The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.131274-22-1, Name is Tri-tert-butylphosphonium tetrafluoroborate, molecular formula is C12H28BF4P. In a Article，once mentioned of 131274-22-1, Computed Properties of C12H28BF4P
Oxidative direct arylation polymerization has recently emerged as a simple, mild, and atom economical homopolymerization method; however, the application of this promising method to unsymmetrical or binary monomer systems, where different C-H reactivities are present, is limited. Two random copolymer families of poly(hexyl thiophene-3-carboxylate), herein referred to as poly(3-hexylesterthiophene) (P3HET), featuring either thieno[3,4-c]pyrrole-4,6-dione (TPD) or 4,4?-dimethyl-2,2?-bithiazole (BTz) comonomers are synthesized by oxidative direct arylation polymerization (oxi-DArP) conditions that enable high regioregularities despite the lack of preactivation of the monomers. Through refinement of the reaction parameters and minimization of auxiliary reagent loadings, polymers with good molecular weights are achieved and the feed ratio is closely correlated to the polymer composition. These random copolymers are evaluated by 1H NMR, SEC, UV-Vis, GIXRD, and SCLC hole mobility analyses to determine the compatibility of this emerging synthetic method with increasingly popular random copolymer architectures.
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.Computed Properties of C12H28BF4P, you can also check out more blogs about131274-22-1
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