CH⋯S hydrogen bonds as the organising force in 2,3-thienyl- and phenyl- or 2,3-dithienyl-substituted propenoic acid aggregates studied by the combination of FT-IR spectroscopy and computations-Reference-Cited by-同舟云学术

CH⋯S hydrogen bonds as the organising force in 2,3-thienyl- and phenyl- or 2,3-dithienyl-substituted propenoic acid aggregates studied by the combination of FT-IR spectroscopy and computations

Published:2011-05 Issue:1-3 Volume:993 Page:259-263
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Csankó K.,Illés L.,Felföldi K.,Kiss J.T.,Sipos P.,Pálinkó I.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference18 articles.

1. Hydrogen bonding interactions of α-phenylcinnamic acid isomers in the liquid phase studied by IR and NMR spectroscopies and computational methods

2. Hydrogen bonded networks of methoxy-substituted α-phenylcinnamic acids studied by spectroscopic and computational methods

3. Changes in the aggregation patterns of Z-2,3-diphenylpropenoic acid and its methyl ester on substituting the olefinic hydrogen with CF3 group—an FT-IR study

4. CH…F hydrogen bonds as the organising force in F-substituted α-phenyl cinnamic acid aggregates studied by the combination of FTIR spectroscopy and computations

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