Photophysics and excited state relaxation dynamics of p-hydroxy and p-amino-substituted benzophenones: a review

Photophysics and excited state relaxation dynamics of p-hydroxy and p-amino-substituted... Very short lifetimes (a few picoseconds) of the lowest excited singlet (S1) state of benzophenone (BP) and p-hydroxybenzophenone (HOBP) suggest that they have π* character in all kinds of solvents. However, in the case of the p-amino-substituted benzophenones (ABPs), the nature of the S1 state, whether it is n–π* or π–π*, depends on the nature of the solvent and the identity of the substituent groups. The lowest excited triplet (T1) state of BP has nπ* character in all kinds of solvents and hence phosphorescence decay is short (a few ms). The T1 state character of HOBP and ABP’s are solvent dependent. In a few cases dual exponential decay of phosphorescence indicates that n–π* and π–π* triplet states lie close to each other. The π–π* type of T1 state has longer phosphorescence lifetime (a few tens of ms). Investigations of the ultrafast relaxation dynamics of 4-N,N-dimethylaminobenzophenoene (DMABP) in different kinds of solvents of varying polarities and viscosities reveal that conversion of the locally excited (LE) state to the twisted intramolecular charge transfer (TICT) state by twisting of the dimethylanilino group is the major process, which is responsible for the efficient non-radiative relaxation mechanism of the S1 state of this molecule and solvation dynamics plays a minor role in it. In self-quenching interaction between the triplet state and its ground state, the n–π* kind of T1 state plays the major role and no triplet exciplex is involved as an intermediate. The T1 state of BP is equally reactive towards hydrogen atom abstraction reaction with the ground state of each of the ABPs either by direct hydrogen atom transfer or by a chargetransfer-coupled proton-transfer mechanism. Exciplex formation has been observed only in the case of the reaction between the T1 state of BP and DMABP. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Research on Chemical Intermediates Springer Journals

Photophysics and excited state relaxation dynamics of p-hydroxy and p-amino-substituted benzophenones: a review

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Publisher
Brill Academic Publishers
Copyright
Copyright © 2005 by VSP
Subject
Chemistry; Inorganic Chemistry; Physical Chemistry; Catalysis
ISSN
0922-6168
eISSN
1568-5675
D.O.I.
10.1163/1568567053147020
Publisher site
See Article on Publisher Site

Abstract

Very short lifetimes (a few picoseconds) of the lowest excited singlet (S1) state of benzophenone (BP) and p-hydroxybenzophenone (HOBP) suggest that they have π* character in all kinds of solvents. However, in the case of the p-amino-substituted benzophenones (ABPs), the nature of the S1 state, whether it is n–π* or π–π*, depends on the nature of the solvent and the identity of the substituent groups. The lowest excited triplet (T1) state of BP has nπ* character in all kinds of solvents and hence phosphorescence decay is short (a few ms). The T1 state character of HOBP and ABP’s are solvent dependent. In a few cases dual exponential decay of phosphorescence indicates that n–π* and π–π* triplet states lie close to each other. The π–π* type of T1 state has longer phosphorescence lifetime (a few tens of ms). Investigations of the ultrafast relaxation dynamics of 4-N,N-dimethylaminobenzophenoene (DMABP) in different kinds of solvents of varying polarities and viscosities reveal that conversion of the locally excited (LE) state to the twisted intramolecular charge transfer (TICT) state by twisting of the dimethylanilino group is the major process, which is responsible for the efficient non-radiative relaxation mechanism of the S1 state of this molecule and solvation dynamics plays a minor role in it. In self-quenching interaction between the triplet state and its ground state, the n–π* kind of T1 state plays the major role and no triplet exciplex is involved as an intermediate. The T1 state of BP is equally reactive towards hydrogen atom abstraction reaction with the ground state of each of the ABPs either by direct hydrogen atom transfer or by a chargetransfer-coupled proton-transfer mechanism. Exciplex formation has been observed only in the case of the reaction between the T1 state of BP and DMABP.

Journal

Research on Chemical IntermediatesSpringer Journals

Published: Jan 1, 2005

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