Oligomers with silicon and transition metal groups: Thermolysis of poly[1,1'-bis( diorganosilylethynyl}ferrocenes] and poly[{(diorganosilylene) diacetylene) dicobalthexacarbonyls] to give iron silicide- and cobalt silicide-based ceramics

被引:48
作者
Corriu, RJP [1 ]
Devylder, N [1 ]
Guerin, C [1 ]
Henner, B [1 ]
Jean, A [1 ]
机构
[1] UNIV MONTPELLIER 2,UNITE MIXTE RECH CNRS 44,UNITE MIXTE CNRS RHONE POULENC,F-34095 MONTPELLIER 05,FRANCE
关键词
poly[(silylene)diacetylenes; iron silicide; multiphase ceramic; pyrolysis; cobalt silicide;
D O I
10.1016/0022-328X(95)05812-4
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The pyrolysis of transition-metal-containing organosilicon-diacetylene oligomers was performed in order to prepare multiphase ceramics. Poly[1,1'-bis(diorganosilylethynyl)ferrocenes] (2) were pyrolysed, under argon, up to 1350 degrees C to give FexSiyCz phases with good yields, owing to the incorporation of the cyclopentadiene groups in the carbon matrix and the participation of nearly all silicon and iron in the ceramic residue. The pyrolysis of poly[{(diorganosilylene) diacetylene} dicobalt hexacarbonyls] (3) at 1350 degrees C gave Co2Si and graphite-like carbon. Evolution of part of the carbon monoxide of 3 in the early stage of the pyrolysis (100 degrees C) showed that the cross-linking of the diacetylene units was induced by reactive cobalt species. Furthermore, at higher temperatures (200-500 degrees C), cobalt clusters catalysed the ceramic formation. Co2Si was shown to result from the reaction of SiC with Co above 1000 degrees C, both formed during the pyrolysis process. Finally, at 1100 degrees C, a carboreduction reaction led to the elimination of the oxygen incorporated in the carbon matrix during the cross-linking process.
引用
收藏
页码:249 / 257
页数:9
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