The Use of Protonation Induced Changes in Carbon-13 NMR Chemical Shifts to Investigate the Solution Microscopic Structure of Partially Protonated Polybasic Molecules
Joseph E. Sarneski, Henry L. Surprenant, Charles N. Reilley
Abstract
Joseph E. Sarneski, Henry L. Surprenant, Charles N. Reilley
Abstract
Changes in the NMR chemical shift of carbon-13 nuclei upon protonation of a nearby basic center are shown to be a useful method of probing the microscopic site of protonation of molecules containing multiple basic centers, such as diethylenetriaminepenta-acetic acid (DTPA). This approach is also shown to support the predominance of the pyridine amine protonated tautomer in the 4-pyridone ↔ 4-hydroxypyridine equilibrium.
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Changes in the NMR chemical shift of carbon-13 nuclei upon protonation of a nearby basic center are shown to be a useful method of probing the microscopic site of protonation of molecules containing multiple basic centers, such as diethylenetriaminepenta-acetic acid (DTPA). This approach is also shown to support the predominance of the pyridine amine protonated tautomer in the 4-pyridone ↔ 4-hydroxypyridine equilibrium.
Key concepts: Protonation, Chemistry, Tautomer, Molecule, Chemical shift, Pyridine, Amine gas treating, Carbon-13 NMR