Crystallography Open Database

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1516039 CIFC70 H78 Au3 Cu2 NP -112.158; 16.063; 18.733
64.59; 83.11; 74.52
3184.6Yip, Sung-Kong; Chan, Chui-Ling; Lam, Wai Han; Cheung, Kung-Kai; Yam, Vivian Wing-Wah
Synthesis, structure and luminescence studies of heterometallic gold(I)-copper(I) and -silver(I) alkynyl clusters/aggregates.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2007, 6, 365-371
1516040 CIFC18 H34 Cr N10 O7 YbP 1 21/n 113.0556; 12.7471; 18.9654
90; 109.859; 90
2968.5Lazarides, Theodore; Davies, Graham M.; Adams, Harry; Sabatini, Cristiana; Barigelletti, Francesco; Barbieri, Andrea; Pope, Simon J. A.; Faulkner, Stephen; Ward, Michael D.
Ligand-field excited states of hexacyanochromate and hexacyanocobaltate as sensitisers for near-infrared luminescence from Nd(iii) and Yb(iii) in cyanide-bridged d-f assemblies.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2007, 6, 1152-1157
1516041 CIFC38 H34P 1 21/n 19.5027; 8.2756; 17.7737
90; 98.642; 90
1381.86Beeby, Andrew; Findlay, Karen S.; Goeta, Andrés E; Porrès, Laurent; Rutter, Simon R.; Thompson, Amber L.
Engineering a twist in 9,10-diethynylanthracenes by steric interactions.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2007, 6, 982-986
1516042 CIFC9 H22 N2 O4P 1 21/n 16.02881; 9.88517; 20.4701
90; 97.8757; 90
1208.43Hasib-ur-Rahman, Muhammad; Larachi, Faïçal
CO2 capture in alkanolamine-RTIL blends via carbamate crystallization: route to efficient regeneration.
Environmental science & technology, 2012, 46, 11443-11450
1516043 CIFC53 H64.5 F12 N5.5 O10 P2P -110.9871; 15.0321; 19.4495
67.41; 87.04; 85.923
2957.3Xing, Hao; Wei, Peifa; Yan, Xuzhou
Supramolecular Side-Chain Poly[2]pseudorotaxanes Formed by Orthogonal Coordination-Driven Self-Assembly and Crown-Ether-Based Host-Guest Interactions.
Organic letters, 2014, 16, 2850-2853
1516044 CIFC117 H122 N4 O2 ZnP -114.274; 16.988; 21.032
67.91; 80.65; 86.6
4662.8Ota, Kensuke; Tanaka, Takayuki; Osuka, Atsuhiro
meso-β Dibenzo[a,g]corannulene-Fused Porphyrins.
Organic letters, 2014, 16, 2974-2977
1516045 CIFC96.89 H88.31 N4 O1.72 ZnP -19.353; 21.838; 38.554
103.231; 90.09; 102.288
7480Ota, Kensuke; Tanaka, Takayuki; Osuka, Atsuhiro
meso-β Dibenzo[a,g]corannulene-Fused Porphyrins.
Organic letters, 2014, 16, 2974-2977
1516046 CIFC96 H98 N4 O2 ZnP -19.7687; 15.6035; 26.497
75.421; 83.382; 87.1181
3881.8Ota, Kensuke; Tanaka, Takayuki; Osuka, Atsuhiro
meso-β Dibenzo[a,g]corannulene-Fused Porphyrins.
Organic letters, 2014, 16, 2974-2977
1516047 CIFC23 H18 O2P -19.661; 9.9907; 10.7602
63.28; 80.45; 70.81
875.9Chagarovsky, Alexey O.; Budynina, Ekaterina M.; Ivanova, Olga A.; Villemson, Elena V.; Rybakov, Victor B.; Trushkov, Igor V.; Melnikov, Mikhail Ya
Reaction of Corey Ylide with α,β-Unsaturated Ketones: Tuning of Chemoselectivity toward Dihydrofuran Synthesis.
Organic letters, 2014, 16, 2830-2833
1516048 CIFC23 H23 N O3P 1 21/c 110.0605; 10.1253; 19.2983
90; 91.597; 90
1965.1Chagarovsky, Alexey O.; Budynina, Ekaterina M.; Ivanova, Olga A.; Villemson, Elena V.; Rybakov, Victor B.; Trushkov, Igor V.; Melnikov, Mikhail Ya
Reaction of Corey Ylide with α,β-Unsaturated Ketones: Tuning of Chemoselectivity toward Dihydrofuran Synthesis.
Organic letters, 2014, 16, 2830-2833
1516049 CIFC21 H23 F N2 OP 1 21/c 19.073; 11.096; 19.557
90; 94.205; 90
1963.6Thirupathi, Nuligonda; Hari Babu, Madala; Dwivedi, Vikas; Kant, Ruchir; Sridhar Reddy, Maddi
Palladium-Catalyzed Tandem Intramolecular Oxy/Amino-Palladation/Isocyanide Insertion: Synthesis of α-Benzofuranyl/Indolylacetamides.
Organic letters, 2014, 16, 2908-2911
1516050 CIFC26 H36 N2 O2P 21 21 2110.5434; 11.509; 19.6411
90; 90; 90
2383.3Seo, Min-Seob; Lee, Ansoo; Kim, Hyunwoo
2,2'-dihydroxybenzil: a stereodynamic probe for primary amines controlled by steric strain.
Organic letters, 2014, 16, 2950-2953
1516051 CIFC18 H19.26 N O5.13P 1 21 18.1308; 17.5736; 11.0262
90; 94.94; 90
1569.65Luo, Zengwei; Wang, Fuqian; Zhang, Jinwen; Li, Xingyao; Zhang, Mengke; Hao, Xincai; Xue, Yongbo; Li, Yan; Horgen, F. David; Yao, Guangmin; Zhang, Yonghui
Cytotoxic alkaloids from the whole plants of Zephyranthes candida.
Journal of natural products, 2012, 75, 2113-2120
1516052 CIFC15 H22 O5P 21 21 217.6345; 13.862; 13.927
90; 90; 90
1473.9Macías, Francisco A; Santana, Alejandro; Yamahata, Azusa; Varela, Rosa M.; Fronczek, Frank R.; Molinillo, José M G
Facile preparation of bioactive seco-guaianolides and guaianolides from Artemisia gorgonum and evaluation of their phytotoxicity.
Journal of natural products, 2012, 75, 1967-1973
1516053 CIFC15.8 H19.6 O4.4P 21 21 217.3918; 29.704; 32.1937
90; 90; 90
7068.6Macías, Francisco A; Santana, Alejandro; Yamahata, Azusa; Varela, Rosa M.; Fronczek, Frank R.; Molinillo, José M G
Facile preparation of bioactive seco-guaianolides and guaianolides from Artemisia gorgonum and evaluation of their phytotoxicity.
Journal of natural products, 2012, 75, 1967-1973
1516054 CIFC15 H20 O5P 21 21 219.0581; 9.5429; 15.5537
90; 90; 90
1344.47Macías, Francisco A; Santana, Alejandro; Yamahata, Azusa; Varela, Rosa M.; Fronczek, Frank R.; Molinillo, José M G
Facile preparation of bioactive seco-guaianolides and guaianolides from Artemisia gorgonum and evaluation of their phytotoxicity.
Journal of natural products, 2012, 75, 1967-1973
1516055 CIFC23.5 H21 O9.5P 1 21 110.876; 6.7384; 14.743
90; 92.481; 90
1079.5Thanh, Van Trinh Thi; Pham, Van Cuong; Mai, Huong Doan Thi; Litaudon, Marc; Guéritte, Françoise; Retailleau, Pascal; Nguyen, Van Hung; Chau, Van Minh
Cytotoxic lignans from fruits of Cleistanthus indochinensis: synthesis of cleistantoxin derivatives.
Journal of natural products, 2012, 75, 1578-1583
1516057 CIFC26 H15 Mo O5 PP 1 21 117.039; 6.2992; 21.025
90; 97.831; 90
2235.6Mao, Yanli; Lim, Kelvin Meng Hui; Ganguly, Rakesh; Mathey, Francois
A new route to a 2-phosphanaphthalene.
Organic letters, 2012, 14, 4974-4975
1516058 CIFC26 H16 Cl O6 P WP 1 21/c 118.4823; 9.4251; 15.2278
90; 114.313; 90
2417.38Mao, Yanli; Lim, Kelvin Meng Hui; Ganguly, Rakesh; Mathey, Francois
A new route to a 2-phosphanaphthalene.
Organic letters, 2012, 14, 4974-4975
1516059 CIFC26 H16 Cl O6 P WP 1 21/n 18.1251; 12.1902; 25.1571
90; 90.472; 90
2491.6Mao, Yanli; Lim, Kelvin Meng Hui; Ganguly, Rakesh; Mathey, Francois
A new route to a 2-phosphanaphthalene.
Organic letters, 2012, 14, 4974-4975
1516060 CIFC16 H20 N2 O3P n a 2140.076; 5.5575; 13.021
90; 90; 90
2900.1Hirschhäuser, Christoph; Parker, Jeremy S.; Perry, Matthew W. D.; Haddow, Mairi F.; Gallagher, Timothy
Spiro-fused pyrrolidine, piperidine, and oxindole scaffolds from lactams.
Organic letters, 2012, 14, 4846-4849
1516061 CIFC17 H22 N2 O3P b c a9.5653; 10.45; 30.655
90; 90; 90
3064.2Hirschhäuser, Christoph; Parker, Jeremy S.; Perry, Matthew W. D.; Haddow, Mairi F.; Gallagher, Timothy
Spiro-fused pyrrolidine, piperidine, and oxindole scaffolds from lactams.
Organic letters, 2012, 14, 4846-4849
1516062 CIFC16 H20 N2 O3P 1 21/n 110.604; 10.38; 13.204
90; 95.551; 90
1446.5Hirschhäuser, Christoph; Parker, Jeremy S.; Perry, Matthew W. D.; Haddow, Mairi F.; Gallagher, Timothy
Spiro-fused pyrrolidine, piperidine, and oxindole scaffolds from lactams.
Organic letters, 2012, 14, 4846-4849
1516063 CIFC12 H12 N2 O2P 1 21/c 16.4277; 10.169; 15.7788
90; 95.698; 90
1026.26Hirschhäuser, Christoph; Parker, Jeremy S.; Perry, Matthew W. D.; Haddow, Mairi F.; Gallagher, Timothy
Spiro-fused pyrrolidine, piperidine, and oxindole scaffolds from lactams.
Organic letters, 2012, 14, 4846-4849
1516064 CIFC15 H19 N OI b a 210.9646; 34.3413; 6.972
90; 90; 90
2625.23Brawn, Ryan A.; Guimarães, Cristiano R W; McClure, Kim F.; Liras, Spiros
An efficient synthesis of bridged heterocycles from an Ir(I) bis-amination/ring-closing metathesis sequence.
Organic letters, 2012, 14, 4802-4805
1516066 CIFC19 H25 N3 O2P 1 21/c 110.5786; 10.5791; 15.5501
90; 104.447; 90
1685.22Tan, Shen H.; Banwell, Martin G.; Willis, Anthony C.; Reekie, Tristan A.
Application of a Raney-cobalt-mediated tandem reductive cyclization protocol to total syntheses of the Aspidosperma alkaloids (±)-limaspermidine and (±)-1-acetylaspidoalbidine.
Organic letters, 2012, 14, 5621-5623
1516067 CIFC20 H29 N3 O2P 1 21/c 111.8836; 10.3003; 15.9702
90; 109.242; 90
1845.62Tan, Shen H.; Banwell, Martin G.; Willis, Anthony C.; Reekie, Tristan A.
Application of a Raney-cobalt-mediated tandem reductive cyclization protocol to total syntheses of the Aspidosperma alkaloids (±)-limaspermidine and (±)-1-acetylaspidoalbidine.
Organic letters, 2012, 14, 5621-5623
1516068 CIFC19 H26 N2 OP n a 2113.7232; 14.9269; 7.6655
90; 90; 90
1570.24Tan, Shen H.; Banwell, Martin G.; Willis, Anthony C.; Reekie, Tristan A.
Application of a Raney-cobalt-mediated tandem reductive cyclization protocol to total syntheses of the Aspidosperma alkaloids (±)-limaspermidine and (±)-1-acetylaspidoalbidine.
Organic letters, 2012, 14, 5621-5623
1516069 CIFC21 H38 O4P 21 21 215.2688; 7.4978; 52.786
90; 90; 90
2085.28Persich, Peter; Kerschbaumer, Julia; Helling, Sandra; Hildmann, Barbara; Wibbeling, Birgit; Haufe, Günter
Transannular O-heterocyclization: a useful tool for the total synthesis of Murisolin and 16,19-cis-Murisolin.
Organic letters, 2012, 14, 5628-5631
1516074 CIFC40 H41 N3 O4P -112.3712; 12.5383; 13.3489
102.471; 100.682; 118.295
1677.5Castellano, Teresa G.; Neo, Ana G.; Marcaccini, Stefano; Marcos, Carlos F.
Enols as feasible acid components in the Ugi condensation.
Organic letters, 2012, 14, 6218-6221
1516075 CIFC19 H24 N2 O3P 21 21 217.9485; 12.166; 17.196
90; 90; 90
1662.9Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J.
The synthesis of melohenine B and a related natural product.
Organic letters, 2012, 14, 6166-6169
1516076 CIFC20 H22 N2 O6P 21 21 217.1383; 10.9101; 23.798
90; 90; 90
1853.4Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J.
The synthesis of melohenine B and a related natural product.
Organic letters, 2012, 14, 6166-6169
1516077 CIFC21 H26 N2 O5P 618.268; 8.268; 48.704
90; 90; 120
2883.3Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J.
The synthesis of melohenine B and a related natural product.
Organic letters, 2012, 14, 6166-6169
1516078 CIFC21 H28 N2 O3P 21 21 217.4222; 9.96; 25.642
90; 90; 90
1895.6Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J.
The synthesis of melohenine B and a related natural product.
Organic letters, 2012, 14, 6166-6169
1516079 CIFC22 H26 N2 O4P 21 21 217.9567; 12.3012; 20.572
90; 90; 90
2013.5Lancefield, Christopher S.; Zhou, Linna; Lébl, Tomas; Slawin, Alexandra M. Z.; Westwood, Nicholas J.
The synthesis of melohenine B and a related natural product.
Organic letters, 2012, 14, 6166-6169
1516081 CIFC14 H17 B F2 N4P -17.3413; 7.5696; 13.1377
96.128; 99.18; 95.256
712.2Lee, Ho Yong; Olasz, András; Chen, Chun-Hsing; Lee, Dongwhan
Three-stage binary switching of azoaromatic polybase.
Organic letters, 2012, 14, 6286-6289
1516082 CIFC29 H20 N2 O7P -110.6771; 13.0878; 18.3378
83.667; 73.144; 75.898
2376.35Kelgtermans, Hans; DobrzaƄska, Liliana; Van Meervelt, Luc; Dehaen, Wim
A fragment-based approach toward substituted trioxa[7]helicenes.
Organic letters, 2012, 14, 5200-5203
1516083 CIFC32 H38 O8P 1 21/c 16.0458; 9.8845; 24.023
90; 95.05; 90
1430Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516084 CIFC40 H54 O8P 1 21/c 116.6322; 9.1956; 12.1051
90; 98.357; 90
1831.73Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516085 CIFC26 H24 O8P 1 21/n 15.271; 14.1093; 15.2301
90; 94.765; 90
1128.7Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516086 CIFC24 H20 O8P 1 21/c 110.8267; 9.5361; 20.2199
90; 97.858; 90
2068Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516087 CIFC6 H5 Br O3P 1 21/n 110.3165; 4.9709; 14.1637
90; 101.925; 90
710.67Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516088 CIFC36 H42 O6C 1 2/c 129.11; 9.5418; 22.962
90; 103.062; 90
6212.9Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516089 CIFC32 H26 O8P 1 21/c 19.5983; 5.4838; 24.21
90; 91.793; 90
1273.7Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516090 CIFC26 H26 O8P 1 21/n 17.7228; 11.0389; 13.6925
90; 97.28; 90
1157.89Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516091 CIFC40 H52 O8P -15.7869; 9.9739; 16.9218
87.166; 81.47; 78.248
945.45Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516092 CIFC12 H12 Br2 O6P 1 21/n 19.6055; 7.7143; 18.8681
90; 93.576; 90
1395.4Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516093 CIFC40 H54 O12P -15.9676; 9.4094; 17.2733
89.735; 85.714; 85.834
964.7Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516094 CIFC32 H26 O8P -16.1693; 9.7194; 11.3573
67.533; 80.008; 86.414
619.77Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377
1516095 CIFC32 H38 O12P -15.946; 10.5168; 12.6676
81.198; 80.39; 81.904
766.41Benniston, Andrew C.; Winstanley, Thomas P. L.; Lemmetyinen, Helge; Tkachenko, Nikolai V.; Harrington, Ross W.; Wills, Corinne
Large Stokes shift fluorescent dyes based on a highly substituted terephthalic acid core.
Organic letters, 2012, 14, 1374-1377

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