Synthetic, structural, photophysical and computational studies on 2-arylethynyl-1,3,2-diazaboroles

Weber, Lothar; Werner, Vanessa; Fox, Mark A.; Marder, Todd B.; Schwedler, Stefanie; Brockhinke, Andreas; Hans-Georg, Stammler; Neumann, Beate

Abstract

New 2-arylalkynyl benzo-1,3,2-diazaboroles, 2-(4′-XC6H4C[triple bond, length as m-dash]C)-1,3-Et2-1,3,2-N2BC6H4 (X =Me 2; MeO 3; MeS 4; Me2N 5), were prepared from B-bromodiazaborole, 2-Br-1,3-Et2-1,3,2-N2BC6H4, with the appropriate lithiated arylacetylene, ArC[triple bond, length as m-dash]CLi. Molecular structures of 2, 3 and 5 were determined by X-ray diffraction studies. UV-vis and luminescence spectroscopic studies on these diazaboroles reveal intense blue/violet fluorescence with very large quantum yields of 0.89–0.99 for 2–5. The experimental findings were complemented by DFT and TD-DFT calculations. The Stokes shift of only 2600 cm−1 for 5, compared to Stokes shifts in the range of 5900–7300 cm−1 for 1–4, is partly explained by the different electronic structures found in 5 compared to 1–4 (X = H). The HOMO is mainly located on the aryl group in 5 and on the diazaborolyl group in 1–4 whereas the LUMOs are largely aryl in character for all compounds. Thus, in contrast to other conjugated systems containing three-coordinate boron centers such as B(Mes)2, (Mes = 2,4,6-Me3C6H2), in which the boron serves as a π-acceptor, the 10-π electron benzodiazaborole moiety appears to function as a π-donor moiety.

Citation

Weber, L., Werner, V., Fox, M. A., Marder, T. B., Schwedler, S., Brockhinke, A., …Neumann, B. (2009). Synthetic, structural, photophysical and computational studies on 2-arylethynyl-1,3,2-diazaboroles. Dalton Transactions, 2009(15), 2823-2831. https://doi.org/10.1039/b821208b

• Journal Article Type: Article
• Acceptance Date: Jan 30, 2009
• Publication Date: Apr 1, 2009
• Deposit Date: Dec 14, 2011
• Publicly Available Date: Apr 30, 2015
• Journal: Dalton Transactions
• Print ISSN: 1477-9226
• Electronic ISSN: 1477-9234
• Publisher: Royal Society of Chemistry
• Peer Reviewed: Peer Reviewed
• Volume: 2009
• Issue: 15
• Pages: 2823-2831
• DOI: https://doi.org/10.1039/b821208b
• Public URL: https://durham-repository.worktribe.com/output/1523992