Supramolecular networks through second-sphere coordination based on 1D metal-4,4′-dipyridyldisulfide coordination polymers and hydrogenfumarate or sulfonate anions

被引:7
|
作者
Carballo, Rosa [1 ]
Fernandez-Hermida, Nuria [1 ]
Lago, Ana B. [1 ]
Rodriguez-Hermida, Sabina [1 ]
Vazquez-Lopez, Ezequiel M. [1 ]
机构
[1] Univ Vigo, Dept Quim Inorgan, Fac Quim, E-36310 Vigo, Galicia, Spain
关键词
Coordination polymers; Metallosupramolecular chemistry; Hydrogenfumarate; Pyridine-3-sulfonate; 4,4 '-Dipyridyldisulfide; METAL-ORGANIC FRAMEWORKS; TWISTED LIGANDS 4,4'-DIPYRIDYLDISULFIDE; CRYSTAL-STRUCTURE; X-RAY; STRUCTURAL DIVERSITY; ABSOLUTE-CONFIGURATION; NEUTRON-DIFFRACTION; SPHERE COORDINATION; WATER SUBSTRUCTURES; MAGNETIC-PROPERTIES;
D O I
10.1016/j.poly.2011.09.008
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Four hydrogen-bonded assemblies of formula [M(dpds)(2)(OH2)(2)]A(2)center dot nH(2)O (A = anion) are described. These assemblies result from the second-sphere coordination interactions between the 1D coordination polymers [M(dpds)(2)(OH2)(2)](2+), M = Zn(II) and Cu(II). dpds = 4,4'-dipyridyldisulfide, and the pyridine-3-sulfonate (3pySO(3)(-)) or hydrogenfumarate (Hfum(-)) anions. Significantly, supramolecular structural variations are observed depending on the presence of water lattice molecules, which formed discrete aggregates when the Hfum(-) anion was used. The effects of geometrical variations in the building blocks are also evident on using Jahn-Teller-distorted divalent Cu(II) ions or regular octahedral species based on Zn(II) ions. The second-sphere effects on the stabilization of the compounds are illustrated by TGA experiments. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:118 / 127
页数:10
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