Crystallography Open Database

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1514481 CIFC54 H64 B F4 N16 O7 P2P 1 21/c 119.726; 15.697; 22.564
90; 101.404; 90
6849Cai, Jiajia; Hay, Benjamin P.; Young, Neil J.; Yang, Xiaoping; Sessler, Jonathan L.
A pyrrole-based triazolium-phane with NH and cationic CH donor groups as a receptor for tetrahedral oxyanions that functions in polar media
Chemical Science, 2013, 4, 1560
1514482 CIFC162 H200 B8 F32 N48 O16 P4P 1 21/n 120.554; 16.552; 31.568
90; 93.445; 90
10720Cai, Jiajia; Hay, Benjamin P.; Young, Neil J.; Yang, Xiaoping; Sessler, Jonathan L.
A pyrrole-based triazolium-phane with NH and cationic CH donor groups as a receptor for tetrahedral oxyanions that functions in polar media
Chemical Science, 2013, 4, 1560
1514483 CIFC57 H74 Cl4 Cu2 N4 S2C 2 2 2114.073; 21.02; 19.083
90; 90; 90
5645Zhang, Shiyu; Warren, Timothy H.
Three coordinate models for the binuclear CuA electron-transfer site
Chemical Science, 2013, 4, 1786
1514484 CIFC58 H76 Cl4 Cu2 N4 S2C 1 2/c 152.089; 8.9421; 35.545
90; 129.297; 90
12813Zhang, Shiyu; Warren, Timothy H.
Three coordinate models for the binuclear CuA electron-transfer site
Chemical Science, 2013, 4, 1786
1514485 CIFC35 H43 Cl2 Cu N2 SP 1 21/c 19.26; 24.43; 15.506
90; 100.133; 90
3453Zhang, Shiyu; Warren, Timothy H.
Three coordinate models for the binuclear CuA electron-transfer site
Chemical Science, 2013, 4, 1786
1514486 CIFC18 H18 Cl D2 N3 O2P b c a18.9604; 9.3522; 19.2687
90; 90; 90
3416.8Collett, Christopher J.; Massey, Richard S.; Maguire, Oliver R.; Batsanov, Andrei S.; O'Donoghue, AnnMarie C.; Smith, Andrew D.
Mechanistic insights into the triazolylidene-catalysed Stetter and benzoin reactions: role of the N-aryl substituent
Chemical Science, 2013, 4, 1514
1514487 CIFC19 H20 Cl D2 N3 O2P b c a19.2697; 9.5129; 19.6896
90; 90; 90
3609.3Collett, Christopher J.; Massey, Richard S.; Maguire, Oliver R.; Batsanov, Andrei S.; O'Donoghue, AnnMarie C.; Smith, Andrew D.
Mechanistic insights into the triazolylidene-catalysed Stetter and benzoin reactions: role of the N-aryl substituent
Chemical Science, 2013, 4, 1514
1514488 CIFC18 H17 Cl D2 F N3 O2P b c a18.8845; 9.4266; 19.2915
90; 90; 90
3434.2Collett, Christopher J.; Massey, Richard S.; Maguire, Oliver R.; Batsanov, Andrei S.; O'Donoghue, AnnMarie C.; Smith, Andrew D.
Mechanistic insights into the triazolylidene-catalysed Stetter and benzoin reactions: role of the N-aryl substituent
Chemical Science, 2013, 4, 1514
1514489 CIFC35 H48 Cl2 Fe N O2P 1 21/n 110.1903; 12.5783; 27.2498
90; 96.4952; 90
3470.4Wong, Janice L.; Sánchez, Raúl Hernández; Logan, Jennifer Glancy; Zarkesh, Ryan A.; Ziller, Joseph W.; Heyduk, Alan F.
Disulfide reductive elimination from an iron(iii) complex
Chemical Science, 2013, 4, 1906
1514490 CIFC40 H76 Fe N3 O2 Si4P 1 21/c 111.9269; 17.5744; 24.1583
90; 111.583; 90
4708.7Wong, Janice L.; Sánchez, Raúl Hernández; Logan, Jennifer Glancy; Zarkesh, Ryan A.; Ziller, Joseph W.; Heyduk, Alan F.
Disulfide reductive elimination from an iron(iii) complex
Chemical Science, 2013, 4, 1906
1514491 CIFC75.5 H98 Cl8 Fe2 N2 O8P -114.8709; 15.747; 17.9214
94.0663; 111.428; 95.5142
3863Wong, Janice L.; Sánchez, Raúl Hernández; Logan, Jennifer Glancy; Zarkesh, Ryan A.; Ziller, Joseph W.; Heyduk, Alan F.
Disulfide reductive elimination from an iron(iii) complex
Chemical Science, 2013, 4, 1906
1514492 CIFC43 H55 Cl4 Fe N2 O5P 1 21/n 112.6068; 24.431; 16.6177
90; 111.803; 90
4752.1Wong, Janice L.; Sánchez, Raúl Hernández; Logan, Jennifer Glancy; Zarkesh, Ryan A.; Ziller, Joseph W.; Heyduk, Alan F.
Disulfide reductive elimination from an iron(iii) complex
Chemical Science, 2013, 4, 1906
1514493 CIFC66 H90 Fe2 N4 O4P 1 21/c 114.1943; 14.2798; 17.1104
90; 113.995; 90
3168.4Wong, Janice L.; Sánchez, Raúl Hernández; Logan, Jennifer Glancy; Zarkesh, Ryan A.; Ziller, Joseph W.; Heyduk, Alan F.
Disulfide reductive elimination from an iron(iii) complex
Chemical Science, 2013, 4, 1906
1514494 CIFC45 H58 Fe N5 O2P 1 21 114.0101; 15.7187; 19.934
90; 97.6912; 90
4350.4Wong, Janice L.; Sánchez, Raúl Hernández; Logan, Jennifer Glancy; Zarkesh, Ryan A.; Ziller, Joseph W.; Heyduk, Alan F.
Disulfide reductive elimination from an iron(iii) complex
Chemical Science, 2013, 4, 1906
1514495 CIFC26 H27 Cu3 N8 O0P -111.4287; 11.7031; 12.918
64.005; 89.783; 71.129
1450.1Wang, Jun-Hao; Li, Mian; Li, Dan
A dynamic, luminescent and entangled MOF as a qualitative sensor for volatile organic solvents and a quantitative monitor for acetonitrile vapour
Chemical Science, 2013, 4, 1793
1514496 CIFC20 H21 Cu3 N8 O0P -111.4262; 11.4509; 12.5243
66.62; 89.182; 69.908
1398.37Wang, Jun-Hao; Li, Mian; Li, Dan
A dynamic, luminescent and entangled MOF as a qualitative sensor for volatile organic solvents and a quantitative monitor for acetonitrile vapour
Chemical Science, 2013, 4, 1793
1514497 CIFC22 H26 Cu3 N8 O2P -111.4964; 11.3571; 12.9352
115.386; 91.133; 69.305
1409.92Wang, Jun-Hao; Li, Mian; Li, Dan
A dynamic, luminescent and entangled MOF as a qualitative sensor for volatile organic solvents and a quantitative monitor for acetonitrile vapour
Chemical Science, 2013, 4, 1793
1514498 CIFC22 H26 Cu3 N8 O2P -111.5152; 11.312; 12.6953
114.171; 91.497; 68.347
1386.93Wang, Jun-Hao; Li, Mian; Li, Dan
A dynamic, luminescent and entangled MOF as a qualitative sensor for volatile organic solvents and a quantitative monitor for acetonitrile vapour
Chemical Science, 2013, 4, 1793
1514499 CIFC24 H29 Cu3 N8 O2P -111.4723; 11.4569; 13.1199
64.295; 89.824; 110.147
1434.83Wang, Jun-Hao; Li, Mian; Li, Dan
A dynamic, luminescent and entangled MOF as a qualitative sensor for volatile organic solvents and a quantitative monitor for acetonitrile vapour
Chemical Science, 2013, 4, 1793
1514500 CIFC26 H33 Cu3 N8P -111.4507; 11.6026; 13.2025
65.36; 71.368; 71.461
1475.62Wang, Jun-Hao; Li, Mian; Li, Dan
A dynamic, luminescent and entangled MOF as a qualitative sensor for volatile organic solvents and a quantitative monitor for acetonitrile vapour
Chemical Science, 2013, 4, 1793
1514501 CIFC22 H24 Cu3 N9 OP -111.37; 11.4274; 12.1912
67.952; 87.743; 69.803
1370.45Wang, Jun-Hao; Li, Mian; Li, Dan
A dynamic, luminescent and entangled MOF as a qualitative sensor for volatile organic solvents and a quantitative monitor for acetonitrile vapour
Chemical Science, 2013, 4, 1793
1514502 CIFC49 H38 N2 O6P -18.947; 14.538; 14.887
75.26; 78.85; 82.01
1829.06Cheriya, Rijo T.; Mallia, Ajith R.; Hariharan, Mahesh
Light harvesting vesicular donor–acceptor scaffold limits the rate of charge recombination in the presence of an electron donor
Energy & Environmental Science, 2014, 7, 1661
1514503 CIFC15 Cl2 N5 Ni O8P 4/n m m :29.2584; 9.2584; 14.1473
90; 90; 90
1212.68Cho, Jaeheung; Kang, Hye Yeon; Liu, Lei V.; Sarangi, Ritimukta; Solomon, Edward I.; Nam, Wonwoo
Mononuclear nickel(II)-superoxo and nickel(III)-peroxo complexes bearing a common macrocyclic TMC ligand.
Chemical science (Royal Society of Chemistry : 2010), 2013, 4, 1502-1508
1514504 CIFC15 H33 Cl N5 Ni O6P 1 c 17.7299; 7.7263; 17.8514
90; 100.673; 90
1047.7Cho, Jaeheung; Kang, Hye Yeon; Liu, Lei V.; Sarangi, Ritimukta; Solomon, Edward I.; Nam, Wonwoo
Mononuclear nickel(II)-superoxo and nickel(III)-peroxo complexes bearing a common macrocyclic TMC ligand.
Chemical science (Royal Society of Chemistry : 2010), 2013, 4, 1502-1508
1514505 CIFC42 H44 F6 Ir N2 O2 P2P 6319.437; 19.437; 18.1371
90; 90; 120
5934.13Schramm, York; Barrios-Landeros, Fabiola; Pfaltz, Andreas
Discovery of an iridacycle catalyst with improved reactivity and enantioselectivity in the hydrogenation of dialkyl ketimines
Chemical Science, 2013, 4, 2760
1514506 CIFC26 H19 Br N2 O2 SP 21 21 218.6182; 12.4254; 20.8694
90; 90; 90
2234.79Li, Meiling; Woods, Philip A.; Smith, Martin D.
Cation-directed enantioselective synthesis of quaternary-substituted indolenines
Chemical Science, 2013, 4, 2907
1514507 CIFC27 H19 N3P 1 21/c 112.6892; 9.9361; 16.3936
90; 102.515; 90
2017.81Li, Meiling; Woods, Philip A.; Smith, Martin D.
Cation-directed enantioselective synthesis of quaternary-substituted indolenines
Chemical Science, 2013, 4, 2907
1514508 CIFC72 H2 Cl16P -111.049; 13.43; 18.364
105.567; 91.091; 106.254
2507Tan, Yuan-Zhi; Li, Jia; Du, Ming-Yue; Lin, Shui-Chao; Xie, Su-Yuan; Lu, Xin; Huang, Rong-Bin; Zheng, Lan-Sun
Exohedrally stabilized C70 isomer with adjacent pentagons characterized by crystallography
Chemical Science, 2013, 4, 2967
1514509 CIFC368 H360 B16 Co8 F64 N72 O40C 1 2/c 127.658; 39.485; 42.581
90; 106.741; 90
44531Whitehead, Martina; Turega, Simon; Stephenson, Andrew; Hunter, Christopher A.; Ward, Michael D.
Quantification of solvent effects on molecular recognition in polyhedral coordination cage hosts
Chemical Science, 2013, 4, 2744
1514510 CIFC23 H21 N O6P 1 21 116.5029; 7.0004; 17.5337
90; 103.817; 90
1967Corbett, Michael T.; Johnson, Jeffrey S.
Enantioselective synthesis of hindered cyclic dialkyl ethers via catalytic oxa-Michael/Michael desymmetrization.
Chemical science (Royal Society of Chemistry : 2010), 2013, 4, 2828-2832
1514511 CIFC28 H40 O6P 21 21 2111.3881; 13.7611; 15.9461
90; 90; 90
2499Liffert, Raphael; Hoecker, Johannes; Jana, Chandan K.; Woods, Tom M.; Burch, Patrick; Jessen, Henning J.; Neuburger, Markus; Gademann, Karl
Withanolide A: synthesis and structural requirements for neurite outgrowth
Chemical Science, 2013, 4, 2851
1514512 CIFC27 H29 Br2 N O4P 21 21 216.4731; 9.867; 41.104
90; 90; 90
2625.3Wang, Hengbin; Guptill, David M.; Alvarez, Adrian Varela; Musaev, Djamaladdin G.; Davies, Huw M. L.
Rhodium-catalyzed enantioselective cyclopropanation of electron deficient alkenes.
Chemical science (Royal Society of Chemistry : 2010), 2013, 4, 2844-2850
1514513 CIFC21 H21 Br O4P 21 21 216.0402; 15.4144; 20.729
90; 90; 90
1930Wang, Hengbin; Guptill, David M.; Alvarez, Adrian Varela; Musaev, Djamaladdin G.; Davies, Huw M. L.
Rhodium-catalyzed enantioselective cyclopropanation of electron deficient alkenes.
Chemical science (Royal Society of Chemistry : 2010), 2013, 4, 2844-2850
1514514 CIFC40 H52 Cl4 F24 N3 O8 P4 Rh2P 1 21/n 112.7242; 20.3878; 23.2389
90; 97.497; 90
5977.1Powers, David C.; Chambers, Matthew B.; Teets, Thomas S.; Elgrishi, Noémie; Anderson, Bryce L.; Nocera, Daniel G.
Halogen Photoelimination from Dirhodium Phosphazane Complexes via Chloride-Bridged Intermediates.
Chemical science (Royal Society of Chemistry : 2010), 2013, 4, 2880
1514515 CIFC25 H26 Cl2 F25 N3 O8 P4 Rh2P 110.1595; 10.386; 12.0283
73.962; 69.049; 71.477
1104.74Powers, David C.; Chambers, Matthew B.; Teets, Thomas S.; Elgrishi, Noémie; Anderson, Bryce L.; Nocera, Daniel G.
Halogen Photoelimination from Dirhodium Phosphazane Complexes via Chloride-Bridged Intermediates.
Chemical science (Royal Society of Chemistry : 2010), 2013, 4, 2880
1514516 CIFC26 H29 Cl2 F24 N3 O9 P4 Rh2P 1 21/c 112.0403; 19.3984; 20.6248
90; 106.961; 90
4607.7Powers, David C.; Chambers, Matthew B.; Teets, Thomas S.; Elgrishi, Noémie; Anderson, Bryce L.; Nocera, Daniel G.
Halogen Photoelimination from Dirhodium Phosphazane Complexes via Chloride-Bridged Intermediates.
Chemical science (Royal Society of Chemistry : 2010), 2013, 4, 2880
1514517 CIFC25 H26 Cl4 F25 N3 O8 P4 Rh2P 1 21/c 112.2025; 21.385; 20.398
90; 98.351; 90
5266.4Powers, David C.; Chambers, Matthew B.; Teets, Thomas S.; Elgrishi, Noémie; Anderson, Bryce L.; Nocera, Daniel G.
Halogen Photoelimination from Dirhodium Phosphazane Complexes via Chloride-Bridged Intermediates.
Chemical science (Royal Society of Chemistry : 2010), 2013, 4, 2880
1514518 CIFC33 H37 Cl4 F24 N3 O9 P4 Rh2P -110.7825; 15.2029; 18.7253
87.983; 80.065; 73.223
2894.5Powers, David C.; Chambers, Matthew B.; Teets, Thomas S.; Elgrishi, Noémie; Anderson, Bryce L.; Nocera, Daniel G.
Halogen Photoelimination from Dirhodium Phosphazane Complexes via Chloride-Bridged Intermediates.
Chemical science (Royal Society of Chemistry : 2010), 2013, 4, 2880
1514519 CIFC62 H135 Mn Mo6 N6 O26P c c a23.3192; 28.2; 30.215
90; 90; 90
19869Yvon, Carine; Macdonell, Andrew; Buchwald, Saskia; Surman, Andrew J.; Follet, Noémie; Alex, Jennifer; Long, De-Liang; Cronin, Leroy
A collection of robust methodologies for the preparation of asymmetric hybrid Mn‒Anderson polyoxometalates for multifunctional materials
Chemical Science, 2013, 4, 3810
1514520 CIFC94 H152 Mn Mo6 N9 O26P -118.0136; 26.3164; 26.5199
113.089; 102.13; 100.729
10790.7Yvon, Carine; Macdonell, Andrew; Buchwald, Saskia; Surman, Andrew J.; Follet, Noémie; Alex, Jennifer; Long, De-Liang; Cronin, Leroy
A collection of robust methodologies for the preparation of asymmetric hybrid Mn‒Anderson polyoxometalates for multifunctional materials
Chemical Science, 2013, 4, 3810
1514521 CIFC80 H153 Mn Mo6 N8 O28P 1 21/c 127.455; 29.007; 24.974
90; 94.45; 90
19829Yvon, Carine; Macdonell, Andrew; Buchwald, Saskia; Surman, Andrew J.; Follet, Noémie; Alex, Jennifer; Long, De-Liang; Cronin, Leroy
A collection of robust methodologies for the preparation of asymmetric hybrid Mn‒Anderson polyoxometalates for multifunctional materials
Chemical Science, 2013, 4, 3810
1514522 CIFC80 H155 Mn Mo6 N8 O29P n m a28.257; 21.8128; 16.5796
90; 90; 90
10219.1Yvon, Carine; Macdonell, Andrew; Buchwald, Saskia; Surman, Andrew J.; Follet, Noémie; Alex, Jennifer; Long, De-Liang; Cronin, Leroy
A collection of robust methodologies for the preparation of asymmetric hybrid Mn‒Anderson polyoxometalates for multifunctional materials
Chemical Science, 2013, 4, 3810
1514523 CIFC19 H25 N O4P 1 21 18.3357; 11.294; 9.9646
90; 103.551; 90
912Wasil, Zahida; Pahirulzaman, Khomaizon A. K.; Butts, Craig; Simpson, Thomas J.; Lazarus, Colin M.; Cox, Russell J.
One pathway, many compounds: heterologous expression of a fungal biosynthetic pathway reveals its intrinsic potential for diversity
Chemical Science, 2013, 4, 3845
1514524 CIFC19 H23 N O4P 1 21 17.3372; 22.647; 20.618
90; 90.112; 90
3426Wasil, Zahida; Pahirulzaman, Khomaizon A. K.; Butts, Craig; Simpson, Thomas J.; Lazarus, Colin M.; Cox, Russell J.
One pathway, many compounds: heterologous expression of a fungal biosynthetic pathway reveals its intrinsic potential for diversity
Chemical Science, 2013, 4, 3845
1514525 CIFC13 H19 N O3P 1 21 19.0939; 30.695; 9.139
90; 94.405; 90
2543.5Wasil, Zahida; Pahirulzaman, Khomaizon A. K.; Butts, Craig; Simpson, Thomas J.; Lazarus, Colin M.; Cox, Russell J.
One pathway, many compounds: heterologous expression of a fungal biosynthetic pathway reveals its intrinsic potential for diversity
Chemical Science, 2013, 4, 3845
1514526 CIFC17 H17 Cl3 N2 O3P -19.7614; 10.2988; 10.4722
80.745; 71.023; 89.009
981.91Cui, Sunliang; Zhang, Yan; Wang, Dahai; Wu, Qifan
Rh(iii)-catalyzed C–H activation/[4 + 3] cycloaddition of benzamides and vinylcarbenoids: facile synthesis of azepinones
Chemical Science, 2013, 4, 3912
1514527 CIFC35 H61 B11 Br6 F P Ru SiP -111.8239; 14.7954; 15.4075
99.322; 110.839; 91.577
2475.17Fasulo, Meg E.; Lipke, Mark C.; Tilley, T. Don
Structural and mechanistic investigation of a cationic hydrogen-substituted ruthenium silylene catalyst for alkene hydrosilation
Chemical Science, 2013, 4, 3882
1514528 CIFC30.5 H23.25 Co F6 N5.75 O6 S2P -19.8107; 12.2952; 13.4212
93.235; 91.814; 91.35
1615.01Nippe, Michael; Khnayzer, Rony S.; Panetier, Julien A.; Zee, David Z.; Olaiya, Babatunde S.; Head-Gordon, Martin; Chang, Christopher J.; Castellano, Felix N.; Long, Jeffrey R.
Catalytic proton reduction with transition metal complexes of the redox-active ligand bpy2PYMe
Chemical Science, 2013, 4, 3934
1514529 CIFC33 H30.5 B0.5 F11 N7 Ni O0.5 P1.5P 1 21/n 111.605; 26.456; 12.584
90; 114.443; 90
3517.3Nippe, Michael; Khnayzer, Rony S.; Panetier, Julien A.; Zee, David Z.; Olaiya, Babatunde S.; Head-Gordon, Martin; Chang, Christopher J.; Castellano, Felix N.; Long, Jeffrey R.
Catalytic proton reduction with transition metal complexes of the redox-active ligand bpy2PYMe
Chemical Science, 2013, 4, 3934
1514530 CIFC33 H27 Cu F6 N7 O6 S2P -19.9247; 13.1783; 14.849
66.577; 80.638; 81.873
1752.01Nippe, Michael; Khnayzer, Rony S.; Panetier, Julien A.; Zee, David Z.; Olaiya, Babatunde S.; Head-Gordon, Martin; Chang, Christopher J.; Castellano, Felix N.; Long, Jeffrey R.
Catalytic proton reduction with transition metal complexes of the redox-active ligand bpy2PYMe
Chemical Science, 2013, 4, 3934

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