A new application about (1S,2S)-Cyclohexane-1,2-diamine

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.Recommanded Product: 21436-03-3, you can also check out more blogs about21436-03-3

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.21436-03-3, Name is (1S,2S)-Cyclohexane-1,2-diamine, molecular formula is C6H14N2. In a Article,once mentioned of 21436-03-3, Recommanded Product: 21436-03-3

Electrochemical oxidation is described as a very efficient polymerization procedure for the heterogenization of metallic chiral catalysts. From chromium chiral complexes based on salen-thiophene ligands, this methodology provided an efficient access to various polymers. Recovered as insoluble powders, these materials were tested in different enantioselective heterogeneous catalytic reactions. Structural modifications were introduced on the salen core in order to evaluate their influence on redox polymer properties and on the enantioselectivity of the catalysis. Electrochemical experiments showed the particular stability of these deposited materials at the electrode surface and SEM analyses suggested the influence of the electropolymerization conditions on their morphology.

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.Recommanded Product: 21436-03-3, you can also check out more blogs about21436-03-3

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare