Macrocycle-based metal ion complexation: a study of the lanthanide contraction effect towards hexacyclohexanocucurbit[6]uil
Xiao Qin, Xin‐Long Ni, Jing‐Xu Hu, Kai Chen, Yun‐Qian Zhang, Carl Redshaw, Qian‐Jiang Zhu, Sai‐Feng Xue, Zhu Tao
Abstract
Xiao Qin, Xin‐Long Ni, Jing‐Xu Hu, Kai Chen, Yun‐Qian Zhang, Carl Redshaw, Qian‐Jiang Zhu, Sai‐Feng Xue, Zhu Tao
Abstract
In the present study, the lanthanide(III) contraction effect induced coordination architectures of HCyHQ[6] have been studied. The results, including fifteen crystal structures, indicate that although lanthanide metal ions have similar chemical properties mostly, their slightly different ionic radii play a key role in the formation of different supramolecular self-assembly types of HCyHQ[6]. As a result, the ionic radius-dependent complexes of HCyHQ[6] can be structurally classified into four groups: HCyHQ[6]-pair, HCyHQ[6]-molecular bowl, Ln–HCyHQ[6] one dimensional coordination polymer, and HCyHQ[6]-molecular capsule.
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In the present study, the lanthanide(III) contraction effect induced coordination architectures of HCyHQ[6] have been studied. The results, including fifteen crystal structures, indicate that although lanthanide metal ions have similar chemical properties mostly, their slightly different ionic radii play a key role in the formation of different supramolecular self-assembly types of HCyHQ[6]. As a result, the ionic radius-dependent complexes of HCyHQ[6] can be structurally classified into four groups: HCyHQ[6]-pair, HCyHQ[6]-molecular bowl, Ln–HCyHQ[6] one dimensional coordination polymer, and HCyHQ[6]-molecular capsule.
Key concepts: Lanthanide, Lanthanide contraction, Ionic radius, Supramolecular chemistry, Metal, Ionic bonding, Ion, Metal ions in aqueous solution