Immobilization of Chiral Ruthenium(II) Complex and Its Catalytic Application in Enantioselective Transfer Hydrogenation
β Scribed by Nie Chun-Fa; Suo Ji-Shuan
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 68 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0256-7660
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β¦ Synopsis
Chiral Ru-BsDPEN, (1R,2R)-N-p-benzenesulfonyl-1,2-diphenylethylenediamine, catalyst has been immobilized on a mesoporous molecular sieve of MCM-41 type successfully. A hybrid mesoporous molecular sieve was synthesized using a precursor bearing benzene group, which in organosilica were sulfonylated and reacted with (1R,2R)-1,2-diphenylethylenediamine and [RuCl 2 (p-cymene)] 2 successively to afford immobilized catalyst. The Brunauer-Emmett-Teller (BET) surface area and Barrett-Joyner-Halenda (BJH) pore size decreased after immobilization of catalyst onto the mesoporous material. Enantioselective transfer hydrogenation of ketones catalyzed by immobilized catalyst showed the highest yield of 22.36% and e.e. value of 31.47% by using acetophenone as substrate when reaction time was 48 and 16 h respectively.
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract A new and safer methodology has been developed for the synthesis of bis(pyrazolβ1βyl)methane ligands (NN). Several ligands containing different phenyl groups on the central carbon atom have been obtained. Ruthenium derivatives of the type [Ru(arene)Cl(NN)]BPh~4~ (arene = benzene, __p__β