A new application about (R)-4-Hydroxydinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepine 4-oxide

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Safety of (R)-4-Hydroxydinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepine 4-oxide, you can also check out more blogs about39648-67-4

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.39648-67-4, Name is (R)-4-Hydroxydinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepine 4-oxide, molecular formula is C20H13O4P. In a Article,once mentioned of 39648-67-4, Safety of (R)-4-Hydroxydinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepine 4-oxide

A new method is developed whereby the enantiomeric composition of a chiral analyte is determined by steady-state fluorescence anisotropy. A theoretical model is presented showing that the measured anisotropy of an enantiomeric mixture in the presence of a chiral selector is dependent on the selectivity, the concentration of free selector, and the enantiomeric composition. Furthermore, for a given system the relationship between the measured anisotropy and the enantiomeric composition is predicted to be linear. The prediction of a linear relationship was confirmed experimentally by examining mixed enantiomeric compositions of 1,1?binaphthyl-2,2?-diylhydrogen phosphate in the presence of beta- and alpha-cyclodextrin. The enantiomeric compositions of four solutions of mixed enantiomers were determined based on a 2-point calibration with an average absolute error of less than 2%.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Safety of (R)-4-Hydroxydinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepine 4-oxide, you can also check out more blogs about39648-67-4

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare