Abstract
Tantallacarborane trimethyl complexes show diverse reactivity patterns toward isonitriles. Reaction of [η1:η5-(Me2NCH2CH2)C2B9H10]TaMe3 (1) with 1-adamantyl isonitrile (AdNC) led to the clean formation of an imido complex, [σ:η5-(MeNCH2CH2)C2B9H10]Ta(═NAd)(THF) (2) with elimination of methane and 2-methylpropene, whereas treatment of [η1:η5-{(CH2)5NCH2CH2}C2B9H10]TaMe3 (3) with AdNC under the same reaction conditions gave the cage B–H activated product {σ:η1:η5-[(CH2)5NCHCH2](CHMe2)C2B9H9}Ta(═NAd)(THF) (4). An equimolar reaction of 1 with R1NC (R1 = Cy, Ad), followed by 1 equiv of R2NC (R2 = Xyl, Cy), afforded the imido amido complexes [η1:η5-(Me2NCH2CH2)C2B9H10]Ta(═NR1)[N(CMe═CMe2)R2] (R1 = Ad, R2 = Cy (5); R1 = Cy, R2 = Xyl (6)). If 2 equiv of 2,6-dimethylphenyl isonitrile (XylNC) was used in the above reaction, the cage B–H alkylation products [η1:η5-(Me2NCH2CH2)C2B9H9]Ta(═NR1)[N(Xyl){CHC(Me2)C(Me)═NXyl}] (R1 = Cy (7), Ad (8)) were isolated. On the other hand, η2-iminoacyl imido complexes [η1:η5-(Me2NC...
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