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• W2009444906 abstract "The highly delocalized distribution of the MOs in C60 has been analyzed with the aid of extended Hückel calculations and their graphic representations. Symmetry and perturbation theory arguments rationalize the MO correlations in terms of the implosion of 12 C5 rings distributed at the vertices of an expanded icosahedron. In particular, two distinguishable σ and π C60 subsets are each split into 30 filled and 30 empty MOs belonging to the same species under Ih symmetry. As a major difference, whereas 30 new CC σ bonds add to the 60 pre-existing C5 endocyclic bonds, some partial π bonding at the 6:6 edges of C60 occurs at the expense of π bonding at the 5:6 edges. This point has been clarified by referring to the electronic structure of the simpler molecule [5]-radialene which typifies the MO response to the idea of π resonance. An overview at the CC bonding/ antibonding roles in all of the π MOs simplifies understanding their possible interactions with the frontier MOs of typical transition metal fragments. The model complexes considered involve the η2-coordination of the C2ν fragment (PH3)2Pt to C60 in 6:1, 2:1 and 1:1 ratios. The MO analysis highlights the electronic causes of the deformation from sphericity of C60 when a metal is attached to one or more 6:6 edge. Attempts to explore alternative, but as yet unsynthesized coordination modes have also been made." @default.
• W2009444906 created "2016-06-24" @default.
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• W2009444906 date "1994-09-01" @default.
• W2009444906 modified "2023-10-12" @default.
• W2009444906 title "A pictorial MO description of Buckminsterfullerene and its interactions with transition metal fragments" @default.
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• W2009444906 doi "https://doi.org/10.1016/0022-328x(94)88168-5" @default.
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