TY - JOUR
T1 - Transient absorption spectroscopy on spiropyran monolayers using nanosecond pump-probe Brewster angle reflectometry
AU - Siebenhofer, Bernhard
AU - Gorelik, Sergey
AU - Lear, Martin J.
AU - Song, Hong Yan
AU - Nowak, Christoph
AU - Hobley, Jonathan
PY - 2013
Y1 - 2013
N2 - 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.
AB - 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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U2 - 10.1039/c3pp25397j
DO - 10.1039/c3pp25397j
M3 - Article
C2 - 23396378
AN - SCOPUS:84876924055
SN - 1474-905X
VL - 12
SP - 848
EP - 853
JO - Photochemical and Photobiological Sciences
JF - Photochemical and Photobiological Sciences
IS - 5
ER -