Fluorescence-Lifetime Imaging and Super-Resolution Microscopies Shed Light on the Directed- and Self-Assembly of Functional Porphyrins onto Carbon Nanotubes and Flat Surfaces

Detalhes bibliográficos
Autor(a) principal: Mao, Boyang
Data de Publicação: 2017
Outros Autores: Calatayud, David G., Mirabello, Vincenzo, Kuganathan, Navaratnarajah, Ge, Haobo, Jacobs, Robert M. J., Shepherd, Ashley M., Martins, J. A. R., De la Serna, Jorge Bernardino, Hodges, Benjamin J., Botchway, Stanley W., Pascu, Sofia I.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/51137
Resumo: Functional porphyrins have attracted intense attention due to their remarkably high extinction coefficients in the visible region and potential for optical and energy-related applications. Two new routes to functionalised SWNTs have been established using a bulky Zn-II-porphyrin featuring thiolate groups at the periphery. We probed the optical properties of this zinc(II)-substituted, bulky aryl porphyrin and those of the corresponding new nano-composites with single walled carbon nanotube (SWNTs) and coronene, as a model for graphene. We report hereby on: i) the supramolecular interactions between the pristine SWNTs and Zn-II-porphyrin by virtue of pi-pi stacking, and ii) a novel covalent binding strategy based on the Bingel reaction. The functional porphyrins used acted as dispersing agent for the SWNTs and the resulting nanohybrids showed improved dispersibility in common organic solvents. The synthesized hybrid materials were probed by various characterisation techniques, leading to the prediction that supramolecular polymerisation and host-guest functionalities control the fluorescence emission intensity and fluorescence lifetime properties. For the first time, XPS studies highlighted the differences in covalent versus non-covalent attachments of functional metalloporphyrins to SWNTs. Gas-phase DFT calculations indicated that the Zn-II-porphyrin interacts non-covalently with SWNTs to form a donor-acceptor complex. The covalent attachment of the porphyrin chromophore to the surface of SWNTs affects the absorption and emission properties of the hybrid system to a greater extent than in the case of the supramolecular functionalisation of the SWNTs. This represents a synthetic challenge as well as an opportunity in the design of functional nanohybrids for future sensing and optoelectronic applications.
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spelling Fluorescence-Lifetime Imaging and Super-Resolution Microscopies Shed Light on the Directed- and Self-Assembly of Functional Porphyrins onto Carbon Nanotubes and Flat Surfacescarbon nanotubesnanostructuresoptically active materialsself-assemblysuper-resolution STED imagingCiências Naturais::Ciências QuímicasScience & TechnologyFunctional porphyrins have attracted intense attention due to their remarkably high extinction coefficients in the visible region and potential for optical and energy-related applications. Two new routes to functionalised SWNTs have been established using a bulky Zn-II-porphyrin featuring thiolate groups at the periphery. We probed the optical properties of this zinc(II)-substituted, bulky aryl porphyrin and those of the corresponding new nano-composites with single walled carbon nanotube (SWNTs) and coronene, as a model for graphene. We report hereby on: i) the supramolecular interactions between the pristine SWNTs and Zn-II-porphyrin by virtue of pi-pi stacking, and ii) a novel covalent binding strategy based on the Bingel reaction. The functional porphyrins used acted as dispersing agent for the SWNTs and the resulting nanohybrids showed improved dispersibility in common organic solvents. The synthesized hybrid materials were probed by various characterisation techniques, leading to the prediction that supramolecular polymerisation and host-guest functionalities control the fluorescence emission intensity and fluorescence lifetime properties. For the first time, XPS studies highlighted the differences in covalent versus non-covalent attachments of functional metalloporphyrins to SWNTs. Gas-phase DFT calculations indicated that the Zn-II-porphyrin interacts non-covalently with SWNTs to form a donor-acceptor complex. The covalent attachment of the porphyrin chromophore to the surface of SWNTs affects the absorption and emission properties of the hybrid system to a greater extent than in the case of the supramolecular functionalisation of the SWNTs. This represents a synthetic challenge as well as an opportunity in the design of functional nanohybrids for future sensing and optoelectronic applications.S.I.P. and S.W.B. thank The Royal Society and STFC for funding. B.Y.M. thanks the University of Bath for a studentship (ORS). J.B.d.l.S. acknowledges support for a European Union Marie Curie Career Integration Grant. Dr. Rory L. Arrowsmith is thanked for the initial stages of the DFT calculations of the ZnII-porphyrin. Dr. Amy Kieran is thanked for initial experiments in porphyrin synthesis. The authors thank EPSRC National Service for computational chemistry software and High Performance Computational facilities at Imperial College London for support and computational facilities. Professors Jeremy K. M. Sanders and Paul Raithy are acknowledged for training, helpful discussions in supramolecular chemistry, and porphyrin supramolecular chemistry, as well as mentorship to S.I.P. and her group. Dr. Gabriele Kociok-Kohn is thanked for assistance with X-ray diffraction. B.J.H. and S.I.P. thank EPSRC for funding from the CDT in Sustainable Chemical Technologies. The S.I.P. group thanks the EPSRC for funding, as a member of the Centre of Graphene Science. The authors thank EPSRC National Service for Mass Spectrometry at Swansea and EPSRC National Service for Crystallography at Southampton for data collection. The authors also acknowledge the ERC for the Consolidator Grant O2SENSE.info:eu-repo/semantics/publishedVersionWileyUniversidade do MinhoMao, BoyangCalatayud, David G.Mirabello, VincenzoKuganathan, NavaratnarajahGe, HaoboJacobs, Robert M. J.Shepherd, Ashley M.Martins, J. A. R.De la Serna, Jorge BernardinoHodges, Benjamin J.Botchway, Stanley W.Pascu, Sofia I.2017-07-212017-07-21T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/51137eng0947-653910.1002/chem.20160523228444700http://onlinelibrary.wiley.com/doi/10.1002/chem.201605232/abstractinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:52:10Zoai:repositorium.sdum.uminho.pt:1822/51137Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:51:13.964670Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Fluorescence-Lifetime Imaging and Super-Resolution Microscopies Shed Light on the Directed- and Self-Assembly of Functional Porphyrins onto Carbon Nanotubes and Flat Surfaces
title Fluorescence-Lifetime Imaging and Super-Resolution Microscopies Shed Light on the Directed- and Self-Assembly of Functional Porphyrins onto Carbon Nanotubes and Flat Surfaces
spellingShingle Fluorescence-Lifetime Imaging and Super-Resolution Microscopies Shed Light on the Directed- and Self-Assembly of Functional Porphyrins onto Carbon Nanotubes and Flat Surfaces
Mao, Boyang
carbon nanotubes
nanostructures
optically active materials
self-assembly
super-resolution STED imaging
Ciências Naturais::Ciências Químicas
Science & Technology
title_short Fluorescence-Lifetime Imaging and Super-Resolution Microscopies Shed Light on the Directed- and Self-Assembly of Functional Porphyrins onto Carbon Nanotubes and Flat Surfaces
title_full Fluorescence-Lifetime Imaging and Super-Resolution Microscopies Shed Light on the Directed- and Self-Assembly of Functional Porphyrins onto Carbon Nanotubes and Flat Surfaces
title_fullStr Fluorescence-Lifetime Imaging and Super-Resolution Microscopies Shed Light on the Directed- and Self-Assembly of Functional Porphyrins onto Carbon Nanotubes and Flat Surfaces
title_full_unstemmed Fluorescence-Lifetime Imaging and Super-Resolution Microscopies Shed Light on the Directed- and Self-Assembly of Functional Porphyrins onto Carbon Nanotubes and Flat Surfaces
title_sort Fluorescence-Lifetime Imaging and Super-Resolution Microscopies Shed Light on the Directed- and Self-Assembly of Functional Porphyrins onto Carbon Nanotubes and Flat Surfaces
author Mao, Boyang
author_facet Mao, Boyang
Calatayud, David G.
Mirabello, Vincenzo
Kuganathan, Navaratnarajah
Ge, Haobo
Jacobs, Robert M. J.
Shepherd, Ashley M.
Martins, J. A. R.
De la Serna, Jorge Bernardino
Hodges, Benjamin J.
Botchway, Stanley W.
Pascu, Sofia I.
author_role author
author2 Calatayud, David G.
Mirabello, Vincenzo
Kuganathan, Navaratnarajah
Ge, Haobo
Jacobs, Robert M. J.
Shepherd, Ashley M.
Martins, J. A. R.
De la Serna, Jorge Bernardino
Hodges, Benjamin J.
Botchway, Stanley W.
Pascu, Sofia I.
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Mao, Boyang
Calatayud, David G.
Mirabello, Vincenzo
Kuganathan, Navaratnarajah
Ge, Haobo
Jacobs, Robert M. J.
Shepherd, Ashley M.
Martins, J. A. R.
De la Serna, Jorge Bernardino
Hodges, Benjamin J.
Botchway, Stanley W.
Pascu, Sofia I.
dc.subject.por.fl_str_mv carbon nanotubes
nanostructures
optically active materials
self-assembly
super-resolution STED imaging
Ciências Naturais::Ciências Químicas
Science & Technology
topic carbon nanotubes
nanostructures
optically active materials
self-assembly
super-resolution STED imaging
Ciências Naturais::Ciências Químicas
Science & Technology
description Functional porphyrins have attracted intense attention due to their remarkably high extinction coefficients in the visible region and potential for optical and energy-related applications. Two new routes to functionalised SWNTs have been established using a bulky Zn-II-porphyrin featuring thiolate groups at the periphery. We probed the optical properties of this zinc(II)-substituted, bulky aryl porphyrin and those of the corresponding new nano-composites with single walled carbon nanotube (SWNTs) and coronene, as a model for graphene. We report hereby on: i) the supramolecular interactions between the pristine SWNTs and Zn-II-porphyrin by virtue of pi-pi stacking, and ii) a novel covalent binding strategy based on the Bingel reaction. The functional porphyrins used acted as dispersing agent for the SWNTs and the resulting nanohybrids showed improved dispersibility in common organic solvents. The synthesized hybrid materials were probed by various characterisation techniques, leading to the prediction that supramolecular polymerisation and host-guest functionalities control the fluorescence emission intensity and fluorescence lifetime properties. For the first time, XPS studies highlighted the differences in covalent versus non-covalent attachments of functional metalloporphyrins to SWNTs. Gas-phase DFT calculations indicated that the Zn-II-porphyrin interacts non-covalently with SWNTs to form a donor-acceptor complex. The covalent attachment of the porphyrin chromophore to the surface of SWNTs affects the absorption and emission properties of the hybrid system to a greater extent than in the case of the supramolecular functionalisation of the SWNTs. This represents a synthetic challenge as well as an opportunity in the design of functional nanohybrids for future sensing and optoelectronic applications.
publishDate 2017
dc.date.none.fl_str_mv 2017-07-21
2017-07-21T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/51137
url http://hdl.handle.net/1822/51137
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0947-6539
10.1002/chem.201605232
28444700
http://onlinelibrary.wiley.com/doi/10.1002/chem.201605232/abstract
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Wiley
publisher.none.fl_str_mv Wiley
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