Convenient and Efficient Suzuki Miyaura Coupling Reactions of Meso-Halogenated BODIPYs
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In this study, we synthesized new conjugated BODIPY compounds with potential fluorescence by treated the BODIPY compound containing bromine in the meso position with different boronic acids. BODIPY cores derived from meso position are used in interesting applications such as pH probe and redox sensors.
- Leen, V., Yuan, P., Wang, L., Boens, N., Dehaen, W. (2012). Synthesis of Meso-Halogenated BODIPYs and Access to Meso-Substituted Analogues. Organic Letters, 14 (24) 6150-6153. https://doi.org/10.1021/ol3028225
- Derin, Y., Yılmaz, R. F:, Baydilek, I. H., Atalay, V. E., Ozdemir, A., Tutar,A. (2018). Synthesis Electrochemical/Photophysical Properties and Computational Investigation of 3,5- dialkyl BODIPY Fluorophores. Inorganica Chimica Acta, 482, 130-135. https://doi.org/10.1016/j.ica.2018.06.006
- Lakshmi, V., Ravikanth, M. (2012). Brominated Boron Dipyrrins. Synthesis, Structure, Spectral an Electrochemical Properties. Dalton Transactions, 41, 5903-5911. https://doi.org/10.1039/C2DT00019A
- Suzuki, A. (2002). Cross-coupling Reactions via Organoboranes. Journal of Organometallic Chemistry 653 (1-2) 83-90. https://doi.org/10.1016/S0022-328X(02)01269-X