Photodissociation of C 3 H 5 Br and C 4 H 7 Br at 234 nm
The photodissociation dynamics of cyclopropyl bromide ($C_3H_5Br$) and cyclobutyl bromide ($C_4H_7Br$) at 234 nm was investigated. A two-dimensional photofragment ion-imaging technique coupled with a [2+1] resonanceenhanced multiphoton ionization scheme was utilized to obtain speed and angular distr...
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Veröffentlicht in: | Bulletin of the Korean Chemical Society 2012, Vol.33 (1), p.143-148 |
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creator | Kim, Hyun-Kook Paul, Dababrata Hong, Ki-Ryong Cho, Ha-Na Lee, Kyoung-Seok Kim, Tae-Kyu |
description | The photodissociation dynamics of cyclopropyl bromide ($C_3H_5Br$) and cyclobutyl bromide ($C_4H_7Br$) at 234 nm was investigated. A two-dimensional photofragment ion-imaging technique coupled with a [2+1] resonanceenhanced multiphoton ionization scheme was utilized to obtain speed and angular distributions of the nascent $Br(^2P_{3/2})$ and $Br^*(^2P_{1/2})$ atoms. The recoil anisotropies for the Br and $Br^*$ channels were measured to be ${\beta}_{Br}=0.92{\pm}0.03$ and ${\beta}_{Br^*}=1.52{\pm}0.04$ for $C_3H_5Br$ and ${\beta}_{Br}=1.10{\pm}0.03$ and ${\beta}_{Br^*}=1.49{\pm}0.05$ for $C_4H_7Br$. The relative quantum yield for Br was found to be ${\Phi}_{Br}=0.13{\pm}0.03$ and for $C_3H_5Br$ and $C_4H_7Br$, respectively. The soft radical limit of the impulsive model adequately modeled the related energy partitioning. The nonadiabatic transition probability from the 3A' and 4A' potential energy surfaces was estimated and discussed. |
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A two-dimensional photofragment ion-imaging technique coupled with a [2+1] resonanceenhanced multiphoton ionization scheme was utilized to obtain speed and angular distributions of the nascent $Br(^2P_{3/2})$ and $Br^*(^2P_{1/2})$ atoms. The recoil anisotropies for the Br and $Br^*$ channels were measured to be ${\beta}_{Br}=0.92{\pm}0.03$ and ${\beta}_{Br^*}=1.52{\pm}0.04$ for $C_3H_5Br$ and ${\beta}_{Br}=1.10{\pm}0.03$ and ${\beta}_{Br^*}=1.49{\pm}0.05$ for $C_4H_7Br$. The relative quantum yield for Br was found to be ${\Phi}_{Br}=0.13{\pm}0.03$ and for $C_3H_5Br$ and $C_4H_7Br$, respectively. The soft radical limit of the impulsive model adequately modeled the related energy partitioning. The nonadiabatic transition probability from the 3A' and 4A' potential energy surfaces was estimated and discussed.</description><identifier>ISSN: 0253-2964</identifier><identifier>EISSN: 1229-5949</identifier><language>kor</language><ispartof>Bulletin of the Korean Chemical Society, 2012, Vol.33 (1), p.143-148</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4024</link.rule.ids></links><search><creatorcontrib>Kim, Hyun-Kook</creatorcontrib><creatorcontrib>Paul, Dababrata</creatorcontrib><creatorcontrib>Hong, Ki-Ryong</creatorcontrib><creatorcontrib>Cho, Ha-Na</creatorcontrib><creatorcontrib>Lee, Kyoung-Seok</creatorcontrib><creatorcontrib>Kim, Tae-Kyu</creatorcontrib><title>Photodissociation of C 3 H 5 Br and C 4 H 7 Br at 234 nm</title><title>Bulletin of the Korean Chemical Society</title><addtitle>Bulletin of the Korean chemical society</addtitle><description>The photodissociation dynamics of cyclopropyl bromide ($C_3H_5Br$) and cyclobutyl bromide ($C_4H_7Br$) at 234 nm was investigated. A two-dimensional photofragment ion-imaging technique coupled with a [2+1] resonanceenhanced multiphoton ionization scheme was utilized to obtain speed and angular distributions of the nascent $Br(^2P_{3/2})$ and $Br^*(^2P_{1/2})$ atoms. The recoil anisotropies for the Br and $Br^*$ channels were measured to be ${\beta}_{Br}=0.92{\pm}0.03$ and ${\beta}_{Br^*}=1.52{\pm}0.04$ for $C_3H_5Br$ and ${\beta}_{Br}=1.10{\pm}0.03$ and ${\beta}_{Br^*}=1.49{\pm}0.05$ for $C_4H_7Br$. The relative quantum yield for Br was found to be ${\Phi}_{Br}=0.13{\pm}0.03$ and for $C_3H_5Br$ and $C_4H_7Br$, respectively. The soft radical limit of the impulsive model adequately modeled the related energy partitioning. The nonadiabatic transition probability from the 3A' and 4A' potential energy surfaces was estimated and discussed.</description><issn>0253-2964</issn><issn>1229-5949</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>JDI</sourceid><recordid>eNqNyrEKwjAQgOEgChbtO9ziWEhzSdobtShFBzu4l2otBmsCXt4fi_gATj8f_DOR5EpRZkjTXCRSGcwUWb0UKbO7SoNY2AIpEWXzCDH0jjncXBdd8BAGqAChBgO7N3S-n6gnFl9GUKjBv9ZiMXQj39NfV2Jz2F-qOns6jq71PY_tcXs6K5krWVq0SCjJ4L_fB0u2MeE</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Kim, Hyun-Kook</creator><creator>Paul, Dababrata</creator><creator>Hong, Ki-Ryong</creator><creator>Cho, Ha-Na</creator><creator>Lee, Kyoung-Seok</creator><creator>Kim, Tae-Kyu</creator><scope>JDI</scope></search><sort><creationdate>2012</creationdate><title>Photodissociation of C 3 H 5 Br and C 4 H 7 Br at 234 nm</title><author>Kim, Hyun-Kook ; Paul, Dababrata ; Hong, Ki-Ryong ; Cho, Ha-Na ; Lee, Kyoung-Seok ; Kim, Tae-Kyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kisti_ndsl_JAKO2012086363930953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2012</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Hyun-Kook</creatorcontrib><creatorcontrib>Paul, Dababrata</creatorcontrib><creatorcontrib>Hong, Ki-Ryong</creatorcontrib><creatorcontrib>Cho, Ha-Na</creatorcontrib><creatorcontrib>Lee, Kyoung-Seok</creatorcontrib><creatorcontrib>Kim, Tae-Kyu</creatorcontrib><collection>KoreaScience</collection><jtitle>Bulletin of the Korean Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Hyun-Kook</au><au>Paul, Dababrata</au><au>Hong, Ki-Ryong</au><au>Cho, Ha-Na</au><au>Lee, Kyoung-Seok</au><au>Kim, Tae-Kyu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photodissociation of C 3 H 5 Br and C 4 H 7 Br at 234 nm</atitle><jtitle>Bulletin of the Korean Chemical Society</jtitle><addtitle>Bulletin of the Korean chemical society</addtitle><date>2012</date><risdate>2012</risdate><volume>33</volume><issue>1</issue><spage>143</spage><epage>148</epage><pages>143-148</pages><issn>0253-2964</issn><eissn>1229-5949</eissn><abstract>The photodissociation dynamics of cyclopropyl bromide ($C_3H_5Br$) and cyclobutyl bromide ($C_4H_7Br$) at 234 nm was investigated. A two-dimensional photofragment ion-imaging technique coupled with a [2+1] resonanceenhanced multiphoton ionization scheme was utilized to obtain speed and angular distributions of the nascent $Br(^2P_{3/2})$ and $Br^*(^2P_{1/2})$ atoms. The recoil anisotropies for the Br and $Br^*$ channels were measured to be ${\beta}_{Br}=0.92{\pm}0.03$ and ${\beta}_{Br^*}=1.52{\pm}0.04$ for $C_3H_5Br$ and ${\beta}_{Br}=1.10{\pm}0.03$ and ${\beta}_{Br^*}=1.49{\pm}0.05$ for $C_4H_7Br$. The relative quantum yield for Br was found to be ${\Phi}_{Br}=0.13{\pm}0.03$ and for $C_3H_5Br$ and $C_4H_7Br$, respectively. The soft radical limit of the impulsive model adequately modeled the related energy partitioning. The nonadiabatic transition probability from the 3A' and 4A' potential energy surfaces was estimated and discussed.</abstract><oa>free_for_read</oa></addata></record> |
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title | Photodissociation of C 3 H 5 Br and C 4 H 7 Br at 234 nm |
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