For experimental details of the synthesis and analytical data of compounds 3, 5, 6, and 8, 1H and 13C NMR, and absorption and emission spectra of compounds 5, 6, and 8, solid state emission spectra of compounds 5 and 6, X-ray structural data of compound 5a, and DFT/TDDFT calculations of compounds 5 and 6, see below.
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Emission solvatochromic, solid-state and aggregation-induced emissive α-pyrones and emission-tuneable 1H-pyridines by Michael addition–cyclocondensation sequences
Natascha Breuer, Irina Gruber, Christoph Janiak and Thomas J. J. Müller
Beilstein J. Org. Chem. 2019, 15, 2684–2703. https://doi.org/10.3762/bjoc.15.262
How to Cite
Breuer, N.; Gruber, I.; Janiak, C.; Müller, T. J. J. Beilstein J. Org. Chem. 2019, 15, 2684–2703. doi:10.3762/bjoc.15.262
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Citations to This Article
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- Ji Ram, V.; Goel, A.; Pratap, R. Application of pyranones in material sciences. Isolated Pyranones; Elsevier, 2022; pp 247–252. doi:10.1016/b978-0-12-821216-5.00009-1
- Nguyen Tien, T. A.; Miliutina, M.; Radolko, J.; Thom, R.; Dang, T. T.; Ehlers, P.; Langer, P. Synthesis of chromeno[2,3-c]pyrrol-9(2H)-ones by domino Michael-Claisen-SNAr reactions of amino acid esters with 2-chlorophenylpropynones. Tetrahedron 2022, 104, 132608. doi:10.1016/j.tet.2021.132608
- Olutas, M.; Sağırlı, A. Solvatochromic and solid-state emissive azlactone-based AIEE-active organic dye: Synthesis, photophysical properties and color-conversion LED application. Journal of Molecular Liquids 2020, 313, 113482. doi:10.1016/j.molliq.2020.113482