15617-19-3Relevant articles and documents
Giant Concentric Metallosupramolecule with Aggregation-Induced Phosphorescent Emission
Li, Yiming,Huo, Gui-Fei,Liu, Bingqing,Song, Bo,Zhang, Yuan,Qian, Xiaomin,Wang, Heng,Yin, Guang-Qiang,Filosa, Alexander,Sun, Wenfang,Hla, Saw Wai,Yang, Hai-Bo,Li, Xiaopeng
supporting information, p. 14638 - 14648 (2020/09/15)
Fluorescent metallosupramolecules have received considerable attention due to their precisely controlled dimensions as well as the tunable photophysical and photochemical properties. However, phosphorescent analogues are still rare and limited to small structures with low-temperature phosphorescence. Herein, we report the self-assembly and photophysical studies of a giant, discrete metallosupramolecular concentric hexagon functionalized with six alkynylplatinum(II) bzimpy moieties. With a size larger than 10 nm and molecular weight higher than 26000 Da, the assembled terpyridine-based supramolecule displayed phosphorescent emission at room temperature. Moreover, the supramolecule exhibited enhanced aggregation-induced phosphorescent emission compared to the ligand by tuning the aggregation states through intermolecular interactions and significant enhancement of emission to CO2 gas.
Synthesis and properties of new phosphorescent red light-excitable platinum(II) and palladium(II) complexes with schiff bases for oxygen sensing and triplet-triplet annihilation-based upconversion
Borisov, Sergey M.,Saf, Robert,Fischer, Roland,Klimant, Ingo
, p. 1206 - 1216 (2013/04/10)
New Pt(II) and Pd(II) complexes with donor-acceptor Schiff bases are conveniently prepared in only two steps. The complexes efficiently absorb in the red part of the spectrum (ε > 105 M-1 cm -1) and show moderate to strong
Synthesis and characterisation of mixed ligand Pt(ii) and Pt(iv) oxadiazoline complexes
Sarju, Julien,Arbour, Jannine,Sayer, James,Rohrmoser, Benjamin,Scherer, Wolfgang,Wagner, Gabriele
, p. 5302 - 5312 (2009/02/06)
The nitrile ligands in trans-[PtX2(PhCN)2] (X = Cl, Br, I) undergo sequential 1,3 dipolar cycloadditions with nitrones R 1R2C=N+(Me)-O- (R1 = H, R2 = Ph; R1 = CO2Et, R2 = CH 2CO2Et) to selectively form the Δ4-1,2,4- oxadiazoline complexes trans-[PtX2(PhCN) {N=C(Ph)-O-N(Me)-CR 1R2}] or trans-[PtX2{N=C(Ph)-O-N(Me)-CR 1R2}2] in high yields. The reactivity of the mixed ligand complexes trans-[PtX2(PhCN){N=C(Ph)-O-N(Me)-CR 1R2}] towards oxidation and ligand substitution was studied in more detail. Oxidation with Cl2 or Br2 provides the Pt(iv) species trans-[PtX2Y2(PhCN){N=C(Ph)-O-N(Me)- CH(Ph)}] (X, Y = Cl, Br). The mixed halide complex (X = Cl, Y = Br) undergoes halide scrambling in solution to form trans-[PtX(4-n)Y n(PhCN){N=C(Ph)-O-N(Me)-CH(Ph)}] as a statistical mixture. Ligand substitution in trans-[PtCl2(PhCN){N=C(Ph)-O-N(Me)-CR 1R2}] allows for selective replacement of the coordinated nitrile by nitrogen heterocycles such as pyridine, DMAP or 1-benzyl-2- methylimidazole to produce mixed ligand Pt(ii) complexes of the type trans- [PtX2(heterocycle){N=C(Ph)-O-N(Me)-CR1R2}]. All compounds were characterised by elemental analysis, mass spectrometry, IR and 1H, 13C and 195Pt NMR spectroscopy. Single-crystal X-ray structural analysis of (R,S)-trans-[PtBr 2{N=C(Ph)-O-N(Me)-CH(Ph)}2] and trans-[PtCl 2(C5H5N){N=C(Ph)-O-N(Me)-CH(Ph)}] confirms the molecular structure and the trans configuration of the heterocycles relative to each other. The Royal Society of Chemistry.
