Exploring 3D non-interpenetrated metal-organic framework with malonate-bridged Co(II) coordination polymer: structural elucidation and theoretical study

被引:3
|
作者
Hossain, Anowar [1 ]
Mandal, Tripti [1 ]
Mitra, Monojit [1 ]
Manna, Prankrishna [1 ]
Bauza, Antonio [2 ]
Frontera, Antonio [2 ]
Seth, Saikat Kumar [3 ]
Mukhopadhyay, Subrata [1 ]
机构
[1] Jadavpur Univ, Dept Chem, Kolkata, India
[2] Univ Illes Balears, Dept Quim, Palma De Mallorca, Baleares, Spain
[3] Jadavpur Univ, Dept Phys, Kolkata, India
关键词
Bi-layer network; coordination polymer; DFT study; metal organic framework; tetranuclear Co-Cluster; HIRSHFELD SURFACE-ANALYSIS; ANION-PI INTERACTIONS; LONE PAIR-PI; CRYSTAL-STRUCTURES; WEAK FORCES; COMPLEXES M; CU(II); LIGAND; ASSEMBLIES; DIVERSITY;
D O I
10.1080/01411594.2017.1326603
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
A Co(II)-based coordination polymer with tetranuclear cobalt(II)-malonate cluster has been easily generated by aqueous medium self-assembly from Cobalt(II) chloride hexahydrate and malonic acid. The structure exhibits a non-interpenetrating, highly undulating two-dimensional (2D) bi-layer network with (4,4) topology. The crystal structure is composed of infinite interdigitated 2D metal-organic bi-layers which extended to an intricate 3D framework through the interbilayer hydrogen bonds. We have studied energetically by means of Density Functional Theory (DFT) calculations the H-bonding interactions that connect the 2D metal-organic bi-layers. The finite theoretical models have been used to compute conventional O-H center dot center dot center dot O and unconventional C-H center dot center dot center dot O interactions which plays a key role to build 3D architecture.
引用
收藏
页码:1193 / 1204
页数:12
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