J
José Elguero
Researcher at Spanish National Research Council
Publications - 1374
Citations - 31355
José Elguero is an academic researcher from Spanish National Research Council. The author has contributed to research in topics: Hydrogen bond & Tautomer. The author has an hindex of 69, co-authored 1346 publications receiving 29017 citations. Previous affiliations of José Elguero include Université Paul Cézanne Aix-Marseille III & Complutense University of Madrid.
Papers
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Journal ArticleDOI
N‐polyazolylmethanes. 1. Synthesis and nmr study of N,N′‐diazolylmethanes
Sebastian Juliá,Pilar Sala,José Del Mazo,Manuel Sancho,Carmen Ochoa,José Elguero,Jean-Pierre Fayet,M. C. Vertut +7 more
TL;DR: In this paper, the relative amounts of isomeric mixtures obtained with asymmetric azoles or with equimolar mixtures of azoles are compared with literature results on monoalkylation of azole.
Journal ArticleDOI
Charge-Transfer Complexes between Dihalogen Compounds and Electron Donors
TL;DR: In this article, a theoretical study of charge transfer complexes formed by dihalogen compounds (F2, Cl2, Br2, FBr, FCl, and ClBr) and electron donors (FH, OH2, NH3, CO, NCH, and C2H2) has been carried out.
Journal ArticleDOI
Molecular Complexes between Silicon Derivatives and Electron-Rich Groups
TL;DR: In this paper, theoretical calculations on a series of SiXY3-ZW complexes, where X and Y are H, F, and Cl, and Z corresponds to an electron donor atom (ZW ) NH3, NCH, CNH, OH2, FH), were performed.
Book ChapterDOI
Basicity and Acidity of Azoles
Javier Catalán,José Elguero +1 more
TL;DR: In this paper, a large collection of solution data and a thoroughly updated discussion of thermodynamic, kinetic, and structural results of aromatic azoles is provided. But the main focus of this paper is on the parent structure on theoretical grounds.
Journal ArticleDOI
Carbon-13 Magnetic Resonance Studies of Azoles. Tautomerism, Shift Reagent Effects, and Solvent Effects
TL;DR: The effects of substitution, lanthanide-shift reagents, solvent changes, and tautomerism were investigated in this article, where it was concluded that chemical shifts are of limited value to ascertain the positions of tautomers.