Crystallography Open Database

Result: there are 11338 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 2022

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 114 | Next 100 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
1566599 CIFC31 H37 Cl2 Cr F2 N2 O2P 1 21/c 114.4764; 14.5398; 15.5208
90; 109.539; 90
3078.75Tian, Jiliang; Zhang, Xingwang; Liu, Shaofeng; Li, Zhibo
Chromium complexes supported by NNO-tridentate ligands: an unprecedented activity with the requirement of a small amount of MAO
Polymer Chemistry, 2022, 13, 1852-1860
1566600 CIFC36 H48 Ca Gd K O3P 1 21/c 19.2772; 13.9703; 26.2056
90; 90.079; 90
3396.4Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566601 CIFC36 H48 Ca Er K O3P 1 21/c 19.2555; 13.9514; 26.113
90; 90.709; 90
3371.6Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566602 CIFC36 H48 Ca Dy K O3P 1 21/c 19.2628; 13.9533; 26.1417
90; 90.377; 90
3378.7Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566603 CIFC36 H48 Ca Ho K O3P 1 21/c 19.2613; 13.9568; 26.1226
90; 90.566; 90
3376.4Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566604 CIFC36 H48 Ca K O3 TmP 1 21/c 19.2649; 13.9648; 26.111
90; 90.8583; 90
3377.9Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566605 CIFC36 H48 Ca K O3 TbP 1 21/c 19.2738; 13.9561; 26.155
90; 90.302; 90
3385.1Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566606 CIFC36 H48 Ca K O3 YbP 1 21/c 19.2602; 13.9561; 26.1046
90; 90.935; 90
3373.2Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566607 CIFC92 H166 Fe N4 O28 Si16P 21 21 2116.2474; 17.2899; 46.6858
90; 90; 90
13114.8Zong, Zhaohui; Hao, Aiyou; Xing, Pengyao; Zhao, Yanli
Chiral Molecular Nanosilicas
Chemical Science, 2022
1566608 CIFC92 H182 Fe N4 O32 Si16P 1 21 116.9205; 17.5657; 21.7093
90; 90.98; 90
6451.5Zong, Zhaohui; Hao, Aiyou; Xing, Pengyao; Zhao, Yanli
Chiral Molecular Nanosilicas
Chemical Science, 2022
1566609 CIFC76.5 Fe N4 O27.5 S2 Si16I 1 2 137.4731; 17.2234; 42.6209
90; 103.053; 90
26797.4Zong, Zhaohui; Hao, Aiyou; Xing, Pengyao; Zhao, Yanli
Chiral Molecular Nanosilicas
Chemical Science, 2022
1566610 CIFCl Ga6 K3 Mn2 S12P 3 1 c10.9208; 10.9208; 6.1774
90; 90; 120
638.04Liu, Bin-Wen; Pei, Shao-Min; Jiang, Xiao-Ming; Guo, Guo-Cong
Broad transparency and wide band gap achieved in a magnetic infrared nonlinear optical chalcogenide by suppressing d-d transitions.
Materials horizons, 2022, 9, 1513-1517
1566611 CIFC28 H41 F O4P 1 21 110.3779; 7.2974; 33.47
90; 98.797; 90
2504.9Jiang, Liyin; Sarró, Pau; Teo, Wei Jie; Llop, Jordi; Suero, Marcos
Catalytic alkene skeletal modification for the construction of fluorinated tertiary stereocenters
Chemical Science, 2022
1566612 CIFC26 H39 F O4C 1 2 114.7648; 6.0876; 26.974
90; 96.281; 90
2409.9Jiang, Liyin; Sarró, Pau; Teo, Wei Jie; Llop, Jordi; Suero, Marcos
Catalytic alkene skeletal modification for the construction of fluorinated tertiary stereocenters
Chemical Science, 2022
1566613 CIFC227 H209 Ag6 Au19 B2 F8 O17 P6 S17P -120.4536; 20.7898; 33.6586
72.945; 82.104; 63.917
12289Shi, Wan-Qi; Guan, Zong-Jie; Li, Jiao-Jiao; Han, Xu-Shuang; Wang, Quan-Ming
Site-Specified Doping of Silver Atoms into Au25 Nanocluster as Directed by Ligand Binding Preference
Chemical Science, 2022
1566614 CIFC66 H72 N4 Ni Si4P -111.7807; 11.8079; 22.9033
80.502; 78.053; 71.215
2934.25Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566615 CIFC34 H29 N2 Si2P -110.31; 12.326; 12.941
77.219; 79.312; 79.801
1560Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566616 CIFC83 H103 N7 Ni5 Si4P -113.9645; 14.7686; 24.4091
89.5959; 79.412; 63.052
4394.3Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566617 CIFC73 H85 N5 Ni2 Si4P -114.392; 22.272; 22.51
97.75; 95.438; 102.855
6912Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566618 CIFC35 H48 N PP -110.677; 11.8045; 12.4452
96.831; 101.037; 111.157
1405.1Chen, Zicong; Gu, Changxue; Yuen, On Ying; So, Chau Ming
Palladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates at the C–Cl site
Chemical Science, 2022
1566619 CIFC42 H34 B F3 P2 SeP -19.6724; 12.8821; 14.5407
84.961; 77.687; 74.085
1701.43Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566620 CIFC43 H39 B F3 O3 P2 RhP -19.1533; 13.0253; 33.273
83.172; 88.634; 79.181
3868.8Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566621 CIFC36.96 H31.91 B0.95 F2.87 I0.05 P2 Se0.95P n a 2114.5444; 19.8328; 11.0256
90; 90; 90
3180.4Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566622 CIFC15 H16 B F3 K O0.5 PP -15.6907; 21.5917; 26.847
78.455; 89.976; 89.948
3232Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566623 CIFC91 H144 O10P -111.9787; 17.3956; 22.0177
110.06; 90.8994; 101.377
4207.6Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566624 CIFC16 H16 F10 O2P 1 21/a 111.164; 5.0419; 15.9267
90; 91.317; 90
896.2Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566625 CIFC108 H108 F60 O12C 1 2/c 169.979; 13.9205; 24.2019
90; 96.4154; 90
23428.5Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566626 CIFC81 H94 F30 O10P 1 21/a 123.6441; 22.5243; 31.147
90; 95.0726; 90
16522.9Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566627 CIFC91 H94 F50 O10P -120.9282; 22.7403; 24.2682
98.976; 98.951; 114.017
10108.6Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566628 CIFC90.65 H93.56 F50 O10P 1 21/n 122.9793; 21.8597; 40.474
90; 102.22; 90
19870Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566629 CIFC18 H26 Cd N4 O6 P2 S4P -17.2387; 9.6411; 10.4545
81.448; 75.399; 70.165
662.56Tan, Yee Seng; Yeo, Chien Ing; Kwong, Huey Chong; Tiekink, Edward R. T.
Unusual {⋯HNC <sub>2</sub> O⋯HC <sub> <i>n</i> </sub> O}, <i>n</i> = 1 or 2, synthons predominate in the molecular packing of one-dimensional coordination polymers, {Cd[S <sub>2</sub> P(OR) <sub>2</sub> ] <sub>2</sub> ( <sup>3</sup> LH <sub>2</sub> )} <sub> <i>n</i> </sub> , for R = Me and Et, but are precluded when R = i-Pr; <sup>3</sup> LH <sub>2</sub> = <i>N</i> , <i>N</i> ′-bis(3-pyridylmethyl)oxalamide
CrystEngComm, 2022, 24, 2992-3004
1566630 CIFC26 H42 Cd N4 O6 P2 S4P -19.9154; 12.3655; 15.4749
106.08; 99.172; 91.827
1794.03Tan, Yee Seng; Yeo, Chien Ing; Kwong, Huey Chong; Tiekink, Edward R. T.
Unusual {⋯HNC <sub>2</sub> O⋯HC <sub> <i>n</i> </sub> O}, <i>n</i> = 1 or 2, synthons predominate in the molecular packing of one-dimensional coordination polymers, {Cd[S <sub>2</sub> P(OR) <sub>2</sub> ] <sub>2</sub> ( <sup>3</sup> LH <sub>2</sub> )} <sub> <i>n</i> </sub> , for R = Me and Et, but are precluded when R = i-Pr; <sup>3</sup> LH <sub>2</sub> = <i>N</i> , <i>N</i> ′-bis(3-pyridylmethyl)oxalamide
CrystEngComm, 2022, 24, 2992-3004
1566631 CIFC22 H34 Cd N4 O6 P2 S4P -19.0611; 9.2065; 10.5703
82.436; 77.672; 64.113
774.27Tan, Yee Seng; Yeo, Chien Ing; Kwong, Huey Chong; Tiekink, Edward R. T.
Unusual {⋯HNC <sub>2</sub> O⋯HC <sub> <i>n</i> </sub> O}, <i>n</i> = 1 or 2, synthons predominate in the molecular packing of one-dimensional coordination polymers, {Cd[S <sub>2</sub> P(OR) <sub>2</sub> ] <sub>2</sub> ( <sup>3</sup> LH <sub>2</sub> )} <sub> <i>n</i> </sub> , for R = Me and Et, but are precluded when R = i-Pr; <sup>3</sup> LH <sub>2</sub> = <i>N</i> , <i>N</i> ′-bis(3-pyridylmethyl)oxalamide
CrystEngComm, 2022, 24, 2992-3004
1566632 CIFC78 H78 N6 O3P -114.2538; 17.1903; 17.3592
79.038; 72.546; 68.828
3767.7Fang, Lingyi; Zhang, Yuyan; Ren, Ming; Xie, Xinrui; Li, Tianyu; Yuan, Yi; Zhang, Jing; Wang, Peng
A triple helicene based molecular semiconductor characteristic of a fully fused conjugated backbone for perovskite solar cells
Energy & Environmental Science, 2022, 15, 1630-1637
1566633 CIFC15 H15 N3 O SP 1 21/n 16.6492; 13.731; 15.329
90; 101.032; 90
1373.7Kshtriya, Vivekshinh; Koshti, Bharti; Mehmood, Tahir; Singh, Ramesh; Joshi, Khashti Ballabh; Bandyopadhyay, Sujoy; Boukhvalov, Danil W.; Reddy, J. Prakasha; Gour, Nidhi
A new aggregation induced emission enhancement (AIEE) dye which self-assembles to panchromatic fluorescent flowers and has application in sensing dichromate ions.
Soft matter, 2022, 18, 3019-3030
1566663 CIFC36 H37 K N3 O3 P2 Ru SP c a 2112.6529; 18.7504; 15.5836
90; 90; 90
3697.2Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566664 CIFC100 H83 N6 O3 P6 Ru2P 1 21/c 114.8971; 22.753; 28.6172
90; 100.332; 90
9542.6Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566665 CIFC51 H48 Cl N4 O2 P3 RuP b c n25.849; 19.5041; 21.0152
90; 90; 90
10595Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566666 CIFC23 H27 B O3P n a 2112.912; 10.1397; 15.597
90; 90; 90
2042Wei, Yu-Bai; Luo, Dong; Xiong, Xiao; Huang, Yong-Liang; Xie, Mo; Lu, Weigang; Li, Dan
Biomimetic Mimicry of Formaldehyde-Induced DNA–Protein Crosslinks in the Confined Space of Metal–Organic Framework
Chemical Science, 2022
1566667 CIFC23 H27 B O3P 1 21/n 112.4943; 9.9586; 16.762
90; 95.6616; 90
2075.5Wei, Yu-Bai; Luo, Dong; Xiong, Xiao; Huang, Yong-Liang; Xie, Mo; Lu, Weigang; Li, Dan
Biomimetic Mimicry of Formaldehyde-Induced DNA–Protein Crosslinks in the Confined Space of Metal–Organic Framework
Chemical Science, 2022
1566668 CIFC16 H29 N O6 SP 21 21 215.46991; 10.15896; 34.3303
90; 90; 90
1907.69Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566669 CIFC18 H22 O2 SP n a 219.3374; 6.0661; 28.5106
90; 90; 90
1614.89Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566670 CIFC15 H20 Cl N O3 SP -15.0188; 9.6241; 16.1198
89.487; 85.132; 82.136
768.5Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566671 CIFC10 H18 O4 S2P 1 21/n 16.4691; 11.4368; 8.7387
90; 102.114; 90
632.143Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566672 CIFC11 H14 O3 SP -15.72076; 8.13039; 11.8424
91.8184; 91.4466; 103.412
535.219Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566673 CIFC10 H11 F O3 SP 1 c 15.7165; 12.1828; 14.7356
90; 91.722; 90
1025.77Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566674 CIFC15 H27 N O6 SP 1 21/c 111.1742; 16.6182; 10.3665
90; 116.394; 90
1724.34Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566675 CIFC10 H18 O4 S2P 1 21/c 16.09765; 8.92648; 22.0926
90; 91.4743; 90
1202.11Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566676 CIFC15 H17 N O2 SP 1 21/c 19.0612; 15.82137; 10.2622
90; 114.837; 90
1335.12Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566677 CIFC25 H30 O8 SP 1 21 110.04584; 19.87397; 12.32816
90; 95.9688; 90
2447.98Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566678 CIFC23 H27 B O3P n a 2112.912; 10.1397; 15.597
90; 90; 90
2042wu, Fu-Peng; Wu, Xiao-Feng
Catalyst-Controlled Selective Borocarbonylation of Benzylidenecyclopropanes: Regiodivergent Synthesis of γ-Vinylboryl Ketones and β-Cyclopropylboryl Ketones
Chemical Science, 2022
1566679 CIFC23 H27 B O3P 1 21/n 112.4943; 9.9586; 16.762
90; 95.6616; 90
2075.5wu, Fu-Peng; Wu, Xiao-Feng
Catalyst-Controlled Selective Borocarbonylation of Benzylidenecyclopropanes: Regiodivergent Synthesis of γ-Vinylboryl Ketones and β-Cyclopropylboryl Ketones
Chemical Science, 2022
1566680 CIFC50.5 H47 Co O3 P2P 1 21/n 19.9652; 18.349; 23.3602
90; 96.462; 90
4244.3Martínez-Carrión, Alicia; Romero-Navarro, Andrés; Núñez-Rico, José Luis; Gutiérrez, Albert; Grabulosa, Arnald; Vidal-Ferran, Anton
Valorisation of mixtures of linear alkenes using cobalt-mediated isomerisation and hydroformylation chemistries
Catalysis Science & Technology, 2022, 12, 3219-3227
1566681 CIFC45 H32 Co2 O7 P2P -110.8578; 11.6947; 17.4282
106.744; 95.84; 112.496
1900.9Martínez-Carrión, Alicia; Romero-Navarro, Andrés; Núñez-Rico, José Luis; Gutiérrez, Albert; Grabulosa, Arnald; Vidal-Ferran, Anton
Valorisation of mixtures of linear alkenes using cobalt-mediated isomerisation and hydroformylation chemistries
Catalysis Science & Technology, 2022, 12, 3219-3227
1566682 CIFC16 H19 N O6 SP 21 21 218.0346; 12.621; 16.5455
90; 90; 90
1677.79Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566683 CIFC16 H19 N O6 SP 1 21 110.1269; 8.043; 10.8756
90; 114.408; 90
806.66Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566684 CIFC17 H26 F6 N3 O7 S2P 1 21 111.0402; 9.5966; 12.5085
90; 115.079; 90
1200.32Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566685 CIFC16 H20 N2 O6 SP 21 21 218.1051; 14.1921; 15.2659
90; 90; 90
1756.01Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566686 CIFC160 H218 N8 O49 S8P 1 21 113.5261; 12.674; 25.4683
90; 99.78; 90
4302.6Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566687 CIFC1220 H968 B11.95 Cu24 F47.82 N52 O104P 1 21/n 118.838; 32.458; 64.439
90; 94.55; 90
39277Domoto, Yuya; Yamamoto, Kidai; Horie, Shumpei; Yu, Zhengsu; Fujita, Makoto
Multiplication of weak chiral inductions for excellent control over the helical orientation of discrete topologically chiral (M3L2)n polyhedra
Chemical Science, 2022
1566688 CIFC29.4 H40.8 Cl8.8 N2 P2 PdP 1 21/n 115.262; 12.8154; 20.9917
90; 108.535; 90
3892.8Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566689 CIFC26 H40 B2 N2 P2P -19.1591; 11.3142; 15.1394
103.273; 102.525; 105.201
1408Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566690 CIFC28 H34 F6 N2 O6 P2 Pd S2P -111.2734; 12.1729; 13.5903
73.9005; 72.8892; 73.6404
1671.4Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566691 CIFC17 H21 B F2 N4 OP 21 21 218.9883; 11.1112; 17.485
90; 90; 90
1746.2Zeng, Lintao; Chen, Tianhong; Zhu, Beitong; Koo, Seyoung; Tang, Yonghe; Lin, Weiying; James, Tony D.; Kim, Jong Seung
A molecular recognition platform for the simultaneous sensing of diverse chemical weapons
Chemical Science, 2022
1566692 CIFC15 H19 B F2 N4P 4110.5675; 10.5675; 13.404
90; 90; 90
1496.9Zeng, Lintao; Chen, Tianhong; Zhu, Beitong; Koo, Seyoung; Tang, Yonghe; Lin, Weiying; James, Tony D.; Kim, Jong Seung
A molecular recognition platform for the simultaneous sensing of diverse chemical weapons
Chemical Science, 2022
1566693 CIFC16 H17 B F2 N4 OP -16.9141; 9.2485; 12.7582
93.651; 101.649; 97.353
789.08Zeng, Lintao; Chen, Tianhong; Zhu, Beitong; Koo, Seyoung; Tang, Yonghe; Lin, Weiying; James, Tony D.; Kim, Jong Seung
A molecular recognition platform for the simultaneous sensing of diverse chemical weapons
Chemical Science, 2022
1566694 CIFC83 H135 As7 K La2 O6 Si8P -115.7346; 18.2731; 19.7473
106.435; 102.572; 100.222
5139Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566695 CIFC96 H164 As14 Ce2 K2 O12 Si8P -111.223; 16.579; 18.693
72.888; 89.816; 73.008
3166Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566696 CIFC80 H132 As7 K Nd2 O6 Si8P -115.6899; 18.4469; 20.1223
111.299; 104.839; 100.119
5006.3Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566697 CIFC77 H129 As3 K Nd2 O6 Si8P -111.7764; 17.4676; 26.292
84.855; 79.39; 71.581
5040.7Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566698 CIFC58 H102 As7 K2 Nd O12 Si4P 1 21/n 114.2709; 31.995; 17.4941
90; 98.678; 90
7896.3Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566699 CIFC77 H132 As7 Ce2 K O6 Si8P 1 21/n 120.0117; 18.0444; 27.5019
90; 96.273; 90
9871.5Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566700 CIFC74 H138 As14 K2 Nd2 O12 Si8C 1 2/c 141.591; 13.2497; 19.5306
90; 95.516; 90
10712.9Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566701 CIFC43 H40 Au N O6P 21 21 219.9306; 13.2468; 27.4297
90; 90; 90
3608.3Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566702 CIFC38 H24 N O2 PP 21 21 2111.8935; 12.6595; 18.8734
90; 90; 90
2841.7Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566703 CIFC41.17 H29.17 Au Cl3.5 N O3P 21 21 2112.999; 13.954; 22.15
90; 90; 90
4018Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566704 CIFC42 H32 Au Cl4 N O3P 21 21 2112.578; 13.7123; 21.0398
90; 90; 90
3628.8Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566705 CIFC42 H36 Au N O5P 21 21 219.9266; 13.1669; 27.3976
90; 90; 90
3580.9Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566706 CIFH66 Mo60 Na8 O187I 41/a c d :223.5571; 23.5571; 61.035
90; 90; 90
33870.6Li, xuexin; Ji, Tuo; Gao, Jun-Yang; Chen, Wei-Chao; Yuan, Ye; Sha, Haoyan; Faller, Roland; Shan, Guo-Gang; Shao, Kui-Zhan; Wang, Xinlong; Su, Zhong-Min
An Unprecedented Fully Reduced {MoV60} Polyoxometalate: From All-Inorganic Molecular Light-Absorber Model to Improved Photoelectronic Performance
Chemical Science, 2022
1566707 CIFC54.5 H53 B Cl P2 SP -18.8424; 11.4067; 24.8662
81.957; 80.897; 69.046
2303.2Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566708 CIFC29.25 H31.5 B Cl0.5 F4 P2 Pt SP b a m20.9374; 10.9959; 14.9555
90; 90; 90
3443.14Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566709 CIFC28 H28 Cl O P2 Rh SP 21 21 2110.4581; 14.2792; 17.4031
90; 90; 90
2598.86Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566710 CIFC54 H53 B Cl P2 Rh SP 1 21/n 110.9915; 34.1432; 12.5533
90; 99.76; 90
4642.9Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566711 CIFC45.5 H36 Cl F7 P3 Rh SP -19.1404; 12.3384; 19.4965
102.063; 92.077; 103.656
2080.95Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566712 CIFC43 H32 F4 O3 P2 S2P 1 21/n 112.4956; 28.031; 12.6611
90; 119.324; 90
3866.48Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566713 CIFC56 H59 B P2 Pt SP 1 21/c 116.6775; 15.3273; 19.3126
90; 102.496; 90
4819.76Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566714 CIFC47 H35 F13 N2 O8 P2 Pt S5P 1 21/c 123.6369; 12.7303; 18.9449
90; 98.297; 90
5640.95Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566715 CIFC32 H39 B2 F8 N O2 P2 Pt SP -110.727; 13.1882; 15.143
65.687; 75.111; 75.546
1861.41Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566718 CIF
HKL
Paper
C21 H18 N2 OC 1 2/c 130.3989; 8.7177; 14.0581
90; 115.367; 90
3366.3Meenatchi, C. Selva; Athimoolam, S.; Suresh, J.; Priya, R. Vishnu; Rubina, S. Raja; Bhandari, S. R.
(<i>E</i>)-5-(4-Methylbenzylidene)-1-phenyl-4,5,6,7-tetrahydro-1<i>H</i>-indazol-4-one
IUCrData, 2022, 7, x220283
1566719 CIFC20 H56 Bi2 Br10 N4P -112.4378; 13.2166; 14.021
97.835; 93.139; 90.289
2279.7Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566720 CIFC20 H56 Ag Bi Br8 N4P -18.4797; 8.7683; 13.9411
73.253; 88.908; 87.415
991.56Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566721 CIFC20 Ag Bi Br8 N8C m m m8.774; 27.47; 8.771
90; 90; 90
2114Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566722 CIFC25 H69 Br9 N5 Pb2P -111.996; 13.422; 17.477
72.658; 70.158; 77.179
2503.7Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566723 CIFC25 H70 Br9 N5 Pb2P -111.975; 13.366; 17.472
72.618; 70.213; 77.258
2488.9Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566724 CIFC23 H23 Cl N2 O2P 1 21 19.6064; 7.9331; 13.748
90; 101.106; 90
1028.09Xiao, Lu; Li, Bo; Xiao, Fan; Fu, Cong; Wei, Liang; Dang, Yanfeng; Dong, Xiu-Qin; Wang, Chun-Jiang
Stereodivergent Synthesis of Enantioenriched Azepino[3,4,5-cd]-Indoles via Cooperative Cu/Ir-Catalyzed Asymmetric Allylic Alkylation and Intramolecular Friedel-Crafts Reaction
Chemical Science, 2022
1566725 CIFC23 H23 Cl N2 O2P 21 21 219.2992; 18.0846; 24.744
90; 90; 90
4161.26Xiao, Lu; Li, Bo; Xiao, Fan; Fu, Cong; Wei, Liang; Dang, Yanfeng; Dong, Xiu-Qin; Wang, Chun-Jiang
Stereodivergent Synthesis of Enantioenriched Azepino[3,4,5-cd]-Indoles via Cooperative Cu/Ir-Catalyzed Asymmetric Allylic Alkylation and Intramolecular Friedel-Crafts Reaction
Chemical Science, 2022
1566726 CIFC23 H23 Cl N2 O2P 21 21 219.11893; 17.37833; 50.2087
90; 90; 90
7956.66Xiao, Lu; Li, Bo; Xiao, Fan; Fu, Cong; Wei, Liang; Dang, Yanfeng; Dong, Xiu-Qin; Wang, Chun-Jiang
Stereodivergent Synthesis of Enantioenriched Azepino[3,4,5-cd]-Indoles via Cooperative Cu/Ir-Catalyzed Asymmetric Allylic Alkylation and Intramolecular Friedel-Crafts Reaction
Chemical Science, 2022
1566727 CIFC23 H30 N4 O2P 1 21/c 116.0767; 12.9097; 10.9767
90; 99.712; 90
2245.51Zhan, Yi-Zhou; Meng, Huan; Shu, Wei
Rapid Access to t-Butylalkylated Olefins Enabled by Ni-Catalyzed Intermolecular Regio- and trans-Selective Cross-Electrophile t-Butylalkylation of Alkynes
Chemical Science, 2022
1566728 CIF
HKL
Paper
C15 H14 Cl N5 O2P 1 21 17.1533; 11.936; 9.004
90; 98.128; 90
761.1Song, Jingjing; Jiang, Xinyu; Wang, Ziyi; Pei, Jingyao; Li, Hongsen
4-Chloro-5-(dimethylamino)-2-[(5-phenyl-1,3,4-oxadiazol-2-yl)methyl]pyridazin-3(2<i>H</i>)-one
IUCrData, 2022, 7, x220342
1566729 CIF
HKL
Paper
C16 H9 N O2 SP 1 21/c 14.60717; 20.7275; 12.6444
90; 91.911; 90
1206.81Abdallah, Amira E. M.; Elgemeie, Galal H.; Jones, Peter G.
3-(Benzo[<i>d</i>]thiazol-2-yl)-2<i>H</i>-chromen-2-one
IUCrData, 2022, 7, x220332

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 114 | Next 100 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!