Journal article
Pyrolysis of fulvenallene (C7H6) and fulvenallenyl (C7H5): Theoretical kinetics and experimental product detection
G Da Silva, AJ Trevitt, M Steinbauer, P Hemberger
Chemical Physics Letters | ELSEVIER SCIENCE BV | Published : 2011
Abstract
Fulvenallene and fulvenallenyl are the respective C7H 6 and C7H5 global minima, yet their importance to combustion has only recently emerged. We have studied the pyrolysis of these species theoretically to obtain rate constants and compare our results to pyrolysis mass spectrometry experiments for product identification. Master equation modeling reveals that fulvenallene rapidly dissociates to fulvenallenyl + H, and that fulvenallenyl dissociates to form propargyl plus diacetylene, with lesser amounts of i-C5H3 (CH2CCCCH)/n- C5H3 (CHCCHCCH) plus acetylene. Photoionization mass spectrometry experiments using a pyrolysis source on the fulvenallene precursor phthalide identify products consiste..
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Awarded by Verband der Chemischen Industrie
Funding Acknowledgements
The experimental work was carried out at the VUV beamline of the Swiss Light Source of the Paul Scherrer Institute. Experimental work was funded by the German Science Foundation (Fi575/7-2). MS acknowledges a fellowship by the 'Fonds der Chemischen Industrie'. AJT acknowledges funding through the Australian Research Council (DP1094135). Computational resources provided by the Victorian Partnership for Advanced Computing (VPAC). We are grateful to Prof. Ingo Fischer for helpful discussions.