Synthesis and Properties of Novel Asymmetrical Porphyrin with [p-(4-Flourobenzoyloxy)-M-Ethyloxy]phenyl and its Lanthanide Complexes

2011 ◽  
Vol 308-310 ◽  
pp. 643-646
Author(s):  
Xiao Ling Cui ◽  
Xin Ming Shi ◽  
Shi You Li
Keyword(s):  
Lanthanide Complexes ◽  
Room Temperature ◽  
Molar Conductance ◽  
Bidentate Ligand ◽  
Quantum Yields ◽  
Luminescence Spectra ◽  
Tetradentate Ligand ◽  
Rare Earth Ion ◽  
Elemental Analyses ◽  
Band Fluorescence

A series of lanthanide complexes with acetylacetonate and a new asymmetrical 5-[p-(4-fluorobenzoyloxy)-m-ethyloxy]phenyl-10,15,20-triphenylporphyrin were prepared and characterized by elemental analyses, molar conductance, UV-Vis, IR, 1H NMR, luminescence spectra and themal analysis. Quantum yields of Q band fluorescence are in the region 0.073-0.097 at room temperature. Complexes have higher stability (decompose until 211°C). The structure that both the porphyrin behaved as a tetradentate ligand and acetylacetonate as a bidentate ligand are coordinated to a rare earth ion also has been proposed.

Enhanced Luminescence of Terbium Complexes with 2,3-Pyrazinedicarboxylate by Y(III) Doping

2013 ◽  
Vol 750-752 ◽  
pp. 1007-1010
Author(s):  
Ai Ling Wang ◽  
Hai Xia Zhang ◽  
Kai Kong ◽  
Huan Huan Li ◽  
Hua Wang ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Lanthanide Complexes ◽  
The Self ◽  
Lanthanide Ions ◽  
Quantum Yields ◽  
Luminescence Spectra ◽  
Intramolecular Energy Transfer ◽  
Enhanced Luminescence ◽  
Yttrium Complexes ◽  
Terbium Complexes

Ten kinds of terbium doped inert yttrium complexes with 2,3-pyrazinedicarboxylate (2,3-pzdc2-) have been synthesized. Characterization results indicate that the complexes have the compositions of Tb (pzdc)1.55H2O and TbxYy(pzdc)1.55H2O (x:y=0.10:0.90; 0.20:0.80; 0.30:0.70; 0.40:0.60; 0.60:0.40; 0.70:0.30; 0.80:0.20; 0.90:0.10). IR spectra show that the lanthanide ions coordinate with the carboxylic oxygen atoms and nitrogen atoms of the ligands. Luminescence spectra show that the Y(III) ions can remarkably increase the luminescent intensities of terbium complexes. And Tb0.7Y0.3(pzdc)1.55H2O exhibits the strongest luminescent emission. Furthermore, the doped lanthanide complexes show longer luminescence lifetimes and higher quantum yields. The enhanced luminescence efficiencies of Tb3+ions in the doped complexes may result from intramolecular energy transfer as well as the decrease of the self-quench of the Tb3+ions induced by the doped Y(III) ions.

Synthesis, spectroscopy, surface photovoltage, and electrochemical properties of porphyrin compound liquid crystals

2005 ◽  
Vol 09 (04) ◽  
pp. 231-239 ◽  
Author(s):  
Miao Yu ◽  
Guo F. Liu ◽  
Xiao L. Cui
Keyword(s):  
Liquid Crystalline ◽  
Molar Conductance ◽  
Quantum Yields ◽  
Surface Photovoltage ◽  
Luminescence Spectra ◽  
Redox Potentials ◽  
Visible Absorption ◽  
Surface Photovoltage Spectroscopy ◽  
Uv Visible ◽  
Hexagonal Columnar

Two series of porphyrin liquid crystalline compounds, meso-tetra-[(p-alkacyloxy-m-ethyloxy)phenyl]porphyrin ( TPAMEP ), and [5-(p-alkacyloxy) phenyl-10,15,20-tri-phenyl] porphyrin ( APTPP ) are synthesized and display a hexagonal columnar discotic columnar ( Col h ) phase. Their structure and properties were studied by elemental analysis, molar conductance, UV-visible and infrared spectra. Luminescence spectra of the compounds were discussed. Quantum yields of the Q band are in the region 0.007935-0.05847. The electrochemical studies show that the redox potentials do not change with the variation of the chain length. The surface photovoltage (SPV) response of the compounds was investigated by means of surface photovoltage spectroscopy (SPS) and field-induced surface photovoltage spectroscopy (FISPS), and the bands are analogous with the UV-visible absorption spectra.

scholarly journals Synthesis, Characterization and Antibacterial Activity Study of Cobalt(II), Nickel(II), Copper(II), Palladium(II), Cadmium(II) and Platinum(IV) Complexes with 4-Amino-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazole-3-thione

2021 ◽  
Vol 21 (6) ◽  
pp. 1514
Author(s):  
Waleed Abbas Jawad ◽  
Asim Alaa Abd Al-Hussein Balakit ◽  
Mahmoud Najim Abid Al-Jibouri
Keyword(s):  
Antibacterial Activity ◽  
Metal Complexes ◽  
Thermal Analyses ◽  
Free Ligand ◽  
Molar Conductance ◽  
Bidentate Ligand ◽  
Ring Closure ◽  
Tetrahedral Geometry ◽  
Visible Spectra ◽  
Elemental Analyses

New transition metal complexes of cobalt(II), nickel(II), copper(II), palladium(II), cadmium(II), and platinum(IV) with bidentate ligand 4-amino-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazole-3-thiol were synthesized and characterized by microelemental analyses (CHNS), Fourier-transform infrared (FT-IR), UV-Visible spectra, molar conductance, magnetic susceptibility and thermal analyses (TG-DSC). The ligand was synthesized by ring closure of potassium-2-(3,4,5-trimethoxybenzoyl) hydrazine carbodithioate with an excess amount of hydrazine, and then was acidified using hydrochloric acid. The ligand was used as Lewis bases to prepare metal complexes through the reaction of ratio (1:2) metal:ligand. The ligand was characterized by 1H-NMR and 13C-NMR and the previously described methods to identify the complexes. The results obtained from spectra and elemental analyses indicated the tetrahedral geometry around Cd(II) ion, square-planar for Cu(II) and Pd(II), and octahedral geometry around Co(II), Ni(II), and Pt(IV). All the metal complexes showed significant antibacterial activity in comparison with the free ligand. The antibacterial test of the platinum(IV) complex showed higher activity than other metal complexes against bacteria Staphylococcus aureus (G-positive) and Escherichia coli (G-negative).

scholarly journals Preparation and Properties of Rhodium(III) Complexes with the Tetradentate Ligand N,N'-Bis(2'-pyridinecarboxamide)-1,8-naphthalene

1994 ◽  
Vol 49 (1) ◽  
pp. 111-118 ◽  
Author(s):  
Evy Manessi-Zoupa ◽  
Theodoros F. Zafiropoulos ◽  
Spyros P. Perlepes
Keyword(s):  
Solid State ◽  
Chelating Agent ◽  
Bidentate Ligand ◽  
Octahedral Complex ◽  
Tetradentate Ligand ◽  
Conductivity Measurements ◽  
Nmr Studies ◽  
X Ray ◽  
H Nmr ◽  
Elemental Analyses

AbstractSynthetic procedures are described that allow access to a number of new Rh(III) complexes with the tetradentate bis-amide ligand N,N'-bis(2'-pyridinecarboxamide)-1,8-naphthalene (LH2). These complexes have the formulae Rh(LH2)Cl3, Na[RhLX2] • H2O (X = Cl, CN) and [RhLA2]ClO4 (A = pyridine, 1-methylbenzotriazole). The compounds have been characterized by elemental analyses, conductivity measurements, X-ray powder patterns, spectroscopic (IR, UV/VIS, 1H NMR) studies and electrochemical methods. The neutral amide behaves as a bis-bidentate ligand in the oligomeric or polymeric, octahedral complex Rh(LH2,)Cl3. Monomeric, trans octahedral structures are assigned for the complexes of L2− in the solid state; the doubly deprotonated ligand acts as a tetradentate chelating agent with the four nitrogens as ligating atoms.

scholarly journals Guidelines for measurement of luminescence spectra and quantum yields of inorganic and organometallic compounds in solution and solid state (IUPAC Technical Report)

2016 ◽  
Vol 88 (7) ◽  
pp. 701-711 ◽  
Author(s):  
Hitoshi Ishida ◽  
Jean-Claude Bünzli ◽  
Andrew Beeby
Keyword(s):  
Solid State ◽  
Organic Compounds ◽  
Room Temperature ◽  
Inorganic Compounds ◽  
Organometallic Compounds ◽  
Quantum Yields ◽  
Luminescence Spectra ◽  
Room Temperature Phosphorescence ◽  
Emission Data ◽  
Technical Report

AbstractGuidelines for measuring the luminescence of inorganic compounds, metal complexes, and organometallic compounds are described. Common textbooks and manuals describing luminescence measurements are usually targeted for organic compounds, and are not always suitable for inorganic and organometallic compounds, which emit room-temperature phosphorescence. The report describes problems that researchers may confront while recording emission data and elaborates clear procedures to avoid these problems and provide adequate standardized protocols.

Eu3+ Ion Luminescence Spectra from Lanthanide Sesquioxides Exhibiting Three Different Crystal Structures

1992 ◽  
Vol 46 (2) ◽  
pp. 273-276 ◽  
Author(s):  
G. Chen ◽  
R. G. Haire ◽  
J. R. Peterson
Keyword(s):  
Crystal Structure ◽  
Crystal Structures ◽  
Room Temperature ◽  
Luminescence Spectra ◽  
Spectral Splitting ◽  
The Eu

We have investigated the Eu3+ ion luminescence spectra from different host crystals of the lanthanide sesquioxides exhibiting either the A, B, or C form. The Eu3+ ion luminescence spectra from B-type Eu2O3 and from Eu3+-doped A-type La2O3 and C-type Lu2O3 were obtained at room temperature. It is suggested that the luminescence from f-f transitions in the Eu3+ ion can be used to determine the crystal structure, because the different Eu3+ ion site symmetries in the different crystal structures give rise to different characteristic spectral splitting patterns.

Photoluminescence of Erbium-Diffused Silicon

1996 ◽  
Vol 422 ◽  
Author(s):  
H. Horiguchi ◽  
T. Kinone ◽  
R. Saito ◽  
T. Kimura ◽  
T. Ikoma
Keyword(s):  
Room Temperature ◽  
Crystalline Silicon ◽  
Luminescence Spectra ◽  
Main Peak ◽  
Silicon Substrates ◽  
Annealing Atmosphere ◽  
Full Width ◽  
Half Maximum ◽  
Strong Luminescence ◽  
Fine Structures

AbstractErbium films are evaporated on crystalline silicon substrates and are thermally diffused into silicon in an Ar+02 or H2 flow. Very sharp Er3+-related luminescence peaks are observed around 1.54 μ m.The main peak as well as the fine structures of the luminescence spectra depend on the annealing atmosphere, suggesting different luminescence centers. The full width at half maximum (FWHM) of the main peaks is ≤ 0.5nm at 20K. Thermal diffusion with Al films on top of the Er films is found to increase the intensity of the Er3+-related peaks greatly. The temperature dependence between 20 K and room temperature is relatively small, and a strong luminescence is obtained at room temperature.

scholarly journals The behaviour of visual purple at low temperature

1941 ◽  
Vol 179 (977) ◽  
pp. 151-159 ◽  
Keyword(s):  
Aqueous Solution ◽  
Low Temperature ◽  
Low Temperatures ◽  
Room Temperature ◽  
Absorption Curve ◽  
Quantum Yields

Visual purple is soluble and stable in a mixture of glycerol and water (3:1). At room temperature the spectrum of such a solution is identical with that of the aqueous solution. At — 73° C the peak of the absorption curve is higher and narrower than at room temperature, and it is shifted towards longer waves. The product of photodecomposition at — 73° C has a spectrum in ­ dependent of pH and is at low temperatures thermostable and photostable, but at room temperature it decomposes therm ally to indicator yellow. The primary product appears to be identical with transient orange. The quantum yields of the photoreaction at low and at room temperature are of the same order.

Basic Chromium(III) Carboxylates: Reactions of Chromium(III) Chloride with Some Carboxylic Acids

1979 ◽  
Vol 34 (10) ◽  
pp. 1369-1372 ◽  
Author(s):  
Ramesh Kapoor
Keyword(s):  
Acetic Anhydride ◽  
General Formula ◽  
Carboxylic Acids ◽  
Magnetic Measurements ◽  
Molar Conductance ◽  
Strong Affinity ◽  
Elemental Analyses

Abstract Anhydrous chromium(III) chloride reacts with pure carboxylic acids (RCOOH where R = CH3, C2H5, n-C3H7, CH2Cl, CHCl2 and CCl3) to give basic trinuclear chromium(III) carboxylates of the general formula [Cr3O(OOCR)6]+Cl-. The reaction of CrCl3 with acetic anhydride, however, gives a partially substituted product, CrCl(OOCCH3)2.The formation of basic carboxylates has been attributed to the strong affinity of Cr3+ ions for water that they can abstract it even from pure carboxylic acids. Their addition compounds with ammonia have also been prepared. The compounds have been characterized by their elemental analyses, IR, molar conductance and magnetic measurements.

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