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3-(4-氯苯基)-1-(4-硝基苯基)苯并[f]喹啉

3-(4-Chloro-phen-yl)-1-(4-nitro-phen-yl)benzo[f]quinoline.

作者信息

Wang Shu-Liang, Li Qing, Wang Xiang-Shan, Tu Shu-Jiang

机构信息

School of Chemistry and Chemical Engineering, Xuzhou Normal University, Xuzhou Jiangsu 221116, People's Republic of China.

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2009 Aug 12;65(Pt 9):o2137. doi: 10.1107/S1600536809031122.

DOI:10.1107/S1600536809031122
PMID:21577547
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2970097/
Abstract

In the title compound, C(25)H(15)ClN(2)O(2), the pyridine ring is inclined at angles of 6.89 (7), 4.24 (9) and 66.98 (4)° with respect to the naphthalene, chloro-phenyl and nitro-phenyl rings, respectively. The two substituent aromatic rings make a dihedral angle of 71.1 (1)° with one another. C-H⋯π and π-π stacking are present in the crystal structure; the π-π stacking [centroid-centroid distance between the pyridyl rings of adjacent mol-ecules= 3.7838 (11) Å] links the mol-ecules into dimers, while the C-H⋯Cg type π-ring inter-actons link the mol-ecules into a chain structure along c.

摘要

在标题化合物C₂₅H₁₅ClN₂O₂中,吡啶环相对于萘环、氯苯环和硝基苯环的倾斜角度分别为6.89(7)°、4.24(9)°和66.98(4)°。两个取代芳香环之间的二面角为71.1(1)°。晶体结构中存在C—H⋯π和π - π堆积作用;π - π堆积作用[相邻分子吡啶环之间的质心 - 质心距离 = 3.7838(11)Å]将分子连接成二聚体,而C—H⋯Cg型π - 环相互作用将分子沿c轴连接成链状结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59b0/2970097/e32028807749/e-65-o2137-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59b0/2970097/0f2b440c9945/e-65-o2137-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59b0/2970097/e32028807749/e-65-o2137-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59b0/2970097/0f2b440c9945/e-65-o2137-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59b0/2970097/e32028807749/e-65-o2137-fig2.jpg

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本文引用的文献

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Acta Crystallogr Sect E Struct Rep Online. 2009 Apr 18;65(Pt 5):o1074. doi: 10.1107/S1600536809013713.
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Discovery of the first non-peptide full agonists for the human bradykinin B(2) receptor incorporating 4-(2-picolyloxy)quinoline and 1-(2-picolyl)benzimidazole frameworks.
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Novel quinazoline-quinoline alkaloids with cytotoxic and DNA topoisomerase II inhibitory activities.具有细胞毒性和DNA拓扑异构酶II抑制活性的新型喹唑啉-喹啉生物碱。
Bioorg Med Chem Lett. 2004 Mar 8;14(5):1193-6. doi: 10.1016/j.bmcl.2003.12.048.
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