| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1323603 | Journal of Organometallic Chemistry | 2011 | 4 Pages |
Treatment of [Ru(CHR)Cl2(PCy3)2] (Cy = cyclohexyl) with Tl[N(Pr2iPO)2] and AgLOEt (LOEt− = [CpCo{P(O)(OEt)2}3]−) afforded the Ru carbene complexes [Ru(CHPh)(PCy3)Cl{N(Pr2iPO)2}] (1) and [LOEtRu(CHR)(PCy3)Cl] (2), respectively. Chloride abstraction of complex 2 with TlPF6 in MeCN afforded [LOEtRu(CHPh)(PCy3)(MeCN)][PF6] (3). Complexes 1 and 2 are capable of catalyzing ring-closing metathesis of diethyl 1,2-diallylmalonate. The crystal structure of complex 2 has been determined.
Graphical abstractTreatment of [Ru(CHR)Cl2(PCy3)2] (Cy = cyclohexyl) with Tl[N(Pr2iPO)2] and AgLOEt (LOEt− = [CpCo{P(O)(OEt)2}3]−) afforded the Ru carbene complexes [Ru(CHPh)(PCy3)Cl{N(Pr2iPO)2}] (1) and [LOEtRu(CHR)(PCy3)Cl] (2), respectively, which can catalyze the ring-closing metathesis of diethyl 1,2-diallylmalonate.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Ru carbene complexes supported by chelating PO ligands. ► Structurally characterized Ru carbene complex with an oxygen tripod ligand. ► Catalysts for ring-closing metathesis of diethyl diallylmalonate.
