Magnetic superexchange switching by transformation of trigonal bipyramid into square pyramid in Cu(II)-nitroxide complex

IF 3.3 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Kseniya Maryunina, Koyo Yamaguchi, Katsuya Inoue, Arkady A. Samsonenko, Sergey L. Veber, Kristina Smirnova, Artem Bogomyakov, Gleb Letyagin, Galina Romanenko, Vitaliy A Morozov
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引用次数: 0

Abstract

The reaction of Cu(hfac)2 and imino nitroxide 2-(pyridin-4-yl)-4,4,5,5,5-tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl (IN) gives the complex [Cu2(hfac)4(IN)]n (1), which has the structure of a chain-polymer with side branches. IN, acting as a μ3-O,N,N-tridentate ligand, bridges the intrachain Cu atoms through the ONO atoms of the nitroxide groups and the NIm atoms of the imidazoline ring of IN, while the NPy atom of the pyridine cycle binds to the branching Cu atom. The specific disorder of the imino nitroxide fragment in IN and the intrachain Cu(hfac)2 moieties makes the structure of 1 almost similar to that of the complex [Cu2(hfac)4(NN)]n (2) with nitronyl nitroxide NN, an analog of IN. Thermally induced hysteretic change in the χT value (T↓ = 109 K and T↑ = 119 K) and transformations of EPR spectra were found for the complex 1. Applying pressure above 1.9 kbar not only completly suppresses this magnetic anomaly, but also manifests significant differences in the magnetic behavior of the low-temperature and pressure-stabilized modifications at χT(T) curve. Comparing magnetostructural correlations for 1 at atmospheric and hydrostatic pressure with those for an analogue of nitronyl nitroxide 2 using quantum chemical calculations made it possible to clarify the nature of the magnetic anomaly. It was established that the magnetic transition of 1 is related to the transformation of the trigonal-bipyramidal environment of the branched Cu atom into a square-pyramidal one with a change in the position of the NPy atom of the pyridine ring from equatorial to axial. EPR spectroscopy clearly indicates the changes of g-tensor components of the branching Cu2+ ion, while the giso parameter remaining almost unchanged. Magnetic anomaly in 1 revealed by SQUID magnetometry is a unique case of switching the indirect magnetic superexchange {Cu2+...IN} through the pyridine fragment during the rearengement of peripheral fragments of the structure.
Cu(II)-氮氧化物配合物中三角双棱锥转化为方形棱锥的磁超交换开关
Cu(hfac)2与亚硝基2-(吡啶-4-基)-4,4,5,5,5-四甲基-4,5-二氢- 1h -咪唑-1-氧(IN)反应得到配合物[Cu2(hfac)4(IN)]n(1),该配合物具有带侧支的链式聚合物结构。IN作为一种μ3-O,N,N-三齿配体,通过氮氧基的ONO原子和IN的咪唑啉环的NIm原子桥接链内Cu原子,而吡啶环的NPy原子与支链Cu原子结合。in中亚硝基氮氧化物片段和链内Cu(hfac)2基团的特殊无序性使得1的结构几乎与与in类似的硝基氮氧化物NN的配合物[Cu2(hfac)4(NN)]n(2)的结构相似。发现配合物1的χT值(T↓= 109 K, T↑= 119 K)和EPR谱发生了热致滞后变化。施加高于1.9 kbar的压力不仅完全抑制了这种磁异常,而且在χT(T)曲线上表现出低温和压力稳定的磁行为差异显著。利用量子化学计算将大气和静水压力下1的磁结构相关性与硝基氮氧化物2的类似物的磁结构相关性进行比较,使澄清磁异常的性质成为可能。结果表明,1的磁跃迁与支链Cu原子的三角-双锥体环境转变为方锥体环境有关,与吡啶环NPy原子的位置由赤道向轴向变化有关。EPR光谱清晰地显示了支化Cu2+离子的g张量分量的变化,而giso参数基本保持不变。SQUID磁强计揭示的1区的磁异常是一个切换间接磁超交换{Cu2+…IN}通过吡啶片段在结构的外围片段的重新排列。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
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