dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorFac Integradas Catolicas Palmas
dc.date.accessioned2014-05-20T15:20:28Z
dc.date.available2014-05-20T15:20:28Z
dc.date.created2014-05-20T15:20:28Z
dc.date.issued2007-03-01
dc.identifierJournal of Thermal Analysis and Calorimetry. Dordrecht: Springer, v. 87, n. 3, p. 789-792, 2007.
dc.identifier1388-6150
dc.identifierhttp://hdl.handle.net/11449/31755
dc.identifier10.1007/s10973-006-7863-0
dc.identifierWOS:000244823700035
dc.identifier3300223970814448
dc.identifier7471310113999140
dc.identifier7927677053650819
dc.identifier8534138813417161
dc.identifier0000-0002-0057-7964
dc.identifier0000-0003-1574-681X
dc.description.abstractSynthesis, spectroscopic characterization and thermal behavior of pyrazolate-bridged palladium complexes [Pd(mu-Pz)(2)](n) (1), [Pd(mu-mPz)(2)](n) (2), [Pd(mu-dmPz)(2)](n) (3), [Pd(mu-IPz)(2)](n) (4) {pyrazolate (Pz(-)), 4-methylpyrazolate (mPz(-)), 3,5-dimethylpyrazolate (dmPz(-)), 4-iodopyrazolate (IPz(-))} have been described in this work. The exobidentate coordination mode of pyrazolato ligands in 1-4 was inferred on basis of IR spectroscopic evidences. TG investigations indicated that the introduction of substituents at the 4 position in the pyrazolyl moiety into coordination polymers do not affect significantly their thermal stability, whereas at the 3 and 5 position reduced the stability of the main chain. Metal palladium was the final product of the thermal decompositions, which was identified by X-ray powder diffraction.
dc.languageeng
dc.publisherSpringer
dc.relationJournal of Thermal Analysis and Calorimetry
dc.relation2.209
dc.relation0,587
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectcoordination polymers
dc.subjectDTA
dc.subjectpalladium(II)
dc.subjectpyrazolates
dc.subjectTG
dc.titleSynthesis, spectral and thermal studies on pyrazolate-bridged palladium(II) coordination polymers
dc.typeArtículos de revistas


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