Coordination complexes with the redox active tetrathiafulvalene based imino-pyrazine ligand: syntheses, a radical cation salt, crystal structures and electrochemistry

被引:23
作者
Cosquer, Goulven [1 ]
Pointillart, Fabrice [1 ]
Le Gal, Yann [1 ]
Golhen, Stephane [1 ]
Cador, Olivier [1 ]
Ouahab, Lahcene [1 ]
机构
[1] Univ Rennes 1, CNRS, URI Sci Chim Rennes, UMR Organomet & Mat Mol 6226, F-35042 Rennes, France
关键词
TRANSITION-METAL-COMPLEXES; CU-II; MOLECULAR-METALS; TTF DERIVATIVES; ORGANIC DONOR; MN-II; HEXAFLUOROACETYLACETONATE; CONSTRUCTION; VERSATILE; SERIES;
D O I
10.1039/b815865g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The tetrathiafulvalene based 2-immino-pyrazine derivative (TTF-CHN-2-pyz) (1) was synthesized and characterized. Its radical cation salt (1(center dot+)PF(6)(-)) was prepared as single crystals by electrocrystallisation. 1(center dot+)PF(6)(-) crystallizes in the triclinic P (1) over bar space group. Four 1 : 2 bis(hexafluoroacetylacetonate)M(II) complexes coordinated with I were prepared (M = Mn for 2, M = Co for 3, M = Cu for 4 and M = Zn for 5). Complex 2 crystallizes in the monoclinic C2/c space group, complexes 4 and 5 crystallize in the triclinic space group P (1) over bar. Two pyrazine N atoms from two different donors are coordinated in cis configuration for 2 and trans configuration for 4 and 5 to the metallic ion of M(hfac)(2) (hfac(-)=hexafluoroacetylacetonate anion). The manganese atom adopts a pseudo-compressed octahedral geometry while the copper and the zinc ions adopt axially elongated octahedral geometries. Both crystal packing structures and electrochemical properties are appropriate for their potential use as starting molecular bricks for conducting and magnetic materials.
引用
收藏
页码:3495 / 3502
页数:8
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