Anion-controlled isostructurality and structural diversity in cadmium coordination polymers of 2-aminobenzonitrile

被引:0
|
作者
Notash, Behrouz [1 ]
Tilenoie, Ommolbanin Barzegar [1 ]
机构
[1] Shahid Beheshti Univ, Dept Inorgan Chem, Tehran 1983969411, Iran
关键词
Anion-controlled; Coordination polymer; Isostructurality; Structural diversity; Cadmium; Hirshfeld surface analysis; 2-Aminobenzonitrile; METAL-ORGANIC FRAMEWORK; LUMINESCENCE PROPERTIES; BONDING INTERACTIONS; CRYSTAL-STRUCTURES; SILVER COMPLEXES; LIGAND; PHOTOLUMINESCENCE; 1D; HYDROGEN; NETWORKS;
D O I
10.1016/j.molstruc.2024.137582
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Using 2-aminobenzonitrile (2-ABN) and different anions, four one-dimensional coordination polymers of the formulae [Cd(2-ABN)2Br2]n (1), [Cd(2-ABN)2I2]n (2), [Cd(2-ABN)(H2O) (NO3)2]n (3), and {[Cd(2-ABN)2(H2O)2] (ClO4)2}n (4) were synthesized and structurally characterized by FT-IR, PXRD, TGA, Elemental analysis and single-crystal X-ray diffraction. According to our structural analysis, the 2-aminobenzonitrile ligand can act as a monodentate and bridge mu 2-N,N ' ligand. In isostructural compounds 1 and 2, the 2-ABN ligand was coordinated only through the Nnitrile to the metal center and a 1D ribbon chain is obtained through bridged halide anions. While compound 3 and 4 includes 1D helical and double chain structural motif due to the (mu 2-N,N ') ligand coordination mode, respectively. Our results prove that anions can play an essential role in the final structural motif of cadmium coordination polymers. Also, Hirshfeld surface analysis was performed to investigate intermolecular interactions in compounds 1-4.
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页数:10
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