Iridium(III)porphyrin arrays with tuneable photophysical properties

Bibliographic Details
Main Author: Castro, M. Cidália R.
Publication Date: 2020
Other Authors: Sedrine, Nabiha Ben, Monteiro, Teresa, Machado, Ana V.
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10773/37336
Summary: The photophysical properties of iridium(III) porphyrins complexes with two different axial ligands (Cl(CO) and bipyridine (bpy)) in solution and in cellulose acetate polymer matrix were investigated. The axial ligands substitution was made aiming to evaluate the photophysical properties and the solubility in different solvents. Therefore, dissimilar from the free porphyrin, non-polar solvents (as toluene) favours the quantum yield of iridium(III)porphyrins and ligands with a more extended π-conjugated compound as bpy results in higher yields. Moreover, despite all the porphyrins reveals a negative solvatochromism, the substitution of Cl(CO) ligand by bpy ligand exhibits similar solubility either on non-polar or polar solvents. The observed photoluminescence (PL) at room temperature appears at NIR region in contrast to the previously reported iridium(III) porphyrins. Comparing with free porphyrin H2TTP, the red/NIR PL spectra of the iridium(III)porphyrins (either in solution and in the polymer matrix) reveals remarkable changes. Particularly, a more significative decrease of the red/NIR intensity ratio was detected for [Ir(ttp)(bpy)2] 2 where the maxima of the NIR emission can be adjusted under suitable excitation wavelength.
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spelling Iridium(III)porphyrin arrays with tuneable photophysical propertiesIridium porphyrinAxial ligand effectsOptical sensorNIR photoluminescenceThe photophysical properties of iridium(III) porphyrins complexes with two different axial ligands (Cl(CO) and bipyridine (bpy)) in solution and in cellulose acetate polymer matrix were investigated. The axial ligands substitution was made aiming to evaluate the photophysical properties and the solubility in different solvents. Therefore, dissimilar from the free porphyrin, non-polar solvents (as toluene) favours the quantum yield of iridium(III)porphyrins and ligands with a more extended π-conjugated compound as bpy results in higher yields. Moreover, despite all the porphyrins reveals a negative solvatochromism, the substitution of Cl(CO) ligand by bpy ligand exhibits similar solubility either on non-polar or polar solvents. The observed photoluminescence (PL) at room temperature appears at NIR region in contrast to the previously reported iridium(III) porphyrins. Comparing with free porphyrin H2TTP, the red/NIR PL spectra of the iridium(III)porphyrins (either in solution and in the polymer matrix) reveals remarkable changes. Particularly, a more significative decrease of the red/NIR intensity ratio was detected for [Ir(ttp)(bpy)2] 2 where the maxima of the NIR emission can be adjusted under suitable excitation wavelength.Elsevier2023-04-24T14:31:34Z2020-07-05T00:00:00Z2020-07-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/37336eng1386-142510.1016/j.saa.2020.118309Castro, M. Cidália R.Sedrine, Nabiha BenMonteiro, TeresaMachado, Ana V.info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-06T04:45:14Zoai:ria.ua.pt:10773/37336Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T14:19:07.043125Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Iridium(III)porphyrin arrays with tuneable photophysical properties
title Iridium(III)porphyrin arrays with tuneable photophysical properties
spellingShingle Iridium(III)porphyrin arrays with tuneable photophysical properties
Castro, M. Cidália R.
Iridium porphyrin
Axial ligand effects
Optical sensor
NIR photoluminescence
title_short Iridium(III)porphyrin arrays with tuneable photophysical properties
title_full Iridium(III)porphyrin arrays with tuneable photophysical properties
title_fullStr Iridium(III)porphyrin arrays with tuneable photophysical properties
title_full_unstemmed Iridium(III)porphyrin arrays with tuneable photophysical properties
title_sort Iridium(III)porphyrin arrays with tuneable photophysical properties
author Castro, M. Cidália R.
author_facet Castro, M. Cidália R.
Sedrine, Nabiha Ben
Monteiro, Teresa
Machado, Ana V.
author_role author
author2 Sedrine, Nabiha Ben
Monteiro, Teresa
Machado, Ana V.
author2_role author
author
author
dc.contributor.author.fl_str_mv Castro, M. Cidália R.
Sedrine, Nabiha Ben
Monteiro, Teresa
Machado, Ana V.
dc.subject.por.fl_str_mv Iridium porphyrin
Axial ligand effects
Optical sensor
NIR photoluminescence
topic Iridium porphyrin
Axial ligand effects
Optical sensor
NIR photoluminescence
description The photophysical properties of iridium(III) porphyrins complexes with two different axial ligands (Cl(CO) and bipyridine (bpy)) in solution and in cellulose acetate polymer matrix were investigated. The axial ligands substitution was made aiming to evaluate the photophysical properties and the solubility in different solvents. Therefore, dissimilar from the free porphyrin, non-polar solvents (as toluene) favours the quantum yield of iridium(III)porphyrins and ligands with a more extended π-conjugated compound as bpy results in higher yields. Moreover, despite all the porphyrins reveals a negative solvatochromism, the substitution of Cl(CO) ligand by bpy ligand exhibits similar solubility either on non-polar or polar solvents. The observed photoluminescence (PL) at room temperature appears at NIR region in contrast to the previously reported iridium(III) porphyrins. Comparing with free porphyrin H2TTP, the red/NIR PL spectra of the iridium(III)porphyrins (either in solution and in the polymer matrix) reveals remarkable changes. Particularly, a more significative decrease of the red/NIR intensity ratio was detected for [Ir(ttp)(bpy)2] 2 where the maxima of the NIR emission can be adjusted under suitable excitation wavelength.
publishDate 2020
dc.date.none.fl_str_mv 2020-07-05T00:00:00Z
2020-07-05
2023-04-24T14:31:34Z
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/10773/37336
url http://hdl.handle.net/10773/37336
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1386-1425
10.1016/j.saa.2020.118309
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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