A photofunctional platform of bis-terpyridine ruthenium complex-linked coordination polymers with structural diversity
Solvothermal syntheses of the bis(4′-carboxyl-2,2′:6′,2′′-terpyridine) ruthenium complex [Ru(tpyCOO − ) 2 ] as a linker and different metal anions as nodes constructed a family of ten novel coordination polymers (CPs) with different topological types, ranging from one-dimensional (1D) chains and two...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2022-12, Vol.1 (47), p.2563-2569 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Solvothermal syntheses of the bis(4′-carboxyl-2,2′:6′,2′′-terpyridine) ruthenium complex [Ru(tpyCOO
−
)
2
] as a linker and different metal anions as nodes constructed a family of ten novel coordination polymers (CPs) with different topological types, ranging from one-dimensional (1D) chains and two-dimensional (2D) networks to three-dimensional (3D) frameworks. The structural diversity of CPs is achieved by the various coordinating geometries of metal nodes, including 3d transition (monometallic or bimetallic), lanthanide, and group 4 (zirconium and hafnium) metal anions. The Ru complex linker plays the role of a light-harvesting unit and renders multifarious photofunctions to the CP materials. While the ytterbium CP (
Yb-Ru
) exhibits near-infrared emission upon visible-light excitation, the 2D bimetallic Co/Ni CPs (
Co
x
-Ni
y
-Ru
) and 3D interpenetrated copper CP (
Cu-Ru
) show high to modest efficiencies toward the photocatalytic hydrogen evolution reaction. We suggest the series of new CPs with versatile structural traits as a unique platform for the research of photocatalysis and other photonic functional applications.
A family of novel coordination polymers (CPs) with topological diversity has been prepared based on a bis-terpyridine ruthenium linker. They provide a unique platform for the development of multifarious photofunctions. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d2ta07219j |