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Ring Expansion Alkyne Metathesis Polymerization.
Beauchamp, Andrew M; Chakraborty, Jhonti; Ghiviriga, Ion; Abboud, Khalil A; Lester, Daniel W; Veige, Adam S.
Afiliação
  • Beauchamp AM; Department of Chemistry, Center for Catalysis, University of Florida, Gainesville, Florida 32611, United States.
  • Chakraborty J; Department of Chemistry, Center for Catalysis, University of Florida, Gainesville, Florida 32611, United States.
  • Ghiviriga I; Department of Chemistry, Center for NMR Spectroscopy, University of Florida, Gainesville, Florida 32611, United States.
  • Abboud KA; Department of Chemistry, Center for Catalysis, University of Florida, Gainesville, Florida 32611, United States.
  • Lester DW; Polymer Characterization Research Technology Platform, University of Warwick, Coventry CV4 7AL, U.K.
  • Veige AS; Department of Chemistry, Center for Catalysis, University of Florida, Gainesville, Florida 32611, United States.
J Am Chem Soc ; 145(41): 22796-22802, 2023 Oct 18.
Article em En | MEDLINE | ID: mdl-37812163
The synthesis, characterization, and preliminary activity of an unprecedented tethered alkylidyne tungsten complex for ring expansion alkyne metathesis polymerization (REAMP) are reported. The tethered alkylidyne 7 is generated rapidly by combining alkylidyne W(CtBu)(CH2tBu)(O-2,6-i-Pr2C6H3)2 (6) with 1 equiv of an yne-ol proligand (5). Characterized by NMR studies and nuclear Overhauser effect spectroscopy, complex 7 is a dimer. Each metal center contains a tungsten-carbon triple bond tethered to the metal center via an alkoxide ligand. The polymerization of the strained cycloalkyne 3,8-didodecyloxy-5,6-dihydro-11,12-didehydrodibenzo[a,e]-[8]annulene, 8, to generate cyclic polymers was demonstrated. Size exclusion chromatography (SEC) and intrinsic viscosity (η) measurements confirm the polymer's cyclic topology.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article