Influence of methoxy- and nitro-substitutions in the aromatic ring on proton donation ability in hydrogen bond and on the amino group parameters of free and H-bonded molecules of 2-aminopyrimidine-Reference-Cited by-同舟云学术

Influence of methoxy- and nitro-substitutions in the aromatic ring on proton donation ability in hydrogen bond and on the amino group parameters of free and H-bonded molecules of 2-aminopyrimidine

Published:2008-06 Issue:1-3 Volume:882 Page:9-23
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Borisenko V.E.,Krekov S.A.,Fomenko M.Yu.,Koll A.,Lipkovski P.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference22 articles.

1. Chemistry of Hetero Cyclic Compounds;Ivanskiy,1978

2. Dynamic, electrooptical and energetic nonequivalency of NH bonds in 1:1 and 1:2 complexes of aminopyridines with proton acceptors

3. The influence of hetero-substitution in the aromatic ring of amino pyrimidine on amino group characteristics in free and H-bonded molecules

4. Dynamic and electrooptical non-equivalency of amino group NH bonds of anisidines in H-bonded 1:1 and 1:2 complexes with proton acceptors

5. The Chemist’s Companion. A Handbook of Practical Date Techniques and Referents. A Wiley – Interscience publication;Gordon,1972

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