摘要：

The photoelectron spectra of 1,5-cyclooctadiyne (2) and of 1,6-dithiacyclodeca-3,8-diyne (3) have been recorded. The first four (2) or six (3) PE. bands have been assigned as follows; in increasing order of ionization potentials: The relative sequence and the positions of the PE. bands are explained in terms of through-bond and through-space interactions between the basis π-orbitals and σ-orbitals of appropriate symmetry behaviour.An analysis of the PE. spectroscopic data for cyclooctyne (1) and for (2) indicates that a cis-bend of the acetylene moiety by θ < 20° leads to a split in energy of the in-plane and out-of-plane basis π-orbitals which is smaller than ∽ 0.2 eV. This is in agreement with the predictions derived from semiempirical models (MINDO/2, SPINDO) and qualitative orbital arguments. However, it is shown by using orbital localization procedures, that the rationales underlying the two semiempirical models differ significantly.

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