Bis-cyclometallated iridium(III) complexes bearing pyridineimine and salicylimine ancillary ligands : synthesis, characterization and applications

Two stable diastereomeric atropisomers of a cyclometallated iridium complex containing a pyrene functionalized pyridineimine ligand have been isolated. These are the first fully characterized examples of metal containing atropisomers in which the rotational axis is not between two chelating atoms. T...

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Main Author: Howarth, Ashlee Joanna
Language:English
Published: University of British Columbia 2014
Online Access:http://hdl.handle.net/2429/48396
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spelling ndltd-UBC-oai-circle.library.ubc.ca-2429-483962018-01-05T17:27:30Z Bis-cyclometallated iridium(III) complexes bearing pyridineimine and salicylimine ancillary ligands : synthesis, characterization and applications Howarth, Ashlee Joanna Two stable diastereomeric atropisomers of a cyclometallated iridium complex containing a pyrene functionalized pyridineimine ligand have been isolated. These are the first fully characterized examples of metal containing atropisomers in which the rotational axis is not between two chelating atoms. The atropisomers can be converted thermally via a rocking motion of the pyrene moiety. A new mechanism for enhanced phosphorescence emission in the solid state (EPESS) in cyclometallated Ir complexes with the general formula [Ir(C^N)₂(N^O)] involving distortion of the six-membered chelate ring of the ancillary ligand is proposed. Photophysical and computational studies show that neither π-stacking nor restricted rotation cause the observed EPESS in these complexes and that ligand distortions in the triplet excited state are responsible for EPESS. Bis-cyclometallated Ir(III) complexes with the general formula Ir(ppz)₂(N^XPyrene) where X = N or O are shown. Modifications on the ancillary ligand containing pyrene drastically affect the emission lifetimes observed (2 μs to 104 μs). Extended emission lifetimes in these complexes compared to model complexes result from reversible electronic energy transfer or the observation of pyrene (³LC) phosphorescence. A combination of steady state and time-resolved spectroscopic techniques are used to observe reversible electronic energy transfer between the cyclometallated iridium core and the pyrene moiety in the complexes [Ir(ppz)₂(N^NPyrene)][PF₆]. Replacing the N^NPyrene ligand with an N^OPyrene ligand results in long-lived pyrene phosphorescence. Reversible electronic energy transfer as well as 3pyrene emission is observed and characterized in a PMMA film. Science, Faculty of Chemistry, Department of Graduate 2014-07-17T15:12:39Z 2015-01-31T00:00:00Z 2014 2014-09 Text Thesis/Dissertation http://hdl.handle.net/2429/48396 eng Attribution-NonCommercial-NoDerivs 2.5 Canada http://creativecommons.org/licenses/by-nc-nd/2.5/ca/ University of British Columbia
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language English
sources NDLTD
description Two stable diastereomeric atropisomers of a cyclometallated iridium complex containing a pyrene functionalized pyridineimine ligand have been isolated. These are the first fully characterized examples of metal containing atropisomers in which the rotational axis is not between two chelating atoms. The atropisomers can be converted thermally via a rocking motion of the pyrene moiety. A new mechanism for enhanced phosphorescence emission in the solid state (EPESS) in cyclometallated Ir complexes with the general formula [Ir(C^N)₂(N^O)] involving distortion of the six-membered chelate ring of the ancillary ligand is proposed. Photophysical and computational studies show that neither π-stacking nor restricted rotation cause the observed EPESS in these complexes and that ligand distortions in the triplet excited state are responsible for EPESS. Bis-cyclometallated Ir(III) complexes with the general formula Ir(ppz)₂(N^XPyrene) where X = N or O are shown. Modifications on the ancillary ligand containing pyrene drastically affect the emission lifetimes observed (2 μs to 104 μs). Extended emission lifetimes in these complexes compared to model complexes result from reversible electronic energy transfer or the observation of pyrene (³LC) phosphorescence. A combination of steady state and time-resolved spectroscopic techniques are used to observe reversible electronic energy transfer between the cyclometallated iridium core and the pyrene moiety in the complexes [Ir(ppz)₂(N^NPyrene)][PF₆]. Replacing the N^NPyrene ligand with an N^OPyrene ligand results in long-lived pyrene phosphorescence. Reversible electronic energy transfer as well as 3pyrene emission is observed and characterized in a PMMA film. === Science, Faculty of === Chemistry, Department of === Graduate
author Howarth, Ashlee Joanna
spellingShingle Howarth, Ashlee Joanna
Bis-cyclometallated iridium(III) complexes bearing pyridineimine and salicylimine ancillary ligands : synthesis, characterization and applications
author_facet Howarth, Ashlee Joanna
author_sort Howarth, Ashlee Joanna
title Bis-cyclometallated iridium(III) complexes bearing pyridineimine and salicylimine ancillary ligands : synthesis, characterization and applications
title_short Bis-cyclometallated iridium(III) complexes bearing pyridineimine and salicylimine ancillary ligands : synthesis, characterization and applications
title_full Bis-cyclometallated iridium(III) complexes bearing pyridineimine and salicylimine ancillary ligands : synthesis, characterization and applications
title_fullStr Bis-cyclometallated iridium(III) complexes bearing pyridineimine and salicylimine ancillary ligands : synthesis, characterization and applications
title_full_unstemmed Bis-cyclometallated iridium(III) complexes bearing pyridineimine and salicylimine ancillary ligands : synthesis, characterization and applications
title_sort bis-cyclometallated iridium(iii) complexes bearing pyridineimine and salicylimine ancillary ligands : synthesis, characterization and applications
publisher University of British Columbia
publishDate 2014
url http://hdl.handle.net/2429/48396
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