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Synthesis and Reactivity of the [NCCCO]- Cyanoketenate Anion.
Wang, Tongtong; Guo, Zhuangzhuang; English, Laura E; Stephan, Douglas W; Jupp, Andrew R; Xu, Maotong.
Afiliação
  • Wang T; School of Chemical Science and Engineering, Tongji University, 1239 Siping Rd, Shanghai, China, 200092.
  • Guo Z; School of Chemical Science and Engineering, Tongji University, 1239 Siping Rd, Shanghai, China, 200092.
  • English LE; School of Chemistry, University of Birmingham, Edgbaston, Birmingham, West Midlands, UK, B15 2TT.
  • Stephan DW; Department of Chemistry, University of Toronto, 80 St. George St., Toronto, Ontario, Canada, M5S3H6.
  • Jupp AR; School of Chemistry, University of Birmingham, Edgbaston, Birmingham, West Midlands, UK, B15 2TT.
  • Xu M; School of Chemical Science and Engineering, Tongji University, 1239 Siping Rd, Shanghai, China, 200092.
Angew Chem Int Ed Engl ; 63(20): e202402728, 2024 May 13.
Article em En | MEDLINE | ID: mdl-38483891
ABSTRACT
Cyanoketene is a fundamental molecule that is actively being searched for in the interstellar medium. Its deprotonated form (cyanoketenate) is a heterocumulene that is isoelectronic to carbon suboxide whose structure has been the subject of debate. However, the investigation of cyanoketene and its derivatives is hampered by the lack of practical synthetic routes to these compounds. We report the first synthesis of the cyanoketenate anion in [K(18-crown-6)][NCCCO] (1) as a stable molecule on a multigram scale in excellent yields (>90 %). The structure of this molecule is probed crystallographically and computationally. We also explore the protonation of 1, and its reaction with triphenylsilylchloride and carbon dioxide. In all cases, anionic dimers are formed. The cyanoketene could be synthesized and crystallographically characterized when stabilized by a N-heterocyclic carbene. The cyanoketenate is a very useful unsaturated building block containing N, C and O atoms that can now be explored with relative ease and will undoubtedly unlock more interesting reactivity.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl / Angew. Chem. (Int. ed., Internet) / Angewandte Chemie (International ed. Internet) Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl / Angew. Chem. (Int. ed., Internet) / Angewandte Chemie (International ed. Internet) Ano de publicação: 2024 Tipo de documento: Article