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Laser-induced- and dispersed-fluorescence studies of rhodamine 590 and 640 ions formed by electrospray ionization: observation of fluorescence from highly-excited vibrational levels of S states
The gas-phase fluorescence excitation and emission properties of rhodamine 590 (R590) and rhodamine 640 (R640) cations were studied using a novel instrument that allows extension of optical excitation to the UV region. Ions were generated by an electrospray ion source, and desolvated ions were accum...
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Published in: | Physical chemistry chemical physics : PCCP 2018-10, Vol.2 (42), p.26859-26869 |
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Main Author: | |
Format: | Article |
Language: | |
Online Access: | Get full text |
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Summary: | The gas-phase fluorescence excitation and emission properties of rhodamine 590 (R590) and rhodamine 640 (R640) cations were studied using a novel instrument that allows extension of optical excitation to the UV region. Ions were generated by an electrospray ion source, and desolvated ions were accumulated in a room-temperature quadrupole ion-trap. In addition to the well-known S
1
-S
0
transition observed for both dyes, two ultraviolet (UV) bands (that have not been reported previously) were observed for R590. When compared with transitions observed for the dyes in methanol solutions, the S
1
-S
0
transitions in the gas phase are shifted to significantly higher energies. These shifts suggest that the S
1
states for both dyes are more stabilized by favorable solvent interactions than the S
0
states. The UV bands observed for R590 were assigned to the transitions involving the higher-energy S
3
and S
n
states. The DF spectra obtained upon UV excitation are similar to those recorded for S
1
excitation; however, the emission after UV excitation is shifted slightly to the red region. These observations are consistent with the emission from high-vibrational levels of the S
1
state formed upon fast internal conversion from S
3
or S
n
.
In vacuo
, the absence of collisions extends the lifetimes of vibrationally-excited S
1
states, allowing fluorescence from these states to be observed. A similar DF spectrum was also observed for the UV excitation of R640, suggesting that fluorescence from vibrationally hot S
1
states is a general phenomenon for ions in the gas phase.
Fluorescence spectra of vibrationally very "hot" S
1
states were observed for the first time under gas phase conditions. |
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ISSN: | 1463-9076 1463-9084 |
DOI: | 10.1039/c8cp04067b |