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A mild, efficient and catalyst-free thermoreversible ligation system based on dithiooxalates

Pahnke, Kai; Haworth, Naomi L.; Brandt, Josef; Paulmann, Uwe; Richter, Christian; Schmidt, Friedrich G.; Lederer, Albena; Coote, Michelle; Barner-Kowollik, Christopher

Description

We demonstrate a novel and ready to prepare thermoreversible hetero Diels–Alder dilinker on the basis of dithiooxalates, enabling the mild, rapid and catalyst-free linkage of diverse diene species under ambient conditions for applications in the fields of, for example, modular ligation, self-healing or recyclable materials and surface modification amongst others. The linker was studied using quantum chemical calculations, and experimentally in small molecular reactions via UV/Vis spectroscopy,...[Show more]

dc.contributor.authorPahnke, Kai
dc.contributor.authorHaworth, Naomi L.
dc.contributor.authorBrandt, Josef
dc.contributor.authorPaulmann, Uwe
dc.contributor.authorRichter, Christian
dc.contributor.authorSchmidt, Friedrich G.
dc.contributor.authorLederer, Albena
dc.contributor.authorCoote, Michelle
dc.contributor.authorBarner-Kowollik, Christopher
dc.date.accessioned2017-01-13T01:49:13Z
dc.date.available2017-01-13T01:49:13Z
dc.identifier.issn1759-9954
dc.identifier.urihttp://hdl.handle.net/1885/111767
dc.description.abstractWe demonstrate a novel and ready to prepare thermoreversible hetero Diels–Alder dilinker on the basis of dithiooxalates, enabling the mild, rapid and catalyst-free linkage of diverse diene species under ambient conditions for applications in the fields of, for example, modular ligation, self-healing or recyclable materials and surface modification amongst others. The linker was studied using quantum chemical calculations, and experimentally in small molecular reactions via UV/Vis spectroscopy, mass spectrometry and NMR as well as in step-growth polymerizations with diene-difunctional building blocks – characterized via (temperature dependent) SEC and HT NMR – as an example for efficient polymer ligation.
dc.description.sponsorshipC. B.-K., M. L. C. and A. L. are grateful for continued support from and the excellent collaboration with Evonik Industries. C. B.-K. additionally acknowledges continued support from the KIT via the Helmholtz association (BIFTM and STN programs) as well as the German Research Council (DFG).
dc.format.mimetypeapplication/pdf
dc.publisherRoyal Society of Chemistry
dc.rights© The Royal Society of Chemistry 2016. http://www.sherpa.ac.uk/romeo/issn/1759-9954/..."Author's post-print on author's personal website, institutional repository, open access repository, scholarly communications networks that comply with International Association of STM Publishers sharing principles" from SHERPA/RoMEO site (as at 23/01/17).
dc.sourcePolymer Chemistry
dc.titleA mild, efficient and catalyst-free thermoreversible ligation system based on dithiooxalates
dc.typeJournal article
local.identifier.citationvolume7
dc.date.issued2016
local.publisher.urlhttp://www.rsc.org/
local.type.statusAccepted Version
local.contributor.affiliationHaworth, N. L., ARC Centre of Excellence for Electromaterials Science, Research School of Chemistry, The Australian National University
local.contributor.affiliationCoote, M. L., ARC Centre of Excellence for Electromaterials Science, Research School of Chemistry, The Australian National University
local.identifier.essn1759-9962
local.bibliographicCitation.issue19
local.bibliographicCitation.startpage3244
local.bibliographicCitation.lastpage3250
local.identifier.doi10.1039/C6PY00470A
dcterms.accessRightsOpen Access
dcterms.accessRightsOpen Access
CollectionsANU Research Publications

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