Understanding of Photo-Induced Reversible Rearrangement from Borepin to Borirane.

Abstract

The first reversible photoisomerization between a borepin and a borirane was reported in the photo-induced reactions of B(npy)Ar2 (npy=2-(naphthalen-1-yl) pyridine, Ar=phenyl or electron rich aryl; S. Wang, et al. Angew. Chem. Int. Ed. 2019, 58, 6683-6687). In this work, the detailed mechanisms of the unprecedented reversible photoisomerization between the borepin (compound a) and the borirane (compound b) of B(npy)Ph2 in the first excited singlet (S1 ) state and the ground (S0 ) state were studied by carrying out calculations with the complete active space self-consistent field (CASSCF) and its second-order perturbation (CASPT2) methods combined with time-dependent density functional theory (TD-DFT). The calculation results show that photoexcitation of a-S0 at 365 nm and b-S0 at 450 nm populate their S1 state with evident charge transfer characteristics. The photoisomerization is triggered in the S1 state and ends in the S0 state, at which the intersection points in a (S1 /S0 )x intersection seam participate in and promote phenyl migration and ring-closure processes. Furthermore, we reveal that the not large energy difference (less than 0.6 eV) and similar conjugation properties of π electrons between a-S0 and b-S0 are responsible for their unique photo-reversible reactivity, compared with those of the isomers of the thermally reversible compound B(ppy)Mes2 . Our results contribute to an understanding of the excited-state reactivity of organoboron compounds and will be useful to support the design of new boron-based photo-responsive materials.