Structural investigations of three triazines: solution-state NMR studies of internal rotation and structural information from solid-state NMR, plus a full structure determination from powder x-ray diffraction in one case

• Published in: Magnetic resonance in chemistry Vol. 41; no. 5; pp. 324 - 336
• Main Authors: Birkett, Helen E., Cherryman, Julian C., Chippendale, A. Margaret, Evans, John S. O., Harris, Robin K., James, Mark, King, Ian J., McPherson, Graham J.
• Format: Journal Article
• Language: English
• Published: Chichester, UK John Wiley & Sons, Ltd 01.05.2003; Wiley
• Subjects: 13C NMR; 15N NMR; 1H NMR; Chemistry; Chemistry, Multidisciplinary; Chemistry, Physical; conformation; magic-angle spinning; NMR; Physical Sciences; powder XRD; rotamers; Science & Technology; Spectroscopy; structure solution; Technology; triazines; RESTRICTED ROTATIONS; SERIES; N-15; SHIELDING TENSORS; 4,6-BIS-(N,N-DIALKYLAMINO)-S-TRIAZINES; conformation; SUBSTITUTED TRIAZINES; magic-angle spinning; NMR; triazines; H-1 NMR; C-13; rotamers; structure solution; N-15 NMR; powder XRD; C-13 NMR; SPECTRA; 2,4,6-TRIS-(N,N-DIALKYLAMINO)-S-TRIAZINES
• ISSN: 0749-1581; 1097-458X
• DOI: 10.1002/mrc.1185

Three model 2,4,6‐tris(amino)‐1,3,5‐triazines, structurally related to a dyestuff molecule previously studied by NMR, were synthesized in order to enable the effects of rotamer exchange on the NMR spectra to be investigated in more detail. Two of the compounds are novel. Internal rotation of the triazine ring substituents was studied by variable‐temperature solution‐state 1H, 13C and 15N NMR spectroscopy. All the expected rotamers were detected for each molecule. Rotamer exchange rates varied from slow to fast over the temperature range −40 to 90 °C, as observed for the dyestuff molecule itself. Solid‐state 13C and 15N NMR provided information about the structures of the solid molecules. A full crystal structure determination from high‐resolution powder x‐ray diffraction was achieved for one of the molecules using simulated annealing techniques. Ab initio MO and 15N NMR chemical shift calculations, based on energy‐minimized structures derived from the x‐ray structure determination, enabled the effect of intermolecular hydrogen bonding on the 15N NMR chemical shifts to be studied. The results compared favourably with the experimental solid‐state 15N NMR shifts. Copyright © 2003 John Wiley & Sons, Ltd.