Reduction of 1,3,5,7-Cyclooctatetraene by a Molecular Calcium Hydride: An Even Electron Polarised Insertion/Deprotonation Mechanism

Michael Hill; Andrew Wilson; Mary Mahon; Laurent Maron; Emma Richards

doi:10.1039/C9CC02418B

Reduction of 1,3,5,7-Cyclooctatetraene by a Molecular Calcium Hydride: An Even Electron Polarised Insertion/Deprotonation Mechanism

Michael Hill, Andrew Wilson, Mary Mahon, Laurent Maron, Emma Richards

Research output: Contribution to journal › Article › peer-review

24 Citations (SciVal)

Abstract

Reaction of a dimeric β-diketiminato calcium hydride with 1,3,5,7-cyclooctatetraene enables two electron aromatisation of the [8]annulene to provide an inverse sandwich dicalcium cyclooctatetraenyl derivative. This reactivity does not proceed through sequential single electron transfer but via a consecutive polarised Ca-H/CC insertion and deprotonation pathway that occurs at the intact dimeric hydride reagent.

Original language	English
Pages (from-to)	5732-5735
Number of pages	4
Journal	Chemical Communications
Volume	55
Issue number	40
Early online date	17 Apr 2019
DOIs	https://doi.org/10.1039/C9CC02418B
Publication status	Published - 18 May 2019

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
General Chemistry
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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10.1039/C9CC02418BLicence: CC BY-NC

Cite this

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title = "Reduction of 1,3,5,7-Cyclooctatetraene by a Molecular Calcium Hydride: An Even Electron Polarised Insertion/Deprotonation Mechanism",

abstract = "Reaction of a dimeric β-diketiminato calcium hydride with 1,3,5,7-cyclooctatetraene enables two electron aromatisation of the [8]annulene to provide an inverse sandwich dicalcium cyclooctatetraenyl derivative. This reactivity does not proceed through sequential single electron transfer but via a consecutive polarised Ca-H/CC insertion and deprotonation pathway that occurs at the intact dimeric hydride reagent.",

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T1 - Reduction of 1,3,5,7-Cyclooctatetraene by a Molecular Calcium Hydride: An Even Electron Polarised Insertion/Deprotonation Mechanism

AU - Hill, Michael

AU - Wilson, Andrew

AU - Mahon, Mary

AU - Maron, Laurent

AU - Richards, Emma

PY - 2019/5/18

Y1 - 2019/5/18

N2 - Reaction of a dimeric β-diketiminato calcium hydride with 1,3,5,7-cyclooctatetraene enables two electron aromatisation of the [8]annulene to provide an inverse sandwich dicalcium cyclooctatetraenyl derivative. This reactivity does not proceed through sequential single electron transfer but via a consecutive polarised Ca-H/CC insertion and deprotonation pathway that occurs at the intact dimeric hydride reagent.

AB - Reaction of a dimeric β-diketiminato calcium hydride with 1,3,5,7-cyclooctatetraene enables two electron aromatisation of the [8]annulene to provide an inverse sandwich dicalcium cyclooctatetraenyl derivative. This reactivity does not proceed through sequential single electron transfer but via a consecutive polarised Ca-H/CC insertion and deprotonation pathway that occurs at the intact dimeric hydride reagent.

UR - https://www.scopus.com/pages/publications/85065830138

U2 - 10.1039/C9CC02418B

DO - 10.1039/C9CC02418B

M3 - Article

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IS - 40

ER -

Reduction of 1,3,5,7-Cyclooctatetraene by a Molecular Calcium Hydride: An Even Electron Polarised Insertion/Deprotonation Mechanism

Abstract

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Nucleophilic alkaline earth boryls: from conception and theory to application

Augmentation of Alkaline Earth Reactivity: An FLP Analogy

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Reduction of 1,3,5,7-Cyclooctatetraene by a Molecular Calcium Hydride: An Even Electron Polarised Insertion/Deprotonation Mechanism

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Projects

Nucleophilic alkaline earth boryls: from conception and theory to application

Augmentation of Alkaline Earth Reactivity: An FLP Analogy

Cite this