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First synthesis and electronic properties of ring-alkynylated phenothiazines
✍ Scribed by Thomas J.J. Müller
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 226 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
3-mono-and 3,7-bis(alkynylated) phenothiazines 7 and 8 can be readily synthesized from the corresponding phenothiazinyl carbaldehydes. The monoalkynylated phenothiazines 7 are dimerized or cross-coupled to give highly fluorescent phenothiazinyl-terminated redox active dumbbells 9 and 10 that display large Stokes shifts. Compound 9 reveals a strong electronic coupling of the phenothiazinyl moieties according to cyclic voltammetry.
📜 SIMILAR VOLUMES
Oligo)phenothiazinyl nitriles were synthesized in good to very good yields from bromo (oligo)phenothiazines via the Beller cyanation protocol either under conductive or under dielectric heating using NMP as a solvent. Their electronic properties were determined by absorption and emission spectroscop