Cyclobutane to diolefin trausfcmations prauoted by transition-metal compounds, such as 1-s the isomerisation of quadricyclaues to norbornadienes and of cube type moleculestoring cleaved products, 495 have recently attracted cmsiderable attention. Lately, we' and The details of the preparation of th
On the nature of carbenoids generated from bicyclo[1.1.0]butanes and transition metal complexes
β Scribed by R. Noyori
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 341 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
In valence bond description, a complex of a transition metal MxLn (x = oxidation number, L = ligand) and a carbene :CRR' (R, R' = H or carbon function) exists as a resonance hybrid consisting of the ylene form Ia and the two polar contributors, the metal-bonded carbanion Ib (ylide) and the metal-bonded carbocation Ic (inverse ylide).
2 The relative significance of the canonical forms is determined by the nature of the metal, its ligands, and the carbene substituents
π SIMILAR VOLUMES
Pentacyclic (CH)a hydrocarbon 1 can be viewed not only as the most highly condensed valence isomer of cyclooctatetraene, but also as a formal (2+2) dimer of tetrahedrane. The effective cyclic conjugation of two bicyclo[l.l.O]butsne rings in 1 should form the basis for interesting spectral properties