n → π* and chalcogen bonds in azole-substituted isoindole derivatives: a combined crystallographic and computational study

Azole-substituted epoxyisoindole derivatives exhibit diverse noncovalent interactions, including n → π*, hydrogen, and chalcogen bonds, which govern their crystal packing and conformational preferences.

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Publication Details

Journal
CrystEngComm
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ce00673b
Citations
1
Primary Topic
Crystallography and molecular interactions
Type
article
Field-Weighted Citation Impact
1.75

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article

n → π* and chalcogen bonds in azole-substituted isoindole derivatives: a combined crystallographic and computational study

Rosa M. Gomila, Федор И. Зубков, И. А. Колесник, В. И. Поткин et al.
1 citations
CrystEngComm
Crystallography and molecular interactions
1.75
article

n → π* and chalcogen bonds in azole-substituted isoindole derivatives: a combined crystallographic and computational study

Rosa M. Gomila, Федор И. Зубков, И. А. Колесник, В. И. Поткин, Vladimir P. Zaytsev, Antonio Frontera, Eugeniya V. Nikitina, Mikhail S. Grigoriev
article en
1 citations

Abstract

Azole-substituted epoxyisoindole derivatives exhibit diverse noncovalent interactions, including n → π*, hydrogen, and chalcogen bonds, which govern their crystal packing and conformational preferences.

CrystEngCommVol. 27(37)
Peoples' Friendship University of Russia (RU), Demos (US), National Academy of Sciences of Belarus (BY), Frumkin Institute of Physical Chemistry and Electrochemistry Russian Academy of Sciences (RU), Universitat de les Illes Balears (ES)
Belarusian Republican Foundation for Fundamental Research, Ministerio de Ciencia y Tecnología, Russian Science Foundation, Agencia Estatal de Investigación
Openalex Percentile: Top 14%
Crystallography and molecular interactions
1.75
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n → π* and chalcogen bonds in azole-substituted isoindole derivatives: a combined crystallographic and computational study — Rosa M. Gomila, Федор И. Зубков, et al. · CrystEngComm (2025) | TGRS Research Map | TGRS