Abstract
We report the synthesis, characterization, and scope of a new versatile emissive molecular probe functionalized with a 1,10-phenanthroline moiety containing methylserotonin groups as binding sites for metal ion recognition. The synthesis, characterization, and evaluation of the in vitro imaging capability of the iridium(III) and ruthenium(II) complexes [Ir(ppy)2(N-N)](+) and [Ru(bpy)2(N-N)](2+), in which ppyis 2-phenylpyridine, bpyis 2,2'-bipyridine, and N-N is a 1,10-phenanthroline ligand functionalized with two methylserotonin groups to serve as binding sites for metal ion recognition, is reported. The uptake of these compounds by living freshwater fish (Carassius auratus) was studied by fluorescence microscopy, and the cytotoxicity of ligand N-N and [Ru(bpy)2(N-N)](2+) in this species was also investigated.
Original language | English |
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Pages (from-to) | 679-692 |
Number of pages | 14 |
Journal | JBIC Journal of Biological Inorganic Chemistry |
Volume | 18 |
Issue number | 6 |
DOIs | |
Publication status | Published - Aug 2013 |
Keywords
- Cellular imaging
- Cyclometalated complexes
- Dyes
- Serotonin
- Time-dependent density functional theory
- bis(o methylserotonin)
- fluorescent dye
- iridium complex
- ruthenium complex
- unclassified drug
- animal cell
- animal experiment
- animal tissue
- article
- binding site
- chemical structure
- complex formation
- controlled study
- cytotoxicity test
- erythrocyte
- fluorescence microscopy
- goldfish
- ligand binding
- molecular imaging
- molecular probe
- molecular recognition
- molecular stability
- nonhuman
- photochemical quenching
- physical chemistry
- priority journal
- Carassius auratus
- Animals
- Fluorescent Dyes
- Goldfish
- Iridium
- Microscopy, Fluorescence
- Models, Biological
- Models, Molecular
- Molecular Structure
- Organometallic Compounds
- Photochemical Processes
- Quantum Theory
- Ruthenium
- Tissue Distribution