Jiang, Qiuju et al. published their research in Nano Energy in 2022 | CAS: 128-08-5

1-Bromopyrrolidine-2,5-dione (cas: 128-08-5) belongs to organobromine compounds. Bromine is more electronegative than carbon (2.9 vs 2.5). Consequently, the carbon in a carbon–bromine bond is electrophilic, i.e. alkyl bromides are alkylating agents. The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.Safety of 1-Bromopyrrolidine-2,5-dione

Reducing steric hindrance around electronegative atom in polymer simultaneously enhanced efficiency and stability of organic solar cells was written by Jiang, Qiuju;Han, Pengwei;Ning, Haijun;Jiang, Jiaquan;Chen, Hui;Xiao, Yonghong;Ye, Chun-Rong;Chen, Jinming;Lin, Man;He, Feng;Huang, Xiao-Chun;Wu, Qinghe. And the article was included in Nano Energy in 2022.Safety of 1-Bromopyrrolidine-2,5-dione This article mentions the following:

Uncovering the underlying rules that determine efficiency and device stability of polymer donors is crucially important for future rational design of new materials. By reducing bulkiness of alkyl chain in NTI, we synthesized polymer donor PNTB-HD. The PNTB-HD:N3 based photovoltaic device exhibits the highest PCE of 18.15% that is among the best efficiency in binary devices. More encouragingly, it demonstrates much better device thermal stability than PNTB-2T and the most widely used polymer PM6. Compared with PNTB-2T, PNTB-HD has more condensed packing and stronger tendency to preassembly in chloroform solution that is reason for simultaneously enhancement of efficiency and thermal stability. Single crystal data further revealed reducing alkyl chain bulkiness in NTI could significantly enhance short interaction of C=O…H-C between adjacent mols. that provide useful information to understand the phys. property variation of two polymers. This study revealed reducing steric hindrance around electroneg. atom is an effective strategy for designing high-performance polymers donors. In the experiment, the researchers used many compounds, for example, 1-Bromopyrrolidine-2,5-dione (cas: 128-08-5Safety of 1-Bromopyrrolidine-2,5-dione).

1-Bromopyrrolidine-2,5-dione (cas: 128-08-5) belongs to organobromine compounds. Bromine is more electronegative than carbon (2.9 vs 2.5). Consequently, the carbon in a carbon–bromine bond is electrophilic, i.e. alkyl bromides are alkylating agents. The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.Safety of 1-Bromopyrrolidine-2,5-dione

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary