Five organic salts assembled from carboxylic acids and bis-imidazole derivatives through collective noncovalent interactions

被引:8
|
作者
Jin, Shouwen [1 ]
Guo, Jianzhong [2 ]
Liu, Li [2 ]
Wang, Daqi [3 ]
机构
[1] Zhejiang A&F Univ, Tianmu Coll, Linan 311300, Peoples R China
[2] Zhejiang A&F Univ, Fac Sci, Linan 311300, Peoples R China
[3] Liaocheng Univ, Dept Chem, Liaocheng 252059, Peoples R China
关键词
Crystal structure; 3D framework; Hydrogen bonds; Noncovalent interactions; Bis-imidazoles; Carboxylic acids; PROTON-TRANSFER COMPOUNDS; PI-PI-STACKING; DICARBOXYLIC-ACIDS; HYDROGEN-BONDS; SUPRAMOLECULAR SYNTHESIS; 5-SULFOSALICYLIC ACID; BUILDING-BLOCKS; CRYSTAL; COCRYSTALS; PYRIDINE;
D O I
10.1016/j.molstruc.2011.08.010
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Five multicomponent crystals of bis(imidazole) derivatives have been prepared with 5-nitrosalicylic acid, 5-sulfosalicylic acid, and phthalic acid. The five crystalline forms reported are organic salts of which the crystal structures have all been determined by X-ray diffraction. The results presented herein indicate that the strength and directionality of the N-H center dot center dot center dot O, O-H center dot center dot center dot O, and N-H center dot center dot center dot N hydrogen bonds (ionic or neutral) between carboxylic acids and ditopic imidazoles are sufficient to bring about the formation of binary organic salts. All supramolecular architectures of the organic salts 1-5 involve extensive O-H center dot center dot center dot O, and N-H center dot center dot center dot O hydrogen bonds as well as other noncovalent interactions. The role of weak and strong noncovalent interactions in the crystal packing is ascertained. These noncovalent interactions combined, all the complexes displayed 3D framework structure. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:227 / 236
页数:10
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