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  1. B200 工学部/工学研究科
  2. B200a 雑誌掲載論文
  3. 学術雑誌

Macromolecular helicity induction and static helicity memory of poly(biphenylylacetylene)s bearing aromatic pendant groups and their use as chiral stationary phases for high‐performance liquid chromatography

http://hdl.handle.net/2237/0002002161
0cce06c6-6ab9-4700-88cc-5cdb3bfcef3c
名前 / ファイル ライセンス アクション
Ikai-rev.pdf Ikai-rev.pdf (831 KB)
 Download is available from 2023/1/31.
Item type itemtype_ver1(1)
公開日 2022-03-08
タイトル
タイトル Macromolecular helicity induction and static helicity memory of poly(biphenylylacetylene)s bearing aromatic pendant groups and their use as chiral stationary phases for high‐performance liquid chromatography
言語 en
著者 Ikai, Tomoyuki

× Ikai, Tomoyuki

en Ikai, Tomoyuki

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Okuda, Shogo

× Okuda, Shogo

en Okuda, Shogo

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Yashima, Eiji

× Yashima, Eiji

en Yashima, Eiji

Search repository
アクセス権
アクセス権 embargoed access
アクセス権URI http://purl.org/coar/access_right/c_f1cf
権利
言語 en
権利情報 "This is the peer reviewed version of the following article: [ Ikai, T, Okuda, S, Yashima, E. Macromolecular helicity induction and static helicity memory of poly(biphenylylacetylene)s bearing aromatic pendant groups and their use as chiral stationary phases for high-performance liquid chromatography. Chirality. 2022; 34( 2): 306- 316. doi:10.1002/chir.23399], which has been published in final form at [https://doi.org/10.1002/chir.23399]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited."
内容記述
内容記述 Two novel poly(biphenylylacetylene)s (PBPAs) bearing achiral alkylphenyl groups at the 4′-position of the biphenyl pendant through ester linkers with different sequences were synthesized by the rhodium-catalyzed polymerization of the corresponding monomers. The influence of the alkylphenyl pendants and the ester sequences on the macromolecular helicity induction and subsequent static helicity memory was investigated. In addition, the chiral recognition ability as chiral stationary phases for high-performance liquid chromatography of the helicity-memorized PBPAs was also examined. Both polymers formed almost perfect right- and left-handed helical conformations through noncovalent chiral interactions with enantiomeric alcohols, and their induced macromolecular helicities were completely retained (“memorized”) after removal of the helix inducer. A PBPA bearing a 4-n-butylphenoxycarbonyl pendant group with a static helicity memory showed a remarkably high chiral recognition ability toward a wide variety of chiral aromatics, including simple point chiral compounds, axially chiral biaryls, a chiral spiro compound, helicenes, and planar chiral cyclophanes, particularly under the reversed-phase conditions.
言語 en
内容記述タイプ Abstract
出版者
言語 en
出版者 Wiley
言語
言語 eng
資源タイプ
資源タイプresource http://purl.org/coar/resource_type/c_6501
タイプ journal article
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
関連情報
関連タイプ isVersionOf
関連識別子
識別子タイプ DOI
関連識別子 https://doi.org/10.1002/chir.23399
収録物識別子
収録物識別子タイプ PISSN
収録物識別子 0899-0042
書誌情報 en : Chirality

巻 34, 号 2, p. 306-316, 発行日 2022-02
ファイル公開日
日付 2023-02-01
日付タイプ Available
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