Studies of the Mechanism of the Jaffé Reaction, II: Configurational and Conformational Studies Using <sup>1</sup>H and <sup>13</sup>C NMR Spectroscopy

Kovar, Karl‐Artur; Rupp, K. A.

doi:10.1002/ardp.19843170615

Cited by 3 publications

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“…In the present spectrophotometric study, the 1:1 red and 2: l orange colored complexes were easily identified by their corresponding absorption maxima near 490 nanometers and 390 nanometers, respectively (6). Upon the addition of excess creatinine to alkaline picrate blank Solutions, a mixture of l : l and 2: l complexes readily formed.…”

Section: Discussionmentioning

confidence: 51%

Jaffe’ Reaction Products

Ng¹,

Blass²

1986

Clinical Chemistry and Laboratory Medicine

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Polarographic and spectrophotometric studies of the interaction of creatinine with alkaline picrate have been undertaken in sodium hydroxide concentrations ranging between 0.95 and 4.5 mol/1. Red colored l : l and orange colored 2 : l creatinine-picrate complexes readily formed along with orange colored 1:1:1 creatinine-picrate-hydroxide complexes. The red and orange colored complexes were easily identified by their corresponding absorption maxima near 490 nanometers and 390 nanometers, respectively.Alkaline picrate polarograms showed three well-defined nitro group reduction waves with approximate halfwave potentials of -0.60 volts, -0.77 volts, and -0.91 volts. Increased concentrations of hydroxide and/ or creatinine resulted in a decreased diffusion current for reduction waves l -3 and the appearance of a fourth reduction wave, with an approximate half-wave potential of -1.24 volts. Further increases in base and/or creatinine concentration resulted in the disappearance of reduction waves 1 -3, with only reduction wave 4 remaining. Based upon the experimental data, a tri-nitro anion structure has been assigned for the 2: l complex.

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Section: Discussionmentioning

confidence: 51%