The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.224311-51-7, Name is 2-(Di-tert-Butylphosphino)biphenyl, molecular formula is C20H27P. In a Review，once mentioned of 224311-51-7, Product Details of 224311-51-7
The discovery, in the mid 1990s, that certain cobalt, ruthenium and copper complexes could effectively control the radical polymerization of a number of polar olefins, allowing for the facile synthesis of complex macromolecular architectures, fostered an intense search for increasingly better performing catalysts. As a consequence, several metal complexes were designed and tested. This article presents an organized and detailed overview of the most significant developments in the use of transition metal compounds to initiate, mediate and control radical polymerization, i.e., atom transfer radical polymerization or organometallic mediated radical polymerization. The catalysts have been classified according to the group of the periodic table to which the relative metal centers belong. Their catalytic performance, the mechanism with which they are supposed to operate, the structure-reactivity correlations as well as the type of monomers and experimental conditions employed are described. The use and the role of non-transition metal complexes in controlled radical polymerization are also discussed.
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 224311-51-7, you can also check out more blogs about224311-51-7
Reference：
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate