Chemical Speciation and Coordination Behavior of 8‑Hydroxyquinoline-2-carboxylic Acid with Divalent Cations in Aqueous Solution: An Irving-Williams Series Study. [PDF]
Baryłka A +12 more
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Precise Carboxylic Acid-Functionalized Polyesters in Reprocessable Vitrimers. [PDF]
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The rsmA mutant from Pseudomonas aeruginosa ID4365 is a non-virulent strain that is suitable for pyocyanin and phenazine-1-carboxylic acid production. [PDF]
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Bifunctional Iminophosphorane Superbases Enable the Highly Enantioselective Sulfa-Michael Addition to Fully Substituted Cyclopropene Carboxylic Acid Derivatives. [PDF]
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Acidity of Carboxylic Acids: A Rebuttal and Redefinition
Journal of the American Chemical Society, 2001A recent theory of ionization of carboxylic acids divided the process of ionization into two steps and attributed the main importance to the electrostatic potential of the acid molecule. The origin of the acidity was thus seen in the high energy of the acid molecule and not in the stabilization of the anion by resonance.
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Behavior of carboxylic acids and carboxylic anhydrides in sulfuric acid
Canadian Journal of Chemistry, 1967The behavior of some carboxylic acids and anhydrides in sulfuric acid has been investigated by cryoscopic and conductimetric measurements in 100% H2SO4, cryoscopic measurements in aqueous H2SO4, and conductimetric titrations in dilute oleum.The previously established behavior of acetic anhydride in dehydrating sulfuric acid, [Formula: see text]is ...
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This chapter discusses carboxylic acids that generally have high mobilities compared with those of proteins. Carboxylic acids used as model substances for checking both theoretical aspects and correct functioning of the equipment are separated qualitatively and quantitatively by isotachophoresis.
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Phenanthrene-4-carboxylic Acid and 1,2-Dihydrophenanthrene-4-carboxylic Acid
Acta Crystallographica Section C Crystal Structure Communications, 1998Phenanthrene-4-carboxylic acid, C15H10O2, crystallized in the centrosymmetric space group P2(1)/n, while 1,2-dihydrophenanthrene-4-carboxylic acid, C15H12O2, crystallized in the centrosymmetric space group Pbca. In each structure, there is a single type of hydrogen bond: it is of the cyclic dimer type about a center of symmetry.
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Carboxylic Acid Reductase Can Catalyze Ester Synthesis in Aqueous Environments
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