First synthesis and electronic properties of diphenothiazine dumbbells bridged by heterocycles
✍ Scribed by Franz, Adam W. ;Popa, Larisa N. ;Rominger, Frank ;Müller, Thomas J. J.
- Book ID
- 118265802
- Publisher
- Royal Society of Chemistry
- Year
- 2009
- Tongue
- English
- Weight
- 396 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1477-0520
- DOI
- 10.1039/b814850c
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
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
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