d'Aquino Andrea I, Cheng Ho Fung, Barroso-Flores Joaquín, Kean Zachary S, Mendez-Arroyo Jose, McGuirk C Michael, Mirkin Chad A
Department of Chemistry and International Institute for Nanotechnology , Northwestern University , 2145 Sheridan Road , Evanston , Illinois 60208 , United States.
Centro Conjunto de Investigación en Química Sustentable , UAEM-UNAM , Carretera Toluca-Atlacomulco Km 14.5, Personal de la UNAM, Unidad San Cayetano , Toluca , Estado de México C.P. 50200 , México.
Inorg Chem. 2018 Apr 2;57(7):3568-3578. doi: 10.1021/acs.inorgchem.7b02745. Epub 2018 Jan 5.
Macrocycles capable of host-guest chemistry are an important class of structures that have attracted considerable attention because of their utility in chemical separations, analyte sensing, signal amplification, and drug delivery. The deliberate design and synthesis of such structures are rate-limiting steps in utilizing them for such applications, and coordination-driven supramolecular chemistry has emerged as a promising tool for rapidly making large classes of such systems with attractive molecular recognition capabilities and, in certain cases, catalytic properties. A particularly promising subset of such systems are stimuli-responsive constructs made from hemilabile ligands via the weak-link approach (WLA) to supramolecular coordination chemistry. Such structures can be reversibly toggled between different shapes, sizes, and charges based upon small-molecule and elemental-anion chemical effectors. In doing so, one can deliberately change their recognition properties and both stoichiometric and catalytic chemistries, thereby providing mimics of allosteric enzymes. The vast majority of structures made to date involve two-state systems, with a select few being able to access three different states. Herein, we describe the synthesis of a new allosterically regulated four-state macrocycle assembled via the WLA. The target structure was made via the stepwise assembly of ditopic bidentate hemilabile N-heterocyclic carbene thioether (NHC,S) and phosphino thioether (P,S) ligands at Pt metal nodes. The relatively simple macrocycle displays complex dynamic behavior when addressed with small-molecule effectors, and structural switching can be achieved with several distinct molecular cues. Importantly, each state was fully characterized by multinuclear NMR spectroscopy and, in some cases, single-crystal X-ray diffraction studies and density functional theory computational models. This new structure opens the door to complex multicue switching reminiscent of multistate chemoswitches that could be important in controlling stoichiometric and catalytic transformations as well as generating molecular logic systems.
能够进行主客体化学的大环化合物是一类重要的结构,因其在化学分离、分析物传感、信号放大和药物递送中的应用而备受关注。此类结构的精心设计与合成是将其用于这些应用的限速步骤,而配位驱动的超分子化学已成为一种有前景的工具,可快速制备大量具有吸引人的分子识别能力且在某些情况下具有催化性质的此类体系。此类体系中一个特别有前景的子集是通过超分子配位化学的弱连接方法(WLA)由半不稳定配体构建的刺激响应性结构。基于小分子和元素阴离子化学效应物,此类结构可以在不同形状、大小和电荷之间可逆切换。这样一来,人们可以有意改变它们的识别性质以及化学计量和催化化学性质,从而提供变构酶的模拟物。迄今为止制备的绝大多数结构涉及双态体系,只有少数能够达到三种不同状态。在此,我们描述了一种通过WLA组装的新型变构调节四态大环化合物的合成。目标结构是通过在铂金属节点上逐步组装双齿双位点半不稳定N - 杂环卡宾硫醚(NHC,S)和膦硫醚(P,S)配体而构建的。当用小分子效应物处理时,这种相对简单的大环化合物表现出复杂的动态行为,并且可以通过几种不同的分子线索实现结构切换。重要的是,每种状态都通过多核核磁共振光谱进行了全面表征,在某些情况下还通过单晶X射线衍射研究和密度泛函理论计算模型进行了表征。这种新结构为复杂的多线索切换打开了大门,让人联想到多态化学开关,这在控制化学计量和催化转化以及生成分子逻辑系统方面可能很重要。