1389326-06-0Relevant academic research and scientific papers
Reactions and properties of the dinuclear molybdenum complex [(η5-C5H3)2(CMe 2)(SiMe2)]Mo2(CO)6
Zhu, Bo-Lin,Xu, Shan-Sheng,Zhou, Xiu-Zhong,Wang, Bai-Quan
, p. 57 - 65 (2012)
Reactions of the title complex (1), which features the rigid doubly-bridged biscyclopentadienyl ligand and the unusually long Mo-Mo bond in the structure, with a variety of classic substrates are explored. Complex 1 reacts with I 2 in CH2Cl2 to give the expected Mo-Mo cleaved product [(η5-C5H3)2(CMe 2)(SiMe2)]Mo2(CO)6I2 (2A) with a Mo-Mo distance of 5.329 A?. While the same reaction in benzene forms the product 2B, which has the same structural formula as 2A but a different conformation, in which the Mo-Mo distance is 6.442 A?. Reaction of 1 with Ph2E2 (E = S, Se) in refluxing toluene or under UV irradiation yields products with the carbonyls completely removed, [(η5-C5H3)2(CMe 2)(SiMe2)]Mo2(EPh)2(μ-EPh) 2 (3a-b). Reaction of 1 with [Et2NC(S)S]2 results in the di-substituted product [(η5-C5H 3)2(CMe2)(SiMe2)]Mo 2(CO)4(Et2NC(S)S)2 (4). Reaction of 1 with C2Ph2 affords the acetylene-bridged derivative [(η5-C5H3)2(CMe 2)(SiMe2)]Mo2(CO)4(μ-C 2Ph2) (5). Reaction of 1 with an excess of PPh3 in refluxing toluene only provides the mono-substituted derivative [(η5-C5H3)2(CMe 2)(SiMe2)]Mo2(CO)5(PPh3) (6), while the reaction of 1 with excess P(OPh)3 under the same conditions produces not only the mono-substituted derivative [(η5-C5H3)2(CMe 2)(SiMe2)]Mo2(CO)5(P(OPh) 3) (7), but also the di-substituted derivative [(η5- C5H3)2(CMe2)(SiMe 2)]Mo2(CO)4(P(OPh)3)2 (8). The reactivity and properties of the doubly-bridged molybdenum complex 1 and the corresponding non-bridged and singly-bridged analogs are compared. The molecular structures of 2A, 2B, 3a, 5 and 8 have been determined by single crystal X-ray diffraction.
