Cadmium dicarboxylate coordination polymers incorporating a long-spanning organodiimine: in situ alkene isomerization and an unprecedented chiral 658 two-dimensional network

被引:37
作者
Martin, David P. [1 ,2 ]
Supkowski, Ronald M. [3 ]
LaDuca, Robert L. [1 ,2 ]
机构
[1] Michigan State Univ, Lyman Briggs Coll, E Lansing, MI 48825 USA
[2] Michigan State Univ, Dept Chem, E Lansing, MI 48825 USA
[3] Kings Coll, Dept Chem & Phys, Wilkes Barre, PA 18711 USA
关键词
METAL-ORGANIC FRAMEWORKS; CRYSTAL-STRUCTURES; MAGNETIC-PROPERTIES; HYDROGEN STORAGE; LIGANDS; CONSTRUCTION; FLUORESCENCE; ADSORPTION; SEPARATION; DESIGN;
D O I
10.1039/b812265b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reaction of cadmium nitrate, maleic acid, and N, N'-bis(4-pyridylmethyl) piperazine (bpmp) in a methanol/water mixed solvent system at 25 degrees C resulted in an unexpected in situ isomerization and formation of {[Cd(fumarate)(bpmp)(H2O)(2)] center dot 2H(2)O}(n) (1), which exhibits a system of mutually interpenetrated [Cd(fumarate)(bpmp)(H2O)](n) grid-like coordination polymer layers. A similar reaction using cadmium chloride and succinic acid produced {[Cd(succinate)(bpmp)(CH3OH)] center dot 2H(2)O}(n) (2), which manifests a chiral two-dimensional coordination polymer network with an unprecedented 658 topology. The differences in the conformations of the four-carbon dicarboxylate tethers (anti in 1, gauche in 2) and cadmium coordination environment (octahedral in 1, pentagonal bipyramidal in 2) play a significant role in structure direction during self-assembly. Thermal properties of 1 and 2 are also reported.
引用
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页码:514 / 520
页数:7
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