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dc.contributor.authorYang, J. M.zh_CN
dc.contributor.authorYang, L. J.zh_CN
dc.contributor.authorYu, Y. X.zh_CN
dc.contributor.authorCheng, X.zh_CN
dc.contributor.authorZhang, Y.zh_CN
dc.contributor.author余煜玺zh_CN
dc.date.accessioned2013-12-12T02:03:04Z
dc.date.available2013-12-12T02:03:04Z
dc.date.issued2009-12-10zh_CN
dc.identifier.citationChemical Journal of Chinese Universities-Chinese, 2009,30(12):2525-2529zh_CN
dc.identifier.issn0251-0790zh_CN
dc.identifier.otherISI:000273792900040zh_CN
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/59044
dc.description.abstractPolyaluminocarbosilanes (PACS) with different Al contents were synthesized by reacting liquid polyearbosilane(LPCS) with aluminum acetylacetonate[Al(AcAc)(3)]. Compared with those reported in literatures, this route is considered to be more convenient and safer since no circulating reflux is needed. It was shown that the composition and structure of LPCS heated and kept at the synthesis temperature of PACS remained fairly stable. The chemical elemental analysis results of PACS indicated that through this route the Al contents were almost fully introduced into PACS from Al(AcAc)(3), and with the increasing of Al contents, the O contents also increased. Furthermore, the formation of AlO(4), AlO(5) and AlO(6) was confirmed by (27)Al MAS NMR results. On the base of the structure analysis it was suggested that LPCS reacted with Al(AcAc)(3) by consuming Si-H bonds. Then Si-O-Al crosslinking bonds were formed, leading to the increases of the number average molecular weight and the polydispersion index in molecular weight with the increase of Al contents in PACS.zh_CN
dc.language.isoen_USzh_CN
dc.subjectHIGH-STRENGTHzh_CN
dc.subjectPYROLYSISzh_CN
dc.titleSynthesis and Characterization of Liquid Polycarbosilane-derived Polyaluminocarbosilanezh_CN
dc.typeArticlezh_CN


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