Crystal structure and Hirshfeld surface analysis of N-[2-(5-methylfuran-2-yl)phenyl]-3-nitroN-[(3-nitrophenyl)sulfonyl]benzenesulfonamide

In the title compound, C23H17N3O9S2, C-H...O hydrogen bonds link adjacent molecules in a three-dimensional network, while π-π stacking interactions, with centroid-centroid distances of 3.8745 (9) Å, between the furan and an arene ring of one of the two (3-nitrophenyl)sulfonyl groups, result in chains parallel to the a axis. The Hirshfeld surface analysis indicates that O...H/H...O (40.1%), H...H (27.5%) and C...H/H...C (12.4%) interactions are the most significant contributors to the crystal packing. © 2023 International Union of Crystallography. All rights reserved.

Авторы
Mammadova G.Z. , Annadurdyyeva S. , Burkin G.M. , Khrustalev V.N. , Akkurt M. , Yıldırım S.Ö. , Bhattarai A.
Журнал
Acta Crystallographica Section E: Crystallographic Communications
Издательство
International Union of Crystallography
Номер выпуска
Pt 5
Язык
Английский
Страницы
499-503
Статус
Опубликовано
Ссылка
Внешняя ссылка
DOI
10.1107/S2056989023003523
Том
79
Год
2023
Организации
  • 1 Excellence Center, Baku State University, Z. Xalilov Str. 23, Baku, Az 1148, Azerbaijan
  • 2 Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St., Moscow, 117198, Russian Federation
  • 3 Zelinsky Institute of Organic Chemistry of RAS, 4, 7 Leninsky Prospect, Moscow, 119991, Russian Federation
  • 4 Department of Physics, Faculty of Sciences, Erciyes University, Kayseri, 38039, Turkey
  • 5 Department of Physics, Faculty of Science, Eskisehir Technical University, Yunus Emre Campus, Eskisehir, 26470, Turkey
  • 6 Department of Chemistry, M.M.A.M.C. (Tribhuvan University), Biratnagar, Nepal
Ключевые слова
crystal structure; Hirshfeld surface analysis; hydrogen bonds; sulfonamides; π-π stacking interactions
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