Extracurricular laboratory: Synthetic route of 110-52-1

When you point to this article, it is believed that you are also very interested in this compound(110-52-1)Application of 110-52-1 and due to space limitations, I can only present the most important information.

Application of 110-52-1. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 1,4-Dibromobutane, is researched, Molecular C4H8Br2, CAS is 110-52-1, about Two new anion exchange membranes based on poly(bis-arylimidazolium) ionenes blend polybenzimidazole. Author is Yu, Na; Dong, Jianhao; Wang, Tingting; Jin, Yaping; Tang, Weiqin; Yang, Jingshuai.

The development of polymer membranes with excellent alk. stability and high hydroxide conductivity is a huge challenge to fuel cells. Herein, two blend membranes based on poly(bis-arylimidazolium)s (i.e. Ppbim and Ptpim) and polybenzimidazole (PBI) are prepared and used as anion exchange membranes. Ppbim and Ptpim ionenes are synthesized from bis-imidazole compounds (i.e. pbim and tpim) and α,α’-dibromo-p-xylene via the Menshutkin reaction, while pbim and tpim are synthesized from 2-phenylbenzimidazole (or 2,4,5-triphenylimidazole) with 1,4-dibromobutane through the nucleophilic substitution reaction. The physicochem. properties such as water uptake, ion exchange capacity, swelling, tensile strength and conductivity can be adjusted by changing the molar ratio of pbim (or tpim) to PBI in the blend membranes. Comparing with Ppbim, Ptpim containing bulky tri-Ph groups exhibits better alk. stability due to the steric hindrance effect of tri-Ph groups. The tech. feasibility of the Ptpim-51%PBI membrane for the anion exchange membrane fuel cell is demonstrated by the polarization curves. This work provides a straightforward method to synthesize water-insoluble ether-free polymers with dicationic groups in the polymer repeat unit.

When you point to this article, it is believed that you are also very interested in this compound(110-52-1)Application of 110-52-1 and due to space limitations, I can only present the most important information.

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