Synthesis, characterization and surface enhanced Raman spectroscopy study of a new family of different substituted cruciform molecular systems deposited on gold nanoparticles

Rodrigo Sánchez-González, Elizabeth Imbarack, Constanza Suazo, Juan Pablo Soto, PATRICIO ALEJANDRO LEYTON BONGIORNO, Santiago Sánchez-Cortés, Marcelo Campos-Vallette

Resultado de la investigación: Contribución a una revistaArtículorevisión exhaustiva

1 Cita (Scopus)

Resumen

In this work, the adsorption and orientation on gold nanoparticles (AuNps) of a new family of cruciform systems consisting of thiophene rings and imino groups were studied. The structural modification and its influence on the adsorbate-substrate interaction were evaluated by UV–Vis spectroscopy and Surface Enhanced Raman Spectroscopy (SERS). The absence of SERS spectrum for (N,N′-bis(4-(trifluoromethyl)benzylidene)-2,5-di (thiophene-2-yl)-1,4-diaminobenzene) CFF shows that the inclusion of a trifluoromethyl group (-CF3) on the benzylidene fragment limits the interaction of the CFF system with the gold substrate, in contrast, to that obtained for (N, N′-dibenzylidene-2,5-di (thiophene-2-yl) -1,4-diaminobenzene) 2-CF and (N, N′-bis (4-methoxybenzylidene) -2,5-di (thiophene-2yl) -1,4-diaminobenzene) CMF, where the adsorption took place preferentially through the thiophene rings, resulting in partial quinoidization. On the other hand, the interaction for compound (N, N′-bis (4-methylenepyridinyl) -2,5-di (thiophene-2-yl) -1,4-diaminobenzene) CPy with the surface was conducted by means of the pyridinic fragments. The systematic modification of the bifunctional cruciform systems, with groups of different nature, makes it possible to rationalize the structural aspects that directly influence the adsorbate-substrate interaction and molecular orientation on gold substrates. These structural parameters are the basis to the development of stable molecular assemblies, which can act as basic building blocks in the manufacture of molecular switches.

Idioma originalInglés
PublicaciónJournal of Raman Spectroscopy
DOI
EstadoAceptada/en prensa - 2021
Publicado de forma externa

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