Ultrafast Internal Conversion Dynamics of 2-Chloropyridine by Femtosecond Time-Resolved Photoelectron Imaging
O644; Ultrafast internal conversion dynamics of 2-chloropyridine were studied by femtosecond time-resolved photoelectron imaging spectroscopy coupled with time-resolved mass spectroscopy. The ultrafast internal conversion from the second excited state (S2) to the first excited state (S1) via an adja...
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Veröffentlicht in: | Wuli huaxue xuebao 2012-11, Vol.28 (11), p.2543-2548 |
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creator | Ahmed-Yousif, GHAZAl Xue-Jun, QIU Chao-Chao, QIN Jin-You, LONG Bumaliya, ABULIMITI Bing, ZHANG |
description | O644; Ultrafast internal conversion dynamics of 2-chloropyridine were studied by femtosecond time-resolved photoelectron imaging spectroscopy coupled with time-resolved mass spectroscopy. The ultrafast internal conversion from the second excited state (S2) to the first excited state (S1) via an adjacent conical intersection within (162±5) fs was clearly observed from the time-dependence of the photoelectron spectra. The subsequent deactivations involved the coupling of S2/S0(the ground state) and S1/S0 conical intersections, which occurred on a timescale of about (5.5±0.3) ps, and led to the internal conversion to the ground state from the S2 and S1 states. |
doi_str_mv | 10.3866/PKU.WHXB201208135 |
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R. China; Graduate University of Chinese Academy of Sciences, Beijing 100049, P. R. China</creatorcontrib><description>O644; Ultrafast internal conversion dynamics of 2-chloropyridine were studied by femtosecond time-resolved photoelectron imaging spectroscopy coupled with time-resolved mass spectroscopy. The ultrafast internal conversion from the second excited state (S2) to the first excited state (S1) via an adjacent conical intersection within (162±5) fs was clearly observed from the time-dependence of the photoelectron spectra. The subsequent deactivations involved the coupling of S2/S0(the ground state) and S1/S0 conical intersections, which occurred on a timescale of about (5.5±0.3) ps, and led to the internal conversion to the ground state from the S2 and S1 states.</description><identifier>ISSN: 1000-6818</identifier><identifier>DOI: 10.3866/PKU.WHXB201208135</identifier><language>eng</language><publisher>Graduate University of Chinese Academy of Sciences, Beijing 100049, P. R. China</publisher><ispartof>Wuli huaxue xuebao, 2012-11, Vol.28 (11), p.2543-2548</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.wanfangdata.com.cn/images/PeriodicalImages/wlhxxb/wlhxxb.jpg</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Ahmed-Yousif, GHAZAl</creatorcontrib><creatorcontrib>Xue-Jun, QIU</creatorcontrib><creatorcontrib>Chao-Chao, QIN</creatorcontrib><creatorcontrib>Jin-You, LONG</creatorcontrib><creatorcontrib>Bumaliya, ABULIMITI</creatorcontrib><creatorcontrib>Bing, ZHANG</creatorcontrib><creatorcontrib>中国科学院武汉物理与数学研究所, 波谱与原子分子物理国家重点实验室, 武汉 430071; 中国科学院研究生院, 北京 100049,State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics, Chinese Academy of Sciences, Wuhan 430071, P. R. China; Graduate University of Chinese Academy of Sciences, Beijing 100049, P. R. China</creatorcontrib><title>Ultrafast Internal Conversion Dynamics of 2-Chloropyridine by Femtosecond Time-Resolved Photoelectron Imaging</title><title>Wuli huaxue xuebao</title><description>O644; Ultrafast internal conversion dynamics of 2-chloropyridine were studied by femtosecond time-resolved photoelectron imaging spectroscopy coupled with time-resolved mass spectroscopy. The ultrafast internal conversion from the second excited state (S2) to the first excited state (S1) via an adjacent conical intersection within (162±5) fs was clearly observed from the time-dependence of the photoelectron spectra. The subsequent deactivations involved the coupling of S2/S0(the ground state) and S1/S0 conical intersections, which occurred on a timescale of about (5.5±0.3) ps, and led to the internal conversion to the ground state from the S2 and S1 states.</description><issn>1000-6818</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpV0E1PwjAcBvAeNBHRD-CtN0_DvkBbjjrlJZJIDERvS9f9CyNbS9oJ7Ns7ghdPz-XJkzw_hB4oGXAlxNPyfT34mn2_MEIZUZSPrlCPEkISoai6Qbcx7gjhhArVQ_W6aoK2OjZ47hoITlc49e4AIZbe4dfW6bo0EXuLWZJuKx_8vg1lUTrAeYsnUDc-gvGuwKuyhuQToq8OUODl1jceKjBN6Hbmtd6UbnOHrq2uItz_ZR-tJ2-rdJYsPqbz9HmRGCZZk3BQhghaDHWh5VjkXFsCSg4JU8WYSlA8l1RTAyNpcigoCMZyAEJzK63kivfR42X3qJ3VbpPt_M_5WsyO1fZ0ys8ytCMRXZNemib4GAPYbB_KWoc2oyQ7a2adZvZPk_8CPWhs8A</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>Ahmed-Yousif, GHAZAl</creator><creator>Xue-Jun, QIU</creator><creator>Chao-Chao, QIN</creator><creator>Jin-You, LONG</creator><creator>Bumaliya, ABULIMITI</creator><creator>Bing, ZHANG</creator><general>Graduate University of Chinese Academy of Sciences, Beijing 100049, P. R. China</general><general>State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics, Chinese Academy of Sciences, Wuhan 430071 P. R. China</general><scope>AAYXX</scope><scope>CITATION</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20121101</creationdate><title>Ultrafast Internal Conversion Dynamics of 2-Chloropyridine by Femtosecond Time-Resolved Photoelectron Imaging</title><author>Ahmed-Yousif, GHAZAl ; Xue-Jun, QIU ; Chao-Chao, QIN ; Jin-You, LONG ; Bumaliya, ABULIMITI ; Bing, ZHANG</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c272t-3e8c061d4ada796b3af0e874028d917e83b71a1ce57cbed1e622bee01bf7f7383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Ahmed-Yousif, GHAZAl</creatorcontrib><creatorcontrib>Xue-Jun, QIU</creatorcontrib><creatorcontrib>Chao-Chao, QIN</creatorcontrib><creatorcontrib>Jin-You, LONG</creatorcontrib><creatorcontrib>Bumaliya, ABULIMITI</creatorcontrib><creatorcontrib>Bing, ZHANG</creatorcontrib><creatorcontrib>中国科学院武汉物理与数学研究所, 波谱与原子分子物理国家重点实验室, 武汉 430071; 中国科学院研究生院, 北京 100049,State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics, Chinese Academy of Sciences, Wuhan 430071, P. R. China; Graduate University of Chinese Academy of Sciences, Beijing 100049, P. R. China</creatorcontrib><collection>CrossRef</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Wuli huaxue xuebao</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ahmed-Yousif, GHAZAl</au><au>Xue-Jun, QIU</au><au>Chao-Chao, QIN</au><au>Jin-You, LONG</au><au>Bumaliya, ABULIMITI</au><au>Bing, ZHANG</au><aucorp>中国科学院武汉物理与数学研究所, 波谱与原子分子物理国家重点实验室, 武汉 430071; 中国科学院研究生院, 北京 100049,State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics, Chinese Academy of Sciences, Wuhan 430071, P. R. 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The subsequent deactivations involved the coupling of S2/S0(the ground state) and S1/S0 conical intersections, which occurred on a timescale of about (5.5±0.3) ps, and led to the internal conversion to the ground state from the S2 and S1 states.</abstract><pub>Graduate University of Chinese Academy of Sciences, Beijing 100049, P. R. China</pub><doi>10.3866/PKU.WHXB201208135</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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title | Ultrafast Internal Conversion Dynamics of 2-Chloropyridine by Femtosecond Time-Resolved Photoelectron Imaging |
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