摘要
Reaction of the bis(diphenylphosphino sulfide)-methanide anion (S similar to C similar to S) with [Ir(cyclooctene)(2)Cl](2) dimer complex affords an 18-VE Ir(III) hydrido complex. DFT calculations suggest that formation of this hydrido species results from the insertion of the highly reactive 16-VE Ir(I) complex [Ir(SCS-)(cyclooctene)] into one of the C-H bonds of'the phenyl group of a pendant phosphino sulfide ligand. The DFT results also point to the easy access to unsaturated intermediates, explaining the experimentally observed facile displacement of the cyclooctene ligand by PPh(3).
- 出版日期2009-3-23