反铁磁性
席夫碱
化学
配体(生物化学)
星团(航天器)
结晶学
链条(单位)
铁磁性
产量(工程)
甘氨酸
丙氨酸
立体化学
冷凝
缩合反应
材料科学
物理
氨基酸
热力学
有机化学
凝聚态物理
计算机科学
程序设计语言
天文
冶金
催化作用
生物化学
受体
作者
Emmanouil Κ. Charkiolakis,David Gracia,M. Cervera,Marco Evangelisti,Constantinos J. Milios
标识
DOI:10.1002/chem.202500911
摘要
The solvothermal reaction between FeCl3·6H2O, NiCl2·6H2O, 2-hydroxynaphthaldehyde, and glycine (gly) in MeOH results in the formation of the trinuclear heterometallic cluster [FeΙΙΙ 2NiΙΙ(L1)4(MeOH)4] (1) in good yield, while the same reaction upon replacing gly with methyl-alanine (mAla), results in the formation of the closely related quasi 1D coordination polymer {[FeΙΙΙ 2NiΙΙ(L2)4(MeOH)2]n} (2) (L1, L2: the dianionic form of the Schiff-base ligand derived from the condensation of 2-hydroxynaphthaldehyde and gly (L1 for 1), or mAla (L2 for 2)). The structure of 1 describes a linear trimetallic {FeIII 2Ni} unit, whereas complex 2 consists of repeating linear {FeIII 2Ni} units with each one connected to two neighboring units via four coordination bonds, forming a quasi-1D chain. The structural similarity between complex 1 and the repeating unit of complex 2 is remarkable. However, their magnetic properties differ significantly, with complex 1 displaying dominant ferromagnetic interactions, and complex 2 showing antiferromagnetic interactions.
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