1. Reactions and properties of the dinuclear molybdenum complex [(η 5-C5H3)2(CMe2)(SiMe2)]Mo2(CO)6
- Author
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Zhu, Bo-Lin, Xu, Shan-Sheng, Zhou, Xiu-Zhong, and Wang, Bai-Quan
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CHEMICAL reactions , *MOLYBDENUM compounds , *METAL complexes , *LIGANDS (Chemistry) , *CHEMICAL bonds , *MOLECULAR structure , *CHEMICAL derivatives - Abstract
Abstract: 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 I2 in CH2Cl2 to give the expected Mo–Mo cleaved product [(η 5-C5H3)2(CMe2)(SiMe2)]Mo2(CO)6I2 (2A) with a Mo–Mo distance of 5.329Å. 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 6.442Å. Reaction of 1 with Ph2E2 (E=S, Se) in refluxing toluene or under UV irradiation yields products with the carbonyls completely removed, [(η 5-C5H3)2(CMe2)(SiMe2)]Mo2(EPh)2(μ-EPh)2 (3a–b). Reaction of 1 with [Et2NC(S)S]2 results in the di-substituted product [(η 5-C5H3)2(CMe2)(SiMe2)]Mo2(CO)4(Et2NC(S)S)2 (4). Reaction of 1 with C2Ph2 affords the acetylene-bridged derivative [(η 5-C5H3)2(CMe2)(SiMe2)]Mo2(CO)4(μ-C2Ph2) (5). Reaction of 1 with an excess of PPh3 in refluxing toluene only provides the mono-substituted derivative [(η 5-C5H3)2(CMe2)(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 [(η 5-C5H3)2(CMe2)(SiMe2)]Mo2(CO)5(P(OPh)3) (7), but also the di-substituted derivative [(η 5-C5H3)2(CMe2)(SiMe2)]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. [Copyright &y& Elsevier]
- Published
- 2012
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