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Enantioseparation on helical poly(diphenylacetylene)s bearing optically-active pendants: Effects of differences in higher-order structures of kinetically-trapped and thermodynamically-stable states on chiral recognition ability.
- Source :
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Journal of chromatography. A [J Chromatogr A] 2022 Jul 19; Vol. 1675, pp. 463164. Date of Electronic Publication: 2022 May 25. - Publication Year :
- 2022
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Abstract
- An optically-active poly(diphenylacetylene) (PDPA) bearing carboxy pendant groups with left-handed helicity memory (M-h-poly-1), synthesized using the noncovalent helicity-induction-and-memory strategy, was converted into a PDPA bearing optically-active pendant groups through an amide bonding (M-h <subscript>KT</subscript> -poly-2S), while maintaining the left-handed helicity memory, by reaction with (S)-1-phenylethylamine ((S)-2) using a condensing reagent at room temperature. Its chiral recognition ability was investigated as a chiral stationary phase (CSP) for high-performance liquid chromatography (HPLC). M-h <subscript>KT</subscript> -poly-2S exhibited significantly different chiral recognition ability towards racemates compared to the previously reported corresponding helical PDPA bearing the same optically-active pendant groups (M-h <subscript>TS</subscript> -poly-2S) (prepared by the reaction of an optically-inactive PDPA bearing carboxy pendants with (S)-2, followed by thermal annealing, to induce a left-handed helical structure in the polymer main chain). Although the main chains of both M-h <subscript>KT</subscript> -poly-2S and M-h <subscript>TS</subscript> -poly-2S formed almost completely left-handed helical structures, their higher-order structures varied slightly, as confirmed by various spectroscopic methods (UV-Vis, circular dichroism (CD), IR, and vibrational CD). M-h <subscript>KT-TS</subscript> -poly-2S, the PDPA formed on the thermal annealing of M-h <subscript>KT</subscript> -poly-2S, exhibited the same higher-order structure and chiral discrimination ability as M-h <subscript>TS</subscript> -poly-2S. Therefore, slight differences in the higher-order structures of the kinetically-trapped metastable state (M-h <subscript>KT</subscript> -poly-2S) and the thermodynamically-stable state (M-h <subscript>TS</subscript> -poly-2S), due to differences in synthetic procedures, significantly impact their chiral recognition abilities as CSPs, even with identical primary structures and helix-sense of the polymer main chain.<br />Competing Interests: Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Katsuhiro Maeda has patent issued to Kanazawa University.<br /> (Copyright © 2022 Elsevier B.V. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 1873-3778
- Volume :
- 1675
- Database :
- MEDLINE
- Journal :
- Journal of chromatography. A
- Publication Type :
- Academic Journal
- Accession number :
- 35660321
- Full Text :
- https://doi.org/10.1016/j.chroma.2022.463164