Effect of Ligand Structural Isomerism in Formation of Calcium Coordination Networks

被引:58
|
作者
Plonka, Anna M. [2 ]
Banerjee, Debasis [1 ]
Parise, John B. [2 ,3 ]
机构
[1] SUNY Stony Brook, ESS, Dept Chem, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Dept Geosci, Stony Brook, NY 11794 USA
[3] Brookhaven Natl Lab, Photon Source Div, Upton, NY 11973 USA
基金
美国国家科学基金会;
关键词
METAL-ORGANIC FRAMEWORK; SELECTIVE GAS-ADSORPTION; POLYMERS; COMPLEXES; 1D; PH; TRANSFORMATION; TEMPERATURE; TOPOLOGIES; CONVERSION;
D O I
10.1021/cg300093h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Using different structural isomers (2,5-; 2,4-; 2;6-; 3,4-; 3,5-) of pyridinedicarboxylic acid, nine calcium-based coordination networks were synthesized under hydro-/ solvothermal conditions and/or were produced via solvent recrystallization of previously synthesized compounds. The coordination networks reported were characterized using single crystal X-ray diffraction and thermal methods. They show diverse structural topologies, depending on the ligand geometry and coordinated solvent molecules, with inorganic connectivity motifs ranging from isolated octahedra to infinite chains, layer and a three-dimensional dense framework. The as-synthesized and desolvated networks further show structural transformation to hydrated phases through dissolution/reformation pathways. The process is likely driven by the high hydration energy of the calcium metal center.
引用
收藏
页码:2460 / 2467
页数:8
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