scholarly journals Coordination Reactions and Noncovalent Interactions of Polyamines with Nucleotides in Binary Systems and with Nucleotides and Copper(II) Ion in Ternary Systems

2010 ◽  
Vol 2010 ◽  
pp. 1-13 ◽  
Author(s):  
Lechoslaw Lomozik ◽  
Anna Gasowska ◽  
Grzegorz Krzysko ◽  
Romualda Bregier-Jarzebowska
Keyword(s):  
Binary Systems ◽  
Noncovalent Interactions ◽  
Ternary Systems ◽  
Coordination Sites ◽  
Protonated Amine ◽  
Overall Stability ◽  
Methylene Groups ◽  
Amine Groups ◽  
Mode Of Coordination ◽  
Phosphate Groups

Interactions of nucleotides (AMP, CMP) and 1,2-diaminopropane (tn-1) or 2-methyl-1,2-diaminopropane (tn-2) in metal-free systems as well as in the systems including copper(II) ions were studied. The composition and overall stability constants of the complexes formed were determined by the potentiometric method, whereas the interaction centres and coordination sites were identified by spectroscopic methods. It was found that phosphate groups of nucleotides and the protonated amine groups of polyamines are the centres of interaction. The differences in the interactions with the polyamines which act as models of biogenic amines are impacted by the presence of lateral chains (methylene groups) in tn-1 and tn-2. In the ternary systems with Cu(II) ions, the heteroligand complexes are mainly of the ML⋯L’ type, in which the protonated polyamine is engaged in noncovalent interactions with the anchoring Cu(II)-nucleotide complex. The complexes formed in the Cu/NMP)/tn-1 system are more stable than those formed in the system with tn-2. The mode of coordination in the complex is realised mainly through the phosphate groups of the nucleotide with involvement of the endocyclic nitrogen atoms in a manner which depends upon the steric conditions and in particular on the number of the methylene groups in the polyamine molecule.

scholarly journals The Influence of pH on Complexation Process of Copper(II) Phosphoethanolamine to Pyrimidine Nucleosides

Materials ◽  
2021 ◽  
Vol 14 (15) ◽  
pp. 4309
Author(s):  
Malwina Gabryel-Skrodzka ◽  
Martyna Nowak ◽  
Klaudia Stachowiak ◽  
Michal Zabiszak ◽  
Kazuma Ogawa ◽  
...  
Keyword(s):  
Equilibrium Constants ◽  
Computer Calculation ◽  
Biological Applications ◽  
Pyrimidine Nucleosides ◽  
Species Formation ◽  
Overall Stability ◽  
Influence Of Ph ◽  
Mode Of Coordination ◽  
Phosphate Groups ◽  
Complexation Process

The influence of pH on the complex formation of phosphoethanolamine and pyrimidine nucleosides (uridine, cytidine and thymidine) with copper(II) ions was studied. All investigations were performed in aqueous solution. The overall stability constants of the complexes and non-covalent compounds were obtained using the potentiometric method with computer calculation of the data. Moreover, equilibrium constants of the reaction were determined. The mode of coordination was obtained using spectroscopic methods. Analysis of the potentiometric and spectroscopic data confirmed the involvement and effectiveness of phosphate groups in species formation as well as the influence of pH on the mode of coordination of the investigated biomaterials. In the next step, studied complexes will be applied as potential biomaterials with biological applications.

Calculation of phase diagrams and thermodynamic properties of 14 additive and reciprocal ternary systems containing Li2CO3, Na2CO3, K2CO3, Li2SO4, Na2SO4, K2SO4, LiOH, NaOH, and KOH

1984 ◽  
Vol 62 (3) ◽  
pp. 457-474 ◽  
Author(s):  
A. D. Pelton ◽  
C. W. Bale ◽  
P. L. Lin
Keyword(s):  
Phase Diagram ◽  
Thermodynamic Properties ◽  
Molten Salt ◽  
Phase Diagrams ◽  
Binary Systems ◽  
Ternary Phase ◽  
Ternary Phase Diagram ◽  
Ternary Systems ◽  
Maximum Error ◽  
Critical Assessment

Phase diagrams and thermodynamic properties of five additive molten salt ternary systems and nine reciprocal molten salt ternary systems containing the ions Li+, Na+, [Formula: see text], OH− are calculated from the thermodynamic properties of their binary subsystems which were obtained previously by a critical assessment of the thermodynamic data and the phase diagrams in these binary systems. Thermodynamic properties of ternary liquid phases are estimated from the binary properties by means of the Conformal Ionic Solution Theory. The ternary phase diagrams are then calculated from these thermodynamic properties by means of computer programs designed for the purpose. It is found that a ternary phase diagram can generally be calculated in this way with a maximum error about twice that of the maximum error in the binary phase diagrams upon which the calculations are based. If, in addition, some reliable ternary phase diagram measurements are available, these can be used to obtain small ternary correction terms. In this way, ternary phase diagram measurements can be smoothed and the isotherms drawn in a thermodynamically correct way. The thermodynamic approach permits experimental data to be critically assessed in the light of thermodynamic principles and accepted solution models. A critical assessment of error limits on all the calculated ternary diagrams is made, and suggestions as to which composition regions merit further experimental study are given.

scholarly journals Two-phase equilibrium in binary and ternary systems II. The system methane-ethylene III. The system methane-ethane-ethylene

1940 ◽  
Vol 176 (964) ◽  
pp. 140-152 ◽  
Keyword(s):  
Phase Equilibrium ◽  
Ternary System ◽  
Binary Systems ◽  
Ternary Systems ◽  
Two Phase ◽  
Composition Diagram ◽  
Wide Range ◽  
Binary And Ternary Systems

The liquid-vapour equilibrium of the system methane-ethylene has been determined at 0, -42 , -78, -88 and -104° C over a wide range of pressures and the results are shown on a pressure-composition-temperature diagram and by a series of pressure-composition curves. The liquid-vapour equilibrium of the ternary system methane-ethane-ethylene has been determined at -104, -78 and 0° C. Values for the two binary systems methane-ethane and methane-ethylene and for the ternary system methane-ethane-ethylene are shown on a composite pressure-composition diagram.

scholarly journals Online process monitoring of a batch distillation by medium field NMR spectroscopy

2021 ◽  
Author(s):  
Anne Friebel ◽  
Erik von Harbou ◽  
Kerstin Münnemann ◽  
Hans Hasse
Keyword(s):  
Process Monitoring ◽  
Binary Systems ◽  
Spectroscopic Analysis ◽  
Ternary Systems ◽  
Ethyl Formate ◽  
Batch Distillation ◽  
Non Invasive ◽  
Robust Measurements ◽  
Online Process Monitoring ◽  
Online Process

Medium field NMR spectrometers are attractive for online process monitoring. Therefore, in the present work, a single-stage laboratory batch distillation still was coupled online with a medium field NMR spectrometer. This enables quantitative non-invasive measurements without calibration. The technique was used for studying isobaric and isothermal residue curves in two ternary systems: (dimethyl sulfoxide + acetonitrile + ethyl formate) and (ethyl acetate + acetone + diethyl ether) and boiling curves and high-boiling azeotropes in two binary systems: (acetic acid + pyridine) and (methanol + diethylamine). The results of the online NMR spectroscopic analysis were compared to results from offline analysis as well as to results from thermodynamic modeling using NRTL parameters that were parametrized with literature data. The new method for online process monitoring gives reliable results and is well-suited for fast and robust measurements of residue curves.

Thermodynamic Calculation of Phase Equilibria in the Mn-RE (RE=Nd, Gd, Dy) Binary Systems

2017 ◽  
Vol 898 ◽  
pp. 1036-1041
Author(s):  
M.H. Rong ◽  
S.D. Lin ◽  
Jiang Wang ◽  
H.Y. Zhou ◽  
G.H. Rao
Keyword(s):  
Magnetic Properties ◽  
Thermodynamic Properties ◽  
Phase Equilibria ◽  
Thermodynamic Calculation ◽  
Binary Systems ◽  
Ternary Systems ◽  
Experimental Information ◽  
Calphad Method ◽  
Self Consistent ◽  
Ternary Intermetallic Compounds

Ternary intermetallic compounds with rare earth elements and transition metals in the RE-Mn-X (X=Si, Ge, Sn etc.) ternary systems show interesting magnetic properties. As key sub-binary systems of the RE-Mn-X (X=Si, Ge, Sn etc.) ternary systems, the information of phase equilibria and thermodynamic properties of the Mn-RE (RE=Nd, Gd, Dy) binary systems are indispensable to explore the RE-Mn-X (X=Si, Ge, Sn etc.) alloys with better magnetic properties. In this work, the experimental data of phase equilibria and thermodynamic properties of the Mn-RE (RE=Nd, Gd, Dy) binary systems in the published literature were reviewed. Based on the available experimental information, thermodynamic calculation of phase equilibria of the Mn-RE (RE=Nd, Gd, Dy) binary systems was performed using the CALPHAD method. As a result, further experimental investigation and thermodynamic optimization would be still necessary in order to develop the self-consistent and compatible thermodynamic database of the RE-Mn-based alloy systems.

Cellulose-g-tetraethylenepentamine Dual-function Imprinted Polymers Selectively and Effectively Adsorb and Remove 4-Nitrophenol and Cr(VI)

2021 ◽  
Author(s):  
Daning Lang ◽  
Xia Xu ◽  
Ronglan Wu ◽  
WEI WANG ◽  
Ming Shi ◽  
...  
Keyword(s):  
Binary Systems ◽  
Competitive Adsorption ◽  
Dual Function ◽  
Imprint Polymer ◽  
Inorganic Contaminants ◽  
Cellulosic Material ◽  
Imprinted Polymer ◽  
Promising Candidate ◽  
Adsorption Sites ◽  
Amine Groups

Abstract A cellulosic material could efficiently and selectively adsorb organic and inorganic contaminants from aqueous solutions without interference from competing adsorption sites. In this study, cellulose-graft-tetraethylenepentamin molecular imprinted polymer (C-TEPA-MIP) was synthesized by using 4-nitrophenol (4-NP) as the template. The C-TEPA-MIP adsorbent could adsorb 4-NP and Cr(VI) simultaneously and selectively, without being affected by the competitive adsorption sites of each of these pollutants. The adsorption of 4-NP was predominantly due to the imprinted sites of 4-NP in C-TEPA-MIP that were located inside of the adsorbent, whereas that of Cr(VI) was primarily due to the amine groups of TEPA found on the surface of the adsorbent. Compared with the non-imprint polymer synthesized without the template, C-TEPA-MIP showed higher selectivity for both 4-NP and Cr(VI) in unitary and binary systems. In addition, C-TEPA-MIP exhibited good stability and recyclability for 4-NP, which makes it a promising candidate material for applications concerning wastewater treatment.

scholarly journals Experimental Investigation and Thermodynamic Calculation of Ni–Al–La Ternary System in Nickel-Rich Region: A New Intermetallic Compound Ni2AlLa

Materials ◽  
2018 ◽  
Vol 11 (12) ◽  
pp. 2396 ◽  
Author(s):  
Jinfa Liao ◽  
Hang Wang ◽  
Tzu-Yu Chen
Keyword(s):  
Ternary System ◽  
Binary Systems ◽  
Ternary Phase ◽  
Ternary Systems ◽  
Rich Region ◽  
Space Group ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Backscattered Electron ◽  
Electron Imaging

The phase equilibrium of the Ni–Al–La ternary system in a nickel-rich region was observed at 800 °C and 1000 °C using scanning electron microscopy backscattered electron imaging, energy dispersive X-ray spectrometry and X-ray diffractometry. The solubility of Al in the Ni5La phase was remeasured at 800 °C and 1000 °C. Herein, we report a new ternary phase, termed Ni2AlLa, confirmed at 800 °C. Its X-ray diffraction (XRD) pattern was indexed and space group determined using Total Pattern Solution (TOPAS), and the suitable lattice parameters were fitted using the Pawley method and selected-area electron diffraction. Ni2AlLa crystallizes in the trigonal system with a space group R3 (no. 146), a = 4.1985 Å and c = 13.6626 Å. A self-consistent set of thermodynamic parameters for the Al–La and Ni–La binary systems and the Ni–Al–La ternary system includes a Ni2AlLa ternary phase, which was optimized using the CALPHAD method. The calculated thermodynamic and phase-equilibria data for the binary and ternary systems are consistent with the literature and measured data.

scholarly journals Ethylenediamine loading into a manganese-based metal–organic framework enhances water stability and carbon dioxide uptake of the framework

2020 ◽  
Vol 7 (3) ◽  
pp. 191934 ◽  
Author(s):  
Aisha Asghar ◽  
Naseem Iqbal ◽  
Leena Aftab ◽  
Tayyaba Noor ◽  
Benson M. Kariuki ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Metal Organic Framework ◽  
Carbon Dioxide Uptake ◽  
Coordination Sites ◽  
Carbon Dioxide Sorption ◽  
Metal Organic ◽  
Amine Groups ◽  
Thermogravimetric Studies ◽  
Original Metal ◽  
Very High

Metal–organic frameworks (MOFs) based on 2,5-dihydroxyterepthalic acid (DOBDC) as the linker show very high CO 2 uptake capacities at low to moderate CO 2 pressures; however, these MOFs often require expensive solvent for synthesis and are difficult to regenerate. We have synthesized a Mn-DOBDC MOF and modified it to introduce amine groups into the structure by functionalizing its metal coordination sites with ethylenediamine (EDA). Repeat framework synthesis was then also successfully performed using recycled dimethylformamide (DMF) solvent. Characterization by elemental analysis, FTIR and thermogravimetric studies suggest that EDA molecules are successfully substituting the original metal-bound DMF. This modification not only enhances the material's carbon dioxide sorption capacity, increasing stability to repeated CO 2 sorption cycles, but also improves the framework's stability to moisture. Moreover, this is one of the first amine-modified MOFs that can demonstrably be synthesized using recycled solvent, potentially reducing the future costs of production at larger scales.

scholarly journals Thermodynamic and Spectroscopic Studies of the Complexes Formed in Tartaric Acid and Lanthanide(III) Ions Binary Systems

Molecules ◽  
2020 ◽  
Vol 25 (5) ◽  
pp. 1121 ◽  
Author(s):  
Michal Zabiszak ◽  
Martyna Nowak ◽  
Zbigniew Hnatejko ◽  
Jakub Grajewski ◽  
Kazuma Ogawa ◽  
...  
Keyword(s):  
Tartaric Acid ◽  
Stability Constants ◽  
Binary Systems ◽  
Equilibrium Constants ◽  
Spectroscopic Studies ◽  
Luminescence Spectroscopy ◽  
Binary Complexes ◽  
Overall Stability ◽  
The Stability

Binary complexes of tartaric acid with lanthanide(III) ions were investigated. The studies have been performed in aqueous solution using the potentiometric method with computer analysis of the data for detection of the complexes set, determination of the stability constants of these compounds. The mode of the coordination of complexes found was determined using spectroscopy, which shows: Infrared, circular dichroism, ultraviolet, visible as well as luminescence spectroscopy. The overall stability constants of the complexes as well as the equilibrium constants of the reaction were determined. Analysis of the equilibrium constants of the reactions and spectroscopic data allowed the effectiveness of the carboxyl groups in the process of complex formation.

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