Liu, Fan’s team published research in Advanced Functional Materials in 2019 | CAS: 111865-47-5

Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide(cas: 111865-47-5) belongs to organobromine compounds.The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. Product Details of 111865-47-5 The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.

The author of 《Hole Transport Materials Based on 6,12-Dihydroindeno[1,2-b]fluorine with Different Periphery Groups: A New Strategy for Dopant-Free Perovskite Solar Cells》 were Liu, Fan; Wu, Fei; Tu, Zongxiao; Liao, Qiuyan; Gong, Yanbin; Zhu, Linna; Li, Qianqian; Li, Zhen. And the article was published in Advanced Functional Materials in 2019. Product Details of 111865-47-5 The author mentioned the following in the article:

Although several hole-transporting materials (HTMs) have been designed to obtain perovskite solar cells (PSCs) devices with high performance, the dopant-free HTMs for efficient and stable PSCs remain rare. Herein, a rigid planar 6,12-dihydroindeno[1,2-b]fluorine (IDF) core with different numbers of bulky periphery groups to construct dopant-free HTMs of IDF-SFXPh, IDF-DiDPA, and IDF-TeDPA is modified. Thanks to the contributions of the planar IDF core and the twisted SFX periphery groups, the dopant-free IDF-SFXPh-based PSCs device achieves a device performance of 17.6%, comparable to the doped 2,2′,7,7′-tetrakis(N,N-di-p-methoxyphenylamine)-9,9′-spirobifluorene (spiro-OMeTAD)-based device (17.6%), with much enhanced device stability under glovebox and ambient conditions. In the experiment, the researchers used Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide(cas: 111865-47-5Product Details of 111865-47-5)

Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide(cas: 111865-47-5) belongs to organobromine compounds.The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. Product Details of 111865-47-5 The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary