Interpretation of the Longitudinal ¹³C Nuclear Spin Relaxation and Chemical Shift Data for Five Bromoazaheterocycles Supported by Nonrelativistic and Relativistic DFT Calculations

Abstract

The longitudinal relaxation times of (13)C nuclei and NOE enhancement factors for 2-bromopyridine (1), 6-bromo-9-methylpurine (2), 3,5-dibromopyridine (3), 2,4-dibromopyrimidine (4), and 2,4,6-tribromopyrimidine (5) have been measured at 25 °C and B0 = 11.7 T. The most important contributions to the overall relaxation rates of nonbrominated carbons, i.e., the relaxation rates due to the (13)C-(1)H dipolar interactions and the shielding anisotropy mechanism, have been separated out. For 3 and 5, additionally, the T2,Q((14)N) values have been established from (14)N NMR line widths. All of these data have been used to determine rotational diffusion tensors for the investigated molecules. The measured saturation recovery curves of brominated carbons have been decomposed into two components to yield relaxation times, which after proper corrections provided parameters characterizing the scalar relaxation of the second kind for (13)C nuclei of (79)Br- and (81)Br-bonded carbons. These parameters and theoretically calculated quadrupole coupling constants for bromine nuclei have allowed the values of one-bond (13)C-(79)Br spin-spin coupling constants to be calculated. Independently, the coupling constants and magnetic shielding constants of the carbon nuclei have been calculated theoretically using the nonrelativistic and relativistic DFT methods F/6-311++G(2d,p)/PCM and so-ZORA/F/TZ2P/COSMO (F = BHandH or B3LYP), respectively. The agreement between the experimental and theoretical values of these parameters is remarkably dependent on the theoretical method used.

Orotic Acid in Water Solution, a DFT and 13C NMR Spectroscopic Study

“…Continuing our NMR studies on solution structures of biologically important compounds, − we devote this work to orotic acid, known also as vitamin B-13, which is an important natural product, structurally related to uracil. In living organisms it is a precursor of pyrimidine bases of nucleic acids .…”