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 Ã 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″)...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of Chemical Physics 1999-01, Vol.110 (2), p.805-816
Hauptverfasser: Bise, Ryan T., Choi, Hyeon, Pedersen, Henrik B., Mordaunt, David H., Neumark, Daniel M.
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 Ã 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 Ã 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 Ã 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 Ã 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 Ã 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 Ã 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 Ã 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 Ã 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 Ã 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 Ã 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 Ã 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 Ã 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