347897-10-3Relevant academic research and scientific papers
Synthesis, NMR and structural studies of cluster derivatives derived from reactions of 1,2,3-triphenyl-1,2,3-triphosphaindan with [Os3(CO)10(μ-H)2]
Ang, Siau-Gek,Zhong, Xinhua,Ang, How-Ghee
, p. 218 - 225 (2007/10/03)
Reactions of 1,2,3-triphenyl-1,2,3-triphosphaindan (I) with [Os3(CO)10(μ-H)2] at various conditions afford a series of osmium carbonyl cluster derivatives: an open bent-chain trinuclear cluster [Os3(CO)9{μ3- η3-PPhC6H4(PPh)2}] (1), a di-substituted bridged trinuclear cluster [Os3(CO)10 {μ-1,3-η2-C6H4(PPh)3}] (2), a 1,3-linked bis-trinuclear hydride cluster {μ3-η3-{(PPh)2C6H 4PPh}] (4), and a closed trinuclear cluster [(μ-H)Os3 (CO)8{C6H4(PPh)3}{μ-η 3-{C6H4(PPh)2PC6 H4}] (5). All the compounds obtained have been fully characterized by spectroscopic methods (IR, FABMS, 1H- and 31P-NMR spectroscopy), and the molecular structures of 3, 4, 5 are established by X-ray crystallography.
Reactions of 1,2,3-triphenyl-1,2,3-triphosphaindan with activated triosmium carbonyl clusters: Characterization and crystal structure of the products
Ang,Zhong,Ang
, p. 1151 - 1158 (2007/10/03)
Reaction of 1,2,3-triphenyl-1,2,3-triphosphaindan (I) with [Os3(CO)11(NCMe)] at room temperature afforded two clusters: mono-substituted trinuclear [Os3(CO)11{1-C6H4 (PPh)3}] 1 and bridged bis-trinuclear [{Os3(CO)11}2{μ-1,3-η2- C6H4(PPh)3}] 2, which can also be prepared by further reaction of 1 with an equimolar amount of [Os3(CO)11(NCMe)]. The reaction at 100°C gave, apart from cluster 2, a di-substituted bridged cluster, [Os3(CO)10{μ-1,3-η2-C6 H4(PPh)3}] 3, and that at 140°C formed a linked pentanuclear cluster, [Os2(CO)6{μ3-η3- PPhC6H4(PPh)2}Os3 (CO)11] 4 and a trinuclear cluster with only two M-M bonds, [Os3(CO)9{μ3-η3- PPhC6H4(PPh)2}] 5 together with 3. Similarly [Os3(CO)10(NCMe)2] reacted with I at room temperature to afford 3 in good yields. The conversion of cluster 1 into 3 can be achieved through pyrolysis of a solution of 1. Cluster 4 exhibits stereochemical non-rigidity in the solution state and exists as two isomers at low temperature. All the new compounds were characterized by spectroscopic and analytical techniques and their structures established by X-ray crystallography.
