We report the study of stimuli-responsive ZnII and FeII coordination polymers (MC34+ or MC24+ with M=Fe2+ or Zn2+ ). These soluble metallopolymers were formed spontaneously by reaction of an organic ligand (C34+ or C24+ ) with one molar equivalent of metal ions. The C34+ and C24+ ligands incorporate two chelating terpyridine groups bridged by a redox responsive hinge featuring two viologen units (viologen=N,N'-dialkyl-4,4'-bipyridinium) linked either with propyl (C34+ ) or ethyl (C24+ ) chains. The viologen units in the polymer chains were reduced (1 e- per viologen group) either by bulk electrolysis or by visible-light irradiation carried out in the presence of a photosensitizer. The 1 e- reduction of the viologen units in the MC24+ polymers induced a slight decrease in the viscosity of the solutions due to a modification of the overall charge carried by the metallopolymers. In strong contrast, reduction of coordination polymers involving propyl linkers (MC34+ ) led to a remarkable increase (≈+400 %) in observed viscosity. This reversible effect was attributed to a folding of the polymer chains triggered by π-dimerization of the photo-generated viologen cation radicals.
Keywords: coordination polymers; redox chemistry; switches; viologen; zinc.
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