Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups.

ABSTRACT: Three compounds with phenyl (1), 4-tert-butylphenyl (2) and 4-N,N-diphenylaminophenyl (3) groups attached to bis(fluoromesityl)boryl ((FMes)₂B) through B-C bonds have been prepared. The restricted rotation about the B-C bonds of boron-bonded aryl rings in solution has been studied by variable-temperature ¹⁹F NMR spectroscopy, and through-space F-F coupling has been observed for 3 at low temperature. Steric congestion inhibits binding of 1 by Lewis bases DABCO and tBu₃P and the activation of H₂ in their presence. Photophysical and electrochemical studies have been carried out on 2, 3, and an analogue of 3 containing a bis(mesityl)boryl ((Mes)₂B) group, namely 4. Both 2 and 3 show bright emission in nonpolar solvents and in the solid-state, very strong electron-accepting ability as measured by cyclic voltammetry, and good air-stability. In addition, 2 displayed unusually long-lived emission (? = 2.47 s) in 2-MeTHF at 77 K. The much stronger acceptor strength of (FMes)₂B than (Mes)₂B leads to significantly red-shifted emission in solution and the solid state, stronger emission solvatochromism, and significantly lower reduction potentials. Theoretical calculations confirm that 2 and 3 tend to form highly twisted excited states with good conjugation between one FMes group and the boron atom, which correlate well with their blue-shifted solid-state emissions and low k_r values in solution.

SUBMITTER: Zhang Z 

PROVIDER: S-EPMC5586071 | biostudies-literature | 2015 Jan

REPOSITORIES: biostudies-literature