Crystallography Open Database
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Searching journal of publication like 'Chem.Commun.' volume of publication is 51
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7117421 | CIF | C25 H27 N2 O6 Pt S | P -1 | 7.2201; 13.2276; 14.0336 70.675; 80.551; 84.13 | 1245.94 | Harriet L. Steel; Sarah L. Allinson; Jane Andre; Michael P. Coogan; James A. Platts Platinum trimethyl bipyridyl thiolates ‒ new, tunable, red- to near IR emitting luminophores for bioimaging applications Chem.Commun., 2015, 51, 11441 |
| 7117422 | CIF | C118 H143 Mg3 N12 | P 63/m | 15.9267; 15.9267; 24.086 90; 90; 120 | 5291.1 | Jani O. Moilanen; Benjamin M. Day; Thomas Pugh; Richard A. Layfield Open-shell doublet character in a hexaazatrinaphthylene trianion complex Chem.Commun., 2015, 51, 11478 |
| 7117423 | CIF | C22 H19 Cl2 F6 N O3 S2 Sb | P -1 | 9.106; 10.58; 15.856 102.819; 97.906; 112.771 | 1330.3 | S. Menichetti; S. Cecchi; P. Procacci; M. Innocenti; L. Becucci; L. Franco; C. Viglianisi Thia-bridged triarylamine heterohelicene radical cations as redox-driven molecular switches Chem.Commun., 2015, 51, 11452 |
| 7117424 | CIF | C21 H17 N O3 S2 | P b c a | 10.641; 14.807; 23.076 90; 90; 90 | 3635.9 | S. Menichetti; S. Cecchi; P. Procacci; M. Innocenti; L. Becucci; L. Franco; C. Viglianisi Thia-bridged triarylamine heterohelicene radical cations as redox-driven molecular switches Chem.Commun., 2015, 51, 11452 |
| 7117425 | CIF | C21 H17 F6 N S2 Sb | P 1 21/n 1 | 8.543; 15.622; 16.383 90; 94.989; 90 | 2178.2 | S. Menichetti; S. Cecchi; P. Procacci; M. Innocenti; L. Becucci; L. Franco; C. Viglianisi Thia-bridged triarylamine heterohelicene radical cations as redox-driven molecular switches Chem.Commun., 2015, 51, 11452 |
| 7117426 | CIF | C24 H22 O Si | P 1 c 1 | 8.624; 15.417; 7.309 90; 104.681; 90 | 940.1 | Ryo Shintani; Hiroki Kurata; Kyoko Nozaki Rhodium-catalyzed intramolecular alkynylsilylation of alkynes Chem.Commun., 2015, 51, 11378 |
| 7117427 | CIF | C58 H64 Cl Mg N2 O Sb | P 1 21/n 1 | 13.7235; 16.6434; 23.277 90; 106.733; 90 | 5091.5 | Alexander Hinz; Axel Schulz; Alexander Villinger Accessing heavy allyl-analogous [(TerN)2E]- (E = Sb, Bi) ions and their reactivity towards ECl3 Chem.Commun., 2015, 51, 11437 |
| 7117428 | CIF | C58 H64 Bi Cl Mg N2 O | P 1 21/n 1 | 13.7359; 16.6363; 23.257 90; 106.645; 90 | 5091.9 | Alexander Hinz; Axel Schulz; Alexander Villinger Accessing heavy allyl-analogous [(TerN)2E]- (E = Sb, Bi) ions and their reactivity towards ECl3 Chem.Commun., 2015, 51, 11437 |
| 7117429 | CIF | C48 H50 Bi Cl2 N2 Sb | P b c a | 14.6206; 15.5222; 18.7038 90; 90; 90 | 4244.7 | Alexander Hinz; Axel Schulz; Alexander Villinger Accessing heavy allyl-analogous [(TerN)2E]- (E = Sb, Bi) ions and their reactivity towards ECl3 Chem.Commun., 2015, 51, 11437 |
| 7117435 | CIF | C13 H10 N2 O | C 1 2/c 1 | 17.9438; 6.3301; 19.758 90; 113.492; 90 | 2058.2 | Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones. Chemical communications (Cambridge, England), 2015, 51, 11658-11661 |
| 7117436 | CIF | C13 H12 N2 O | C 1 2/c 1 | 18.9282; 6.0959; 20.6755 90; 116.768; 90 | 2130 | Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones. Chemical communications (Cambridge, England), 2015, 51, 11658-11661 |
| 7117437 | CIF | C13 H11 Cl N2 O | P 1 21 1 | 13.4732; 9.5123; 19.795 90; 109.801; 90 | 2386.95 | Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones. Chemical communications (Cambridge, England), 2015, 51, 11658-11661 |
| 7117438 | CIF | C14 H14 N2 O S | C 1 2/c 1 | 20.924; 5.7267; 23.879 90; 112.393; 90 | 2645.5 | Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones. Chemical communications (Cambridge, England), 2015, 51, 11658-11661 |
| 7117439 | CIF | C17 H15 Fe N3 | C 1 2/c 1 | 35.793; 5.7087; 13.346 90; 99.709; 90 | 2687.9 | Yadav, Abhimanyu; Verma, Ajay; Patel, Saket; Kumar, Amit; Rathore, Vandana; Meenakshi, ?; Kumar, Shailesh; Kumar, Sangit KO(t)Bu-mediated annulation of acetonitrile with aldehyde: synthesis of substituted dihydropyridin-2(1H)-ones, pyridin-2(1H)-ones, and thiopyridin-2(1H)-ones. Chemical communications (Cambridge, England), 2015, 51, 11658-11661 |
| 7117440 | CIF | C22 H17 N O4 | P -1 | 7.3977; 11.6656; 20.3981 76.247; 83.564; 88.301 | 1699.07 | Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K. A supramolecular approach for designing emissive solid-state carbazole arrays. Chemical communications (Cambridge, England), 2015, 51, 11603-11606 |
| 7117441 | CIF | C46.67 H42 Co2 N3.34 O12 | P 1 21/n 1 | 10.148; 14.9006; 28.1544 90; 92.505; 90 | 4253.2 | Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K. A supramolecular approach for designing emissive solid-state carbazole arrays. Chemical communications (Cambridge, England), 2015, 51, 11603-11606 |
| 7117442 | CIF | C25 H20 Cu N2 O5 | C 1 2/c 1 | 27.7412; 11.114; 15.0069 90; 102.921; 90 | 4509.7 | Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K. A supramolecular approach for designing emissive solid-state carbazole arrays. Chemical communications (Cambridge, England), 2015, 51, 11603-11606 |
| 7117443 | CIF | C50 H47 N5 O12 Zn2 | P 21 21 21 | 10.2867; 17.0328; 26.8808 90; 90; 90 | 4709.8 | Lifshits, Liubov M.; Noll, Bruce C.; Klosterman, Jeremy K. A supramolecular approach for designing emissive solid-state carbazole arrays. Chemical communications (Cambridge, England), 2015, 51, 11603-11606 |
| 7117444 | CIF | C39 H37 Cl N2 O5 Si | P -1 | 9.8459; 10.5371; 19.8151 94.748; 98.528; 110.714 | 1881.2 | Kim, Sooyeon; Fujitsuka, Mamoru; Tohnai, Norimitsu; Tachikawa, Takashi; Hisaki, Ichiro; Miyata, Mikiji; Majima, Tetsuro The unprecedented J-aggregate formation of rhodamine moieties induced by 9-phenylanthracenyl substitution. Chemical communications (Cambridge, England), 2015, 51, 11580-11583 |
| 7117445 | CIF | C30 H34 N6 O8 | P -1 | 9.0281; 11.3963; 16.9166 109.458; 90.63; 102.206 | 1597.7 | Li, Yi-Jin; Li, Xue; Zhang, Shao-Xiao; Zhao, Yu-Long; Liu, Qun Copper(ii)-catalyzed oxidative [3+2] cycloaddition reactions of secondary amines with α-diazo compounds: a facile and efficient synthesis of 1,2,3-triazoles. Chemical communications (Cambridge, England), 2015, 51, 11564-11567 |
| 7117446 | CIF | C22 H18 O3 | P 1 21/c 1 | 8.6642; 20.3575; 10.1977 90; 115.123; 90 | 1628.53 | Khoobi, Mehdi; Molaverdi, Fatemeh; Jafarpour, Farnaz; Abbasnia, Masoumeh; Kubicki, Maciej; Shafiee, Abbas A one-pot domino C-H, C-C activation in coumarins: a fast track to 2,3-diaryl benzo[b]furans. Chemical communications (Cambridge, England), 2015, 51, 11713-11716 |
| 7117447 | CIF | C22 H29 N O6 | P 21 21 21 | 8.4147; 11.96874; 21.5473 90; 90; 90 | 2170.1 | Zhou, Yuhang; Lin, Lili; Yin, Chengkai; Wang, Zhengmeng; Liu, Xiaohua; Feng, Xiaoming The N,N'-dioxide/Ni(ii)-catalyzed asymmetric inverse-electron-demand hetero-Diels-Alder reaction of methyleneindolinones with hetero-substituted alkenes. Chemical communications (Cambridge, England), 2015, 51, 11689-11692 |
| 7117448 | CIF | C30 H49 N O Si2 | P -1 | 12.502; 15.8137; 17.4136 74.497; 75.487; 76.75 | 3162.7 | Liu, Yan-Hua; Liu, Yue-Jin; Yan, Sheng-Yi; Shi, Bing-Feng Ni(ii)-catalyzed dehydrative alkynylation of unactivated (hetero)aryl C-H bonds using oxygen: a user-friendly approach. Chemical communications (Cambridge, England), 2015, 51, 11650-11653 |
| 7117449 | CIF | C54 H50 Cl0 Cu2 F0 N6 P2 | C 1 2/c 1 | 26.589; 17.564; 29.171 90; 106.352; 90 | 13072.1 | Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C. Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers. Chemical communications (Cambridge, England), 2015, 51, 11560-11563 |
| 7117450 | CIF | C144 H124 B4 Cl0 Cu4 F16 N12 O0 P4 | P -1 | 15.189; 15.957; 23.446 107.923; 101.304; 104.447 | 5001.1 | Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C. Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers. Chemical communications (Cambridge, England), 2015, 51, 11560-11563 |
| 7117451 | CIF | C172 H140 B0 Cl0 Cu4 F0 N12 P4 | P -1 | 15.705; 17.816; 21.535 107.871; 104.457; 97.386 | 5413.8 | Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C. Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers. Chemical communications (Cambridge, England), 2015, 51, 11560-11563 |
| 7117452 | CIF | C176 H148 B4 Cl0 Cu4 F16 N12 P4 | P -1 | 15.582; 17.047; 22.619 102.262; 104.435; 102.171 | 5460.5 | Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C. Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers. Chemical communications (Cambridge, England), 2015, 51, 11560-11563 |
| 7117453 | CIF | C146 H128 B4 Cl12 Cu4 F16 N12 P4 | P -1 | 13.887; 15.375; 18.799 101.562; 105.589; 101.967 | 3639.7 | Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C. Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers. Chemical communications (Cambridge, England), 2015, 51, 11560-11563 |
| 7117454 | CIF | C108 H102 B0 Cl0 Cu4 F0 N12 P4 | C 1 2/c 1 | 25.7551; 20.5086; 24.6987 90; 95.409; 90 | 12987.8 | Shen, W.; El Sayed Moussa, M.; Yao, Y.; Lescop, C. Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers. Chemical communications (Cambridge, England), 2015, 51, 11560-11563 |
| 7117455 | CIF | C17 H20 N2 O2 | P -1 | 9.074; 9.586; 10.271 105.491; 97.554; 108.975 | 790.5 | García-González, Ma Carmen; Hernández-Vázquez, Eduardo; Gordillo-Cruz, Raúl E; Miranda, Luis D. Ugi-derived dehydroalanines as a pivotal template in the diversity oriented synthesis of aza-polyheterocycles. Chemical communications (Cambridge, England), 2015, 51, 11669-11672 |
| 7117456 | CIF | C18 H22 N2 O2 | P 1 21/c 1 | 9.1496; 9.3085; 19.945 90; 95.325; 90 | 1691.4 | García-González, Ma Carmen; Hernández-Vázquez, Eduardo; Gordillo-Cruz, Raúl E; Miranda, Luis D. Ugi-derived dehydroalanines as a pivotal template in the diversity oriented synthesis of aza-polyheterocycles. Chemical communications (Cambridge, England), 2015, 51, 11669-11672 |
| 7117457 | CIF | C21 H22 N2 O2 | P -1 | 9.2332; 10.3088; 10.7141 105.017; 100.269; 102.043 | 933.7 | García-González, Ma Carmen; Hernández-Vázquez, Eduardo; Gordillo-Cruz, Raúl E; Miranda, Luis D. Ugi-derived dehydroalanines as a pivotal template in the diversity oriented synthesis of aza-polyheterocycles. Chemical communications (Cambridge, England), 2015, 51, 11669-11672 |
| 7117458 | CIF | C27 H18 O6 | P 1 | 31.1904; 31.2132; 51.976 72.71; 77.555; 60.912 | 42068 | Zentner, Cassandra A.; Lai, Holden W. H.; Greenfield, Joshua T.; Wiscons, Ren A.; Zeller, Matthias; Campana, Charles F.; Talu, Orhan; FitzGerald, Stephen A.; Rowsell, Jesse L. C. High surface area and Z' in a thermally stable 8-fold polycatenated hydrogen-bonded framework. Chemical communications (Cambridge, England), 2015, 51, 11642-11645 |
| 7117459 | CIF | C27 H18 O6 | I 1 2 1 | 31.419; 30.116; 45.32 90; 90.412; 90 | 42881 | Zentner, Cassandra A.; Lai, Holden W. H.; Greenfield, Joshua T.; Wiscons, Ren A.; Zeller, Matthias; Campana, Charles F.; Talu, Orhan; FitzGerald, Stephen A.; Rowsell, Jesse L. C. High surface area and Z' in a thermally stable 8-fold polycatenated hydrogen-bonded framework. Chemical communications (Cambridge, England), 2015, 51, 11642-11645 |
| 7117460 | CIF | C21 H26 O3 | P 21 21 21 | 5.7682; 7.7444; 39.9505 90; 90; 90 | 1784.64 | Akira Matsumoto; Keisuke Asano; Seijiro Matsubara A chiral phosphoric acid catalyst for asymmetric construction of 1,3-dioxanes Chem.Commun., 2015, 51, 11693 |
| 7117465 | CIF | C48 H88 N12 O12 | P 21 21 21 | 9.4643; 19.6586; 31.9809 90; 90; 90 | 5950.2 | Julien Maury; Bryden A. F. Le Bailly; James Raftery; Jonathan Clayden Conformational cooperativity between helical domains of differing geometry in oligoamide-oligourea foldamer chimeras Chem.Commun., 2015, 51, 11802 |
| 7117466 | CIF | C27 H27 N3 O9 S | P -1 | 8.3006; 9.3862; 17.717 86.352; 87.532; 77.772 | 1345.68 | Cong-Shuai Wang; Ren-Yi Zhu; Yu-Chen Zhang; Feng Shi Catalytic chemoselective [3+3] cycloadditions of azomethine ylides with quinone monoimides leading to the construction of a dihydrobenzoxazine scaffold Chem.Commun., 2015, 51, 11798 |
| 7117467 | CIF | C28 H21 Cl2 N3 O7 S | P -1 | 8.4575; 12.5061; 13.4396 80.3987; 85.8752; 78.3825 | 1371.8 | Cong-Shuai Wang; Ren-Yi Zhu; Yu-Chen Zhang; Feng Shi Catalytic chemoselective [3+3] cycloadditions of azomethine ylides with quinone monoimides leading to the construction of a dihydrobenzoxazine scaffold Chem.Commun., 2015, 51, 11798 |
| 7117468 | CIF | C35 H36 Br N3 O3 S | P 1 21 1 | 9.4805; 15.3417; 11.8162 90; 111.93; 90 | 1594.3 | Chao-You Liu; Fu-She Han Organocatalytic asymmetric reaction of indol-2-yl carbinols with enamides: synthesis of chiral 2-indole-substituted 1,1-diarylalkanes Chem.Commun., 2015, 51, 11844 |
| 7117469 | CIF | C31 H10 Al F36 N O4 S | P 1 21/c 1 | 14.2945; 19.666; 19.9786 90; 134.333; 90 | 4017.3 | Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures Chem.Commun., 2015, 51, 11822 |
| 7117470 | CIF | C69.8 H27.6 Al2 Cl3.61 F72 N2 O8 S2 | P 1 21/n 1 | 13.604; 20.135; 16.634 90; 93.113; 90 | 4549.6 | Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures Chem.Commun., 2015, 51, 11822 |
| 7117471 | CIF | C71.56 H27.11 Al2 Cl3.11 F72 N2 O8 S2 | P 1 21/c 1 | 10.415; 15.3696; 28.611 90; 93.362; 90 | 4572 | Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures Chem.Commun., 2015, 51, 11822 |
| 7117472 | CIF | C62 H24 Al2 F72 N2 O8 | P 1 21/c 1 | 27.656; 11.298; 25.57 90; 94.846; 90 | 7961 | Xingyong Wang; Zaichao Zhang; You Song; Yuanting Su; Xinping Wang Bis(phenothiazine)arene diradicaloids: isolation, characterization and crystal structures Chem.Commun., 2015, 51, 11822 |
| 7117473 | CIF | C96 H109 Cl Li N4 O6 P4 Pd Y | P -1 | 13.4049; 15.2317; 22.79 99.348; 98.546; 99.455 | 4455 | Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides Chem.Commun., 2015, 51, 11761 |
| 7117474 | CIF | C96 H109 Cl Li Lu N4 O6 P4 Pd | P 1 21/n 1 | 13.559; 28.87; 22.627 90; 90.84; 90 | 8856 | Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides Chem.Commun., 2015, 51, 11761 |
| 7117475 | CIF | C96 H109 Cl Li Lu N4 O6 P4 Pd | P -1 | 13.332; 15.349; 21.771 88.53; 80.9; 83.96 | 4374.4 | Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides Chem.Commun., 2015, 51, 11761 |
| 7117476 | CIF | C94.4 H105.8 Cl Li Lu N4 O5.6 P4 Pd | P -1 | 13.414; 15.386; 22.048 88.38; 80.4; 84.17 | 4463.2 | Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides Chem.Commun., 2015, 51, 11761 |
| 7117477 | CIF | C124 H124 Li N6 O4 P6 Pd2 Y | P 1 21/c 1 | 28.427; 14.576; 29.04 90; 106.14; 90 | 11559 | Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides Chem.Commun., 2015, 51, 11761 |
| 7117478 | CIF | C124 H124 Li Lu N6 O4 P6 Pd2 | P 1 21/c 1 | 28.3174; 14.561; 29.0288 90; 105.984; 90 | 11506.7 | Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides Chem.Commun., 2015, 51, 11761 |
| 7117479 | CIF | C100 H116 Li N4 O7 P4 Y | P 1 21/c 1 | 14.911; 24.635; 26.155 90; 104.1; 90 | 9318 | Franziska Volcker; Felix M. Muck; Konstantinos D. Vogiatzis; Karin Fink; Peter W. Roesky Bi- and trimetallic rare-earth-palladium complexes ligated by phosphinoamides Chem.Commun., 2015, 51, 11761 |
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