Crystal structure and Hirshfeld surface analysis of ( <i>E</i> )-1-{2,2-dibromo-1-[4-( <i>tert</i> -butyl)phenyl]ethenyl}-2-(3,4-dimethylphenyl)diazene

The title azo compound, C<sub>20</sub>H<sub>22</sub>Br<sub>2</sub>N<sub>2</sub>, crystallizes in the triclinic space group <i>P</i>1 (No. 2) with two independent mol-ecules in the asymmetric unit. The mol-ecular structure was analyzed using spectroscopic and crystallographic techniques, confirming the expected configuration and electronic environment. Hirshfeld surface analysis revealed key non-covalent inter-actions such as C-H⋯π, C-H⋯Br, π-π stacking, and halogen bonding, which consolidate the crystal structure. The study provides valuable insights into the structural features and inter-molecular inter-actions of this brominated azo compound, which may have potential applications in optoelectronic materials, dyes, and mol-ecular switches.

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Publication Details

Journal
Acta Crystallographica Section E Crystallographic Communications
Published
2025-07-01
DOI
https://doi.org/10.1107/s2056989025005390
Primary Topic
Chemical Reactions and Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Crystal structure and Hirshfeld surface analysis of ( E )-1-{2,2-dibromo-1-[4-( tert -butyl)phenyl]ethenyl}-2-(3,4-dimethylphenyl)diazene

Namiq Q. Shikhaliyev, Ali N. Khalilov, Victor N. Khrustalev, A.A. Niyazova et al.
Acta Crystallographica Section E Crystallographic Communications
Chemical Reactions and Mechanisms
article

Crystal structure and Hirshfeld surface analysis of ( E )-1-{2,2-dibromo-1-[4-( tert -butyl)phenyl]ethenyl}-2-(3,4-dimethylphenyl)diazene

Namiq Q. Shikhaliyev, Ali N. Khalilov, Victor N. Khrustalev, A.A. Niyazova, Jonathan Cisterna, Alebel N. Belay, Abel M. Maharramov, Ayten M. Gajar
article en

Abstract

The title azo compound, C<sub>20</sub>H<sub>22</sub>Br<sub>2</sub>N<sub>2</sub>, crystallizes in the triclinic space group <i>P</i>1 (No. 2) with two independent mol-ecules in the asymmetric unit. The mol-ecular structure was analyzed using spectroscopic and crystallographic techniques, confirming the expected configuration and electronic environment. Hirshfeld surface analysis revealed key non-covalent inter-actions such as C-H⋯π, C-H⋯Br, π-π stacking, and halogen bonding, which consolidate the crystal structure. The study provides valuable insights into the structural features and inter-molecular inter-actions of this brominated azo compound, which may have potential applications in optoelectronic materials, dyes, and mol-ecular switches.

Acta Crystallographica Section E Crystallographic CommunicationsVol. 81(8)
Peoples' Friendship University of Russia (RU), Baku State University (AZ), Universidad Católica del Norte (CL), Azerbaijan State University of Economics (AZ), N.D. Zelinsky Institute of Organic Chemistry (RU), Baku Engineering University (AZ), Bahir Dar University (ET)
Baki Dövlət Universiteti
Openalex Percentile: Top 85%
Chemical Reactions and Mechanisms
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