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          <dc:title xml:lang="en">Photodissociation spectrum of cyanobenzene dimer cation. Absence of intermolecular resonance interaction</dc:title>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Ohashi, Kazuhiko</jpcoar:creatorName>
            <jpcoar:familyName xml:lang="en">Ohashi</jpcoar:familyName>
            <jpcoar:givenName xml:lang="en">Kazuhiko</jpcoar:givenName>
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          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Nishiguchi, Masaharu</jpcoar:creatorName>
            <jpcoar:familyName xml:lang="en">Nishiguchi</jpcoar:familyName>
            <jpcoar:givenName xml:lang="en">Masaharu</jpcoar:givenName>
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          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Inokuchi, Yoshiya</jpcoar:creatorName>
            <jpcoar:familyName xml:lang="en">Inokuchi</jpcoar:familyName>
            <jpcoar:givenName xml:lang="en">Yoshiya</jpcoar:givenName>
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          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Sekiya, Hiroshi</jpcoar:creatorName>
            <jpcoar:familyName xml:lang="en">Sekiya</jpcoar:familyName>
            <jpcoar:givenName xml:lang="en">Hiroshi</jpcoar:givenName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Nishi, Nobuyuki</jpcoar:creatorName>
            <jpcoar:familyName xml:lang="en">Nishi</jpcoar:familyName>
            <jpcoar:givenName xml:lang="en">Nobuyuki</jpcoar:givenName>
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          <dc:rights>(c) VSP 1998</dc:rights>
          <jpcoar:subject subjectScheme="NDC">430</jpcoar:subject>
          <datacite:description xml:lang="en">Electronic spectra of a homo-molecular dimer cation, (C6H5CN)2+, are measured by photodissociation spectroscopy in the gas phase. Broad features appeared in the 450–650 nm region are characteristic of π3 → πCN transitions of the C6H5CN+ chromophore. No intense band is observed in the 650–1300 nm region, where other aromatic dimer cations usually show charge resonance bands. Two component molecules of (C6H5CN)2+ cannot take a parallel sandwich configuration suitable for the resonance interaction, because of geometrical constraints due to other stronger interactions.</datacite:description>
          <datacite:description descriptionType="Other">This work was supported in part by a Grant-in-Aid for Scientific Research (No. 09740450) from the Ministry of Education, Science, Sports and Culture of Japan.</datacite:description>
          <datacite:description descriptionType="Other">This is a postprint of an article published by Springer Netherlands in Research on Chemical Intermediates, 1998, available online: http://doi.org/10.1163/156856798X00393</datacite:description>
          <dc:publisher>Springer Netherlands</dc:publisher>
          <datacite:date dateType="Issued">1998-07</datacite:date>
          <dc:language>eng</dc:language>
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          <jpcoar:sourceIdentifier identifierType="ISSN">0922-6168</jpcoar:sourceIdentifier>
          <jpcoar:sourceTitle>Research on Chemical Intermediates</jpcoar:sourceTitle>
          <jpcoar:sourceTitle>Research on Chemical Intermediates</jpcoar:sourceTitle>
          <jpcoar:volume>24</jpcoar:volume>
          <jpcoar:issue>7</jpcoar:issue>
          <jpcoar:pageStart>755</jpcoar:pageStart>
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