Results 191 to 200 of about 21,611 (258)

Near-infrared light-activated <i>Z</i>-to-<i>E</i> isomerization of azobenzene <i>via</i> triplet sensitization from PbS quantum dots. [PDF]

Chem Sci
Feng Y, Luan Q, Zhang S, Xi L, Zhang S, Chen K, Liu T, Hou L.   +7 more
europepmc   +1 more source

Wavelength-dependent photofragmentation of pyrazine. [PDF]

Sci Rep
Payra SS, Thakkar P, Lenka Y, Aravind G.
europepmc   +1 more source

Novel Nitroxide-Substituted Hydrazone Switch: Experimental and Theoretical Insights into Photoswitching Behavior. [PDF]

ACS Org Inorg Au
Kotásková L, Nemec I, Herchel R, Santana VT, Neugebauer P.   +4 more
europepmc   +1 more source

A Multiscale Simulation Framework for Elucidating Photochemical Structure-Activity Relationships of Photoswitchable Ligands in Complex Biomolecular Environments. [PDF]

J Chem Inf Model
Bakhtiiari A, Khavani M, Costa GJ, Liang R.   +3 more
europepmc   +1 more source

Molecular Photogearing for Controlling Rotary Motion at the Nanoscale. [PDF]

Chempluschem
Arpa EM, Durbeej B.
europepmc   +1 more source

Beyond-Kasha Photochemistry in a Heteroleptic Platinum-Dithiolene Complex. [PDF]

J Am Chem Soc
Gazzetto M, Artizzu F, Attar SS, Casanova JT, Marchiò L, Pilia L, Monari A, Deplano P, Cannizzo A.   +8 more
europepmc   +1 more source

The first microseconds of the life of excited heptamethine cyanine revealed by femtosecond stimulated Raman spectroscopy. [PDF]

Commun Chem
Glotz G, Polena J, Khan NM, Mukherjee A, Kloz M, Slavíček P, Klán P.   +6 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

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
openaire   +3 more sources

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
openaire   +2 more sources

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
openaire   +2 more sources