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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.


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ChemInform Abstract: First Synthesis and
✍ Thomas J. J. Mueller 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

First synthesis and electronic propertie
✍ Adam W. Franz; Larisa N. Popa; Thomas J.J. Müller 📂 Article 📅 2008 🏛 Elsevier Science 🌐 French ⚖ 127 KB

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