Academic Journal

3,3′-(Phenylmethylene)bis(1-ethyl-3,4-dihydro-1H-2,1-benzothiazine-2,2,4-trione): single-crystal X-ray diffraction study, quantum-chemical calculations and Hirshfeld surface analysis

التفاصيل البيبلوغرافية
العنوان: 3,3′-(Phenylmethylene)bis(1-ethyl-3,4-dihydro-1H-2,1-benzothiazine-2,2,4-trione): single-crystal X-ray diffraction study, quantum-chemical calculations and Hirshfeld surface analysis
المؤلفون: Mariia O. Shyshkina, Dmitry A. Lega, Liudmyla M. Shemchuk, Irina L. Starchikova, Leonid A. Shemchuk
المصدر: Acta Crystallographica Section E: Crystallographic Communications, Vol 79, Iss 4, Pp 349-355 (2023)
بيانات النشر: International Union of Crystallography, 2023.
سنة النشر: 2023
المجموعة: LCC:Crystallography
مصطلحات موضوعية: 2,1-benzothiazine 2,2-dioxide, keto-enol tautomerism, molecular structure, crystal structure, hirshfeld surface analysis, quantum-chemical calculations, Crystallography, QD901-999
الوصف: The title compound, C27H26N2O6S2, possesses potential antimicrobial, analgesic, and anti-inflammatory activity. This compound has three tautomeric forms, which relative energies were estimated with quantum-chemical calculations. All these tautomers (dienol form 7A, keto–enol form 7B, and diketo form 7C) were optimized by the M06–2X/cc-pVTZ method in a vacuum, using the PCM model with chloroform and DMSO as solvent. The diketo form of the title compound proved to be the most energetically favourable as compared to the keto–enol or dienol forms. The diketo form can exist as three possible stereoisomers with the same configuration of one stereogenic center and different configurations of the stereogenic centers at two other atoms: (R, R, R), (S, R, S) and (R, R, S). The (R, R, S) stereoisomer was found in the crystal phase. It was revealed that the thiazine rings of equivalent benzothiazine fragments have different conformations, (a sofa or a half-chair). The two bicyclic fragments connected through the phenylmethylene group are oriented almost orthogonal to each other, subtending a dihedral angle of 82.16(7)°.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2056-9890
20569890
Relation: http://scripts.iucr.org/cgi-bin/paper?S2056989023002505; https://doaj.org/toc/2056-9890
DOI: 10.1107/S2056989023002505
URL الوصول: https://doaj.org/article/de6e55d4db494fbe819a26e2d95d750d
رقم الانضمام: edsdoj.6e55d4db494fbe819a26e2d95d750d
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20569890
DOI:10.1107/S2056989023002505