Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/8270
DC FieldValueLanguage
dc.contributor.authorCalderón, Verónica-
dc.contributor.authorSchwarz, Gert-
dc.contributor.authorGarcía, Félix-
dc.contributor.authorTapia, María J.-
dc.contributor.authorValente, Artur J. M.-
dc.contributor.authorBurrows, Hugh D.-
dc.contributor.authorGarcía, José Miguel-
dc.date.accessioned2009-02-09T14:31:55Z-
dc.date.available2009-02-09T14:31:55Z-
dc.date.issued2006en_US
dc.identifier.citationJournal of Polymer Science Part A: Polymer Chemistry. 44:21 (2006) 6252-6269en_US
dc.identifier.urihttps://hdl.handle.net/10316/8270-
dc.description.abstractWe report the synthesis and characterization of 10 novel polyamides containing the benzo-18-crown-6 subunit and its dipodal counterpart, along with their properties, and a comparison with homologous polyamides bearing benzo-12-crown-4, benzo-15-crown-5, and the corresponding dipodal systems. The anomalous polymerization of some of the diacid monomers, that leads to insoluble gels under standard Yamazaki polymerization conditions, is described. The gel formation has been attributed to the threading of cyclic oligoamides with a growing polyamide chain to yield rotaxanes, polyrotaxanes, catenanes, or polycatenanes. Polyamide macrocycles have been characterized with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. A route to avoid gel formation, consisting of a lower initial monomer concentration, is also described, along with the polymer properties of the polyamides obtained, including the chemical characterization, mechanical behavior, water sorption, morphology, diffusion data, and permeability of membranes prepared with these polymers. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6252-6269, 2006en_US
dc.language.isoengeng
dc.rightsopenAccesseng
dc.titleSynthesis and characterization of new aromatic polyamides bearing crown ethers and acyclic ethylene oxide units in the pendant structure. III. Benzo-18-crown-6 systems and their open-chain counterpartsen_US
dc.typearticleen_US
dc.identifier.doi10.1002/pola.21710en_US
uc.controloAutoridadeSim-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-4612-7686-
crisitem.author.orcid0000-0003-3127-2298-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
Files in This Item:
File Description SizeFormat
obra.pdf625.1 kBAdobe PDFView/Open
Show simple item record

SCOPUSTM   
Citations

29
checked on May 6, 2024

WEB OF SCIENCETM
Citations 5

29
checked on May 2, 2024

Page view(s)

332
checked on May 7, 2024

Download(s) 50

419
checked on May 7, 2024

Google ScholarTM

Check

Altmetric

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.