Pregled bibliografske jedinice broj: 198578
New Pirkle-Type Chiral Stationary Phases with Limited Approach to Silica Surface
New Pirkle-Type Chiral Stationary Phases with Limited Approach to Silica Surface // 29th International Symposium on high performance liquid phase separations and related techniques
Stockholm, Švedska, 2005. (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
New Pirkle-Type Chiral Stationary Phases with Limited Approach to Silica Surface
Autori
Moslavac Forjan, Davorka ; Vinković, Vladimir
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
29th International Symposium on high performance liquid phase separations and related techniques
/ - , 2005
Skup
HPLC 2005
Mjesto i datum
Stockholm, Švedska, 26.06.2005. - 30.06.2005
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
chiral stationary phase; liquid chromatography
Sažetak
Liquid chromatographic resolution of enantiomers on chiral stationary phases (CSPs) has been known as one of the most convenient and accurate tool for evaluating of purity and preparative separation of enantiomers, recently even on industrial scale. Consequently, various CSPs for this purpose have been developed. Pirkle– type CSPs have been known to separate enantiomers by forming energetically different transient diastereomeric p-donor/p-acceptor complexes. For the effective formation of such complexes between the CSP and racemic analyte, Pirkle– type CSPs have been usually designed to contain p-acidic (acceptor) or/and p-basic (donor) aromatic rings. In study presented here we wish to report the process of developing a new chiral stationary phases derived from the selected amino acids. All CSPs contain a strong p-acidic N-3, 5-dinitrobenzoyl group (DNB), which is expected to interact with various aromatic derivatives, and aromatic p-basic or alkyl group which controlled the approach to silica surface. The chiral selector is covalently bound at silica surface with the spacer which is placed behind the chiral center, so that in stationary phase the chiral hole of selector is ideally open for analytes approach. With such structure the chiral selection of CSPs is remained but the achiral interaction with polar silica surface are substantially diminished.
Izvorni jezik
Engleski
Znanstvena područja
Kemija