Crystal structure, spectroscopic investigations. and quantum chemical calculational studies of N-diphenylphosphino-4-methylpiperidine sulfide

Saraçoğlu H., Sarioz O., Oznergiz S.

JOURNAL OF MOLECULAR STRUCTURE, vol.1063, pp.170-177, 2014 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 1063
  • Publication Date: 2014
  • Doi Number: 10.1016/j.molstruc.2013.12.087
  • Journal Name: JOURNAL OF MOLECULAR STRUCTURE
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.170-177
  • Keywords: Aminophosphines, Chalcogenides, Computational chemistry, Non-linear optics, NMR spectroscopy, NONLINEAR-OPTICAL PROPERTIES, MOLECULAR-STRUCTURE, MONOOXIDIZED BIS(PHOSPHINO)AMINES, EQUILIBRIUM GEOMETRIES, COORDINATION CHEMISTRY, PLATINUM(II) COMPLEXES, HARTREE-FOCK, LIGANDS, AMINOPHOSPHINES, DERIVATIVES
  • Ondokuz Mayıs University Affiliated: Yes

Abstract

The title molecule, N-diphenylphosphino-4-methylpiperidine sulfide (I), has been synthesized and characterized by elemental analysis, H-1 NMR, P-31 NMR, IR and X-ray single-crystal determination. The molecular geometry from X-ray determination, vibrational frequencies and gauge, including atomic orbital (GIAO) H-1 NMR and P-31 NMR chemical shift values of the title compound (I) in the ground state have been calculated using the density functional theory with the 6-31G(d), 6-31G(d,p) and 6-311G(d,p) basis sets. The calculated results show that the optimized geometry can well reproduce the crystal structure, and theoretical vibrational frequencies and chemical shift values show good agreement with experimental values. The predicted nonlinear optical properties of the title compound are greater than those of urea. In addition, DFT calculations of the molecular electrostatic potentials, frontier molecular orbitals of the title compound were carried out at the B3LYP/6-31G(d) level of theory. (C) 2014 Elsevier B.V. All rights reserved.