Franks Andrew T, Peng Degao, Yang Weitao, Franz Katherine J
Department of Chemistry, and ‡Department of Physics, Duke University , Durham, North Carolina 27708, United States.
Inorg Chem. 2014 Feb 3;53(3):1397-405. doi: 10.1021/ic402221x. Epub 2014 Jan 15.
Photoswitching molecules are utilized for a variety of applications where the rapid manipulation of the molecules' chemical properties and spatial orientations allows for new spatiotemporal control over molecular-scale interactions and processes. Here, we present a hydrazone-containing transition metal chelator, HAPI ((E)-N'-[1-(2-hydroxyphenyl)ethyliden]isonicotinoylhydrazide), that displays dual-wavelength photoswitching behavior. Several of its metal complexes, however, are inert to photoreaction and thereby add another layer of control over the photoswitch system. The light-induced twist in HAPI structure is accompanied by a dramatic change in electronic properties as well as chelator strength. This work introduces HAPI as the prototype for a class of molecules with properties that may be optimized for a variety of experimental applications that take advantage of phototriggered molecular changes.
光开关分子被用于各种应用中,在这些应用中,分子化学性质和空间取向的快速操纵能够实现对分子尺度相互作用和过程的新的时空控制。在此,我们展示了一种含腙的过渡金属螯合剂HAPI((E)-N'-[1-(2-羟苯基)亚乙基]异烟酰肼),它表现出双波长光开关行为。然而,它的几种金属配合物对光反应呈惰性,从而为光开关系统增加了另一层控制。HAPI结构中光诱导的扭曲伴随着电子性质以及螯合强度的显著变化。这项工作将HAPI作为一类分子的原型引入,这类分子的性质可针对利用光触发分子变化的各种实验应用进行优化。