Chiral molecular nanosilicas

Molecular nanoparticles including polyoxometalates, proteins, fullerenes and polyhedral oligosiloxane (POSS) are nanosized objects with atomic precision, among which POSS derivatives are the smallest nanosilicas. Incorporation of molecular nanoparticles into chiral aggregates either by chiral matric...

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Main Authors: Zong, Zhaohui, Hao, Aiyou, Xing, Pengyao, Zhao, Yanli
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2022
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Online Access:https://hdl.handle.net/10356/160413
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spelling sg-ntu-dr.10356-1604132023-02-28T20:01:39Z Chiral molecular nanosilicas Zong, Zhaohui Hao, Aiyou Xing, Pengyao Zhao, Yanli School of Physical and Mathematical Sciences Science::Chemistry Chirality Amino-Acids Molecular nanoparticles including polyoxometalates, proteins, fullerenes and polyhedral oligosiloxane (POSS) are nanosized objects with atomic precision, among which POSS derivatives are the smallest nanosilicas. Incorporation of molecular nanoparticles into chiral aggregates either by chiral matrices or self-assembly allows for the transfer of supramolecular chirality, yet the construction of intrinsic chirality with atomic precision in discrete molecules remains a great challenge. In this work, we present a molecular folding strategy to construct giant POSS molecules with inherent chirality. Ferrocenyl diamino acids are conjugated by two or four POSS segments. Hydrogen bonding-driven folding of diamino acid arms into parallel β-sheets facilitates the chirality transfer from amino acids to ferrocene and POSS respectively, disregarding the flexible alkyl spacers. Single crystal X-ray structures, density functional theory (DFT) calculations, circular dichroism and vibrational circular dichroism spectroscopy clearly verify the preferential formation of one enantiomer containing chiral molecular nanosilicas. The chiral orientation and chiroptical properties of POSS show pronounced dependence on the substituents of α-amino acids, affording an alternative way to control the folding behavior and POSS chirality in addition to the absolute configuration of amino acids. Through the kinetic nanoprecipitation protocol, one-dimensional aggregation enables chirality transfer from the molecular scale to the micrometer scale, self-assembling into helices in accordance with the packing propensity of POSS in a crystal phase. This work, by illustrating the construction of chiral molecular nanosilicas, paves a new way to obtain discrete chiral molecular nanoparticles for potential chiroptical applications. Published version This work is supported by the Qilu Young Scholarship Funding of Shandong University, the National Natural Science Foundation of China (21872087 and 21901145), the Natural Science Foundation of Jiangsu Province (BK20190209), and the Youth Cross-Scientific Innovation Group of Shandong University (2020QNQT003). 2022-07-21T06:47:54Z 2022-07-21T06:47:54Z 2022 Journal Article Zong, Z., Hao, A., Xing, P. & Zhao, Y. (2022). Chiral molecular nanosilicas. Chemical Science, 13(14), 4029-4040. https://dx.doi.org/10.1039/d2sc00793b 2041-6520 https://hdl.handle.net/10356/160413 10.1039/d2sc00793b 35440995 2-s2.0-85127834038 14 13 4029 4040 en Chemical Science © 2022 The Author(s). Published by the Royal Society of Chemistry. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry
Chirality
Amino-Acids
spellingShingle Science::Chemistry
Chirality
Amino-Acids
Zong, Zhaohui
Hao, Aiyou
Xing, Pengyao
Zhao, Yanli
Chiral molecular nanosilicas
description Molecular nanoparticles including polyoxometalates, proteins, fullerenes and polyhedral oligosiloxane (POSS) are nanosized objects with atomic precision, among which POSS derivatives are the smallest nanosilicas. Incorporation of molecular nanoparticles into chiral aggregates either by chiral matrices or self-assembly allows for the transfer of supramolecular chirality, yet the construction of intrinsic chirality with atomic precision in discrete molecules remains a great challenge. In this work, we present a molecular folding strategy to construct giant POSS molecules with inherent chirality. Ferrocenyl diamino acids are conjugated by two or four POSS segments. Hydrogen bonding-driven folding of diamino acid arms into parallel β-sheets facilitates the chirality transfer from amino acids to ferrocene and POSS respectively, disregarding the flexible alkyl spacers. Single crystal X-ray structures, density functional theory (DFT) calculations, circular dichroism and vibrational circular dichroism spectroscopy clearly verify the preferential formation of one enantiomer containing chiral molecular nanosilicas. The chiral orientation and chiroptical properties of POSS show pronounced dependence on the substituents of α-amino acids, affording an alternative way to control the folding behavior and POSS chirality in addition to the absolute configuration of amino acids. Through the kinetic nanoprecipitation protocol, one-dimensional aggregation enables chirality transfer from the molecular scale to the micrometer scale, self-assembling into helices in accordance with the packing propensity of POSS in a crystal phase. This work, by illustrating the construction of chiral molecular nanosilicas, paves a new way to obtain discrete chiral molecular nanoparticles for potential chiroptical applications.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Zong, Zhaohui
Hao, Aiyou
Xing, Pengyao
Zhao, Yanli
format Article
author Zong, Zhaohui
Hao, Aiyou
Xing, Pengyao
Zhao, Yanli
author_sort Zong, Zhaohui
title Chiral molecular nanosilicas
title_short Chiral molecular nanosilicas
title_full Chiral molecular nanosilicas
title_fullStr Chiral molecular nanosilicas
title_full_unstemmed Chiral molecular nanosilicas
title_sort chiral molecular nanosilicas
publishDate 2022
url https://hdl.handle.net/10356/160413
_version_ 1759856136842903552