Hall, Lewis Marshall, Tew, David, Pridmore, Natalie Estelle et al. (3 more authors) (2017) A Structurally Characterized Fluoroalkyne. Angewandte Chemie International Edition. pp. 7551-7556. ISSN 1433-7851
Abstract
The facile synthesis of a stable and isolable compound with a fluoroalkynyl group, M−C≡CF, is reported. Reaction of [Ru(C≡CH)(η 5-C 5Me 5)(dppe)] with an electrophilic fluorinating agent (NFSI) results in the formation of the fluorovinylidene complex [Ru(=C=CHF)(η 5-C 5Me 5)(dppe)][N(SO 2Ph) 2]. Subsequent deprotonation with LiN(SiMe 3) 2 affords the fluoroalkynyl complex [Ru(C≡CF)(η 5-C 5Me 5)(dppe)]. In marked contrast to the rare and highly reactive examples of fluoroalkynes that have been reported previously, this compound can be readily isolated and structurally characterized. This has allowed the structure and bonding in the CCF motif to be explored. Further electrophilic fluorination of this species yields the difluorovinylidene complex [Ru(C=CF 2)(η 5-C 5Me 5)(dppe)][N(SO 2Ph) 2].
Metadata
Item Type: | Article |
---|---|
Authors/Creators: |
|
Copyright, Publisher and Additional Information: | © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. This is an author-produced version of the published paper. Uploaded in accordance with the publisher’s self-archiving policy. Further copying may not be permitted; contact the publisher for details |
Keywords: | alkynes,alkynyls,electrophilic fluorination,fluorine,vinylidenes |
Dates: |
|
Institution: | The University of York |
Academic Units: | The University of York > Faculty of Sciences (York) > Chemistry (York) |
Funding Information: | Funder Grant number EPSRC EP/H011455/1 |
Depositing User: | Pure (York) |
Date Deposited: | 01 Jun 2017 08:30 |
Last Modified: | 08 Feb 2025 00:22 |
Published Version: | https://doi.org/10.1002/anie.201702401 |
Status: | Published |
Refereed: | Yes |
Identification Number: | 10.1002/anie.201702401 |
Related URLs: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:117163 |
Download
Filename: Accepted_manuscript_201702401.docx
Description: Accepted-manuscript-201702401