Journal article
Synthesis, characterisation and structural studies of amidinate and guanidinate alkaline earth–transition metal bonded complexes
- Abstract:
- Reaction of magnesium amidinate complexes of the form [{MesC(NR)2}MgBr(OEt2)]2 (R = i Pr, Dipp, Mes) with the potassium salts of transition metal anions K[CpFe(CO)2] (K[Fp]) and K[Co(CO)3(PCy3)](THF)2 gave the complexes {MesC(NR)2}MgFp(THF) and {MesC(NR)2}Mg{Co(CO)3(PCy3)}(THF). Single crystal X-ray diffraction studies of {MesC(NR)2}Mg{Co(CO)3(PCy3)}(THF) for R = i Pr and Dipp confirm these to have Mg‒Co bonds in the solid state. Reaction of the structurally similar magnesium guanidinate complex {Me2NC(NDipp)2}MgI(OEt2) with the aforementioned transition metal anions and additional K[Co(CO)3(PPh3)](THF) gave the series of complexes [{Me2NC(NDipp)2}MgFp]2, {Me2NC(NDipp)2}Mg{Co(CO)3(PCy3)}(OEt2) and {Me2NC(NDipp)2}Mg{Co(CO)3(PPh3)}(OEt2). Structural authentication by X-ray crystallography showed [{Me2NC(NDipp)2}MgFp]2 to be a very rare example of a base-free alkaline earth‒transition bonded complex, having two Mg‒Fe bonds. IR and diffusion NMR spectroscopy were carried out to gain further insight into the solid state and solution phase structures.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Accepted manuscript, pdf, 1.3MB, Terms of use)
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- Publisher copy:
- 10.1016/j.poly.2016.02.028
Authors
- Publisher:
- Elsevier
- Journal:
- Polyhedron More from this journal
- Volume:
- 116
- Pages:
- 64–75
- Publication date:
- 2016-03-26
- Acceptance date:
- 2016-02-19
- DOI:
- EISSN:
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1873-3719
- ISSN:
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0277-5387
- Keywords:
- Pubs id:
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pubs:607500
- UUID:
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uuid:00cab998-05e0-4577-bb60-2be0890384d7
- Local pid:
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pubs:607500
- Source identifiers:
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607500
- Deposit date:
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2016-03-03
- ARK identifier:
Terms of use
- Copyright holder:
- Elsevier Ltd
- Copyright date:
- 2016
- Notes:
- Copyright © 2016 Elsevier Ltd. This is the accepted manuscript version of the article. The final version is available online from Elsevier at: https://doi.org/10.1016/j.poly.2016.02.028
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