Artigo Revisado por pares

S−H Bond Dissociation Enthalpies in Thiophenols: A Time-Resolved Photoacoustic Calorimetry and Quantum Chemistry Study

2002; American Chemical Society; Volume: 106; Issue: 42 Linguagem: Inglês

10.1021/jp025677i

ISSN

1520-5215

Autores

Rui M. Borges dos Santos, Vânia S. F. Muralha, Catarina F. Correia, Rita C. Guedes, Benedito J. Costa Cabral, José A. Martinho Simões,

Tópico(s)

Atmospheric chemistry and aerosols

Resumo

Time-resolved photoacoustic calorimetry (TR-PAC) and quantum chemistry calculations were used to investigate the energetics of sulfur−hydrogen bonds in thiophenol and four para-substituted thiophenols, 4-XC6H4SH (X = CH3, OCH3, Cl, and CF3). The result obtained for the PhS−H gas-phase bond dissociation enthalpy, derived from the PAC experimental results in solution, is 349.4 ± 4.5 kJ mol-1. This value is significantly higher than recent literature values but agrees with a value suggested some 20 years ago in a widely used review. The PAC result also concurs with the value computed at a high theory level, G3(MP2), 346.8 kJ mol-1. The data obtained for the substituted thiophenols support the idea that substituent effects are less pronounced on the S−H bond dissociation enthalpy than on the O−H bond dissociation enthalpy of the corresponding phenols.

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