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Experimental and theoretical investigation of conformational states and noncovalent interactions in crystalline sulfonamides with a methoxyphenyl moiety
Abstrakt
Four sulfonamide derivatives with a methoxyphenyl moiety, namely N-{4-[(2-methoxyphenyl)sulfamoyl] phenyl}acetamide (1a), N-{4-[(3-methoxyphenyl)sulfamoyl]phenyl}acetamide (1b), 4-amino-N-(2- methoxyphenyl)benzenesulfonamide (2a) and 4-amino-N-(3-methoxyphenyl)benzenesulfonamide (2b), have been synthesized and characterized physiochemically by CHNS, MS, FT-IR, 1H NMR, 13C NMR, PXRD and TG methods. Crystal structures were determined by SC-XRD and their conformational and noncovalent interaction properties were examined by both experimental and theoretical (HS, MEPS, NBO, dimerization energy, QTAIM) methods. The conformational flexibility of the bridge connecting two phenyl rings was studied and minimum-energy conformations were theoretically found. The packing architecture and hydrogen bond networks were described by graph set notation. Hirshfeld surface analysis revealed regions of stronger contacts and allowed us to indicate the relative contributions of different noncovalent contacts in the crystal packing. MEPS calculations helped to distinguish the electron rich and electron poor regions and to find the best H-bond donors and acceptors. The use of the QTAIM method enabled us to explain the influence of functional groups and molecular arrangement on the strength of noncovalent interactions in the crystals and overall packing efficiency
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Autorzy (5)
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Mateusz Kowalik
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Jakub Brzeski
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Małgorzata Gawrońska
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Mariusz Makowski
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Informacje szczegółowe
- Kategoria:
- Publikacja w czasopiśmie
- Typ:
- artykuły w czasopismach
- Opublikowano w:
-
CRYSTENGCOMM
nr 23,
strony 6137 - 6162,
ISSN: 1466-8033 - Język:
- angielski
- Rok wydania:
- 2021
- Opis bibliograficzny:
- Kowalik M., Brzeski J., Gawrońska M., Kazimierczuk K., Makowski M.: Experimental and theoretical investigation of conformational states and noncovalent interactions in crystalline sulfonamides with a methoxyphenyl moiety// CRYSTENGCOMM -Vol. 23,iss. 35 (2021), s.6137-6162
- DOI:
- Cyfrowy identyfikator dokumentu elektronicznego (otwiera się w nowej karcie) 10.1039/d1ce00869b
- Weryfikacja:
- Politechnika Gdańska
wyświetlono 92 razy
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