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

Mammadova, Gunay; Annadurdyyeva, Selbi; Burkin, Gleb; Khrustalev, Victor; AKKURT, MEHMET; YILDIRIM, SEMA; Bhattarai, Ajaya

doi:10.1107/s2056989023003523

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

Mammadova G. Z., Annadurdyyeva S., Burkin G. M., Khrustalev V. N., AKKURT M., YILDIRIM S., ...Daha Fazla

Acta Crystallographica Section E: Crystallographic Communications, cilt.79, sa.Pt 5, ss.499-503, 2023 (Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 79 Sayı: Pt 5
Basım Tarihi: 2023
Doi Numarası: 10.1107/s2056989023003523
Dergi Adı: Acta Crystallographica Section E: Crystallographic Communications
Derginin Tarandığı İndeksler: Scopus
Sayfa Sayıları: ss.499-503
Anahtar Kelimeler: crystal structure, sulfonamides, hydrogen bonds, pi-pi stacking interactions, Hirshfeld surface analysis
Erciyes Üniversitesi Adresli: Evet

Özet

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.