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光致发光锌(II)有机配合物中来自轴向前手性配体的不同手性单元。

Distinct chiral units from an axially prochiral ligand in a photoluminescent zinc(II)-organic complex.

作者信息

Zhang Ming-Xing, Chen Xin, Huang Kun-Lin, Zhu Yi, Yang Shan-Shan

机构信息

College of Chemistry, Chongqing Normal University, Chongqing 400047, People's Republic of China.

出版信息

Acta Crystallogr C. 2012 Apr;68(Pt 4):m90-3. doi: 10.1107/S0108270112006051. Epub 2012 Mar 3.

DOI:10.1107/S0108270112006051
PMID:22476142
Abstract

The asymmetric unit of the title compound, poly[(dimethylamine-κN)[μ(3)-(E)-2,6-dimethyl-4-styrylpyridine-3,5-dicarboxylato-κ(3)O(3):O(3'):O(5)]zinc(II)], Zn(C(17)H(13)NO(4))(C(2)H(7)N), consists of one crystallographically independent distorted tetrahedral Zn(II) cation, one (E)-2,6-dimethyl-4-styrylpyridine-3,5-dicarboxylate (mspda(2-)) ligand and one coordinated dimethylamine molecule. Two S- and R-type chiral units are generated from the axially prochiral mspda(2-) ligand through C-H...O hydrogen bonds. The R-type chiral units assemble a left-handed (M) Zn-mspda helical chain, while the right-handed (P) Zn-mspda helical chain is constructed from neighbouring S-type chiral units. The P- and M-type helical chains are interlinked by carboxylate O atoms to form a one-dimensional ladder. Interchain N-H...O hydrogen bonds extend these one-dimensional ladders into a two-dimensional supramolecular architecture. The title compound exhibits luminescence at λ(max) = 432 nm upon excitation at 365 nm.

摘要

标题化合物聚[(二甲胺-κN)[μ(3)-(E)-2,6-二甲基-4-苯乙烯基吡啶-3,5-二羧酸根-κ(3)O(3):O(3′):O(5)]锌(II)],[Zn(C₁₇H₁₃NO₄)(C₂H₇N)]ₙ的不对称单元由一个晶体学独立的扭曲四面体Zn(II)阳离子、一个(E)-2,6-二甲基-4-苯乙烯基吡啶-3,5-二羧酸根(mspda²⁻)配体和一个配位的二甲胺分子组成。通过C-H...O氢键,轴向手性前体mspda²⁻配体产生两个S型和R型手性单元。R型手性单元组装成左手(M)型Zn-mspda螺旋链,而右手(P)型Zn-mspda螺旋链由相邻的S型手性单元构成。P型和M型螺旋链通过羧酸根O原子相互连接形成一维梯子状结构。链间N-H...O氢键将这些一维梯子状结构扩展为二维超分子结构。标题化合物在365 nm激发下在λ(max) = 432 nm处表现出发光。

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引用本文的文献

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