Electronic spectroscopy of benzo[g,h,i]perylene and coronene inside helium nanodroplets

We have recorded the electronic spectra of benzo[g,h,i]perylene and coronene and their van der Waals complexes with argon and oxygen with a helium-nanodroplet depletion spectrometer. These molecules differ by the addition of one and two fused benzene rings to perylene, which was previously studied i...

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Veröffentlicht in:Physical chemistry chemical physics : PCCP 2008-01, Vol.10 (12), p.1648-1657
Hauptverfasser: BIRER, Ozgür, MORESCHINI, Paolo, LEHMANN, Kevin K
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MORESCHINI, Paolo
LEHMANN, Kevin K
description We have recorded the electronic spectra of benzo[g,h,i]perylene and coronene and their van der Waals complexes with argon and oxygen with a helium-nanodroplet depletion spectrometer. These molecules differ by the addition of one and two fused benzene rings to perylene, which was previously studied in helium. The coronene spectrum is similar to a previously reported jet-cooled laser-induced fluorescence (LIF) spectrum. The van der Waals complexes with argon and oxygen show different complexation sites and maximum number of adsorbants. We report a vibronically resolved benzo[g,h,i]perylene S(1)
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These molecules differ by the addition of one and two fused benzene rings to perylene, which was previously studied in helium. The coronene spectrum is similar to a previously reported jet-cooled laser-induced fluorescence (LIF) spectrum. The van der Waals complexes with argon and oxygen show different complexation sites and maximum number of adsorbants. We report a vibronically resolved benzo[g,h,i]perylene S(1) &lt;-- S(0) spectrum. The spectral lines are split in a similar way to that of several molecules studied before. However, surprisingly, while the van der Waals complexes with argon are free of the splitting, the complexes with oxygen retain the splitting, with increased linewidth and splitting. We could also observe the S(2) &lt;-- S(0) origin transition of benzo[g,h,i]perylene which was previously observed by cavity ring down spectroscopy. 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These molecules differ by the addition of one and two fused benzene rings to perylene, which was previously studied in helium. The coronene spectrum is similar to a previously reported jet-cooled laser-induced fluorescence (LIF) spectrum. The van der Waals complexes with argon and oxygen show different complexation sites and maximum number of adsorbants. We report a vibronically resolved benzo[g,h,i]perylene S(1) &lt;-- S(0) spectrum. The spectral lines are split in a similar way to that of several molecules studied before. However, surprisingly, while the van der Waals complexes with argon are free of the splitting, the complexes with oxygen retain the splitting, with increased linewidth and splitting. We could also observe the S(2) &lt;-- S(0) origin transition of benzo[g,h,i]perylene which was previously observed by cavity ring down spectroscopy. While in general the two spectra are quite similar, the relative intensities and spectral shifts of several lines are different.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><pmid>18338065</pmid><doi>10.1039/b717307e</doi><tpages>10</tpages></addata></record>
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subjects Argon - chemistry
Chemistry
Exact sciences and technology
General and physical chemistry
Helium - chemistry
Lasers
Nanotechnology
Oxygen - chemistry
Perylene - analogs & derivatives
Perylene - chemistry
Polycyclic Compounds - chemistry
Spectrum Analysis - methods
Vibration
title Electronic spectroscopy of benzo[g,h,i]perylene and coronene inside helium nanodroplets
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