Selective and efficient synthesis of di-, tri- and tetrasubstituted 1, 10-phenanthrolines
✍ Scribed by Christiane Dietrich-Buchecker; M.Consuelo Jime´nez; Jean-Pierre Sauvage
- Book ID
- 104261285
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 135 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A general synthetic procedure for the preparation of multisubstituted phenanthrolines is presented. Bromination of 1,10-phenanthroline at the 3 and 8 positions, followed by Suzuki coupling reaction and subsequent methylation afford the di-, tri and tetra-substituted phenanthrolines in good yields. These phenanthroline derivatives are useful building blocks in the construction of highly sophisticated molecular architectures.
📜 SIMILAR VOLUMES
## Abstract The synthesis and the photophysical properties of a series of tetrasubstituted phenanthroline (phen) ruthenium complexes of the type [Ru(tbbpy)~2~(phen‐R~4~)]^2+^ (tbbpy = 4,4′‐di‐__tert__‐butyl‐2,2′‐bipyridine; phen = 1,10‐phenanthroline; R represents the substitution at 3‐, 5‐, 6‐ and
## Abstract For Abstract see ChemInform Abstract in Full Text.