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Transient absorption spectroscopy on spiropyran monolayers using nanosecond pump—probe Brewster angle reflectometry
Author(s) -
Bernhard Siebenhofer,
Sergey Gorelik,
Martin J. Lear,
Hong Song,
Christoph Nowak,
Jonathan Hobley
Publication year - 2013
Publication title -
photochemical and photobiological sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.699
H-Index - 101
eISSN - 1474-9092
pISSN - 1474-905X
DOI - 10.1039/c3pp25397j
Subject(s) - spiropyran , merocyanine , nanosecond , ultrafast laser spectroscopy , photochemistry , monolayer , photochromism , absorption spectroscopy , materials science , spectroscopy , chemistry , microsecond , absorption (acoustics) , analytical chemistry (journal) , optics , laser , physics , nanotechnology , quantum mechanics , composite material , chromatography
Self-assembled monolayers of 11-(3',3'-dimethyl-6,8-dinitrospiro[chromene-2,2'-indoline]-1'-yl) undecanoic acid (amphiphilic spiropyran) at the air-water interface are studied using Brewster angle reflectometry. Transient kinetics of the spiropyran to merocyanine conversion are recorded in a UV-pump, VIS-probe configuration. By varying the probe wavelength using an optical parametric oscillator, we are able to reconstruct absorption spectra of intermediate states with a time-resolution of 10 nanoseconds, limited by the temporal convolution of the two laser pulses. After UV irradiation, spiropyran converts to merocyanine in two stages. The first occurs within a timescale of several tens of nanoseconds and is heavily convoluted with the system response time, whereas the second stage occurs over a few hundred nanoseconds. During the rise time there is a small red shift in the transient absorption spectrum of ~20 nm. We assign the red shift and the slower kinetics to the isomerization of a merocyanine isomer cis about the central methine bond to those that are trans about the same bond.

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