A vibrational study of di-i-propoxyphosphoryl benzylisothiourea

¹Centro Técnico Científico, Pontificia Universidade Católica do Rio de Janeiro-PUC-Rio, Brazil. tellez@postmaster.co.uk

Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy

|May 4, 2000

Abstract:

The Fourier transform infrared and Raman spectra of di-i-propoxyphosphoryl benzylisothiourea (DPB) (1) in the solid state and in solutions of CCl4, CHCl3, CHBr3, CH2Cl2, C2H4Cl2, C2H4Br2 and THF were studied. In the IR spectra, the effects of different concentrations were also investigated. The behavior of the nu(NH), delta(NH), delta(HNH), nu(C=N) and nu(P=O) normal modes suggests the existence of a tautomerism between the phosphorylamine (I) and N-phosphorylimine (II) structures: [structures: see text] The data show the presence of different delta(NH) and delta(HNH) bendings and nu(C=N) normal modes in the solid state as a result of inter and intramolecular hydrogen bonding. The experimental approximate frequencies assignments were done for this compound, and were confirmed by a normal coordinate analysis carried out for several fragments of phosphorylamine and N-phosphorylimine structures.

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