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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Stepped spin crossover in Fe(III) halogen substituted quinolylsalicylaldimine complexes
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Stepped spin crossover in Fe(III) halogen substituted quinolylsalicylaldimine complexes

机译:Fe(III)卤素取代的喹啉基水杨基醛亚胺络合物中的逐步自旋交叉

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The reaction of Fe(NCS)(3) prepared in situ in MeOH with Hqsal-X (Hqsal-X = 5-X-N-quinolylsalicylaldimine) in CH2Cl2 yields the Fe-III complexes, [Fe(qsal-X)(2)]NCS.solvent (X = F 1; X = Cl, 2, Br, 3 solvent = MeOH; X = I, solvent = 0.25CH(2)Cl(2)center dot 0.5MeOH 4) in moderate to good yields. IR spectroscopy confirms that NCS- acts as a counteranion only and that the qsal-X ligand is bound to the Fe-III centre. SQUID magnetometric studies reveal stepped hysteretic spin crossover in 1 and 2, which is abrupt in both steps in latter compound. Mossbauer spectroscopic studies of 1 and 2 support these conclusions. The bromo derivative, 3, undergoes half spin crossover up to 340 K while 4 is low spin at all temperatures measured. The spin transition temperature, T-1/2 is found to increase on moving from F to Br. UV-Vis and NMR spectroscopic studies indicate that 1-4 have spin states intermediate between HS and LS in solution. Structural studies show that 1, 2 and 3 crystallize in triclinic P (1) over bar while 4 is in monoclinic P2(1)/c. Crystallographic studies of 1 at 100, 200 and 270 K show that spin crossover proceeds from a [LS-LS] state through a [LS-HS] intermediate to a [HS-HS] state (LS = low spin, S = 1/2, HS = high spin, S = 5/2). Similar results are found for 3 although this time a [LS-IS] state exists at 123 K while a [LS-HS] state is found at 295 K (IS = intermediate spin state where partial spin crossover has occurred). Both 2 and 4 are found to have LS Fe-III centres although the latter contains two crystallographically independent Fe-III centres in the asymmetric unit. The crystal packing in 1-4 consists of extensive pi-pi interactions through the planar qsal-X ligands and CH center dot center dot center dot X (X = O, halogen) and/or X center dot center dot center dot pi (X = halogen) interactions which result in pseudo 3D supramolecular networks. This results in high cooperativity in 1 and 2 and is probably responsible for the hysteretic stepped spin crossover in these compounds.
机译:在MeOH中原位制备的Fe(NCS)(3)与Hqsal-X(Hqsal-X = 5-XN-喹啉基水杨醛亚胺)在CH2Cl2中的反应生成Fe-III配合物,[Fe(qsal-X)(2)] NCS。溶剂(X = F 1; X = Cl,2,Br,3溶剂= MeOH; X = I,溶剂= 0.25CH(2)Cl(2)中心点0.5MeOH 4),产率中等至良好。红外光谱证实,NCS-仅充当抗衡阴离子,并且qsal-X配体与Fe-III中心键合。 SQUID磁力研究表明,在1和2中出现了阶跃磁滞自旋交叉,这在后面的化合物中在两个步骤中都是突变的。 Mossbauer光谱研究1和2支持这些结论。溴衍生物3在最高340 K的温度下经历了一半的自旋交叉,而4在所有测得的温度下均处于低自旋状态。从F到Br,自旋转变温度T-1 / 2升高。 UV-Vis和NMR光谱研究表明1-4的自旋态介于溶液中的HS和LS之间。结构研究表明,1、2和3在三斜晶P(1)上方结晶,而4在单斜晶P2(1)/ c中结晶。在100、200和270 K下的1的晶体学研究表明,自旋交叉从[LS-LS]状态通过[LS-HS]中间体过渡到[HS-HS]状态(LS =低自旋,S = 1 / 2,HS =高自旋,S = 5/2)。尽管这一次[LS-IS]状态在123 K处存在,而[LS-HS]状态在295 K(IS =发生部分自旋交叉的中间自旋状态),但对于3发现了相似的结果。发现2和4都具有LS Fe-III中心,尽管后者在不对称单元中包含两个晶体学独立的Fe-III中心。 1-4中的晶体堆积包括通过平面qsal-X配体和CH中心点中心点中心点X(X = O,卤素)和/或X中心点中心点中心点pi(X =卤素)相互作用,从而产生伪3D超分子网络。这会导致1和2的高协同性,并且可能是这些化合物中滞后的阶跃自旋交叉的原因。

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