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Synthesis, crystal structure, self-assembly of C(60) derivatives bearing rigid pyridine substituents
Microstructures of fullerene derivatives formed via self-assembly strategy facilitate the versatile applications of these zero-dimensional molecules. However, the accurate elucidation of formation mechanism of fullerene microstructures is a challenge issue. A novel fullerene derivative 2 with rigid...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059989/ https://www.ncbi.nlm.nih.gov/pubmed/35518946 http://dx.doi.org/10.1039/c8ra09893j |
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author | Ai, Min Li, Jie Ji, Zijuan Wang, Chuanhui Li, Rui Dai, Wei Chen, Muqing |
author_facet | Ai, Min Li, Jie Ji, Zijuan Wang, Chuanhui Li, Rui Dai, Wei Chen, Muqing |
author_sort | Ai, Min |
collection | PubMed |
description | Microstructures of fullerene derivatives formed via self-assembly strategy facilitate the versatile applications of these zero-dimensional molecules. However, the accurate elucidation of formation mechanism of fullerene microstructures is a challenge issue. A novel fullerene derivative 2 with rigid pyridine substituent was synthesized and characterized by X-ray crystallography. Using the strategy of liquid–liquid interfacial precipitation, self-assembly of 2 affords a micrometer-sized flowerlike and a discoid morphology. Based on the crystal packing of 2, the proper formation mechanism of different morphologies was proposed. Meanwhile, the photoelectrochemical properties of different morphologies of 2 was also unveiled. |
format | Online Article Text |
id | pubmed-9059989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90599892022-05-04 Synthesis, crystal structure, self-assembly of C(60) derivatives bearing rigid pyridine substituents Ai, Min Li, Jie Ji, Zijuan Wang, Chuanhui Li, Rui Dai, Wei Chen, Muqing RSC Adv Chemistry Microstructures of fullerene derivatives formed via self-assembly strategy facilitate the versatile applications of these zero-dimensional molecules. However, the accurate elucidation of formation mechanism of fullerene microstructures is a challenge issue. A novel fullerene derivative 2 with rigid pyridine substituent was synthesized and characterized by X-ray crystallography. Using the strategy of liquid–liquid interfacial precipitation, self-assembly of 2 affords a micrometer-sized flowerlike and a discoid morphology. Based on the crystal packing of 2, the proper formation mechanism of different morphologies was proposed. Meanwhile, the photoelectrochemical properties of different morphologies of 2 was also unveiled. The Royal Society of Chemistry 2019-01-23 /pmc/articles/PMC9059989/ /pubmed/35518946 http://dx.doi.org/10.1039/c8ra09893j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Ai, Min Li, Jie Ji, Zijuan Wang, Chuanhui Li, Rui Dai, Wei Chen, Muqing Synthesis, crystal structure, self-assembly of C(60) derivatives bearing rigid pyridine substituents |
title | Synthesis, crystal structure, self-assembly of C(60) derivatives bearing rigid pyridine substituents |
title_full | Synthesis, crystal structure, self-assembly of C(60) derivatives bearing rigid pyridine substituents |
title_fullStr | Synthesis, crystal structure, self-assembly of C(60) derivatives bearing rigid pyridine substituents |
title_full_unstemmed | Synthesis, crystal structure, self-assembly of C(60) derivatives bearing rigid pyridine substituents |
title_short | Synthesis, crystal structure, self-assembly of C(60) derivatives bearing rigid pyridine substituents |
title_sort | synthesis, crystal structure, self-assembly of c(60) derivatives bearing rigid pyridine substituents |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059989/ https://www.ncbi.nlm.nih.gov/pubmed/35518946 http://dx.doi.org/10.1039/c8ra09893j |
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