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Photodissociation dynamics of 1-naphthol
The photodissociation of 1-naphthol at 193 and 248 nm was studied using multimass ion imaging techniques under collisionless conditions. Only one dissociation channel was observed, i.e. H atom elimination. The translational energy distributions show two components at both wavelengths. The slow compo...
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Published in: | Molecular physics 2008-02, Vol.106 (2-4), p.233-237 |
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cites | cdi_FETCH-LOGICAL-c346t-71a279a9eaeb8a954c703ad236f8481e2bd3568b3fea28c29b54ebc1da5eac093 |
container_end_page | 237 |
container_issue | 2-4 |
container_start_page | 233 |
container_title | Molecular physics |
container_volume | 106 |
creator | Tseng, C.-M. Lee, Y. T. Ni, C.-K. |
description | The photodissociation of 1-naphthol at 193 and 248 nm was studied using multimass ion imaging techniques under collisionless conditions. Only one dissociation channel was observed, i.e. H atom elimination. The translational energy distributions show two components at both wavelengths. The slow component corresponds to the dissociation from the ground electronic state after internal conversion, and the fast component results from the dissociation on the electronic excited state. Comparison with the photodissociation of phenol was made. |
doi_str_mv | 10.1080/00268970701765803 |
format | article |
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Comparison with the photodissociation of phenol was made.</description><identifier>ISSN: 0026-8976</identifier><identifier>EISSN: 1362-3028</identifier><identifier>DOI: 10.1080/00268970701765803</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><subject>1-naphthol ; multimass ion imaging ; phenol ; photodissociation</subject><ispartof>Molecular physics, 2008-02, Vol.106 (2-4), p.233-237</ispartof><rights>Copyright Taylor & Francis Group, LLC 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c346t-71a279a9eaeb8a954c703ad236f8481e2bd3568b3fea28c29b54ebc1da5eac093</citedby><cites>FETCH-LOGICAL-c346t-71a279a9eaeb8a954c703ad236f8481e2bd3568b3fea28c29b54ebc1da5eac093</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Tseng, C.-M.</creatorcontrib><creatorcontrib>Lee, Y. 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The slow component corresponds to the dissociation from the ground electronic state after internal conversion, and the fast component results from the dissociation on the electronic excited state. Comparison with the photodissociation of phenol was made.</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/00268970701765803</doi><tpages>5</tpages></addata></record> |
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source | Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Science and Technology Collection (Reading list) |
subjects | 1-naphthol multimass ion imaging phenol photodissociation |
title | Photodissociation dynamics of 1-naphthol |
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