Anion-Coordination-Assisted Assembly of Supramolecular Charge-Transfer Complexes Based on Tris(urea) Ligands

被引:5
|
作者
Zhang, Dan [1 ]
Hou, Le-Kai [1 ]
Zhang, Qiang [2 ]
He, Jia-Wei [2 ]
Feng, Hong-Jian [2 ]
Wuerthner, Frank [3 ,4 ]
Yang, Xiao-Juan [1 ]
Wu, Biao [1 ]
机构
[1] Northwest Univ, Minist Educ, Key Lab Synthet & Nat Funct Mol Chem, Coll Chem & Mat Sci, Xian 710127, Peoples R China
[2] Northwest Univ, Sch Phys, Xian 710127, Peoples R China
[3] Univ Wurzburg, Ctr Nanosyst Chem, D-97074 Wurzburg, Germany
[4] Univ Wurzburg, Inst Organ Chem, D-97074 Wurzburg, Germany
基金
中国国家自然科学基金;
关键词
anions; charge transfer; pi interactions; oligo(urea) ligands; sulfate; METAL-ORGANIC FRAMEWORK; ELECTRICAL-CONDUCTIVITY; BUILDING-BLOCKS; DONOR; CHEMISTRY; CRYSTAL; CATION; FLUORESCENCE; VIOLOGEN;
D O I
10.1002/chem.201905021
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Charge-transfer (CT) complexes, formed by noncovalent bonding between electron-rich (donor, D) and electron-deficient (acceptor, A) molecules (or moieties) have attracted considerable attention due to their fascinating structures and potential applications. Herein, we demonstrate that anion coordination is a promising strategy to promote CT complex formation between anion-binding, electron-rich tris(urea) donor ligands (D) and electron-deficient viologen cation acceptors (A), which form co-crystals featuring infinite ..........DADA......or discrete (circular DADA or three-decker DAD) pi-stacking interactions. These CT complexes were studied by X-ray diffraction, UV/Vis spectroscopy, electric conductivity measurements, charge displacement curve (CDC) calculations, and DFT computations.
引用
收藏
页码:1414 / 1421
页数:8
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