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Boron-Doped C(24) Fullerenes for Alkyl Functionalization or Potential Polymerization

[Image: see text] Replacing a single carbon atom in C(24) with a boron atom allows the functionalization of one additional carbon atom. Such a process involves little energy cost with regard to the structure of the fullerene. Two such replacements are required if the fullerenes are to act as “pearls...

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Autores principales: Hurst, M. Owen, Hurst, Michael O., Fortenberry, Ryan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641310/
https://www.ncbi.nlm.nih.gov/pubmed/31457943
http://dx.doi.org/10.1021/acsomega.7b01767
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author Hurst, M. Owen
Hurst, Michael O.
Fortenberry, Ryan C.
author_facet Hurst, M. Owen
Hurst, Michael O.
Fortenberry, Ryan C.
author_sort Hurst, M. Owen
collection PubMed
description [Image: see text] Replacing a single carbon atom in C(24) with a boron atom allows the functionalization of one additional carbon atom. Such a process involves little energy cost with regard to the structure of the fullerene. Two such replacements are required if the fullerenes are to act as “pearls on a string”. This work shows trends for increasingly higher levels of carbon replacement with boron as well as hydrogenation, methylation, and ethylation of a subsequent carbon atom in such a boron-doped small fullerene. Additionally, dimers are shown to be stable, and the linking ethyl groups actually stabilize the overall structure more than when the ethyl groups are on the surface of the structure and are not serving as linkers. Such stringed fullerenes would certainly have applications to materials science if polymers could be made from these stringed pearls and would be suitable for neutron radiation shielding in spacecraft or spacesuits.
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spelling pubmed-66413102019-08-27 Boron-Doped C(24) Fullerenes for Alkyl Functionalization or Potential Polymerization Hurst, M. Owen Hurst, Michael O. Fortenberry, Ryan C. ACS Omega [Image: see text] Replacing a single carbon atom in C(24) with a boron atom allows the functionalization of one additional carbon atom. Such a process involves little energy cost with regard to the structure of the fullerene. Two such replacements are required if the fullerenes are to act as “pearls on a string”. This work shows trends for increasingly higher levels of carbon replacement with boron as well as hydrogenation, methylation, and ethylation of a subsequent carbon atom in such a boron-doped small fullerene. Additionally, dimers are shown to be stable, and the linking ethyl groups actually stabilize the overall structure more than when the ethyl groups are on the surface of the structure and are not serving as linkers. Such stringed fullerenes would certainly have applications to materials science if polymers could be made from these stringed pearls and would be suitable for neutron radiation shielding in spacecraft or spacesuits. American Chemical Society 2018-01-25 /pmc/articles/PMC6641310/ /pubmed/31457943 http://dx.doi.org/10.1021/acsomega.7b01767 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Hurst, M. Owen
Hurst, Michael O.
Fortenberry, Ryan C.
Boron-Doped C(24) Fullerenes for Alkyl Functionalization or Potential Polymerization
title Boron-Doped C(24) Fullerenes for Alkyl Functionalization or Potential Polymerization
title_full Boron-Doped C(24) Fullerenes for Alkyl Functionalization or Potential Polymerization
title_fullStr Boron-Doped C(24) Fullerenes for Alkyl Functionalization or Potential Polymerization
title_full_unstemmed Boron-Doped C(24) Fullerenes for Alkyl Functionalization or Potential Polymerization
title_short Boron-Doped C(24) Fullerenes for Alkyl Functionalization or Potential Polymerization
title_sort boron-doped c(24) fullerenes for alkyl functionalization or potential polymerization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641310/
https://www.ncbi.nlm.nih.gov/pubmed/31457943
http://dx.doi.org/10.1021/acsomega.7b01767
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