Cyclic aminomethylphosphines as ligands. Rational design and unpredicted findings

2017 ◽  
Vol 89 (3) ◽  
pp. 293-309 ◽  
Author(s):  
Andrey A. Karasik ◽  
Elvira I. Musina ◽  
Anna S. Balueva ◽  
Igor D. Strelnik ◽  
Oleg G. Sinyashin

Abstract:Rational design of title ligands and their transition metal complexes gave the high effective catalysts for hydrogen economy and perspective “stimuli-responsive” luminescent materials. Together with the above novel cyclic aminomehtylphospine ligands have showed a row of unpredicted properties like spontaneous formation of macrocyclic molecules, unique reversible slitting of macrocycles on to the smaller cycles, rapid interconversion of the isomers catalyzed by both acids and transitional metals, bridging behavior of usually chelating ligands and unexpected high influence of handling substituents on N-atoms on to the catalytic and luminescent properties of P-complexes.

2020 ◽  
Vol 5 (10) ◽  
pp. 1578-1605
Author(s):  
Baoning Li ◽  
Zhenjie Liang ◽  
Huijie Yan ◽  
Yongguang Li

Organoplatinum(ii) complexes with various π-conjugated ligands exhibit intriguing luminescent properties and they are a promising candidate to construct smart luminescent materials in optical devices, chemical sensors, and bio-imaging.


2020 ◽  
Author(s):  
Xin-Yue Lou ◽  
Nan Song ◽  
Ying-Wei Yang

Abstract Tunable luminescent materials are becoming more and more important owing to their broad application potential in various fields. Here we construct a pillar[5]arene-based hybrid material with stimuli-responsive luminescent properties and ion sensing abilities from a pyridine-modified conjugated pillar[5]arene and a planar chromophore oligo(phenylenevinylene) upon coordination of Cd (II) metal cores. This new material not only shows an optimized luminescence due to the minimized π-π stacking and efficient charge transfer (CT) properties benefitting from the existence of pillar[5]arene rings, but also exhibits tunable multicolor emission induced by different external stimuli including solvent, ions, and acid, indicating great application potential as a fluorescent sensory material especially for Fe3+. With this pillar[5]arene-based dual-ligand hybrid material, valid optimization and regulation on the fluorescence of the original chromophore have been achieved, which demonstrates a plausible strategy for the design of tunable solid-state luminescent materials and also a prototypical model for the effective regulation of fluorescent properties of planar π systems using synthetic macrocycles-based building blocks.


2018 ◽  
Vol 2018 ◽  
pp. 1-7
Author(s):  
Xiangwei Sun ◽  
Feiyue Wu ◽  
Yan Luo ◽  
Mengjun Huang ◽  
Yuntao Li ◽  
...  

Dysprosium (Dy) ternary complex was prepared using 5-sulfosalicylic acid (SSA) as the first ligand and 1,10-phenanthroline (Phen) as the second ligand, denoted as Dy(SSA)3Phen. The complex was blended with tri-cellulose acetate (TCA) via a cosolvent method to obtain polymer luminescent materials. The composition and structure of the rare-earth complex were characterized by means of elemental analysis, infrared (IR) spectra, and thermogravimetric analysis (TGA). The fluorescence spectra displayed this pure Dy(SSA)3Phen complex, and the TCA/Dy(SSA)3Phen composites all emit blue light. The (90/10) composite possesses fine luminescent properties with quantum yield of 33.5% and thermal stability for potential usage as blue fluorescent materials.


2021 ◽  
Author(s):  
Chunguang Zhai ◽  
Xiu Yin ◽  
Shifeng Niu ◽  
Mingguang Yao ◽  
Shuhe Hu ◽  
...  

Abstract Developing a universal strategy to design new piezochromic luminescent materials with desirable properties remains challenging. Here, we report that insertion of a non-emissive molecule into a donor (perylene) and acceptor (TCNB) binary cocrystal can realize fine manipulation of intermolecular interactions between perylene and TCNB for desirable piezochromic luminescent properties. A continuous pressure-induced emission enhancement up to 3 GPa and a blue shift from 655 nm to 619 nm have been observed in perylene-TCNB cocrystals upon THF insertion, in contrast to the red-shifted and quenched emission observed when compressing perylene-TCNB cocrystals and other cocrystals reported earlier. By combining experiment with theory, it is further revealed that the inserted non-emissive THF forms blue-shifted H-bonds with neighboring TCNB molecules and promote a conformation change of perylene molecules upon compression, causing the blue-shifted and enhanced emission. This strategy remains valid when inserting other molecules as non-emissive component into perylene-TCNB cocrystals for abnormal piezochromic luminescent behaviors. Our strategy could also be extended to other cocrystals with different donor-acceptor components, opening a new way for designing novel piezochromic luminescent materials for future applications.


Author(s):  
Kaitao Yu ◽  
Lifang Wei ◽  
Jiaqi Shen

The series of luminescent materials of Eu3 +, Tb3 + doped Li2SrSiO4 were synthesized by a high-temperature solid-state method. The phase purity of the samples was measured by X-ray powder diffraction (XRD). The luminescent properties of the samples were studied by UV-visible excitation spectra and emission spectra The It is found that the strong absorption of Eu3 + doped Li2-xSr1-xEuxSiO4 is from the 250 ~ 290 nm charge transfer band of Eu3 + and the 7F0 → 5L6 absorption transition of 393 nm. The strongest emission of the emission spectra at 393 nm is 614 nm and 701 nm, respectively, from the 5D0 → 7F2 and 5D0 → 7F4 transitions of Eu3 +. Tb3 + doped sample Li2-xSr1-xTb xSiO4 excitation spectrum is mainly composed of Tb3 + ion fd transition and charge transfer band composed of broadband, the strongest absorption at 269 nm, the emission of the main emission of 5D4 → 7F5 transition (542 nm).


2019 ◽  
Vol 91 (21) ◽  
pp. 14029-14035
Author(s):  
Miao Yang ◽  
Chunrong Ma ◽  
Shushu Ding ◽  
Yujie Zhu ◽  
Guoyue Shi ◽  
...  

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