PIRKLE-TYPE COLUMNS
Exclusive to Regis, we offer additional chiral phases with Pirkle-Type (or commonly
referred to as brush-type) chemistries. Pirkle chiral stationary phases generally
fall into three classes: π-electron acceptor/π-electron donors, the π-electron
acceptors and the π-electron donors. With Pirkle phases, chiral recognition
occurs at binding sites. Major binding sites are classified as π -basic or π -acidic
aromatic rings, acidic sites, basic sites, and steric interaction sites. Aromatic
rings are potential sites for π - π interactions. Acidic sites supply hydrogens
for potential intermolecular hydrogen bonds; the hydrogen is often an amido
proton (N-H) from an amide, carbamate, urea, or amine. Basic sites, such as
π-electrons, sulfinyl or phosphinyl oxygens, and hydroxy or ether oxygens, may
also be involved in hydrogen bond formation. Steric interactions may also occur
between large groups.
Advantages of the Pirkle-Type Chiral Stationary Phases
• Long lasting, robust columns
• Covalently bonded selector
• Compatible with strong solvents for cleaning
• Compatible with SFC and SMB applications
• High Capacity
*Phenylglycine*
Phenylglycine, a π-acceptor chiral phase, is covalently bonded to 5 µm aminopropyl silica. Phenylglycine columns are available in both L- and D- configurations to invert elution order. This CSP resolves a wide variety of compounds containing π-basic groups, including: aryl-substituted cyclic sulfoxides, bi-β-naphthol and its analogs, α-indanol and α-tetralol analogs, and aryl-substituted hydantoins.
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