首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Influence of aliphatic spacer group on adsorption mechanisms of phosphonate derivatives of l-phenylalanine: Surface-enhanced Raman, Raman, and infrared studies
Authors:E Podstawka  A Kudelski  LM Proniewicz
Institution:a Laser Raman Laboratory, Regional Laboratory of Physicochemical Analysis and Structural Research, Jagiellonian University, ul. Ingardena 3, 30-060 Krakow, Poland
b Faculty of Chemistry, University of Warsaw, ul. L. Pasteura 1, 02-093 Warsaw, Poland
c Institute of Organic Chemistry, Biochemistry and Biotechnology, Wroclaw Technical University, ul. Wybrze?e Wyspiańskiego 27, 50-370 Wroclaw, Poland
d Chemical Physics Division, Faculty of Chemistry, Jagiellonian University, ul. Ingardena 3, 30-060 Krakow, Poland
Abstract:The nature of phosphonopeptides containing N-terminal l-phenylalanine (l-Phe), namely l-Phe-dl-NH-CH(CH(CH3)2)-PO3H2 (A), l-Phe-l-NH-CH(CH3)-PO3H2 (B), and l-Phe-dl-NH-CH(CH2CH2COOH)-PO3H2 (C) (Fig. 1 presents molecular structure of these molecules), adsorbed on electrochemically roughened and colloidal silver surfaces has been explored by surface-enhanced Raman spectroscopy (SERS). To reveal adsorption mechanism of these species on the basis of their SERS spectra at first Fourier-transform Raman (FT-RS) and absorption infrared (FT-IR) spectra of non-adsorbed molecules were measured. Examination of enhancement, frequency shifts, and changes in relative intensities of SERS bands due to adsorption and surface roughens variation reveals that the tilted compounds adsorb on the electrochemically roughened silver substrate in similar way, while they behave differently on the colloidal silver surface. A stronger enhancement of in-plane ring vibrations of the l-Phe ring, i.e., ν3 and ν18b (B2), over these of the A2 symmetry in all SERS spectra on the electrochemically roughened silver substrate suggests that the ring interacts with this surface adopting slightly deflect orientation from the perpendicular one. Also, enhancement of Pdouble bond; length as m-dashO and -CH2-/-CH3 fragments vibrations points out that they are involved in adsorption process on this substrate. This conclusion was drawn on the basis of the enhancement of 1274-1279 and 1138-1152 (ν(Pdouble bond; length as m-dashO)), 1393-1400 (δ(CH) + ρb(CNH2) + ν(C-Cdouble bond; length as m-dashO) + δ(CH3)), ∼1455 (δ(CCH3/CCH2) + ρb(CH3/CH2), and 1505-1512 cm−1 (δ(CH2) + Phe(ν19a)) bands. Although a relative intensity ratio of these bands in the presented SERS spectra is different. On the other hand, on the colloidal silver nanoparticles, the aromatic ring of all molecules is lying flat or takes almost parallel orientation to this surface. Besides, A interacts also via P-terminal group (568, 765, 827, 1040, and 1150 cm−1), whereas B mainly through NH2-C-(Cdouble bond; length as m-dashO)-CNH-(712 and 1255 cm−1). In the case of C, it adsorbs on the silver colloidal surface mainly through the aromatic ring of l-Phe, while other fragments of the molecule are in close proximity to this surface as comes off the weak enhancement of bands due to the aliphatic vibrations.
Keywords:Surface enhanced Raman scattering  SERS  Fourier-transform Raman scattering  FT-RS  Fourier-transform infrared spectroscopy  FT-IR  Silver colloid  Electrochemically roughened silver substrate  l-Phenylalanine phosphonate derivatives" target="_blank">l-Phenylalanine phosphonate derivatives
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号