Upon UV irradiation of the hydrogen-bond confined crystal state of a dithienylhexafluorocyclopentene with (R)-N-phenylethylamide substituents, the photochemical cyclization reaction proceeds diastereoselectively to form the coloured, closed-ring isomer with 97% de.</p
The understanding of the intimate electronic processes in photochromes is essential to optimize the ...
Nine 1-[2-(1-substituted)ethyl-3-benzothienyl]-2-(2-methyl-3-benzothienyl) hexafluorocyclopentenes (...
Diarylethene photochromic switches use light to drive structural changes through reversible electroc...
Upon UV irradiation of the hydrogen-bond confined crystal state of a dithienylhexafluorocyclopentene...
1,2-Dithienylethene compounds (DTEs) reversibly interconvert between two isomeric forms, referred to...
1,2-Dithienylethenes (DTEs) and the related ‘hexatriene’ derivative are a robust family of P-Type ph...
The photophysical properties of a series of dithienylethenes, free or blocked in an ideal photoactiv...
Molecular systems with integrated chemical reactivity and photochromic functions are potentially ben...
Dithienylethene (DTE) molecular photoswitches have shown to be excellent candidates in the design of...
Guiding light: Enantioselectivity is obtained for the photocyclization of a photochromic dithienylet...
The diarylethene chromophore is commonly used in light-triggered molecular switches. The chromophore...
Compounds that undergo reversible photochemical transformations have been investigated for use in op...
The understanding of the intimate electronic processes in photochromes is essential to optimize the ...
The photoswitching and competitive processes of the referent photochromic diarylethene derivative 1,...
A cyanine-based dithienylethene is developed. Its photoisomerization shows that (1) the irradiation ...
The understanding of the intimate electronic processes in photochromes is essential to optimize the ...
Nine 1-[2-(1-substituted)ethyl-3-benzothienyl]-2-(2-methyl-3-benzothienyl) hexafluorocyclopentenes (...
Diarylethene photochromic switches use light to drive structural changes through reversible electroc...
Upon UV irradiation of the hydrogen-bond confined crystal state of a dithienylhexafluorocyclopentene...
1,2-Dithienylethene compounds (DTEs) reversibly interconvert between two isomeric forms, referred to...
1,2-Dithienylethenes (DTEs) and the related ‘hexatriene’ derivative are a robust family of P-Type ph...
The photophysical properties of a series of dithienylethenes, free or blocked in an ideal photoactiv...
Molecular systems with integrated chemical reactivity and photochromic functions are potentially ben...
Dithienylethene (DTE) molecular photoswitches have shown to be excellent candidates in the design of...
Guiding light: Enantioselectivity is obtained for the photocyclization of a photochromic dithienylet...
The diarylethene chromophore is commonly used in light-triggered molecular switches. The chromophore...
Compounds that undergo reversible photochemical transformations have been investigated for use in op...
The understanding of the intimate electronic processes in photochromes is essential to optimize the ...
The photoswitching and competitive processes of the referent photochromic diarylethene derivative 1,...
A cyanine-based dithienylethene is developed. Its photoisomerization shows that (1) the irradiation ...
The understanding of the intimate electronic processes in photochromes is essential to optimize the ...
Nine 1-[2-(1-substituted)ethyl-3-benzothienyl]-2-(2-methyl-3-benzothienyl) hexafluorocyclopentenes (...
Diarylethene photochromic switches use light to drive structural changes through reversible electroc...