1073340-48-3Relevant academic research and scientific papers
Highly intense fluorescent diarylboron diketonate
Nagai, Atsushi,Kokado, Kenta,Nagata, Yuuya,Arita, Manabu,Chujo, Yoshiki
, p. 8605 - 8607 (2008)
(Chemical Equation Presented) Diarylboron diketonates were successfully prepared by the reaction of 1,3-diketone derivatives and arylboron compounds such as triphenylborane [BPh3] and fluorobis(pentafluorophenyl)borane diethyl etherate [(C6F6)2BF·OEt 2]. The fluorescent emission of their complexes took place depending on the substituent of the arylboron moiety. In particular, a boron 1,3-bis(4-methoxyphenyl)-1,3-diketonate chelated by a strong electron-withdrawing C6F5 group exhibited the most intense fluorescence.
