Electric Literature of 244-76-8, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 244-76-8, Name is 9H-Pyrido[2,3-b]indole, molecular formula is C11H8N2. In a Article，once mentioned of 244-76-8
Carbazole compounds modified with a pyridoindole moiety were examined as thermally stable high triplet energy host materials for tris[1-(2,4-diisopropyldibenzo[b,d]furan-3-yl)-2-phenylimidazole] (Ir(dbi)3) based blue phosphorescent organic light-emitting diodes. A well-known carbazole compound, N,N?-dicarbazolyl-3,5-benzene, was substituted with one or two pyridoindole moieties to develop the thermally stable host materials for Ir(dbi)3 blue triplet emitters. Remarkably high glass transition temperature of 196 C and thermal decomposition temperature of 486 C in addition to high triplet energy of 2.89 eV were achieved by the pyridoindole modification. The pyridoindole modified carbazole compounds also delivered high quantum efficiency of 25.4% in the blue phosphorescent devices by doping Ir(dbi)3.
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.Electric Literature of 244-76-8, you can also check out more blogs about244-76-8
Reference：
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles