scholarly journals Synthesis, Photoluminescence and Electrical Study of Pyrazolone-Based Azomethine Ligand Zn(II) Complexes

Materials ◽  
2020 ◽  
Vol 13 (24) ◽  
pp. 5698
Author(s):  
Alexey Gusev ◽  
Elena Braga ◽  
Andrey Tyutyunik ◽  
Vladimir Gurchenko ◽  
Maria Berezovskaya ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Solid State ◽  
Electrical Properties ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Sandwich Structure ◽  
High Thermal Stability ◽  
Quantum Yields ◽  
X Ray ◽  
Electrical Study

New luminescent zinc complexes were obtained by reaction of pyrazolone-based azomethine ligands with Zn(CH3COO)2·2H2O. Complexes fully characterized by elemental analysis, FTIR, ES–MS, NMR, and single crystal X-ray analysis. Title complexes in the solid state demonstrate tunable luminescence from blue to orange by varying of substituents on the aromatic ring. Quantum yields are in the 0.03 to 0.49 range. TGA data shows that obtained complexes demonstrate high thermal stability and can be used as electroluminescent materials. The electrical properties of the complexes under study were considered in the ITO-Zncomplex-Al “sandwich” structure.

scholarly journals 1-[N-Methyl-N-(Phenyl)amino]-3- (4-Methylphenyl)Thiourea

Molbank ◽  
10.3390/m1052 ◽  
2019 ◽  
Vol 2019 (1) ◽  
pp. M1052 ◽  
Author(s):  
Chien Yeo ◽  
Edward Tiekink
Keyword(s):  
Hydrogen Bond ◽  
Solid State ◽  
Hydrogen Bonds ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Title Compound ◽  
Molecular Conformation ◽  
Phenyl Hydrazine ◽  
X Ray ◽  
X Ray Crystallography

The title compound, 1-[N-methyl-N-(phenyl)amino]-3-(4-methylphenyl)thiourea (1), was synthesized by the reaction of 1-methyl-1-phenyl hydrazine and 4-tolyl isothiocyanate, and was characterized by spectroscopy (1H and 13C{1H} NMR, IR, and UV), elemental analysis as well as by single crystal X-ray crystallography. In the solid state, the molecule exists as the thioamide tautomer and features an anti-disposition of the thioamide–N–H atoms; an intramolecular N–H⋯N hydrogen bond is noted. The molecular conformation resembles that of the letter L. In the molecular packing, thioamide-N1–H⋯S1(thione) hydrogen bonds lead to centrosymmetric eight-membered {⋯HNCS}2 synthons. The dimers are assembled into a supramolecular layer in the bc-plane by phenyl- and methyl-C–H⋯π(phenyl) interactions.

N–O Bond Cleavage During the Deprotonation of N,O-Bis(trimethylsilyl)hydroxylamine

2008 ◽  
Vol 63 (3) ◽  
pp. 339-341 ◽  
Author(s):  
Ajay Venugopal ◽  
Alexander Willner ◽  
Norbert W. Mitzel
Keyword(s):  
Solid State ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Bond Cleavage ◽  
State Structure ◽  
X Ray Diffraction ◽  
Solid State Structure ◽  
X Ray ◽  
Potassium Hydride ◽  
Oxygen Atoms

The reaction of N,O-bis(trimethylsilyl)hydroxylamine with potassium hydride in pentane affords a product of the formula {K6[OSiMe3]4[ON(SiMe3)2]2}, resulting from deprotonation followed by N-O bond cleavage and 1,2-silylshift. The compound was characterised by elemental analysis and by single crystal X-ray diffraction. The aggregate consists of a K3O3 bis-cubane core, with N(SiMe3)2 groups at the oxygen atoms shared by the two cubes, andMe3Si groups attached to the four O vertices. Two weak K···N interactions are also detected in the solid state structure.

scholarly journals The Role of Percent Volume Buried in the Characterization of Copper(I) Complexes for Lighting Purposes

Molecules ◽  
2020 ◽  
Vol 25 (11) ◽  
pp. 2647 ◽  
Author(s):  
Murat Alkan-Zambada ◽  
Edwin C. Constable ◽  
Catherine E. Housecroft
Keyword(s):  
Solid State ◽  
Single Crystal ◽  
Quantum Yields ◽  
X Ray ◽  
Photophysical Behavior

The usefulness of percent volume buried (%Vbur) as a readily quantifiable property is investigated with regard to [Cu(NN)(PP)]+ complexes of interest for lighting purposes. Photoluminescence quantum yields (PLQYs) and single crystal X-ray structures of 100 reported compounds were assembled, %Vbur of the ligand systems were calculated and analyzed for correlations. We found that increased shielding of the central Cu(I) cation relying on shared contributions of both (NN) and (PP) ligand systems led to increased PLQYs. These findings are of relevance for future characterizations of Cu(I)-based complexes and their photophysical behavior in the solid-state.

Synthesis, characterization, and luminescence modulation of a rare barium-tetracarboxylate framework with I2O1 connectivity

CrystEngComm ◽  
2014 ◽  
Vol 16 (37) ◽  
pp. 8706-8709 ◽  
Author(s):  
Xiao Chen ◽  
Sha He ◽  
Feiyan Chen ◽  
Yunlong Feng
Keyword(s):  
Thermal Stability ◽  
Ion Exchange ◽  
Single Crystal ◽  
Luminescence Intensity ◽  
High Thermal Stability ◽  
Solvothermal Reaction ◽  
Tetracarboxylic Acid ◽  
X Ray ◽  
Organic Framework

Solvothermal reaction of a tetracarboxylic acid with Ba(NO3)2 afforded a barium–organic framework whose single crystal X-ray structure was characterized to have I2O1 connectivity and 1 D channels 15.1 Å in diameter. This MOF has high thermal stability up to 540 °C, and its luminescence intensity can be modulated by ion exchange.

Synthesis, Characterization, and Crystal Structures of Three cis/trans Pyridine - Cyclopalladated Ferrocenylimine Complexes, and Their Catalysis in Suzuki Reactions

2007 ◽  
Vol 60 (3) ◽  
pp. 190 ◽  
Author(s):  
Chen Xu ◽  
Jun-Fang Gong ◽  
Yan-Hui Zhang ◽  
Yu Zhu ◽  
Yang-Jie Wu
Keyword(s):  
Solid State ◽  
Ir Spectra ◽  
Single Crystal ◽  
1H Nmr ◽  
Elemental Analysis ◽  
Phenylboronic Acid ◽  
Suzuki Reaction ◽  
X Ray ◽  
Suzuki Reactions ◽  
Aryl Bromides

Three new pyridine–cyclopalladated ferrocenylimine complexes 2a–c have been easily prepared and characterized by elemental analysis, ESI-MS, 1H NMR, and IR spectra. Their detailed structures are determined by single-crystal X-ray analysis. Palladacycle 2a is found to be a cis complex in the solid state, while 2b and 2c are trans complexes. These complexes were found to be efficient for the Suzuki reaction of aryl bromides with phenylboronic acid. Typically, using 0.2 mol% of 2c in the presence of 1.5 equivalents of K2CO3 as base in toluene at 100°C provided the coupled products in good to excellent yields.

scholarly journals Synthesis, characterization and thermal behaviour of solid state compounds of 4-methoxybenzoate with Manganese, Nickel and Copper

2005 ◽  
Vol 30 (1) ◽  
pp. 15-20 ◽  
Author(s):  
E. C. Rodrigues ◽  
A. C. Vallejo ◽  
E.Y. Ionashiro ◽  
G. Bannach ◽  
M. Ionashiro
Keyword(s):  
Thermal Stability ◽  
Thermal Analysis ◽  
Thermal Decomposition ◽  
Differential Thermal Analysis ◽  
Infrared Spectroscopy ◽  
Solid State ◽  
Thermal Behaviour ◽  
Elemental Analysis ◽  
X Ray

Solid state M-L compounds, where M stands for bivalent Mn, Ni, Cu and L is 4-methoxybenzoate, have been synthesized. Simultaneous thermogravimetry - differential thermal analysis (TG-DTA), X-ray powder diffractometry, infrared spectroscopy, elemental analysis and complexometry were used to characterize and to study the thermal behaviour of these compounds. The results led to information about the composition, dehydration, thermal stability and thermal decomposition of the isolated compounds.

Synthesis, Characterization, Structure and Thermal Decomposition of a Ag(I) Complex Derived from 3-Pyridinesulfonate and 1,4-Bis(2-Methyl-Imidazol-1-Yl)Butane

2014 ◽  
Vol 934 ◽  
pp. 86-90
Author(s):  
Xiao Min Hao ◽  
Gang Chen ◽  
Chang Sheng Gu
Keyword(s):  
Thermal Stability ◽  
Thermal Decomposition ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Luminescent Property ◽  
Title Complex ◽  
Single Crystal Diffraction ◽  
X Ray ◽  
Triclinic System ◽  
Novel Complex

A novel complex of [Ag (bib)(3-pySO3)] n (3-pySO3:3-pyridinesulfonate; bib 1, 4-bis (2-methyl-imidazol-1-yl) butane) was synthesized and characterized by elemental analysis, IR, X-ray single crystal diffraction. The title complex belongs to triclinic system with space group P-1, a=7.8030(16)Å, b=8.0070(16)Å, c=10.742(2)Å,α=84.64(3)°,β=82.33(3)°,γ=82.76(3)°, V=657.8(2)Å3, Z=2, Dc=1.894g/cm3, μ= 1.697mm-1, F(000)= 374. Final indices is R =0.0480, wR =0.1169. Thermal stability and luminescent property of compound have also been investigated.

Synthesis, structure, fluorescence, and electrochemical properties of a binuclear Ag(I) complex with 1,4-bis(benzo[d]oxazol-2-yl)butane as a ligand

2020 ◽  
Vol 75 (4) ◽  
pp. 353-357
Author(s):  
Lixian Xia ◽  
Geng Zhang ◽  
Xinzhao Xia ◽  
Yagang Li ◽  
Jiao Wang ◽  
...  
Keyword(s):  
Solid State ◽  
Ir Spectroscopy ◽  
Oxygen Atom ◽  
Single Crystal ◽  
Electrochemical Properties ◽  
Elemental Analysis ◽  
Cyclic Voltammograms ◽  
X Ray Diffraction ◽  
Coordination Environment ◽  
X Ray

AbstractReaction of 1,4-bis(benzo[d]oxazol-2-yl)butane (BBO) with [Ag(CH3CN)4(ClO4)] afforded a new binuclear silver(I) complex, with composition [Ag2(BBO)2(ClO4)2], characterized by elemental analysis, UV/Vis and IR spectroscopy, and single-crystal X-ray diffraction. The results show that the Ag(I) complex consists of a centrosymmetric dimetallacyclic structure assembled from two Ag(I) atoms and two bridging BBO ligands. The coordination environment of silver(I) complex can be described as distorted trigonal planar, with one oxygen atom from a perchlorate anion and two nitrogen atoms from two BBO ligands. The luminescence properties of the ligand and the Ag(I) complex were studied in the solid state. The emission peaks of the Ag(I) complex are attributed to ligand-centered transitions. There is no effect of the complexation except for a partial quenching. The cyclic voltammograms of the Ag(I) complex indicated an irreversible Ag+/Ag couple.

Synthesis, X-ray characterization and DFT studies of bis-N-imidazolylpyrimidine salts: the prominent role of hydrogen bonding and anion–π interactions

CrystEngComm ◽  
2014 ◽  
Vol 16 (38) ◽  
pp. 9043-9053 ◽  
Author(s):  
Francisca Orvay ◽  
Antonio Bauzá ◽  
Miquel Barceló-Oliver ◽  
Angel García-Raso ◽  
Joan J. Fiol ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Solid State ◽  
Single Crystal ◽  
Elemental Analysis ◽  
Dft Studies ◽  
X Ray Diffraction ◽  
X Ray ◽  
Π Interactions ◽  
New Compounds

Five new compounds have been synthesized and characterized by elemental analysis, IR, NMR and single-crystal X-ray diffraction. They present interesting assemblies in the solid state dominated by H-bonding and anion–π interactions.

Study of the polymerization of high-performance polymers by electrons and x-rays: 1. The case of polypropargylic-butanedioldimethacrylate systems

1995 ◽  
Vol 7 (2) ◽  
pp. 157-180 ◽  
Author(s):  
Marie-Florence Grenier-Loustalot ◽  
Vincent Denizot ◽  
Daniel Beziers
Keyword(s):  
Thermal Stability ◽  
Solid State ◽  
Carbon Fibre ◽  
High Performance ◽  
Thermal Polymerization ◽  
High Thermal Stability ◽  
X Rays ◽  
X Ray ◽  
High Performance Polymers ◽  
Pure Resin

We have investigated the polymerization of polypropargylic butanedioldimeth-acrylate derivatives using electron and x-ray irradiation. The results obtained with the pure resin and carbon-fibre-based composites were compared in terms of kinetics, mechanisms and properties with those obtained by thermal polymerization. Data gathered using a panoply of solid state physicochemical techniques have shown that these polymers are good systems for obtaining composites having high thermal stability at temperatures higher than 350°C.

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