Ultrafast time-resolved spectroscopy of diarylethene-based photoswitchable deoxyuridine nucleosides

Photoswitches based on the diarylethene architecture have been attracting considerable attention for the investigation and control of a variety of biological processes. The reversible photoisomerization reaction between their open- and closed-ring forms can be selectively addressed by irradiation wi...

Full description

Saved in:
Bibliographic Details
Main Authors: Buckup, Tiago (Author) , Sarter, Christopher (Author) , Volpp, Hans-Robert (Author) , Jäschke, Andres (Author) , Motzkus, Marcus (Author)
Format: Article (Journal)
Language:English
Published: November 10, 2015
In: The journal of physical chemistry letters
Year: 2015, Volume: 6, Issue: 23, Pages: 4717-4721
ISSN:1948-7185
DOI:10.1021/acs.jpclett.5b01949
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/acs.jpclett.5b01949
Get full text
Author Notes:Tiago Buckup, Christopher Sarter, Hans-Robert Volpp, Andres Jäschke, Marcus Motzkus
Description
Summary:Photoswitches based on the diarylethene architecture have been attracting considerable attention for the investigation and control of a variety of biological processes. The reversible photoisomerization reaction between their open- and closed-ring forms can be selectively addressed by irradiation with light of two markedly different wavelengths. In this work, the dynamics of the photochromic ring-opening reaction of four novel diarylethene-based photoswitchable deoxyuridine nucleosides is investigated by femtosecond transient absorption. Upon photoexcitation with sub-20 fs pulses in the first absorption band (500 nm), all four photoswitches showed a fast ballistic excited-state deactivation within less than 500 fs toward the S1/S0 conical intersection. Transient data was globally analyzed, and a relaxation kinetic model with a branching between open and closed ring forms without any loss channels was derived. Ring-opening quantum yields, Φr-o, were found to strongly depend on the substituents (R), ranging from 0.64 (dUPSI: R = 2-naphthyl) to 0.30 (dUPSIV: R = 2-pyridyl).
Item Description:Gesehen am 20.10.2020
Physical Description:Online Resource
ISSN:1948-7185
DOI:10.1021/acs.jpclett.5b01949