Distortion isomerism in ferrous thiourea complexes-II(1) thermodynamics and kinetics
Author
dc.contributor.author
Latorre, R.
Author
dc.contributor.author
Costamagna, J.
Author
dc.contributor.author
Frank, E.
Author
dc.contributor.author
Abeledo, C.
Author
dc.contributor.author
Frankel, R.
Admission date
dc.date.accessioned
2018-12-20T15:10:03Z
Available date
dc.date.available
2018-12-20T15:10:03Z
Publication date
dc.date.issued
1979
Cita de ítem
dc.identifier.citation
Journal of Inorganic and Nuclear Chemistry, Volumen 41, Issue 5, 1979, Pages 649-655
Identifier
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00221902
Identifier
dc.identifier.other
10.1016/0022-1902(79)80349-8
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/158119
Abstract
dc.description.abstract
Mössbauer spectroscopy as a function of temperature of Fe(II)(N,N′-dicyclohexyl-thiourea)6(ClO4)2(FeDCTU) shows the existence of two isomeric forms A and B which coexist in the temperature range 200 < T < 300 K. The relative concentrations of A and B were studied as a function of time at different temperatures in the coexistence region. From the equilibrium constant as a function of temperature we obtain the following thermodynamic parameters: ΔH = −4520 ± 120 cal/mol and δS = 20 ± 0.1 e.u. The kinetics seem to follow an ordinary first order law but with an unusual temperature dependence of the rate constant k1. The results are discussed in terms of hydrogen bonded interactions between the perchlorate anions and the cyclohexylthiourea moieties.