Characterization of Chiral Carbonaceous Nanotubes Prepared from Four Coiled Tubular 4,4'-biphenylene-silica Nanoribbons

Four dipeptides derived from phenylalanine were synthesized, which can self-assemble into twisted nanoribbon in deionized water. The handedness of the organic self-assemblies was controlled by the chirality of the phenylalanine at the terminals. Coiled 4,4'-biphenylene bridged polybissilsesquio...

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Main Authors: Shuwei Lin, Yitai Fu, Yunsen Sang, Yi Li, Baozong Li, Yonggang Yang
Format: Article
Language:English
Published: AIMS Press 2014-04-01
Series:AIMS Materials Science
Subjects:
Online Access:http://www.aimspress.com/Materials/article/166/fulltext.html
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author Shuwei Lin
Yitai Fu
Yunsen Sang
Yi Li
Baozong Li
Yonggang Yang
author_facet Shuwei Lin
Yitai Fu
Yunsen Sang
Yi Li
Baozong Li
Yonggang Yang
author_sort Shuwei Lin
collection DOAJ
description Four dipeptides derived from phenylalanine were synthesized, which can self-assemble into twisted nanoribbon in deionized water. The handedness of the organic self-assemblies was controlled by the chirality of the phenylalanine at the terminals. Coiled 4,4'-biphenylene bridged polybissilsesquioxane tubular nanoribbons were prepared using the organic self-assemblies as the templates. The circular dichroism spectra indicated that the biphenylene rings preferred to twist in one-handedness within the walls of the samples. After carbonization and removal of silica, single-handed coiled carbonaceous tubular nanoribbons were obtained. The Raman spectra indicated that the carbon was amorphous. The diffuse reflectance circular dichroism spectra indicated the tubular carbonaceous nanoribbons exhibited optical activity.
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spelling doaj.art-25c2e4a68ef44154a1ca2f458f3fdcb02022-12-22T00:18:08ZengAIMS PressAIMS Materials Science2372-04842014-04-011111010.3934/matersci.2013.1.120140101Characterization of Chiral Carbonaceous Nanotubes Prepared from Four Coiled Tubular 4,4'-biphenylene-silica NanoribbonsShuwei Lin0Yitai Fu1Yunsen Sang2Yi Li3Baozong Li4Yonggang Yang5Jiangsu Key Laboratory of Advanced Functional Polymer Design and Application, Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P. R. ChinaJiangsu Key Laboratory of Advanced Functional Polymer Design and Application, Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P. R. ChinaJiangsu Key Laboratory of Advanced Functional Polymer Design and Application, Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P. R. ChinaJiangsu Key Laboratory of Advanced Functional Polymer Design and Application, Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P. R. ChinaJiangsu Key Laboratory of Advanced Functional Polymer Design and Application, Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P. R. ChinaJiangsu Key Laboratory of Advanced Functional Polymer Design and Application, Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, P. R. ChinaFour dipeptides derived from phenylalanine were synthesized, which can self-assemble into twisted nanoribbon in deionized water. The handedness of the organic self-assemblies was controlled by the chirality of the phenylalanine at the terminals. Coiled 4,4'-biphenylene bridged polybissilsesquioxane tubular nanoribbons were prepared using the organic self-assemblies as the templates. The circular dichroism spectra indicated that the biphenylene rings preferred to twist in one-handedness within the walls of the samples. After carbonization and removal of silica, single-handed coiled carbonaceous tubular nanoribbons were obtained. The Raman spectra indicated that the carbon was amorphous. The diffuse reflectance circular dichroism spectra indicated the tubular carbonaceous nanoribbons exhibited optical activity.http://www.aimspress.com/Materials/article/166/fulltext.htmlSelf-assemblyChiralityNanostructuresSol-gel growthCarbonaceous materials
spellingShingle Shuwei Lin
Yitai Fu
Yunsen Sang
Yi Li
Baozong Li
Yonggang Yang
Characterization of Chiral Carbonaceous Nanotubes Prepared from Four Coiled Tubular 4,4'-biphenylene-silica Nanoribbons
AIMS Materials Science
Self-assembly
Chirality
Nanostructures
Sol-gel growth
Carbonaceous materials
title Characterization of Chiral Carbonaceous Nanotubes Prepared from Four Coiled Tubular 4,4'-biphenylene-silica Nanoribbons
title_full Characterization of Chiral Carbonaceous Nanotubes Prepared from Four Coiled Tubular 4,4'-biphenylene-silica Nanoribbons
title_fullStr Characterization of Chiral Carbonaceous Nanotubes Prepared from Four Coiled Tubular 4,4'-biphenylene-silica Nanoribbons
title_full_unstemmed Characterization of Chiral Carbonaceous Nanotubes Prepared from Four Coiled Tubular 4,4'-biphenylene-silica Nanoribbons
title_short Characterization of Chiral Carbonaceous Nanotubes Prepared from Four Coiled Tubular 4,4'-biphenylene-silica Nanoribbons
title_sort characterization of chiral carbonaceous nanotubes prepared from four coiled tubular 4 4 biphenylene silica nanoribbons
topic Self-assembly
Chirality
Nanostructures
Sol-gel growth
Carbonaceous materials
url http://www.aimspress.com/Materials/article/166/fulltext.html
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