Combination of primary amide and dipyrrin for the elaboration of extended architectures built upon both coordination and hydrogen bonding

被引:49
作者
Baudron, Stephane A. [1 ]
Salazar-Mendoza, Domingo [1 ]
Hosseini, Mir Wais [1 ]
机构
[1] Univ Strasbourg, Inst Le Bel, CNRS UMR 7140, Chim Coordinat Organ Lab, F-67000 Strasbourg, France
来源
CRYSTENGCOMM | 2009年 / 11卷 / 07期
关键词
METAL-ORGANIC FRAMEWORKS; MOLECULAR TECTONICS; BONDED NETWORKS; CRYSTAL-STRUCTURES; COMPLEXES; DESIGN; CHEMISTRY; STRATEGY; MOTIFS; NANOSTRUCTURES;
D O I
10.1039/b901167f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The 5-(benzamide) dipyrrin, a ditopic tecton bearing two different interaction poles, i.e. a primary amide as H-bond donor and acceptor and a deprotonated dipyrrin unit as a strong chelating group leads in the presence of metal cations (Cu(II), Zn(II..)) or metal complexes ([Cu(II)-acac](+) and [Co(III)salen](+))to homo-and heteroleptic complexes. The latter behave as metallo-organic tectons and generate in the crystalline phase molecular networks. Whereas the homoleptic Cu complex leads to the formation of a 2-D network, its Zn analogue forms a 1-D ribbon type architecture owing to the presence of capping dioxane molecules. For the heteroleptic complexes, in the case of the Cu-acac, a 1-D network resulting from bridging of H-bonded dimers of dimers by dioxane molecules is observed whereas for the Co-salen, due to the salen ligand offering further hydrogen bonding capabilities, two different solvates with different connectivity patterns have been obtained.
引用
收藏
页码:1245 / 1254
页数:10
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