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Different types of electron transfers (ETs) underlie the versatile use of various solid viologen-derived compounds, which is still insufficiently understood and difficult to control. Here, we demonstrate an effective strategy for modulating the key ET process in crystalline metalloviologen compounds (MVCs). By adjusting the coordinated transition metal ions bearing different electronic structures (e.g., , , ), three MVCs (i.e., , , and ) with highly consistent coordination environments have been synthesized successfully. Surprisingly, whether the photochromism (energy-induced ET mechanism) or the specific analyte recognition (molecule-induced ET mechanism), compound exhibits obvious photochromic behavior and differential dimethylamine detection. Combined detailed structural analysis with theoretical calculations, such unique ion-dependent properties, were correlated to the fine modulation of the electron density of the bipyridinium cores by metal ions. Additionally, thanks to the delicate recognition of dimethylamine vapor, a convenient test strip was prepared as a sensitive biogenic amine sensor for evaluating the real-time freshness of seafood.
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http://dx.doi.org/10.1021/acs.inorgchem.4c02210 | DOI Listing |
Inorg Chem
September 2024
Key Laboratory of Surface & Interface Science of Polymer Materials of Zhejiang Province, School of Chemistry and Chemical Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, P. R. China.
Different types of electron transfers (ETs) underlie the versatile use of various solid viologen-derived compounds, which is still insufficiently understood and difficult to control. Here, we demonstrate an effective strategy for modulating the key ET process in crystalline metalloviologen compounds (MVCs). By adjusting the coordinated transition metal ions bearing different electronic structures (e.
View Article and Find Full Text PDFDalton Trans
April 2024
State Key Laboratory Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Science, Fuzhou 350002, P. R. China.
Metalloviologens, as emerging electron-transfer photochromic compounds, have shown intriguing properties such as radiochromism, photochromism and photoconductance. However, only a limited number of them have been reported so far. Exploration of new metalloviologens is strongly desired.
View Article and Find Full Text PDFJ Am Chem Soc
February 2021
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, People's Republic of China.
Charge-separated states with a lifetime scale of seconds or longer not only favor studies using various steady-state analysis techniques but are important for light-energy conversion and other applications. Through a steric-hindrance-induced method, unprecedented photoinduced generation of a partially charge separated (PCS) state with a lifetime of days has been detected in the "visual" mode during the decay of excited states to a commonly observed fully charge separated (FCS) state for viologen analogues. One pale yellow 4,4'-bipyridine-based metalloviologen compound, with an interannular dihedral angle of 1.
View Article and Find Full Text PDFDalton Trans
April 2012
Department of Chemistry, Faculty of Science, Kyushu University, Hakozaki 6-10-1, Fukuoka 812-8581, Japan.
A new Pt(II)-based metalloviologen analog, [PtCl(Mepytpy)](2+) (abbreviated as PV(2+); Mepytpy(+) = 4'-(4-methyl-pyridinio)-2,2':6',2''-terpyridine), was synthesized and its spectroscopic and electrochemical properties were investigated. The structures of Mepytpy(+) and PV(2+) were solved by single-crystal X-ray diffraction analysis. Electrochemical studies in DMF (N,N-dimethylformamide) revealed that both the first and second reduction potentials of PV(2+) (E = -0.
View Article and Find Full Text PDFChem Commun (Camb)
April 2005
Max Planck Institute of Colloids and Interfaces, D-14424, Potsdam, Germany.
A metallosupramolecular coordination polyelectrolyte prepared by the reaction of cobalt(II) with a novel bisterpyridine ligand has been assembled as the active component in electrochromic films by sequential deposition using electrostatic layer-by-layer self-assembly.
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