A novel one-pot process for the preparation of linear and hyperbranched polycarbonates of various diols and triols using dimethyl carbonate. Issue 21 (21st February 2017)
- Record Type:
- Journal Article
- Title:
- A novel one-pot process for the preparation of linear and hyperbranched polycarbonates of various diols and triols using dimethyl carbonate. Issue 21 (21st February 2017)
- Main Title:
- A novel one-pot process for the preparation of linear and hyperbranched polycarbonates of various diols and triols using dimethyl carbonate
- Authors:
- Sun, Jingjiang
Aly, Kamal Ibrahim
Kuckling, Dirk - Abstract:
- Abstract : A novel one-pot method for preparation of high molecular-weight linear and hyperbranched polycarbonates from diols and triols with dimethyl carbonate. Abstract : A new eco-friendly strategy for the preparation of linear and hyperbranched polycarbonates was developed. Our work referred to a one-pot condensation polymerization of various alcohols (diols and triols) with equivalent amounts of eco-friendly dimethyl carbonate (DMC) at 120 °C, atmospheric pressure and in 1, 4-dioxane solution using 4-dimethylaminopyridine (DMAP) or lithium acetylacetonate (LiAcac) as a catalyst. Polymer chains were built by pure transesterification of hydroxyl and methyl carbonate chain ends, and the single byproduct (methanol) was removed using a pressure-equalized addition funnel filled with 4 Å molecular sieves as the crucial equipment in this work. Using this strategy, hyperbranched polycarbonates with high molar masses ( M n up to 10 000 g mol −1 and M w up to 64 000 g mol −1 ) and high hydroxyl end group contents (up to 94%) were successfully prepared using dimethyl carbonate instead of toxic phosgene or phosgene-based monomers for the first time. In addition, linear aliphatic polycarbonates of various diols were also synthesized with M n up to 16 000 g mol −1 and low molar mass distributions ( Đ M < 1.70). Another eco-friendly aspect of this work was the use of equimolar amounts of DMC to avoid waste and the disposal of excess DMC; in a classic 2-step polycondensation forAbstract : A novel one-pot method for preparation of high molecular-weight linear and hyperbranched polycarbonates from diols and triols with dimethyl carbonate. Abstract : A new eco-friendly strategy for the preparation of linear and hyperbranched polycarbonates was developed. Our work referred to a one-pot condensation polymerization of various alcohols (diols and triols) with equivalent amounts of eco-friendly dimethyl carbonate (DMC) at 120 °C, atmospheric pressure and in 1, 4-dioxane solution using 4-dimethylaminopyridine (DMAP) or lithium acetylacetonate (LiAcac) as a catalyst. Polymer chains were built by pure transesterification of hydroxyl and methyl carbonate chain ends, and the single byproduct (methanol) was removed using a pressure-equalized addition funnel filled with 4 Å molecular sieves as the crucial equipment in this work. Using this strategy, hyperbranched polycarbonates with high molar masses ( M n up to 10 000 g mol −1 and M w up to 64 000 g mol −1 ) and high hydroxyl end group contents (up to 94%) were successfully prepared using dimethyl carbonate instead of toxic phosgene or phosgene-based monomers for the first time. In addition, linear aliphatic polycarbonates of various diols were also synthesized with M n up to 16 000 g mol −1 and low molar mass distributions ( Đ M < 1.70). Another eco-friendly aspect of this work was the use of equimolar amounts of DMC to avoid waste and the disposal of excess DMC; in a classic 2-step polycondensation for polycarbonate synthesis excess DMC is a prerequisite in order to obtain high molar masses. … (more)
- Is Part Of:
- RSC advances. Volume 7:Issue 21(2017)
- Journal:
- RSC advances
- Issue:
- Volume 7:Issue 21(2017)
- Issue Display:
- Volume 7, Issue 21 (2017)
- Year:
- 2017
- Volume:
- 7
- Issue:
- 21
- Issue Sort Value:
- 2017-0007-0021-0000
- Page Start:
- 12550
- Page End:
- 12560
- Publication Date:
- 2017-02-21
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7ra01317e ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 55.xml