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The Synthesis and Reactivity of New μ 2- and μ 3-Aminophosphinidene Cobalt Complexes

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Abstract

The reaction of K[Co(CO)4] and PCl2(TMP) at −5°C leads to the unstable and reactive μ-phosphinidene complex [Co2(CO)6{μ-P(TMP)}] (1), while the same reaction carried out at 35°C gives the chlorophosphido and phosphinidene bridged cluster [Co3(CO)7{μ-P(Cl)TMP}{μ 3-P(TMP)}] (2) (TMP=2,2,6,6-tetramethylpiperidyl). Compound 1 reacts with dppm (dppm=bis(diphenyl- phosphino)methane) and [Co2(CO)8] to form the more stable substitution product [Co2(CO)4{μ-P(TMP)}(μ-dppm)] (3) and [Co4(CO)7(μ-CO)3{μ 3-P(TMP)}] (4) respectively. The first example of a cationic μ 3-phosphinidene cluster compound [Co3(CO)9{μ 3-P(TMP)}][AlCl4] (5) is obtained from reaction of 3 with AlCl3. The X-ray structures of clusters 2 and 5 are discussed.

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Correspondence to Arthur J. Carty.

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Sánchez-Nieves, J., Sterenberg, B.T., Udachin, K.A. et al. The Synthesis and Reactivity of New μ 2- and μ 3-Aminophosphinidene Cobalt Complexes. Journal of Cluster Science 15, 151–162 (2004). https://doi.org/10.1023/B:JOCL.0000027399.01179.fe

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  • DOI: https://doi.org/10.1023/B:JOCL.0000027399.01179.fe

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