A new application about 2,2-Biphenol

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.Product Details of 1806-29-7, you can also check out more blogs about1806-29-7

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1806-29-7, Name is 2,2-Biphenol, molecular formula is C12H10O2. In a Article,once mentioned of 1806-29-7, Product Details of 1806-29-7

Synthesis and study of an ortho-phenol polymer, a highly functionalized polyphenylene, have been conducted. A dibromo ortho-biphenol monomer was synthesized and its homocoupling in the presence of Ni(1,5-cyclooctadiene)2 followed by hydrolysis led to the formation of an ortho-phenol polymer. This polymer was soluble in common organic solvents. It was characterized by gel permeation chromatography, UV-vis, IR, 1H and 13C NMR spectroscopic methods. The use of this polymer in the Lewis acid-catalyzed reaction of phenylacetylene with benzaldehyde in the presence of diethylzinc was studied. It was found that the polymer when treated with 1/4 equiv. (relative to the phenol unit of the polymer) of Ti(OiPr)4 generated a much more active Lewis acid catalyst than when treated with excess Ti(OiPr)4. This indicates that different types of catalytic sites in the polymer have been produced under these conditions.

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.Product Details of 1806-29-7, you can also check out more blogs about1806-29-7

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare