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Zeitschrift für Physikalische Chemie

International journal of research in physical chemistry and chemical physics

Editor-in-Chief: Rademann, Klaus


IMPACT FACTOR 2018: 0.975
5-year IMPACT FACTOR: 1.021

CiteScore 2018: 1.20

SCImago Journal Rank (SJR) 2018: 0.327
Source Normalized Impact per Paper (SNIP) 2018: 0.391

Online
ISSN
2196-7156
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Volume 229, Issue 10-12

Issues

Femtosecond Infrared Spectroscopy of Aroylperoxide Photofragmentation – Site Selective Decarboxylation

Hendrik Vennekate / Christian Reichardt / Arne Walter / Harald Fuest / Jörg Schroeder / Dirk Schwarzer
Published Online: 2015-07-10 | DOI: https://doi.org/10.1515/zpch-2015-0629

Abstract

The ultrafast photofragmentation of acetyl-benzoyl peroxide (ABPO) and 2-naphthoyl-benzoyl peroxide (NBPO) after UV excitation at 266 nm is studied by mid-infrared transient absorption spectroscopy. 13C-isotopic labelling is employed to unravel the primary fragmentation paths. For NBPO it appears that excitation of the benzoyloxy part causes decarboxylation exclusively at that site. In ABPO the acetyloxy part completely decarboxylates upon 266 nm excitation while only 80% – 85% of the benzoyloxyl radicals formed decarboxylate. The remaining radicals either combine with methyl radicals to methylbenzoate within about 30 ps or survive on the time scale of the experiment (1.5 ns). Photofragmentation of ABPO occurs from the S1-state whose lifetime is about 200 fs. All fragmentation products including CO2 also appear on this time scale.

Keywords: Reaction Dynamics; Photochemistry; Femtosecond IR Spectroscopy

About the article

Accepted: 2015-06-07

Received: 2015-04-17

Published Online: 2015-07-10

Published in Print: 2015-10-28


Citation Information: Zeitschrift für Physikalische Chemie, Volume 229, Issue 10-12, Pages 1799–1814, ISSN (Online) 2196-7156, ISSN (Print) 0942-9352, DOI: https://doi.org/10.1515/zpch-2015-0629.

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©2015 Walter de Gruyter Berlin/Boston.Get Permission

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