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Article: Preparation and properties of novel triphenylpyridine-containing hyperbranched polyimides derived from 2,4,6-tris(4-aminophenyl)pyridine under microwave irradiation

TitlePreparation and properties of novel triphenylpyridine-containing hyperbranched polyimides derived from 2,4,6-tris(4-aminophenyl)pyridine under microwave irradiation
Authors
KeywordsHyperbranched
Microwave irradiation
Polyimides
Triamines
Triphenylpyridine
Issue Date2010
PublisherWiley - V C H Verlag GmbH & Co KGaA.
Citation
Macromolecular Chemistry And Physics, 2010, v. 211 n. 16, p. 1803-1813 How to Cite?
AbstractA novel BB′ 2-type triamine was synthesized for the first time and employed to prepare a series of amine- and anhydride-terminated triphenylpyridine-containing hyperbranched polyimides under microwave irradiation. The structure of the triamine monomer and polymers were verified by FTIR and 1H NMR spectroscopy. The predominantly amorphous polyimides were soluble inm-cresol, NMP, DMSO, DMAc and DMF at room temperature or upon heating. The polymers showed glass transition temperatures above 310 8C and a 5 and 10% weight-loss temperature above 482 and 559 °C. Tensile strength and modulus were higher than 53.1 MPa and 1.01 GPa, respectively. AM-HBPI- 2 and AD-HBPI-2 showed UV-Vis absorptions in the region 200-400 and 200-350nm and displayed strong purple and blue fluorescence. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Persistent Identifierhttp://hdl.handle.net/10722/139547
ISSN
2023 Impact Factor: 2.5
2023 SCImago Journal Rankings: 0.501
ISI Accession Number ID
Funding AgencyGrant Number
Natural Science Foundation of Hubei Province2008CDB276
Funding Information:

This work was financially supported by the Natural Science Foundation of Hubei Province (No 2008CDB276) The authors also acknowledge the Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials for providing the necessary facilities.

References

 

DC FieldValueLanguage
dc.contributor.authorChen, Wen_HK
dc.contributor.authorYan, Wen_HK
dc.contributor.authorWu, Sen_HK
dc.contributor.authorXu, Zen_HK
dc.contributor.authorYeung, KWKen_HK
dc.contributor.authorYi, Cen_HK
dc.date.accessioned2011-09-23T05:51:32Z-
dc.date.available2011-09-23T05:51:32Z-
dc.date.issued2010en_HK
dc.identifier.citationMacromolecular Chemistry And Physics, 2010, v. 211 n. 16, p. 1803-1813en_HK
dc.identifier.issn1022-1352en_HK
dc.identifier.urihttp://hdl.handle.net/10722/139547-
dc.description.abstractA novel BB′ 2-type triamine was synthesized for the first time and employed to prepare a series of amine- and anhydride-terminated triphenylpyridine-containing hyperbranched polyimides under microwave irradiation. The structure of the triamine monomer and polymers were verified by FTIR and 1H NMR spectroscopy. The predominantly amorphous polyimides were soluble inm-cresol, NMP, DMSO, DMAc and DMF at room temperature or upon heating. The polymers showed glass transition temperatures above 310 8C and a 5 and 10% weight-loss temperature above 482 and 559 °C. Tensile strength and modulus were higher than 53.1 MPa and 1.01 GPa, respectively. AM-HBPI- 2 and AD-HBPI-2 showed UV-Vis absorptions in the region 200-400 and 200-350nm and displayed strong purple and blue fluorescence. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en_HK
dc.languageengen_US
dc.publisherWiley - V C H Verlag GmbH & Co KGaA.-
dc.relation.ispartofMacromolecular Chemistry and Physicsen_HK
dc.subjectHyperbranched-
dc.subjectMicrowave irradiation-
dc.subjectPolyimides-
dc.subjectTriamines-
dc.subjectTriphenylpyridine-
dc.titlePreparation and properties of novel triphenylpyridine-containing hyperbranched polyimides derived from 2,4,6-tris(4-aminophenyl)pyridine under microwave irradiationen_HK
dc.typeArticleen_HK
dc.identifier.emailYeung, KWK:wkkyeung@hkucc.hku.hken_HK
dc.identifier.authorityYeung, KWK=rp00309en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/macp.201000193en_HK
dc.identifier.scopuseid_2-s2.0-77955729984en_HK
dc.identifier.hkuros192180en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-77955729984&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume211en_HK
dc.identifier.issue16en_HK
dc.identifier.spage1803en_HK
dc.identifier.epage1813en_HK
dc.identifier.isiWOS:000281346800009-
dc.publisher.placeGermanyen_HK
dc.identifier.scopusauthoridChen, W=25925712200en_HK
dc.identifier.scopusauthoridYan, W=7402221278en_HK
dc.identifier.scopusauthoridWu, S=13410759900en_HK
dc.identifier.scopusauthoridXu, Z=8401665500en_HK
dc.identifier.scopusauthoridYeung, KWK=13309584700en_HK
dc.identifier.scopusauthoridYi, C=7101997365en_HK
dc.identifier.issnl1022-1352-

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