"Lp⋯synthon" interaction as a reason for the strong amplification of synthon-forming hydrogen bonds. Issue 9 (12th February 2019)

• Record Type: Journal Article
• Authors: Lodochnikova, Olga A.; Latypova, Liliya Z.; Madzhidov, Timur I.; Chmutova, Galina A.; Voronina, Julia K.; Gubaidullin, Aidar T.; Kurbangalieva, Almira R.
• Is Part Of: CrystEngComm. Volume 21:Issue 9(2019)
• Page Start: 1499
• Page End: 1511
• Publication Date: 2019-02-12
• Subjects: Crystals -- Periodicals; Crystal growth -- Periodicals; Crystallography -- Periodicals; Cristaux -- Périodiques; Cristaux -- Croissance -- Périodiques; Cristallographie -- Périodiques; 548
• DOI: 10.1039/c8ce01982g
• Languages: English
• ISSNs: 1466-8033

Abstract

Abstract : A new type of interaction is presented. Abstract : An original supramolecular motif has been found in one of two polymorphic modifications of (3, 4-dichloro-2-oxo-2, 5-dihydrofuran-5-ylsulfonyl)ethanoic acid: above and below the center of the classical carboxyl H-bonded dimer, the sulfonyl groups of two other molecules of the same compound are located. The interaction of the oxygen atoms of these sulfonyl groups with the carboxyl dimer synthon can be named the "lp(lone pair)⋯synthon"-type interaction. A strong amplification of the synthon-forming H-bonds is directly linked to the occurrence of such an interaction. The nature of the interactions is characterized by quantum-chemistry models using R. Bader's theory (QTAIM), the values of electrostatic potentials (MESP), and Pendás's approach based on interacting quantum fragments (IQFs).