Tuning the Photophysical and Excited State Properties of Phosphorescent Iridium(III) Complexes by Polycyclic Unit Substitution

Abstract Two novel N‐embedded polycyclic units functionalized phosphorescent iridium(III) complexes (Ir‐1 and Ir‐2) with substituents in different positions have been prepared. Complex Ir‐1 bearing the substituent at the 3‐position shows a distinct blue shift single‐peak emission (524 nm) with a hig...

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Main Authors: Cuicui Wu, Qiuxia Li, Xinghua Zhang, Dr. Chao Shi, Gang Li, Mingjie Wang, Kang Li, Prof. Dr. Aihua Yuan
Format: Article
Language:English
Published: Wiley-VCH 2019-03-01
Series:ChemistryOpen
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Online Access:https://doi.org/10.1002/open.201900041
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author Cuicui Wu
Qiuxia Li
Xinghua Zhang
Dr. Chao Shi
Gang Li
Mingjie Wang
Kang Li
Prof. Dr. Aihua Yuan
author_facet Cuicui Wu
Qiuxia Li
Xinghua Zhang
Dr. Chao Shi
Gang Li
Mingjie Wang
Kang Li
Prof. Dr. Aihua Yuan
author_sort Cuicui Wu
collection DOAJ
description Abstract Two novel N‐embedded polycyclic units functionalized phosphorescent iridium(III) complexes (Ir‐1 and Ir‐2) with substituents in different positions have been prepared. Complex Ir‐1 bearing the substituent at the 3‐position shows a distinct blue shift single‐peak emission (524 nm) with a higher luminescence efficiency (ΦPL=42 %) and shorter emission lifetime (τ=282 ns) by comparison with 4‐position substitution based complex Ir‐2 (ΦPL=23 %, τ=562 ns), which exhibits a dual‐peak emission (564 nm and 602 nm), and phosphorescence color can be tuned from green to yellow. In addition, DFT calculations demonstrate that unusual ligand‐to‐metal charge transfer (3LMCT) excited state property can be found in Ir‐2, which is in contrast to metal‐to‐ligand charge transfer (3MLCT) excited state character in Ir‐1. This result can be attribute to strong electron‐donating character and 4‐position substitution effect of the unit.
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spelling doaj.art-c7d8b42175b04b4294b5f32cddab249d2023-07-27T14:18:47ZengWiley-VCHChemistryOpen2191-13632019-03-018333934310.1002/open.201900041Tuning the Photophysical and Excited State Properties of Phosphorescent Iridium(III) Complexes by Polycyclic Unit SubstitutionCuicui Wu0Qiuxia Li1Xinghua Zhang2Dr. Chao Shi3Gang Li4Mingjie Wang5Kang Li6Prof. Dr. Aihua Yuan7School of Environmental and Chemical Engineering Jiangsu University of Science and Technology Zhenjiang 212003 P. R. China., .School of Material Science and Engineering Jiangsu University of Science and Technology Zhenjiang 212003 P. R. China.School of Environmental and Chemical Engineering Jiangsu University of Science and Technology Zhenjiang 212003 P. R. China., .School of Environmental and Chemical Engineering Jiangsu University of Science and Technology Zhenjiang 212003 P. R. China., .School of Environmental and Chemical Engineering Jiangsu University of Science and Technology Zhenjiang 212003 P. R. China., .School of Environmental and Chemical Engineering Jiangsu University of Science and Technology Zhenjiang 212003 P. R. China., .School of Environmental and Chemical Engineering Jiangsu University of Science and Technology Zhenjiang 212003 P. R. China., .School of Environmental and Chemical Engineering Jiangsu University of Science and Technology Zhenjiang 212003 P. R. China., .Abstract Two novel N‐embedded polycyclic units functionalized phosphorescent iridium(III) complexes (Ir‐1 and Ir‐2) with substituents in different positions have been prepared. Complex Ir‐1 bearing the substituent at the 3‐position shows a distinct blue shift single‐peak emission (524 nm) with a higher luminescence efficiency (ΦPL=42 %) and shorter emission lifetime (τ=282 ns) by comparison with 4‐position substitution based complex Ir‐2 (ΦPL=23 %, τ=562 ns), which exhibits a dual‐peak emission (564 nm and 602 nm), and phosphorescence color can be tuned from green to yellow. In addition, DFT calculations demonstrate that unusual ligand‐to‐metal charge transfer (3LMCT) excited state property can be found in Ir‐2, which is in contrast to metal‐to‐ligand charge transfer (3MLCT) excited state character in Ir‐1. This result can be attribute to strong electron‐donating character and 4‐position substitution effect of the unit.https://doi.org/10.1002/open.201900041N-embedded complexespolycyclic unitsphosphorescenceiridium complexesphotophysical properties
spellingShingle Cuicui Wu
Qiuxia Li
Xinghua Zhang
Dr. Chao Shi
Gang Li
Mingjie Wang
Kang Li
Prof. Dr. Aihua Yuan
Tuning the Photophysical and Excited State Properties of Phosphorescent Iridium(III) Complexes by Polycyclic Unit Substitution
ChemistryOpen
N-embedded complexes
polycyclic units
phosphorescence
iridium complexes
photophysical properties
title Tuning the Photophysical and Excited State Properties of Phosphorescent Iridium(III) Complexes by Polycyclic Unit Substitution
title_full Tuning the Photophysical and Excited State Properties of Phosphorescent Iridium(III) Complexes by Polycyclic Unit Substitution
title_fullStr Tuning the Photophysical and Excited State Properties of Phosphorescent Iridium(III) Complexes by Polycyclic Unit Substitution
title_full_unstemmed Tuning the Photophysical and Excited State Properties of Phosphorescent Iridium(III) Complexes by Polycyclic Unit Substitution
title_short Tuning the Photophysical and Excited State Properties of Phosphorescent Iridium(III) Complexes by Polycyclic Unit Substitution
title_sort tuning the photophysical and excited state properties of phosphorescent iridium iii complexes by polycyclic unit substitution
topic N-embedded complexes
polycyclic units
phosphorescence
iridium complexes
photophysical properties
url https://doi.org/10.1002/open.201900041
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