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Diversity-oriented approach to functional thiophene dyes by Suzuki coupling-lithiation one-pot sequences

Abstract

Functional thiophenes, e.g. for organic metal-free dye sensitized solar cells (DSSC), are efficiently accessible via a divergent and diversity-oriented synthetic strategy. Here, we present two straightforward, modular and comparative one-pot syntheses of diversely functionalized thiophenes with high yields, namely Suzuki-Lithiation-Formylation-Knoevenagel (SLiForK) sequence and Suzuki-Lithiation-Borylation-Suzuki (SLiBS) sequence, starting from simple molecules. These methods open new avenues to interesting thiophene structure motives with potential applications as pharmaceutical active agents or in molecular electronics, which we have elucidated by a substance library of 21 diversely, mostly unsymmetrically substituted thiophenes. Finally, three novel DSSC dyes were synthesized according the developed one-pot protocols. For illustration DSSC devices sensitized by the selected dyes revealed promising solar cell performances, which were rationalized by photophysical and electrochemical characterization and DFT calculations.

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Publication details

The article was received on 29 Oct 2019, accepted on 03 Dec 2019 and first published on 04 Dec 2019


Article type: Research Article
DOI: 10.1039/C9QO01318K
Org. Chem. Front., 2019, Accepted Manuscript

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    Diversity-oriented approach to functional thiophene dyes by Suzuki coupling-lithiation one-pot sequences

    L. May, S. Daniel and T. J.J. Müller, Org. Chem. Front., 2019, Accepted Manuscript , DOI: 10.1039/C9QO01318K

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