Webb2 jan. 1998 · In contrast, a typical calculated photolysis rate constant for O 3 to generate O(1 D) at 290 to 320 nm is 7.2 × 10 –6 s –1 at a solar zenith angle of 60°. This comparison suggests that the effective light intensity in the chamber experiments is about 110 times that in the atmosphere at a solar zenith angle of 60°. Webb1 sep. 1962 · The photolysis of diazoacetylchymotrypsin. SINGH A, THORNTON ER, WESTHEIMER FH The Journal of Biological Chemistry , 01 Sep 1962, 237: 3006-3008 PMID: 13913310 Share this article Abstract No abstract provided. Citations & impact Impact metrics 55 Citations Jump to Citations Citations of article over time Alternative metrics …
Interactions of a photo-affinity ATP analog with cation-stimulated ...
Webb9 jan. 2014 · Photolysis results in the creation of highly reactive intermediates, mainly carbenes and nitrenes, which will form covalent bonds with receptor proteins and thereby covalently attach the ligand at their receptor-binding site. ... The photolysis of diazoacetylchymotrypsin. J. Biol. Chem.237(9), ... WebbPhotolysis diazo groups Kirmse and Horner160 have shown that the quantum yield, in photolysis with monochromatic light, of C6H5COCHN2 is lowered considerably by the presence of additional double bonds in conjugation with the carbonyl groups and by para- and me aroyl groups attached to the carbon atom of the diazo group. … can rice noodles be used in soup
Photostability and interaction of ascorbic acid in cream …
WebbPhotodissociation, photolysis, photodecomposition, or photofragmentationis a chemical reactionin which moleculesof a chemical compoundare broken down by photons. It is defined as the interaction of one or more photons with one target molecule. Photodissociation is not limited to visible light. WebbRead the latest articles of Journal of Biological Chemistry at ScienceDirect.com, Elsevier’s leading platform of peer-reviewed scholarly literature WebbThe Photolysis of Diazo- acetylchymotrypsin* AJAIB SINGH, EDWARD R. THORNTON, AND F. H. WESTHEIMER From the James Bryant Conant Laboratory, Harvard University Cambridge 58, Massachusetts flanigan and byrd