Results 211 to 220 of about 14,703 (275)

Harnessing light energy with molecules. [PDF]

Beilstein J Org Chem
Han GGD, Nielsen MB, Wegner HA.
europepmc   +1 more source

Light-Controlled Folding and Chiroptical Sensing of G-Quadruplex DNA. [PDF]

J Phys Chem Lett
Matusiak A, Trojnar J, Matczyszyn K, Deiana M, Dudek M.   +4 more
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A Bio-Based Chiroptical Overcrowded Alkene From Flavanone: Photoreactivity and Theoretical Investigation. [PDF]

Chemistry
Limawan DH, Combe A, Bongso A, Dwiputra B, Ivansyah AL, Weber RR, Stindt CN, Roswanda R, Feringa BL.   +8 more
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Thermally Bistable Stiff Stilbene Photoswitches and Polymer Applications. [PDF]

Chem Rec
Imato K.
europepmc   +1 more source

Photoswitchable Silver(I) Complex with Anticancer and Antimicrobial Potential. [PDF]

ACS Omega
Kręcigłowa A, Stolarek-Sipior M, Jagielska P, Kamiński K, Skóra M, Gryl M, Sikorski A, Rak J, Nowakowska M, Szczubiałka K.   +9 more
europepmc   +1 more source

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Photoisomerization of Saccharin

The Journal of Organic Chemistry, 2013
Most known applications of saccharin and saccharyl derivatives and their potential for new uses rely on the thermal and photochemical stability of the saccharyl system. Here, we show that saccharin undergoes structural rearrangement when subjected to a narrow-band ultraviolet irradiation.
Duarte, L., Reva, I. D., Cristiano, Maria Lurdes Santos, Fausto, R.   +3 more
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THE PHOTOISOMERIZATION OF RETINAL*

Photochemistry and Photobiology, 1970
Abstract— –Quantum efficiencies have been measured for the photoisomerization of four stereoisomers of retinal (all‐trans, 13‐cis, 11 cis, and 9‐cis) in two solvents at different wavelengths of irradiation and at various temperatures. In heane at 25°C the quantum efficiencies for isomerization at 365 nm are: 9‐cis to trans, 0.5; 13‐cis to trans, 0.4 ...
A, Kropf, R, Hubbard
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Photoisomerization in Rhodopsin

Biochemistry (Moscow), 2001
This article reviews the primary reaction processes in rhodopsin, a photoreceptive pigment for twilight vision. Rhodopsin has an 11-cis retinal as the chromophore, which binds covalently with a lysine residue through a protonated Schiff base linkage.
H, Kandori, Y, Shichida, T, Yoshizawa
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Octatetraene Photoisomerization

Chemical Reviews, 1993
Bryan E. Kohler
exaly   +2 more sources

Photoisomerization of Perfluoroaryltetrahedranes to Perfluoroarylcyclobutadienes

Journal of the American Chemical Society, 2011
Two perfluoroaryl-substituted cyclobutadiene derivatives, 6 and 7, were prepared as air- and moisture-sensitive red solids by the photochemical isomerization of the corresponding tetrahedranes (4 and 5, respectively). Remarkably, the 9,10-dicyanoanthracene-sensitized photochemical reaction of 4 also proceeded, giving 6, and the mechanism of this ...
Yusuke, Inagaki, Masaaki, Nakamoto, Akira, Sekiguchi   +2 more
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