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Issue 41, 2018
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The Heck reaction as a tool to expand polyoxovanadates towards thiol-sensitive organic–inorganic hybrid fluorescent switches

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Abstract

Among the Lindqvist-type hexavanadates synthesised herein by the palladium-catalysed Heck reactions a C–C cross-coupled organic–inorganic hybrid with the largest conjugated, stilbene-derivatised π ligands is reduced in the presence of thiols producing a remarkable increase in fluorescence intensity with respect to the fully-oxidised variant. This enhanced emission (ON-state) of the reduced species can be switched OFF if the solution is subjected to e.g. air where the species is re-oxidised.

Graphical abstract: The Heck reaction as a tool to expand polyoxovanadates towards thiol-sensitive organic–inorganic hybrid fluorescent switches

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Publication details

The article was received on 07 Jun 2018, accepted on 17 Aug 2018 and first published on 17 Aug 2018


Article type: Communication
DOI: 10.1039/C8DT02340A
Citation: Dalton Trans., 2018,47, 14402-14407

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    The Heck reaction as a tool to expand polyoxovanadates towards thiol-sensitive organic–inorganic hybrid fluorescent switches

    O. Linnenberg, L. Mayerl and K. Yu. Monakhov, Dalton Trans., 2018, 47, 14402
    DOI: 10.1039/C8DT02340A

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