Novel Cyclometalated Iridium(III) Xanthate Complexes and Their Phosphorescence Behavior in the Presence of Metal Ions

2012 ◽  
Vol 67 (9) ◽  
pp. 865-871
Author(s):  
Bihai Tong ◽  
Yaqing Xu ◽  
Jiayan Qiang ◽  
Man Zhang ◽  
Qunbo Mei ◽  
...  
Keyword(s):  
Quantum Yield ◽  
Metal Ions ◽  
Single Crystal ◽  
Photophysical Properties ◽  
Metal Cations ◽  
X Ray Diffraction ◽  
Red Emission ◽  
X Ray ◽  
Emission Lifetime ◽  
Phosphorescence Quantum Yield

Two cyclometalated iridium(III) complexes, Ir(dpppz)(ppz)(ipx) and Ir(ppz)2(ipx) (dpppzH=1- (2,6-dimethylphenoxy)-4-phenylphthalazine, ppzH=4-phenylphthalazinone, ipx=isopropyl xanthate), have been synthesized and characterized by single-crystal X-ray diffraction. The photophysical properties of the two complexes were also investigated. Ir(dpppz)(ppz)(ipx) shows orange-red emission at around 606 nm with a phosphorescence quantum yield of ca. 0.0032 and an emission lifetime of 188 ns, while Ir(ppz)2(ipx) shows orange-red emission at around 599 nm with a phosphorescence quantum yield of ca. 0.00318 and an emission lifetime of 259 ns. The phosphorescence behavior of Ir(ppz)2(ipx) towards different metal cations has also be studied. Its strong phosphorescence is quenched by Hg2+, Cu2+ and Ag+ cations. The interaction ratio with Hg2+ is 1:1

Tuning the Photophysical Properties of Cyclometalated Ir(III) Complexes by a Trifluoroacetyl Group

2012 ◽  
Vol 67 (3) ◽  
pp. 213-218 ◽  
Author(s):  
Bihai Tong ◽  
Jiayan Qiang ◽  
Qunbo Mei ◽  
Hengshan Wang ◽  
Qianfeng Zhang ◽  
...  
Keyword(s):  
Single Crystal ◽  
Electron Acceptor ◽  
Photophysical Properties ◽  
Red Shift ◽  
Luminescence Spectra ◽  
X Ray Diffraction ◽  
X Ray ◽  
Absorption And Luminescence Spectra ◽  
Homo Lumo

Four cationic Ir(III) complexes, [Ir(dpq)2(bpy)]PF6 (1), [Ir(dpq)2(phen)]PF6 (2), [Ir(tfapq)2- (bpy)]PF6 (3), and [Ir(tfapq)2(phen)]PF6 (4) (dpqH = 2,4-diphenylquinoline, tfapqH = 2-(4ʹ-trifluoroacetylphenyl)- 4-phenylquinoline, bpy = 2,2ʹ-bipyridine, phen = 1,10-phenanthroline) have been synthesized and fully characterized. The structure of 4 was also confirmed by single-crystal X-ray diffraction. The electron-acceptor character of the trifluoroacetyl unit leads to a reduced HOMO-LUMO gap and consequently a red-shift of the UV/Vis absorption and luminescence spectra. The solvophobic character of the trifluoroacetyl unit gives rise to a molecule assembly in solution.

A Novel Indole-Containing Diarylethene: Synthesis, Crystal Structure and Photochromism

2017 ◽  
Vol 41 (7) ◽  
pp. 423-426 ◽  
Author(s):  
Chunhong Zheng ◽  
Guanming Liao ◽  
Congbin Fan ◽  
Renjie Wang ◽  
Shouzhi Pu
Keyword(s):  
Crystal Structure ◽  
Quantum Yield ◽  
Single Crystal ◽  
Diffraction Analysis ◽  
Phenyl Group ◽  
X Ray Diffraction ◽  
X Ray ◽  
Meta Position ◽  
Thiophene Moiety ◽  
Photochemical Properties

An indole-containing diarylethene with a trifluoromethyl function at the meta-position of the phenyl group attached to the thiophene moiety was synthesised. Its structure was determined by single-crystal X-ray diffraction analysis and its photochemical properties in solution and in the single crystalline phases were studied. The compound showed relatively high fluorescent modulation efficiency and cyclisation quantum yield.

scholarly journals Synthesis, Crystal Structure, and Luminescence of Cadmium(II) and Silver(I) Coordination Polymers Based on 1,3-Bis(1,2,4-triazol-1-yl)adamantane

Molecules ◽  
2021 ◽  
Vol 26 (17) ◽  
pp. 5400
Author(s):  
Roman D. Marchenko ◽  
Taisiya S. Sukhikh ◽  
Alexey A. Ryadun ◽  
Andrei S. Potapov
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Metal Ions ◽  
Single Crystal ◽  
Diffraction Analysis ◽  
Coordination Polymers ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray

Coordination polymers with a new rigid ligand 1,3-bis(1,2,4-triazol-1-yl)adamantane (L) were prepared by its reaction with cadmium(II) or silver(I) nitrates. Crystal structure of the coordination polymers was determined using single-crystal X-ray diffraction analysis. Silver formed two-dimensional coordination polymer [Ag(L)NO3]n, in which metal ions are linked by 1,3-bis(1,2,4-triazol-1-yl)adamantane ligands, coordinated by nitrogen atoms at positions 2 and 4 of 1,2,4-triazole rings. Layers of the coordination polymer consist of rare 18- and 30-membered {Ag2L2} and {Ag4L4} metallocycles. Cadmium(II) nitrate formed two kinds of one-dimensional coordination polymers depending on the metal-to-ligand ratio used in the synthesis. Coordination polymer [Cd(L)2(NO3)2]n was obtained in case of a 1:2 M:L ratio, while for M:L = 2:1 product {[Cd(L)(NO3)2(CH3OH)]·0.5CH3OH}n was isolated. All coordination polymers demonstrated ligand-centered emission near 450 nm upon excitation at 370 nm.

Cooperative metal–ligand influence on the formation of coordination polymers, and conducting and photophysical properties of Tl(i) β-oxodithioester complexes

2018 ◽  
Vol 47 (45) ◽  
pp. 16264-16278 ◽  
Author(s):  
Chote Lal Yadav ◽  
Gunjan Rajput ◽  
Krishna K. Manar ◽  
Kavita Kumari ◽  
Michael G. B. Drew ◽  
...  
Keyword(s):  
Single Crystal ◽  
Coordination Polymers ◽  
Photophysical Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Polymeric Structures ◽  
Metal Ligand

Eight novel luminescent and semiconducting Tl(i) β-oxodithioester complexes forming 1D/2D coordination polymeric structures were investigated using single crystal X-ray diffraction.

Photoluminescent Characteristics of ZnS Quantum Dots Synthesized in Non-Aqueous-Phase

2013 ◽  
Vol 750-752 ◽  
pp. 991-994
Author(s):  
Jing Liu ◽  
Ming Ying ◽  
Yu Ling Tan ◽  
Bo Xi
Keyword(s):  
Aqueous Solution ◽  
Quantum Dots ◽  
Quantum Yield ◽  
Reaction Medium ◽  
Emission Spectra ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Zinc Blend ◽  
Red Emission ◽  
X Ray

ZnS quantum dots (ZnS QDs) synthesized in aqueous solution is easy to gather a mass, which always results in low quantum yield. So, in this study benzene was used as reaction medium in which ZnS QDs with different hues were synthesized, and the hues of ZnS QDs were depend on the molar ratio of Zn (CH3COO)2 and Na2S·9H2O. The results show the emission spectra of ZnS QDs shifts with the change of the precursor molar ratio but the absorption peak at 310nm is not. The emission peaks centered at 430nm and 580nm at higher molar ratio [Zn2+]/[S2-] with blue-violet emitting phosphors; but, ZnS QDs synthesized at higher molar ratio [S2-]/[Zn2+] have orange-red emission at 580nm only. The X-ray diffraction analysis shows the crystallinity of ZnS QDs is better at [Zn2+]/[S2-]=1:10, which are typical zinc blend with nanorod structure.

scholarly journals The synthesis of a Cu(ii) Schiff base complex using a bidentate N2O2 donor ligand: crystal structure, photophysical properties, and antibacterial activities

RSC Advances ◽  
2019 ◽  
Vol 9 (71) ◽  
pp. 41737-41744 ◽  
Author(s):  
Yaning Guo ◽  
Xiaobing Hu ◽  
Xinli Zhang ◽  
Xiaohua Pu ◽  
Yue Wang
Keyword(s):  
Crystal Structure ◽  
Schiff Base ◽  
Single Crystal ◽  
Schiff Base Ligand ◽  
Photophysical Properties ◽  
Schiff Base Complex ◽  
Antibacterial Activities ◽  
X Ray Diffraction ◽  
Donor Ligand ◽  
X Ray

Reaction of a symmetric compartmental Schiff base ligand (HL) with copper(ii) salt in 2 : 1 M ratio in methanol gave rise to a mononuclear copper(ii) complex, which was characterized by single crystal X-ray diffraction studies.

scholarly journals A synchrotron study of [5,10,15,20-tetrakis(3-cyanophenyl)porphyrinato-κ4N5,N10,N15,N20]copper(II) nitrobenzene trisolvate at 80 K

2016 ◽  
Vol 72 (11) ◽  
pp. 861-866
Author(s):  
Rüdiger W. Seidel ◽  
Richard Goddard ◽  
Thomas Mayer-Gall ◽  
Iris M. Oppel
Keyword(s):  
Single Crystal ◽  
Guest Molecule ◽  
Cyano Group ◽  
Photophysical Properties ◽  
Ring System ◽  
X Ray Diffraction ◽  
X Ray ◽  
Face To Face ◽  
Square Planar ◽  
Derivatives Of

Porphyrin assemblies display interesting photophysical properties and a relatively high thermal stability. Moreover,meso-functionalized porphyrins with virtually fourfold symmetry can be relatively readily synthesized from pyrrole and the appropriate aldehyde. A number of metallo derivatives of 5,10,15,20-tetrakis(4-cyanophenyl)porphyrin, where the N atom of the linear cyano group can act both as a donor for coordination bonds or as an acceptor for hydrogen bonds, have been structurally characterized by single-crystal X-ray analysis. The supramolecular and structural chemistry of the corresponding 2- and 3-cyanophenyl isomers of the parent porphyrin, however, has remained largely unexplored. The crystal structure of [5,10,15,20-tetrakis(3-cyanophenyl)porphyrinato]copper(II) (CuTCNPP) nitrobenzene trisolvate, [Cu(C48H24N8)]·3C6H5NO2, has been determined at 80 K by synchrotron single-crystal X-ray diffraction. CuTCNPP exhibits aC2h-symmetric ααββ conformation, despite an unsymmetrical crystal environment, and is situated on a crystallographic centre of symmetry. The CuIIion adopts a genuine square-planar coordination by the four pyrrole N atoms. The 24-membered porphyrin ring system shows no marked deviation from planarity. In the crystal, the CuTCNPP molecules and two nitrobenzene molecules are face-to-face stacked in an alternating fashion, resulting in corrugated layers. The remaining nitrobenzene guest molecule per CuTCNPP resides in the region between four neighbouring columnar stacks of CuTCNPP and sandwiched nitrobenzene molecules, and is disordered over four positions about a centre of symmetry.

scholarly journals Direct borylation of terrylene and quaterrylene

2020 ◽  
Vol 16 ◽  
pp. 621-627
Author(s):  
Haruka Kano ◽  
Keiji Uehara ◽  
Kyohei Matsuo ◽  
Hironobu Hayashi ◽  
Hiroko Yamada ◽  
...  
Keyword(s):  
Single Crystal ◽  
Diffraction Analysis ◽  
Organic Solvents ◽  
Column Chromatography ◽  
Theoretical Calculations ◽  
Photophysical Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Homo And Lumo ◽  
Post Modification

The preparation of large rylenes often needs the use of solubilizing groups along the rylene backbone, and all the substituents of the terrylenes and quaterrylenes were introduced before creating the rylene skeleton. In this work, we successfully synthesized 2,5,10,13-tetrakis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)terrylene (TB4) by using an iridium-catalyzed direct borylation of C–H bonds in terrylene in 56% yield. The product is soluble in common organic solvents and could be purified without column chromatography. Single crystal X-ray diffraction analysis revealed that the terrylene core is not disturbed by the substituents and is perfectly flat. The photophysical properties of TB4 are also unchanged by the substituents because the carbon atoms at 2,5,10,13-positions have less coefficients on its HOMO and LUMO, estimated by theoretical calculations. Finally, the same borylation reaction was applied for quaterrylene, resulting in the formation of soluble tetra-borylated quaterrylene despite a low yield. The post modification of rylenes enables us to prepare their borylated products as versatile units after creating the rylene skeletons.

scholarly journals New Bis-Pyrazole-Bis-Acetate Based Coordination Complexes: Influence of Counter-Anions and Metal Ions on the Supramolecular Structures

2020 ◽  
Vol 13 (1) ◽  
pp. 288
Author(s):  
Afaf Oulmidi ◽  
Smaail Radi ◽  
Haralampos N. Miras ◽  
Nayarassery N. Adarsh ◽  
Yann Garcia
Keyword(s):  
Metal Ions ◽  
Single Crystal ◽  
Network Structure ◽  
Coordination Complexes ◽  
Supramolecular Structures ◽  
Supramolecular Interactions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sheet Structure ◽  
Hydrogen Bonded

A new flexible bis-pyrazol-bis-acetate ligand, diethyl 2,2’-(pyridine-2,6-diylbis (5-methyl-1H-pyrazole-3,1-diyl))diacetate (L), has been synthesised, and three coordination complexes, namely, [Zn(L)2](BF4)2 (1), [MnLCl2] (2) and [CdLCl2] (3) have been obtained. All ligands and complexes were characterised by IR, mass spectroscopy, thermogravimetric analysis and single-crystal X-ray diffraction. Single crystal X-ray diffraction experiment revealed that the primary supramolecular building block of 1 is a hexagonal chair shaped 0D hydrogen bonded synthon (stabilised by C–H∙∙∙O hydrogen bonding and C=O∙∙∙π interactions), which further built into a 2D corrugated sheet-like architecture having a 3-c net honeycomb topology, and finally extended to a 3D hydrogen bonded network structure having a five nodal 1,3,3,3,7-c net, through C–H∙∙∙F interactions. On the other hand, the two crystallographically independent molecules of 2 exhibited two distinct supramolecular structures such as 2D hydrogen bonded sheet structure and 1D zigzag hydrogen bonded chain, sustained by C–H∙O and C–H∙∙∙Cl interactions, which are further self-assembled into a 3,4-c network structure, and 3 showed a 2D hydrogen bonded sheet structure. The supramolecular structural diversity in these complexes is due to the different conformations adopted by the ligands, which are mainly induced by different metal ions with coordination environments controlled by different anions. Hirshfeld surface analysis was explored for the qualitative and quantitative analysis of the supramolecular interactions.

Electron Microscopy of Shock Loaded Polycrystalline Beryllium

1974 ◽  
Vol 32 ◽  
pp. 506-507 ◽  
Author(s):  
J. M. Galbraith ◽  
L. E. Murr ◽  
A. L. Stevens
Keyword(s):  
Electron Microscopy ◽  
Wave Propagation ◽  
Structural Change ◽  
Single Crystal ◽  
Diffraction Pattern ◽  
Shock Loading ◽  
Slip Systems ◽  
Compression Tests ◽  
X Ray Diffraction ◽  
X Ray

Uniaxial compression tests and hydrostatic tests at pressures up to 27 kbars have been performed to determine operating slip systems in single crystal and polycrystal1ine beryllium. A recent study has been made of wave propagation in single crystal beryllium by shock loading to selectively activate various slip systems, and this has been followed by a study of wave propagation and spallation in textured, polycrystal1ine beryllium. An alteration in the X-ray diffraction pattern has been noted after shock loading, but this alteration has not yet been correlated with any structural change occurring during shock loading of polycrystal1ine beryllium.This study is being conducted in an effort to characterize the effects of shock loading on textured, polycrystal1ine beryllium. Samples were fabricated from a billet of Kawecki-Berylco hot pressed HP-10 beryllium.

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