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Investigation of adsorption mode of a novel group of N-benzylamino(boronphenyl)methylphosphonic acids using SERS.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy (2012-12-25)
Edyta Proniewicz, Natalia Piergies, Yukihiro Ozaki, Younkyoo Kim, Leonard M Proniewicz
RESUMEN

Here, we report a systematic surface-enhanced Raman spectroscopy (SERS) study of the structures of five N-benzylamino(boronphenyl)-methylphosphonic acids: N-benzylamino-(3-boronphenyl)-S-methylphosphonic acid (m-PhS), N-benzylamino-(4-boronphenyl)-S-methylphosphonic acid (p-PhS), N-benzylamino-(2-boronphenyl)-R-methylphosphonic acid (o-PhR), N-benzylamino-(3-boronphenyl)-R-methyl-phosphonic acid (m-PhR), and N-benzylamino-(4-boronphenyl)-R-methylphosphonic acid (p-PhR) adsorbed on nanometer-sized colloidal particles (20-25 nm). For example, we showed that all of these molecules interact with the colloidal surface through a boronophenyl ring, which plane remained vertical on the surface. For p-PhS, a preferential interaction between the P=O bond and the colloidal silver surface is observed to be stronger than for the remaining compounds. The -P(OH)(2) and -B(OH)(2) fragments take part in the adsorption process. However, the B-O bond of p-PhS and p-PhR seemed to be tilted with respect to the silver surface.

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Sigma-Aldrich
Methylphosphonic acid, 98%