Synthesis and characterisation of divalent di(1,3-bis(diphenylphosphano)cyclopentadienyl)lanthanoid and alkaline earth complexes as potential platforms for heterometallic complexes
Daniels, Daisy P., Guo, Zhifang, Shephard, Angus C.G., Deacon, Glen B., Jaroschik, Florian, and Junk, Peter C. (2022) Synthesis and characterisation of divalent di(1,3-bis(diphenylphosphano)cyclopentadienyl)lanthanoid and alkaline earth complexes as potential platforms for heterometallic complexes. Zeitschrift fuer Anorganische und Allgemeine Chemie, 648 (23). e202200251.
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Abstract
New divalent lanthanoid and alkaline earth metal complexes bearing the 1,3-bis(diphenylphosphano)cyclopentadienyl ligand have been synthesised using the redox-transmetallation protolysis (RTP) approach. From the reaction of the corresponding metal, diphenylmercury and the proligand C5H4(PPh2)2, the compounds [M(η5-C5H3(PPh2)2-1,3)2(S)] (with M=Yb, S=(thf)2 or M=Yb, Eu, Ca, Sr, Ba, S=dme) were isolated and characterised by X-ray diffraction and multinuclear NMR spectroscopy. These compounds may provide a platform for early-late heterobimetallic complexes.
Item ID: | 76545 |
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Item Type: | Article (Research - C1) |
ISSN: | 1521-3749 |
Keywords: | alkaline earth, bimetallic complexes, cyclopentadienyl, lanthanide, phosphine |
Copyright Information: | © 2022 The Authors. Zeitschrift für anorganische und allgemeine Chemie published by Wiley-VCH GmbH. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
Funders: | Australian Research Council (ARC) |
Projects and Grants: | ARC DP190100798 |
Date Deposited: | 04 Jan 2023 23:01 |
FoR Codes: | 34 CHEMICAL SCIENCES > 3402 Inorganic chemistry > 340203 F-block chemistry @ 100% |
SEO Codes: | 28 EXPANDING KNOWLEDGE > 2801 Expanding knowledge > 280105 Expanding knowledge in the chemical sciences @ 100% |
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