Synthesis, structural, spectroscopic and electric/dielectric studies of a nanocrystalline Ni(<sc>ii</sc>) complex based on [(1,3-diphenyl-1H-pyrazol-4-yl)methylene]thiocarbonohydrazide

被引:0
作者
Fouad, R. [1 ]
Ali, Tarik E. [2 ]
Assiri, Mohammed A. [2 ]
Shenouda, S. S. [3 ,4 ]
机构
[1] Ain Shams Univ, Fac Educ, Dept Chem, Roxy, Cairo, Egypt
[2] King Khalid Univ, Fac Sci, Dept Chem, POB 9004, Abha 61421, Saudi Arabia
[3] Ain Shams Univ, Fac Educ, Phys Dept, Roxy, Cairo, Egypt
[4] Obour High Inst Engn & Technol, Dept Basic Sci, Obour, Egypt
关键词
AC ELECTRICAL-CONDUCTIVITY; DNA-BINDING AFFINITY; TEMPERATURE-DEPENDENCE; DIELECTRIC-RELAXATION; PD(II) COMPLEXES; METAL-COMPLEXES; NI(II); CU(II); CO(II); CHALCOGENIDE;
D O I
10.1039/d4ra00665h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A Ni2+ nanocomplex based on a heterocyclic ligand containing a pyrazole moiety was developed in this work, and its electric conductivity and dielectric characteristics were studied. The Ni2+ nanocomplex with the general formula [Ni(PyT)(2)(H2O)(2)]Cl-2<middle dot>1/2H(2)O, where PyT = [(1,3-diphenyl-1H-pyrazol-4-yl)methylene]thiocarbonohydrazide, was characterized using various techniques, including elemental and thermal analyses, as well as conductivity, magnetism, TEM, and spectroscopic (FT-IR, UV-Vis and XRD) studies. The results showed that PyT was bonded to the Ni(ii) centers via a neutral bidentate ligand, resulting in an octahedral-shaped, thermally stable mononuclear complex. The frequency response of the dielectric properties and ac conductivity was studied in the range from 200 Hz to 6 kHz. Both dielectric constant and dielectric loss decreased with increasing frequency. In addition, the effect of temperature was investigated in the range of 294.1-363.4 K. The ac conductivity increased with increasing temperature in the range of 294.1-333.5 K. The ac conduction is described as correlated barrier hopping between non-intimate valence alternation pairs. Furthermore, the PyT and Ni(PyT) nanocomplex structures were optimized using theoretical calculations and DFT computations.
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收藏
页码:9747 / 9757
页数:11
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