Publication: A new generation of highly branched polymers: hyperbranched, segmented poly(urethane urea) elastomers
dc.contributor.coauthor | Ünal, S. | |
dc.contributor.coauthor | Sheth, J.P. | |
dc.contributor.coauthor | Wilkes, G.L. | |
dc.contributor.coauthor | Long, T.E. | |
dc.contributor.department | Department of Chemistry | |
dc.contributor.department | Department of Chemistry | |
dc.contributor.kuauthor | Yılgör, Emel | |
dc.contributor.kuauthor | Yılgör, İskender | |
dc.contributor.kuprofile | Researcher | |
dc.contributor.kuprofile | Faculty Member | |
dc.contributor.other | Department of Chemistry | |
dc.contributor.schoolcollegeinstitute | College of Sciences | |
dc.contributor.schoolcollegeinstitute | College of Sciences | |
dc.contributor.yokid | 40527 | |
dc.contributor.yokid | 24181 | |
dc.date.accessioned | 2024-11-09T23:57:25Z | |
dc.date.issued | 2004 | |
dc.description.abstract | A simple oligomeric A 2 + B 2 approach was described for the preparation of segmented, hyperbranched polyureas and poly(urethane urea). The approach utilized an isocyanate end-capped polyether as an oligomeric A 2 monomer and B 3 triamine monomer. The approach can be extended to a large number of telechelic oligomers including poly(dimethylsiloxane) (PDMS) or poly (ethylene glycol) and trifunctional polymer (B 3) to prepare polymeric materials. The similarity in soft segment glass transition behavior and strain hardening character of the hyperbranched systems suggested considerable promise for future applications. | |
dc.description.indexedby | Scopus | |
dc.description.issue | 19 | |
dc.description.openaccess | YES | |
dc.description.publisherscope | International | |
dc.description.volume | 37 | |
dc.identifier.doi | 10.1021/ma049472e | |
dc.identifier.issn | 0024-9297 | |
dc.identifier.link | https://www.scopus.com/inward/record.uri?eid=2-s2.0-4744353870&doi=10.1021%2fma049472e&partnerID=40&md5=df3eb66215408f941be70366bc051127 | |
dc.identifier.quartile | Q1 | |
dc.identifier.scopus | 2-s2.0-4744353870 | |
dc.identifier.uri | http://dx.doi.org/10.1021/ma049472e | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/15274 | |
dc.keywords | Branched polymers | |
dc.keywords | Chemical structures | |
dc.keywords | Hyperbranched systems | |
dc.keywords | Room temperature | |
dc.keywords | Composition | |
dc.keywords | Dynamic mechanical analysis | |
dc.keywords | Elastomers | |
dc.keywords | Glass transition | |
dc.keywords | Hysteresis | |
dc.keywords | Monomers | |
dc.keywords | Polymerization | |
dc.keywords | Strain hardening | |
dc.keywords | Tensile strength | |
dc.keywords | Thermoplastics | |
dc.keywords | Polyurethanes | |
dc.language | English | |
dc.publisher | American Chemical Society (ACS) | |
dc.source | Macromolecules | |
dc.subject | Chemistry | |
dc.title | A new generation of highly branched polymers: hyperbranched, segmented poly(urethane urea) elastomers | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.authorid | 0000-0001-9133-3377 | |
local.contributor.authorid | 0000-0002-7756-4192 | |
local.contributor.kuauthor | Yılgör, Emel | |
local.contributor.kuauthor | Yılgör, İskender | |
relation.isOrgUnitOfPublication | 035d8150-86c9-4107-af16-a6f0a4d538eb | |
relation.isOrgUnitOfPublication.latestForDiscovery | 035d8150-86c9-4107-af16-a6f0a4d538eb |