Synthesis and Characterization of Modified Polydimethylsiloxane Nanomembrane for Chiral Separation

Polydimethylsiloxane-2-[2-tert-Butoxycarbonylamino-(1H-pyrazol-4-yl)-propionylamino] -3-phenyl-propanoic acid (PDMS-BCPA) is a newly developed stereo-specific membrane that interacts with S configuration of enantiomers as chiral recognition sites. In this study, realization of PDMS-BCPA nanomembrane...

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Published inAdvanced Materials Research Vol. 1105; pp. 231 - 236
Main Authors Masdar, Non Daina, Ismail, Syarifah Nursyimi Azlina Syed, Mahmud, Abdul Hadi, Saim, Norashikin, Mohd Ali, Mohd Tajudin, Tajuddin, Ruziyati, Md Jani, Abd Mutalib
Format Journal Article
LanguageEnglish
Published Zurich Trans Tech Publications Ltd 20.05.2015
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Summary:Polydimethylsiloxane-2-[2-tert-Butoxycarbonylamino-(1H-pyrazol-4-yl)-propionylamino] -3-phenyl-propanoic acid (PDMS-BCPA) is a newly developed stereo-specific membrane that interacts with S configuration of enantiomers as chiral recognition sites. In this study, realization of PDMS-BCPA nanomembrane was achieved via anodized aluminum oxide (AAO) template synthesis approach followed by the attachment of synthesized chiral selector (BCPA) using simple immersion method. The effect of surface modification and the attachment with chiral selector were investigated and characterized using Fourier Transform Infrared spectroscopy (FT-IR), Field Emission Scanning Electron Microscopic (FE-SEM) and Atomic Force Microscopic (AFM) methods. The characterization via these methods indicates the synthesized BCPA as chiral selector was successfully attached onto the PDMS surface. The enantioselectivity of PDMS-BCPA nanomembrane was verified by the separation of alpha cypermethrin enantiomer.
Bibliography:Selected, peer reviewed papers from the 2015 5th International Conference on Advanced Materials Research (ICAMR 2015), January 7-8, 2015, Doha, Qatar
ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISBN:3038354724
9783038354727
ISSN:1022-6680
1662-8985
1662-8985
DOI:10.4028/www.scientific.net/AMR.1105.231