147-14-8Relevant articles and documents
Facile one-pot preparation of thermally and photochemically convertible soluble precursors of copper phthalocyanine and naphthalocyanine
Kikukawa, Yuu,Fukuda, Takamitsu,Fuyuhiro, Akira,Ishikawa, Naoto,Kobayashi, Nagao
, p. 8518 - 8520 (2011)
Soluble copper phthalocyanine (CuPc) and naphthalocyanine (CuNc) precursors which can be converted thermally and photochemically into insoluble CuPc and CuNc, respectively, have been synthesized by a one-step reaction using commercially available chemicals. The Royal Society of Chemistry 2011.
(Phthalocyaninato)copper(II) complexes fused with different numbers of 15-crown-5 moieties - Synthesis, spectroscopy, supramolecular structures, and the effects of substituent number and molecular symmetry
Sheng, Ning,Zhang, Yuexing,Xu, Hui,Bao, Meng,Sun, Xuan,Jiang, Jianzhuang
, p. 3268 - 3275 (2007)
Symmetrical (phthalocyaninato)copper(II) complexes Cu(Pc′) [Pc′ = Pc(15C5), Pc(opp-15C5)2, Pc(adj-15C5)2, Pc(15C5) 3; Pc = unsubstituted phthalocyaninate, Pc(15C5) = 2,3-(15-crown-5)phthalocyaninate, Pc(opp-15C5)2 = 2,3,16,17-bis(15-crown-5)phthalocyaninate, Pc(adj-15C5)2 = 2,3,9,10-bis(15-crown-5)phthalocyaninate, Pc(15C5)3 = 2,3,9,10,16,17-tris(15-crown-5)phthalocyaninate] (2-5) have been prepared by the reaction of corresponding heteroleptic bis(phthalocyaninato)europium complexes Eu(Pc)(Pc′) [Pc′ = Pc(15C5), Pc(opp-15C5)2, Pc(adj-15C5)2, Pc(15C5)3, Pc(15C5)4; Pc = unsubstituted phthalocyaninate] with Cu(OAc)2 in dry dmf at 100°C. For the purpose of comparative studies, the symmetrical counterparts CuPc (1) and CuPc(15C5)4 [Pc(15C5)4 = 2,3,9,10,16,17,24, 25-tetrakis(15-crown-5)phthalocyaninate] (7) have also been prepared. These monomeric complexes have been characterized by spectroscopic methods in addition to elemental analysis. Having a series of closely related phthalocyanines with a different number and/or disposition of 15-crown-5 groups at the peripheral positions, the effects of 15-crown-5 substituent number and molecular symmetry on the electronic absorption spectra, infra-red (IR) spectra, and supramolecular structure formation induced by K+ ions have been investigated. Systematic studies on the formation of dimeric supramolecular structures of the series of monomers 2-6 reveal and confirm the previously proposed two-step three-stage process of K+-induced dimerization of phthalocyanines with three or four 15-crown-5 moieties. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.
Magneto-modified catalyst on the base of nanocrystalline CuO
Yermakov,Feduschak,Sedoi,Uimin,Mysik
, p. 2445 - 2447 (2004)
The weakly oxidized nanocrystalline copper powders of different sizes (average particle size of 30 and 100nm) were used as the reactants at copper phthalocyanine (PcCu) formation. The nanocrystalline cupric oxide located at the particles surface serves as a heterogeneous magneto-controlled catalyst. A new effect of acceleration of chemical reaction rate controlled by low external steady magnetic field (~2 kOe) at room temperature was revealed and investigated on an example of formation of a coordination compound of PcCu. The rate of PcCu formation accelerated by 7-8 times after applying of a magnetic field.
Synthesis and characterization of copper phthalocyanine and tetracarboxamide copper phthalocyanine deposited mica-titania pigments
Topuz, Berna Burcu,Guenduez, Guengoer,Mavis, Bora,Colak, Uener
, p. 31 - 37,7 (2013)
Combination pigments were synthesized by the deposition of copper phthalocyanine and tetracarboxamide copper phthalocyanine on a mica-titania pigment in dimethyl formamide solvent to improve color properties. The FT-IR and XRD analyses were performed to observe the crystal transformations of the pigments on the substrate. The stable beta form of copper phthalocyanine normally preferred in paint applications was obtained at 90 °C and 120°C, while tetracarboxamide copper phthalocyanine remained amorphous at all temperatures experimented. Pigment surface morphologies were investigated by SEM analysis. Copper phthalocyanine crystalline rods were observed on the mica-titania substrate, however, the tetracarboxamide copper phthalocyanine pigment did not exhibit any such crystalline structure due to its amorphous structure, which was confirmed by XRD analysis. Furthermore, nitrogen elemental analysis was performed to determine the amount of copper phthalocyanines adsorbed to the mica-titania surfaces at different temperatures. The resulting combination pigments showed enhanced luster, good dispersion, hue, and high color intensity.
Facile, liquid phase preparation of copper phthalocyanine microcrystals by means of thermal conversion of the dimethoxy-substituted solvent soluble phthalocyanine precursors
Fukuda, Takamitsu,Ishikawa, Naoto
, p. 151 - 154 (2014)
A simple procedure for the preparation of microcrystals of insoluble copper phthalocyanine (CuPc) by thermolysis of a dimethoxy-substituted precursor has been developed. Although the morphologies of the resultant microcrystals are practically independent from initial solution concentrations higher than ca. 0.03 mM of the dimethoxy-precursor, crystals with increased width are obtained with increasing the initial concentration of the precursor.
Improvement in the synthesis of metallophthalocyanines using microwave irradiation
Burczyk, Aleksandra,Loupy, André,Bogdal, Dariusz,Petit, Alain
, p. 179 - 188 (2005)
A successful application of microwave irradiation, in which phthalocyanines were synthesized under solventless conditions from 1,2-phthalonitrile or phthalic anhydride and urea in the presence of metal templates is described. It was found that in comparison with conventional heating, the microwave process is a very useful alternative for cyclotetramerization processes because of reduction of the reaction time, better yield, and easy-to-perform procedure. Graphical Abstract.
Stojakovic, Djordje R.,Rajic, Nevenka Z.
, p. 17 - 20 (1990)
-
Elvidge,Linstead
, p. 3536,3541 (1955)
-
Effects of MN4-Type Coordination Structure in Metallophthalocyanine for Bio-Inspired Oxidative Desulfurization Performance
Tan, Amin,Tian, Min,Yang, Yan,Zhang, Gai,Zhang, Yufan
, (2022/02/14)
Oxidative desulfurization (ODS) is the promising new method for super deep desulfurization of fuel oil. The oxidative desulfurization performance of the metal-N4-chelates metallophthalocyanines (MPcs) is related to the chemical properties of conjugate structures and the central metal ions. Herein, a biomimetic catalytic system composed of metallophthalocyanines (MPcR4, M = Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Zn(II); R = -H, -COOH, -NO2, -NH2) and molecular O2 was performed to study the influence of MN4-type coordination structure in metallophthalocyanines for the degradation of dibenzothiophene (DBT) in model oil containing n-octane. The results reveal that the conjugate structures and the center metal ions of metallophthalocyanines played key roles in oxidative desulfurization performance. The inductive effect of different R substituents strongly affected the electron cloud distribution of the conjugate structures and the catalytic performance. Moreover, the catalytic activity of MPcs, which is related to the d electronic configuration and ligand-field effects, does not sequentially increase with the increase in the d electron number of central metal ions.
Nanostructural catalyst: Metallophthalocyanine and carbon nano-onion with enhanced visible-light photocatalytic activity towards organic pollutants
Brzezinski, Krzysztof,Butsyk, Olena,Chaur, Manuel N.,Czyrko-Horczak, Justyna,Echegoyen, Luis,Olejnik, Piotr,Plonska-Brzezinska, Marta E.,Regulska, Elzbieta,Tomczykowa, Monika,Zubyk, Halyna
, p. 10910 - 10920 (2020/03/30)
Metallophthalocyanine (MPc) and carbon nano-onion (CNO) derivatives were synthesized and characterized by using ultraviolet-visible spectroscopy, infrared and Raman spectroscopy, scanning electron microscopy with energy-dispersive X-ray spectroscopy and X-ray powder diffraction. The unmodified CNOs and MPc-CNO derivatives were used as photocatalysts for rhodamine B (RhB) degradation under visible-light irradiation. The photocatalytic studies revealed that the MPc-CNO nanostructural materials simultaneously exhibited a high absorption capacity and an excellent visible-light-driven photocatalytic activity towards RhB. These nanostructures possess great potential for use as active photocatalysts for organic pollutant degradation.
NANOPARTICLE DISPERSION CONTAINING A DYE
-
Page/Page column 16, (2019/07/13)
A method for preparing a dispersion of nanoparticles of a solid organic dye or pigment in a liquid carrier, the method comprising continuously mixing: at least one solution or slurry containing a reactant precursor for the solid organic dye or pigment in an organic or other solvent with the liquid carrier in a counter current or concurrent mixing reactor whereby to obtain reaction of the reactant precursor and formation of the solid organic dye or pigment as a dispersion of nanoparticles in the liquid carrier and solvent mixture; optionally, removing unreacted reactant precursor and/or byproduct from the dispersion when present; and optionally, concentrating the dispersion.