A Multi‐Redox Responsive Cyanometalate‐Based Metallogel

A TTF‐based (TTF=tetrathiafulvalene) tridentate ligand (α‐(4′‐methyl‐4,5‐di‐n‐dodecylthylthiotetrathiafulvalene‐5′‐ylthio)‐ α′‐[2,2,2‐tris(1‐pyrazolyl)ethoxy]‐p‐xylene) (L) with long‐chain alkyl moieties was prepared in order to obtain a new multi‐redox active gelator based on a mixed‐metal octanucl...

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Veröffentlicht in:Chemistry : a European journal 2017-01, Vol.23 (7), p.1502-1506
Hauptverfasser: Mitsumoto, Kiyotaka, Cameron, Jamie M., Wei, Rong‐Jia, Nishikawa, Hiroyuki, Shiga, Takuya, Nihei, Masayuki, Newton, Graham N., Oshio, Hiroki
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Sprache:eng
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Zusammenfassung:A TTF‐based (TTF=tetrathiafulvalene) tridentate ligand (α‐(4′‐methyl‐4,5‐di‐n‐dodecylthylthiotetrathiafulvalene‐5′‐ylthio)‐ α′‐[2,2,2‐tris(1‐pyrazolyl)ethoxy]‐p‐xylene) (L) with long‐chain alkyl moieties was prepared in order to obtain a new multi‐redox active gelator based on a mixed‐metal octanuclear complex [FeIII4NiII4(CN)12(tp)4(L)4](BF4)4 (1). The magnetism, electrochemistry, and gelation behavior of 1 were studied and 1,2‐dichlorobenzene solutions of 1 are shown to display thermoreversible gelation behavior at room temperature. Furthermore, the gel phase of 1 was shown to undergo room‐temperature gel‐to‐sol transformations induced by both the oxidation and reduction of the gelator complex by F4TCNQ or [FeII(Cp*)2], respectively. A new heterometallic, discrete metallogelator based on an octanuclear cyanometallate {Fe4Ni4} complex, supported by long‐chain alkyl ligands with incorporated tetrathiafulvalene moieties, was synthesized. It exhibited thermoreversible gelation behavior at room temperature and redox‐mediated gel‐to‐sol transitions.
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.201605542