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dc.contributor.authorArroyo, Juan Luis
dc.contributor.authorNorambuena, Ángel
dc.contributor.authorReyes, Héctor
dc.contributor.authorValdebenito, Cristián
dc.contributor.authorAbarca, Gabriel
dc.contributor.authorMacLeod-Carey, Desmond
dc.contributor.authorMorales-Verdejo, César A.
dc.date.accessioned2021-03-03T12:27:28Z
dc.date.available2021-03-03T12:27:28Z
dc.date.issued2021-02-01
dc.identifier10.1021/acs.inorgchem.0c02639
dc.identifier.issn00201669
dc.identifier.urihttps://hdl.handle.net/20.500.12728/8637
dc.description.abstractWe show the synthesis and characterization of four heterobimetallic compounds derived from s-indacene of general formula [{(CO)3Mn}-s-Ic-{MCp*}]q with M = Fe, Co, Ni, and Ru; q = 0, 1+. The complexes reported here were characterized by 1H and 13C NMR, elemental analysis and FT-IR. Additionally, the X-ray crystal structure of [(CO)3Mn-s-Ic-FeCp*] (1) and Mössbauer spectra are reported. The heterobimetallic compounds exhibit higher quasireversible redox potentials compared with ferrocene and catocene under the same reaction conditions. The complexes were tested as catalysts on the thermal decomposition of ammonium perchlorate examined by a differential scanning calorimetry technique to study their catalytic behavior. Compound (1) causes a decrease of ammonium perchlorate's decomposition temperature to 315 °C, consequently increasing the heat release by 138 J·g-1. Conversely, [{(CO)3Mn}-s-Ic′-{CoCp*}] (2) presents a higher heat release (2462 J·g-1), comparable to catocene.es_ES
dc.language.isoenes_ES
dc.publisherAmerican Chemical Societyes_ES
dc.subjectCrystal structurees_ES
dc.subjectDecompositiones_ES
dc.subjectDifferential scanning calorimetryes_ES
dc.subjectInorganic compoundses_ES
dc.subjectIron compoundses_ES
dc.subjectOrganometallicses_ES
dc.subjectRedox reactionses_ES
dc.subjectThermolysises_ES
dc.titleHeterobimetallic Catalysts for the Thermal Decomposition of Ammonium Perchlorate: Efficient Burning Rate Catalysts for Solid Rocket Motors and Missileses_ES
dc.typeArticlees_ES


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