Abstract

Many acceptor/donor systems can form excited-state charge-transfer complexes (exciplexes) in photo-induced electron transfer reactions. Exciplex can be detected by their luminescence. In addition, the exciplex luminescence is magneto-sensitive. Here, we employ an approach based on the magnetic field effect on the exciplex of 9,10- dimethylanthracene/N,N-dimethylaniline pair in micro-homogeneous and micro-heterogeneous binary solvents to investigate the effects of the preferential solvation processes on solute molecules in solutions. Micro-homogeneous solvent mixtures of propyl acetate (PA)/butyronitrile (BN) allow for a systematic variation of the static dielectric constants, s , in the range from 6.0 to 24.6. The mixtures of toluene (TO)/dimethylsulfoxide (DMSO) with varying the s values in the range from 4.3 to 15.5 are used as micro-heterogeneous binary solvents. In micro-heterogeneous environment, DMSO molecules get preferentially favoured in the solvation shell, forming micro-clusters surrounding the solute molecules. This solvation effect is reflected in the altered magnetic field effects, lifetimes and dissociation rate constants of the exciplexes.

Highlights

  • Exciplexes, excited-state charge-transfer complexes, are formed in bimolecular photoinduced electron transfer (PET) reactions of excited electron acceptor (A*) and electron donor (D) [1]

  • 2 we show the apparatuses to measure the absorption and fluorescence spectra of acceptor/donor pair of dimethylanthracene/N,N-dimethylaniline before the reader is fully acquainted with the preparations of micro-homogeneous and micro-heterogeneous binary solvents with varying different static dielectric constants

  • By using the Magnetic field effect (MFE) on the exciplexes of DMAnt/DMA system in micro-homogeneous and micro-heterogeneous binary solvents with systematically varying the static dielectric constants, s s, we have been able to demonstrate that the MFE on the exciplex-forming organic acceptor/donor system is a powerful tool to investigate the preferential solvation effects

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Summary

Introduction

Exciplexes, excited-state charge-transfer complexes, are formed in bimolecular photoinduced electron transfer (PET) reactions of excited electron acceptor (A*) and electron donor (D) [1]. The exciplex is formed when the contact distance of A* and D is 6.5 Å while the distance of 10 Å refers to radical ion pair (RIP). The exciplex population can react to a weak external magnetic field [2,3,4, 8,9,10,11,12]. This effect originates from the so-called radical pair mechanism [13, 14]

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