
Journal of Chemical Physics p. 7566 - 7579 (1994)
Update date:2022-08-10
Topics:
Mohrschladt, R.
Schroeder, J.
Schwarzer, D.
Troe, J.
Voehringer, P.
The viscosity dependence of the photoisomerization of trans-stilbeme in compressed liquid ethanol shows deviations from a simple power law description in the viscosity range from 1 to 4 mPa s.Corresponding deviations are observed in the solvents methanol, n-propanol, and n-butanol.This behavior is attributed to a competition between solvent relaxation and barrier crossing in the S1 state of trans-stilbene.The relative time scales of barrier crossing and solvent relaxation change as the pressure increases, because the dielectric relaxation rate of the solvent decreases more rapidly with increasing viscosity than the barrier crossing rate.Consequently, the reaction takes place in an increasingly retarded solvent environment which no longer relaxes completely around the changing charge distribution of the solute along its reaction path, giving rise to "dielectric friction".In contrast to trans-stilbene, the corresponding reaction of diphenylbutadiene in n-alkanols shows a much weaker sensitivity to solute-solvent interaction and, consequently, a simple inverse viscosity dependence of the photoisomerization rate is observed in all alkanols such as described by the Kramers-Smoluchowski theory.This significant difference is probably caused by smaller sudden polarization effects along the reaction path in diphenylbutadiene.The observed dependence of the trans-stilbene barrier crossing rate on pressure is compared either to a model with density dependent effective barrier height, or to a simple continuum model of the frequency dependence of the dielectric friction in the limit of weak coupling.Neither model works well unless a very strong viscosity dependence of the dielectric relaxation time of the solvent (τD<*>η10) is employed to obtain agreement with the observed viscosity dependence of the barrier crossing rate.
View More
Suzhou Zhonghelong Chemical Tech Co., Ltd【License cancellation】
Contact:+86 571-12345678
Address:Dunhuang Road, Suzhou Industrial Park, No.128 building 701 room Mansion
Xinchang Jiu Xin Pharmaceutical Co., Ltd
website:http://www.jiuxinpharm.com
Contact:86 137 5756 8585
Address:Poyang industry Park
Shanghai PengMo Biotechnology Co.,Ltd
website:http://www.pengmobio.lookchem.com
Contact:86-13052359378
Address:No.218 Hai Qu Road.Shanghai.China
Contact:0571-
Address:zhejing
Dayang Chem (Hangzhou) Co.,Ltd.
website:http://www.dycnchem.com
Contact:+86-571-88938639
Address:9/F, Unit 2 Changdi Torch Building, 259# WenSan Road, Xihu District, Hangzhou City 310012, P.R.China
Doi:10.1016/j.catcom.2020.106209
(2021)Doi:10.1021/acs.orglett.8b03661
(2019)Doi:10.1039/b107275g
(2001)Doi:10.1021/acs.joc.0c01369
(2020)Doi:10.1080/00945710009351870
(2000)Doi:10.1023/A:1024781929253
(2003)