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Elucidating The Mechanism Of A Two-step Spin Transition In A Nanoporous Metal-organic Framework

机译:阐明了纳米多孔金属有机骨架中两步自旋转变的机理

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The nanoporous metal-organic framework, Fe(bpe)_2(NCS)_2·3(acetone), SCOF-4(Ac) (where bpe is 1,2-bis(4'-pyridyl)ethane), displays a two-step spin crossover (SCO) transition (65-155 K) that is sensitive to the presence of acetone guest molecules. Structural analyses have revealed a structural phase transition, from tetragonal (P42_1c) to orthorhombic (P2_12_12), associated with the spin transition that defines a checkerboard-like ordering of spin sites at the high-spin:low-spin plateau. The reversible desorption of the acetone guest species is accompanied by a complex series of structural phase transitions that describe a dramatic flexing of the structure. The thermal trapping of a metastable state with ~20-25% high-spin character was observed both magnetically and structurally upon rapid quenching of SCOF-4(Ac) to 10 and 25 K, respectively. The light-induced excited spin state trapping (LIESST) effects for SCOF-4(Ac) show a 55% excitation of a metastable HS state at 10 K and a characteristic T(LIESST) value of 52 K.
机译:纳米多孔金属有机骨架Fe(bpe)_2(NCS)_2·3(丙酮),SCOF-4(Ac)(其中bpe为1,2-双(4'-吡啶基)乙烷)显示出两个对丙酮客体分子的存在敏感的逐步自旋交联(SCO)跃迁(65-155 K)。结构分析表明,从四方(P42_1c)到正交(P2_12_12)的结构相变与自旋跃迁相关,自旋跃迁定义了高自旋:低自旋高原上自旋位点的棋盘状排序。丙酮客体物质的可逆解吸伴随着一系列复杂的结构相变,描述了结构的剧烈弯曲。在将SCOF-4(Ac)快速淬灭至10 K和25 K时,在磁性和结构上均观察到具有〜20-25%高自旋特性的亚稳态热陷阱。 SCOF-4(Ac)的光诱导激发自旋态俘获(LIESST)效应显示在10 K时亚稳态HS态的激发率为55%,特征T(LIESST)值为52K。

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