Synthesis of copper halide coordination polymers with ligands formed by in situ cyclization of 2-aminopyrimidine and ethanol

被引：15

作者：

Bi, Minghui ^{[1
]}

Li, Guanghua ^{[1
]}

Hua, Jia ^{[1
]}

Lin, Yingjie ^{[1
]}

Cao, Junjun ^{[1
]}

Shi, Zhan ^{[1
]}

Feng, Shouhua ^{[1
]}

机构：

[1] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China

来源：

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY | 2008年 / 07期

关键词：

coordination polymers; copper; halides; in situ cyclization;

D O I：

10.1002/ejic.200701126

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The design and synthesis of coordination polymers from transition metals and organic ligands have been extensively studied for their crystallographic diversity and potential applications. Recently, the synthesis of coordination polymers by hydro(solvo) thermal in situ metal/ligand reactions has drawn great interest because of its potential to generate novel coordination architectures and new organic reactions. As described in our manuscript, the nitrogen heterocyclic 2,3-dihydroimidazo[1,2-a]pyrimidine (C6H7N3) ligand was synthesized by an in situ reaction starting from 2-aminopyrimidine and ethanol. At the same time, two luminescent copper halide coordination polymers, (CuCl)(3)C6H7N3 and (CuI)(2)C6H7N3, were assembled under solvothermal conditions. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008).

引用

页码：1035 / 1038

页数：4

共 36 条

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