Synthesis, Characterization and Single Crystal X-Ray Structures of Trifluroacetylacetonate Copper(II) Complexes

被引:2
|
作者
Kumari, Neha [1 ]
Bahadur, Vir [2 ]
Butcher, Raymond J. [3 ]
Kumbhar, Anupa A. [1 ]
机构
[1] Savitribai Phule Pune Univ, Dept Chem, Pune 411007, Maharashtra, India
[2] CSIR, Natl Chem Lab, Dr Homi Bhabha Marg, Pune 411008, Maharashtra, India
[3] Howard Univ, Dept Chem, 2400 Sixth St NW, Washington, DC 20059 USA
关键词
Copper(II) complexes; Crystal structure; Cyclic voltammetry; DABCO; Pyridine; Trifluoroacetylacetone; COORDINATION POLYMERS; BETA-DIKETONE; CATALYST; LIGANDS; STABILITY;
D O I
10.1007/s10870-022-00937-1
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
Three Cu(II) complexes of 1,1,1-trifluoroacetylacetonate, viz. [Cu(TFACAC)(2)(MeOH)] (1), [Cu(TFACAC)(2)(py)] (2) and [Cu(TFACAC)(2)(DABCO)] (3) were synthesized and characterized by elemental analysis, IR, UV-Visible spectroscopy and cyclic voltammetry. Structures of complexes 1-3 were established by single crystal X-ray diffraction wherein 1 and 2 adapt square pyramidal geometry. Complex 1 crystallizes in triclinic space group P-(1), with a = 8.5059(6) angstrom, b = 9.3025(7) angstrom, c = 10.9906(8) angstrom, alpha = 75.684(2)degrees, beta = 73.191(2)degrees, gamma = 64.992(2)degrees, and Z = 2. X-ray crystallographic studies revealed that in complex 1, both, TFACC ligands and coordinated methanol are disordered over two conformations giving a combination of two isomers with cis to trans isomer ratio of 0.538:0.462. In complex 3 DABCO is acting as a bridging ligand connecting two Cu(II) centers thereby forming a 1-D polymer chain with each copper in octahedral coordination. The cyclic voltammograms of 1 and 3 give a quasi-reversible Cu(II)/Cu(I) peak with E-1/2 + 0.01 V and - 0.05 V respectively whereas complex 2 gives a one electron reversible Cu(II)/Cu(I) couple at E-1/2 = - 0.25 V. [GRAPHICS] .
引用
收藏
页码:525 / 533
页数:9
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