Competing Intramolecular N?H???O=C and Extended Intermolecular Network in 1-(4-chlorobenzoyl)-3-(2-methyl-4-oxopentan-2-yl) Thiourea Analyzed by Experimental and Theoretical Methods

SAEED, AAMER; KHURSHID, A.; JASINSKI, J. P.; POZZI, C. GUSTAVO; FANTONI, ADOLFO; ERBEN, MAURICIO FEDERICO

CHEMICAL PHYSICS

ELSEVIER SCIENCE BV

Lugar: Amsterdam; Año: 2014 vol. 431 p. 39 - 46

0301-0104

The synthesis of a novel 1-acyl-thiourea species (C14H17N2O2SCl), has been tailored in such a way that two distinct N-H···O=C intramolecular competing hydrogen bonds are feasible. The X-ray structure analysis as well as the vibrational (FT-IR and FT-Raman) data reveal that the S conformation is preferred, with the C=O and C=S bonds of the acyl-thiourea group pointing in opposite directions. The preference for the intramolecular N-H···O=C hydrogen bond within the -C(O)NHC(S)NH- core is confirmed. The Natural Bond Orbital and the Atom in Molecule approaches demonstrate that a strong hyperconjugative lpO---> <sigma>*(N-H) remote interaction between the acyl and the thioamide NAH groups is responsible for the stabilization of the S conformation. Intermolecular interactions have been characterized in the periodic system electron density and the topological analysis reveals the presence of an extended intermolecular network in the crystal, including a Cl···N interaction playing a relevant role in crystal packing.