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2D-Coordination Polymers Based on Rare-Earth Propionates of Layered Topology Demonstrate Polytypism and Controllable Single-Crystal-to-Single-Crystal Phase Transitions

机译:基于稀土拓扑结构的2D协调聚合物表明了多液氮和可控单晶对单晶相变

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摘要

A series of rare-earth propionate based complexes [Ln(2)(H2O)(2)Prop(6)] (Ln = Y, Ho-Lu) were synthesized in the form of two polymorphs (alpha and beta), both being layered 2D-coordination polymers with identical geometries of the single layers. The polymorphs differ from each other in the layer arrangement, and therefore they are considered the first example of polytypes among aliphatic rare-earth carboxylates. Strategies toward the controllable crystallization of each polytype have been developed. The beta polytype undergoes an irreversible single-crystal-to-single-crystal (SCSC) phase transition to the alpha polytype upon cooling, whereas a can be artificially converted into beta via mechanical treatment. The performed DFT calculations reveal the alpha polytype to be more energetically favorable by 13 kJ per 1 mol of unit cells that is determined predominantly by the difference between energies of weak interlayer van der Waals interactions for the two polytypes. A low interlayer interaction energy makes it possible to use mechanical exfoliation to obtain a crystal surface of atomic smoothness suitable for mechanical decoration.
机译:一系列稀土基丙酸盐基络合物[LN(2)(H2O)(2)支本(2)支点(6)](LN = Y,HO-LU)以两种多晶型(α和β)的形式合成层叠的2D配位聚合物,单层的相同几何形状。多晶型物在层排列中彼此不同,因此它们被认为是脂族稀土羧酸盐之间的多阱的第一例。已经开发了每个聚贸易可控制结晶的策略。在冷却时,β聚型经历不可逆的单晶 - 单晶(SCSC)相转变至α聚型,而A可以通过机械处理人工转化为β。所进行的DFT计算显示α多型以每1摩尔单位细胞的13kJ更有利,其单位细胞主要由两种聚晶体的相互作用的相互作用的能量之间的差异确定。低层间相互作用能量使得可以使用机械剥离来获得适于机械装饰的原子平滑度的晶体表面。

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