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Relevant bibliographies by topics / 6-pyridine-dicarboxylic acid

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Academic literature on the topic '6-pyridine-dicarboxylic acid'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "6-pyridine-dicarboxylic acid"

1

Hildebrand, U., K. Taraz, and H. Budzikiewicz. "6-(Hydroxythio) carbonyIpyridin-2-carbonsäure und Pyridin-2-carbon- säure-6-monothiocarbonsäure als biosynthetische Zwischenstufen bei der Bildung von Pyridin-2,6-di(monothiocarbonsäure) aus Pyridin-2,6- dicarbonsäure [1] / 6-(Hydroxythio)carbonylpyridine-2-carboxylic Acid and Pyridine-2-carboxylic Acid-6- monothiocarboxylic Acid as Interm ediates in the Biosynthesis of Pyridine-2,6-di(monothiocarboxylic Acid) from Pyridine-2,6-dicarboxylic Acid [1]." Zeitschrift für Naturforschung C 41, no. 7-8 (1986): 691–94. http://dx.doi.org/10.1515/znc-1986-7-805.

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Abstract It is shown by feeding experiments with [3-2H]pyridine-2,6 -dicarboxylic acid that 6 -(hydroxythio)carbonylpyridine-2-carboxylic acid and pyridine-2 -carboxylic acid-6-m onothiocarboxylic acid are intermediates in the biosynthesis of pyridine-2,6 -di(monothiocarboxylic acid) from pyridine-2,6 -dicarboxylic acid produced by Pseudomonas putida. Thus the series of biosynthetic steps - COOH → - CO - SOH → COSH has been demonstrated for the first time.

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2

Smith, Graham, Katherine E. Baldry, Karl A. Byriel, and Colin H. L. Kennard. "Molecular Cocrystals of Carboxylic Acids. XXV The Utility of Urea in Structure Making with Carboxylic Acids and the Crystal Structures of a Set of Six Adducts with Aromatic Acids." Australian Journal of Chemistry 50, no. 7 (1997): 727. http://dx.doi.org/10.1071/c96199.

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Molecular adducts of urea with six aromatic carboxylic acids have been prepared and characterized by using X-ray diffraction methods and infrared spectroscopy. These compounds are with 5-nitrosalicylic acid [(C7H5NO5)2(CH4N2O)] (1), 3,5-dinitrosalicylic acid [(C7H4N2O7)(CH4N2O)] (2), 4-aminobenzoic acid [(C7H7NO2)2(CH4N2O)] (3), o-phthalic acid [(C8H6O4)(CH4N2O)] (4), pyrazine-2,3-dicarboxylic acid [(C4H4N2O4)(CH4N2O)] (5) and pyridine-2,6-dicarboxylic acid [(C7H5NO4)(CH4N2O)2] (6). In the majority of the adducts, all six potential interactive sites on the urea molecules are utilized in hydrog

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3

Novoa de Armas, Héctor, Oswald M. Peeters, Norbert M. Blaton, et al. "6-Methyl-4-phenylthieno[2,3-b]pyridine-2,5-dicarboxylic acid." Acta Crystallographica Section E Structure Reports Online 59, no. 4 (2003): o450—o452. http://dx.doi.org/10.1107/s1600536803005464.

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4

Han, Lizhi, Longyi Jin, Enbo Wang, and Zhongmin Su. "Synthesis and characterization of two isostructural 3d–4f coordination compounds based on pyridine-2,6-dicarboxylic acid and 4,4′-bipyridine." Acta Crystallographica Section C Structural Chemistry 75, no. 6 (2019): 723–27. http://dx.doi.org/10.1107/s2053229619006004.

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The design and synthesis of 3d–4f heterometallic coordination polymers have attracted much interest due to the intriguing diversity of their architectures and topologies. Pyridine-2,6-dicarboxylic acid (H2pydc) has a versatile coordination mode and has been used to construct multinuclear and heterometallic compounds. Two isostructural centrosymmetric 3d–4f coordination compounds constructed from pyridine-2,6-dicarboxylic acid and 4,4′-bipyridine (bpy), namely 4,4′-bipyridine-1,1′-diium diaquabis(μ2-pyridine-2,6-dicarboxylato)tetrakis(pyridine-2,6-dicarboxylato)bis[4-(pyridin-4-yl)pyridinium]co

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Cowan, John A., Judith A. K. Howard, Garry, J. McIntyre, Samuel M. F. Lo, and Ian D. Williams. "Variable-temperature neutron diffraction studies of the short, strong hydrogen bonds in the crystal structure of pyridine-3,5-dicarboxylic acid." Acta Crystallographica Section B Structural Science 61, no. 6 (2005): 724–30. http://dx.doi.org/10.1107/s0108768105030077.

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Pyridine-3,5-dicarboxylic acid has been studied by single-crystal neutron diffraction at 15 and 296 K. Pyridine-3,5-dicarboxylic acid, in which the carboxylic acid protons have been replaced by deuterons, has also been studied at 15, 150 and 296 K. The protonated structure contains a short N...H...O hydrogen bond [N...O 2.523 (2) Å at 15 K]. Temperature-dependent proton migration occurs where the N—H distance in the hydrogen bond changes from 1.213 (4) Å at 15 K to 1.308 (6) Å at 300 K. In the deuterated structure the overall hydrogen-bond length increased [N...O 2.538 (3) Å at 15 K] and the m

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6

Kremer, Marius, and Ulli Englert. "Zn and Ni complexes of pyridine-2,6-dicarboxylates: crystal field stabilization matters!" Acta Crystallographica Section E Crystallographic Communications 75, no. 6 (2019): 903–11. http://dx.doi.org/10.1107/s2056989019007461.

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Six reaction products of ZnII and NiII with pyridine-2,6-dicarboxylic acid (H2Lig1), 4-chloropyridine-2,6-dicarboxylic acid (H2Lig2) and 4-hydroxypyridine-2,6-dicarboxylic acid (H2Lig3) are used to pinpoint the structural consequences of crystal field stabilization by an incomplete d shell. The pseudo-octahedral ZnII coordination sphere in bis(6-carboxypicolinato)zinc(II) trihydrate, [Zn(C7H4NO4)2]·3H2O or [Zn(HLig1)2]·3H2O, (1), is significantly less regular than that about NiII in the isostructural compound bis(6-carboxypicolinato)nickel(II) trihydrate, [Ni(C7H4NO4)2]·3H2O or [Ni(HLig1)2]·3H

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7

Napitupulu, Mery, Geoffrey A. Lawrance, Guy J. Clarkson, and Peter Moore. "Methyl 2-[N-(2′-Pyridylmethyl)carbamyl]pyridine-6-carboxylate: A Precursor for Unsymmetrical Diamide Ligands." Australian Journal of Chemistry 59, no. 11 (2006): 796. http://dx.doi.org/10.1071/ch06310.

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Methyl 2-[N-(2′-pyridylmethyl)carbamyl]pyridine-6-carboxylate (H1), prepared by reaction of a 1:1 ratio of the methyl diester of pyridine-2,6-dicarboxylic acid and 2-aminomethylpyridine, can form 1:2 M:L complexes by acting as a tridentate ligand, as exemplified by a crystal structure analysis of [CoIII(1)2](ClO4) where each ligand is coordinated by the amido group and its two flanking pyridine groups, with the ester group, a relatively poor donor, remaining unbound. The acid formed upon ester hydrolysis, hydrogen 2-[N-(2′-pyridylmethyl)carbamyl]pyridine-6-carboxylate (H22), has been isolated

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8

Ghalia, Mohamed H., Mohamed Abd El-Hamid, Mohamed A. Zweil, Abd El-Galil E. Amr, and Shimaa A. Moafi. "Synthesis and Reactions of New Chiral Linear and Macrocyclic Tetraand Penta-peptide Candidates." Zeitschrift für Naturforschung B 67, no. 8 (2012): 806–18. http://dx.doi.org/10.5560/znb.2012-0116.

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9a A series of linear and macrocyclic pentapeptide derivatives have been prepared via the coupling of pyridine-2,6-dicarboxylic acid (1) or pyridine-2,6-dicarbonyl dichloride (2) with appropriate amino acid methyl esters. The coupling of 1or 2with aminoacid methyl esters gave the corresponding pyridine dipeptide methyl esters 3, which were hydrolyzed with sodium hydroxide to the corresponding acids 4. The latter compounds 4were coupled with other amino acid methyl esters to afford the corresponding tetrapeptide esters 5, which were hydrolyzed with sodium hydroxide to the corresponding acids 6.

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9

Liu, Haixing, and Ying Liu. "Study on a structure of pyridine-2, 6-dicarboxylic acid calcium boric acid hydrate, C7H16BCaNO12." IOP Conference Series: Earth and Environmental Science 769, no. 2 (2021): 022061. http://dx.doi.org/10.1088/1755-1315/769/2/022061.

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10

Park, Hyunjin, Myong Yong Choi, Cheol Joo Moon, and Tae Ho Kim. "Crystal structure ofN-[2-(cyclohexylsulfanyl)ethyl]quinolinic acid imide." Acta Crystallographica Section E Crystallographic Communications 73, no. 9 (2017): 1372–74. http://dx.doi.org/10.1107/s2056989017012142.

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The title compound, C15H18N2O2S {systematic name: 6-[2-(cyclohexylsulfanyl)ethyl]-5H-pyrrolo[3,4-b]pyridine-5,7(6H)-dione}, was obtained from the reaction of pyridine-2,3-dicarboxylic anhydride (synonym: quinolinic anhydride) with 2-(cyclohexylsulfanyl)ethylamine. The dihedral angle between the mean plane of the cyclohexyl ring and the quinolinic acid imide ring is 25.43 (11)°. In the crystal, each molecule forms two C—H...O hydrogen bonds and one weak C—O...π [O...ring centroid = 3.255 (2) Å] interaction with neighbouring molecules to generate a ladder structure along theb-axis direction. The

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Book chapters on the topic "6-pyridine-dicarboxylic acid"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with pyridine-4-hydroxy-2,6-dicarboxylic acid." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_484.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with pyridine-2,5-dicarboxylic acid and 1,10-phenanthroline." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_255.

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3

Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand nickel(II) complex with pyridine-2,5-dicarboxylic acid and 2,2′-bipyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_254.

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4

Devikala, Sundaramurthy, and Johnson Maryleedarani Abisharani. "Addition of Organic Compounds in Gelatin-biopolymer Gel Electrolyte for Enhanced Dye-sensitized Solar Cells." In Advances in Solar Photovoltaic Energy Systems. IntechOpen, 2024. http://dx.doi.org/10.5772/intechopen.1003045.

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This chapter introduced a new series of organic compound additives like thiophene 2,5-dicarboxylic acid (TDA), sulfanilamide (SAA), 2,6-diamino pyridine (DAP), dibenzo-18-crown-6 (DBC) and 2,6-pyridine dicarboxylic acid (PDA) with gelatin/KI/I2 consist gel polymer electrolytes for dye-sensitized solar cells (DSSCs) application. Nowadays, it is focusing on biopolymers for preparing gel electrolytes for DSSCs application which is a conventional renewable energy source. Biopolymers are abundant in nature, and they are non-toxic, thermally stable, environmentally friendly, low-cost, and have good

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