Photoinduced E to Z isomerization of tetraphenylethylene derivatives within organometallic supramolecular assemblies

被引:15
|
作者
Liu, Xiao-Xu [1 ]
Li, Yang [1 ]
Li, Xin [1 ]
Hahn, F. Ekkehardt [1 ,2 ]
Han, Ying-Feng [1 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Xian 710127, Peoples R China
[2] Westfalische Wilhelms Univ Munster, Inst Anorganicshe & Anal Chem, Corrensstr 30, D-48149 Munster, Germany
关键词
N-heterocyclic carbene; tetraphenylethylene; photochemical isomerization; fluorescence; EZI process; AGGREGATION-INDUCED EMISSION; E/Z ISOMERS; CONJUGATED POLY(TETRAPHENYLETHENE); PURE STEREOISOMERS; FLUORESCENCE; MODULATION; BEHAVIOR; LIGANDS; BOND;
D O I
10.1007/s11426-021-1041-8
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Isolation of E-1,2-bis(4-bromophenyl)-1,2-diphenyl-ethylene from the E/Z isomer mixture obtained by a McMurry coupling reaction and reaction of this isomer with imidazole followed by N-alkylation with nBuBr and anion exchange yielded the bisimidazolium tetraphenylethylene (TPE) derivative H-2-E-1(PF6)(2). The reaction of H-2-E-1(PF6)(2) with Ag2O yielded the di-nuclear metallarectangle [Ag-2(E-1)(2)](PF6)(2) where the two bis-NHC donors E-1 bridge two silver atoms. Irradiation of [Ag-2(E-1)(2)](PF6)(2) leads to E/Z isomerization of the di-NHC ligand and formation of Z-1 in the mononuclear complex [Ag(Z-1)]PF6. Demetallation of the di-NHC ligand with NH4Cl/NH4PF6 yielded bisimidazolium salt H-2-Z-1(PF6)(2). The unique isomerization of the E-TPE derivative into its Z-isomer via metal complex formation/irradiation/demetallation cannot be achieved by irradiation of the individual imidazolium salt. The emissive properties of the TPE complexes [Ag-2(E-1)(2)](PF6)(2) and [Ag(Z-1)]PF6 have been investigated.
引用
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页码:1709 / 1715
页数:7
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