Jiang Wenjing, Jiao Chengqi, Meng Yinshan, Zhao Liang, Liu Qiang, Liu Tao
State Key Laboratory of Fine Chemicals , Dalian University of Technology , 2 Linggong Rd. , 116024 , Dalian , China . Email:
Chem Sci. 2017 Oct 30;9(3):617-622. doi: 10.1039/c7sc03401f. eCollection 2018 Jan 21.
The preparation of single-chain magnets (SCMs) with photo-switchable bistable states is essential for the development of high-density photo-recording devices. However, the reversible switching of the SCM behavior upon light irradiation is a formidable challenge. Here we report a well-isolated double zigzag chain {[Fe(bpy)(CN)][Co(phpy)]}·2HO (bpy = 2,2'-bipyridine, phpy = 4-phenylpyridine), which exhibits reversible redox reactions with interconversion between FeIIILS(μ-CN)CoIIHS(μ-NC)FeIIILS (LS = low-spin, HS = high-spin) and FeIIILS(μ-CN)CoIIILS(μ-NC)FeIILS linkages under alternating irradiation with 808 and 532 nm lasers. The bidirectional photo-induced metal-to-metal charge transfer results in significant changes of anisotropy and intrachain magnetic interactions, reversibly switching the SCM behavior. The on-switching SCM behavior driven by light irradiation at 808 nm could be reversibly switched off by irradiation at 532 nm. The results provide an additional and independent way to control the bistable states of SCMs by switching in the 0 → 1 → 0 sequence, with potential applications in high density storage and molecular switches.
制备具有光可切换双稳态的单链磁体(SCM)对于高密度光记录设备的发展至关重要。然而,在光照射下SCM行为的可逆切换是一项艰巨的挑战。在此,我们报道了一种高度隔离的双锯齿链{[Fe(bpy)(CN)][Co(phpy)]}·2HO(bpy = 2,2'-联吡啶,phpy = 4-苯基吡啶),它在808和532 nm激光交替照射下表现出可逆的氧化还原反应,FeIIILS(μ-CN)CoIIHS(μ-NC)FeIIILS(LS = 低自旋,HS = 高自旋)和FeIIILS(μ-CN)CoIIILS(μ-NC)FeIILS键之间发生相互转换。双向光诱导的金属到金属电荷转移导致各向异性和链内磁相互作用的显著变化,从而可逆地切换SCM行为。由808 nm光照射驱动的开启状态的SCM行为可以通过532 nm照射可逆地关闭。这些结果提供了一种额外的、独立的方法,通过按0 → 1 → 0顺序切换来控制SCM的双稳态,在高密度存储和分子开关方面具有潜在应用。