Chemical Science, 2021, 12, 4747-4752
1560504 CIFC26 H32 Cl2 O5P 21 21 217.4407; 11.6989; 28.3425
90; 90; 90
2467.16Lu, Xiao-Long; Qiu, Yuanyou; Yang, Baochao; He, Haibing; Gao, Shuanhu
Asymmetric total synthesis of (+)-xestoquinone and (+)-adociaquinones A and B
Chemical Science, 2021, 12, 4747-4752
1560527 CIFC40 H52 B20P 32 2 111.3287; 11.3287; 29.3678
90; 90; 120
3264.1Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560528 CIFC18 H38 B20 Cl2C 1 2/c 133.909; 13.6784; 13.6791
90; 108.58; 90
6014Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560529 CIFC22 H46 B20 Cl2P 21 21 2111.7538; 12.8616; 21.8976
90; 90; 90
3310.3Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560530 CIFC44 H60 B20P 1 21/n 111.4361; 19.1205; 21.4742
90; 94.001; 90
4684.2Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560531 CIFC27 H54.5 B20 O0.25P -113.3453; 16.5248; 18.4539
82.5401; 78.3148; 83.5363
3935.9Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560532 CIFC30 H60 B20C 1 2/c 124.2513; 10.403; 18.2107
90; 120.094; 90
3975Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560533 CIFC22 H48 B20P 21 21 2110.3911; 13.0014; 24.381
90; 90; 90
3293.8Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560534 CIFC26 H56 B20P 1 21/n 113.3754; 13.4901; 19.9071
90; 91.104; 90
3591.3Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560535 CIFC24 H54 B20P 1 21/n 113.2519; 11.98; 21.8685
90; 105.683; 90
3342.5Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560536 CIFC26 H62 B20 Si2P -111.326; 12.468; 15.493
108.096; 95.522; 104.001
1982.7Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560537 CIFC38 H59 B20P -111.6972; 13.3199; 15.5282
75.8963; 79.1092; 66.3809
2138.51Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560538 CIFC27 H48 B20P 1 21/c 111.0591; 17.981; 17.9274
90; 92.3086; 90
3562Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560539 CIFC14 H30 B10P 1 21/c 111.1066; 27.939; 12.8423
90; 90.244; 90
3985Zhang, Jie; Xie, Zuowei
Tandem [4 + 2]/[2 + 2] cycloaddition of o-carboryne with enynes: facile construction of carborane-fused tricyclics
Chemical Science, 2021, 12, 5616-5620
1560599 CIFC30 H18 N4 SR -3 :H25.7763; 25.7763; 17.9852
90; 90; 120
10348.7Liu, Tiantian; Chen, Xiaojie; Zhao, Juan; Wei, Weichun; Mao, Zhu; Wu, William; Jiao, Shibo; Liu, Yang; Yang, Zhiyong; Chi, Zhenguo
Hybridized local and charge-transfer excited state fluorophores enabling organic light-emitting diodes with record high efficiencies close to 20%
Chemical Science, 2021, 12, 5171-5176
1560600 CIFC47 H52 Cl2 N4 SP -110.6634; 10.9432; 18.341
88.604; 83.994; 82.942
2112.2Liu, Tiantian; Chen, Xiaojie; Zhao, Juan; Wei, Weichun; Mao, Zhu; Wu, William; Jiao, Shibo; Liu, Yang; Yang, Zhiyong; Chi, Zhenguo
Hybridized local and charge-transfer excited state fluorophores enabling organic light-emitting diodes with record high efficiencies close to 20%
Chemical Science, 2021, 12, 5171-5176
1560601 CIFC64 H72 N4 SP -112.041; 15.9608; 16.4529
114.757; 104.294; 93.279
2735.8Liu, Tiantian; Chen, Xiaojie; Zhao, Juan; Wei, Weichun; Mao, Zhu; Wu, William; Jiao, Shibo; Liu, Yang; Yang, Zhiyong; Chi, Zhenguo
Hybridized local and charge-transfer excited state fluorophores enabling organic light-emitting diodes with record high efficiencies close to 20%
Chemical Science, 2021, 12, 5171-5176
1560602 CIFC29 H23 F O5P 1 21 19.9631; 9.1494; 13.3605
90; 102.001; 90
1191.28Zheng, Haifeng; Wang, Rui; Wang, Kan; Wherritt, Daniel; Arman, Hadi; Doyle, Michael P.
Formal [4 + 4]-, [4 + 3]-, and [4 + 2]-cycloaddition reactions of donor‒acceptor cyclobutenes, cyclopropenes and siloxyalkynes induced by Brønsted acid catalysis
Chemical Science, 2021, 12, 4819-4824
1560603 CIFC15 H15 F O2P 1 21/n 17.3867; 19.0785; 9.3357
90; 111.972; 90
1220.09Zheng, Haifeng; Wang, Rui; Wang, Kan; Wherritt, Daniel; Arman, Hadi; Doyle, Michael P.
Formal [4 + 4]-, [4 + 3]-, and [4 + 2]-cycloaddition reactions of donor‒acceptor cyclobutenes, cyclopropenes and siloxyalkynes induced by Brønsted acid catalysis
Chemical Science, 2021, 12, 4819-4824
1560604 CIFC28 H20 F N O4P 1 21/c 112.28538; 20.3181; 8.91344
90; 99.0372; 90
2197.31Zheng, Haifeng; Wang, Rui; Wang, Kan; Wherritt, Daniel; Arman, Hadi; Doyle, Michael P.
Formal [4 + 4]-, [4 + 3]-, and [4 + 2]-cycloaddition reactions of donor‒acceptor cyclobutenes, cyclopropenes and siloxyalkynes induced by Brønsted acid catalysis
Chemical Science, 2021, 12, 4819-4824
1560605 CIFC44 H49 Cl2 Na O6P -19.6802; 11.1157; 19.9995
74.62; 88.918; 78.973
2035.5Wang, Xinya; Wang, Xiaohua; Zhen, Nuo; Gu, Jin; Zhang, Hao; Dong, Bo; Wang, Feng; Liu, Heng
Sodium complexes bearing cavity-like conformations: a highly active and well-controlled catalytic system for macrolactone homo- and copolymerization
Polymer Chemistry, 2021, 12, 1957-1966
1560621 CIFC56.08 H50 Cl12.16 N4 Ni SbP -19.2156; 20.0257; 21.5606
114.68; 94.469; 98.787
3528.32Miyagawa, Kazuya; Hisaki, Ichiro; Fukui, Norihito; Shinokubo, Hiroshi
Redox-induced reversible [2 + 2] cycloaddition of an etheno-fused diporphyrin
Chemical Science, 2021, 12, 5224-5229
1560622 CIFC254 H248 N16 Ni4P -121.0654; 22.4572; 25.0542
104.279; 98.423; 111.649
10298.3Miyagawa, Kazuya; Hisaki, Ichiro; Fukui, Norihito; Shinokubo, Hiroshi
Redox-induced reversible [2 + 2] cycloaddition of an etheno-fused diporphyrin
Chemical Science, 2021, 12, 5224-5229
1560703 CIFC38 H32 Cl2 Ir N8 PtC 1 2/c 113.0437; 24.3865; 28.8657
90; 101.971; 90
8982.2Wu, Si-Hai; Ma, Dian-Xue; Gong, Zhong-Liang; Ma, Junjie; Shao, Jiang-Yang; Yang, Rong; Zhong, Yu-Wu
Synthesis, Photophysical, and Computational Studies of a Bridged Ir^III^-Pt^II^ Heterodimetallic Complex
Crystals, 2021, 11, 236
1560704 CIFC23 H30 N2 O5C 1 2 119.5794; 9.9646; 12.819
90; 113.599; 90
2291.84Chear, Nelson Jeng-Yeou; León, Francisco; Sharma, Abhisheak; Kanumuri, Siva Rama Raju; Zwolinski, Grant; Abboud, Khalil A.; Singh, Darshan; Restrepo, Luis F.; Patel, Avi; Hiranita, Takato; Ramanathan, Surash; Hampson, Aidan J.; McMahon, Lance R.; McCurdy, Christopher R.
Exploring the Chemistry of Alkaloids from Malaysian Mitragyna speciosa (Kratom) and the Role of Oxindoles on Human Opioid Receptors
Journal of Natural Products, 2021
1560705 CIFC11 H8 O5P 1 21/n 14.9167; 16.6655; 11.2024
90; 98.726; 90
907.29Norman, Edward Owen; Tuohey, Hayden; Pizzi, David; Saidah, Milane; Bell, Rachael; Brkljača, Robert; White, Jonathan M.; Gasser, Robin B.; Taki, Aya C.; Urban, Sylvia
Phytochemical Profiling and Biological Activity of the Australian Carnivorous Plant, <i>Drosera magna</i>.
Journal of natural products, 2021
1560706 CIF
HKL
Paper
C19 H22 F N5 OP b c a10.6982; 19.8473; 16.7642
90; 90; 90
3559.5Andreev, Stanislav; Schollmeyer, Dieter; Koch, Pierre
1-{3-[(7-Fluoro-9<i>H</i>-pyrimido[4,5-<i>b</i>]indol-4-yl)(methyl)amino]piperidin-1-yl}propan-1-one
IUCrData, 2021, 6, x210159
1560707 CIF
HKL
Paper
C30 H31 N O3 S2P -4 21 c25.375; 25.375; 8.6456
90; 90; 90
5566.82Vinotha, G.; Sundar, T. V.; Sharmila, N.
13-Benzyl-4,11-dihydroxy-1,8-diphenyl-2,9-dithia-13-azadispiro[4.1.4.3]tetradecan-6-one
IUCrData, 2021, 6, x210210
1560708 CIF
HKL
Paper
C28 H24 N3 O6.5P 1 21/c 118.248; 10.304; 27.541
90; 101.41; 90
5076.1Li, Yu-Long; Zhou, Jin; Jiang, Hong; Sun, Hong-Shun; Li, Rui-Zhe; Liu, Sha-Li; Zhang, Xu-Dong
Dimethyl 3,3'-[(4-nitrophenyl)methylene]bis(1<i>H</i>-indole-2-carboxylate) ethanol hemisolvate
IUCrData, 2021, 6, x210057
1560717 CIFC17.5 H29 N9 Ni O0.5 S2P 1 21/n 114.8018; 16.4349; 19.1348
90; 102.494; 90
4544.6Rubín-Osanz, Marcos; Lambert, François; Shao, Feng; Rivière, Eric; Guillot, Régis; Suaud, Nicolas; Guihéry, Nathalie; Zueco, David; Barra, Anne-Laure; Mallah, Talal; Luis, Fernando
Chemical tuning of spin clock transitions in molecular monomers based on nuclear spin-free Ni(ii)
Chemical Science, 2021, 12, 5123-5133
1560718 CIFC38 H38 Cl6 N8 S6P -110.2559; 15.7584; 16.1989
67.534; 71.56; 75.75
2271.55Ding, Yanjun; Alimi, Lukman O.; Moosa, Basem; Maaliki, Carine; Jacquemin, Johan; Huang, Feihe; Khashab, Niveen M.
Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages
Chemical Science, 2021, 12, 5315-5318
1560719 CIFC45 H45 N8 S6P 1 21/n 112.8314; 15.7916; 21.178
90; 92.517; 90
4287.12Ding, Yanjun; Alimi, Lukman O.; Moosa, Basem; Maaliki, Carine; Jacquemin, Johan; Huang, Feihe; Khashab, Niveen M.
Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages
Chemical Science, 2021, 12, 5315-5318
1560720 CIFC42 H48 N8 S6P c a 2114.1011; 14.1412; 41.847
90; 90; 90
8344.6Ding, Yanjun; Alimi, Lukman O.; Moosa, Basem; Maaliki, Carine; Jacquemin, Johan; Huang, Feihe; Khashab, Niveen M.
Selective adsorptive separation of cyclohexane over benzene using thienothiophene cages
Chemical Science, 2021, 12, 5315-5318
1560721 CIFCa3 Ge3 O12 Zn ZrI a -3 d12.5541; 12.5541; 12.5541
90; 90; 90
1978.59Su, C.; Fang, L.; Ao, L.; Chen, J.; Sun, C.; Yang, A.; Tang, Y.; Liu, L.
Structure, Raman spectra and microwave dielectric properties of novel garnet-type Ca3MZrGe3O12 (M = Co, Zn) ceramics
Journal of Asian Ceramic Societies, 2021, 9, 424-432
1560722 CIFCa3 Co Ge3 O12 ZrI a -3 d12.5199; 12.5199; 12.5199
90; 90; 90
1962.47Su, C.; Fang, L.; Ao, L.; Chen, J.; Sun, C.; Yang, A.; Tang, Y.; Liu, L.
Structure, Raman spectra and microwave dielectric properties of novel garnet-type Ca3MZrGe3O12 (M = Co, Zn) ceramics
Journal of Asian Ceramic Societies, 2021, 9, 424-432
1560723 CIFC26 H46 N3 P Si3P 1 21/n 111.204; 17.824; 15.275
90; 97.916; 90
3021.4Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Interconversion between a silaimine and an aminosilylene supported by an iminophosphonamide ligand.
Chemical communications (Cambridge, England), 2021, 57, 3203-3206
1560724 CIFC32 H52 N3 P Se Si3P 1 21/n 110.9693; 19.9448; 15.9939
90; 91.8748; 90
3497.3Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Interconversion between a silaimine and an aminosilylene supported by an iminophosphonamide ligand.
Chemical communications (Cambridge, England), 2021, 57, 3203-3206
1560725 CIFC20 H28 Cl N2 P Se SiC 1 2/c 115.6803; 10.0386; 42.425
90; 92.403; 90
6672.2Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Interconversion between a silaimine and an aminosilylene supported by an iminophosphonamide ligand.
Chemical communications (Cambridge, England), 2021, 57, 3203-3206
1560726 CIFC6 H14 Cl N2 Na O6P 1 2/n 19.1493; 10.1833; 13.22
90; 108.244; 90
1169.8Prakash, Prabhat; Ardhra, Shylendran; Fall, Birane; Zdilla, Michael J.; Wunder, Stephanie L.; Venkatnathan, Arun
Solvate sponge crystals of (DMF)3NaClO4: reversible pressure/temperature controlled juicing in a melt/press-castable sodium-ion conductor
Chemical Science, 2021, 12, 5574-5581
1560727 CIFC130 H93 Br4 Co F12 N27 Ni4 O12 S4P 1 21/c 131.1965; 18.5947; 28.7563
90; 110.013; 90
15673.9Scott, Aaron J.; Vallejo, Julia; Sarkar, Arup; Smythe, Lucy; Regincós Martí, E.; Nichol, Gary S.; Klooster, Wim T.; Coles, Simon J.; Murrie, Mark; Rajaraman, Gopalan; Piligkos, Stergios; Lusby, Paul J.; Brechin, Euan K.
Exploiting host‒guest chemistry to manipulate magnetic interactions in metallosupramolecular M4L6 tetrahedral cages
Chemical Science, 2021, 12, 5134-5142
1560728 CIFC154 H126 Cl4 F18 N38 Ni5 O18 S6C 1 2/c 131.8614; 20.267; 26.4739
90; 114.773; 90
15521.9Scott, Aaron J.; Vallejo, Julia; Sarkar, Arup; Smythe, Lucy; Regincós Martí, E.; Nichol, Gary S.; Klooster, Wim T.; Coles, Simon J.; Murrie, Mark; Rajaraman, Gopalan; Piligkos, Stergios; Lusby, Paul J.; Brechin, Euan K.
Exploiting host‒guest chemistry to manipulate magnetic interactions in metallosupramolecular M4L6 tetrahedral cages
Chemical Science, 2021, 12, 5134-5142
1560729 CIFC126 H84 Cl4 F18 Mn N24 Ni4 O18 S6C 1 2/c 132.5915; 19.6893; 26.8651
90; 116.807; 90
15386.7Scott, Aaron J.; Vallejo, Julia; Sarkar, Arup; Smythe, Lucy; Regincós Martí, E.; Nichol, Gary S.; Klooster, Wim T.; Coles, Simon J.; Murrie, Mark; Rajaraman, Gopalan; Piligkos, Stergios; Lusby, Paul J.; Brechin, Euan K.
Exploiting host‒guest chemistry to manipulate magnetic interactions in metallosupramolecular M4L6 tetrahedral cages
Chemical Science, 2021, 12, 5134-5142
1560730 CIFC147.5 H124 Br2 F24 Fe0.5 N24 Ni4 O29 S7.5C 1 2/c 131.3026; 20.566; 26.4213
90; 112.812; 90
15678.8Scott, Aaron J.; Vallejo, Julia; Sarkar, Arup; Smythe, Lucy; Regincós Martí, E.; Nichol, Gary S.; Klooster, Wim T.; Coles, Simon J.; Murrie, Mark; Rajaraman, Gopalan; Piligkos, Stergios; Lusby, Paul J.; Brechin, Euan K.
Exploiting host‒guest chemistry to manipulate magnetic interactions in metallosupramolecular M4L6 tetrahedral cages
Chemical Science, 2021, 12, 5134-5142
1560731 CIFC126 H84 Br4 Cu F18 N24 Ni4 O18 S6C 1 2/c 133.6581; 19.3004; 27.7984
90; 119.638; 90
15695.6Scott, Aaron J.; Vallejo, Julia; Sarkar, Arup; Smythe, Lucy; Regincós Martí, E.; Nichol, Gary S.; Klooster, Wim T.; Coles, Simon J.; Murrie, Mark; Rajaraman, Gopalan; Piligkos, Stergios; Lusby, Paul J.; Brechin, Euan K.
Exploiting host‒guest chemistry to manipulate magnetic interactions in metallosupramolecular M4L6 tetrahedral cages
Chemical Science, 2021, 12, 5134-5142
1560732 CIFC132 H88 F24 N26 Ni4 O24 S8C 1 2/c 131.7631; 20.376; 26.2656
90; 114.263; 90
15497.7Scott, Aaron J.; Vallejo, Julia; Sarkar, Arup; Smythe, Lucy; Regincós Martí, E.; Nichol, Gary S.; Klooster, Wim T.; Coles, Simon J.; Murrie, Mark; Rajaraman, Gopalan; Piligkos, Stergios; Lusby, Paul J.; Brechin, Euan K.
Exploiting host‒guest chemistry to manipulate magnetic interactions in metallosupramolecular M4L6 tetrahedral cages
Chemical Science, 2021, 12, 5134-5142
1560733 CIFC151 H120 Cl4 F21 Fe N36 Ni4 O21 S7C 1 2/c 131.6627; 20.3859; 26.5585
90; 114.491; 90
15600.4Scott, Aaron J.; Vallejo, Julia; Sarkar, Arup; Smythe, Lucy; Regincós Martí, E.; Nichol, Gary S.; Klooster, Wim T.; Coles, Simon J.; Murrie, Mark; Rajaraman, Gopalan; Piligkos, Stergios; Lusby, Paul J.; Brechin, Euan K.
Exploiting host‒guest chemistry to manipulate magnetic interactions in metallosupramolecular M4L6 tetrahedral cages
Chemical Science, 2021, 12, 5134-5142
1560734 CIFC138 H105 Cl4 Co F18 N28 Ni4 O19 S6P 1 21/n 120.4016; 29.7181; 26.8106
90; 91.1568; 90
16251.9Scott, Aaron J.; Vallejo, Julia; Sarkar, Arup; Smythe, Lucy; Regincós Martí, E.; Nichol, Gary S.; Klooster, Wim T.; Coles, Simon J.; Murrie, Mark; Rajaraman, Gopalan; Piligkos, Stergios; Lusby, Paul J.; Brechin, Euan K.
Exploiting host‒guest chemistry to manipulate magnetic interactions in metallosupramolecular M4L6 tetrahedral cages
Chemical Science, 2021, 12, 5134-5142
1560748 CIFC12 H20 Cl2 N4 O2 SP 1 21/n 16.966; 20.504; 11.68
90; 98.372; 90
1650.5Takahashi, Masae; Kowada, Mitsuru; Matsui, Hiroshi; Kwon, Eunsang; Ikemoto, Yuka
Temperature-Dependent Low-Frequency Vibrations of Thiamine Crystal Containing Hydrated Ions.
The journal of physical chemistry. A, 2021, 125, 1837-1844
1560749 CIFC68 H65 Dy O P4 S4P -111.2686; 12.7447; 21.7296
89.265; 88.319; 83.122
3096.8Thomas-Hargreaves, Lewis R.; Giansiracusa, Marcus J.; Gregson, Matthew; Zanda, Emanuele; O'Donnell, Felix; Wooles, Ashley J.; Chilton, Nicholas F.; Liddle, Stephen T.
Correlating axial and equatorial ligand field effects to the single-molecule magnet performances of a family of dysprosium bis-methanediide complexes
Chemical Science, 2021, 12, 3911-3920
1560750 CIFC54 H49 O P4 S4 YP 1 21/n 110.8536; 22.5853; 21.0093
90; 99.013; 90
5086.5Thomas-Hargreaves, Lewis R.; Giansiracusa, Marcus J.; Gregson, Matthew; Zanda, Emanuele; O'Donnell, Felix; Wooles, Ashley J.; Chilton, Nicholas F.; Liddle, Stephen T.
Correlating axial and equatorial ligand field effects to the single-molecule magnet performances of a family of dysprosium bis-methanediide complexes
Chemical Science, 2021, 12, 3911-3920
1560751 CIFC116 H120 Dy2 K2 O8 P8 S8P -113.521; 20.9074; 22.2017
71.645; 79.408; 84.373
5849.94Thomas-Hargreaves, Lewis R.; Giansiracusa, Marcus J.; Gregson, Matthew; Zanda, Emanuele; O'Donnell, Felix; Wooles, Ashley J.; Chilton, Nicholas F.; Liddle, Stephen T.
Correlating axial and equatorial ligand field effects to the single-molecule magnet performances of a family of dysprosium bis-methanediide complexes
Chemical Science, 2021, 12, 3911-3920
1560752 CIFC76 H92 K N2 O8 P4 S4 YP -111.9072; 12.5346; 26.216
81.43; 83.556; 84.318
3831.2Thomas-Hargreaves, Lewis R.; Giansiracusa, Marcus J.; Gregson, Matthew; Zanda, Emanuele; O'Donnell, Felix; Wooles, Ashley J.; Chilton, Nicholas F.; Liddle, Stephen T.
Correlating axial and equatorial ligand field effects to the single-molecule magnet performances of a family of dysprosium bis-methanediide complexes
Chemical Science, 2021, 12, 3911-3920
1560753 CIFC116 H120 K2 O8 P8 S8 Y2P -113.4728; 20.8633; 22.1735
71.523; 79.315; 84.386
5803.8Thomas-Hargreaves, Lewis R.; Giansiracusa, Marcus J.; Gregson, Matthew; Zanda, Emanuele; O'Donnell, Felix; Wooles, Ashley J.; Chilton, Nicholas F.; Liddle, Stephen T.
Correlating axial and equatorial ligand field effects to the single-molecule magnet performances of a family of dysprosium bis-methanediide complexes
Chemical Science, 2021, 12, 3911-3920
1560754 CIFC93 H116 Dy K N4 O7 P4 Si4P 1 21/n 113.23949; 23.5137; 30.0645
90; 97.5329; 90
9278.6Thomas-Hargreaves, Lewis R.; Giansiracusa, Marcus J.; Gregson, Matthew; Zanda, Emanuele; O'Donnell, Felix; Wooles, Ashley J.; Chilton, Nicholas F.; Liddle, Stephen T.
Correlating axial and equatorial ligand field effects to the single-molecule magnet performances of a family of dysprosium bis-methanediide complexes
Chemical Science, 2021, 12, 3911-3920
1560755 CIFC62 H70 Dy Na O6 P4 S4P 1 21/c 114.1523; 30.8391; 15.6028
90; 110.56; 90
6376Thomas-Hargreaves, Lewis R.; Giansiracusa, Marcus J.; Gregson, Matthew; Zanda, Emanuele; O'Donnell, Felix; Wooles, Ashley J.; Chilton, Nicholas F.; Liddle, Stephen T.
Correlating axial and equatorial ligand field effects to the single-molecule magnet performances of a family of dysprosium bis-methanediide complexes
Chemical Science, 2021, 12, 3911-3920
1560756 CIFC62 H70 Gd Na O6 P4 S4P 1 21/c 114.1998; 30.9404; 15.6211
90; 110.508; 90
6428.1Thomas-Hargreaves, Lewis R.; Giansiracusa, Marcus J.; Gregson, Matthew; Zanda, Emanuele; O'Donnell, Felix; Wooles, Ashley J.; Chilton, Nicholas F.; Liddle, Stephen T.
Correlating axial and equatorial ligand field effects to the single-molecule magnet performances of a family of dysprosium bis-methanediide complexes
Chemical Science, 2021, 12, 3911-3920
1560757 CIFC72 H84 Dy K N2 O7 P4 S4P -115.0677; 15.8625; 17.3285
97.435; 91.979; 116.19
3665.66Thomas-Hargreaves, Lewis R.; Giansiracusa, Marcus J.; Gregson, Matthew; Zanda, Emanuele; O'Donnell, Felix; Wooles, Ashley J.; Chilton, Nicholas F.; Liddle, Stephen T.
Correlating axial and equatorial ligand field effects to the single-molecule magnet performances of a family of dysprosium bis-methanediide complexes
Chemical Science, 2021, 12, 3911-3920
1560758 CIFC62 H70 Na O6 P4 S4 YP 1 21/c 114.155; 30.9664; 15.632
90; 110.731; 90
6408.3Thomas-Hargreaves, Lewis R.; Giansiracusa, Marcus J.; Gregson, Matthew; Zanda, Emanuele; O'Donnell, Felix; Wooles, Ashley J.; Chilton, Nicholas F.; Liddle, Stephen T.
Correlating axial and equatorial ligand field effects to the single-molecule magnet performances of a family of dysprosium bis-methanediide complexes
Chemical Science, 2021, 12, 3911-3920
1560759 CIFC26 H24 F6 N2 O6 Pd2P 1 21/n 117.9432; 15.8649; 21.6563
90; 114.273; 90
5619.8Tóth, Balázs L.; Monory, Anna; Egyed, Orsolya; Domján, Attila; Bényei, Attila; Szathury, Bálint; Novák, Zoltán; Stirling, András
The ortho effect in directed C‒H activation
Chemical Science, 2021, 12, 5152-5163
1560760 CIFC35 H30 F6 N2 O7 Pd2F d d 237.712; 13.024; 15.254
90; 90; 90
7492Tóth, Balázs L.; Monory, Anna; Egyed, Orsolya; Domján, Attila; Bényei, Attila; Szathury, Bálint; Novák, Zoltán; Stirling, András
The ortho effect in directed C‒H activation
Chemical Science, 2021, 12, 5152-5163
1560761 CIFC33 H26 F6 N2 O7 Pd2P 1 21/c 119.2535; 8.0799; 21.9245
90; 93.765; 90
3403.4Tóth, Balázs L.; Monory, Anna; Egyed, Orsolya; Domján, Attila; Bényei, Attila; Szathury, Bálint; Novák, Zoltán; Stirling, András
The ortho effect in directed C‒H activation
Chemical Science, 2021, 12, 5152-5163
1560762 CIFC34 H26 F6 N2 O8 Pd2C 1 2/c 132.598; 12.5843; 22.685
90; 128.447; 90
7288.2Tóth, Balázs L.; Monory, Anna; Egyed, Orsolya; Domján, Attila; Bényei, Attila; Szathury, Bálint; Novák, Zoltán; Stirling, András
The ortho effect in directed C‒H activation
Chemical Science, 2021, 12, 5152-5163
1560763 CIFC37 H34 F6 N2 O7 Pd2F d d 237.337; 13.419; 15.197
90; 90; 90
7614Tóth, Balázs L.; Monory, Anna; Egyed, Orsolya; Domján, Attila; Bényei, Attila; Szathury, Bálint; Novák, Zoltán; Stirling, András
The ortho effect in directed C‒H activation
Chemical Science, 2021, 12, 5152-5163
1560764 CIFC17 H14 F3 N O4 PdC 1 2/c 120.9754; 13.1973; 15.3039
90; 125.008; 90
3469.9Tóth, Balázs L.; Monory, Anna; Egyed, Orsolya; Domján, Attila; Bényei, Attila; Szathury, Bálint; Novák, Zoltán; Stirling, András
The ortho effect in directed C‒H activation
Chemical Science, 2021, 12, 5152-5163
1560765 CIFC42 H26 N2P 1 21/c 113.9636; 12.6503; 17.3356
90; 103.979; 90
2971.5Dhbaibi, Kais; Abella, Laura; Meunier-Della-Gatta, Sylvia; Roisnel, Thierry; Vanthuyne, Nicolas; Jamoussi, Bassem; Pieters, Grégory; Racine, Benoît; Quesnel, Etienne; Autschbach, Jochen; Crassous, Jeanne; Favereau, Ludovic
Achieving high circularly polarized luminescence with push‒pull helicenic systems: from rationalized design to top-emission CP-OLED applications
Chemical Science, 2021, 12, 5522-5533
1560766 CIFC42 H22 N2 O4C 1 2/c 118.9074; 9.4843; 18.9118
90; 97.294; 90
3363.9Dhbaibi, Kais; Abella, Laura; Meunier-Della-Gatta, Sylvia; Roisnel, Thierry; Vanthuyne, Nicolas; Jamoussi, Bassem; Pieters, Grégory; Racine, Benoît; Quesnel, Etienne; Autschbach, Jochen; Crassous, Jeanne; Favereau, Ludovic
Achieving high circularly polarized luminescence with push‒pull helicenic systems: from rationalized design to top-emission CP-OLED applications
Chemical Science, 2021, 12, 5522-5533
1560767 CIFC44 H22 N2P 41 21 214.6129; 14.6129; 29.4748
90; 90; 90
6294Dhbaibi, Kais; Abella, Laura; Meunier-Della-Gatta, Sylvia; Roisnel, Thierry; Vanthuyne, Nicolas; Jamoussi, Bassem; Pieters, Grégory; Racine, Benoît; Quesnel, Etienne; Autschbach, Jochen; Crassous, Jeanne; Favereau, Ludovic
Achieving high circularly polarized luminescence with push‒pull helicenic systems: from rationalized design to top-emission CP-OLED applications
Chemical Science, 2021, 12, 5522-5533
1560800 CIFC23 H28.5 Cl1.5 N8 O0.25 S2 ZnC 1 2/c 114.257; 11.4474; 17.156
90; 108.496; 90
2655.3Gilleran, John A.; Yu, Xin; Blayney, Alan J.; Bencivenga, Anthony F.; Na, Bing; Augeri, David J.; Blanden, Adam R.; Kimball, S. David; Loh, Stewart N.; Roberge, Jacques Y.; Carpizo, Darren R.
Benzothiazolyl and Benzoxazolyl Hydrazones Function as Zinc Metallochaperones to Reactivate Mutant p53.
Journal of medicinal chemistry, 2021, 64, 2024-2045
1560801 CIFC32 H30 N8 O S2 ZnP 1 21/c 110.3073; 29.5898; 9.8383
90; 90.5116; 90
3000.5Gilleran, John A.; Yu, Xin; Blayney, Alan J.; Bencivenga, Anthony F.; Na, Bing; Augeri, David J.; Blanden, Adam R.; Kimball, S. David; Loh, Stewart N.; Roberge, Jacques Y.; Carpizo, Darren R.
Benzothiazolyl and Benzoxazolyl Hydrazones Function as Zinc Metallochaperones to Reactivate Mutant p53.
Journal of medicinal chemistry, 2021, 64, 2024-2045
1560802 CIFC30 H28 O10P 21 21 218.381; 9.3907; 32.0572
90; 90; 90
2523.01Li, Yu-Ting; Yang, Chan; Wu, Yan; Lv, Jun-Jiang; Feng, Xiao; Tian, Xiaofei; Zhou, Zhengzheng; Pan, Xiaoyan; Liu, Shuwen; Tian, Li-Wen
Axial Chiral Binaphthoquinone and Perylenequinones from the Stromata of <i>Hypocrella bambusae</i> Are SARS-CoV-2 Entry Inhibitors.
Journal of natural products, 2021, 84, 436-443
1560803 CIFC30 H32 O12P 21 21 2113.1752; 17.53391; 23.9821
90; 90; 90
5540.17Li, Yu-Ting; Yang, Chan; Wu, Yan; Lv, Jun-Jiang; Feng, Xiao; Tian, Xiaofei; Zhou, Zhengzheng; Pan, Xiaoyan; Liu, Shuwen; Tian, Li-Wen
Axial Chiral Binaphthoquinone and Perylenequinones from the Stromata of <i>Hypocrella bambusae</i> Are SARS-CoV-2 Entry Inhibitors.
Journal of natural products, 2021, 84, 436-443
1560804 CIFC20 H28 O5P 21 21 217.9582; 23.6809; 10.0261
90; 90; 90
1889.49Xue, Peng-Hui; Zhang, Nan; Liu, Da; Zhang, Qing-Ran; Duan, Jing-Shi; Yu, Ya-Qin; Li, Jin-Yan; Cao, Shi-Jie; Zhao, Feng; Kang, Ning; Qiu, Feng
Cytotoxic and Anti-Inflammatory Sesquiterpenes from the Whole Plants of <i>Centipeda minima</i>.
Journal of natural products, 2021, 84, 247-258
1560805 CIFC20 H26 O5P 1 21 111.1415; 8.1158; 20.8793
90; 95.962; 90
1877.74Xue, Peng-Hui; Zhang, Nan; Liu, Da; Zhang, Qing-Ran; Duan, Jing-Shi; Yu, Ya-Qin; Li, Jin-Yan; Cao, Shi-Jie; Zhao, Feng; Kang, Ning; Qiu, Feng
Cytotoxic and Anti-Inflammatory Sesquiterpenes from the Whole Plants of <i>Centipeda minima</i>.
Journal of natural products, 2021, 84, 247-258
1560806 CIFC24 H36 O6P 21 21 216.6873; 15.0723; 24.1896
90; 90; 90
2438.14Xue, Peng-Hui; Zhang, Nan; Liu, Da; Zhang, Qing-Ran; Duan, Jing-Shi; Yu, Ya-Qin; Li, Jin-Yan; Cao, Shi-Jie; Zhao, Feng; Kang, Ning; Qiu, Feng
Cytotoxic and Anti-Inflammatory Sesquiterpenes from the Whole Plants of <i>Centipeda minima</i>.
Journal of natural products, 2021, 84, 247-258

Left arrow Left arrow First | Left arrow Previous 500 | of 27 | Next 500 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!