Crystallography Open Database

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1518738 CIFC19.5 H18.5 As3 Cl6.5 S6P n m a20.703; 9.885; 14.702
90; 90; 90
3008.8Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518739 CIFC24 H24 Cl3 S6 Sb3R -3 c :H14.2066; 14.2066; 33.41
90; 90; 120
5839.7Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518740 CIFC36 H42 As3 Cl3 S6P -110.0055; 12.424; 16.522
81.285; 88.456; 84.579
2020.9Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518741 CIFC30 H42 As3 Cl3 S6R -3 :H16.413; 16.413; 23.8
90; 90; 120
5552.4Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518742 CIFC24 H30 Cl3 S6 Sb3P 1 21/n 116.0971; 11.4604; 16.3368
90; 91.867; 90
3012.2Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518743 CIFC30 H42 Cl3 S6 Sb3R -3 :H16.458; 16.458; 23.9449
90; 90; 120
5616.9Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W.
Self-assembled trinuclear arsenic and antimony macrobicycles
Chem. Sci., 2015, 6, 2444
1518744 CIFC32 H30 N8 O5 Zn4P 42/m c m11.5382; 11.5382; 25.813
90; 90; 90
3436.5Lin, Rui-Biao; Li, Tai-Yang; Zhou, Hao-Long; He, Chun-Ting; Zhang, Jie-Peng; Chen, Xiao-Ming
Tuning fluorocarbon adsorption in new isoreticular porous coordination frameworks for heat transformation applications
Chem. Sci., 2015, 6, 2516
1518745 CIFC34 H32 N8 O5 Zn4P 42/m c m11.517; 11.517; 34.474
90; 90; 90
4573Lin, Rui-Biao; Li, Tai-Yang; Zhou, Hao-Long; He, Chun-Ting; Zhang, Jie-Peng; Chen, Xiao-Ming
Tuning fluorocarbon adsorption in new isoreticular porous coordination frameworks for heat transformation applications
Chem. Sci., 2015, 6, 2516
1518753 CIFC37 H31 Cu F12 N4P -112.1667; 12.1867; 13.5954
81.549; 77.873; 65.444
1788.5Tomson, Neil C.; Williams, Kamille D.; Dai, Xuliang; Sproules, Stephen; DeBeer, Serena; Warren, Timothy H.; Wieghardt, Karl
Re-evaluating the Cu K pre-edge XAS transition in complexes with covalent metal–ligand interactions
Chem. Sci., 2015, 6, 2474
1518754 CIFC16 H6 F12 N2I 41/a :236.71; 36.71; 4.9148
90; 90; 90
6623.3Tomson, Neil C.; Williams, Kamille D.; Dai, Xuliang; Sproules, Stephen; DeBeer, Serena; Warren, Timothy H.; Wieghardt, Karl
Re-evaluating the Cu K pre-edge XAS transition in complexes with covalent metal–ligand interactions
Chem. Sci., 2015, 6, 2474
1518755 CIFC18 H27 Au B Cl N2 O2P 1 21/n 111.295; 10.512; 16.9583
90; 102.328; 90
1967.1Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518756 CIFC53 H79 Au B Cl N4 O4P 1 21/c 115.396; 14.4925; 24.966
90; 100.935; 90
5469.4Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518757 CIFC19 H27 B F3 Li N2 O5 SP -15.9513; 10.9562; 17.3953
96.176; 93.242; 97.646
1114.73Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518758 CIFC26 H39 B Cl N2 O2 RhP 1 21/c 116.46; 13.8072; 11.9483
90; 104.628; 90
2627.4Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518759 CIFC33 H47 B Cl Ir N2 O2C 1 2/c 135.4699; 10.667; 18.1337
90; 115.404; 90
6197.6Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei
Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors
Chem. Sci., 2015, 6, 2893
1518761 CIFC25 H23 F12 Fe2 O10P -19.507; 11.729; 16.605
102.703; 96.771; 112.595
1625Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518762 CIFC35 H25 F24 Fe3 O14P 1 21 19.7834; 20.8414; 12.0955
90; 102.57; 90
2407.2Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518763 CIFC35 H25 F24 Fe3 O14P 1 21 19.7979; 20.819; 12.0998
90; 102.659; 90
2408.2Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518764 CIFC35 H19 F30 Fe3 O14C 1 2/c 120.934; 13.481; 17.739
90; 92.848; 90
5000Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518765 CIFC25 H23 F12 Fe Mn O10P -19.464; 11.8255; 16.508
102.022; 97.859; 112.682
1618.3Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518766 CIFC35 H25 F24 Fe Ni2 O14P 1 21 19.7682; 20.7583; 12.0575
90; 103.126; 90
2381Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V.
Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors
Chem. Sci., 2015, 6, 2835
1518779 CIFC38 H34 Cl2 Ir N P2I b a m30.868; 17.517; 24.155
90; 90; 90
13061Liu, Chong; Xie, Jian-Hua; Tian, Gui-Long; Li, Wei; Zhou, Qi-Lin
Highly efficient hydrogenation of carbon dioxide to formate catalyzed by iridium(iii) complexes of imine‒diphosphine ligands
Chem. Sci., 2015, 6, 2928
1518780 CIFGa1.67 O10 P2.5 Zn0.83C 1 2/m 116.767; 19.047; 10.248
90; 127.038; 90
2612.5Wu, Junbiao; Tao, Chunyao; Li, Yi; Li, Jiyang; Yu, Jihong
Methyl viologen-templated zinc gallophosphate zeolitic material with dual photo-/thermochromism and tuneable photovoltaic activity
Chem. Sci., 2015, 6, 2922
1518781 CIFC63 H59 B F29 Fe N3 P2P -112.7767; 13.894; 38.0545
90.4567; 92.9881; 96.475
6702.5Darmon, Jonathan M.; Kumar, Neeraj; Hulley, Elliott B.; Weiss, Charles J.; Raugei, Simone; Bullock, R. Morris; Helm, Monte L.
Increasing the rate of hydrogen oxidation without increasing the overpotential: a bio-inspired iron molecular electrocatalyst with an outer coordination sphere proton relay
Chem. Sci., 2015, 6, 2737
1518782 CIFC38 H55 Co N2 O4P 1 21/n 117.569; 10.302; 19.781
90; 100.629; 90
3518.8Zhao, Yaguang; Yu, Mengmeng; Zhang, Shuailin; Wu, Zhenqiang; Liu, Yuchu; Peng, Chi-How; Fu, Xuefeng
A well-defined, versatile photoinitiator (salen)Co‒CO2CH3for visible light-initiated living/controlled radical polymerization
Chem. Sci., 2015, 6, 2979
1518784 CIFC16 H29 B I N3C 1 2/c 117.3182; 19.7092; 12.0924
90; 120.773; 90
3546.3Chauvier, Clément; Tlili, Anis; Das Neves Gomes, Christophe; Thuéry, Pierre; Cantat, Thibault
Metal-free dehydrogenation of formic acid to H2and CO2using boron-based catalysts
Chem. Sci., 2015, 6, 2938
1518785 CIFC17 H30 B N3 O4P 21 21 217.1546; 12.8526; 20.4294
90; 90; 90
1878.59Chauvier, Clément; Tlili, Anis; Das Neves Gomes, Christophe; Thuéry, Pierre; Cantat, Thibault
Metal-free dehydrogenation of formic acid to H2and CO2using boron-based catalysts
Chem. Sci., 2015, 6, 2938
1518786 CIFC23 H17 NP n a 217.4701; 19.7919; 11.1894
90; 90; 90
1654.32Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J.
Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters
Chem. Sci., 2015, 6, 2843
1518787 CIFC58 H46 F6 Ir N4 O PP n a 2113.128; 37.8916; 10.29
90; 90; 90
5118.7Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J.
Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters
Chem. Sci., 2015, 6, 2843
1518788 CIFC44 H32 F6 Ir N4 PP 1 21/n 115.0877; 13.1747; 18.093
90; 96.094; 90
3576.1Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J.
Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters
Chem. Sci., 2015, 6, 2843
1518789 CIFC76 H60 F6 Ir N4 PP -110.8073; 13.5065; 20.8777
80.953; 86.577; 78.797
2950.9Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J.
Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters
Chem. Sci., 2015, 6, 2843
1518821 CIFC65 H80 Au N OP -111.6132; 14.7425; 16.9669
87.393; 71.112; 80.062
2707Ming Tong, Glenna So; Chan, Kaai Tung; Chang, Xiaoyong; Che, Chi-Ming
Theoretical studies on the photophysical properties of luminescent pincer gold(iii) arylacetylide complexes: the role of π-conjugation at the C-deprotonated [C^N^C] ligand
Chem. Sci., 2015, 6, 3026
1518822 CIFC35 H34 Au B Mn O2 PP -110.071; 11.844; 13.4
86.394; 79.387; 74.371
1512.8Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518823 CIFC43 H40 Au B Mn O2 PC 1 2/c 141.848; 10.898; 15.941
90; 91.024; 90
7269Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518824 CIFC30 H29 Au B Mn N O2 P SP 1 21/n 113.491; 13.559; 16.412
90; 101.959; 90
2937Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518825 CIFC46 H40 Au B3 Cl8 Mn2 O4P 1 21/c 118.435; 33.798; 17.288
90; 113.832; 90
9853Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518826 CIFC98 H85 Ag2 B6 Cl16 F Mn4 O8P -112.2946; 13.8214; 16.0619
88.083; 67.993; 83.916
2516.2Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518827 CIFC53 H48 Ag B3 Cl8 Mn2 O4P 1 21/n 111.184; 36.556; 13.609
90; 93.434; 90
5554Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518828 CIFC46 H40 Ag B3 Cl8 Mn2 O4P 1 21/c 118.444; 33.901; 17.285
90; 113.909; 90
9880Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518829 CIFC53 H48 B3 Cl8 Cu Mn2 O4P 1 21/n 111.0743; 36.198; 13.711
90; 93.21; 90
5488Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518830 CIFC55 H50 B3 Cl12 Cu2 Mn3 O6P -111.952; 14.576; 20.573
70.672; 73.21; 68.233
3084Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518831 CIFC67 H62 B3 Cl8 Cu2 Mn3 O6P -111.301; 14.461; 21.311
97.172; 96.19; 102.139
3345.8Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518832 CIFC75 H50 Au B F24 P2P -112.38; 15.772; 18.327
83.065; 74.699; 81.63
3402.1Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong
Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments
Chem. Sci., 2015, 6, 2989
1518843 CIFC22 H23 N O3P 1 21/n 16.0325; 20.594; 14.3515
90; 97.425; 90
1768Faustino, Hélio; Varela, Iván; Mascareñas, José L.; López, Fernando
Gold(i)-catalyzed [2 + 2 + 2] cycloaddition of allenamides, alkenes and aldehydes: a straightforward approach to tetrahydropyrans
Chem. Sci., 2015, 6, 2903
1518844 CIFC25 H27 N O3P 1 21/n 110.6026; 12.0053; 16.5199
90; 105.806; 90
2023.27Faustino, Hélio; Varela, Iván; Mascareñas, José L.; López, Fernando
Gold(i)-catalyzed [2 + 2 + 2] cycloaddition of allenamides, alkenes and aldehydes: a straightforward approach to tetrahydropyrans
Chem. Sci., 2015, 6, 2903
1518845 CIFC24 H25 N O3P 1 21/c 119.6584; 6.7792; 14.62
90; 104.609; 90
1885.39Faustino, Hélio; Varela, Iván; Mascareñas, José L.; López, Fernando
Gold(i)-catalyzed [2 + 2 + 2] cycloaddition of allenamides, alkenes and aldehydes: a straightforward approach to tetrahydropyrans
Chem. Sci., 2015, 6, 2903
1518846 CIFC10 H9 Br Cl N O2P 1 21 15.928; 7.6682; 11.3533
90; 95.944; 90
513.31Zhu, Cheng-Liang; Tian, Jun-Shan; Gu, Zhen-Yuan; Xing, Guo-Wen; Xu, Hao
Iron(ii)-catalyzed asymmetric intramolecular olefin aminochlorination using chloride ion
Chem. Sci., 2015, 6, 3044
1518866 CIFC11 H9 Dy N3 O6P 1 21/c 113.672; 7.313; 12.481
90; 94.296; 90
1244.4Yin, Dan-Dan; Chen, Qi; Meng, Yin-Shan; Sun, Hao-Ling; Zhang, Yi-Quan; Gao, Song
Slow magnetic relaxation in a novel carboxylate/oxalate/hydroxyl bridged dysprosium layer
Chem. Sci., 2015, 6, 3095
1518867 CIFC11 H9 N3 O6 YP 1 21/c 113.655; 7.278; 12.428
90; 94.424; 90
1231.4Yin, Dan-Dan; Chen, Qi; Meng, Yin-Shan; Sun, Hao-Ling; Zhang, Yi-Quan; Gao, Song
Slow magnetic relaxation in a novel carboxylate/oxalate/hydroxyl bridged dysprosium layer
Chem. Sci., 2015, 6, 3095
1518869 CIFC42 H34 N6 O10P -18.8838; 20.6864; 22.5136
68.276; 78.717; 89.509
3760Martinez-Cuezva, Alberto; Pastor, Aurelia; Cioncoloni, Giacomo; Orenes, Raul-Angel; Alajarin, Mateo; Symes, Mark D.; Berna, Jose
Versatile control of the submolecular motion of di(acylamino)pyridine-based [2]rotaxanes
Chem. Sci., 2015, 6, 3087

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