Related Products of 1196-19-6, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.1196-19-6, Name is 3-(Bromomethyl)benzo[b]thiophene, molecular formula is C9H7BrS. In a article£¬once mentioned of 1196-19-6
Synthesis, characterization, and photophysical properties of cyclometalated N-Heterocyclic carbene Platinum(II) complexes
Thiophene and benzothiophene ligands containing N-heterocyclic carbene (NHC) moieties were used to synthesize five and six-membered Pt(II) metallacycles. Ligand scaffolding was synthesized using two methods. The ligands were synthesized using a coupling reaction, utilizing Cu2O as the catalyst or were synthesized using a nucleophilic substitution reaction. The ligands were then metalated by chelate-assisted C?H activation. The synthesis, characterization, reactivity, and photophysical properties of these NHC-functionalized, cyclometalated products are reported.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 1196-19-6
Reference£º
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem