Marinova Maya, Torres-Werlé Maria, Taupier Grégory, Maisse-François Aline, Achard Thierry, Boeglin Alex, Dorkenoo Kokou Dodzi Honorat, Bellemin-Laponnaz Stéphane
Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), CNRS-Université de Strasbourg, 23 rue du Loess BP 43, F-67034 Strasbourg, France.
ACS Omega. 2019 Feb 5;4(2):2676-2683. doi: 10.1021/acsomega.8b03484. eCollection 2019 Feb 28.
We report an extensive study on the coordination behavior of chiral ditopic bridging ligands, which lead to metallosupramolecular polymers in the presence of Zn(II) and Cu(II) in solution. With the help of UV-vis and circular dichroism spectroscopies, we show that the metallopolymer sequence can be controlled by chirality and by the choice of the metal ion. Although the formation of a block metallopolymer proceeds through the assembly of homoleptic complexes, an alternate metallopolymer may be obtained only when heteroleptic complexes are formed. This demonstrates how the prevalent coordination geometries at metal centers may be used to control the sequences of the metallopolymers.
我们报告了一项关于手性双齿桥连配体配位行为的广泛研究,该配体在溶液中与锌(II)和铜(II)存在时会形成金属超分子聚合物。借助紫外可见光谱和圆二色光谱,我们表明金属聚合物序列可以通过手性和金属离子的选择来控制。尽管嵌段金属聚合物的形成是通过同配络合物的组装进行的,但只有当形成异配络合物时才能获得交替金属聚合物。这证明了金属中心普遍存在的配位几何结构可如何用于控制金属聚合物的序列。