VTechWorks staff will be away for the winter holidays starting Tuesday, December 24, 2024, through Wednesday, January 1, 2025, and will not be replying to requests during this time. Thank you for your patience, and happy holidays!
 

Imparting functional variety to cellulose ethers via olefin cross-metathesis

dc.contributor.authorDong, Yifanen
dc.contributor.authorEdgar, Kevin J.en
dc.contributor.departmentSustainable Biomaterialsen
dc.contributor.departmentChemistryen
dc.contributor.departmentMacromolecules Innovation Instituteen
dc.date.accessed2016-03-17en
dc.date.accessioned2016-03-18T22:24:52Zen
dc.date.available2016-03-18T22:24:52Zen
dc.date.issued2015-04-09en
dc.description.abstractOlefin cross-metathesis is a valuable new approach for imparting functional variety to cellulose ethers. Starting from commercially available ethyl cellulose, terminally unsaturated alkyl groups were appended as metathesis handles by reaction with allyl chloride, 5-bromo-1-pentene, 7-bromo-1-heptene and 11-bromo-1-undecene, employing sodium hydride catalyst. These olefin-terminal ethyl cellulose derivatives were then subjected to olefin cross-metathesis with a variety of electron-poor olefin substrates, including acrylic acid and acrylate esters under optimized conditions (5–10 mol% Hoveyda-Grubbs’ 2nd generation catalyst, 37 °C, 2 h). The effects of varying the length of the ω-unsaturated alkyl handle, and of the solvent systems used were evaluated. Ethyl cellulose containing a pent-4-enyl substituent performed best in cross metathesis reactions and a hept-6-enyl substituent gave similarly good results. Ethyl cellulose with allyl substituents gave low to moderate metathesis conversion (<50%), possibly due to steric effects and the proximity of the ether oxygen to the terminal olefin. Interestingly, longer tethers (undec-10-enyl) gave high conversions (up to 90%) but relatively slow reactions (ca. 12 h needed for high conversion). While limited in this study by the relatively low DS (OH) of the starting commercial ethyl cellulose materials, this methodology has strong promise for introduction of diverse functionality to cellulose ethers in chemospecific and mild fashion, enabling amorphous solid dispersion and other applications.en
dc.description.notesContains supporting information fileen
dc.description.notes2015 Royal Society of Chemistry Open Access Gold Articleen
dc.description.sponsorshipNational Science Foundation (U.S.)en
dc.format.extent12 p.en
dc.format.mimetypeapplication/pdfen
dc.identifier.citationDong, Y., & Edgar, K. J. (2015). Imparting functional variety to cellulose ethers via olefin cross-metathesis. Polymer Chemistry, 6(20), 3816-3827. doi:10.1039/C5PY00369Een
dc.identifier.doihttps://doi.org/10.1039/C5PY00369Een
dc.identifier.issn1759-9954en
dc.identifier.issue20en
dc.identifier.other2015_Dong_Imparting_functional_variety_to_cell.pdfen
dc.identifier.otherImparting_functional_variety_supp.pdfen
dc.identifier.otherDMR-1308276en
dc.identifier.urihttp://hdl.handle.net/10919/64952en
dc.identifier.volume6en
dc.language.isoen_USen
dc.publisherThe Royal Society of Chemistryen
dc.rightsCreative Commons Attribution-NonCommercial 3.0 Unporteden
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/en
dc.titleImparting functional variety to cellulose ethers via olefin cross-metathesisen
dc.title.serialPolymer Chemistryen
dc.typeArticle - Refereeden
dc.type.dcmitypeTexten

Files

Original bundle
Now showing 1 - 2 of 2
Loading...
Thumbnail Image
Name:
2015_Dong_Imparting_functional_variety_to_cell.pdf
Size:
1.39 MB
Format:
Adobe Portable Document Format
Description:
Loading...
Thumbnail Image
Name:
Imparting_functional_variety_supp.pdf
Size:
421.81 KB
Format:
Adobe Portable Document Format
Description: