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Philipp Bielec Lucien Eisenburger H. Lars Deubner Daniel Günther Florian Kraus Oliver Oeckler Wolfgang Schnick 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(3):850-853
Based on the known linking options of their fundamental building unit, that is the SiN4 tetrahedron, nitridosilicates belong to the inorganic compound classes with the greatest structural variability. Although facilitating the discovery of novel Si–N networks, this variability represents a challenge when targeting non‐stoichometric compounds. Meeting this challenge, a strategy for targeted creation of vacancies in highly condensed nitridosilicates by exchanging divalent M2+ for trivalent M3+ using the ion exchange approach is reported. As proof of concept, the first Sc and U nitridosilicates were prepared from α‐Ca2Si5N8 and Sr2Si5N8. Powder X‐ray diffraction (XRD) and synchrotron single‐crystal XRD showed random vacancy distribution in Sc0.2Ca1.7Si5N8, and partial vacancy ordering in U0.5xSr2?0.75xSi5N8 with x≈1.05. The high chemical stability of U nitridosilicates makes them interesting candidates for immobilization of actinides. 相似文献
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