Bi-analyte SERS with isotopically edited dyes

Isotopically substituted rhodamine dyes provide ideal probes for the study of single-molecule surface enhanced Raman scattering (SM-SERS) events through multiple-analyte techniques. Isotopic editing should, in principle, provide probes that have identical chemical properties (and surface chemistries...

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Veröffentlicht in:Physical chemistry chemical physics : PCCP 2008-01, Vol.10 (28), p.4147-4153
Hauptverfasser: BLACKIE, E, LE RU, E. C, MEYER, M, TIMMER, M, BURKETT, B, NORTHCOTE, P, ETCHEGOIN, P. G
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Sprache:eng
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Zusammenfassung:Isotopically substituted rhodamine dyes provide ideal probes for the study of single-molecule surface enhanced Raman scattering (SM-SERS) events through multiple-analyte techniques. Isotopic editing should, in principle, provide probes that have identical chemical properties (and surface chemistries); while exhibiting at the same time distinct Raman features which enable us to identify single-molecule SERS events. We present here a specific example of two-analyte SM-SERS based on the isotopic substitution of a methyl ester rhodamine dye. The dyes are carefully characterized (in both standard and SERS conditions) to confirm experimentally their similar chemical properties. We then demonstrate their utility for bi-analyte SERS (BiASERS) experiments and, as an example, highlight the transition from a single, to a few, to many molecules in the statistics of SM-SERS signals.
ISSN:1463-9076
1463-9084
DOI:10.1039/b803738h