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Relevant bibliographies by topics / Anion oxalate

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Academic literature on the topic 'Anion oxalate'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Anion oxalate"

1

Hind, A. R., S. K. Bhargava, W. Van Bronswijk, S. C. Grocott, and S. L. Eyer. "On the Aqueous Vibrational Spectra of Alkali Metal Oxalates." Applied Spectroscopy 52, no. 5 (1998): 683–91. http://dx.doi.org/10.1366/0003702981944355.

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Fourier transform infrared attenuated total reflectance and Fourier transform Raman spectra of the series of aqueous alkali metal oxalates—lithium oxalate (Li2C2O4), sodium oxalate (Na2C2O4), potassium oxalate (K2C2O4), rubidium oxalate (Rb2C2O4), and cesium oxalate (Cs2C2O4)—are presented for the first time. Fourier transform Raman spectra of the solid oxalates are also presented for the first time. The solid and aqueous oxalate ions are assumed to possess D2 h and D2 d symmetry, respectively, and the assignment of fundamental vibrational modes is made accordingly. The effect of increasing al

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2

Yin, Xia, Song-Liang Cai, Sheng-Run Zheng, Jun Fan, and Wei-Guang Zhang. "A new two-dimensional cadmium coordination polymer with 1H-imidazole-4-carboxylate and oxalate." Acta Crystallographica Section C Crystal Structure Communications 68, no. 7 (2012): m177—m180. http://dx.doi.org/10.1107/s0108270112023153.

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The title compound, poly[aqua(μ2-1H-imidazole-4-carboxylato-κ3N3,O:O′)hemi(μ2-oxalato-κ4O1,O2:O1′,O2′)cadmium(II)], [Cd(C4H3N2O2)(C2O4)0.5(H2O)]n, exhibits a two-dimensional network. The CdIIcation is coordinated to one N atom and two carboxylate O atoms from two 1H-imidazole-4-carboxylate (Himc) ligands, two carboxylate O atoms from the bridging oxalate anion and one ligated water molecule; these six donor atoms form a distorted octahedral configuration. The oxalate anion lies on a centre of inversion. The Himc ligands connect the CdIIcations to form –Cd–Himc–Cd–Himc–Cd– zigzag chains, with a

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Diop, Mouhamadou Birame, Libasse Diop, Laurent Plasseraud та Thierry Maris. "Crystal structure of 2-methyl-1H-imidazol-3-ium aquatrichlorido(oxalato-κ2O,O′)stannate(IV)". Acta Crystallographica Section E Crystallographic Communications 71, № 5 (2015): 520–22. http://dx.doi.org/10.1107/s2056989015005988.

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The tin(IV) atom in the complex anion of the title salt, (C4H7N2)[Sn(C2O4)Cl3(H2O)], is in a distorted octahedral coordination environment defined by three chlorido ligands, an oxygen atom from a water molecule and two oxygen atoms from a chelating oxalate anion. The organic cation is linked through a bifurcated N—H...O hydrogen bond to the free oxygen atoms of the oxalate ligand of the complex [Sn(H2O)Cl3(C2O4)]−anion. Neighbouring stannate(IV) anions are linked through O—H...O hydrogen bonds involving the water molecule and the two non-coordinating oxalate oxygen atoms. In combination with a

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4

Sharma, Ashwani K., and Tej P. Singh. "Structure of oxalate-substituted diferric mare lactoferrin at 2.7 Å resolution." Acta Crystallographica Section D Biological Crystallography 55, no. 11 (1999): 1792–98. http://dx.doi.org/10.1107/s0907444999009439.

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Lactoferrin binds two Fe3+ and two CO^{2-}_{3} ions with high affinity. It can also bind other metal ions and anions. In order to determine the perturbations in the environments of the binding sites in the N and C lobes and elsewhere in the protein, the crystal structure of oxalate-substituted diferric mare lactoferrin has been determined at 2.7 Å resolution. The final model has a crystallographic R factor of 21.3% for all data in the resolution range 17.0–2.7 Å. The substitution of an oxalate anion does not perturb the overall structure of the protein, but produces several significant changes

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Li, Zhi-Feng, Yi-Chao Zhang, Xiao-Qin Hu та Chun-Xiang Wang. "Crystal structure of poly[μ6-adipato-diaquadi-μ2-oxalato-didysprosium(III)]". Acta Crystallographica Section E Structure Reports Online 70, № 12 (2014): m399—m400. http://dx.doi.org/10.1107/s1600536814024544.

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In the title coordination polymer, [Dy2(C6H8O4)(C2O4)2(H2O)2]n, the asymmetric unit consists of one Dy3+cation, one half of an adipate anion, two halves of oxalate anions and one coordinating water molecule. The adipate and oxalate ions are located on centres of inversion. The Dy3+cation has a distorted tricapped trigonal–prismatic geometry and is coordinated by nine O atoms, four belonging to three adipate anions, four to two oxalate anions and one from an aqua ligand. The cations are bridged by adipate ligands, generating a two-dimensional network parallel to (010). This network is further e

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Gerencser, G. A., M. A. Cattey, and G. A. Ahearn. "Sulfate/oxalate exchange by lobster hepatopancreatic basolateral membrane vesicles." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 269, no. 3 (1995): R572—R577. http://dx.doi.org/10.1152/ajpregu.1995.269.3.r572.

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Purified basolateral membrane vesicles (BLMV) were prepared from lobster hepatopancreas by osmotic disruption and discontinuous sucrose gradient centrifugation. Radiolabeled sulfate uptake was stimulated by 10 mM intravesicular oxalate compared with gluconate-loaded vesicles. Sulfate/oxalate exchange was not affected by transmembrane valinomycin-induced potassium diffusion potentials (inside negative or inside positive), suggesting electroneutral anion transport. Sulfate uptake was not stimulated by the similar carboxylic anions formate, succinate, oxaloacetate, or ketoglutarate. Sulfate influ

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Gapinska, Agata, Alan J. Lough, and Ulrich Fekl. "Coordination compounds containing bis-dithiolene-chelated molybdenum(IV) and oxalate: comparison of terminal with bridging oxalate." Acta Crystallographica Section E Crystallographic Communications 73, no. 8 (2017): 1202–7. http://dx.doi.org/10.1107/s205698901701026x.

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Two coordination compounds containing tetra-n-butylammonium cations and bis-tfd-chelated molybdenum(IV) [tfd2− = S2C2(CF3)2 2−] and oxalate (ox2−, C2O4 2−) in complex anions are reported, namely bis(tetra-n-butylammonium) bis(1,1,1,4,4,4-hexafluorobut-2-ene-2,3-dithiolato)oxalatomolybdate(IV)–chloroform–oxalic acid (1/1/1), (C16H36N)2[Mo(C4F6S2)2(C2O4)]·CHCl3·C2H2O4 or (N n Bu4)2[Mo(tfd)2(ox)]·CHCl3·C2H2O4, and bis(tetra-n-butylammonium) μ-oxalato-bis[bis(1,1,1,4,4,4-hexafluorobut-2-ene-2,3-dithiolato)molybdate(IV)], (C16H36N)2[Mo2(C4F6S2)4(C2O4)] or (N n Bu4)2[(tfd)2Mo(μ-ox)Mo(tfd)2]. They co

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Freel, Robert W., Marguerite Hatch, and N. D. Vaziri. "Conductive pathways for chloride and oxalate in rabbit ileal brush-border membrane vesicles." American Journal of Physiology-Cell Physiology 275, no. 3 (1998): C748—C757. http://dx.doi.org/10.1152/ajpcell.1998.275.3.c748.

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To evaluate the possibility that an apical membrane conductive pathway for oxalate is present in the rabbit distal ileum, we studied oxalate ([14C]oxalate) and chloride (36Cl) uptake into brush-border membrane vesicles enriched 15- to 18-fold in sucrase activity. Voltage-sensitive pathways for oxalate and chloride were identified by the stimulation of uptake provided by an inwardly directed potassium diffusion potential in the presence of valinomycin. Additionally, outwardly directed oxalate (or chloride) gradients stimulated [14C]oxalate (or36Cl) uptake to a greater degree in the absence of v

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Ko, Narae, Felix Knauf, Zhirong Jiang, Daniel Markovich, and Peter S. Aronson. "Sat1 is dispensable for active oxalate secretion in mouse duodenum." American Journal of Physiology-Cell Physiology 303, no. 1 (2012): C52—C57. http://dx.doi.org/10.1152/ajpcell.00385.2011.

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Mice deficient for the apical membrane oxalate transporter SLC26A6 develop hyperoxalemia, hyperoxaluria, and calcium oxalate stones due to a defect in intestinal oxalate secretion. However, the nature of the basolateral membrane oxalate transport process that operates in series with SLC26A6 to mediate active oxalate secretion in the intestine remains unknown. Sulfate anion transporter-1 (Sat1 or SLC26A1) is a basolateral membrane anion exchanger that mediates intestinal oxalate transport. Moreover, Sat1-deficient mice also have a phenotype of hyperoxalemia, hyperoxaluria, and calcium oxalate s

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Yusenko, Elena, Evgeniya Polyntseva, Anna Lyzhova, and Olga Kalyakina. "Determination of Oxalate and Some Inorganic Anions in Green and Black Tea." Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences 67, no. 4-5 (2013): 429–32. http://dx.doi.org/10.2478/prolas-2013-0076.

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Abstract Oxalate concentration differs in various daily consumed food products. The role of oxalic acid in the human body is very significant, as its compounds are responsible for the stability of biological membranes. However, insoluble calcium and magnesium oxalates can be accumulated in the body in the form of kidney stones. Oxalate concentration has been measured by high performance liquid, gas after derivatization and ion chromatography (IC). The most effective method for the simultaneous determination of oxalate and inorganic anions is ion chromatography with conductometric detection. He

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Dissertations / Theses on the topic "Anion oxalate"

1

Gohel, Mayur Danny Indulal. "Urinary polyanions important in urinary calcium oxalate crystallization." Thesis, Hong Kong : University of Hong Kong, 1997. http://sunzi.lib.hku.hk/hkuto/record.jsp?B18736841.

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Hamilton, Jenna Victoria. "On the Structure of Metal Oxalate Anions: Theory and Experiment." Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32208.

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Anionic metal-oxalate complexes have been generated in the gas phase and an attempt at determining plausible structures were made. Two different experimental techniques were coupled to mass spectrometry: Infrared Multiphoton Dissociation (IRMPD) and ion mobility. Both techniques were compared to theoretical structures calculated using various levels of theory. With the use of IRMPD, frequencies were generated for each complex and compared to theoretical frequencies. Plausible structures for all complexes were found using the M-series of density functional levels of the theory when the 6-311+gd

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3

Amos, Jacques. "Anion oxalyle équivalent : Alkylation fonctionnalisante stéréospécifique en série stéroïde." Nancy 1, 1990. http://docnum.univ-lorraine.fr/public/SCD_T_1990_0493_AMOS.pdf.

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L'ester glycidique α-chloré dérivé de la 5α-cholestan-3-one se transpose thermiquement pour conduire exclusivement à un cétoester chloré à halogène équatorial. Celui-ci peut être transformé stéréospécifiquement en α-hydroxycétoester à hydroxyle axial, par passage par un époxyéther. Les réactions de l'ester glycidique α-chloré et du cétoester chloré avec les amines fournissent un accès stéréospécifique aux aminocétoesters diastéréoisomères comportant le groupe aminé dans les configurations respectives équatoriales et axiales<br>α-chloroglycidic ester derived from 5α-cholestan-3-one was thermall

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4

Brady, James Peter. "An examination of the applicability of hydrotalcite for removing oxalate anions from Bayer process solutions." Thesis, Queensland University of Technology, 2011. https://eprints.qut.edu.au/46165/1/James_Brady_Thesis.pdf.

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Hydrotalcite and thermally activated hydrotalcites were examined for their potential as methods for the removal of oxalate anions from Bayer Process liquors. Hydrotalcite was prepared and characterised by a number of methods, including X-ray diffraction, thermogravimetric analysis, nitrogen adsorption analysis and vibrational spectroscopy. Thermally activated hydrotalcites were prepared by a low temperature method and characterised using X-ray diffraction, nitrogen adsorption analysis and vibrational spectroscopy. Oxalate intercalated hydrotalcite was prepared by two methods and analysed with

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5

Beck, Jan-Philipp. "Regulation des Sulfat-Anionen-Transporters-1, sat-1, in Caco2-Zellen durch Oxalat und dessen Vorstufen." Doctoral thesis, 2014. http://hdl.handle.net/11858/00-1735-0000-0023-9940-C.

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Book chapters on the topic "Anion oxalate"

1

Ebisuno, S., H. Koul, L. Renzulli, M. Menon, and C. Scheid. "Oxalate Transport in LLC-PK1 Cells: Evidence for Oxalate Transport by Anion Exchange." In Urolithiasis 2. Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2556-1_9.

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2

Manoharan, M., F. Sörgel, P. O. Schwille, H. Hofmann, and A. Sigel. "Determination of urinary oxalate by anion chromatography — a preliminary report." In Pathogenese und Klinik der Harnsteine XI. Steinkopff, 1985. http://dx.doi.org/10.1007/978-3-642-72385-8_37.

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3

Pardasani, R. T., and P. Pardasani. "Magnetic properties of oxalato bridged dinuclear copper(II) complex containing bis(2-pyridylcarbonyl)-amide anion." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_587.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of oxalato bridged dinuclear copper(II) anhydrous complex containing bis(2-pyridylcarbonyl)-amide anion." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_588.

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5

Ma, J. F., W. Zhang, and Z. Zhao. "Regulatory mechanisms of Al-induced secretion of organic acids anions — Involvement of ABA in the Al-induced secretion of oxalate in buckwheat." In Plant Nutrition. Springer Netherlands, 2001. http://dx.doi.org/10.1007/0-306-47624-x_235.

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6

Liu, Chen, Guorui Jia, Daijiang Zou, and Jianbin Wang. "Research on the Attenuation Mechanism of the Lithium Battery with Computational Chemistry and Surface/Interface Detection Methods." In Advances in Transdisciplinary Engineering. IOS Press, 2023. http://dx.doi.org/10.3233/atde230447.

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One of important strategies to improve the ranges of battery electric vehicles is to develop and apply batteries with high energy density. Lithium-rich layered oxide cathode material is one of the most important methods to improve the energy density of batteries. However, there are two bottlenecks in the material: the voltage attenuation of structural transformation and the violent electrolyte decomposition on high voltage. In this study, a spherical Li1.2Mn0.54Co0.13Ni0.13O2 cathode material (LLO) was investigated. The cycle performance of the LLO cathode in various LiBOB electrolytes was com

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Sposito, Garrison. "Soil Humus." In The Chemistry of Soils. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780190630881.003.0007.

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Biomoleculesare compounds synthesized to sustain the life cycles of organisms. In soil humus, they are usually products of litter degradation, root excretion, and microbial metabolism, ranging in molecular structure from simple organic acids to complex biopolymers. Organic acids are among the best-characterized biomolecules. Table 3.1 lists five aliphatic (meaning the C atoms are arranged in open-chain structures) organic acids associated commonly with the soil microbiome. These acids contain the unit R—COOH, where COOH is the carboxyl groupand R represents either H or an organic moiety. The c

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Reports on the topic "Anion oxalate"

1

Kyser, E. Effect of Oxalate on the Recycle of Neptunium Filtrate Solution by Anion Exchange. Office of Scientific and Technical Information (OSTI), 2004. http://dx.doi.org/10.2172/890156.

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Crowder, M., and R. Pierce. LAB-SCALE DEMONSTRATION OF PLUTONIUM PURIFICATION BY ANION EXCHANGE, PLUTONIUM (IV) OXALATE PRECIPITATION, AND CALCINATION TO PLUTONIUM OXIDE TO SUPPORT THE MOX FEED MISSION. Office of Scientific and Technical Information (OSTI), 2012. http://dx.doi.org/10.2172/1049687.

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