Solid‐State Ion Migration in the Preyssler‐Type Phosphotungstate for the Preparation of the Dipotassium Cation‐Encapsulated Derivative

Solid‐State Ion Migration in the Preyssler‐Type Phosphotungstate for the Preparation of the Dipotassium Cation‐Encapsulated Derivative
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普雷斯勒型磷钨酸盐中的固态离子迁移用于制备二钾阳离子包封衍生物

DOI:
10.1002/zaac.202000217
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发表时间:
2020
期刊:
Zeitschrift fuer anorganische und allgemeine Chemie
影响因子:
--
通讯作者:
Sadakane Masahiro
Sadakane Masahiro
中科院分区:
--
文献类型:
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作者:
Wihadi Muh. Nur Khoiru;Sadakane Masahiro

文献摘要

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本文报道了Na包封的Preyssler型磷钨酸盐K盐K14[P5 W30 O 110 Na(side)(H2O)]和K14[P5 W30 O 110 Na(center)]的热驱动固态转变。K14[P5 W30 O 110 Na(side)(H2O)]在其中一个侧腔中含有一个Na+和一个配位H2O分子,而K14[P5 W30 O 110 Na(center)]在中心腔中含有一个Na+。K14[P5 W30 O 110 Na(side)(H2O)]的加热产生[P5 W30 O 110 Na(center)]14-、[P5 W30 O 110 K(center)]14-和[P5 W30 O 110 K(side)2]13-。[P5 W30 O 110 K(中心)]14-和[P5 W30 O 110 K(侧)2]13-分别在中心腔中含有单K+和在两个侧腔中含有双K+。[P5 W30 O 110 Na(中心)]14-的钾盐加热产生[P5 W30 O 110 K(中心)]14-和[P5 W30 O 110 K(侧)2]13-。这些结果表明,在200-500 °C下加热导致Na+和K+的迁移,而没有分子的崩溃。K14[P5 W30 O 110 Na(side)(H2O)]通过反复固态加热成功转化为K12 Na [P5 W30 O 110 K(side)2],该固态加热通过在H2O中溶解和干燥而定期中断。
The heat‐driven solid‐state transformations of K salts of the Na‐encapsulated Preyssler‐type phosphotungstates, K14[P5W30O110Na(side)(H2O)] and K14[P5W30O110Na(center)], are reported herein. K14[P5W30O110Na(side)(H2O)] contains one Na+in one of the side cavities and a coordinating H2O molecule while K14[P5W30O110Na(center)] contains one Na+in the central cavity. The heating of K14[P5W30O110Na(side)(H2O)] produces [P5W30O110Na(center)]14–, [P5W30O110K(center)]14–, and [P5W30O110K(side)2]13–. [P5W30O110K(center)]14–and [P5W30O110K(side)2]13–contain mono‐K+in the central cavity and di‐K+in both side cavities, respectively. The heating of potassium salt of [P5W30O110Na(center)]14–produces [P5W30O110K(center)]14–and [P5W30O110K(side)2]13–. These results indicate that heating, at 200–500 °C, causes the migrations of Na+and K+, without the collapse of the molecule. K14[P5W30O110Na(side)(H2O)] was successfully converted to K12Na[P5W30O110K(side)2] by repeated solid‐state heating, which was periodically interrupted by dissolution, in H2O, and drying.