13479-54-4Relevant articles and documents
Synthesis and characterization of surfactant assisted copper nanomaterials
Murali Krishna,Hussain Reddy,Rashmitha,Sravanthi,Sujathamma
, p. 2700 - 2706 (2020/11/23)
In this work, a simple and low cost synthetic method for four different copper nanomaterials having uniform shape and size using copper(II) acetate and cis-bis(glycinato)copper(II) complex in presence of non-ionic surfactants Tween-80 and Triton X-100 in the presence of ascorbic acid as reducing agent is described. The synthesized nanomaterials were characterized using FT-IR, UV-visible, powder XRD, EDX and SEM techniques. The characterization data reveals that all the copper nanomaterials formed are less than 30 nm size with spherical shape.
ATR-FTIR spectroscopic investigation of the cis- and trans-bis-(α-amino acids) copper(II) complexes
Berestova, Tatyana V.,Kuzina, Lyudmila G.,Amineva, Natalya A.,Faizrakhmanov, Ilshat S.,Massalimov, Ismail A.,Mustafin, Akhat G.
, p. 260 - 266 (2017/03/09)
The crystalline phases of the trans-(a) and cis-(b)-isomers of bis-(α-amino acids) copper(II) complexes [Cu(bL)2] 1–5 (bL - bidentate ligand: gly (1), S-ala (2), R,S-val (3), (±)-thr (4), R,S-phe (5)) were studied by ATR-FTIR spectroscopy in the mid region IR spectrum. It was established that asymmetric νas(COO) and symmetric νs(COO) stretching vibrations of carboxylic groups of 1–5 are sensitive to change of the geometric structure and have a different maxima for the trans(a)- and cis(b)-isomers. It found that νas(COO) and νs(COO) stretching vibrations of cis-isomers are broadened and shifted to longer wavelengths (b) as compared with trans-isomers (a). Shown that peculiarities of crystal packing molecules of geometric isomers may affect on carboxylate stretching vibration bis-α-amino acids complexes copper(II) 1–5 a,b.
An efficient copper catalyzed formylation of amines utilizing CO2 and hydrogen
Kumar, Subodh,Jain, Suman L.
, p. 64277 - 64279 (2015/02/19)
Trans-Bis-(glycinato)copper(ii) complex was found to be a highly active, economical and efficient heterogeneous catalyst for the formylation of amines utilizing CO2 and hydrogen under solvent free conditions. This journal is
Thermally induced oxidative decarboxylation of copper complexes of amino acids and formation of strecker aldehyde
Nashalian, Ossanna,Yaylayan, Varoujan A.
, p. 8518 - 8523 (2014/11/26)
In the Maillard reaction, independent degradations of amino acids play an important role in the generation of amino-acid-specific products, such as Strecker aldehydes or their Schiff bases. Such oxidative decarboxylation reactions are expected to be enhan
Thermally induced oxidative decarboxylation of copper complexes of amino acids and formation of strecker aldehyde
Nashalian, Ossanna,Yaylayan, Varoujan A.
, p. 8518 - 8523 (2015/04/22)
In the Maillard reaction, independent degradations of amino acids play an important role in the generation of amino-acid-specific products, such as Strecker aldehydes or their Schiff bases. Such oxidative decarboxylation reactions are expected to be enhan
Method for Producing Amino Acid Chelate Compounds, Amino Acid Chelate Compounds and Use of Amino Acid Chelate Compounds
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Paragraph 0066-0073, (2014/02/16)
A method for producing amino acid chelate compounds, characterized in that metal oxides and/or metal carbonates and/or metal sulfates and/or metal chlorides and/or metal hydroxides in solid form are activated mechanically and then the activated metal oxides and/or metal carbonates and/or metal hydroxides and/or metal sulfates and/or metal chlorides are brought together with amino acids in solid form and converted to amino acid chelate compounds in a solid-state reaction.
Non-GMO metal amino acid chelates and non-GMO metal amino acid chelate-containing compositions
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Page/Page column 5, (2008/06/13)
Non-GMO metal amino acid chelate compositions, non-GMO formulations containing non-GMO metal amino acid chelates, methods of preparing non-GMO metal amino acid chelates, and methods of administering non-GMO metal amino acid chelates are provided. Specifically, the present invention provides a non-GMO metal amino acid chelate composition, comprising amino acid chelates having a naturally occurring amino acid to metal molar ratio of from about 1:1 to 4:1, wherein both the amino acid and the source of the metal used to form the amino acid chelate are non-GMO.
Method for preparation of metal organic acid chelates
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Page column 3-4, (2008/06/13)
A method is disclosed where organic acid chelates can be made by reacting an organic acid ligand with a metal compound in a non aqueous environment. The chelate is thereafter recovered by means of filtration or evaporation.
A thermochemical study of the solid-state coordination reactions of two α-amino acids with copper(II) acetate
Di, You-Ying,Qu, Song-Sheng,Liu, Yi,Wen, De-Cai,Tang, Hou-Kuan,Li, Lin-Wei
, p. 115 - 119 (2008/10/08)
The two solid-state coordination reactions CuAc2·H2O(s) + 2Ala(s) → trans-Cu(Ala)2(s) + 2HAc(1) + H2O(1) (1) CuAc2·H2O(s) + 2Gly(s) → trans-Cu(Gly)2·H2O(s) + 2HAc(1) (2) have been studied by solution calorimetry. The molar dissolution enthalpies of the reactants and the products in some solvents (such as 2 mol 1-1 HCl or its solutions) of these solid-solid coordination reactions have been measured by an isoperibol solution calorimeter. The standard molar formation enthalpies of [trans-Cu(Ala)2(s), 298.15 K] and [trans-Cu(Gly)2(s), 298.15 K] have been determined to be - 1015.42 ± 0.06 and 1252.36 ± 0.05 kJ mol-1, respectively, from the results of the molar dissolution enthalpies and other auxiliary thermodynamic data.
Syntheses, Structures, and Thermal Behavior of Cu(hfacac) Complexes Derived from Ethanolamines
Pinkas, Jiri,Huffman, John C.,Bollinger, John C.,Streib, William E.,Baxter, David V.,Chisholm, Malcolm H.,Caulton, Kenneth G.
, p. 2930 - 2937 (2008/10/09)
A series of novel precursors for MOCVD of metallic copper have been synthesized and structurally characterized. These precursors are composed of Cu(hfacac)2, which serves as a volatile source of Cu, and amino alcohols, which act as reductants and anchor firmly to the copper center through the amine unit. In some cases, a proton transfer from the coordinated alcohol to the hfacac ligand results in the formation of an alkoxide unit and the release of the free Hhfacac. Metallic copper films can be deposited by MOCVD at 300 °C without any external reductant. Crystal data: Cu(hfacac)2·C7H8 (-103 °C), a = 6.510(6) A, b = 8.594(7) A, c = 18.478(15) A, orthorhombic space group Pmnn, Z = 2; Cu(hfacac)2(H2NCH2CH2OH) (-158 °C), a = 13.145(1)A, b = 13.418(1) A, c= 11.245(1) A, α = 110.39(1)°, β= 99.12(1)°, γ = 97.90(1)°, triclinic space group P1, Z = 4; [Cu(hfacac)(Me2NCH2CH2O)]2 (-153 °C), a = 9.259(2) A, b = 12.011(3) A, c = 6.304(1) A, α = 91.19(1)°, β = 106.66(1)°, γ = 74.83(1)°, triclinic space group P1, Z = 1 ; Cu(hfacac)[N(CH2CH2OH)2(CH2CH 2O)]·MeOH (-168 °C), a - 10.075(4) A, b = 8.611(4) A, c = 19.259(9) A, β= 99.82(2)°, monoclonic space group P21/m, Z = 4.