Meunier Antoine, Singleton Michael L, Kauffmann Brice, Granier Thierry, Lautrette Guillaume, Ferrand Yann, Huc Ivan
Université de Bordeaux, CNRS, Bordeaux Institut National Polytechnique, CBMN (UMR 5248), IECB 2 Rue Robert Escarpit 33600 Pessac France
Université de Bordeaux, CNRS, INSERM, Institut Européen de Chimie et Biologie (UMS 3033) 2 Rue Robert Escarpit 33600 Pessac France.
Chem Sci. 2020 Oct 12;11(44):12178-12186. doi: 10.1039/d0sc05143h.
As metalloproteins exemplify, the chemical and physical properties of metal centers depend not only on their first but also on their second coordination sphere. Installing arrays of functional groups around the first coordination sphere of synthetic metal complexes is thus highly desirable, but it remains a challenging objective. Here we introduce a novel approach to produce tailored second coordination spheres. We used bioinspired artificial architectures based on aromatic oligoamide foldamers to construct a rigid, modular and well-defined environment around a metal complex. Specifically, aza-aromatic monomers having a tethered [2Fe-2S] cluster have been synthesized and incorporated in conical helical foldamer sequences. Exploiting the modularity and predictability of aromatic oligoamide structures allowed for the straightforward design of a conical architecture able to sequester the metal complex in a confined environment. Even though no direct metal complex-foldamer interactions were purposely designed in this first generation model, crystallography, NMR and IR spectroscopy concurred to show that the aromatic oligoamide backbone alters the structure and fluxional processes of the metal cluster.
正如金属蛋白所例证的那样,金属中心的化学和物理性质不仅取决于其一阶配位层,还取决于其二阶配位层。因此,在合成金属配合物的一阶配位层周围安装官能团阵列是非常可取的,但这仍然是一个具有挑战性的目标。在这里,我们介绍一种产生定制二阶配位层的新方法。我们使用基于芳香族寡酰胺折叠体的仿生人工结构,在金属配合物周围构建一个刚性、模块化且定义明确的环境。具体而言,已合成了带有连接的[2Fe-2S]簇的氮杂芳香族单体,并将其纳入锥形螺旋折叠体序列中。利用芳香族寡酰胺结构的模块化和可预测性,能够直接设计出一种锥形结构,该结构能够将金属配合物隔离在一个受限环境中。尽管在第一代模型中没有特意设计金属配合物与折叠体之间的直接相互作用,但晶体学、核磁共振和红外光谱都一致表明,芳香族寡酰胺主链改变了金属簇的结构和动态过程。