One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time. 81058-27-7, Name is (2R,3R,4S,5R,6R)-2-Bromo-6-((pivaloyloxy)methyl)tetrahydro-2H-pyran-3,4,5-triyl tris(2,2-dimethylpropanoate), formurla is C26H43BrO9. In a document, author is Aguiar de Souza, Isabela Cristina, introducing its new discovery. Name: (2R,3R,4S,5R,6R)-2-Bromo-6-((pivaloyloxy)methyl)tetrahydro-2H-pyran-3,4,5-triyl tris(2,2-dimethylpropanoate).
Investigation of cobalt(III)-phenylalanine complexes for hypoxia-activated drug delivery
Four cobalt(iii)-phenylalanine complexes, [Co(Phe)(py(2)en)](ClO4)(2)center dot H2O (1), [Co(Phe)(TPA)](ClO4)(2)center dot H2O (2), [Co(Phe)(py(2)enMe(2))](ClO4)(2)center dot H2O (3) and [Co(bipy)(2)(Phe)](ClO4)(2)center dot H2O (4), were investigated as prototype models for hypoxia-activated delivery of melphalan – a phenylalanine derivative anticancer drug of the class of nitrogen mustards. Single crystal X-ray diffraction analysis provided the molecular structures of 1-4, as a single isomer/conformer. According with NMR and theoretical calculations, the solid-state structures of 2 and 4 are maintained in solutions. For complexes 1 and 3, though, a mixture of isomers was found in DMSO solutions: Delta-cis alpha(exo,exo) and Delta-cis beta(1)(exo,exo) for 1 (3 : 2 ratio), and Delta-cis alpha(exo,exo) and Delta-cis alpha(exo,exo) for 3 (5 : 1 ratio). Theoretical calculations point to a re-equilibration reaction of the solid-state Delta-cis beta(1) isomer of 1 in solution. Electrochemical analysis revealed a correlation between the electron-donor capacity of the ancillary ligands and the redox potentials of the complexes. The potentials varied from +0.01 for 1 to +0.31 V vs. SHE for 4 in aqueous media and indicate that reduction should be achieved in biological media. The integrity of the complexes in pH 5.5 and 7.4 buffered solutions was confirmed by UV-Vis monitoring up to 24 h at 25 degrees C. Reduction by ascorbic acid (AA) shows an O-2-dependent dissociation of the L-Phe for complexes 1-3, with higher conversion rates at pH 7.4. For complex 4, a fast dissociation of L-Phe was observed, with conversion rates unaffected by the pH and presence of O-2.
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Reference:
Chiral nitrogen ligands in late transition metal-catalysed asymmetric synthesis¡ªI. Addressing the problem of ligand lability in rhodium-catalysed hydrosilations,
,Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis