Near Infrared Phosphorescent Dinuclear Ir(III) Complex Exhibiting Unusually Slow Intersystem Crossing and Dual Emissive Behavior.
Marsel Z ShafikovAndrey V ZaytsevAlfiya F SuleymanovaFabian BrandlAleksandra KowalczykMagdalena GapińskaKonrad KowalskiValery N KozhevnikovRafał CzerwieniecPublished in: The journal of physical chemistry letters (2020)
A dinuclear iridium(III) complex IrIr shows dual emission consisting of near infrared (NIR) phosphorescence (λmax = 714 nm, CH2Cl2, T = 300 K) and green fluorescence (λmax = 537 nm). The NIR emission stems from a triplet state (T1) localized on the ditopic bridging ligand (3LC). Because of the dinuclear molecular structure, the phosphorescence efficiency (ΦPL = 3.5%) is high compared to those of other known red/NIR-emitting iridium complexes. The weak fluorescence stems from the lowest excited singlet state (S1) of 1LC character. The occurrence of fluorescence is ascribed to relatively slow intersystem crossing (ISC) from state S1 (1LC) to the triplet manifold. The measured ISC rate corresponds to a time constant τISC of 2.1 ps, which is an order of magnitude longer than those usually found for iridium complexes. This slow ISC rate can be explained in terms of the LC character and large energy separation (0.57 eV) of the respective singlet and triplet excited states. IrIr is internalized by live HeLa cells as evidenced by confocal luminescence microscopy.
Keyphrases
- energy transfer
- photodynamic therapy
- quantum dots
- simultaneous determination
- room temperature
- liquid chromatography
- fluorescence imaging
- mass spectrometry
- drug release
- single molecule
- fluorescent probe
- light emitting
- induced apoptosis
- cell cycle arrest
- optical coherence tomography
- risk assessment
- high resolution
- tandem mass spectrometry
- oxidative stress
- solid phase extraction
- high throughput
- high resolution mass spectrometry
- high speed
- raman spectroscopy
- endoplasmic reticulum stress
- pi k akt
- ionic liquid