scholarly journals Monotelechelic Poly(oxa)norbornenes by Ring-Opening Metathesis Polymerization Using Direct End-Capping and Cross-Metathesis

2010 ◽  
Vol 43 (1) ◽  
pp. 213-221 ◽  
Author(s):  
John B. Matson ◽  
Robert H. Grubbs
Keyword(s):  
Ring Opening ◽  
Ring Opening Metathesis Polymerization ◽  
Metathesis Polymerization ◽  
Cross Metathesis ◽  
End Capping

scholarly journals Application of olefin metathesis in the synthesis of functionalized polyhedral oligomeric silsesquioxanes (POSS) and POSS-containing polymeric materials

2019 ◽  
Vol 15 ◽  
pp. 310-332 ◽  
Author(s):  
Patrycja Żak ◽  
Cezary Pietraszuk
Keyword(s):  
Olefin Metathesis ◽  
Ring Opening ◽  
Polymeric Materials ◽  
Acyclic Diene Metathesis ◽  
Polyhedral Oligomeric Silsesquioxanes ◽  
Ring Opening Metathesis Polymerization ◽  
Metathesis Polymerization ◽  
Cross Metathesis ◽  
Terminal Olefins ◽  
Synthesized Materials

This mini-review summarizes the applications of olefin metathesis in synthesis and functionalization of polyhedral oligomeric silsesquioxanes (POSS) and POSS-containing polymeric materials. Three types of processes, i.e., cross metathesis (CM) of vinyl-substituted POSS with terminal olefins, acyclic diene metathesis (ADMET) copolymerization of divinyl-substituted POSS with α,ω-dienes and ring-opening metathesis polymerization (ROMP) of POSS-substituted norbornene (or other ROMP susceptible cycloolefins) are discussed. Emphasis was put on the synthetic and catalytic aspects rather than on the properties and applications of synthesized materials.

scholarly journals Molecular Weight Control via Cross Metathesis in Photo‐Redox Mediated Ring‐Opening Metathesis Polymerization

2020 ◽  
Vol 132 (23) ◽  
pp. 9159-9164
Author(s):  
Victoria K. Kensy ◽  
Rachel L. Tritt ◽  
Farihah M. Haque ◽  
Laura M. Murphy ◽  
Daniel B. Knorr ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Ring Opening ◽  
Weight Control ◽  
Ring Opening Metathesis Polymerization ◽  
Metathesis Polymerization ◽  
Molecular Weight Control ◽  
Cross Metathesis

Bis-mixed-carbene ruthenium-thiolate-alkylidene complexes: synthesis and olefin metathesis activity

2015 ◽  
Vol 44 (4) ◽  
pp. 1724-1733 ◽  
Author(s):  
Fatme Dahcheh ◽  
Douglas W. Stephan
Keyword(s):  
Olefin Metathesis ◽  
Ring Opening ◽  
Ring Opening Metathesis Polymerization ◽  
Metathesis Polymerization ◽  
Cross Metathesis ◽  
Vinyl Sulfides ◽  
Alkylidene Complexes

A series of bis-carbene Ru-hydride species were prepared and subsequently shown to react with aryl-vinyl-sulfides to give the corresponding biscarbene-alkylidene complexes. The activities of these species for ring-opening metathesis polymerization, ring-closing and cross-metathesis are reported. While these systems are shown to exhibit modest metathesis activities, the reactivity is enhanced in the presence of BCl3.

scholarly journals Molecular Weight Control via Cross Metathesis in Photo‐Redox Mediated Ring‐Opening Metathesis Polymerization

2020 ◽  
Vol 59 (23) ◽  
pp. 9074-9079 ◽  
Author(s):  
Victoria K. Kensy ◽  
Rachel L. Tritt ◽  
Farihah M. Haque ◽  
Laura M. Murphy ◽  
Daniel B. Knorr ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Ring Opening ◽  
Weight Control ◽  
Ring Opening Metathesis Polymerization ◽  
Metathesis Polymerization ◽  
Molecular Weight Control ◽  
Cross Metathesis

scholarly journals α,ω-Epoxide, Oxetane, and Dithiocarbonate Telechelic Copolyolefins: Access by Ring-Opening Metathesis/Cross-Metathesis Polymerization (ROMP/CM) of Cycloolefins in the Presence of Functional Symmetric Chain-Transfer Agents

Polymers ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 1241 ◽  
Author(s):  
Elise Vanbiervliet ◽  
Stéphane Fouquay ◽  
Guillaume Michaud ◽  
Frédéric Simon ◽  
Jean-François Carpentier ◽  
...  
Keyword(s):  
Ring Opening ◽  
Chain Transfer ◽  
Operating Conditions ◽  
Metathesis Polymerization ◽  
Cross Metathesis ◽  
Cyclic Olefins ◽  
Low Viscosity ◽  
End Capping ◽  
Thermal Signature ◽  
Symmetric Chain

Epoxide- and oxetane-α,ω-telechelic (co)polyolefins have been successfully synthesized by the tandem ring-opening metathesis polymerization (ROMP)/cross-metathesis (CM) of cyclic olefins using Grubbs’ second-generation catalyst (G2) in the presence of a bifunctional symmetric alkene epoxide- or oxetane-functionalized chain-transfer agent (CTA). From cyclooctene (COE), trans,trans,cis-1,5,9-cyclododecatriene (CDT), norbornene (NB), and methyl 5-norbornene-2-carboxylate (NBCOOMe), with bis(oxiran-2-ylmethyl) maleate (CTA 1), bis(oxetane-2-ylmethyl) maleate (CTA 2), or bis(oxetane-2-ylmethyl) (E)-hex-3-enedioate (CTA 3), well-defined α,ω-di(epoxide or oxetane) telechelic PCOEs, P(COE-co-NB or -NBCOOMe)s, and P(NB-co-CDT)s were isolated under mild operating conditions (40 or 60 °C, 24 h). The oxetane CTA 3 and the epoxide CTA 1 were revealed to be significantly more efficient in the CM step than CTA 2, which apparently inhibits the reaction. Quantitative dithiocarbonatation (CS2/LiBr, 40 °C, THF) of an α,ω-di(epoxide) telechelic P(NB-co-CDT) afforded a convenient approach to the analogous α,ω-bis(dithiocarbonate) telechelic P(NB-co-CDT). The nature of the end-capping function of the epoxide/oxetane/dithiocarbonate telechelic P(NB-co-CDT)s did not impact their thermal signature, as measured by DSC. These copolymers also displayed a low viscosity liquid-like behavior and a shear thinning rheological behavior.

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