Issue 6, 1990
From the journal:

Journal of the Chemical Society, Perkin Transactions 2

The tautomeric equilibria of thio analogues of nucleic acid bases. Part 3. Ultraviolet photoelectron spectra of 2-thiouracil and its methyl derivatives

Alan R. Katritzky,   Miroslaw Szafran  and  Geneviève Pfister-Guillouzo  

Abstract

The photoelectron spectra of 2-thiouracil and four monoalkyl and four dimethyl derivatives were recorded using He(I) and He(II) excitations. The assignments of the photoelectron bands were based on relative band intensity variations, on the results of AM1 calculations, and by comparisons with uracil and its methyl derivatives. The photoelectron spectrum of 2-methyl-2-thiouracil gave evidence of two forms in tautomeric equilibrium in the gas phase.

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Article information

DOI
https://doi.org/10.1039/P29900000871
Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1990, 871-876

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The tautomeric equilibria of thio analogues of nucleic acid bases. Part 3. Ultraviolet photoelectron spectra of 2-thiouracil and its methyl derivatives

A. R. Katritzky, M. Szafran and G. Pfister-Guillouzo, J. Chem. Soc., Perkin Trans. 2, 1990, 871 DOI: 10.1039/P29900000871

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