Manganese Silylene Hydride Complexes: Synthesis and Reactivity with Ethylene to Afford Silene Hydride Complexes Journal Articles uri icon

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abstract

  • AbstractReaction of the ethylene hydride complex trans‐[(dmpe)2MnH(C2H4)] (1) with Et2SiH2 at 20 °C afforded the silylene hydride [(dmpe)2MnH(=SiEt2)] (2 a) as the trans‐isomer. By contrast, reaction of 1 with Ph2SiH2 at 60 °C afforded [(dmpe)2MnH(=SiPh2)] (2 b) as a mixture of the cis (major) and trans (minor) isomers, featuring a Mn‐H‐Si interaction in the former. The reaction to form 2 b also yielded [(dmpe)2MnH2(SiHPh2)] (3 b); [(dmpe)2MnH2(SiHR2)] (R=Et (3 a) and Ph (3 b)) were accessed cleanly by reaction of 2 a and 2 b with H2, and the analogous reactions with D2 afforded [(dmpe)2MnD2(SiHR2)] exclusively. Both 2 a and 2 b engaged in unique reactivity with ethylene, generating the silene hydride complexes cis‐[(dmpe)2MnH(R2Si=CHMe)] (R=Et (4 a), Ph (4 b)). Compounds trans2 a, cis2 b, 3 b, and 4 b were crystallographically characterized, and bonding in 2 a, 2 b, 4 a, and 4 b was probed computationally.

publication date

  • May 22, 2017