LASER INDUCED FLUORESCENCE SPECTRUM OF PERYLENE IN LARGE HELIUM CLUSTERS
dc.creator | Radcliff, Matthew R. | en_US |
dc.creator | Higgins, J. | en_US |
dc.creator | Reho, J. | en_US |
dc.creator | Lehmann, K. K. | en_US |
dc.creator | Scoles, G. | en_US |
dc.date.accessioned | 2006-06-15T19:05:57Z | |
dc.date.available | 2006-06-15T19:05:57Z | |
dc.date.issued | 1998 | en_US |
dc.identifier | 1998-RJ-09 | en_US |
dc.identifier.uri | http://hdl.handle.net/1811/18985 | |
dc.description | Author Institution: Department of Chemistry, Princeton University | en_US |
dc.description.abstract | Helium Cluster Isolation Spectroscopy as a method of investigating molecular aggregates offers the advantages of extremely low temperatures (0.37 K), control of aggregation, and very weak solvent perturbation effects. Perylene, a molecule comprised of five benzene rings, is a model compound to study the effect of molecular aggregation (e.g., excitation transfer and proximity effects) in a class of molecules which have been frequently investigated in the solid state and in thin films. So far we have measured the monomer spectrum, resolving its vibronic structure up to $1500 cm^{-1}$ in the $S_{1}$ electronic state. The average shift of the bands is approximately $+47 cm^{-1}$ while their zero phonon lines vary in both width and structure, the former reaching values as low as several GHz. We are presently searching for the dimer spectrum. | en_US |
dc.format.extent | 94501 bytes | |
dc.format.mimetype | image/jpeg | |
dc.language.iso | English | en_US |
dc.publisher | Ohio State University | en_US |
dc.title | LASER INDUCED FLUORESCENCE SPECTRUM OF PERYLENE IN LARGE HELIUM CLUSTERS | en_US |
dc.type | article | en_US |
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