4.7 Article

An aggregation induced emission active bis-heteroleptic ruthenium(ii) complex for luminescence light-up detection of pyrophosphate ions

Journal

DALTON TRANSACTIONS
Volume 52, Issue 9, Pages 2592-2602

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2dt03469g

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A red emissive ruthenium(ii) complex L1[PF6](2) has been developed and characterized, which exhibits an aggregation-induced emission (AIE) enhancement and forms nano-aggregates in water and polyethylene glycol media. The AIE properties are attributed to weak supramolecular interactions between the ligands. The complex shows high selectivity towards pyrophosphate ions (PPi) and can be used for intracellular PPi imaging.
A red emissive ruthenium(ii) complex 1[PF6](2) of an amino ethanol substituted 1,10-phenanthroline-based ligand (L1) has been developed and characterized by spectroscopic analysis and single-crystal X-ray diffraction. Complex 1 shows an aggregation-induced emission (AIE) enhancement and forms nano-aggregates in the poor solvent water and highly dense polyethylene glycol (PEG) media. The possible reason behind the AIE properties may be the rigidity gained through weak supramolecular interactions between neighbouring phenanthroline ligands and PF6- counterions. The AIE properties were supported by UV-vis and photoluminescence (PL) spectroscopy and dynamic light scattering (DLS) studies to substantiate the formation of nano-aggregates and to understand the morphology of the aggregated particles, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies were performed. Compound 1[PF6](2) was highly selective towards pyrophosphate ions (PPi) over other phosphates such as ATP, ADP, AMP and H2PO4- ions and other competitive anions in the PL spectroscopic channel in acetonitrile. The PL titrations of 1[PF6](2) with PPi in CH3CN furnished the association constant K-a = 1.08 x 10(4) M-1 and the detection limit was calculated as low as 1.54 mu M. The PPi detection has been established through the unique H-bonding interaction, supported by H-1 NMR titration. Finally, the cytotoxicity study and bioimaging were carried out for biological application. The complex shows very low cytotoxicity and good biocompatibility and is suitable for intracellular PPi imaging.

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