A highly selective off–on fluorescent chemodosimeter for Hg2+ based on a anthracene–bis(phosphinesulfide) conjugate†
Abstract
A chemodosimeter Ph2P(![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) S)NP(–S–CH2–anthracene)Ph2 (L1), featuring the methylanthracenyl moiety covalently linked to one of the two S atoms of an S,S′-tetraphenyldithioimidodiphosphinate (L) unit exhibited good selectivity and sensitivity for Hg2+ in an aqueous environment. The chemical reaction involved differs from those reported in the literature for other Hg2+ chemodosimeters: the binding of Hg2+ induces the cleavage of the PS–CH2 bond to form the stable neutral complex [HgL2] and an emissive anthracenyl derivative. The X-ray crystal structure of L1 is reported (CCDC number 919620).
S)NP(–S–CH2–anthracene)Ph2 (L1), featuring the methylanthracenyl moiety covalently linked to one of the two S atoms of an S,S′-tetraphenyldithioimidodiphosphinate (L) unit exhibited good selectivity and sensitivity for Hg2+ in an aqueous environment. The chemical reaction involved differs from those reported in the literature for other Hg2+ chemodosimeters: the binding of Hg2+ induces the cleavage of the PS–CH2 bond to form the stable neutral complex [HgL2] and an emissive anthracenyl derivative. The X-ray crystal structure of L1 is reported (CCDC number 919620).
 
                



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