Kobayashi Fumiya, Komatsumaru Yuki, Akiyoshi Ryohei, Nakamura Masaaki, Zhang Yingjie, Lindoy Leonard F, Hayami Shinya
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.
Inorg Chem. 2020 Dec 7;59(23):16843-16852. doi: 10.1021/acs.inorgchem.0c00818. Epub 2020 Oct 1.
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.
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。