Aminobenzonitrile isomers-mediated self-assembly of mixed-ligand silver(I) coordination architectures: Synthesis, structural characterization and properties

被引:14
|
作者
Liu, Fu-Jing [1 ,2 ]
Sun, Di [1 ,2 ]
Li, Yun-Hua [1 ,2 ]
Hao, Hong-Jun [1 ,2 ]
Luo, Geng-Geng [3 ]
Huang, Rong-Bin [1 ,2 ]
Zheng, Lan-Sun [1 ,2 ]
机构
[1] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Dept Chem, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[3] Huaqiao Univ, Inst Mat Phys Chem, Xiamen 361021, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Silver(I); Aminobenzonitrile ligand; 3,5-Dinitrobenzoic acid; Ag center dot center dot center dot Ag interaction; Photoluminescence; ARGENTOPHILIC INTERACTIONS; CRYSTAL-STRUCTURES; AG(I) COMPLEXES; IR-SPECTRA; POLYMER; FRAMEWORKS; SACCHARINATE; LUMINESCENCE; NETWORKS; FUNCTIONALITY;
D O I
10.1016/j.molstruc.2011.01.035
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
Three mixed-ligand coordination compounds (CCs) of the formula {[Ag(p-abn)(dnca)]center dot H2O}(n) (1), {[Ag(o-abn)(dnca)]-H2O}(n) (2), and {[Ag(m-abn)(4))]center dot(dnca)center dot H2O} (3) (where p-abn = 4-aminobenzonitrile, o-abn = 2-aminobenzonitrile, m-abn = 3-aminobenzonitrile, Hdnca = 3,5-dinitrobenzoic acid) were synthesized by reactions of Ag2O and aminobenzonitrile ligands with Hdnca under the ammoniacal condition. All CCs have been structurally characterized by element analysis, IR and X-ray single-crystal diffraction. The aminobenzonitrile acts as bidentate ligand in both 1 and 2, and as monodentate ligand in 3. As the change of the relative position of amino and cyano groups of aminobenzonitrile ligands, the dimensionality of 1-3 decreases from 2D to 0D mainly due to the steric effect of the substituted groups, which indicates that aminobenzonitrile isomers play important roles in the formation of the diverse coordination architectures. The three CCs exhibit photoluminescent emissions in the solid state at room temperature. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:158 / 163
页数:6
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