Crystallography Open Database

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Searching journal of publication like 'New Journal of Chemistry' volume of publication is 42

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7057930 CIFC43 H52 O12 S4P 1 21/c 120.44879; 26.48153; 18.22756
90; 116.44; 90
8838.06Landovský, T.; Dvořáková, H.; Eigner, V.; Babor, M.; Krupička, M.; Kohout, M.; Lhoták, P.
Chemoselective oxidation of phenoxathiin-based thiacalix[4]arene and the stereoselective alkylation of products
New Journal of Chemistry, 2018, 42, 20074
7057931 CIFC63 H66.78 Cl6 O11.39 S4P -112.1853; 13.2193; 21.7629
99.283; 96.0609; 107.455
3255.9Landovský, T.; Dvořáková, H.; Eigner, V.; Babor, M.; Krupička, M.; Kohout, M.; Lhoták, P.
Chemoselective oxidation of phenoxathiin-based thiacalix[4]arene and the stereoselective alkylation of products
New Journal of Chemistry, 2018, 42, 20074
7057932 CIFC85 H77 Eu3 N10 O22P 1 21/n 114.5999; 17.7683; 31.8703
90; 90.663; 90
8267.1Yang, Shuai-Liang; Yuan, Yue-Ying; Sun, Pei-Pei; Lin, Tian; Zhang, Chen-Xi; Wang, Qing-Lun
3D water-stable europium metal organic frameworks as a multi-responsive luminescent sensor for high-efficiency detection of Cr2O72−, MnO4−, Cr3+ ions and SDBS in aqueous solution
New Journal of Chemistry, 2018, 42, 20137
7057933 CIFC34 H28 N4 O5I b a 216.631; 30.14; 6.24
90; 90; 90
3127.9Mandal, Jayanta; Ghorai, Pravat; Brandão, Paula; Pal, Kunal; Karmakar, Parimal; Saha, Amrita
An aminoquinoline based biocompatible fluorescent and colourimetric pH sensor designed for cancer cell discrimination
New Journal of Chemistry, 2018, 42, 19818
7057934 CIFC28 H28 N2 O5P -18.7731; 12.3585; 12.5316
96.327; 103.909; 106.988
1237.26Yue, Guizhou; Wu, Yao; Dou, Zhengjie; Chen, Huabao; Yin, Zhongqiong; Song, Xu; He, ChangLiang; Wang, Xianxiang; Feng, Juhua; Zhang, Zuming; Zou, Ping; Lu, Cuifen
Synthesis of spiropyrrolidine oxindoles via Ag-catalyzed stereo- and regioselective 1,3-dipolar cycloaddition of indole-based azomethine ylides with chalcones
New Journal of Chemistry, 2018, 42, 20024
7057935 CIFC27 H18 O9P 1 21/n 112.2928; 13.0408; 27.679
90; 93.341; 90
4429.6Das, Debarati; Roy, Sandipan; Biradha, Kumar
Crystal engineering with isosteric triether and triamine linked aromatic tri-carboxylic acids: iso-structurality and synthon interplay in their co-crystals and salts with bis(pyridyl) derivatives
New Journal of Chemistry, 2018, 42, 19953
7057936 CIFC70 H70 N8 O16P -16.874; 12.86; 18.821
103.912; 97.77; 100.062
1562.6Das, Debarati; Roy, Sandipan; Biradha, Kumar
Crystal engineering with isosteric triether and triamine linked aromatic tri-carboxylic acids: iso-structurality and synthon interplay in their co-crystals and salts with bis(pyridyl) derivatives
New Journal of Chemistry, 2018, 42, 19953
7057937 CIFC38 H33 N5 O7P -19.179; 13.799; 14.211
109.83; 100.42; 97.41
1630Das, Debarati; Roy, Sandipan; Biradha, Kumar
Crystal engineering with isosteric triether and triamine linked aromatic tri-carboxylic acids: iso-structurality and synthon interplay in their co-crystals and salts with bis(pyridyl) derivatives
New Journal of Chemistry, 2018, 42, 19953
7057938 CIFC51 H41 N7 O6P -19.192; 13.0507; 19.469
76.186; 83.285; 69.384
2121.4Das, Debarati; Roy, Sandipan; Biradha, Kumar
Crystal engineering with isosteric triether and triamine linked aromatic tri-carboxylic acids: iso-structurality and synthon interplay in their co-crystals and salts with bis(pyridyl) derivatives
New Journal of Chemistry, 2018, 42, 19953
7057939 CIFC38 H33 N5 O7 SP -19.017; 11.28; 16.817
97.49; 91.87; 92.38
1693Das, Debarati; Roy, Sandipan; Biradha, Kumar
Crystal engineering with isosteric triether and triamine linked aromatic tri-carboxylic acids: iso-structurality and synthon interplay in their co-crystals and salts with bis(pyridyl) derivatives
New Journal of Chemistry, 2018, 42, 19953
7057940 CIFC27 H23 N3 O7P 1 21/c 126.2114; 7.6705; 26.7036
90; 118.679; 90
4710.2Das, Debarati; Roy, Sandipan; Biradha, Kumar
Crystal engineering with isosteric triether and triamine linked aromatic tri-carboxylic acids: iso-structurality and synthon interplay in their co-crystals and salts with bis(pyridyl) derivatives
New Journal of Chemistry, 2018, 42, 19953
7057941 CIFC41 H40 N2 O12P -17.014; 15.896; 17.428
82.57; 87.049; 79.316
1892.7Das, Debarati; Roy, Sandipan; Biradha, Kumar
Crystal engineering with isosteric triether and triamine linked aromatic tri-carboxylic acids: iso-structurality and synthon interplay in their co-crystals and salts with bis(pyridyl) derivatives
New Journal of Chemistry, 2018, 42, 19953
7057942 CIFC39 H28 N2 O9P -17.433; 9.101; 22.827
88.73; 87.969; 84.49
1535.8Das, Debarati; Roy, Sandipan; Biradha, Kumar
Crystal engineering with isosteric triether and triamine linked aromatic tri-carboxylic acids: iso-structurality and synthon interplay in their co-crystals and salts with bis(pyridyl) derivatives
New Journal of Chemistry, 2018, 42, 19953
7057943 CIFC40 H35 N5 O6P -18.4; 13.02; 15.42
92.7; 98.8; 96.2
1653Das, Debarati; Roy, Sandipan; Biradha, Kumar
Crystal engineering with isosteric triether and triamine linked aromatic tri-carboxylic acids: iso-structurality and synthon interplay in their co-crystals and salts with bis(pyridyl) derivatives
New Journal of Chemistry, 2018, 42, 19953
7057944 CIFC37 H28 N2 O10 S2P -17.8654; 9.5964; 22.652
92.607; 97.703; 95.618
1683.2Das, Debarati; Roy, Sandipan; Biradha, Kumar
Crystal engineering with isosteric triether and triamine linked aromatic tri-carboxylic acids: iso-structurality and synthon interplay in their co-crystals and salts with bis(pyridyl) derivatives
New Journal of Chemistry, 2018, 42, 19953
7059038 CIFC26 H17.54 N3 O4.27P -19.9987; 14.262; 15.699
97.42; 97.333; 108.183
2075.3Villada, Juan D.; D’Vries, Richard F.; Macías, Mario; Zuluaga, Fabio; Chaur, Manuel N.
Structural characterization of a fluorescein hydrazone molecular switch with application towards logic gates
New Journal of Chemistry, 2018, 42, 18050
7059039 CIFC39 H31 N5 O3 SP 1 21 110.0344; 8.1177; 20.1951
90; 97.782; 90
1629.87Yadav, Neetu; Singh, Ashok Kumar
Dicarbohydrazide based chemosensors for copper and cyanide ions via a displacement approach
New Journal of Chemistry, 2018, 42, 6023
7059040 CIFC31 H27 N5 O5 SC 1 2/c 130.297; 12.301; 16.64
90; 112; 90
5750Yadav, Neetu; Singh, Ashok Kumar
Dicarbohydrazide based chemosensors for copper and cyanide ions via a displacement approach
New Journal of Chemistry, 2018, 42, 6023
7059041 CIFC29 H23 O5 S Sb WP 1 21/n 110.355; 28.23; 10.896
90; 115.85; 90
2866Landman, Marilé; Jansen van Rensburg, Armand; van Rooyen, Petrus H.; Conradie, Marrigje M.; Conradie, Jeanet
Triphenylstibine-substituted Fischer carbene complexes of tungsten(0): synthesis, structure, DFT and electrochemistry
New Journal of Chemistry, 2018, 42, 7301
7059042 CIFC33 H25 O5 S2 Sb WP -19.587; 11.959; 15.924
71.22; 75.47; 66.92
1573.8Landman, Marilé; Jansen van Rensburg, Armand; van Rooyen, Petrus H.; Conradie, Marrigje M.; Conradie, Jeanet
Triphenylstibine-substituted Fischer carbene complexes of tungsten(0): synthesis, structure, DFT and electrochemistry
New Journal of Chemistry, 2018, 42, 7301
7059043 CIFC29 H23 O6 Sb WP -110.584; 10.93; 14.073
101.23; 91.88; 118.69
1386Landman, Marilé; Jansen van Rensburg, Armand; van Rooyen, Petrus H.; Conradie, Marrigje M.; Conradie, Jeanet
Triphenylstibine-substituted Fischer carbene complexes of tungsten(0): synthesis, structure, DFT and electrochemistry
New Journal of Chemistry, 2018, 42, 7301
7059044 CIFC30 H26 N O5 Sb WP 1 21/n 110.482; 28.043; 10.666
90; 115.58; 90
2828Landman, Marilé; Jansen van Rensburg, Armand; van Rooyen, Petrus H.; Conradie, Marrigje M.; Conradie, Jeanet
Triphenylstibine-substituted Fischer carbene complexes of tungsten(0): synthesis, structure, DFT and electrochemistry
New Journal of Chemistry, 2018, 42, 7301
7059045 CIFC27 H22 Br N3 O4 SP b c a14.158; 14.747; 23.048
90; 90; 90
4812Poomathi, Nataraj; Balaji, Ravichandran; Maheswari, Narayanan Uma; Mathivanan, Narayanasamy; Perumal, Paramasivan T.; Balasubramanian, Kalpattu K.; Barathi, Veluchamy Amutha; Ramakrishna, Seeram
Brønsted acid catalysed eco friendly synthesis of quaternary centred C-3 functionalized oxindole derivatives
New Journal of Chemistry, 2018, 42, 14817
7059046 CIFC20 H20 Cl2 F N5 O9 RuP -110.442; 16.4514; 16.4752
65.968; 82.841; 87.442
2564.7Kostin, Gennadiy A.; Mikhailov, Artem A.; Kuratieva, Natalia V.; Pishchur, Denis P.; Makhinya, Alexander N.
High thermal stability of the Ru‒ON (MS1) linkage isomer of the ruthenium nitrosyl complex [RuNO(Py)4F](ClO4)2 with the trans NO‒Ru‒F coordinate
New Journal of Chemistry, 2018, 42, 18928
7059121 CIFC10 H8 N6 O4 SnI 1 2/c 111.9805; 9.1305; 12.6134
90; 116.631; 90
1233.4Karmakar, Anirban; Hazra, Susanta; Rúbio, Guilherme M. D. M.; Guedes da Silva, M. Fátima C.; Pombeiro, Armando J. L.
Packing polymorphism in 3-amino-2-pyrazinecarboxylate based tin(ii) complexes and their catalytic activity towards cyanosilylation of aldehydes
New Journal of Chemistry, 2018, 42, 17513
7059122 CIFC10 H8 N6 O4 SnP 1 21/c 18.2366; 9.4181; 16.5098
90; 100.057; 90
1261.04Karmakar, Anirban; Hazra, Susanta; Rúbio, Guilherme M. D. M.; Guedes da Silva, M. Fátima C.; Pombeiro, Armando J. L.
Packing polymorphism in 3-amino-2-pyrazinecarboxylate based tin(ii) complexes and their catalytic activity towards cyanosilylation of aldehydes
New Journal of Chemistry, 2018, 42, 17513
7059123 CIFC17 H18 N4 OP 1 21/c 111.141; 11.137; 13.176
90; 104.481; 90
1582.9Huang, Ying; Min, Wei; Wu, Qiu-Wen; Sun, Jing; Shi, Da-Hua; Yan, Chao-Guo
Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities
New Journal of Chemistry, 2018, 42, 16211
7059124 CIFC17 H18 F N3 O3P 1 21/c 18.9286; 12.5329; 14.6928
90; 90.562; 90
1644.1Huang, Ying; Min, Wei; Wu, Qiu-Wen; Sun, Jing; Shi, Da-Hua; Yan, Chao-Guo
Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities
New Journal of Chemistry, 2018, 42, 16211
7059125 CIFC25 H30 N2 O2P 1 21/c 18.3608; 15.3765; 19.0562
90; 114.853; 90
2223Huang, Ying; Min, Wei; Wu, Qiu-Wen; Sun, Jing; Shi, Da-Hua; Yan, Chao-Guo
Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities
New Journal of Chemistry, 2018, 42, 16211
7059126 CIFC23 H23 N3 O3A e a 225.339; 10.4719; 15.6589
90; 90; 90
4155Huang, Ying; Min, Wei; Wu, Qiu-Wen; Sun, Jing; Shi, Da-Hua; Yan, Chao-Guo
Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities
New Journal of Chemistry, 2018, 42, 16211
7059127 CIFC27 H25 Cl N2 O2P -19.624; 10.925; 11.808
85.813; 81.37; 71.045
1160.5Huang, Ying; Min, Wei; Wu, Qiu-Wen; Sun, Jing; Shi, Da-Hua; Yan, Chao-Guo
Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities
New Journal of Chemistry, 2018, 42, 16211
7059128 CIFC20 H24 Cl N3 O3P 1 21/c 18.0048; 10.8582; 23.772
90; 93.426; 90
2062.5Huang, Ying; Min, Wei; Wu, Qiu-Wen; Sun, Jing; Shi, Da-Hua; Yan, Chao-Guo
Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities
New Journal of Chemistry, 2018, 42, 16211
7059129 CIFC21 H22 N2 O2P 1 21/c 18.3445; 18.8273; 11.5601
90; 90.495; 90
1816.1Huang, Ying; Min, Wei; Wu, Qiu-Wen; Sun, Jing; Shi, Da-Hua; Yan, Chao-Guo
Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities
New Journal of Chemistry, 2018, 42, 16211
7059130 CIFC19 H20 N4 O3P 1 21/c 111.5941; 7.55; 22.5636
90; 97.25; 90
1959.3Huang, Ying; Min, Wei; Wu, Qiu-Wen; Sun, Jing; Shi, Da-Hua; Yan, Chao-Guo
Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities
New Journal of Chemistry, 2018, 42, 16211
7059131 CIFC16 H16 N4 OP -17.8537; 10.0186; 10.4353
73.18; 70.237; 72.218
719.76Huang, Ying; Min, Wei; Wu, Qiu-Wen; Sun, Jing; Shi, Da-Hua; Yan, Chao-Guo
Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities
New Journal of Chemistry, 2018, 42, 16211

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