Top Picks: new discover of 1H-Indole-6-carboxylic acid

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 1670-82-2

Synthetic Route of 1670-82-2, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1670-82-2, Name is 1H-Indole-6-carboxylic acid, molecular formula is C9H7NO2. In a Article,once mentioned of 1670-82-2

A novel electrochromic material, poly(indole-6-carboxylic acid) (PIn), and its application in electrochromic devices (ECDs) are discussed. PIn was switched between yellow in the reduced state and green in the oxidized state. Electrochromic switching of PIn film shows that it has fast switching time and high optical contrast. ECD based on PIn and poly(3,4-ethylenedioxythiophene) (PEDOT) was also fabricated and characterized. The response time of this device was found to be 1.0 s and the optical contrast was 45%. The coloration efficiency (CE) was calculated to be 510 cm2 C-1. Clear change from green (neutral) to blue-violet color (oxidized) of ECD is demonstrated with robust cycle life. These results provide an avenue for applications of polyindole family in electrochromic devices. Crown Copyright

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 1670-82-2

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