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Rhenium fac-Tricarbonyl Bisimine Chalcogenide Complexes: Synthesis, Photophysical Studies, and Confocal and
Till Neumann1, Vadde Ramu1, Julie Bertin1
1Laboratoire des biomolécules, LBM, Département de chimie, Ecole normale supérieure, PSL University, Sorbonne Université, CNRS, 75005 Paris, France.
New rhenium carbonyl complexes with pyta or tapy ligands show potential for cellular imaging. Their long fluorescence lifetimes in cells suggest applications in advanced microscopy techniques.
Area of Science:
- Coordination Chemistry
- Bioinorganic Chemistry
- Photophysics
Background:
- Rhenium carbonyl complexes are investigated for their unique photophysical properties.
- Heteroaromatic N∧N ligands and thiolate/selenoate ligands offer tunable characteristics.
- Cellular imaging requires stable probes with distinct photophysical behavior.
Purpose of the Study:
- To synthesize and characterize novel rhenium carbonyl complexes.
- To evaluate the stability and photophysical properties of these complexes, particularly selenolate derivatives.
- To assess their potential for cellular imaging and time-resolved microscopy.
Main Methods:
- Synthesis and characterization of rhenium carbonyl complexes.
- Photophysical property measurements (stability, fluorescence).
- Cellular imaging studies in A549 cells using 405 nm excitation.
- Colocalization studies and fluorescence lifetime measurements.
Main Results:
- Successful preparation and characterization of pyta/tapy-based rhenium carbonyl complexes with thiolate/selenoate ligands.
- Selenolate complexes exhibit distinct stability and photophysical properties compared to chloride and benzenethiolate analogues.
- Two complexes were successfully imaged in A549 cells, showing lysosomal accumulation.
- Significant, variable fluorescence lifetimes were observed in cellular environments, with notable increases from solution to solid state.
Conclusions:
- The synthesized rhenium complexes demonstrate promising characteristics for bioimaging applications.
- Their long and variable fluorescence lifetimes indicate potential for time-resolved microscopy.
- Lysosomal localization suggests specific cellular uptake mechanisms for these novel probes.
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