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Helium Nanodroplet Infrared Spectroscopy of the Tropyl Radical RUHR-UNIVERSITÄT BOCHUM FAKULTÄT FÜR CHEMIE UND BIOCHEMIE Lehrstuhl für Physikalische Chemie II Matin Kaufmann
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Motivation The Tropyl Radical Reaction intermediate for the formation of PAHs (polycyclic aromatic hydrocarbons) -Organic chemistry and synthesis 1 -Combustion reactions and soot formation 2 -The interstellar mid-IR spectrum suggests presence of PAHs in outer space 3 Cycloheptatrienyl (Tropyl): C 7 H 7 ∙ [1] C. Chatgilialoglu, A. Studer; John Wiley & Sons: Chichester 2012 [2] D. Trogolo et al.; J. Phys. Chem. A 2014, 118, 427 [3] L. J. Allamandola et al.; Astrophys. J., Suppl. Ser. 1989, 71, 733
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Motivation C 7 H 7 Isomers Tropyl Benzyl X (-16.8 kcal/mol) 1 [1] R. G. Satink et al.; J. Am. Chem. Soc. 2003, 125, 15714
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Previous Work Spectroscopy of Tropyl
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Previous Work Electronic State Degeneracy of Tropyl I. Sioutis et al.; J. Chem. Phys. 2008, 128, 84311
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Previous Work Experimental Data from LIF Spectroscopy
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Experimental Setup Helium Droplet Machine pick-up cells Rough Pump Gate Valve AirVacuum O-ring seal Water cooled copper electrodes Ta filament / Quartz tube Sample
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Pyrolysis of Bitropyl Mass Spectra +
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Experimental Data IR Spectrum Bitropyl IR Intensity Depletion
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Experimental Data IR Spectrum Tropyl IR Intensity Depletion 3052.93057.4
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Jahn-Teller Effect Symmetry Considerations CH stretch vibrations: IR active Electronic ground state: Vanishing Integral Rule: Vibronic coupling: Check of IR activity: → Vibronic Coupling generates a splitting into two 2-fold degenerate transitions
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Experimental Data Mass Spectra Comparison
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Experimental Data IR Spectrum Comparison Depletion
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Conclusion T. Koenig, J. C. Chan; J. Am. Chem. Soc. 1978, 100, 2240
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Acknowledgements Douberly Lab at the University of Georgia: Gary Doublery, Bernadette Broderick, Chris Moradi, Joe Brice, Alaina Brown and Peter Franke Havenith Lab at the Ruhr-Universität Bochum: Martina Havenith, Gerhard Schwaab, Theo Fischer, Devendra Mani, Daniel Leicht, Raffael Schwan
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