Costil Romain, Crespi Stefano, Pfeifer Lukas, Feringa Ben L
Stratingh Institute for Chemistry, Zernike Institute for Advanced Materials, University of Groningen, Nijenborgh 4, 9747, AG, Groningen, The Netherlands.
Chemistry. 2020 Jun 23;26(35):7783-7787. doi: 10.1002/chem.202002051. Epub 2020 Jun 3.
The preparation, assembly and dynamic properties of photoswitchable bisphosphine ligands based on the stiff-stilbene scaffold are reported. Directional bonding and coordination-induced assembly allow complexation of these ligands with palladium(II), resulting in the formation of discrete metallo-supramolecular entities. While the Z isomer forms a simple bidentate metallo-macrocycle, an intricate double helicate figure-of-eight dimer is observed with the E ligand. Topologically 3D complexes can thus be obtained from 2D ligands. Upon irradiation with UV light, isomerization of the ligands allows control of the architecture of the formed complexes, resulting in a light-triggered modulation of the supramolecular topology. Furthermore, a mechanistic investigation unveiled the dynamic nature of the helicate chirality, where a transmission of motion from the palladium centers yields an "eight-to-eight" inversion.
报道了基于刚性二苯乙烯支架的光开关双膦配体的制备、组装及动态性质。定向键合和配位诱导组装使这些配体与钯(II)络合,从而形成离散的金属超分子实体。Z异构体形成简单的双齿金属大环,而E配体则形成复杂的双螺旋8字形二聚体。因此,可以从二维配体获得拓扑三维配合物。用紫外光照射时,配体的异构化可控制所形成配合物的结构,从而实现超分子拓扑结构的光触发调制。此外,机理研究揭示了螺旋手性的动态本质,其中钯中心的运动传递导致“八到八”反转。