Abstract
Novel silylated hydroborate clusters comprising the closo-decaborate cage were prepared and characterized by 1H, 13C, 11B, 29Si NMR and mass spectroscopy ESI. The synthesis of such silylated clusters was achieved using reactive derivatives of [B 10H10]2-, [1-B10H9N 2]- and [2-B10H9CO]-. These silylated decaborate clusters constitute a new class of precursors that can be covalently anchored onto various silica supports without any prior surface modification. As a proof of concept, the synthesized precursors were successfully anchored on mesoporous silica, SBA-15 type, in different percentages, where the mesoporous material retained its structure. All materials modified with closo-decaborate were characterized by 11B and 29Si solid state NMR, XRD, TEM and nitrogen sorption. This journal is © the Partner Organisations 2014.
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CITATION STYLE
Abi-Ghaida, F., Laila, Z., Ibrahim, G., Naoufal, D., & Mehdi, A. (2014). New triethoxysilylated 10-vertex closo-decaborate clusters. Synthesis and controlled immobilization into mesoporous silica. Dalton Transactions, 43(34), 13087–13095. https://doi.org/10.1039/c4dt00772g
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