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Novel benzimidazole salts for lithium ion battery electrolytes: effects of substituents. T. Sriana, E. G. Leggesse, J. C. Jiang , Phys. Chem. Chem. Phys. , 2015 , 17 , 16462

Boratriazines: inducing luminescence through boron incorporation into a terpy-type framework. Muhammad Yousaf, Nathan J. Yutronkie, Raúl Castañeda, Jacob A. Klein, Jaclyn Brusso , New J. Chem. , 2017 , 41 , 12218

[¹⁸F]-Group 13 fluoride derivatives as radiotracers for positron emission tomography. Kantapat Chansaenpak, Boris Vabre, François. P. Gabbaï , Chem. Soc. Rev. , 2016 , 45 , 954

Colorimetric and ratiometric fluorescence sensing of water based on 9-methyl pyrido[3,4-b]indole-boron trifluoride complex. Toshiaki Enoki, Yousuke Ooyama , Dalton Trans. , 2019 , 48 , 2086

[¹⁸F]–NHC–BF3 adducts as water stable radio-prosthetic groups for PET imaging. Kantapat Chansaenpak, Mengzhe Wang, Zhanhong Wu, Rehmat Zaman, Zibo Li, François P. Gabbaï , Chem. Commun. , 2015 , 51 , 12439

Trifluoroborate-modification of both pyridine and N-alkyldiarylamine-based π-conjugated polymer films: tuning the electronic communication and the mean conjugated length based on two types of nitrogen in the conjugated main segments. Shotaro Hayashi, Atsushi Asano, Toshio Koizumi , RSC Adv. , 2013 , 3 , 7375

Synthesis and reactivity of alkynyl boron compounds. Soumilee Nandy, Swagata Paul, Kanak Kanti Das, Parveen Kumar, Debraj Ghorai, Santanu Panda , Org. Biomol. Chem. , 2021 , 19 , 7276

Hydroelementation of diynes. Jędrzej Walkowiak, Jakub Szyling, Adrian Franczyk, Rebecca L. Melen , Chem. Soc. Rev. , 2022 , 51 , 869

Computational study on C–B homolytic bond dissociation enthalpies of organoboron compounds. JiaoYang Wang, WenRui Zheng, LanLan Ding, YingXing Wang , New J. Chem. , 2017 , 41 , 1346

Selection of boron reagents for Suzuki–Miyaura coupling. Alastair J. J. Lennox, Guy C. Lloyd-Jones , Chem. Soc. Rev. , 2014 , 43 , 412