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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.
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页码:1193 / 1204
页数:12
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