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Luminescent Pincer Platinum(II) Complexes with Emission Quantum Yields up to Almost Unity: Photophysics, Photoreductive CC Bond Formation, and Materials Applications
Luminescent pincer‐type PtII complexes supported by C‐deprotonated π‐extended tridentate RC^N^NR′ ligands and pentafluorophenylacetylide ligands show emission quantum yields up to almost unity. Femtosecond time‐resolved fluorescence measurements and time‐dependent DFT calculations together reveal...
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Published in: | Angewandte Chemie International Edition 2015-02, Vol.54 (7), p.2084-2089 |
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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: | Luminescent pincer‐type PtII complexes supported by C‐deprotonated π‐extended tridentate RC^N^NR′ ligands and pentafluorophenylacetylide ligands show emission quantum yields up to almost unity. Femtosecond time‐resolved fluorescence measurements and time‐dependent DFT calculations together reveal the dependence of excited‐state structural distortions of [Pt(RC^N^NR′)(CC‐C6F5)] on the positional isomers of the tridentate ligand. Pt complexes [Pt(R‐C^N^NR′)(CC‐Ar)] are efficient photocatalysts for visible‐light‐induced reductive CC bond formation. The [Pt(R‐C^N^NR′)(CC‐C6F5)] complexes perform strongly as phosphorescent dopants for green‐ and red‐emitting organic light‐emitting diodes (OLEDs) with external quantum efficiency values over 22.1 %. These complexes are also applied in two‐photon cellular imaging when incorporated into mesoporous silica nanoparticles (MSNs).
Multipurpose platinum: A phosphorescent PtII complex 1 with an emission quantum yield of 0.99 is employed as a catalyst for visible‐light‐induced reductive CC bond formation and as a dopant in organic light‐emitting diodes with an external quantum efficiency of 22.8 %. Encapsulating 1 in mesoporous SiO2 for two‐photon‐excited cellular imaging has been demonstrated. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201408940 |