2016
DOI: 10.1039/c6cp05110c
|View full text |Cite
|
Sign up to set email alerts
|

Triplet state formation and quenching dynamics of 2-mercaptobenzothiazole in solution

Abstract: An adduct-mediated triplet energy transfer from a triplet thione to an alkene is observed with time-resolved vibrational absorption spectroscopy.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
8
0

Year Published

2016
2016
2022
2022

Publication Types

Select...
8

Relationship

4
4

Authors

Journals

citations
Cited by 14 publications
(9 citation statements)
references
References 50 publications
1
8
0
Order By: Relevance
“…It is at first sight surprising that the T 2 → T 1 IC, which occurs with a time constant of ∼11 ps, is slower by an order of magnitude than the ISC rate. However, similar time scales have been reported for IC between the triplet states of various aromatic ketones and attributed to either thermal , or kinetic equilibrium. For Bzp in solution, we propose that the IC rate will be dictated by the vibrational energy transfer (VET) rate to the solvent, which quenches the rapid exchange between the T 2 and T 1 states by relaxation to the minimum on the T 1 state.…”
supporting
confidence: 71%
“…It is at first sight surprising that the T 2 → T 1 IC, which occurs with a time constant of ∼11 ps, is slower by an order of magnitude than the ISC rate. However, similar time scales have been reported for IC between the triplet states of various aromatic ketones and attributed to either thermal , or kinetic equilibrium. For Bzp in solution, we propose that the IC rate will be dictated by the vibrational energy transfer (VET) rate to the solvent, which quenches the rapid exchange between the T 2 and T 1 states by relaxation to the minimum on the T 1 state.…”
supporting
confidence: 71%
“…This procedure gave good agreement between experimental and calculated infrared frequencies for the compounds of interest in this study. 9,39 Calculations of absorption spectra of the carbon centered addition radical (denoted as QS-MMA for the reaction with MMA) used time-dependent density functional theory (TDDFT) with the 6-311++G(3df,3pd) basis set. Enthalpies of activation for addition reactions of the various aromatic thiyl radical with styrene illustrated in Figure 1 were calculated using the CAM-B3LYP density functional, 40 with the 6-311++G(d,p) basis set, because reliable transition states for the addition reaction could not be obtained with the B3LYP method.…”
Section: Methodsmentioning
confidence: 99%
“…In this way, reaction pathways may be observed on timescales from hundreds of femtoseconds up to tens of milliseconds. [29][30][31] The resulting advantage is dynamic real-time tracking of short-and longer-lived intermediates, typically spanning picosecond to microsecond lifetimes, allowing iden-tication and kinetic analyses for species impossible to observe with steady state techniques.…”
Section: Introductionmentioning
confidence: 99%