http://www.cnr.it/ontology/cnr/individuo/prodotto/ID329761
Ring-opening metathesis polymerization of a diolefinic [2]-catenane-copper(i) complex: An easy route to polycatenanes (Articolo in rivista)
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- Ring-opening metathesis polymerization of a diolefinic [2]-catenane-copper(i) complex: An easy route to polycatenanes (Articolo in rivista) (literal)
- Anno
- 2015-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/ma502392v (literal)
- Alternative label
J.A. Berrocal, L.M. Pitet, M.M.L. Nieuwenhuizen, L.Mandolini, E.W. Meijer, S. Di Stefano (2015)
Ring-opening metathesis polymerization of a diolefinic [2]-catenane-copper(i) complex: An easy route to polycatenanes
in Macromolecules (Online); ACS, American chemical society, Washington, DC (Stati Uniti d'America)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- J.A. Berrocal, L.M. Pitet, M.M.L. Nieuwenhuizen, L.Mandolini, E.W. Meijer, S. Di Stefano (literal)
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- Dipartimento di Chimica, Sapienza Università di Roma and Istituto CNR di Metodologie Chimiche (IMC-CNR), Sapienza Università di Roma, P.le A. Moro 5, Rome, I-00185, Italy; Institute for Complex Molecular Systems, Eindhoven University of Technology, P.O. Box 513, MB Eindhoven, 5600, Netherlands (literal)
- Titolo
- Ring-opening metathesis polymerization of a diolefinic [2]-catenane-copper(i) complex: An easy route to polycatenanes (literal)
- Abstract
- A dilute (30 mM) dichloromethane solution of
the copper(I) complex 1·Cu+ of a [2]-catenane composed of
two identical 28-membered macrocyclic alkenes featuring a
phenanthroline moiety in the backbone was subjected to ringopening
metathesis polymerization (ROMP) with secondgeneration
Grubbs catalyst. Shortly after mixing of reactants,
the dark red solution transformed into a gel. The bis-
(phenanthroline)copper(I) units were effectively preserved
during ROMP, as evinced by spectroscopic analysis. This
implies that the putative metal alkylidene pseudorotaxane
intermediates did not undergo dethreading processes but were involved in ring-chain equilibria strongly biased toward the ring
products at the low monomer concentration employed in the ROMP reactions. MALDI-TOF mass spectra of the reaction
mixtures obtained at an early stage of the reaction revealed a distribution of interlocked oligomers (1·Cu+)n(PF6
-)n-1 with n up
to 7, with no traces of peaks ascribable to open chain species. Rheological and mechanical analyses of the gel products provided
independent evidence in support of the conclusion that the fraction of linear species in the polymer is negligible. Indications were
obtained that the major portion of the polymeric material is composed of fully interlocked species. (literal)
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