Institute of Inorganic Chemistry, RWTH Aachen University, 52074, Aachen, Germany.
Jülich-Aachen Research Alliance (JARA-FIT) and Peter Grünberg Institute 6, Forschungszentrum Jülich, 52425, Jülich, Germany.
Chemistry. 2018 Dec 3;24(67):17767-17778. doi: 10.1002/chem.201803531. Epub 2018 Nov 8.
A series of unprecedented supramolecular associates of phenylarsonate-capped {M Pd O }-type (M=Co, Ni and Zn) polyoxopalladates with α-cyclodextrins (α-CD) was obtained and characterized in the solid state (single-crystal X-ray diffraction (XRD), FT-IR spectroscopy, elemental and thermogravimetric (TGA) analyses), in aqueous solution ( H and C NMR) and in the gas phase (ESI-MS). The non-covalent host-guest interactions between the organopolyoxoanions and α-CD rings alter the O coordination environment of a 3d transition metal ion (M ) situated at the center of a cuboid polyoxododecapalladate shell. This synthetically controlled "chemical pressure" effectively induces axial distortion of the otherwise cubic polyoxopalladate environment between two trans-positioned α-CD moieties. Its effect on the magnetic properties and the electronic structure of the Co derivative was assessed in a combined SQUID magnetometry, EPR, X-ray magnetic circular/linear dichroism (XMCD/XMLD), and X-ray absorption near-edge structure (XANES) spectroscopy study.
获得了一系列前所未有的苯胂酸封端的 {M Pd O }-型(M=Co、Ni 和 Zn)多氧多钯酸盐与α-环糊精(α-CD)的超分子配合物,并在固态(单晶 X 射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)、元素和热重分析(TGA))、水溶液( H 和 C NMR)和气相(ESI-MS)中进行了表征。有机多氧多阴离子与α-CD 环之间的非共价主客体相互作用改变了位于十二面多氧多钯酸壳中心的 3d 过渡金属离子(M)的 O 配位环境。这种合成控制的“化学压力”有效地诱导了两个反位 α-CD 部分之间立方多氧多钯酸环境的轴向畸变。在 SQUID 磁强计、EPR、X 射线磁圆/线二色性(XMCD/XMLD)和 X 射线吸收近边结构(XANES)光谱研究中评估了其对 Co 衍生物磁性能和电子结构的影响。