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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Synthesis and isolation of non-chromophore cage-rearranged silsesquioxanes from base-catalyzed reactions
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Synthesis and isolation of non-chromophore cage-rearranged silsesquioxanes from base-catalyzed reactions

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The nucleophilicity of both ortho-and meta-nitrophenolate anions is strong enough to give substituted products, but their basicity also facilitates cage-rearrangement reactions in polyhedral oligomeric silsesquioxanes (POSS). Anions having a stronger basicity, but weaker nucleophilicity, such as CO32-, gave products only from cage-rearrangement, with the cage expansion products being isolable in multi-gram quantities using conventional column chromatography.

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