Controlling supramolecular chirality of two-component hydrogels by J-and H-aggregation of building blocks

While manipulating the helicity of nanostructures is a challenging task, it attracts great research interest on account of its crucial role in better understanding the formation mechanisms of helical systems. For the supramolecular chirality in self-assembly systems, one challenge is how to understa...

Full description

Bibliographic Details
Main Authors: Liu, Guofeng, Sheng, Jianhui, Wu, Hongwei, Yang, Chaolong, Yang, Guangbao, Li, Yongxin, Ganguly, Rakesh, Zhu, Liangliang, Zhao, Yanli
Other Authors: School of Materials Science & Engineering
Format: Journal Article
Language:English
Published: 2020
Subjects:
Online Access:https://hdl.handle.net/10356/137697
_version_ 1826124859644575744
author Liu, Guofeng
Sheng, Jianhui
Wu, Hongwei
Yang, Chaolong
Yang, Guangbao
Li, Yongxin
Ganguly, Rakesh
Zhu, Liangliang
Zhao, Yanli
author2 School of Materials Science & Engineering
author_facet School of Materials Science & Engineering
Liu, Guofeng
Sheng, Jianhui
Wu, Hongwei
Yang, Chaolong
Yang, Guangbao
Li, Yongxin
Ganguly, Rakesh
Zhu, Liangliang
Zhao, Yanli
author_sort Liu, Guofeng
collection NTU
description While manipulating the helicity of nanostructures is a challenging task, it attracts great research interest on account of its crucial role in better understanding the formation mechanisms of helical systems. For the supramolecular chirality in self-assembly systems, one challenge is how to understand the origin of supramolecular chirality and inherent helicity information on nanostructures regulated by functionality-oriented stacking modes (such as J- and H-aggregation) of building blocks. Herein, two-component hydrogels were prepared by phenylalanine-based enantiomers and achiral bis(pyridinyl) derivatives, where helical nanofibers with inverse handedness as well as controllable helical pitch and diameter were readily obtained through stoichiometric coassembly of these building blocks. The helix inversion was achieved by the transition between the J- and H-aggregation of bis(pyridinyl) derivatives, which was collectively confirmed by circular dichroism, scanning electron microscopy, Fourier transform infrared spectroscopy, and single X-ray crystallography. Interestingly, the helical coassemblies with opposite handedness could be obtained not only from the enantiomeric building blocks but also from the chiral monomers with the same configurational chirality by exchanging achiral additives. This work provides insight into the origin and helicity inversion of supramolecular chirality in molecular self-assembly systems and may shine light on the precise fabrication of chiral nanostructures for potential applications in smart display devices, optoelectronics, and biological systems.
first_indexed 2024-10-01T06:27:15Z
format Journal Article
id ntu-10356/137697
institution Nanyang Technological University
language English
last_indexed 2024-10-01T06:27:15Z
publishDate 2020
record_format dspace
spelling ntu-10356/1376972020-06-01T10:01:44Z Controlling supramolecular chirality of two-component hydrogels by J-and H-aggregation of building blocks Liu, Guofeng Sheng, Jianhui Wu, Hongwei Yang, Chaolong Yang, Guangbao Li, Yongxin Ganguly, Rakesh Zhu, Liangliang Zhao, Yanli School of Materials Science & Engineering School of Physical and Mathematical Sciences Science::Chemistry Chirality Nanostructures While manipulating the helicity of nanostructures is a challenging task, it attracts great research interest on account of its crucial role in better understanding the formation mechanisms of helical systems. For the supramolecular chirality in self-assembly systems, one challenge is how to understand the origin of supramolecular chirality and inherent helicity information on nanostructures regulated by functionality-oriented stacking modes (such as J- and H-aggregation) of building blocks. Herein, two-component hydrogels were prepared by phenylalanine-based enantiomers and achiral bis(pyridinyl) derivatives, where helical nanofibers with inverse handedness as well as controllable helical pitch and diameter were readily obtained through stoichiometric coassembly of these building blocks. The helix inversion was achieved by the transition between the J- and H-aggregation of bis(pyridinyl) derivatives, which was collectively confirmed by circular dichroism, scanning electron microscopy, Fourier transform infrared spectroscopy, and single X-ray crystallography. Interestingly, the helical coassemblies with opposite handedness could be obtained not only from the enantiomeric building blocks but also from the chiral monomers with the same configurational chirality by exchanging achiral additives. This work provides insight into the origin and helicity inversion of supramolecular chirality in molecular self-assembly systems and may shine light on the precise fabrication of chiral nanostructures for potential applications in smart display devices, optoelectronics, and biological systems. NRF (Natl Research Foundation, S’pore) MOE (Min. of Education, S’pore) 2020-04-09T02:59:54Z 2020-04-09T02:59:54Z 2018 Journal Article Liu, G., Sheng, J., Wu, H., Yang, C., Yang, G., Li, Y., . . . Zhao, Y. (2018). Controlling supramolecular chirality of two-component hydrogels by J-and H-aggregation of building blocks. Journal of the American Chemical Society, 140(20), 6467-6473. doi:10.1021/jacs.8b03309 0002-7863 https://hdl.handle.net/10356/137697 10.1021/jacs.8b03309 29733593 2-s2.0-85046822549 20 140 6467 6473 en Journal of the American Chemical Society © 2018 American Chemical Society. All rights reserved.
spellingShingle Science::Chemistry
Chirality
Nanostructures
Liu, Guofeng
Sheng, Jianhui
Wu, Hongwei
Yang, Chaolong
Yang, Guangbao
Li, Yongxin
Ganguly, Rakesh
Zhu, Liangliang
Zhao, Yanli
Controlling supramolecular chirality of two-component hydrogels by J-and H-aggregation of building blocks
title Controlling supramolecular chirality of two-component hydrogels by J-and H-aggregation of building blocks
title_full Controlling supramolecular chirality of two-component hydrogels by J-and H-aggregation of building blocks
title_fullStr Controlling supramolecular chirality of two-component hydrogels by J-and H-aggregation of building blocks
title_full_unstemmed Controlling supramolecular chirality of two-component hydrogels by J-and H-aggregation of building blocks
title_short Controlling supramolecular chirality of two-component hydrogels by J-and H-aggregation of building blocks
title_sort controlling supramolecular chirality of two component hydrogels by j and h aggregation of building blocks
topic Science::Chemistry
Chirality
Nanostructures
url https://hdl.handle.net/10356/137697
work_keys_str_mv AT liuguofeng controllingsupramolecularchiralityoftwocomponenthydrogelsbyjandhaggregationofbuildingblocks
AT shengjianhui controllingsupramolecularchiralityoftwocomponenthydrogelsbyjandhaggregationofbuildingblocks
AT wuhongwei controllingsupramolecularchiralityoftwocomponenthydrogelsbyjandhaggregationofbuildingblocks
AT yangchaolong controllingsupramolecularchiralityoftwocomponenthydrogelsbyjandhaggregationofbuildingblocks
AT yangguangbao controllingsupramolecularchiralityoftwocomponenthydrogelsbyjandhaggregationofbuildingblocks
AT liyongxin controllingsupramolecularchiralityoftwocomponenthydrogelsbyjandhaggregationofbuildingblocks
AT gangulyrakesh controllingsupramolecularchiralityoftwocomponenthydrogelsbyjandhaggregationofbuildingblocks
AT zhuliangliang controllingsupramolecularchiralityoftwocomponenthydrogelsbyjandhaggregationofbuildingblocks
AT zhaoyanli controllingsupramolecularchiralityoftwocomponenthydrogelsbyjandhaggregationofbuildingblocks