The polymerization of bio-renewable terpenes such as b-ocimene (O), b-myrcene (M), and b-farnesene (F) promoted by CoCl2(PCyPh2)2 (1) in combination with modified methylalumoxane at room temperature is reported. Stereoregular polymers of O, M, and F were obtained. 1 also promoted, showing good stereoselectivity, the copolymerization of O and M with butadiene (B) in a wide range of compositions by suitably varying the alimentation feed: up to 67 and 75 mol% of O and M incorporated for poly(ocimene-butadiene) and poly(myrcene-butadiene) copolymers, respectively. These new materials with elastomeric properties (glass transition temperatures observed in the range of-5.7 to-72.5 8C) were fully characterized by differential scanning calorimetry, size exclusion chromatography, and nuclear magnetic resonance spectroscopy (1H, 13C, and two-dimensional experiments).

NEW ELASTOMERIC MATERIALS FROM BIOMASS: STEREOSELECTIVE POLYMERIZATION OF LINEAR TERPENES AND THEIR COPOLYMERIZATION WITH BUTADIENE BY USING A COBALT COMPLEX WITH PHOSPHANE LIGANDS

Lamparelli, David Hermann;Paradiso, Veronica;Capacchione, Carmine
2020-01-01

Abstract

The polymerization of bio-renewable terpenes such as b-ocimene (O), b-myrcene (M), and b-farnesene (F) promoted by CoCl2(PCyPh2)2 (1) in combination with modified methylalumoxane at room temperature is reported. Stereoregular polymers of O, M, and F were obtained. 1 also promoted, showing good stereoselectivity, the copolymerization of O and M with butadiene (B) in a wide range of compositions by suitably varying the alimentation feed: up to 67 and 75 mol% of O and M incorporated for poly(ocimene-butadiene) and poly(myrcene-butadiene) copolymers, respectively. These new materials with elastomeric properties (glass transition temperatures observed in the range of-5.7 to-72.5 8C) were fully characterized by differential scanning calorimetry, size exclusion chromatography, and nuclear magnetic resonance spectroscopy (1H, 13C, and two-dimensional experiments).
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11386/4894857
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