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包含阳离子半夹心配合物的有机金属离子塑性晶体

Organometallic Ionic Plastic Crystals Incorporating Cationic Half-Sandwich Complexes.

作者信息

Inoue Ryota, Sumitani Ryo, Honda Hisashi, Kuwahara Daisuke, Goo Zi Lang, Sugimoto Kunihisa, Mochida Tomoyuki

机构信息

Department of Chemistry, Graduate School of Science, Kobe University, 1-1 Rokkodai, Nada, Kobe, Hyogo 657-8501, Japan.

Graduate School of Nanobioscience, Yokohama City University, Kanazawa-ku, Yokohama 236-0027, Japan.

出版信息

Inorg Chem. 2024 Aug 5;63(31):14770-14778. doi: 10.1021/acs.inorgchem.4c02523. Epub 2024 Jul 26.

Abstract

Ionic plastic crystals (IPCs), characterized by nearly spherical molecular ions, exhibit remarkable solid-state characteristics including high ionic conductivity. However, most IPCs are organic onium salts. Incorporating organometallic half-sandwich complexes into IPCs is challenging owing to their low-symmetry structures. This paper introduces a novel series of IPCs composed of salts derived from half-sandwich organometallic complexes. We synthesized five salts of [Ru(Cp)(tmeda)(CO)]X (tmeda = ,,','-tetramethyl-1,2-ethanediamine, X = anion) with different anions and examined their phase behavior, crystal structures, and molecular motion in the solid-state. Salts featuring the CPFSA (= 1,1,2,2,3,3-hexafluoropropane-1,3-disulfonimide), B(CN), and FSA (= (FSO)N) anions underwent phase transitions to an IPC phase with a CsCl-type structure in the temperature range of 327-364 K. Employing smaller anions led to an increase in the transition temperature. In each salt, the coordination number, representing the number of anions surrounding one cation, remained eight in IPC and low-temperature phases. However, salts containing smaller anions (CFBF and PF) displayed a rotator phase rather than the IPC phase. In these cases, the coordination numbers were six at low temperatures.

摘要

离子塑性晶体(IPCs)以近乎球形的分子离子为特征,具有包括高离子电导率在内的显著固态特性。然而,大多数IPCs是有机鎓盐。由于其低对称结构,将有机金属半夹心配合物引入IPCs具有挑战性。本文介绍了一系列由半夹心有机金属配合物衍生的盐组成的新型IPCs。我们合成了五种[Ru(Cp)(tmeda)(CO)]X(tmeda = N,N,N',N'-四甲基-1,2-乙二胺,X = 阴离子)的不同阴离子盐,并研究了它们的相行为、晶体结构以及固态下的分子运动。以CPFSA(= 1,1,2,2,3,3-六氟丙烷-1,3-二磺酰亚胺)、B(CN)和FSA(= (FSO₂)₂N)为阴离子的盐在327 - 364 K的温度范围内经历了向具有CsCl型结构的IPCs相的相变。使用较小的阴离子会导致转变温度升高。在每种盐中,代表围绕一个阳离子的阴离子数量的配位数在IPCs相和低温相中均保持为8。然而,含有较小阴离子(CF₃BF₄和PF₆)的盐呈现出旋转相而非IPCs相。在这些情况下,低温时配位数为6。

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