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Donor–π–acceptor fluorophores that consist of an electron‐donating amino group and an electron‐accepting triarylborane moiety generally exhibit substantial solvatochromism in their fluorescence while retaining high fluorescence quantum yields even in polar media. Herein, we report a new family of this compound class, which bears ortho‐P(=X)R2‐substituted phenyl groups (X=O or S) as a photodissociative module. The P=X moiety that intramolecularly coordinates to the boron atom undergoes dissociation in the excited state, giving rise to dual emission from the corresponding tetra‐ and tricoordinate boron species. The susceptibility of the systems to photodissociation depends on the coordination ability of the P=O and P=S moieties, whereby the latter facilitates dissociation. The intensity ratios of the dual emission bands are sensitive to environmental parameters, including temperature, solution polarity, and the viscosity of the medium. Moreover, precise tuning of the P(=X)R2 group and the electron‐donating amino moiety led to single‐molecule white emission in solution. [ABSTRACT FROM AUTHOR]

Olefin–borane π‐complexes have been postulated as intermediates for the addition of frustrated Lewis pairs (FLP) to olefins. In the present study, we have employed this weak interaction to modulate the electronic properties of boron‐based π‐electron materials. A series of donor–π–acceptor (D–π–A) fluorophores that contain an alkenyl‐bridged diarylboryl group is synthesized. A crystallographic analysis revealed that the olefin and boron moieties are held in close proximity. Upon addition of a Lewis base to a solution of these D–π–A fluorophores, an FLP‐type addition occurs with concurrent significant changes in the absorption and emission properties. The FLP‐type reaction shifts the reaction site from the Lewis‐acidic boron atom to a carbocationic center, and thereby even facilitates a reaction with bulky Lewis bases. For example, a tricyclohexylphosphine adduct thus generated exhibits temperature‐dependent reversible dissociation/association behavior. These results provide a design strategy for stimuli‐responsive emissive boron‐based materials. [ABSTRACT FROM AUTHOR]

Keywords: Boron; Donor-Acceptor Systems; Excited State; Fluorescence; Stimulus-Responsiveness EN Boron Donor-Acceptor Systems Excited State Fluorescence Stimulus-Responsiveness 1 1 1 06/20/23 20230626 NES 230626 B Dual-emissive b triarylborane-based donor- -acceptor fluorophores sensitive to environmental parameters, including temperature, solvent polarity, and viscosity of the medium, are reported by Shigehiro Yamaguchi and co-workers in their Research Article (e202303725). Boron, Donor-Acceptor Systems, Excited State, Fluorescence, Stimulus-Responsiveness Back Cover: Photodissociative Modules that Control Dual-Emission Properties in Donor- -Acceptor Organoborane Fluorophores (Angew. [Extracted from the article]