AI Article Synopsis

  • Two new dinuclear Ru(ii) complexes have been created using different ligands and attached to gold nanoparticles (AuNPs), resulting in novel water-soluble conjugates.
  • The Ru(ii)-AuNP conjugates maintain desirable properties for cellular uptake and are effectively internalized by HeLa cervical cancer cells.
  • Although the gold conjugates show lower luminescence due to energy transfer quenching, they are more tolerated by cells compared to the free complexes, highlighting their potential for bioimaging applications.

Article Abstract

Two new dinuclear Ru(ii) polypyridyl complexes containing an alkyl disulphide functionalised bipyridine-based ligand and either 1,10-phenanthroline (phen) or 1,4,5,8-tetraazaphenanthrene (TAP) as ancillary ligands have been synthesised and characterised. Their attachment onto the surface of gold nanoparticles (AuNPs, average diameter of ca. 2.5 nm) resulted in the formation of two new water-soluble Ru(ii)-AuNP conjugates that combine the advantageous properties of both moieties. Both free complexes show the attractive photophysical properties of Ru(ii) polypyridyl complexes and a rapid cellular uptake in HeLa cervical cancer cells. However, their corresponding gold conjugates displayed lower quantum yields than those determined for the free complexes presumed to be due to an energy transfer quenching of the Ru(ii) luminescence by interaction with the gold surface. Despite their diminished luminescence, confocal fluorescence microscopy studies revealed that the Ru(ii)-AuNP conjugates are successfully internalised into HeLa cells and better tolerated than their free complex counterparts after 24 h incubation, which makes them potential luminescent nanomaterials for bioimaging applications.

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http://dx.doi.org/10.1039/d0dt02754eDOI Listing

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Article Synopsis
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  • Excitation at 470 nm does not trigger ligand release or noticeable luminescence at room temperature, but luminescence is detected at 77 K when excited near the MLCT bands.
  • The complexes show non-cytotoxic behavior in cancer cells, linked to their stability and failure to produce reactive oxygen species, including findings from MTT assays and ICP-MS analyses.
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The preparation, electrochemistry and photophysical properties of a heteroleptic chromium(III) polypyridyl complex [Cr(TMP)(dppn)] () containing two 3,4,7,8-tetramethyl-1,10-phenanthroline (TMP) ligands and the π-extended benzodipyrido[3,2-a:2',3'-]phenazine (dppn) ligand are reported. The visible absorption spectrum of reveals distinct bands between 320 and 420 nm characteristic of dppn-based ligand-centered transitions, with found to be nonemissive in aqueous solution but weakly luminescent in aerated acetonitrile solution. Transient visible absorption (TrA) spectroscopy reveals that 400 nm excitation of leads to initial population of a ligand-to-metal charge transfer (LMCT) state which evolves within tens of ps to form a dppn-localized intraligand (IL) state which persists for longer than 7 ns and efficiently sensitizes singlet oxygen.

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