Complexes of [Re(CO)3Cl] with different oxidation states of the polyfunctional bmtz/H2bmtz ligand system (bmtz=3,6-bis(2-pyrimidyl)-1,2,4,5-tetrazine)

被引:13
作者
Frantz, S
Kaim, W
Fiedler, J
Duboc, C
机构
[1] Univ Stuttgart, Inst Anorgan Chem, D-70550 Stuttgart, Germany
[2] Acad Sci Czech Republ, J Heyrovsky Inst Phys Chem, CZ-18223 Prague, Czech Republic
[3] CNRS, MPI, Grenoble High Magnet Field Lab, F-38042 Grenoble 9, France
关键词
cyclic voltammetry; EPR; rhenium complexes; spectroelectrochemistry; tetrazine ligands;
D O I
10.1016/j.ica.2004.03.056
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Combining fac-[Re(CO)(3)Cl] with components of the ligand redox system bmtz/bmtz(-)-/H(2)bmtz/H(2)bmtz(-) (bmtz = 3,6-bis(2-pyrimidyl)-1,2,4,5-tetrazine) has led to the isolation of the complexes (H(2)bmtz)Re(CO)(3)Cl, (mu-H(2)bmtz)[Re(CO)(3)Cl](2) and (mu-bmtz)[Re(CO)(3)Cl](2). Other species characterized were (bmtz)Re(CO)(3)Cl (UV/Vis, IR), [(H(2)bmtz)Re(CO)(3)Cl](.-) (UV/Vis, IR, EPR), {(mu-H(2)bmtz)[Re(CO)(3)Cl](2)}(.-) (UV/Vis, IR, EPR) and {(mu-bmtz)[Re(CO)(3)Cl](2)}(.-) (UV/Vis, IR, X band and high-field EPR). The results confirm bmtz as very strong and H(2)bmtz as moderate n acceptor ligand versus one or two chelate-bonded low-valent metal centers. Reactivity is observed in terms of oxidative proton and reductive chloride dissociation. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:3657 / 3665
页数:9
相关论文
共 35 条
[1]   High-frequency (245 GHz) and X-band EPR study of stable dicopper radical complexes [J].
Barra, AL ;
Brunel, LC ;
Baumann, F ;
Schwach, M ;
Moscherosch, M ;
Kaim, W .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1999, (21) :3855-3857
[2]   EPR SPECTROSCOPY AT VERY HIGH-FIELD [J].
BARRA, AL ;
BRUNEL, LC ;
ROBERT, JB .
CHEMICAL PHYSICS LETTERS, 1990, 165 (01) :107-109
[3]   Multistep redox sequences of azopyridyl (L) bridged reaction centres in stable radical complex ions {(μ-L)[MCl(η5-C5Me5)]2}•+, M = Rh or Ir:: spectroelectrochemistry and high-frequency EPR spectroscopy [J].
Frantz, S ;
Reinhardt, R ;
Greulich, S ;
Wanner, M ;
Fiedler, J ;
Duboc-Toia, C ;
Kaim, W .
DALTON TRANSACTIONS, 2003, (17) :3370-3375
[4]   Multifrequency EPR study and density functional g-tensor calculations of persistent organorhenium radical complexes [J].
Frantz, S ;
Hartmann, H ;
Doslik, N ;
Wanner, M ;
Kaim, W ;
Kümmerer, HJ ;
Denninger, G ;
Barra, AL ;
Duboc-Toia, C ;
Fiedler, J ;
Ciofini, I ;
Urban, C ;
Kaupp, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (35) :10563-10571
[5]  
FRANTZ S, 2003, THESIS U STUTTGART
[6]  
FRANTZ S, IN PRESS INORG CHIM
[7]  
Glöckle M, 2001, Z ANORG ALLG CHEM, V627, P1441, DOI 10.1002/1521-3749(200107)627:7<1441::AID-ZAAC1441>3.0.CO
[8]  
2-R
[9]   Dicopper(I) complexes with reduced states of 3,6-bis(2′-pyrimidyl)-1,2,4,5-tetrazine:: Crystal structures and spectroscopic properties of the free ligand, a radical species, and a complex of the 1,4-dihydro form [J].
Glöckle, M ;
Hübler, K ;
Kümmerer, HJ ;
Denninger, G ;
Kaim, W .
INORGANIC CHEMISTRY, 2001, 40 (10) :2263-2269
[10]   PROTON-INDUCED SWITCHING OF METAL METAL INTERACTIONS IN DINUCLEAR RUTHENIUM AND OSMIUM COMPLEXES BRIDGED BY 2,2'-BIS(2-PYRIDYL)BIBENZIMIDAZOLE [J].
HAGA, M ;
ANO, T ;
KANO, K ;
YAMABE, S .
INORGANIC CHEMISTRY, 1991, 30 (20) :3843-3849