Photodissociation spectroscopy and dynamics of the methylthio radical (CH3S)
The photodissociation spectroscopy and dynamics of the CH3S and CD3S radicals have been investigated using fast radical beam photofragment spectroscopy of the à 2A1←X̃ 2E electronic band (T0≅26 400 cm−1) and an unstructured band near 45 600 cm−1. At all energies, only one major channel, CH3(X̃ 2A2″)...
Gespeichert in:
Veröffentlicht in: | Journal of Chemical Physics 1999-01, Vol.110 (2), p.805-816 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 816 |
---|---|
container_issue | 2 |
container_start_page | 805 |
container_title | Journal of Chemical Physics |
container_volume | 110 |
creator | Bise, Ryan T. Choi, Hyeon Pedersen, Henrik B. Mordaunt, David H. Neumark, Daniel M. |
description | The photodissociation spectroscopy and dynamics of the CH3S and CD3S radicals have been investigated using fast radical beam photofragment spectroscopy of the à 2A1←X̃ 2E electronic band (T0≅26 400 cm−1) and an unstructured band near 45 600 cm−1. At all energies, only one major channel, CH3(X̃ 2A2″)+S(3Pj), was observed. Photofragment yield spectra for the à 2A1←X̃ 2E electronic band show resolved vibrational progressions extending well beyond those seen in laser-induced fluorescence studies of this band. Photofragment translational energy distributions yield the S(3Pj) fine-structure distribution for each vibrational level of the CH3 product. Photofragment angular distributions were found to be highly anisotropic (β=−0.2 to −1.0±0.1) with increasing anisotropy at higher photon energies. The results yield a refined heat of formation for CH3S (1.346±0.018 eV) as well as the mechanism by which the à 2A1 state is predissociated. Results at 45 600 cm−1 imply that dissociation occurs on the repulsive B̃ 2A2 state. |
doi_str_mv | 10.1063/1.478048 |
format | Article |
fullrecord | <record><control><sourceid>crossref_osti_</sourceid><recordid>TN_cdi_crossref_primary_10_1063_1_478048</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1063_1_478048</sourcerecordid><originalsourceid>FETCH-LOGICAL-c183t-4616eb060a2efff97c47ba6ff6ff8f46e52c69ae93d571a546e7a1aa9aca0cb43</originalsourceid><addsrcrecordid>eNotUMFKAzEUDKJgrYKfEG_1sPVlkyaboxRrhYKCeg6vbxM20m7KJpf9e1cqDAwMwzAzjN0LWArQ8kkslWlANRdsJqCxldEWLtkMoBaV1aCv2U3OPwAgTK1mbPfRpZLamHOiiCWmnueTpzKkTOk0cuxb3o49HiNlngIvnedHX7rxULqY-IBtJDzwxXorPx9v2VXAQ_Z3_zxn35uXr_W22r2_vq2fdxWJRpZKaaH9HjRg7UMI1pAye9QhTGiC0n5Vk7borWxXRuBqUgwKRIuEQHsl5-zhnJtyiS5TLJ46Sn0_FXd1Y2sJk2dx9tA0JQ8-uNMQjziMToD7e8oJd35K_gJxiVuH</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Photodissociation spectroscopy and dynamics of the methylthio radical (CH3S)</title><source>AIP Journals Complete</source><source>AIP Digital Archive</source><creator>Bise, Ryan T. ; Choi, Hyeon ; Pedersen, Henrik B. ; Mordaunt, David H. ; Neumark, Daniel M.</creator><creatorcontrib>Bise, Ryan T. ; Choi, Hyeon ; Pedersen, Henrik B. ; Mordaunt, David H. ; Neumark, Daniel M.</creatorcontrib><description>The photodissociation spectroscopy and dynamics of the CH3S and CD3S radicals have been investigated using fast radical beam photofragment spectroscopy of the à 2A1←X̃ 2E electronic band (T0≅26 400 cm−1) and an unstructured band near 45 600 cm−1. At all energies, only one major channel, CH3(X̃ 2A2″)+S(3Pj), was observed. Photofragment yield spectra for the à 2A1←X̃ 2E electronic band show resolved vibrational progressions extending well beyond those seen in laser-induced fluorescence studies of this band. Photofragment translational energy distributions yield the S(3Pj) fine-structure distribution for each vibrational level of the CH3 product. Photofragment angular distributions were found to be highly anisotropic (β=−0.2 to −1.0±0.1) with increasing anisotropy at higher photon energies. The results yield a refined heat of formation for CH3S (1.346±0.018 eV) as well as the mechanism by which the à 2A1 state is predissociated. Results at 45 600 cm−1 imply that dissociation occurs on the repulsive B̃ 2A2 state.</description><identifier>ISSN: 0021-9606</identifier><identifier>EISSN: 1089-7690</identifier><identifier>DOI: 10.1063/1.478048</identifier><language>eng</language><publisher>United States</publisher><subject>40 CHEMISTRY ; CHEMICAL REACTION YIELD ; DEUTERIUM COMPOUNDS ; ELECTRONIC STRUCTURE ; FLUORESCENCE ; FORMATION HEAT ; ISOTOPE EFFECTS ; ORGANIC COMPOUNDS ; ORGANIC SULFUR COMPOUNDS ; PHOTOLYSIS ; PHYSICS ; RADICALS</subject><ispartof>Journal of Chemical Physics, 1999-01, Vol.110 (2), p.805-816</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c183t-4616eb060a2efff97c47ba6ff6ff8f46e52c69ae93d571a546e7a1aa9aca0cb43</citedby><cites>FETCH-LOGICAL-c183t-4616eb060a2efff97c47ba6ff6ff8f46e52c69ae93d571a546e7a1aa9aca0cb43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,886,27929,27930</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/289230$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Bise, Ryan T.</creatorcontrib><creatorcontrib>Choi, Hyeon</creatorcontrib><creatorcontrib>Pedersen, Henrik B.</creatorcontrib><creatorcontrib>Mordaunt, David H.</creatorcontrib><creatorcontrib>Neumark, Daniel M.</creatorcontrib><title>Photodissociation spectroscopy and dynamics of the methylthio radical (CH3S)</title><title>Journal of Chemical Physics</title><description>The photodissociation spectroscopy and dynamics of the CH3S and CD3S radicals have been investigated using fast radical beam photofragment spectroscopy of the à 2A1←X̃ 2E electronic band (T0≅26 400 cm−1) and an unstructured band near 45 600 cm−1. At all energies, only one major channel, CH3(X̃ 2A2″)+S(3Pj), was observed. Photofragment yield spectra for the à 2A1←X̃ 2E electronic band show resolved vibrational progressions extending well beyond those seen in laser-induced fluorescence studies of this band. Photofragment translational energy distributions yield the S(3Pj) fine-structure distribution for each vibrational level of the CH3 product. Photofragment angular distributions were found to be highly anisotropic (β=−0.2 to −1.0±0.1) with increasing anisotropy at higher photon energies. The results yield a refined heat of formation for CH3S (1.346±0.018 eV) as well as the mechanism by which the à 2A1 state is predissociated. Results at 45 600 cm−1 imply that dissociation occurs on the repulsive B̃ 2A2 state.</description><subject>40 CHEMISTRY</subject><subject>CHEMICAL REACTION YIELD</subject><subject>DEUTERIUM COMPOUNDS</subject><subject>ELECTRONIC STRUCTURE</subject><subject>FLUORESCENCE</subject><subject>FORMATION HEAT</subject><subject>ISOTOPE EFFECTS</subject><subject>ORGANIC COMPOUNDS</subject><subject>ORGANIC SULFUR COMPOUNDS</subject><subject>PHOTOLYSIS</subject><subject>PHYSICS</subject><subject>RADICALS</subject><issn>0021-9606</issn><issn>1089-7690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNotUMFKAzEUDKJgrYKfEG_1sPVlkyaboxRrhYKCeg6vbxM20m7KJpf9e1cqDAwMwzAzjN0LWArQ8kkslWlANRdsJqCxldEWLtkMoBaV1aCv2U3OPwAgTK1mbPfRpZLamHOiiCWmnueTpzKkTOk0cuxb3o49HiNlngIvnedHX7rxULqY-IBtJDzwxXorPx9v2VXAQ_Z3_zxn35uXr_W22r2_vq2fdxWJRpZKaaH9HjRg7UMI1pAye9QhTGiC0n5Vk7borWxXRuBqUgwKRIuEQHsl5-zhnJtyiS5TLJ46Sn0_FXd1Y2sJk2dx9tA0JQ8-uNMQjziMToD7e8oJd35K_gJxiVuH</recordid><startdate>19990108</startdate><enddate>19990108</enddate><creator>Bise, Ryan T.</creator><creator>Choi, Hyeon</creator><creator>Pedersen, Henrik B.</creator><creator>Mordaunt, David H.</creator><creator>Neumark, Daniel M.</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>19990108</creationdate><title>Photodissociation spectroscopy and dynamics of the methylthio radical (CH3S)</title><author>Bise, Ryan T. ; Choi, Hyeon ; Pedersen, Henrik B. ; Mordaunt, David H. ; Neumark, Daniel M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c183t-4616eb060a2efff97c47ba6ff6ff8f46e52c69ae93d571a546e7a1aa9aca0cb43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>40 CHEMISTRY</topic><topic>CHEMICAL REACTION YIELD</topic><topic>DEUTERIUM COMPOUNDS</topic><topic>ELECTRONIC STRUCTURE</topic><topic>FLUORESCENCE</topic><topic>FORMATION HEAT</topic><topic>ISOTOPE EFFECTS</topic><topic>ORGANIC COMPOUNDS</topic><topic>ORGANIC SULFUR COMPOUNDS</topic><topic>PHOTOLYSIS</topic><topic>PHYSICS</topic><topic>RADICALS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bise, Ryan T.</creatorcontrib><creatorcontrib>Choi, Hyeon</creatorcontrib><creatorcontrib>Pedersen, Henrik B.</creatorcontrib><creatorcontrib>Mordaunt, David H.</creatorcontrib><creatorcontrib>Neumark, Daniel M.</creatorcontrib><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Journal of Chemical Physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bise, Ryan T.</au><au>Choi, Hyeon</au><au>Pedersen, Henrik B.</au><au>Mordaunt, David H.</au><au>Neumark, Daniel M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photodissociation spectroscopy and dynamics of the methylthio radical (CH3S)</atitle><jtitle>Journal of Chemical Physics</jtitle><date>1999-01-08</date><risdate>1999</risdate><volume>110</volume><issue>2</issue><spage>805</spage><epage>816</epage><pages>805-816</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><abstract>The photodissociation spectroscopy and dynamics of the CH3S and CD3S radicals have been investigated using fast radical beam photofragment spectroscopy of the à 2A1←X̃ 2E electronic band (T0≅26 400 cm−1) and an unstructured band near 45 600 cm−1. At all energies, only one major channel, CH3(X̃ 2A2″)+S(3Pj), was observed. Photofragment yield spectra for the à 2A1←X̃ 2E electronic band show resolved vibrational progressions extending well beyond those seen in laser-induced fluorescence studies of this band. Photofragment translational energy distributions yield the S(3Pj) fine-structure distribution for each vibrational level of the CH3 product. Photofragment angular distributions were found to be highly anisotropic (β=−0.2 to −1.0±0.1) with increasing anisotropy at higher photon energies. The results yield a refined heat of formation for CH3S (1.346±0.018 eV) as well as the mechanism by which the à 2A1 state is predissociated. Results at 45 600 cm−1 imply that dissociation occurs on the repulsive B̃ 2A2 state.</abstract><cop>United States</cop><doi>10.1063/1.478048</doi><tpages>12</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9606 |
ispartof | Journal of Chemical Physics, 1999-01, Vol.110 (2), p.805-816 |
issn | 0021-9606 1089-7690 |
language | eng |
recordid | cdi_crossref_primary_10_1063_1_478048 |
source | AIP Journals Complete; AIP Digital Archive |
subjects | 40 CHEMISTRY CHEMICAL REACTION YIELD DEUTERIUM COMPOUNDS ELECTRONIC STRUCTURE FLUORESCENCE FORMATION HEAT ISOTOPE EFFECTS ORGANIC COMPOUNDS ORGANIC SULFUR COMPOUNDS PHOTOLYSIS PHYSICS RADICALS |
title | Photodissociation spectroscopy and dynamics of the methylthio radical (CH3S) |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-13T04%3A20%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Photodissociation%20spectroscopy%20and%20dynamics%20of%20the%20methylthio%20radical%20(CH3S)&rft.jtitle=Journal%20of%20Chemical%20Physics&rft.au=Bise,%20Ryan%20T.&rft.date=1999-01-08&rft.volume=110&rft.issue=2&rft.spage=805&rft.epage=816&rft.pages=805-816&rft.issn=0021-9606&rft.eissn=1089-7690&rft_id=info:doi/10.1063/1.478048&rft_dat=%3Ccrossref_osti_%3E10_1063_1_478048%3C/crossref_osti_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |