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Synthesis,characterization, powder XRD and antimicrobial-antioxidant activity evaluation of trivalent transition metal macrocyclic complexes
Institution:1. Department of Chemistry, National Institute of Technology, Kurukshetra 136 119, India;2. Department of Microbiology, Kurukshetra University, Kurukshetra 136 119, India
Abstract:The in vitro antimicrobial and antioxidant activities of metal complexes derived from 1,8-diaminonaphthalene and 5,5-dimethylcyclohexane-1,3-dione were evaluated. The complexes were synthesized by template method in the presence of trivalent metal salts, resulting in the formation of tetraaza macrocyclic complexes of the type M (C36H36N4) X] X2, where M = Cr(III), Fe(III) and X = Cl, NO3, CH3COO. The synthesized complexes were characterized with the aid of elemental analyses, molar conductance measurements, magnetic susceptibility measurements, electronic, IR, mass and powder XRD studies. Based on various studies, a five-coordinated square pyramidal geometry was proposed for these complexes. The X-ray diffraction studies suggest a monoclinic crystal system for the complexes.
Keywords:Template  Infrared  5  5-Dimethylcyclohexane-1  3-dione  Spectroscopic  Antioxidant  X-ray diffraction  B  M  "}  {"#name":"keyword"  "$":{"id":"kw0040"}  "$$":[{"#name":"text"  "_":"Bohr magneton  DMF"}  {"#name":"keyword"  "$":{"id":"kw0050"}  "$$":[{"#name":"text"  "$$":[{"#name":"italic"  "_":"N"}  {"#name":"__text__"  "_":"  "}  {"#name":"italic"  "_":"N"}  {"#name":"__text__"  "_":"-dimethylformamide  DMSO"}  {"#name":"keyword"  "$":{"id":"kw0060"}  "$$":[{"#name":"text"  "_":"dimethylsulfoxide  DOTA"}  {"#name":"keyword"  "$":{"id":"kw0070"}  "$$":[{"#name":"text"  "_":"tetraazacyclododecanetetra-acetic acid  MRI"}  {"#name":"keyword"  "$":{"id":"kw0080"}  "$$":[{"#name":"text"  "_":"Magnetic Resonance Imaging  DNA"}  {"#name":"keyword"  "$":{"id":"kw0090"}  "$$":[{"#name":"text"  "_":"deoxyribonucleic acid  IR"}  {"#name":"keyword"  "$":{"id":"kw0100"}  "$$":[{"#name":"text"  "_":"Infrared  DPPH"}  {"#name":"keyword"  "$":{"id":"kw0110"}  "$$":[{"#name":"text"  "_":"2  2-diphenyl-1-picrylhydrazyl  MTCC"}  {"#name":"keyword"  "$":{"id":"kw0120"}  "$$":[{"#name":"text"  "_":"microbial-type culture collection  IMTECH"}  {"#name":"keyword"  "$":{"id":"kw0130"}  "$$":[{"#name":"text"  "_":"Institute of Microbial Technology  MIC"}  {"#name":"keyword"  "$":{"id":"kw0140"}  "$$":[{"#name":"text"  "_":"minimum inhibitory concentration  MHA"}  {"#name":"keyword"  "$":{"id":"kw0150"}  "$$":[{"#name":"text"  "_":"Mueller–Hinton agar  EDTA"}  {"#name":"keyword"  "$":{"id":"kw0160"}  "$$":[{"#name":"text"  "_":"Ethylenediaminetetraacetic acid  XRD"}  {"#name":"keyword"  "$":{"id":"kw0170"}  "$$":[{"#name":"text"  "_":"X-ray diffraction  NMR"}  {"#name":"keyword"  "$":{"id":"kw0180"}  "$$":[{"#name":"text"  "_":"Nuclear Magnetic Resonance  ESR"}  {"#name":"keyword"  "$":{"id":"kw0190"}  "$$":[{"#name":"text"  "_":"Electron Spin Resonance  DFT"}  {"#name":"keyword"  "$":{"id":"kw0200"}  "$$":[{"#name":"text"  "_":"Density Functional Theory  HOMO"}  {"#name":"keyword"  "$":{"id":"kw0210"}  "$$":[{"#name":"text"  "_":"Highest Occupied Molecular Orbital  LUMO"}  {"#name":"keyword"  "$":{"id":"kw0220"}  "$$":[{"#name":"text"  "_":"Lowest Unoccupied Molecular Orbital
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