Novel Co(II), Ni(II) and Cu(II) complexes involving a 2-thienyl and trifluoromethyl containing symmetrically-substituted tetradentate Schiff-base ligand: Syntheses, structures, electrochemical and computational studies

被引:11
作者
Ahumada, Guillermo [1 ,2 ]
Fuentealba, Mauricio [3 ]
Roisnel, Thierry [2 ]
Kahlal, Samia [2 ]
Carrillo, David [1 ]
Cordova, Ricardo [1 ]
Saillard, Jean-Yves [2 ]
Hamon, Jean-Rene [2 ]
Manzur, Carolina [1 ]
机构
[1] Pontificia Univ Catolica Valparaiso, Inst Quim, Fac Ciencias, Lab Quim Inorgan, Campus Curauma,Ave Univ 330, Valparaiso, Chile
[2] Univ Rennes, CNRS, ISCR, UMR 6226, F-35000 Rennes, France
[3] Pontificia Univ Catolica Valparaiso, Lab Cristalog, Inst Quim, Fac Ciencias, Campus Curauma,Ave Univ 330, Valparaiso, Chile
关键词
Thiophene-based Schiff base complex; N2O2-ligand; Cyclic voltammetry; Single-crystal X-ray diffraction; DFT and TD-DFT calculations; NONLINEAR-OPTICAL PROPERTIES; CRYSTAL-STRUCTURES; DERIVATIVES; CHEMISTRY; SYSTEM;
D O I
10.1016/j.poly.2018.05.048
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Here, we report three novel metal(II) complexes (M = Co, 3a: Ni, 3b; Cu, 3c) involving a symmetrically substituted N2O2-tetradentate Schiff base ligand bearing trifluoromethyl and 2-thienyl substituents. Complexes 3a-c were readily synthesized upon reaction of the diprotic Schiff base proligand with the appropriate hydrated metal(II) acetates, and isolated as neutral, air and thermally stable solids in good to excellent yields (>65-85%). All the complexes have been well characterized using elemental analysis and different spectroscopic tools (ESI+ HRMS, FT-IR, UV-Vis), and single crystal X-ray diffraction analysis for 3b and 3c. Their crystal structures revealed a four-coordinate square planar geometry at the Ni(II) and Cu(II) metal ions, with two nitrogen and two oxygen atoms as donors. Complexes 3a-c displayed similar cyclic voltammetric behavior, exhibiting one anodic and one cathodic wave, both irreversible and of different intensity. They were tentatively assigned to M(II)/M(III) and M(II)/M(I) redox couples, respectively. No deposits of polymeric films on the electrode surface were observed. Structural, electrochemical and electronic parameters of the complexes have been rationalized on the ground of DFT and TD-DFT computation. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:279 / 286
页数:8
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