Exploring the effect of chain length of bridging ligands in coordination complexes and polymers derived from mixed ligand systems of pyridylnicotinamides and dicarboxylates

被引:14
作者
Kumar, D. Krishna [1 ]
机构
[1] Cent Salt & Marine Chem Res Inst, CSIR, Analyt Sci Discipline, Bhavnagar 364002, Gujarat, India
关键词
Crystal engineering; Hydrogen bonding; Mixed ligand systems; Supramolecular chemistry; X-ray crystal structures; METAL-ORGANIC FRAMEWORKS; HYDROGEN-BONDING BACKBONE; LIGATING TOPOLOGIES; CRYSTAL-STRUCTURES; COUNTER ANIONS; NETWORK; DESIGN; SINGLE; CHANNELS; HELIX;
D O I
10.1016/j.ica.2008.08.033
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The supramolecular structural diversities in mixed ligand systems derived from a series of dicarboxylate anions with varying chain lengths and N-donor exo-bidentate ligand equipped with hydrogen bonding capable amide backbone with Co(II)/Zn(II) metal centers are analyzed. In this context, two complexes namely (Co(L1)(2)(malonate)(H2O)(2)} (1a), {Zn(L1)(2)(malonate)(H2O)(2)} (1b) and one coordination polymer namely {[Co(mu-L1)(mu-glutarate)(H2O)] center dot H2O}(n) (4) (where L1 = N-(4-pyridyl)nicotinamide) have been synthesized and crystallographically characterized. The main aim of this work is to explore the effects of chain lengths of the anionic carboxylate ligands such as malonate, succinate, maleate, and glutarate, in determining the final architecture of coordination compounds based on the mixed ligands. Analyses of the structures revealed that the length of the bridging ligands have prominent effect in the formation of hierarchical structures. (C) 2008 Elsevier B. V. All rights reserved.
引用
收藏
页码:1767 / 1771
页数:5
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