Synthesis, characterization and structure of novel Vanadium (III) complexes: Investigation of electrochemical application

电化学 循环伏安法 计时安培法 微分脉冲伏安法 正交晶系 玻璃碳 氧化还原 无机化学 核化学 分析化学(期刊) 化学 晶体结构 结晶学 物理化学 有机化学 电极
作者
Sateesha M. Kannakatte,Mallikarjunagouda B. Patil,Mounesha M. Nayak,Lokanath K. Neratur,Mungalimane K. Amshumali
出处
期刊:Materials Chemistry and Physics [Elsevier]
卷期号:301: 127577-127577 被引量:1
标识
DOI:10.1016/j.matchemphys.2023.127577
摘要

From the prospective of possible electrochemical application of vanadium complexes, here, we report the two novel vanadium complexes. Namely, Tp*VO(3,5-Me2pzH)2(CH3CN) (1) (where, Tp* = hydro tris(3,5-dimethylpyrazolyl)borate and Tp*VTp*(2) these complexes were prepared in a good yield starting from V(III) chloride and hydro tris (3, 5 dimethyl pyrazolyl) borate. Both the complexes were characterized by NMR, Mass, and FTIR spectroscopy. In addition, cyclic voltammetry is used to investigate electrochemical processes of 1 and 2. The electrochemical active species exhibits two noteworthy redox peaks and exhibits considerable catalytic action towards glassy carbon electrodes with a composite of multi-walled carbon nanotubes (MWCNTs). Moreover, the complex1/MWCNTs/GC electrode detects the H2O2 in PBS (pH 7) electrolyte solution by cyclic voltametry (CA), differential pulse voltametry (DPV) and chronoamperometry (CA) techniques; Under the optimal conditions, the reduction peak current is linear to the H2O2 concentration in the ranges, detection limit for; CA: 50–500 μmol; 4.5 μmol L−1, CV: 50–400 μmol; 9.5 μmol L−1, DPV: 50–500 μmol; 8.3 μmol L−1. Single-crystal XRD analysis revealed that complex 1 crystallized in the orthorhombic space group P212121with lattice parameters a = 11.960(4) Å, b = 12.571(4) Å, c = 20.465(7)Å, Z = 4. In addition, distorted octahedral geometry was observed around the vanadium metal centre. Surface morphology of the complexes was probed by scanning electron microscopy (SEM).

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