Xu Fei, Li Gang-Mei, Wang A-Ni, Han Song-De, Pan Jie, Wang Guo-Ming
College of Chemistry and Chemical Engineering, Qingdao University, Shandong 266071, P. R. China.
Dalton Trans. 2021 Dec 14;50(48):18089-18096. doi: 10.1039/d1dt02899e.
Hybrid photochromic materias (HPMs), especially crystalline HPMs (CHPMs), have been widely investigated due to their feasibility in maintaining the advantages of each constituent and genearating captivating photomodulated functionality. Metal-organic complexes (MOCs), as promising candidates for fabricating CHPMs, have attracted the interest of researchers. The molecular predesign of ligands plays a crucial role in yielding MOC-based CHPMs with tunable photochromic functionality. Hitherto, a great majority of CHPMs are driven by photosensitive ligands. However, the complicated synthesis and high cost of photosensitive ligands obviously prevent the macro-synthesis and future application of these CHPMs. Thus, it is indispensable to explore novel branches of CHPMs. Herein, we report a series of photochromic solid materials bearing modulated photochromic properties by hybridizing metal chlorides with a nonphotosensitive coplanar dipyridine unit 1,10-phenanthroline (phen) and its derivative 5-chloro-1,10-phenanthroline (5-Cl-phen). The resulting hybrids, [ZnCl(phen)] (1), [CdCl(phen)] (2), [PbCl(phen)] (3), [ZnCl(HO)(5-Cl-phen)]Cl·2HO (4), [CdCl(5-Cl-phen)] (5) and [PbCl(5-Cl-phen)] (6), exhibit distinct structures from the isolated molecular complexes (1 and 4) to the hybrid chain (2, 3, 5 and 6) because of the distinct coordination mode of central metal ions and chloride ions. After photo-irradiation with a Xe-lamp, all complexes, as expected, exhibited apparent color change because of the photoinduced electron transfer (ET) between coordinated chloride ions (Cl) as electron donors (EDs) and the coordinated coplanar phen and 5-Cl-phen species as electron acceptors (EAs). More importantly, the photochromic performance of the title complexes could be modulated by phen and 5-Cl-phen. This study provides a general and facile way for modulating the structure and photochromic performance of hybrid metal chlorides with phen or phen-based derivatives under the synergy of crystalline engineering strategy and ET mechanism.
混合光致变色材料(HPMs),尤其是晶体HPMs(CHPMs),因其在保持各组分优势以及产生引人注目的光调制功能方面的可行性而受到广泛研究。金属有机配合物(MOCs)作为制备CHPMs的有前景的候选材料,已引起研究人员的兴趣。配体的分子预设计在产生具有可调光致变色功能的基于MOC的CHPMs中起着关键作用。迄今为止,绝大多数CHPMs由光敏配体驱动。然而,光敏配体复杂的合成过程和高成本显然阻碍了这些CHPMs的大规模合成和未来应用。因此,探索CHPMs的新分支是必不可少的。在此,我们报道了一系列通过将金属氯化物与非光敏共平面二吡啶单元1,10 - 菲咯啉(phen)及其衍生物5 - 氯 - 1,10 - 菲咯啉(5 - Cl - phen)杂交而具有调制光致变色性质的光致变色固体材料。所得的配合物,[ZnCl(phen)](1)、[CdCl(phen)](2)、[PbCl(phen)](3)、[ZnCl(HO)(5 - Cl - phen)]Cl·2HO(4)、[CdCl(5 - Cl - phen)](5)和[PbCl(5 - Cl - phen)](6),由于中心金属离子和氯离子不同的配位模式,呈现出从孤立分子配合物(1和4)到混合链(2、3、5和6)的不同结构。在用氙灯进行光照射后,正如预期的那样,所有配合物由于作为电子供体(EDs)的配位氯离子(Cl)与作为电子受体(EAs)的配位共平面phen和5 - Cl - phen物种之间的光致电子转移(ET)而呈现出明显的颜色变化。更重要的是,标题配合物的光致变色性能可以通过phen和5 - Cl - phen进行调制。本研究提供了一种通用且简便的方法,可在晶体工程策略和ET机制的协同作用下,用phen或基于phen的衍生物调制混合金属氯化物的结构和光致变色性能。