AI Article Synopsis

  • - The study focuses on a new luminescent chemosensor based on a cationic platinum complex that selectively detects anions, particularly chloride ions, in water, which is significant for analytical and biological chemistry applications.
  • - The platinum complex exhibits strong green phosphorescent emission in response to chloride, showing a high affinity for this anion compared to others, making it promising for quantitative sensing and possibly useful for bioimaging of cell nuclei.
  • - Structural analysis and various spectroscopic techniques reveal that the sensor's selectivity for chloride arises from a unique three-point recognition mechanism involving a direct bonding interaction and additional non-covalent interactions.

Article Abstract

Selective anion sensing by luminescent chemosensors capable of operating in aqueous conditions is a central field of modern supramolecular chemistry that impacts analytical and biological chemistry. A cationic cyclometalated [Pt(N^C^N)NCCH]OTf complex, [N^C^N = 1,3-bis(1-(-tolyl)-benzimidazol-2'-yl)benzene, OTf = triflate], was prepared, structurally described by single-crystal X-ray diffraction and studied in-depth as a luminescent chemosensor for anions in aqueous phase and solid state. A series of related neutral [Pt(N^C^N)X] complexes (X = Cl, ; CN, and I, ) were formed readily upon treatment of with the respective NaX salt in aqueous media and were described structurally by X-ray diffraction. Complex is hydrostable with phosphorescent green emission originated by intraligand transitions, and [d(Pt) → π*(N^C^N)] charge transfer transitions, as evidenced by TD-DFT calculations and lifetime. Additions of halides, pseudohalides, oxyanions, and dicarboxylates to a neutral aqueous solution of modified its green emission intensity with a pronounced affinity ( = 1.5 × 10 M) and turn-on signal toward Cl within the micromolar concentration range. Pt complex is two orders of magnitude more selective for Cl than the other halides, CN and basic oxyanions. Such Cl affinity for a metal-based chemosensor in aqueous media is still rare. On the basis of X-ray crystallographic analysis and multiple spectroscopic tools (NMR, UV-vis, luminescence, MS, lifetimes) the origin of this selectivity hinges on the cooperative three-point recognition involving one coordination bond (Pt-Cl) and two convergent short C-H···Cl contacts. This strong affinity and efficient optical response can be utilized in quantitative Cl sensing in real samples and solid-liquid extractions. Additionally, chloro-Pt complex, may be relevant to bioimaging as a marker for cell nuclei, as revealed by its emission within living cells and intracellular distribution by confocal microscopic studies. These results demonstrate the usefulness of the new water-stable luminescent Pt-N^C^N complexes as effective analytical tools in anion sensing and extraction agents.

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http://dx.doi.org/10.1021/acs.inorgchem.2c04558DOI Listing

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