Conformity of the 7-azaindole dimer cationic potential with photoionization/Coulomb-explosion MS observations and the concerted biprotonic transfer mechanism
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Catalán, J
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Univ Autonoma Madrid, Fac Ciencias, Dept Quim Fis Aplicada, E-28049 Madrid, SpainUniv Autonoma Madrid, Fac Ciencias, Dept Quim Fis Aplicada, E-28049 Madrid, Spain
Catalán, J
[1
]
del Valle, JC
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机构:Univ Autonoma Madrid, Fac Ciencias, Dept Quim Fis Aplicada, E-28049 Madrid, Spain
del Valle, JC
Kasha, M
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机构:Univ Autonoma Madrid, Fac Ciencias, Dept Quim Fis Aplicada, E-28049 Madrid, Spain
Kasha, M
机构:
[1] Univ Autonoma Madrid, Fac Ciencias, Dept Quim Fis Aplicada, E-28049 Madrid, Spain
[2] Florida State Univ, Inst Mol Biophys, Tallahassee, FL 32306 USA
[3] Florida State Univ, Dept Chem, Tallahassee, FL 32306 USA
In this Letter we consider the second laser-pulse time delay experiments of Castleman and co-workers [D.E. Folmer, L. Poth, E.S. Wisniewski, A.W. CastIeman, Jr., Chem. Phys. Lett. 287 (1998) 1; D.E. Folmer, E.S. Wisniewski, S.M. Hurley, A.W. Castleman, Jr., Proc. Natl. Acad. Sci. USA 96 (1999) 12980] as interrogating the (density functional theory) biprotonic phototautomerization as correlated with the cationic doublet ground electronic state potential D-0((+)) for the species produced in the photoionization step. We demonstrate that the 7-AI(H+) cation can result as a product of this photoionization, and is then revealed a Coulomb-explosion time-of-flight mass spectrum (TOF-MS) species. We demonstrate that the mass-119/mass-118 ratios as a function of photoionization, and Coulomb-explosion laser pulse delay can conform to the concerted biprotonic mechanism. The interpretation emphasizes the invasive nature of the TOF-MS technique requirement in studying the excited state of the doubly-H-bonded 7-azaindole dimer. (C) 2000 Elsevier Science B.V. All rights reserved.