Two new silicate structures based on a rhodesite-type heteropolyhedral microporous framework
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Updated: Jun 14, 2026

Discovery and Synthesis Optimization of Isoreticular Al(III) Phosphonate-Based Metal-Organic Framework Compounds Using High-Throughput Methods
Published on: October 6, 2023
Marcella Cadoni1, Giovanni Ferraris
1Dipartimento di Scienze Mineralogiche e Petrologiche, Università di Torino, Via Valperga Caluso 35, I-10125, Torino, Italy.
Abstract:
Two new members of the mero-plesiotype rhodesite series [Sr(2)Na(2)(Si(8)O(19)).4H(2)O, abbreviated as TR09; SrNa(4)(Si(8)O(19)).4H(2)O, TR10] have been hydrothermally synthesized in Teflon-lined autoclaves at 503 K and structurally characterized using X-ray diffraction single-crystal data. The crystal structures were solved by direct methods and refined to R = 0.021 [TR09; 3317 reflections with I(o) > 2sigma(I(o))] and R = 0.033 [TR10; 5007 reflections with I(o) > 2sigma(I(o))]. Both structures are based on a rhodesite-type microporous heteropolyhedral framework, where two types of channels are within the double silicate layer that alternates with an ;octahedral' O sheet. The large Sr(2+) cation constrains to the roughly ellipsoidal shape of the channels. The H(2)O molecules are located both in the O sheets and in the channels, where they are loosely hydrogen bonded. The crystal-chemical features that allow flexibility to the rhodesite-type microporous heteropolyhedral framework and make it interesting for possible technological applications are discussed.
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