Chiral-mesoporous-polypyrrole nanoparticles: Its chiral recognition abilities and use in enantioselective separationElectronic supplementary information (ESI) available: FT-IR and 1H NMR of CMPPY-GluA (Fig. S1) and CMPPY-Phe (Fig. S2). See DOI: 10.1039/c000232a

Autor: Pradip Paik, Aharon Gedanken, Yitzhak Mastai
Zdroj: Journal of Materials Chemistry; 5/28/2010, Vol. 20 Issue 20, p4085-4093, 9p
Abstrakt: Chiral-mesoporous-polypyrrole (CMPPy) nanoparticles are synthesized by templating chiral block copolymers (CBCs) of poly(ethylene oxide), (PEO) and chiral l-/d- glutamic acid [PEO-b-(l-/d-GluA)10] and blocks of chiral l-/d-phenylalanine [PEO-b-(l-/d-Phe)10]. The well ordered chiral mesopores of nanoparticles are characterized by HRTEM and BET. The CMPPy nanoparticles have well organized pores with sizes ca.3.5–3.7 nm in diameter and with a high surface area. These CMPPy nanoparticles are able to recognize chiral molecules. Using the selective chiral recognition abilities, the chiral resolution of the copolymer-extracted CMPPy nanoparticles and the chiral separation kinetics using a racemic mixture of valine are probed by circular dichroism (CD) and optical polarimetry. Further, the chiral resolution of the CMPPy is confirmed with a racemic mixture of alanine. The chiral selectivity factor is 5.05 for a specific enantiomer which is adsorbed preferably by the CMPPy. These results allow a new approach towards the enantiomeric separation and other enantiomeric applications of novel CMPPy. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index