Rodríguez-Jiménez Santiago, Brooker Sally
Department of Chemistry and the MacDiarmid Institute for Advanced Materials and Nanotechnology, University of Otago , P.O. Box 56, Dunedin 9054, New Zealand.
Inorg Chem. 2017 Nov 20;56(22):13697-13708. doi: 10.1021/acs.inorgchem.7b01338. Epub 2017 Nov 7.
A new family of mononuclear [Fe(Rdpt)(NCE)] complexes (E = S, Se, or BH) is formed by 1:2 reaction of [Fe(pyridine)(NCE)] with the monotopic pyridyl triazole ligand 4-(4-methylphenyl)-3-(2-pyridinyl)-5-phenyl-4H-1,2,4-triazole (tolpyph). The three complexes are obtained as six different solvatomorphs: [Fe(tolpyph)(NCS)]·HO (1·HO), 1·1.5CHOH·0.5HO, [Fe(tolpyph)(NCSe)] (2), 2·1.5HO, [Fe(tolpyph)(NCBH)] (3), and 3·HO. Single-crystal X-ray diffraction reveals that 1·1.5CHOH·0.5HO and 2 are high-spin (HS) at 100 K, while 3 is low-spin (LS) at 100 K and HS at 373 K. Compound 3 is the first structurally characterized example of an [Fe(Rdpt)(NCE)]-type complex with NCBH co-ligand: the crystal packing is dominated by aromatic stacking interactions. Solid-state magnetic measurements show that 1·HO and 2·1.5HO remain HS down to 50 K, whereas 3·HO undergoes spin crossover (SCO) with a T of 309 K, slightly above room temperature. A literature survey of analogous trans-[Fe(Rdpt)(NCX)]-type complexes (53 distinct crystal structures) shows that for the complexes that are SCO active in the solid state the Fe-N≡C(X) angle is usually close to straight, 162-178°, whereas it is usually lower, 142-159°, for the complexes that remain HS. UV-vis studies in CHCl solution show that in each case the use of a 6:1 ratio of tolpyph/Fe(II) is required to ensure the iron(II) is present in solution as [Fe(tolpyph)(NCE)]. Interestingly, using this ratio, all three compounds are SCO-active in CDCl solution-in dramatic contrast to the solid-state findings. Specifically, while compounds 1 and 2 are not SCO-active in the solid state (they remain HS), they undergo gradual SCO in CDCl solution, with T values of 290 and 310 K, respectively. In CDCl solution, compound 3 has a T value of 288 K, which is 21 K lower than in the solid state. These results highlight the differences between solid state (ligand field; crystal packing) and solution (ligand field; solvation) effects on SCO, with the latter studies revealing room-temperature SCO for all three of these complexes.
通过[Fe(吡啶)(NCE)]与单齿吡啶基三唑配体4-(4-甲基苯基)-3-(2-吡啶基)-5-苯基-4H-1,2,4-三唑(tolpyph)按1:2反应,形成了一个新的单核[Fe(Rdpt)(NCE)]配合物家族(E = S、Se或BH)。这三种配合物以六种不同的溶剂化物形式获得:[Fe(tolpyph)(NCS)]·H₂O (1·H₂O)、1·1.5CH₃OH·0.5H₂O、[Fe(tolpyph)(NCSe)] (2)、2·1.5H₂O、[Fe(tolpyph)(NCBH)] (3)和3·H₂O。单晶X射线衍射表明,1·1.5CH₃OH·0.5H₂O和2在100 K时为高自旋(HS),而3在100 K时为低自旋(LS),在373 K时为HS。化合物3是第一个具有结构表征的含NCBH共配体的[Fe(Rdpt)(NCE)]型配合物:晶体堆积以芳香堆积相互作用为主。固态磁性测量表明,1·H₂O和2·1.5H₂O在低至50 K时仍保持HS,而3·H₂O在309 K时发生自旋交叉(SCO),略高于室温。对类似的反式-[Fe(Rdpt)(NCX)]型配合物(53个不同的晶体结构)的文献调查表明,对于在固态中具有SCO活性的配合物,Fe-N≡C(X)角通常接近直线,为162 - 178°,而对于保持HS的配合物,该角度通常较低,为142 - 159°。在CHCl₃溶液中的紫外可见研究表明,在每种情况下,需要使用tolpyph/Fe(II)为6:1的比例以确保铁(II)在溶液中以[Fe(tolpyph)(NCE)]形式存在。有趣的是,使用该比例时,所有三种化合物在CDCl₃溶液中均具有SCO活性——这与固态结果形成了鲜明对比。具体而言,虽然化合物1和2在固态中不具有SCO活性(它们保持HS),但它们在CDCl₃溶液中经历逐渐的SCO,T值分别为290和310 K。在CDCl₃溶液中,化合物3的T值为288 K,比在固态中低21 K。这些结果突出了固态(配体场;晶体堆积)和溶液(配体场;溶剂化)对SCO影响的差异,后者的研究揭示了这三种配合物在室温下均具有SCO。