Synthetic Route of 16096-33-6, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 16096-33-6, Name is 1-Phenyl-1H-indole, molecular formula is C14H11N. In a Article，once mentioned of 16096-33-6
Acridine and carbazole derived electron donors, 8,8-dimethyl-5-phenyl-8,13-dihydro-5H-indolo[2,3-c]acridine (4IA) and 13,13-dimethyl-11-phenyl-11,13-dihydro-5H-indole[2,3-b]acridine(3IA), were synthesized as strong donor moieties of thermally activated delayed fluorescent (TADF) emitters. The new donor moiety was included in the molecular structure of diphenyltriazine based TADF emitter to study the effect of geometrical structure of the donor on the photophysical and device characteristics of TADF emitters. The 4IA donor was better than the 3IA donor for small singlet-triplet energy splitting and TADF emission. TADF behavior was observed only in the 4IA based TADF emitter due to geometrical structure. A TADF emitter having the 4IA based donor moiety exhibited a blue color coordinate of (0.21, 0.31) and a quantum efficiency of 13.7%.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Synthetic Route of 16096-33-6, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 16096-33-6, in my other articles.
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