ExploringOxonitridosilicate Synthesis: From OxideZeolites to Nitride Frameworks

In this study, we synthesized the first CAN (<b><i>can</i></b>crinite)-typed zeolite-like oxonitridosilicates, <i>Ln</i><sub>5</sub>Ca<sub>9</sub>O<sub>2</sub>(SiNO<sub>3</sub>)[Si<sub>12</sub>N<sub>24</sub>] (<i>Ln</i> = La and Ce). The crystal structure of La<sub>5</sub>Ca<sub>9</sub>O<sub>2</sub>(SiNO<sub>3</sub>)[Si<sub>12</sub>N<sub>24</sub>] was determined through single-crystal X-ray diffraction (SCXRD) data and neutron powder diffraction (NPD) data refinement. The compound crystallizes in hexagonal space group <i>P</i>6<sub>3</sub><i>mc</i> (No. 186) with <i>a</i> = 12.9875(2) Å, <i>c</i> = 5.2072(1) Å, and <i>Z</i> = 1. The anionic framework of La<sub>5</sub>Ca<sub>9</sub>O<sub>2</sub>(SiNO<sub>3</sub>)[Si<sub>12</sub>N<sub>24</sub>] is entirely constructed from [SiN<sub>4</sub>] tetrahedra, forming larger-sized composite building units, <i>t-can</i> and <i>t-ato</i>. The Ca<sup>2+</sup> cations in the <i>t-can</i> cage contribute to balancing the charge difference originating from N<sup>3–</sup> substitution for O<sup>2–</sup> in La<sub>5</sub>Ca<sub>9</sub>O<sub>2</sub>(SiNO<sub>3</sub>)[Si<sub>12</sub>N<sub>24</sub>], which was revealed by the charge density difference calculation. The Ce<sup>3+</sup>-doped La<sub>5</sub>Ca<sub>9</sub>O<sub>2</sub>(SiNO<sub>3</sub>)[Si<sub>12</sub>N<sub>24</sub>] shows a broad-band orange-red emission peaking at λ = 630 nm under UV light excitation.

Publication Details

Journal
Figshare
Published
2025-02-04
DOI
https://doi.org/10.1021/acs.inorgchem.4c04210.s001
Primary Topic
Zeolite Catalysis and Synthesis
Type
article
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article

ExploringOxonitridosilicate Synthesis: From OxideZeolites to Nitride Frameworks

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Zeolite Catalysis and Synthesis
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ExploringOxonitridosilicate Synthesis: From OxideZeolites to Nitride Frameworks

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Abstract

In this study, we synthesized the first CAN (<b><i>can</i></b>crinite)-typed zeolite-like oxonitridosilicates, <i>Ln</i><sub>5</sub>Ca<sub>9</sub>O<sub>2</sub>(SiNO<sub>3</sub>)[Si<sub>12</sub>N<sub>24</sub>] (<i>Ln</i> = La and Ce). The crystal structure of La<sub>5</sub>Ca<sub>9</sub>O<sub>2</sub>(SiNO<sub>3</sub>)[Si<sub>12</sub>N<sub>24</sub>] was determined through single-crystal X-ray diffraction (SCXRD) data and neutron powder diffraction (NPD) data refinement. The compound crystallizes in hexagonal space group <i>P</i>6<sub>3</sub><i>mc</i> (No. 186) with <i>a</i> = 12.9875(2) Å, <i>c</i> = 5.2072(1) Å, and <i>Z</i> = 1. The anionic framework of La<sub>5</sub>Ca<sub>9</sub>O<sub>2</sub>(SiNO<sub>3</sub>)[Si<sub>12</sub>N<sub>24</sub>] is entirely constructed from [SiN<sub>4</sub>] tetrahedra, forming larger-sized composite building units, <i>t-can</i> and <i>t-ato</i>. The Ca<sup>2+</sup> cations in the <i>t-can</i> cage contribute to balancing the charge difference originating from N<sup>3–</sup> substitution for O<sup>2–</sup> in La<sub>5</sub>Ca<sub>9</sub>O<sub>2</sub>(SiNO<sub>3</sub>)[Si<sub>12</sub>N<sub>24</sub>], which was revealed by the charge density difference calculation. The Ce<sup>3+</sup>-doped La<sub>5</sub>Ca<sub>9</sub>O<sub>2</sub>(SiNO<sub>3</sub>)[Si<sub>12</sub>N<sub>24</sub>] shows a broad-band orange-red emission peaking at λ = 630 nm under UV light excitation.

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