Lipase-catalyzed ring-opening polymerization of trimethylene carbonate

ABSTRACT: This work was directed at extending the use of lipase-catalyzed ring-opening polymerizations to cyclic carbonate monomers. Of the seven lipases screened for bulk trimethylene carbonate (TMC) polymerization (70°C, 120 h), Novozym-435 from Candida antarctica gave almost quantitative monomer...

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Main Authors: Kirpal S Bisht, Yuri Y Svirkin, Lori A Henderson, Richard A Gross, David L Kaplan, Graham Swift
Other Authors: The Pennsylvania State University CiteSeerX Archives
Format: Text
Language:English
Published: 1997
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Online Access:http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1084.7008
http://homepages.rpi.edu/%7Egrossr/_doc/publication/Macromolecules%201997%2030%207735%20ma9708858.pdf
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spelling ftciteseerx:oai:CiteSeerX.psu:10.1.1.1084.7008 2023-05-15T13:59:47+02:00 Lipase-catalyzed ring-opening polymerization of trimethylene carbonate Kirpal S Bisht Yuri Y Svirkin Lori A Henderson Richard A Gross David L Kaplan Graham Swift The Pennsylvania State University CiteSeerX Archives 1997 application/pdf http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1084.7008 http://homepages.rpi.edu/%7Egrossr/_doc/publication/Macromolecules%201997%2030%207735%20ma9708858.pdf en eng http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1084.7008 http://homepages.rpi.edu/%7Egrossr/_doc/publication/Macromolecules%201997%2030%207735%20ma9708858.pdf Metadata may be used without restrictions as long as the oai identifier remains attached to it. http://homepages.rpi.edu/%7Egrossr/_doc/publication/Macromolecules%201997%2030%207735%20ma9708858.pdf text 1997 ftciteseerx 2020-05-03T00:30:48Z ABSTRACT: This work was directed at extending the use of lipase-catalyzed ring-opening polymerizations to cyclic carbonate monomers. Of the seven lipases screened for bulk trimethylene carbonate (TMC) polymerization (70°C, 120 h), Novozym-435 from Candida antarctica gave almost quantitative monomer conversion (97%) and poly(TMC) with a Mn ) 15 000 (Mw/Mn ) 2.2) with no apparent decarboxylation during propagation. The lipases from Pseudomonas species (AK and PS-30) and porcine pancreas (PPL) also exhibited high monomer conversions (>80%, 120 h) but gave lower molecular weight polymers with broad polydispersity. Analyses by 1 H-NMR spectroscopy suggested that poly(TMC) prepared by Novozym-435-catalyzed polymerization had terminal -CH2OH functionalities at both chain ends. A monotonic increase in monomer conversion with time and the rapid increase in Mn as a function of monomer conversion for Novozym-435-catalyzed TMC bulk polymerization at 70°C suggest that the polymerization has chain-type propagation kinetics. An increase in conversion above 66% did not substantially change Mn. The percent conversion was larger when the reaction temperature was increased from 45 to 55°C. Further increase in the reaction temperature from 55 to 85°C did not give higher percent conversion values. The molecular weight decreased substantially as the reaction temperature was increased from 55 to 85°C (Mn from 24 400 to 5 900). The highest poly(TMC) molecular weight (Mn ) 24 400) was obtained by conducting the polymerization at 55°C. Monomer conversion and molecular weight as a function of the percent reaction water content (w/w) were investigated. Increasing the water content resulted in enhanced polymerization rates and decreased molecular weights. Separation of the oligomeric products from polymerizations of TMC in dried dioxane and toluene catalyzed by porcine pancreatic lipase led to the isolation of di-and triadducts of trimethylene carbonate. Based on the symmetrical structure of these products and the end-group structure of ... Text Antarc* Antarctica Unknown
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description ABSTRACT: This work was directed at extending the use of lipase-catalyzed ring-opening polymerizations to cyclic carbonate monomers. Of the seven lipases screened for bulk trimethylene carbonate (TMC) polymerization (70°C, 120 h), Novozym-435 from Candida antarctica gave almost quantitative monomer conversion (97%) and poly(TMC) with a Mn ) 15 000 (Mw/Mn ) 2.2) with no apparent decarboxylation during propagation. The lipases from Pseudomonas species (AK and PS-30) and porcine pancreas (PPL) also exhibited high monomer conversions (>80%, 120 h) but gave lower molecular weight polymers with broad polydispersity. Analyses by 1 H-NMR spectroscopy suggested that poly(TMC) prepared by Novozym-435-catalyzed polymerization had terminal -CH2OH functionalities at both chain ends. A monotonic increase in monomer conversion with time and the rapid increase in Mn as a function of monomer conversion for Novozym-435-catalyzed TMC bulk polymerization at 70°C suggest that the polymerization has chain-type propagation kinetics. An increase in conversion above 66% did not substantially change Mn. The percent conversion was larger when the reaction temperature was increased from 45 to 55°C. Further increase in the reaction temperature from 55 to 85°C did not give higher percent conversion values. The molecular weight decreased substantially as the reaction temperature was increased from 55 to 85°C (Mn from 24 400 to 5 900). The highest poly(TMC) molecular weight (Mn ) 24 400) was obtained by conducting the polymerization at 55°C. Monomer conversion and molecular weight as a function of the percent reaction water content (w/w) were investigated. Increasing the water content resulted in enhanced polymerization rates and decreased molecular weights. Separation of the oligomeric products from polymerizations of TMC in dried dioxane and toluene catalyzed by porcine pancreatic lipase led to the isolation of di-and triadducts of trimethylene carbonate. Based on the symmetrical structure of these products and the end-group structure of ...
author2 The Pennsylvania State University CiteSeerX Archives
format Text
author Kirpal S Bisht
Yuri Y Svirkin
Lori A Henderson
Richard A Gross
David L Kaplan
Graham Swift
spellingShingle Kirpal S Bisht
Yuri Y Svirkin
Lori A Henderson
Richard A Gross
David L Kaplan
Graham Swift
Lipase-catalyzed ring-opening polymerization of trimethylene carbonate
author_facet Kirpal S Bisht
Yuri Y Svirkin
Lori A Henderson
Richard A Gross
David L Kaplan
Graham Swift
author_sort Kirpal S Bisht
title Lipase-catalyzed ring-opening polymerization of trimethylene carbonate
title_short Lipase-catalyzed ring-opening polymerization of trimethylene carbonate
title_full Lipase-catalyzed ring-opening polymerization of trimethylene carbonate
title_fullStr Lipase-catalyzed ring-opening polymerization of trimethylene carbonate
title_full_unstemmed Lipase-catalyzed ring-opening polymerization of trimethylene carbonate
title_sort lipase-catalyzed ring-opening polymerization of trimethylene carbonate
publishDate 1997
url http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1084.7008
http://homepages.rpi.edu/%7Egrossr/_doc/publication/Macromolecules%201997%2030%207735%20ma9708858.pdf
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