Three-Dimensional-Coordination Polymer of Zn(II)-Carboxylate: Structural Elucidation, Photoelectrical Conductivity, and Biological Activity
Author(s) -
Angeera Chandra,
Mrinmay Das,
Kunal Pal,
Srikanta Jana,
Basudeb Dutta,
Partha Pratim Ray,
Kuladip Jana,
Chittaranjan Sinha
Publication year - 2019
Publication title -
acs omega
Language(s) - English
Resource type - Journals
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b01745
Subject(s) - ligand (biochemistry) , carboxylate , crystallography , chemistry , supramolecular chemistry , benzene , bridging ligand , polymer , crystal structure , conductivity , coordination polymer , stereochemistry , organic chemistry , biochemistry , receptor
A newly designed mixed-ligand coordination polymer [Zn 4 (bdc) 4 (ppmh) 2 (H 2 O)] n ( 1 ) (H 2 bdc = 1,4-benzene dicarboxylic acid, ppmh = N -pyridin-2-yl- N '-pyridin-4-ylmethylene-hydrazine) has been characterized using different physicochemical techniques. The structure has been confirmed by single crystal X-ray diffraction measurements. There are two pyridyl-N and one hydrazino-imine-N donor centers in ppmh , where two pyridyl-Ns bind simultaneously to two Zn(II) to serve as a bridging agent to form a coordination polymer. The 1,4-benzene dicarboxylato ( bdc ) is ligated via the aromatic dicarboxylato-O to form a one-dimensional (1D) chain. These two 1D chains about Zn(II) constitute a two-dimensional structure, which undergoes noncovalent interactions (C-H···π and π···π) to generate a three-dimensional supramolecular assembly. Electrical conductivity of 1 is higher by 1 order (1.37 × 10 -6 S/cm) than that of the free ligand, ppmh (6.2 × 10 -7 S/cm). Especially, the responsivity of the compound 1 was 56.21 mA/W, which is 11 times higher than that of the ligand ppmh (5.12 mA/W). The specific detectivity of the compound was 2.17 × 10 10 Jones, which is also almost 10 times higher with respect to the specific detectivity of the ligand-based device (4.53 × 10 9 Jones). The results show that the compound can be valuable for optoelectronic fields. The biological studies suggest that compound 1 is antibacterial as well as a promising anticancer agent (LD 50 , 42.2 μg/mL against HepG2 cells), while ligands remain silent. Investigation of the mechanism of the cell killing activity of compound 1 accounts the generation of intracellular reactive oxygen species.
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