Raman and surface-enhanced Raman studies of α-aminophosphinic inhibitors of metalloenzymes

Here, we report the nature of new di‐α‐amino (L1–L3) and α‐amino‐α‐hydroxyphosphinic (L4–L6) acids, which are considered potential inhibitors of the aminopeptidase N, adsorbed on a colloidal silver surface by means of surface‐enhanced Raman scattering (SERS) spectroscopy. In order to reveal the adsorption mechanism of these species from their SERS spectra, Fourier‐transform Raman (FT‐RS) spectra of these nonadsorbed molecules were measured. By examining the enhancement, shift in wavenumbers, and changes in breadth of the SERS bands due to the adsorption process, we revealed that the tilted compounds interact with the colloidal silver substrate mainly through the benzene ring, amino group, and phosphinic moiety in the following way. The benzene ring of L2 and L3 is ‘standing up’ on the colloidal silver surface, and the CN bond is almost vertical to it, while the tilt angle between the OPO bond and this surface is greater than 45°. On the other hand, for L1, L4, and L5, the aromatic ring and CN bond are arranged more or less tilted, and the tilt angle between the OPO bond and the silver substrate is smaller than 45°. The elongation of the bond to the benzene ring, the L6 case, produces an almost horizontal orientation of the benzene ring and the OPO bond on the silver nanoparticles. For these ligands, the complement inhibition IC50 tested in vitro using porcine kidney leucine aminopeptidase was correlated mainly with the behavior of the OPO and CCHN fragments on the silver surface. Copyright © 2009 John Wiley & Sons, Ltd. Here we report the nature of new di‐α‐amino (L1–L3) and α‐amino‐α‐hydroxyphosphinic (L4–L6) acids non‐adsorbed and adsorbed on a colloidal silver surface by means of FT‐RS and SERS, respectively. Examining the enhancement, shift in wavenumbers, and changes in breadth of the bands due to the adsorption process, we show that the tilted compounds interact with the colloidal silver substrate mainly through the benzene ring, amino group, and phosphinic moiety.