Near-Field Scanning Optical Microscopy of Single Fluorescent Dendritic Molecules

Individual dendritic molecules adsorbed on glass containing a single fluorescent rhodamine B core have been observed with near-field scanning optical microscopy (NSOM); height and fluorescence images were obtained simultaneously. The dendritic assemblies can be discriminated from free fluorescent co...

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Veröffentlicht in:The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 1999-12, Vol.103 (51), p.11264-11270
Hauptverfasser: Veerman, Joost A, Levi, Stefano A, van Veggel, Frank C. J. M, Reinhoudt, David N, van Hulst, Niek F
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container_issue 51
container_start_page 11264
container_title The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory
container_volume 103
creator Veerman, Joost A
Levi, Stefano A
van Veggel, Frank C. J. M
Reinhoudt, David N
van Hulst, Niek F
description Individual dendritic molecules adsorbed on glass containing a single fluorescent rhodamine B core have been observed with near-field scanning optical microscopy (NSOM); height and fluorescence images were obtained simultaneously. The dendritic assemblies can be discriminated from free fluorescent cores on the basis of accurate simultaneous localization of both the fluorescent core and the surrounding dendritic shell. There are no significant differences between the photophysical properties of the free and dendritic fluorophores. The full three-dimensional orientation of each individual fluorescent core can be resolved and millisecond time resolution accuracy has been achieved. Most dendritic structures exhibited rotational motion of the fluorescent core on a millisecond−second time scale, revealing intramolecular conformational dynamics.
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