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Ruthenium(II) Polypyridine Complex-Based Aggregation-Induced Emission Luminogen for Rapid and Selective Detection of Phosgene in Solution and in the Gas Phase

A bis-heteroleptic ruthenium­(II) complex, Ru-1, of 4,7-bis­(2-aminoethylamino)-1,10-phenanthroline for selective “turn-on” detection of highly toxic chemical warfare agent phosgene is presented. Probe Ru-1 exhibits aggregation-induced emission (AIE), and the restricted intramolecular motion is resp...

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Bibliographic Details
Published in:Inorganic chemistry 2021-12, Vol.60 (24), p.19175-19188
Main Authors: Sen, Bhaskar, Patra, Sumit Kumar, Khatua, Snehadrinarayan
Format: Article
Language:English
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Summary:A bis-heteroleptic ruthenium­(II) complex, Ru-1, of 4,7-bis­(2-aminoethylamino)-1,10-phenanthroline for selective “turn-on” detection of highly toxic chemical warfare agent phosgene is presented. Probe Ru-1 exhibits aggregation-induced emission (AIE), and the restricted intramolecular motion is responsible for the AIE activity. In a CHCl3/CH3CN [95:5 (v/v)] solvent mixture, a unique self-assembled vesicular structure was formed after aggregation, which was supported by transmission electron microscopy, field emission scanning electron microscopy, and atmoic force microscopy studies. Probe Ru-1 showed a rapid and highly selective luminescence turn-on response for phosgene over other competitive chemical warfare agents with a low detection limit (13.9 nM) in CH3CN. The 2-aminoethylamino groups in Ru-1 act as a reacting site for nucleophilic addition to the carbonyl center of phosgene and undergo intramolecular cyclization. The final product of the phosgene-mediated reaction, Ru-1-Phos, contains 2-imidazolidinone groups, which has been confirmed by electrospray ionization mass spectometry and 1H nuclear magnetic resonance (NMR) spectroscopy. 1H NMR titration of Ru-1 with phosgene supported the reaction mechanism and also pointed to the simultaneous reaction of phosgene at two 2-aminoethylamino sites. For the first time, the crystal structure of the phosgene reaction product, Ru-1-Phos, containing the cyclized 2-imidazolidinone group was confirmed by single-crystal X-ray diffraction, which indubitably validates the reaction mechanism. Triplet state time-dependent density functional theory calculations showed that the weak luminescence of Ru-1 was mostly due to the population of the non-emissive 3MC state. The cyclization reaction with phosgene and the corresponding 2-imidazolidinone product formation populated the emissive 3MLCT state in Ru-1-Phos and is the key reason for the enhanced luminescence. Furthermore, a low-cost portable test paper strip has been fabricated with Ru-1 for the real-time selective monitoring of phosgene gas at the nanomolar level.
ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.1c02987