Resonance Assisted Chalcogen Bonding as a New Synthon in the Design of Dyes
Atash V. Gurbanov, Maxim L. Kuznetsov, Kamran T. Mahmudov⧫, Armando J. L. Pombeiro, Giuseppe Resnati
Abstract
Intramolecular chalcogen bonding in arylhydrazones of sulfamethizole is strengthened by conjugation in the π-system of a noncovalent five-membered ring. The S⋅⋅⋅O distance in the sulfamethizole moiety of these compounds ranges from 2.698(3) to 2.806(15) Å, which indicates its strong dependence on the attached arylhydrazone fragments. Information on the nature of the intramolecular chalcogen bond was afforded by DFT calculations.
Topics & Concepts
ChalcogenIntramolecular forceSynthonMoietyRing (chemistry)ChemistryNon-covalent interactionsCrystallographyStereochemistryMoleculeOrganic chemistryHydrogen bondStructural and Chemical Analysis of Organic and Inorganic CompoundsCrystallography and molecular interactionsSynthesis and Characterization of Heterocyclic Compounds