Simple Alkaline‐Earth Metal Catalysts for Effective Alkene Hydrogenation. Issue 46 (15th October 2018)
- Record Type:
- Journal Article
- Title:
- Simple Alkaline‐Earth Metal Catalysts for Effective Alkene Hydrogenation. Issue 46 (15th October 2018)
- Main Title:
- Simple Alkaline‐Earth Metal Catalysts for Effective Alkene Hydrogenation
- Authors:
- Bauer, Heiko
Alonso, Mercedes
Fischer, Christian
Rösch, Bastian
Elsen, Holger
Harder, Sjoerd - Abstract:
- Abstract: Alkaline earth metal amides (AeN′′2 : Ae=Ca, Sr, Ba, N′′=N(SiMe3 )2 ) catalyze alkene hydrogenation (80–120 °C, 1–6 bar H2, 1–10 mol % cat.), with the activity increasing with metal size. Various activated C=C bonds (styrene, p ‐MeO‐styrene, α‐Me‐styrene, Ph2 C=CH2, trans ‐stilbene, cyclohexadiene, 1‐Ph‐cyclohexene), semi‐activated C=C bonds (Me3 SiCH=CH2, norbornadiene), or non‐activated (isolated) C=C bonds (norbornene, 4‐vinylcyclohexene, 1‐hexene) could be reduced. The results show that neutral Ca or Ba catalysts are active in the challenging hydrogenation of isolated double bonds. For activated alkenes (e.g. styrene), polymerization is fully suppressed due to fast protonation of the highly reactive benzyl intermediate by N′′H (formed in the catalyst initiation). Using cyclohexadiene as the H source, the first Ae metal catalyzed H‐transfer hydrogenation is reported. DFT calculations on styrene hydrogenation using CaN′′2 show that styrene oligomerization competes with styrene hydrogenation. Calculations also show that protonation of the benzylcalcium intermediate with N′′H is a low‐energy escape route, thus avoiding oligomerization. Abstract : Keep it simple : The widely used, easily accessible, alkaline earth metal amides M(NR2 )2 (M=Ca, Sr, Ba, R=SiMe3 ) are highly active alkene hydrogenation catalysts. Alkene oligomerization is fully suppressed by trapping the reactive intermediate with R2 NH. A first example of Group 2 metal hydrogen transfer catalysis isAbstract: Alkaline earth metal amides (AeN′′2 : Ae=Ca, Sr, Ba, N′′=N(SiMe3 )2 ) catalyze alkene hydrogenation (80–120 °C, 1–6 bar H2, 1–10 mol % cat.), with the activity increasing with metal size. Various activated C=C bonds (styrene, p ‐MeO‐styrene, α‐Me‐styrene, Ph2 C=CH2, trans ‐stilbene, cyclohexadiene, 1‐Ph‐cyclohexene), semi‐activated C=C bonds (Me3 SiCH=CH2, norbornadiene), or non‐activated (isolated) C=C bonds (norbornene, 4‐vinylcyclohexene, 1‐hexene) could be reduced. The results show that neutral Ca or Ba catalysts are active in the challenging hydrogenation of isolated double bonds. For activated alkenes (e.g. styrene), polymerization is fully suppressed due to fast protonation of the highly reactive benzyl intermediate by N′′H (formed in the catalyst initiation). Using cyclohexadiene as the H source, the first Ae metal catalyzed H‐transfer hydrogenation is reported. DFT calculations on styrene hydrogenation using CaN′′2 show that styrene oligomerization competes with styrene hydrogenation. Calculations also show that protonation of the benzylcalcium intermediate with N′′H is a low‐energy escape route, thus avoiding oligomerization. Abstract : Keep it simple : The widely used, easily accessible, alkaline earth metal amides M(NR2 )2 (M=Ca, Sr, Ba, R=SiMe3 ) are highly active alkene hydrogenation catalysts. Alkene oligomerization is fully suppressed by trapping the reactive intermediate with R2 NH. A first example of Group 2 metal hydrogen transfer catalysis is given. … (more)
- Is Part Of:
- Angewandte Chemie international edition. Volume 57:Issue 46(2018)
- Journal:
- Angewandte Chemie international edition
- Issue:
- Volume 57:Issue 46(2018)
- Issue Display:
- Volume 57, Issue 46 (2018)
- Year:
- 2018
- Volume:
- 57
- Issue:
- 46
- Issue Sort Value:
- 2018-0057-0046-0000
- Page Start:
- 15177
- Page End:
- 15182
- Publication Date:
- 2018-10-15
- Subjects:
- alkaline earth metals -- alkenes -- DFT calculations -- hydrogenation
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3773 ↗
http://www.interscience.wiley.com/jpages/1433-7851 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/anie.201810026 ↗
- Languages:
- English
- ISSNs:
- 1433-7851
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11498.xml