Publication:
Synthesis and characterization of poly(p‐phenylene)‐graft‐poly(ε‐caprolactone) copolymers by combined ring‐opening polymerization and cross‐coupling processes

dc.contributor.authorYurteri, Seda
dc.contributor.authorCianga, Ioan
dc.contributor.authorDegirmenci, Mustafa
dc.contributor.authorYagci, Yusuf
dc.date.accessioned2026-01-25T04:47:16Z
dc.date.issued2004-06-01
dc.description.abstractAbstract2,5‐Dibromo‐1,4‐(dihydroxymethyl)benzene was used as initiator in ring‐opening polymerization of ε‐caprolactone in the presence of stannous octoate (Sn(Oct)2) catalyst. The resulting poly(ε‐caprolactone) (PCL) macromonomer, with a central 2,5‐dibromo‐1,4‐diphenylene group, was used in combination with 1,4‐dibromo‐2,5‐dimethylbenzene for a Suzuki coupling in the presence of Pd(PPh3)4 as catalyst or using the system NiCl2/bpy/PPh3/Zn for a Yamamoto‐type polymerization. The poly(p‐phenylenes) (PPP) obtained, with PCL side chains, have solubility properties similar to those of the starting macromonomer, ie soluble in common organic solvents at room temperature. The new polymers were characterized by 1H and 13C NMR and UV spectroscopy and also by GPC measurements. The thermal behaviour of the precursor PCL macromonomer and the final poly(p‐phenylene)‐graft‐poly(ε‐caprolactone) copolymers were investigated by thermogravimetric analysis and differential scanning calorimetry analyses and compared. Copyright © 2004 Society of Chemical Industry
dc.description.urihttps://doi.org/10.1002/pi.1554
dc.description.urihttps://dx.doi.org/10.1002/pi.1554
dc.identifier.doi10.1002/pi.1554
dc.identifier.eissn1097-0126
dc.identifier.endpage1225
dc.identifier.issn0959-8103
dc.identifier.openairedoi_dedup___::6589ae3ccef38e4f5459e6e6a06a1bce
dc.identifier.startpage1219
dc.identifier.urihttps://hdl.handle.net/11527/45996
dc.identifier.volume53
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofPolymer International
dc.rightsCLOSED
dc.titleSynthesis and characterization of poly(p‐phenylene)‐graft‐poly(ε‐caprolactone) copolymers by combined ring‐opening polymerization and cross‐coupling processes
dc.typeArticle
dspace.entity.typePublication

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