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Selective Synthesis of a Series of Isostructural M II Cu I Heterobimetallic Complexes Spontaneously Assembled by an Unsymmetrical Naphthyridine-Based Ligand
Ist Teil von
Chemistry : a European journal, 2018-07, Vol.24 (41), p.10329-10333
Ort / Verlag
Germany: Wiley Blackwell (John Wiley & Sons)
Erscheinungsjahr
2018
Quelle
Wiley Blackwell Single Titles
Beschreibungen/Notizen
Metal-metal cooperation is integral to the function of many enzymes and materials, and model complexes hold enormous potential for providing insights into the capabilities of analogous multimetallic cores. However, the selective synthesis of heterobimetallic complexes still presents a significant challenge, especially for systems that hold the metals in close proximity and feature open or reactive coordination sites for both metals. To address this issue, a rigid, naphthyridine-based dinucleating ligand featuring distinct binding environments was synthesized. This ligand enables the selective synthesis of a series of M
Cu
bimetallic complexes (M=Mn, Fe, Co, Ni, Cu, Zn), in which each metal center exclusively occupies its preferred binding pocket, from simple chloride salts. The precision of this selectivity is evident from cyclic voltammetry, ESI-MS and anomalous X-ray diffraction measurements.
Sprache
Englisch
Identifikatoren
ISSN: 0947-6539
eISSN: 1521-3765
DOI: 10.1002/chem.201802623
Titel-ID: cdi_osti_scitechconnect_1457513
Format
–
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