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一种具有弯曲并五苯基面板的芳香族胶束:苝二酰亚胺染料和石墨烯纳米片的封装

An aromatic micelle with bent pentacene-based panels: encapsulation of perylene bisimide dyes and graphene nanosheets.

作者信息

Ito Kenta, Nishioka Tomoya, Akita Munetaka, Kuzume Akiyoshi, Yamamoto Kimihisa, Yoshizawa Michito

机构信息

Laboratory for Chemistry and Life Science , Institute of Innovative Research , Tokyo Institute of Technology , 4259 Nagatsuta, Midori-ku , Yokohama 226-8503 , Japan . Email:

出版信息

Chem Sci. 2020 Jun 5;11(26):6752-6757. doi: 10.1039/d0sc01748e. eCollection 2020 Jul 14.

DOI:10.1039/d0sc01748e
PMID:32953033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7472825/
Abstract

For exploitation of a new class of aromatic micelles, we synthesized a bent pentacene-based amphiphilic molecule through Diels-Alder reaction. The amphiphiles bearing two trimethylammonium tethers assemble into a spherical aromatic micelle, with an average core diameter of 1.5 nm, in water at room temperature. The new aromatic micelle efficiently encapsulates perylene bisimide (PBI) dyes and graphene nanosheets (GNS) in water. The encapsulated PBI dyes form a parallel stacked dimer, exhibiting characteristic absorption and emission bands. In addition, the encapsulated GNS are composed of few-layer graphene sheets with an average lateral size of ∼7 nm, as confirmed by Raman spectroscopy. The resultant, aqueous host-guest complexes are stable even after three weeks in water under ambient conditions.

摘要

为了开发一类新型的芳香族胶束,我们通过狄尔斯-阿尔德反应合成了一种基于并五苯的弯曲两亲分子。带有两个三甲基铵链的两亲分子在室温下于水中组装成平均核心直径为1.5纳米的球形芳香族胶束。这种新型芳香族胶束能在水中有效地包封苝二酰亚胺(PBI)染料和石墨烯纳米片(GNS)。被包封的PBI染料形成平行堆叠的二聚体,呈现出特征性的吸收和发射带。此外,经拉曼光谱证实,被包封的GNS由平均横向尺寸约为7纳米的少层石墨烯片组成。即使在环境条件下于水中放置三周后,所得的水相主客体复合物依然稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/4344fcaad10b/d0sc01748e-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/46ff210c54e6/d0sc01748e-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/fd07462b77f8/d0sc01748e-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/c7d30c59bbaa/d0sc01748e-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/cb0c4f35b838/d0sc01748e-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/426a7fc5ef43/d0sc01748e-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/4344fcaad10b/d0sc01748e-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/46ff210c54e6/d0sc01748e-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/0e8fb0058300/d0sc01748e-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/fd07462b77f8/d0sc01748e-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/c7d30c59bbaa/d0sc01748e-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/cb0c4f35b838/d0sc01748e-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/426a7fc5ef43/d0sc01748e-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150c/7472825/4344fcaad10b/d0sc01748e-f7.jpg

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本文引用的文献

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A Redox-Active Heterocyclic Capsule: Radical Generation, Oxygenation, and Guest Uptake/Release.一种氧化还原活性杂环胶囊:自由基生成、氧化和客体摄取/释放。
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