Title of article
First synthesis and electronic properties of cyano(oligo)phenothiazines
Author/Authors
Franz، نويسنده , , Adam W. and Popa، نويسنده , , Larisa N. and Müller، نويسنده , , Thomas J.J.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2008
Pages
4
From page
3300
To page
3303
Abstract
(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 spectroscopy and cyclic voltammetry. Cyano(oligo)phenothiazines display large Stokes-shifts (5800–8300 cm−1) and substantial quantum yields (11–27%). Their reversible oxidation potentials are considerably shifted anodically due to the electron-withdrawing character of the cyano group.
Keywords
Microwave chemistry , Cyclovoltammetry , fluorescence , cyanation , PALLADIUM , Phenothiazine
Journal title
Tetrahedron Letters
Serial Year
2008
Journal title
Tetrahedron Letters
Record number
1859252
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