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卤素取代对前所未有的突变铁自旋交叉配合物中N O席夫碱配体的影响。

Halogen Substitution Effects on N O Schiff Base Ligands in Unprecedented Abrupt Fe Spin Crossover Complexes.

作者信息

Phonsri Wasinee, Macedo David S, Vignesh Kuduva R, Rajaraman Gopalan, Davies Casey G, Jameson Guy N L, Moubaraki Boujemaa, Ward Jas S, Kruger Paul E, Chastanet Guillaume, Murray Keith S

机构信息

School of Chemistry, Building 23, Monash University, Clayton, Victoria, 3800, Australia.

IITB-Monash Research Academy, IIT Bombay, Mumbai, 400076, India.

出版信息

Chemistry. 2017 May 23;23(29):7052-7065. doi: 10.1002/chem.201700232. Epub 2017 May 5.

Abstract

A family of halogen-substituted Schiff base iron(II) complexes, [Fe (qsal-X) ], (qsal-X=5-X-N-(8-quinolyl)salicylaldimines)) in which X=F (1), Cl (2), Br (3) or I (4) has been investigated in detail. Compound 1 shows a temperature invariant high spin state, whereas the others all show abrupt spin transitions, at or above room temperature, namely, 295 K (X=I) up to 342 K (X=Br), these being some of the highest T values obtained, to date, for Fe N/O species. We have recently reported subtle symmetry breaking in [Fe (qsal-Cl) ] 2 with two spin transition steps occurring at 308 and 316 K. A photomagnetic study reveals almost full HS conversion of [Fe (qsal-I) ] 4 at low temperature (T(LIESST)=54 °K). The halogen substitution effects on the magnetic properties, as well as the crystal packing of the [Fe (qsal-X) ] compounds and theoretical calculations, are discussed in depth, giving important knowledge for the design of new spin crossover materials. In comparison to the well known iron(III) analogues, [Fe (qsal-X) ] , the two extra π-π and P4AE interactions found in [Fe (qsal-X) ] compounds, are believed to be accountable for the spin transitions occurring at ambient temperatures.

摘要

我们对一系列卤素取代的席夫碱铁(II)配合物[Fe(qsal-X)](qsal-X = 5-X-N-(8-喹啉基)水杨醛亚胺)进行了详细研究,其中X = F(1)、Cl(2)、Br(3)或I(4)。化合物1呈现出温度不变的高自旋态,而其他化合物在室温及以上均呈现出突然的自旋转变,即从295 K(X = I)到342 K(X = Br),这些是迄今为止铁氮/氧物种所获得的一些最高T值。我们最近报道了[Fe(qsal-Cl)]₂中存在微妙的对称性破缺,在308和316 K发生了两个自旋转变步骤。光磁研究表明,[Fe(qsal-I)]₄在低温下(T(LIESST)=54 K)几乎完全发生高自旋转变。深入讨论了卤素取代对磁性的影响,以及[Fe(qsal-X)]化合物的晶体堆积和理论计算,为新型自旋交叉材料的设计提供了重要知识。与著名的铁(III)类似物[Fe(qsal-X)]相比,[Fe(qsal-X)]化合物中发现的两种额外的π-π和P4AE相互作用被认为是室温下自旋转变的原因。

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