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Silver nanoparticles were synthesized using solution combustion method with citric acid as fuel. The prepared silver nanoparticles exhibit fcc crystalline structure with particle size of ~50 nm. The morphology and purity of the silver nanoparticles were also studied by high-resolution transmission electron microscopy (HRTEM) and energy dispersive X-ray analysis (EDX). Surface-enhanced Raman scattering (SERS) spectra of 2,6-dicarbethoxy-3,5-bis(pyridine-3-yl)tetrahydro-1,4-thiazine-1,1-dioxide (DBTD) adsorbed on silver nanoparticles were investigated. Orientation of DBTD on silver nanoparticles has been inferred from normal Raman spectrum (nRs) and SERS spectral feature. The observed spectral feature evidenced that DBTD would adsorb on silver surface with tilted orientation through the lone pair electrons of C–N, C=O, S=O, and pyridine ring. The present investigation has been a model system to deduce the interaction of drugs with DNA.

International audienceSurface-enhanced infrared (IR) absorption spectroscopic technique has been employed to investigate the orientation of 2,3-bis(chloromethyl) anthracene-1,4,9,10-tetraone (BCMAT) on copper nanoparticles (NPs). Copper NPs have been prepared by the chemical reduction method. The observed ring stretching modes show higher downshifts, broader bandwidths, and higher enhancement. The observed features in out-of-plane and in-plane CH deformation modes indicate that the BCMAT molecules may be adsorbed in a "flat-on" orientation on the copper NPs. The observed lower enhancement factor of the in-plane C=O deformation mode and C=O stretching mode and the higher enhancement factor of out-of-plane C=O deformation mode elucidate that the BCMAT molecules are adsorbed on the copper NPs in a "flat-on" orientation. All these observations show that BCMAT is adsorbed on copper NPs through the pi-anthraquinone ring system in a "flat-on" orientation

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