TY - JOUR
T1 - Effect of Pressure on the Proton-Transfer Rate from a Photoacid to a Solvent. 2. DCN2 in Propanol
AU - Genosar, Liat
AU - Leiderman, Pavel
AU - Koifman, Nahum
AU - Huppert, Dan
PY - 2004/1/15
Y1 - 2004/1/15
N2 - The reversible proton dissociation and geminate recombination of photoacids is studied as a function of pressure in liquid propanol. For this purpose we used a strong photoacid, 5,8-dicyano-2-naphthol (DCN2) (pK a* ∼ -4.5 in water), capable of transferring a proton to alcohols. The time-resolved emission data are explained by the reversible diffusion-influenced chemical reaction model. At low pressure, the proton-transfer rate slightly increases with pressure whereas, at high pressure, the rate constant decreases significantly as the pressure increases. The pressure dependence is explained using an approximate stepwise two-coordinate proton-transfer model. The model is compared with the Landau-Zener curve-crossing proton tunneling formulation. Decrease of the proton-transfer rate at high-pressures reflects the solvent-controlled limit, and the increase in rate at low-pressures reflects the proton tunneling nonadiabatic limit. The results are compared with our recent studies of the pressure dependence of proton transfer from 2-naphthol-6-sulfonate (2N6S) to water and DCN2 to ethanol. Though in 2N6S-water, the proton transfer is controlled by proton tunneling, in our current work we find that, at high pressure, the solvent controls the rate of the process.
AB - The reversible proton dissociation and geminate recombination of photoacids is studied as a function of pressure in liquid propanol. For this purpose we used a strong photoacid, 5,8-dicyano-2-naphthol (DCN2) (pK a* ∼ -4.5 in water), capable of transferring a proton to alcohols. The time-resolved emission data are explained by the reversible diffusion-influenced chemical reaction model. At low pressure, the proton-transfer rate slightly increases with pressure whereas, at high pressure, the rate constant decreases significantly as the pressure increases. The pressure dependence is explained using an approximate stepwise two-coordinate proton-transfer model. The model is compared with the Landau-Zener curve-crossing proton tunneling formulation. Decrease of the proton-transfer rate at high-pressures reflects the solvent-controlled limit, and the increase in rate at low-pressures reflects the proton tunneling nonadiabatic limit. The results are compared with our recent studies of the pressure dependence of proton transfer from 2-naphthol-6-sulfonate (2N6S) to water and DCN2 to ethanol. Though in 2N6S-water, the proton transfer is controlled by proton tunneling, in our current work we find that, at high pressure, the solvent controls the rate of the process.
UR - http://www.scopus.com/inward/record.url?scp=1642444698&partnerID=8YFLogxK
U2 - 10.1021/jp035099l
DO - 10.1021/jp035099l
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AN - SCOPUS:1642444698
SN - 1089-5639
VL - 108
SP - 309
EP - 319
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 2
ER -