Electric Literature of 16096-33-6, 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. 16096-33-6, Name is 1-Phenyl-1H-indole, molecular formula is C14H11N. In a Article，once mentioned of 16096-33-6
New carbazole- and phenylindole-based low molecular weight derivatives were synthesized and characterized. The compounds could form homogeneous amorphous materials (layers). The electron photoemission spectra of the layers of the synthesized compounds showed ionization potentials of 5.75-5.95 eV. The derivatives were tested as host materials in green and blue phosphorescent OLEDs with tris(2-phenylpyridine)iridium(III) and iridium(III)[bis(4,6- difluorophenyl)-pyridinato-N,C2?]picolinate, correspondingly, as the guests. One of the green OLEDs demonstrated current efficiency of 20.9 cd/A and power efficiency of 6.8 lm/W at 100 cd/m2. An efficient blue OLED showed a maximum brightness of 1160 cd/m2, and current efficiency of 9.4 cd/A with power efficiency of 4 lm/W at 100 cd/m2.
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 16096-33-6, you can also check out more blogs about16096-33-6
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