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Multicomponent Synthesis of Poly(α-aminophosphine chalcogenide)s and Subsequent Depolymerization.
Lamberink-Ilupeju, Jan-Willem; Willans, Mathew J; Gilroy, Joe B; Noël, James J; Blacquiere, Johanna M; Ragogna, Paul J.
Afiliação
  • Lamberink-Ilupeju JW; Department of Chemistry, The University of Western Ontario, London, Ontario N6A 587, Canada.
  • Willans MJ; Department of Chemistry, The University of Western Ontario, London, Ontario N6A 587, Canada.
  • Gilroy JB; Department of Chemistry, The University of Western Ontario, London, Ontario N6A 587, Canada.
  • Noël JJ; Department of Chemistry, The University of Western Ontario, London, Ontario N6A 587, Canada.
  • Blacquiere JM; Surface Science Western, The University of Western Ontario, London, Ontario N6G 0J3, Canada.
  • Ragogna PJ; Department of Chemistry, The University of Western Ontario, London, Ontario N6A 587, Canada.
Inorg Chem ; 62(37): 15104-15109, 2023 Sep 18.
Article em En | MEDLINE | ID: mdl-37678149
ABSTRACT
Multicomponent reactions of primary phosphines (R-PH2), diimines (R'-N═C(H)-R-(H)C═N-R'), and chalcogens (O2, S8) generate poly(α-aminophosphine chalcogenide)s (4-7) through step-growth polymerization. Characterization of the linear polymers using 31P{1H} diffusion-ordered NMR spectroscopy (DOSY) experiments aided in determining the molecular weight (Mw) of the material. Subjecting the polyphosphine oxide or sulfide to reducing conditions in the presence of a Lewis acid resulted in complete depolymerization of the polymers, quantitatively releasing the 1° phosphine and diimine (2) starting materials, with concomitant reduction of diimine to diamine (9).

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