کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1324012 | 977316 | 2006 | 11 صفحه PDF | دانلود رایگان |

Thermal reaction of [Ru3(CO)12] with PH2Mes (Mes = mesityl) in refluxing toluene afforded mesitylphosphinidene-capped ruthenium carbonyl clusters, [Ru3(CO)9(μ-H)2(μ3-PMes)] (1), [Ru3(CO)8(PH2Mes)(μ-H)2(μ3-PMes)] (2), [Ru3(CO)9(μ3-PMes)2] (3), [Ru4(CO)10(μ-CO)(μ4-PMes)2] (4), and [Ru5(CO)10H2(μ4-PMes)(μ3-PMes)2] (5). All products were fully characterized and structurally confirmed by X-ray crystal structure analysis. Complexes 2–4 were also obtained in high yields by stepwise reaction starting from 1. Fluxional behavior of carbonyl groups was observed in case of 4. Complex 5 reveals a new type of skeletal structure, bicapped-octahedron having μ3- and μ4-phosphinidene ligands at the capping positions. Similar reaction of [Os3(CO)12] with PH2Mes yielded a phosphido-bridged osmium cluster [Os3(CO)10(μ-H)(μ-PHMes)] (6) and a phosphinidene-capped cluster [Os3(CO)9(μ-H)2(μ3-PMes)] (7).
Mesitylphosphinidene-capped tri, tetra, and pentaruthenium clusters were obtained by the thermal reaction of [Ru3(CO)12] with PH2Mes. The pentaruthenium cluster [Ru5(CO)10H2(μ4-PMes)(μ3-PMes)2] was found to adopt a novel bicapped octahedral framework. Stepwise and high-yield transformation among the products were also found. A similar reaction of [Os3(CO)12] with PH2Mes exclusively afforded trinuclear clusters.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 691, Issue 4, 1 February 2006, Pages 726–736