Controlling Catenation in Germanium(I) Chemistry through Hemilability. (9th June 2021)
- Record Type:
- Journal Article
- Title:
- Controlling Catenation in Germanium(I) Chemistry through Hemilability. (9th June 2021)
- Main Title:
- Controlling Catenation in Germanium(I) Chemistry through Hemilability
- Authors:
- Caise, Alexa
Griffin, Liam P.
Heilmann, Andreas
McManus, Caitilín
Campos, Jesús
Aldridge, Simon - Abstract:
- Abstract: We present a novel approach for constructing chains of Group 14 metal atoms linked by unsupported metal–metal bonds that exploits hemilabile ligands to generate unsaturated metal sites. The formation/nature of catenated species (oligo‐dimetallynes) can be controlled by the use of (acidic/basic) "protecting groups" and through variation of the ligand scaffold. Reduction of Ar NiPr2 GeCl (Ar NiPr2 =2, 6‐( i Pr2 NCH2 )2 C6 H3 )—featuring hemilabile N i Pr2 donors—yields (Ar NiPr2 Ge)4 (2 ), which contains a tetrameric Ge4 chain. 2 represents a novel type of a linear homo‐catenated Ge I compound featuring unsupported E−E bonds. Trapping experiments reveal that a key structural component is the central two‐way Ge=Ge donor‐acceptor bond: reactions with IMe4 and W(CO)5 (NMe3 ) give the base‐ or acid‐stabilized digermynes (Ar NiPr2 Ge(IMe4 ))2 (4 ) and (Ar NiPr2 Ge{W(CO)5 })2 (5 ), respectively. The use of smaller N ‐donors leads to stronger Ge‐N interactions and quenching of catenation behaviour: reduction of Ar NEt2 GeCl gives the digermyne (Ar NEt2 Ge)2, while the unsymmetrical system Ar NEt2 GeGeAr NiPr2 dimerizes to give tetranuclear (Ar NEt2 GeGeAr NiPr2 )2 through aggregation at the N i Pr2 ‐ligated Ge I centres. Abstract : A new approach for the rational construction of chains of Group 14 metal atoms linked by unsupported metal–metal bonds is reported, which exploits hemilabile ancillary ligands to generate unsaturated metal sites. The resulting oligo‐dimetallyneAbstract: We present a novel approach for constructing chains of Group 14 metal atoms linked by unsupported metal–metal bonds that exploits hemilabile ligands to generate unsaturated metal sites. The formation/nature of catenated species (oligo‐dimetallynes) can be controlled by the use of (acidic/basic) "protecting groups" and through variation of the ligand scaffold. Reduction of Ar NiPr2 GeCl (Ar NiPr2 =2, 6‐( i Pr2 NCH2 )2 C6 H3 )—featuring hemilabile N i Pr2 donors—yields (Ar NiPr2 Ge)4 (2 ), which contains a tetrameric Ge4 chain. 2 represents a novel type of a linear homo‐catenated Ge I compound featuring unsupported E−E bonds. Trapping experiments reveal that a key structural component is the central two‐way Ge=Ge donor‐acceptor bond: reactions with IMe4 and W(CO)5 (NMe3 ) give the base‐ or acid‐stabilized digermynes (Ar NiPr2 Ge(IMe4 ))2 (4 ) and (Ar NiPr2 Ge{W(CO)5 })2 (5 ), respectively. The use of smaller N ‐donors leads to stronger Ge‐N interactions and quenching of catenation behaviour: reduction of Ar NEt2 GeCl gives the digermyne (Ar NEt2 Ge)2, while the unsymmetrical system Ar NEt2 GeGeAr NiPr2 dimerizes to give tetranuclear (Ar NEt2 GeGeAr NiPr2 )2 through aggregation at the N i Pr2 ‐ligated Ge I centres. Abstract : A new approach for the rational construction of chains of Group 14 metal atoms linked by unsupported metal–metal bonds is reported, which exploits hemilabile ancillary ligands to generate unsaturated metal sites. The resulting oligo‐dimetallyne chains feature alternating single and double metal–metal bonds. … (more)
- Is Part Of:
- Angewandte Chemie. Volume 133:Number 28(2021)
- Journal:
- Angewandte Chemie
- Issue:
- Volume 133:Number 28(2021)
- Issue Display:
- Volume 133, Issue 28 (2021)
- Year:
- 2021
- Volume:
- 133
- Issue:
- 28
- Issue Sort Value:
- 2021-0133-0028-0000
- Page Start:
- 15734
- Page End:
- 15740
- Publication Date:
- 2021-06-09
- Subjects:
- catenation -- germanium -- hemilabile -- low-valent compounds -- pincer ligand
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ange.202104643 ↗
- Languages:
- English
- ISSNs:
- 0044-8249
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24036.xml