Synthesis and characterization of the [Ru3O(CH3COO)6(py)2(BPE)Ru(bpy)2Cl](PF6)2 dimer

被引:5
|
作者
Nikolaou, Sofia [2 ]
Tomazela, Daniela M. [3 ]
Eberlin, Marcos N. [3 ]
Toma, Henrique E. [1 ]
机构
[1] Univ Sao Paulo, Inst Quim, BR-05513970 Sao Paulo, Brazil
[2] Univ Sao Paulo, Dept Quim & Fis, Fac Ciencias Farmaceut Ribeirao Preto, BR-14040903 Ribeirao Preto, Brazil
[3] Univ Estadual Campinas, UNICAMP, Inst Quim, BR-13083970 Campinas, Brazil
基金
巴西圣保罗研究基金会;
关键词
D O I
10.1007/s11243-008-9156-x
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The polymetallic [Ru3O(CH3COO)(6)(py)(2)(BPE)Ru( bpy)(2)Cl](PF6)(2) complex (bpy = 2,2'-bipyridine, BPE = trans- 1,2-bis(4-pyridil) ethylene and py = pyridine) was assembled by the combination of an electroactive [Ru3O] moiety with a [ Ru( bpy) 2( BPE) Cl] photoactive centre, and its structure was determined using positive ion electrospray (ESI-MS) and tandem mass (ESI-MS/MS) spectrometry. The [Ru3O(CH3COO)(6)(py)(2)(BPE)Ru(bpy)(2)Cl] (2+) doubly charged ion of m/z 732 was mass-selected and subject to 15 eV collision-induced dissociation, leading to a specific dissociation pattern, diagnostic of the complex structure. The electronic spectra display broad bands at 409, 491 and 692 nm ascribed to the [Ru(bpy)(2)(BPE)] charge-transfer bands and to the [Ru3O] internal cluster transitions. The cyclic voltammetry shows five reversible waves at - 1.07 V, 0.13 V, 1.17 V, 2.91 V and - 1.29 V (vs SHE) assigned to the [Ru3O](-1/0/+ 1/+ 2/+3) and to the bpy (0/-1) redox processes; also a wave is observed at 0.96 V, assigned to the Ru (+2/+ 3) pair. Despite the conjugated BPE bridge, the electrochemical and spectroelectrochemical results indicate only a weak coupling through the pi-system, and preliminary photophysical essays showed the compound decomposes under visible light irradiation.
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页码:1059 / 1065
页数:7
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