## Abstract For Abstract see ChemInform Abstract in Full Text.
Synthesis, structure and nonlinear optical properties of some chiral chromophores derived from l-proline
โ Scribed by Richard D.A Hudson; Anthony R Manning; John F Gallagher; Maria-Helena Garcia; Nelson Lopes; Inge Asselberghs; Roel Van Boxel; Andre Persoons
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 231 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
A series of chiral donor-p-acceptor chromophores with potential for nonlinear optical activity has been synthesised utilising a donor derived from L-proline as the source of chirality. The compounds feature both organic and organometallic acceptor end groups and were assessed for second harmonic generation by the Kurtz powder technique and in one case by hyper-Raleigh scattering.
๐ SIMILAR VOLUMES
New chiral porphyrins were obtained in reasonable yields in three steps, starting from the ฮฑฮฒฮฑฮฒ atropisomer of mesotetrakis(o-aminophenyl)porphyrin (TAPP). These potential catalysts for the enantioselective epoxidation of alkenes were obtained by the reaction of different linkers on the same L- prol