A General Pathway to Heterobimetallic Triple‐Decker Complexes. Issue 7 (30th January 2020)
- Record Type:
- Journal Article
- Title:
- A General Pathway to Heterobimetallic Triple‐Decker Complexes. Issue 7 (30th January 2020)
- Main Title:
- A General Pathway to Heterobimetallic Triple‐Decker Complexes
- Authors:
- Piesch, Martin
Dielmann, Fabian
Reichl, Stephan
Scheer, Manfred - Abstract:
- Abstract: A systematic study on the reactivity of the triple‐decker complex [(Cp'''Co)2 (μ, η 4 :η 4 ‐C7 H8 )] (A ) (Cp'''=1, 2, 4‐tritertbutyl‐cyclopentadienyl) towards sandwich complexes containing cyclo ‐P3, cyclo ‐P4, and cyclo ‐P5 ligands under mild conditions is presented. The heterobimetallic triple‐decker sandwich complexes [(Cp*Fe)(Cp'''Co)(μ, η 5 :η 4 ‐P5 )] (1 ) and [(Cp'''Co)(Cp'''Ni)(μ, η 3 :η 3 ‐P3 )] (3 ) (Cp*=1, 2, 3, 4, 5‐pentamethylcyclopentadienyl) were synthesized and fully characterized. In solution, these complexes exhibit a unique fluxional behavior, which was investigated by variable temperature NMR spectroscopy. The dynamic processes can be blocked by coordination to {W(CO)5 } fragments, leading to the complexes [(Cp*Fe)(Cp'''Co)(μ3, η 5 :η 4 :η 1 ‐P5 ){W(CO)5 }] (2 a ), [(Cp*Fe)(Cp'''Co)(μ4, η 5 :η 4 :η 1 :η 1 ‐P5 ){(W(CO)5 )2 }] (2 b ), and [(Cp'''Co)(Cp'''Ni)(μ3, η 3 :η 2 :η 1 ‐P3 ){W(CO)5 }] (4 ), respectively. The thermolysis of 3 leads to the tetrahedrane complex [(Cp'''Ni)2 (μ, η 2 :η 2 ‐P2 )] (5 ). All compounds were fully characterized using single‐crystal X‐ray structure analysis, NMR spectroscopy, mass spectrometry, and elemental analysis. Abstract : From double to triple : A synthetic route to otherwise inaccessible heterometallic triple‐decker complexes is reported (see scheme). The cobalt complex [(Cp'''Co)2 (toluene)] (Cp'''=1, 2, 4‐tritertbutyl‐cyclopentadienyl) as a source for unsaturated {Cp'''Co} fragments was reacted with theAbstract: A systematic study on the reactivity of the triple‐decker complex [(Cp'''Co)2 (μ, η 4 :η 4 ‐C7 H8 )] (A ) (Cp'''=1, 2, 4‐tritertbutyl‐cyclopentadienyl) towards sandwich complexes containing cyclo ‐P3, cyclo ‐P4, and cyclo ‐P5 ligands under mild conditions is presented. The heterobimetallic triple‐decker sandwich complexes [(Cp*Fe)(Cp'''Co)(μ, η 5 :η 4 ‐P5 )] (1 ) and [(Cp'''Co)(Cp'''Ni)(μ, η 3 :η 3 ‐P3 )] (3 ) (Cp*=1, 2, 3, 4, 5‐pentamethylcyclopentadienyl) were synthesized and fully characterized. In solution, these complexes exhibit a unique fluxional behavior, which was investigated by variable temperature NMR spectroscopy. The dynamic processes can be blocked by coordination to {W(CO)5 } fragments, leading to the complexes [(Cp*Fe)(Cp'''Co)(μ3, η 5 :η 4 :η 1 ‐P5 ){W(CO)5 }] (2 a ), [(Cp*Fe)(Cp'''Co)(μ4, η 5 :η 4 :η 1 :η 1 ‐P5 ){(W(CO)5 )2 }] (2 b ), and [(Cp'''Co)(Cp'''Ni)(μ3, η 3 :η 2 :η 1 ‐P3 ){W(CO)5 }] (4 ), respectively. The thermolysis of 3 leads to the tetrahedrane complex [(Cp'''Ni)2 (μ, η 2 :η 2 ‐P2 )] (5 ). All compounds were fully characterized using single‐crystal X‐ray structure analysis, NMR spectroscopy, mass spectrometry, and elemental analysis. Abstract : From double to triple : A synthetic route to otherwise inaccessible heterometallic triple‐decker complexes is reported (see scheme). The cobalt complex [(Cp'''Co)2 (toluene)] (Cp'''=1, 2, 4‐tritertbutyl‐cyclopentadienyl) as a source for unsaturated {Cp'''Co} fragments was reacted with the sandwich complexes [Cp*Fe(η 5 ‐P5 )], [Cp'''Co((η 4 ‐P4 )] and [Cp'''Ni(η 3 ‐P3 )] to form novel heterobimetallic triple‐decker complexes. … (more)
- Is Part Of:
- Chemistry. Volume 26:Issue 7(2020)
- Journal:
- Chemistry
- Issue:
- Volume 26:Issue 7(2020)
- Issue Display:
- Volume 26, Issue 7 (2020)
- Year:
- 2020
- Volume:
- 26
- Issue:
- 7
- Issue Sort Value:
- 2020-0026-0007-0000
- Page Start:
- 1518
- Page End:
- 1524
- Publication Date:
- 2020-01-30
- Subjects:
- cobalt -- cyclo-Pn ligands -- iron -- nickel -- triple-decker complexes
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201905240 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12757.xml