From a 1, 2-azaborinine to large BN-PAHs via electrophilic cyclization: synthesis, characterization and promising optical properties. Issue 1 (20th August 2020)

• Record Type: Journal Article
• Authors: Appiarius, Yannik; Stauch, Tim; Lork, Enno; Rusch, Pascal; Bigall, Nadja C.; Staubitz, Anne
• Is Part Of: Organic chemistry frontiers. Volume 8:Issue 1(2021)
• Page Start: 10
• Page End: 17
• Publication Date: 2020-08-20
• Subjects: Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1039/d0qo00723d
• Languages: English
• ISSNs: 2052-4110

Abstract

Abstract : A synthetic approach towards boron-nitrogen substituted polycyclic aromatic hydrocarbons ( BN -PAHs) via electrophilic cyclization is described and it is shown that the variation of the rings' connectivity may tune the emission wavelengths effectively. Abstract : We present a convergent synthetic route towards boron–nitrogen containing polycyclic aromatic hydrocarbons ( BN -PAHs) that allowed us to synthesize six derivatives. Starting from the conjunction of a 1, 2-azaborinine nucleophile and various aryl electrophiles, the key step was the extension of the aromatic system via an electrophilic ring closure of the respective alkyne precursors. Our route allows the use of substituted PAH precursors to be circumvented, which are often unavailable. Instead, it builds up the BN -PAHs solely from easily accessible monocycles. All derivatives were emissive in solution and solid state with quantum yields up to Φ lum = 0.40 and small Stokes shifts. The emission wavelengths in solid state were notably dependent on the connectivity of the rings. Due to excimer formation in one derivative, its emission was significantly redshifted with a comparatively slow secondary photoluminescence (PL) decay.