Abstract
The formation of thiyl radicals from [Cp*RuIII{κ3SSS′-tpdt }] (1A) and [Cp*RuIII{κ3SSN-apdt}] (1B) {Cp* = η5-C5Me5; tpdt = S(CH2CH2S-)2; apdt = HN(CH2CH2S-)2} has been initiated by thiolate alkylation or oxidation with iodine. Subsequent electron transfer processes yielded disulfide-bridged dinuclear complexes. The mechanistic pathways of these processes will be discussed.
Original language | English |
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Pages (from-to) | 3267-3276 |
Number of pages | 10 |
Journal | Journal of Organometallic Chemistry |
Volume | 692 |
Issue number | 15 |
DOIs | |
Publication status | Published - Jul 1 2007 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
- Materials Chemistry
Keywords
- Cyclopentadienyl ruthenium
- Disulfide bridge
- Methylation
- Thiolate
- Thiyl radical