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Di-orthometallated triphenyl phosphite iridium complex as a ‘turn-on’ phosphorescent chemodosimeter probe for silver ions
A di-orthometallated triphenyl phosphite iridium complex Ir(dttpit)(phen)Cl (dttpitH2 = tris (2, 4-di-tert-butylphenyl) phosphite, phen = phenanthroline), has been synthesied and characterized. The crystal structure was determined by X-ray crystallography. The photoluminescence spectrum of Ir(dttpit...
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Published in: | Inorganic chemistry communications 2018-12, Vol.98, p.62-67 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A di-orthometallated triphenyl phosphite iridium complex Ir(dttpit)(phen)Cl (dttpitH2 = tris (2, 4-di-tert-butylphenyl) phosphite, phen = phenanthroline), has been synthesied and characterized. The crystal structure was determined by X-ray crystallography. The photoluminescence spectrum of Ir(dttpit)(phen)Cl in CH3CN shows emission maximum at 528 nm. In 0.01 wt% PMMA films, its quantum yields and lifetime are 0.16 and 1.78 μs, respectively. The emission of Ir(dttpit)(phen)Cl at 528 exhibits 1393% enhance upon addition of Ag+ in CH3CN/H20. The ratio of Ir(dttpit)(phen)Cl responding to Ag+ is 1:1, and the limit of detection is 0.13 μM. Ir(dttpit)(phen)Cl is a highly selective chemosensor for Ag+ over other metal ions. The interaction between the chlorine atom and Ag+ is responsible for the highly selective and sensitive phosphorescent senor for Ag+.
A di-orthometallated triphenyl phosphite iridium complex Ir(dttpit)(phen)Cl has been synthesized and fully characterized. The phosphorescence behaviour of Ir(dttpit)(phen)Cl toward different metal cations have also be studied which indicating a strong phosphorescence enhance by Ag+. The interaction ratio with Ag+ is 1:1. [Display omitted]
•An iridium complex with di-orthometallated triphenyl phosphite has been synthesized.•Ir(dttpit)(phen)Cl is a ‘turn-on’ phosphorescent chemodosimeter probe for Ag+.•The detection mechanism has been proved. |
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ISSN: | 1387-7003 1879-0259 |
DOI: | 10.1016/j.inoche.2018.10.003 |