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Identification of Serine Conformers by Matrix-Isolation IR Spectroscopy Aided by Near-Infrared Laser-Induced Conformational Change, 2D Correlation Analysis, and Quantum Mechanical Anharmonic Computations.
Najbauer, Eszter E; Bazsó, Gábor; Apóstolo, Rui; Fausto, Rui; Biczysko, Malgorzata; Barone, Vincenzo; Tarczay, György.
Afiliação
  • Najbauer EE; †Laboratory of Molecular Spectroscopy, Institute of Chemistry, Eötvös University, PO Box 32, H-1518, Budapest 112, Hungary.
  • Bazsó G; †Laboratory of Molecular Spectroscopy, Institute of Chemistry, Eötvös University, PO Box 32, H-1518, Budapest 112, Hungary.
  • Apóstolo R; ‡Department of Chemistry, University of Coimbra, 3004-535 Coimbra, Portugal.
  • Fausto R; ‡Department of Chemistry, University of Coimbra, 3004-535 Coimbra, Portugal.
  • Biczysko M; §Physics Department and International Centre for Quantum and Molecular Structure, Shanghai University, Shanghai, 200444 China.
  • Barone V; ∥Scuola Normale Superiore, Piazza dei Cavalieri 7, I-56126 Pisa, Italy.
  • Tarczay G; †Laboratory of Molecular Spectroscopy, Institute of Chemistry, Eötvös University, PO Box 32, H-1518, Budapest 112, Hungary.
J Phys Chem B ; 119(33): 10496-510, 2015 Aug 20.
Article em En | MEDLINE | ID: mdl-26201050
The conformers of α-serine were investigated by matrix-isolation IR spectroscopy combined with NIR laser irradiation. This method, aided by 2D correlation analysis, enabled unambiguously grouping the spectral lines to individual conformers. On the basis of comparison of at least nine experimentally observed vibrational transitions of each conformer with empirically scaled (SQM) and anharmonic (GVPT2) computed IR spectra, six conformers were identified. In addition, the presence of at least one more conformer in Ar matrix was proved, and a short-lived conformer with a half-life of (3.7 ± 0.5) × 10(3) s in N2 matrix was generated by NIR irradiation. The analysis of the NIR laser-induced conversions revealed that the excitation of the stretching overtone of both the side chain and the carboxylic OH groups can effectively promote conformational changes, but remarkably different paths were observed for the two kinds of excitations.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Teoria Quântica / Serina / Lasers / Conformação Molecular Tipo de estudo: Diagnostic_studies Idioma: En Revista: J Phys Chem B Assunto da revista: QUIMICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Hungria País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Teoria Quântica / Serina / Lasers / Conformação Molecular Tipo de estudo: Diagnostic_studies Idioma: En Revista: J Phys Chem B Assunto da revista: QUIMICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Hungria País de publicação: Estados Unidos