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首页> 外文期刊>Chemistry: A European journal >Tuning the transition temperature and cooperativity of bapbpy-based mononuclear spin-crossover compounds: Interplay between molecular and crystal engineering
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Tuning the transition temperature and cooperativity of bapbpy-based mononuclear spin-crossover compounds: Interplay between molecular and crystal engineering

机译:调整基于bapbpy的单核自旋交联化合物的转变温度和协同作用:分子与晶体工程之间的相互作用

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摘要

In this study, we show that 1) different isomers of the same mononuclear iron(II) complex give materials with different spin-crossover (hereafter SCO) properties, and 2) minor modifications of the bapbpy (bapbpy=N6,N6′- di(pyridin-2-yl)-2,2′-bipyridine-6,6′-diamine) ligand allows SCO to be obtained near room temperature. We also provide a qualitative model to understand the link between the structure of bapbpy-based ligands and the SCO properties of their iron(II) compounds. Thus, seven new trans-[Fe{R _2(bapbpy)}(NCS) _2] compounds were prepared, in which the R 2bapbpy ligand bears picoline (9-12), quin-2-oline (13), isoquin-3-oline (14), or isoquin-1-oline (15) substituents. From this series, three compounds (12, 14, and 15) have SCO properties, one of which (15) occurs at 288 K. The crystal structures of compounds 11, 12, and 15 show that the intermolecular interactions in these materials are similar to those found in the parent compound [Fe(bapbpy)(NCS) _2] (1), in which each iron complex interacts with its neighbors through weak N-H?S hydrogen bonding and π-π stacking. For compounds 12 and 15, hindering groups located near the N-H bridges weaken the N-S intermolecular interactions, which is correlated to non-cooperative SCO. For compound 14, the substitution is further away from the N-H bridges, and the SCO remains cooperative as in 1 with a hysteresis cycle. Optical microscopy photographs show the strikingly different spatio-temporal evolution of the phase transition in the noncooperative SCO compound 12 relative to that found in 1. Heat-capacity measurements were made for compounds 1, 12, 14, and 15 and fitted to the Sorai domain model. The number n of like-spin SCO centers per interacting domain, which is related to the cooperativity of the spin transition, was found high for compounds 1 and 14 and low for compounds 12 and 15. Finally, we found that although both pairs of compounds 11/12 and 14/15 are pairs of isomers their SCO properties are surprisingly different.
机译:在这项研究中,我们表明1)同一单核铁(II)配合物的不同异构体产生的材料具有不同的自旋交联(以下称SCO)性质,以及2)bapbpy的较小修饰(bapbpy = N6,N6'- di (吡啶-2-基)-2,2'-联吡啶-6,6'-二胺)配体允许在室温附近获得SCO。我们还提供了定性模型,以了解基于bapbpy的配体的结构与其铁(II)化合物的SCO性质之间的联系。因此,制备了七个新的反式[[Fe {R _2(bapbpy)}(NCS)_2]化合物,其中R 2bapbpy配体带有甲基吡啶(9-12),喹-2-啉(13),异喹3 -oline(14)或isoquin-1-oline(15)取代基。从该系列中,三种化合物(12、14和15)具有SCO特性,其中一种(15)出现在288K。化合物11、12和15的晶体结构表明,这些材料中的分子间相互作用相似与在母体化合物[Fe(bapbpy)(NCS)_2](1)中发现的那些化合物不同,其中每个铁配合物通过弱NH3S氢键和π-π堆积与相邻元素相互作用。对于化合物12和15,位于N-H桥附近的阻碍基减弱了N-S分子间的相互作用,这与非合作SCO有关。对于化合物14,取代基距离N-H桥更远,并且SCO保持与1相同的滞后循环。光学显微镜照片显示,与在1中发现的相比,非合作SCO化合物12中相变的时空变化显着不同。对化合物1、12、14和15进行了热容量测量,并拟合到Sorai域模型。发现每个相互作用域中与自旋跃迁的协同作用相关的类似自旋SCO中心的数量n,对于化合物1和14较高,而对于化合物12和15较低。最后,我们发现,尽管这两对化合物11/12和14/15是一对异构体,它们的SCO特性令人惊讶地不同。

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