A Scandium Complex Bearing Both Methylidene and Phosphinidene Ligands: Synthesis, Structure, and Reactivity

The scandium complex bearing both methylidene and phosphinidene ligands, [(LSc)2­(μ2-CH2)­(μ2-PDIPP)] (L = [MeC­(NDIPP)­CHC­(NDIPP)­Me]−, DIPP = 2,6-( i Pr)2C6H3) (2), has been synthesized, and its reactivity has been investigated. Reaction of scandium methyl phosphide [LSc­(Me)­{P­(H)­DIPP}] with 1...

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Veröffentlicht in:Organometallics 2015-01, Vol.34 (2), p.470-476
Hauptverfasser: Zhou, Jiliang, Li, Tengfei, Maron, Laurent, Leng, Xuebing, Chen, Yaofeng
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Sprache:eng
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Zusammenfassung:The scandium complex bearing both methylidene and phosphinidene ligands, [(LSc)2­(μ2-CH2)­(μ2-PDIPP)] (L = [MeC­(NDIPP)­CHC­(NDIPP)­Me]−, DIPP = 2,6-( i Pr)2C6H3) (2), has been synthesized, and its reactivity has been investigated. Reaction of scandium methyl phosphide [LSc­(Me)­{P­(H)­DIPP}] with 1 equiv of scandium dimethyl complex [LScMe2] in toluene at 60 °C provided complex 2 in good yield, and the structure of complex 2 was determined by single-crystal X-ray diffraction. Complex 2 easily undergoes nucleophilic addition reactions with CO2, CS2, benzonitrile, and tert-butyl isocyanide. In the above reactions, the unsaturated substrates insert into the Sc–C­(methylidene) bond to give some interesting dianionic ligands while the Sc–P­(phosphinidene) bond remains untouched. The bonding situation of complex 2 was analyzed using DFT methods, indicating a more covalent bond between the scandium ion and the phosphinidene ligand than between the scandium ion and the methyl­idene ligand.
ISSN:0276-7333
1520-6041
DOI:10.1021/om500997j