Ruthenium(II) complexes of some simple classic amine ligands

被引:1
作者
Reeves, GorDan T. [1 ]
Addison, Anthony W. [2 ]
Zeller, Matthias [3 ]
机构
[1] Fairleigh Dickinson Univ, Dept Chem & Pharmaceut Sci, Madison, NJ 07940 USA
[2] Drexel Univ, Dept Chem, Philadelphia, PA 19104 USA
[3] Youngstown State Univ, STaRBURSTT CyberInstrumentat Consortium, Dept Chem, Youngstown, OH 44555 USA
关键词
Ruthenium; Amine; Diimine; X-ray structure; X-RAY STRUCTURE; REDOX POTENTIALS; CHEMISTRY; TRIS(2-PYRIDYLMETHYL)AMINE; FUNCTIONALIZATION; IMIDAZOLE; OXIDATION; SERIES; STATES;
D O I
10.1016/j.ica.2015.04.007
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Several new Ru(II) complexes of tris(2-aminoethyl)amine (Tren) and diethylenetriamine (Dien) have been prepared using Ru(PPh3)(3)Cl-2 and [(CH3)(4)N](2)[Ru(Phen)Cl-4] (1) as starting materials. The reaction of Tren or Dien with Ru(PPh3)(3)Cl-2 leads to the formation of either the [Ru(Tren)(PPh3)Cl]Cl (2) or the Ru(Dien)(PPh3)Cl-2 (4) complex, of which the latter then reacts further with a heterocyclic diimine (N-N) ligand to yield [Ru(Dien)(PPh3)(N-N)]Cl-2. Addition of Tren or Dien to solutions of the [(CH3)(4)N](2)[Ru(Phen)Cl-4] complex replaces the coordinated chlorides with the N-donor ligand, forming [Ru(Tren)Phen](ClO4)(2) (3) and [Ru(Dien)(Phen)Cl]Cl (5) respectively. Redox chemistry shows single-electron Ru(II) --> Ru(III) oxidations over a wide range of potentials. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:185 / 191
页数:7
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