1976•Spectroscopy LettersRequires access

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

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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.

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Available 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.

Key concepts: Protonation, Chemistry, Tautomer, Molecule, Chemical shift, Pyridine, Amine gas treating, Carbon-13 NMR

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