Two mononuclear zinc(II) complexes constructed by two types of phenoxyacetic acid ligands: syntheses, crystal structures and fluorescence properties

2019 ◽  
Vol 74 (11-12) ◽  
pp. 839-845 ◽  
Author(s):  
Jun-Xia Li ◽  
Zhong-Xiang Du ◽  
Juan Wang ◽  
Xun Feng
Keyword(s):  
Halogen Bond ◽  
Three Dimensional ◽  
Luminescent Properties ◽  
Phenoxyacetic Acid ◽  
Photoluminescence Spectra ◽  
X Ray Diffraction ◽  
X Ray ◽  
Mononuclear Complexes ◽  
3D Networks ◽  
Oxygen Atoms

AbstractTwo new mononuclear complexes, [Zn(3-Hcpa)2(H2O)4] (1) and [Zn(3,5,6-tcpa)2(H2O)4] [Zn(3,5,6-tcpa)2(H2O)2] (2) (3-H2cpa = 3-carboxy-phenoxyacetic acid, 3,5,6-Htcpa = 3,5,6-trichloro pyridine-2-oxyacetic acid), were synthesized and structurally characterized. The single-crystal X-ray diffraction analysis showed that in 1 the ZnII ion lies on an inversion center of an octahedron formed by four aqua ligands and two carboxy oxygen atoms of two unidentate 3-Hcpa− anions in trans-arrangement. Complex 2 is a co-crystal consisting of two discrete and stereochemically different complexes: one with an octahedrally, and the other a tetrahedrally coordinated zinc center. The six-coordination about the first ZnII ion comprises four oxygen atoms from water (H2O) molecules and two from the carboxy groups of monodentate trans-related 3,5,6-tcpa− ligands. The four-coordination about the second ZnII ion is comprised of two H2O ligands and two unidentate carboxy oxygen atoms from 3,5,6-tcpa− ligands. O–HLO hydrogen bond and/or ClLCl halogen bond interactions play an important part in construction of the three-dimensional (3D) networks for 1 and 2. The photoluminescence spectra reveal that both 1 and 2 display luminescent properties in the violet region.

Luminescent Properties of Zn2SiO4:Eu3+,Dy3+ Phosphors via Sol-Gel Process

2012 ◽  
Vol 217-219 ◽  
pp. 733-736
Author(s):  
Xiu Mei Han ◽  
Shu Ai Hao ◽  
Ying Ling Wang ◽  
Gui Fang Sun ◽  
Xi Wei Qi
Keyword(s):  
Thermal Analysis ◽  
Ir Spectra ◽  
Sol Gel ◽  
Luminescent Properties ◽  
Photoluminescence Spectra ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sol Gel Process ◽  
Ft Ir

Zn2SiO4:Eu3+, Dy3+ phosphors have been prepared through the sol-gel process. X-ray diffraction (XRD), thermogravimetric and ddifferential thermal analysis (TG-DTA), FT-IR spectra and photoluminescence spectra were used to characterize the resulting phosphors. The results of XRD indicated that the phosphors crystallized completely at 1000oC. In Zn2SiO4:Eu3+,Dy3+ phosphors, the Eu3+ and Dy3+ show their characteristic red(613nm, 5D0-7F2), blue (481nm, 4F9/2–6H15/2) and yellow (577nm, 4F9/2–6H13/2) emissions.

scholarly journals Synthesis, Crystal Structure, and Properties of a New Coordination Polymer Built from N/O-Donor Mixed Ligands

Crystals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 372
Author(s):  
Mei-An Zhu ◽  
Shuai-Shuai Han ◽  
Feng Deng ◽  
Jia-Le Li ◽  
Shui-Sheng Chen
Keyword(s):  
Coordination Polymer ◽  
Weak Interactions ◽  
Three Dimensional ◽  
Luminescent Properties ◽  
Tridentate Ligand ◽  
Supramolecular Polymer ◽  
X Ray Diffraction ◽  
X Ray ◽  
Mixed Ligands ◽  
Benzenedicarboxylic Acid

The coordination polymer, namely, [Cd(H2L)(nobda)]n (1) was prepared by the reaction of Cd(NO3)2·4H2O with 4-amino-1,2-benzenedicarboxylic acid (H2nobda) and 1,4-di(1H-imidazol-4-yl)benzene (H2L), and characterized by single-crystal X-ray diffraction, elemental analysis, infrared (IR) spectroscopy, thermogravimetric analysis, and powder X-ray diffraction (PXRD). The carboxylic acid of H2nobda ligands was completely deprotonated to be nobda2− anions, which act as tridentate ligand to connect the Cd2+ to form two-dimensional (2D) network, while the neutral H2L ligands serve as a linear didentate bridge to connect two adjacent Cd2+ ions upper and down the 2D layer. The adjacent 2D layers were further linked into the three-dimensional (3D) supramolecular polymer by the weak interactions such as hydrogen bonds and π−π stacking interactions. The ultraviolet-visible (UV-vis) absorption spectra and luminescent properties in the solid state at room temperature have been investigated.

Crystal and Molecular Structure of 3-Iodo-2-propynyl-N-butylcarbamate

1997 ◽  
Vol 52 (2) ◽  
pp. 256-258 ◽  
Author(s):  
Evgeni V. Avtomonov ◽  
Rainer Grüning ◽  
Jörg Lorberth
Keyword(s):  
Molecular Structure ◽  
Crystal Structure ◽  
Title Compound ◽  
Crystal And Molecular Structure ◽  
Three Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dimensional Network ◽  
Carbamate Group ◽  
Oxygen Atoms

Abstract The crystal structure of the title compound has been determined by X-ray diffraction methods. Due to the Lewis acidic character of the iodine substituent a “zig-zag” chain is formed via intermolecular interactions (2.933(4) A) between iodine and oxygen atoms of theocarbamate moiety. A three-dimensional network is formed through hydrogen-bridging (2.04 A) between NH-groups and the oxygen atoms of the neighbouring carbamate group of the next molecule.

Metal Ion-Driven Assembly of Two New Coordination Polymers Constructed by Asymmetric Tricarboxylate and Imidazole-Containing Ligands: Syntheses, Crystal Structures, and Luminescent Properties

2015 ◽  
Vol 68 (1) ◽  
pp. 121 ◽  
Author(s):  
Wenlong Liu ◽  
Xueying Wang ◽  
Mengqiang Wu ◽  
Bing Wang
Keyword(s):  
Infrared Spectroscopy ◽  
Coordination Polymers ◽  
Metal Ion ◽  
Three Dimensional ◽  
Luminescent Properties ◽  
Dimensional Structure ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
X Ray ◽  
Dimethyl Benzene

Two new coordination polymers, namely, {[Cd3(bpt)2(bimb)2]·2(H2O)}n (1) and [Zn3(bpt)2(bimb)2]n (2) (bpt = biphenyl-3,4′,5-tricarboxylate, bimb = 1,4-bis(1-imidazol-yl)-2,5-dimethyl benzene), have been obtained under hydrothermal conditions. Their structures have been determined by single-crystal X-ray diffraction analysis and further characterised by elemental analysis and infrared spectroscopy. Complex 1 exhibits a trinodal (4,4,4)-connected topology with Schläfli symbol of (4.62.83)4.(64.82). Complex 2 is also a three-dimensional structure and displays a (3,4,6)-connected topology with Schläfli symbol of (4.62)2.(42.66.85.102).(64.82). It is shown that the asymmetrically tricarboxylate can bear diverse structures regulated by metal ions. The photoluminescence behaviours of compounds 1 and 2 were also discussed.

Structural investigation of one- and three-dimensional lanthanide(III) coordination polymers based on functionalized terpyridine carboxylate and aromatic dicarboxylate ligands

2019 ◽  
Vol 75 (4) ◽  
pp. 422-432 ◽  
Author(s):  
Chao Bai ◽  
Bin Liu ◽  
Huai-Ming Hu ◽  
Jin-Dian Li ◽  
Xiaofang Wang ◽  
...  
Keyword(s):  
Coordination Polymers ◽  
Structural Investigation ◽  
Three Dimensional ◽  
Topological Type ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
One Dimensional ◽  
X Ray ◽  
Lanthanide Coordination Polymers ◽  
3D Networks

Three series of lanthanide coordination polymers, namely catena-poly[[lanthanide(III)-μ2-(benzene-1,2-dicarboxylato)-μ2-[2-(2,2′:6′,2′′-terpyridin-4′-yl)benzoato]] monohydrate], {[Ln(C8H4O4)(C22H14N3O2)]·H2O} n or {[Ln(1,2-bdc)(L)]·H2O} n , with lanthanide (Ln) = dysprosium (Dy, 1), holmium (Ho, 2) and erbium (Er, 3), poly[bis(μ2-benzene-1,3-dicarboxylato)bis[μ2-2-(2,2′:6′,2′′-terpyridin-4′-yl)benzoato]dilanthanide(III)], [Ln2(C8H4O4)2(C22H14N3O2)2] n or [Ln2(1,3-bdc)2(L)2] n , with Ln = gadolinium (Gd, 4), Ho (5) and Er (6), and poly[(μ2-benzene-1,4-dicarboxylato)[μ2-2-(2,2′:6′,2′′-terpyridin-4′-yl)benzoato]lanthanide(III)], [Ln(C8H4O4)(C22H14N3O2)] n or [Ln(1,4-bdc)(L)] n , with Ln = Dy (7), Ho (8), Er (9) and ytterbium (Yb, 10), were synthesized under hydrothermal conditions and characterized by elemental analysis, IR and single-crystal X-ray diffraction. Compounds 1–3 possess one-dimensional loop chains with Ln2(COO)2 units, which are extended into three-dimensional (3D) supramolecular structures by π–π interactions. Isostructural compounds 5 and 6 show 6-connected 3D networks, with pcu topology consisting of Ln2(COO)2 units. Compounds 7–10 display 8-connected 3D frameworks with the topological type rob, consisting of Ln2(COO)2 units. The influence of the coordination orientations of the aromatic dicarboxylate groups on the crystal structures is discussed.

Synthesis and Luminescent Properties of M2P2O7:Eu3+ (M = Ca, Sr, Ba ) Phosphors

2011 ◽  
Vol 399-401 ◽  
pp. 978-981
Author(s):  
Fu Wang Mo ◽  
Rong Fang Wang ◽  
Yu Wei Lan ◽  
Li Ya Zhou ◽  
Tao He ◽  
...  
Keyword(s):  
Luminescent Properties ◽  
Solid State Reaction Method ◽  
Photoluminescence Spectra ◽  
X Ray Diffraction ◽  
Microscopy Observation ◽  
Excitation Peak ◽  
Strong Emission ◽  
X Ray ◽  
Red Phosphors ◽  
Strong Excitation

A series of orange-red phosphors M2P2O7: Eu3+ (M = Ca, Sr, Ba ) were prepared by traditional solid-state reaction method. X-ray diffraction analysis confirmed the formation of Ca2P2O7, Sr2P2O7 and Ba2P2O7. Scanning electron-microscopy observation indicated a narrow size-distribution of about 0.6~1 μm for the particles with a quadrate shape. Photoluminescence spectra of M2P2O7(M = Ca, Sr, Ba ): Eu3+ phosphors showed a strong excitation peak around 393 nm, and Ca2P2O7: Eu3+, Sr2P2O7: Eu3+ and Ba2P2O7: Eu3+ phosphors showed strong emission bands peaking at about 593 nm, which suggests that the Eu3+ ion is occupy the site with center of symmetry.

Microcavity Effects in The Luminescence of GaAs Microcrystals

1992 ◽  
Vol 283 ◽  
Author(s):  
S. Juen ◽  
K. F. Lamprecht ◽  
R. Rodrigues ◽  
R. A. Höpfel
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Electron Diffraction ◽  
Three Dimensional ◽  
Photoluminescence Spectra ◽  
X Ray Diffraction ◽  
Bulk Gaas ◽  
X Ray ◽  
Transmission Electron ◽  
Spectral Enhancement

ABSTRACTExperimental photoluminescence spectra of GaAs microcrystals show pronounced variations compared to the luminescence of bulk GaAs. The observed spectra are explained by spectral enhancement and inhibition of spontaneous emission in a three-dimensional optical resonator formed by a dielectrically confined semiconductor microcrystal. The crystals were produced by pulverization of bulk GaAs, size-separated by sedimentation techniques, and characterized by transmission electron microscopy, electron diffraction and x-ray diffraction.

The crystal structures of sjögrenite and pyroaurite

1967 ◽  
Vol 36 (280) ◽  
pp. 465-479 ◽  
Author(s):  
L. Ingram ◽  
H. F. W. Taylor
Keyword(s):  
Crystal Structures ◽  
Three Dimensional ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Approximate Composition ◽  
Oxygen Atoms

SummaryThe crystal structures of sjögrenite and pyroaurite, two stacking modifications of approximate composition Mg6Fe2(OH)16(CO3).4H2O, have been determined by X-ray diffraction using three-dimensional methods. Sjögrenite is hexagonal, with a 3·13, c 15·66 Å, space group P63/mmc , Z = ¼; pyroaurite is rhombohedral, with aH 3·13, cH 23·49 Å, space group R3̄m or R3m, Z = ⅜. Both structures are based on brucite-like layers, with magnesium and iron distributed among the octahedral positions. The cations appear to be largely disordered, although ordered regions may occur in some crystals. Between the brucite-like layers are the water molecules and carbonate groups. These are statistically arranged, with their oxygen atoms distributed among a larger number of possible sites.

Distortions in tetrahedral copper(I)–phosphine complexes: bis(triphenylphosphine)copper(I) nitrate

1969 ◽  
Vol 47 (8) ◽  
pp. 1440-1441 ◽  
Author(s):  
G. G. Messmer ◽  
Gus J. Palenik
Keyword(s):  
Crystal Structure ◽  
Diffraction Study ◽  
Three Dimensional ◽  
Nitrate Group ◽  
X Ray Diffraction ◽  
X Ray ◽  
Phosphine Complexes ◽  
Ideal Tetrahedron ◽  
Oxygen Atoms

The crystal structure of bis(triphenylphosphine)copper(I) nitrate has been determined by a three-dimensional X-ray diffraction study. The copper(I) atom is bonded to the two phosphines and two oxygen atoms of the nitrate group. However, the molecule is distorted from that of an ideal tetrahedron, with the P—Cu—P angle being 131.1°.

ONE-POT SYNTHESIS OF INTERESTING 3D γ-MnOOH NETWORKS

NANO ◽  
2014 ◽  
Vol 09 (07) ◽  
pp. 1450084 ◽  
Author(s):  
HAIQIU LIU ◽  
YUJIAN JIN ◽  
NA LI ◽  
LILI WANG ◽  
SUNQI LOU ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Solvothermal Method ◽  
Three Dimensional ◽  
Oriented Attachment ◽  
X Ray Diffraction ◽  
One Pot ◽  
X Ray ◽  
Transmission Electron ◽  
3D Networks ◽  
Scanning Electron

Three-dimensional (3D) γ- MnOOH networks are successfully prepared by one-pot solvothermal method without using any catalyst. The samples are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM). It is found that the amounts of urea and H 2 O 2 added, reaction temperature and time have important influences on the samples. It is interesting that the 3D networks are formed from the oriented attachment (OA) of Mn 3 O 4 octahedrons; and that the phase transformation from Mn 3 O 4 to γ- MnOOH occurs via the protonation of Mn 3 O 4. This study is expected to offer a facile approach to the syntheses of new, intricate nanostructures.

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