Aryl-substituents moderate the nature of hydrogen bonds, N–H⋯N versus N–H⋯O, leading to supramolecular chains in the crystal structures of N-arylamino 1,2,3-triazole esters-Reference-Cited by-同舟云学术

Aryl-substituents moderate the nature of hydrogen bonds, N–H⋯N versus N–H⋯O, leading to supramolecular chains in the crystal structures of N-arylamino 1,2,3-triazole esters

Published:2013 Issue:24 Volume:15 Page:4917
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Cunha Anna C.,Ferreira Vitor F.,Jordão Alessandro K.,de Souza Maria C. B. V.,Wardell Solange M. S. V.,Wardell James L.,Tan Peiyu Amelia,Bettens Ryan P. A.,Seth Saikat Kumar,Tiekink Edward R. T.

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2013/CE/C3CE40102B

Reference62 articles.

1. Crystal Engineering: A Holistic View

2. Stereoelectronic Effects of Substituent Groups in the Solid State. Crystal Chemistry of Some Cubanecarboxylic and Phenylpropiolic Acids

3. Substituent effects on aromatic interactions in the solid state

4. Solid State Conformational Preferences of a Flexible Molecular Backbone Derived from Acetone: Dependence on Electron Donating/Withdrawing Ability of Substitutions

5. Competitive Interactions in the Crystal Structures of Benzils Effected by Different Halogen Substitution

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