Design and synthesis of four coordination polymers generated from 2,2′-biquinoline-4,4′-dicarboxylate and aromatic bidentate ligands

被引:29
|
作者
Ye, JW [1 ]
Zhang, P [1 ]
Ye, KQ [1 ]
Zhang, HY [1 ]
Jiang, SM [1 ]
Ye, L [1 ]
Yang, GD [1 ]
Wang, Y [1 ]
机构
[1] Jilin Univ, Coll Chem, Minist Educ, Key Lab Supramol Struct & Mat, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
coordination polymers; zinc; manganese; photoluminescence; magnetism;
D O I
10.1016/j.jssc.2005.11.003
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Four coordination polymers [Zn(bqdc)(phen)](n) (1), [Zn(bqdc)(bpy)(H2O)(n) (2), [Mn(bqdc)(bpy)(H2O)(2)](n) (3) and [Mn(bqdc)(phen) (H2O)(2)](n) (4) (H(2)bqdc = 2,2'-biquinoline-4,4'-dicarboxylic acid, phen = 1,10-phenanthroline and bpy = 2,2'-bipyridyl) have been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction. Crystal data for 1: monoclinic system, C2/c, a = 14.141(3) angstrom, b = 10.021(2) angstrom, c = 18.511(4) angstrom, beta = 103.78(3)degrees, V = 2547.6(9) angstrom(3), Z = 4. Crystal data for 2: monoclinic system, p2(1)/n, a = 13.656(3) angstrom, b = 10.015(2) angstrom, c = 19.127(4) angstrom, beta = 107.13(7)degrees, V = 2500.1(9) angstrom(3), Z = 4. Crystal data for 3: monoclinic system, C2/c, a = 14.5050(8) angstrom, b = 15.1932(8) angstrom, c = 12.7549(6) angstrom, beta = 116.8010(11)degrees, V = 2508.9(2) angstrom(3), Z = 4. Crystal data for 4: monoclinic system, C2/c, a = 14.1732(17) angstrom, b = 16.115(3) angstrom, c = 12.809(3)angstrom, beta = 117.04(3)degrees, V = 2605.7(8) angstrom(3), Z = 4. Single helix-like chains exist in 1. The supramolecular structure of 1 exhibits extended two-dimensional network while 2-4 display extended three-dimensional architectures based on interchain hydrogen bonding and pi-pi interactions. Compounds I and 2 show blue photoluminescence under UV light suggesting that they may be employed to develop luminescent materials. Compounds 3 and 4 show interesting magnetic behaviors. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:438 / 449
页数:12
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