Please use this identifier to cite or link to this item:
http://hdl.handle.net/1942/16784
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | VANDENBERGH, Joke | - |
dc.contributor.author | Tura, Tiago | - |
dc.contributor.author | BAETEN, Evelien | - |
dc.contributor.author | JUNKERS, Tanja | - |
dc.date.accessioned | 2014-05-14T14:42:41Z | - |
dc.date.available | 2014-05-14T14:42:41Z | - |
dc.date.issued | 2014 | - |
dc.identifier.citation | JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 52 (9), p. 1263-1274 | - |
dc.identifier.issn | 0887-624X | - |
dc.identifier.uri | http://hdl.handle.net/1942/16784 | - |
dc.description.abstract | This study presents the development of microreactor protocols for the successful continuous flow end group modification of atom transfer radical polymerization precursor polymers into azide end-capped materials and the subsequent copper-catalyzed azide alkyne click reactions with alkyne polymers, in flow. By using a microreactor, the reaction speed of the azidation of poly(butyl acrylate), poly(methyl acrylate), and polystyrene can be accelerated from hours to seconds and full end group conversion is obtained. Subsequently, coppercatalyzed click reactions are executed in a flow reactor at 80 C. Good coupling efficiencies are observed and various block copolymer combinations are prepared. Furthermore, the flow reaction can be carried out in only 40 min, while a batch procedure takes several hours to reach completion. The results indicate that the use of a continuous flow reactor for end group modifications as well as click reactions has clear benefits towards the development and improvement of well-defined polymer materials. | - |
dc.description.sponsorship | The authors are grateful for award of the Odysseus project "Precise Polymer Design for the Development of New Materials" by the Fund for Scientific Research-Flanders (FWO). Additional support via the European Science FoundationPrecision Polymer Materials (P2M) program is acknowledged. Also, the authors wish to thank the "Belgian Science Policy" for financial support in the frame of the "Interuniversity Attraction Poles Programme IAP-PAI P7/05" "Functional Supramolecular Systems." | - |
dc.language.iso | en | - |
dc.rights | © 2014 Wiley Periodicals, Inc. | - |
dc.subject.other | atom transfer radical polymerization (ATRP); azidation; click chemistry; click reactions; diblock copolymers; microflow chemistry; microreactor technology; radical polymerization; reversible addition fragmentation chain transfer (RAFT) | - |
dc.title | Polymer End Group Modifications and Polymer Conjugations via " Click" Chemistry Employing Microreactor Technology | - |
dc.type | Journal Contribution | - |
dc.identifier.epage | 1274 | - |
dc.identifier.issue | 9 | - |
dc.identifier.spage | 1263 | - |
dc.identifier.volume | 52 | - |
local.bibliographicCitation.jcat | A1 | - |
dc.description.notes | Junkers, T (reprint author), Univ Hasselt, Inst Mat Res IMO Imomec, Polymer React Design Grp, Agoralaan Bldg D, B-3590 Diepenbeek, Belgium. thomas.junkers@uhasselt.be | - |
local.type.refereed | Refereed | - |
local.type.specified | Article | - |
dc.identifier.doi | 10.1002/pola.27112 | - |
dc.identifier.isi | 000333310800005 | - |
item.fulltext | With Fulltext | - |
item.contributor | VANDENBERGH, Joke | - |
item.contributor | Tura, Tiago | - |
item.contributor | BAETEN, Evelien | - |
item.contributor | JUNKERS, Tanja | - |
item.fullcitation | VANDENBERGH, Joke; Tura, Tiago; BAETEN, Evelien & JUNKERS, Tanja (2014) Polymer End Group Modifications and Polymer Conjugations via " Click" Chemistry Employing Microreactor Technology. In: JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 52 (9), p. 1263-1274. | - |
item.accessRights | Open Access | - |
item.validation | ecoom 2015 | - |
crisitem.journal.issn | 0887-624X | - |
crisitem.journal.eissn | 1099-0518 | - |
Appears in Collections: | Research publications |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
vandenbergh 1.pdf | Published version | 904.74 kB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.