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Isostructurality and Thermal Properties in the Series of Double Complex Salts [M-1(NH3)(6)][M-2(C2O4)(3)]center dot 3H(2)O (M-1 = Co, Ir, M-2 = Fe, Cr)

ИЗОСТРУКТУРНОСТЬ И ТЕРМИЧЕСКИЕ СВОЙСТВА В РЯДУ ДВОЙНЫХ КОМПЛЕКСНЫХ СОЛЕЙ СОСТАВА

  • Preparation of new bimetallic compounds, including double complex salts (DCSs), containing both a platinumgroup metal and a transition metal of the fourth period is of great interest since these compounds can act as precursors of bimetallic materials. One example of using such compounds is the preparation of ultrafine particles of solid solutions of metals or intermetallic compounds on various supports to fabricate highly efficient catalysts with a low content of noble metals. Compounds containing coordinated oxalate anions are important objects of synthetic chemistry and interesting precursors. For example, a lot of attention is given to salts with [M(C2O4)2]2– anions, where M = Co, Ni, Cu, Pt, Pd. On the one hand, the uniqueness of oxalate coordinated anions is due to the fact that they are easily obtained and are stable both in aqueous solutions and in the solid phase; on the other hand, they are thermally decomposed at relatively low temperatures, which makes them promisingPreparation of new bimetallic compounds, including double complex salts (DCSs), containing both a platinumgroup metal and a transition metal of the fourth period is of great interest since these compounds can act as precursors of bimetallic materials. One example of using such compounds is the preparation of ultrafine particles of solid solutions of metals or intermetallic compounds on various supports to fabricate highly efficient catalysts with a low content of noble metals. Compounds containing coordinated oxalate anions are important objects of synthetic chemistry and interesting precursors. For example, a lot of attention is given to salts with [M(C2O4)2]2– anions, where M = Co, Ni, Cu, Pt, Pd. On the one hand, the uniqueness of oxalate coordinated anions is due to the fact that they are easily obtained and are stable both in aqueous solutions and in the solid phase; on the other hand, they are thermally decomposed at relatively low temperatures, which makes them promising precursors for the fabrication of metallic and oxide materials.zeige mehrzeige weniger
  • Синтезирован ряд из четырех изоструктурных двойных комплексных солей, построенных на основе катионов [М1(NH3)6]3+ и анионов [M2(C2O4)3]3-, где M1 = Co, Ir, M2 = Fe, Cr. Соли кристаллизуются в гексагональной пространственной группе симметрии P`3c1. Согласно данным термического анализа в атмосфере аргона, термическая устойчивость (температуры начала разложения обезвоженных продуктов) изучаемых соединений зависит от природы комплексного трисоксалатного аниона и увеличивается в рядах [Ir(NH3)6][Co(C2O4)3] < [Ir(NH3)6][Fe(C2O4)3] < [Ir(NH3)6][Cr(C2O4)3] < [Ir(NH3)6][Ir(C2O4)3] и [Co(NH3)6][Co(C2O4)3] < [Co(NH3)6][Fe(C2O4)3] < [Co(NH3)6][Cr(C2O4)3] < [Co(NH3)6][Ir(C2O4)]. При этом при одинаковом анионе соли гексаммина иридия(III) более устойчивы по сравнению с солями кобальта(III)). При термическом разложении солей [Co(NH3)6][Fe(C2O4)3]·3H2O и [Ir(NH3)6][Fe(C2O4)3] 3H2O в атмосфере водорода образуются твердые растворы Co0,5Fe0,5 и Ir0,5Fe0,5 соответственно.

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Autor*innen:S Pechenyuk, E Vikulova, Y Semushina, I Baidina, E Filatov, Kirill YusenkoORCiD
Dokumenttyp:Zeitschriftenartikel
Veröffentlichungsform:Verlagsliteratur
Sprache:Mehrsprachig
Titel des übergeordneten Werkes (Englisch):Journal of Structural Chemistry
Jahr der Erstveröffentlichung:2019
Organisationseinheit der BAM:6 Materialchemie
6 Materialchemie / 6.3 Strukturanalytik
Verlag:Springer
Jahrgang/Band:60
Ausgabe/Heft:7
Erste Seite:1110
Letzte Seite:1119
DDC-Klassifikation:Technik, Medizin, angewandte Wissenschaften / Ingenieurwissenschaften / Ingenieurwissenschaften und zugeordnete Tätigkeiten
Freie Schlagwörter:Catalysts; Double complex salts; Single-source precursors
Themenfelder/Aktivitätsfelder der BAM:Material
DOI:10.26902/JSC_id42958
URL:https://doi.org/10.1134/S0022476619070060
Verfügbarkeit des Dokuments:Datei im Netzwerk der BAM verfügbar ("Closed Access")
Datum der Freischaltung:12.09.2019
Referierte Publikation:Ja
Datum der Eintragung als referierte Publikation:12.09.2019
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