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在一个同时展现自旋交叉和轨道跃迁行为的双吡啶钴(II)配合物中,水分子诱导的可逆磁开关效应

Water Molecule-Induced Reversible Magnetic Switching in a Bis-Terpyridine Cobalt(II) Complex Exhibiting Coexistence of Spin Crossover and Orbital Transition Behaviors.

作者信息

Kobayashi Fumiya, Komatsumaru Yuki, Akiyoshi Ryohei, Nakamura Masaaki, Zhang Yingjie, Lindoy Leonard F, Hayami Shinya

机构信息

Department of Chemistry, Graduate School of Science and Technology, Kumamoto University, 2-39-1 Kurokami, Chuo-ku, Kumamoto 860-8555, Japan.

Australian Nuclear Science and Technology Organization, Locked Bag 2001, Kirrawee DC, New South Wales 2232, Australia.

出版信息

Inorg Chem. 2020 Dec 7;59(23):16843-16852. doi: 10.1021/acs.inorgchem.0c00818. Epub 2020 Oct 1.

Abstract

The development of molecule-based switchable materials remains an important challenge in the field of molecular science. Achievement of a structural phase transition induced by adsorption/desorption of guest molecules in spin crossover (SCO) Co(II) compounds is of significant interest because of the possibility that the spin state of the magnetic anisotropic high-spin (HS, = 3/2) and low-spin (LS, = 1/2) states can be switched via the induced changes in associated intermolecular interactions. In this study, we demonstrated a reversible magnetic switching associated with spin state conversion, along with a single-crystal to single-crystal (SCSC) phase transition induced by dehydration/rehydration. Co(terpy)·HO (·HO; terpy = 2,2':6',2''-terpyridine) assembles in the solid state via π-π and CH-π interactions involving adjacent terpyridine cores along the direction to form two-dimensional (2D) layered domains. ·HO exhibits gradual and incomplete SCO, from fully HS to ca. 0.5 HS, and the field-induced single-molecule magnet (SMM) behavior attributed to the presence of the anisotropic partial high-spin Co(II) species. ·HO undergoes a SCSC transformation accompanied by a change from the tetragonal space group 4/ to 4/ via a dehydration process. Dehydrated exhibits a reverse thermal hysteresis behavior ( = 287 K; = 270 K) in the gradual SCO region from fully HS to ca. 0.5 HS, followed by an ordinary thermal hysteresis (' = 195 K; ' = 155 K) to fully LS Co(II). A temperature-dependent single-crystal X-ray structural analysis revealed that the reverse hysteresis can be attributed to an order/disorder structural phase transition of the BF anions involving a symmetry breaking to yield the monoclinic space group 2/ and orbital (angular momentum) transition (T). Both the SCSC phase transition and magnetic behavior are switchable by dehydration/rehydration processes; thus again adsorbs water at room temperature to give both the original structure and its magnetic behavior.

摘要

基于分子的可切换材料的开发仍然是分子科学领域的一项重要挑战。在自旋交叉(SCO)钴(II)化合物中,通过客体分子的吸附/解吸诱导结构相变的实现具有重大意义,因为磁各向异性高自旋(HS,S = 3/2)和低自旋(LS,S = 1/2)态的自旋状态有可能通过相关分子间相互作用的诱导变化而切换。在本研究中,我们展示了与自旋态转换相关的可逆磁开关,以及由脱水/再水化诱导的单晶到单晶(SCSC)相变。Co(terpy)·H₂O(·H₂O;terpy = 2,2':6',2''-三联吡啶)在固态中通过涉及沿c方向相邻三联吡啶核的π-π和CH-π相互作用组装,形成二维(2D)层状域。·H₂O表现出从完全HS到约0.5 HS的逐渐且不完全的SCO,以及归因于各向异性部分高自旋Co(II)物种存在的场诱导单分子磁体(SMM)行为。·H₂O通过脱水过程经历SCSC转变,伴随着从四方空间群I4/mmm到I4/mcm的变化。脱水后的产物在从完全HS到约0.5 HS的逐渐SCO区域表现出反向热滞行为(T₁ = 287 K;T₂ = 270 K),随后是到完全LS Co(II)的普通热滞行为(T₁' = 195 K;T₂' = 155 K)。温度依赖性单晶X射线结构分析表明,反向热滞可归因于BF₄⁻阴离子的有序/无序结构相变,涉及对称性破缺以产生单斜空间群P2/m和轨道(角动量)转变(T)。SCSC相变和磁行为均可通过脱水/再水化过程切换;因此,产物在室温下再次吸水,恢复其原始结构及其磁行为。

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