UV polymerization of self-assembled monolayers of a novel diacetylene on silver: A spectroscopic analysis by surface plasmon resonance and surface enhanced Raman scattering
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Giorgetti, E
Muniz-Miranda, M
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机构:INSTM, I-50127 Florence, Italy
Muniz-Miranda, M
Margheri, G
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机构:INSTM, I-50127 Florence, Italy
Margheri, G
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Giusti, A
Sottini, S
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机构:INSTM, I-50127 Florence, Italy
Sottini, S
Alloisio, M
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机构:INSTM, I-50127 Florence, Italy
Alloisio, M
Cuniberti, C
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机构:INSTM, I-50127 Florence, Italy
Cuniberti, C
Dellepiane, G
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机构:INSTM, I-50127 Florence, Italy
Dellepiane, G
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[1] INSTM, I-50127 Florence, Italy
[2] CNR, Ist Sistemi Complessi, I-50127 Florence, Italy
[3] Univ Florence, Dipartimento Chim, I-50019 Sesto Fiorentino, Italy
UV polymerization of self-assembled monolayers of a novel carbazolyl-diacetylene (CDS9) chemisorbed on silver films was demonstrated by surface plasmon resonance (SPR) and surface enhanced Raman scattering (SERS) experiments. SPR tests performed during UV exposure permitted one to observe the growth of the absorption coefficient, associated with the formation of the polymeric backbone. The Raman spectra of polymerized monolayers exhibited the bands associated with the C=C stretching modes of the conjugated backbone, typical of the blue and red polymeric phases usually present in polydiacetylenes, with a clear predominance of the red form. Moreover, the strong surface enhancement of the Raman band corresponding to the aromatic C=C stretching modes suggested that carbazolyl groups arrange nearly perpendicularly to the metal surface. In contrast, the absence of a SERS signal in the region of conjugated C=-C bond stretchings confirmed a polymerization scheme with conjugated triple bonds nearly parallel to the plane of the metal.