Spectroscopic and theoretical studies of some p-substituted α-methylthio-α-diethoxyphosphorylacetophenones

The analysis of the IR carbonyl band of the α-methylthio-α-diethoxyphosphoryl p-substituted acetophenones p-Y-Ph-C(O)CH[SMe][P(O)(OEt)2] (Y = OMe 1, H 2, F 3, Cl 4, Br 5 and NO26), supported by HF/6-31G** ab initio calculations of the α-methylthio-α-diethoxyphosphoryl acetophenone 2, indicated the existence of a single stable c1 conformer in gas phase and in solvents of increasing polarity, along with the presence of a second high energy conformation in gas phase. The c1 conformer presents the (SMe) group in a syn-clinal (gauche) geometry and the [P(O)(OEt2)] group in a quasi-periplanar (quasi-cis) geometry with respect to the carbonyl group, which is stabilized by the synergism of the nS/π*CO and σC-S/π*CO orbital interactions and Oδ−(PO)⋯Cδ+(CO) orbital and Coulombic interactions, acting to increase the carbonyl oxygen negative charge, and in turn facilitates the Oδ−(CO)⋯Pδ+(PO) electrostatic interaction. The negative and almost constant carbonyl frequency shifts (Δν) of ca. −11 cm−1 for compounds 1-6 relative to the parent acetophenones 7-12, in CCl4, corroborate the prevalence of the electronic interactions over the (−Iσ) inductive effect of the α-substituents for the title compounds. The X-ray diffraction analysis for 3 indicates that it exists in the solid state in the c1′ conformation, which is stabilized by the intramolecular Oδ−(1)[CO}⋯ Pδ+(5)[PO] and Hδ+(10)[SMe]⋯Oδ−(6)[PO] orbital and electrostatic (hydrogen bond) interactions. Moreover, these molecules form dimers which are stabilized through intermolecular hydrogen bonds Hδ+(4)[CH]⋯Oδ−(1)[CO], Hδ+(5′)[Ph]⋯ Oδ−(6)[PO] and Hδ+(6′)[Ph]⋯ Oδ−(6)[PO].