Rational Optimization of Bifunctional Organoboron Catalysts for Versatile Polyethers via Ring-Opening Polymerization of Epoxides was written by Qi, Huan;Xie, Rui;Yang, Guan-Wen;Zhang, Yao-Yao;Xu, Cheng-Kai;Wang, Yuhui;Wu, Guang-Peng. And the article was included in Macromolecules (Washington, DC, United States) in 2022.SDS of cas: 57-55-6 This article mentions the following:
Quaternary ammonium and phosphonium borane bifunctional catalysts have shown high catalytic performance in ring-opening polymerization (ROP) of epoxides to produce polyether. Herein, we systematically investigate a series of well-defined organoboron catalysts by varying the electronic and steric properties of the Lewis acidic boron (B) centers, manipulating the steric hindrance on the ammonium cation (N+), adjusting the distance between B and N+, and regulating the nucleic B number of the catalysts. The investigation on the dinuclear catalysts indicated that the reactivity of a given catalyst could be speculated by its B-N-B angle and the B···B distance. We found that the increase of Lewis acidity and the number of B centers of the organoboron catalysts are useful for a high catalytic activity for ROP of epoxides. The Lewis acidity of the B centers was determined using the acceptor numbers, showing an order of borinane (23.4) > BBN (21.7) > BCy2 (18.8) > Bpin (15.5). Moreover, we demonstrated the production of various telechelic polyols in the presence of different chain transfer agents using the organoboron catalysts. The produced telechelic samples have a well-defined terminal functionality with controllable mol. weight Lastly, these organoboron catalysts were utilized to produce block copolymers, allyl-terminated macromonomers, and random copolymers. In the experiment, the researchers used many compounds, for example, 1,2-Propanediol (cas: 57-55-6SDS of cas: 57-55-6).
1,2-Propanediol (cas: 57-55-6) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.SDS of cas: 57-55-6
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts