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Piecing Together Large Polycyclic Aromatic Hydrocarbons and Fullerenes: A Combined ChemTEM Imaging and MALDI-ToF Mass Spectrometry Approach

Motivated by their importance in chemistry, physics, astronomy and materials science, we investigate routes to the formation of large polycyclic aromatic hydrocarbon (PAH) molecules and the fullerene C(60) from specific smaller PAH building blocks. The behaviour of selected PAH molecules under elect...

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Autores principales: Gover, R. K. E., Chamberlain, T. W., Sarre, P. J., Khlobystov, A. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238087/
https://www.ncbi.nlm.nih.gov/pubmed/34195176
http://dx.doi.org/10.3389/fchem.2021.700562
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author Gover, R. K. E.
Chamberlain, T. W.
Sarre, P. J.
Khlobystov, A. N.
author_facet Gover, R. K. E.
Chamberlain, T. W.
Sarre, P. J.
Khlobystov, A. N.
author_sort Gover, R. K. E.
collection PubMed
description Motivated by their importance in chemistry, physics, astronomy and materials science, we investigate routes to the formation of large polycyclic aromatic hydrocarbon (PAH) molecules and the fullerene C(60) from specific smaller PAH building blocks. The behaviour of selected PAH molecules under electron (using transmission electron microscopy, TEM) and laser irradiation is examined, where four specific PAHs—anthracene, pyrene, perylene and coronene—are assembling into larger structures and fullerenes. This contrasts with earlier TEM studies in which large graphene flakes were shown to transform into fullerenes via a top-down route. A new combined approach is presented in which spectrometric and microscopic experimental techniques exploit the stabilisation of adsorbed molecules through supramolecular interactions with a graphene substrate and enable the molecules to be characterised and irradiated sequentially. Thereby allowing initiation of transformation and characterisation of the resultant species by both mass spectrometry and direct-space imaging. We investigate the types of large PAH molecule that can form from smaller PAHs, and discuss the potential of a “bottom-up” followed by “top-down” mechanism for forming C(60).
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spelling pubmed-82380872021-06-29 Piecing Together Large Polycyclic Aromatic Hydrocarbons and Fullerenes: A Combined ChemTEM Imaging and MALDI-ToF Mass Spectrometry Approach Gover, R. K. E. Chamberlain, T. W. Sarre, P. J. Khlobystov, A. N. Front Chem Chemistry Motivated by their importance in chemistry, physics, astronomy and materials science, we investigate routes to the formation of large polycyclic aromatic hydrocarbon (PAH) molecules and the fullerene C(60) from specific smaller PAH building blocks. The behaviour of selected PAH molecules under electron (using transmission electron microscopy, TEM) and laser irradiation is examined, where four specific PAHs—anthracene, pyrene, perylene and coronene—are assembling into larger structures and fullerenes. This contrasts with earlier TEM studies in which large graphene flakes were shown to transform into fullerenes via a top-down route. A new combined approach is presented in which spectrometric and microscopic experimental techniques exploit the stabilisation of adsorbed molecules through supramolecular interactions with a graphene substrate and enable the molecules to be characterised and irradiated sequentially. Thereby allowing initiation of transformation and characterisation of the resultant species by both mass spectrometry and direct-space imaging. We investigate the types of large PAH molecule that can form from smaller PAHs, and discuss the potential of a “bottom-up” followed by “top-down” mechanism for forming C(60). Frontiers Media S.A. 2021-06-14 /pmc/articles/PMC8238087/ /pubmed/34195176 http://dx.doi.org/10.3389/fchem.2021.700562 Text en Copyright © 2021 Gover, Chamberlain, Sarre and Khlobystov. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Gover, R. K. E.
Chamberlain, T. W.
Sarre, P. J.
Khlobystov, A. N.
Piecing Together Large Polycyclic Aromatic Hydrocarbons and Fullerenes: A Combined ChemTEM Imaging and MALDI-ToF Mass Spectrometry Approach
title Piecing Together Large Polycyclic Aromatic Hydrocarbons and Fullerenes: A Combined ChemTEM Imaging and MALDI-ToF Mass Spectrometry Approach
title_full Piecing Together Large Polycyclic Aromatic Hydrocarbons and Fullerenes: A Combined ChemTEM Imaging and MALDI-ToF Mass Spectrometry Approach
title_fullStr Piecing Together Large Polycyclic Aromatic Hydrocarbons and Fullerenes: A Combined ChemTEM Imaging and MALDI-ToF Mass Spectrometry Approach
title_full_unstemmed Piecing Together Large Polycyclic Aromatic Hydrocarbons and Fullerenes: A Combined ChemTEM Imaging and MALDI-ToF Mass Spectrometry Approach
title_short Piecing Together Large Polycyclic Aromatic Hydrocarbons and Fullerenes: A Combined ChemTEM Imaging and MALDI-ToF Mass Spectrometry Approach
title_sort piecing together large polycyclic aromatic hydrocarbons and fullerenes: a combined chemtem imaging and maldi-tof mass spectrometry approach
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238087/
https://www.ncbi.nlm.nih.gov/pubmed/34195176
http://dx.doi.org/10.3389/fchem.2021.700562
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