## Abstract The ionization potentials of methyl‐, __t__‐butyl‐ and trimethylsilyl‐substituted pyridines have been determined by high‐resolution photoelectron spectroscopy. The results are discussed in terms of destabilizing inductive and stabilizing conjugative effects of the substituents, and have
Photoelectron Spectra of Azabenzenes and Azanaphthalenes: I. Pyridine, diazines, s-triazine and s-tetrazine
✍ Scribed by R. Gleiter; E. Heilbronner; V. Hornung
- Book ID
- 102855269
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- German
- Weight
- 955 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The experimental and theoretical basis of a recently proposed reassignment of the bands in the PE. spectra of pyridine, pyridazine, pyrimidine and pyrazine is discussed in detail. A characteristic feature of the derived orbital sequence is that it takes the ‘through‐space’ and ‘through‐bond’ interaction between the ‘lone pair’ basis orbitals explicitly into account. A simple parametrization of the orbital energies, based on HMO‐type models for the π‐orbitals and for the ‘lone pair’ linear combinations, yields excellent agreement with the observed band positions in the PE. spectra of s‐triazine and s‐tetrazine. Our new assignment is compared to those proposed previously.
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