Amplification of the stereochemistry of biomolecular adsorbates by deracemization of chiral domains in bent-core liquid crystals.
Amplification of the stereochemistry of biomolecular adsorbates by deracemization of chiral domains in bent-core liquid crystals.
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DOI:
10.1002/adma.201203302
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发表时间:
2013-01-11
影响因子:
29.4
通讯作者:
Takezoe, Hideo
中科院分区:
文献类型:
--
作者:
Lee, Guksik;Carlton, Rebecca J.;Araoka, Fumito;Abbott, Nicholas L.;Takezoe, Hideo
Chirality is a key concept found in both chemistry and biology, with chiral asymmetries observed in many substances such as tartrates [1] and biological helices, eg, DNA, RNA, and polypeptide. Chirality in liquid crystals (LCs) is commonly induced by the presence of optically active chiral molecules, for instance, by doping non-chiral mesogens with chiral molecules. Such chiral LCs typically form helical suprastructures,[2] which can be either one-dimensional (cholesteric, chiral smectic C, and twist grain boundary phases) or threedimensional (blue phases).[2] In this paper, we move to explore the general but challenging idea of using LCs to amplify biomolecular chirality at surfaces. The study was motivated by the proposal that achiral or racemic LCs, in which chirality is induced by external chiral stimuli such as a chiral surface,[3] might, in the long-term, enable the design of new classes of biotic-abiotic interfaces in which the chirality of biomolecules is reported in the organization of the LCs. Herein we explore this idea using bent-core LCs (BCLCs, also known as banana-shaped liquid crystals).[4, 5] Macroscopic optical activity in the non-chiral BCLC systems has been observed in the B2,[6] B4,[7] and dark conglomerate (DC) phases.[8] The B2 phase is a smectic phase with molecules tilted from the layer normal such that the chirality is defined by the relative orientation of the molecular long axis, the direction
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影响因子:
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Caruso, Frank
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