4,6-BIS-(N,N-DIALKYLAMINO)-S-TRIAZINES AND 2,4,6-TRIS-(N,N-DIALKYLAMINO)-S-TRIAZINES - SYNTHESIS, NMR-SPECTRA AND RESTRICTED ROTATIONS

Citation
Ar. Katritzky et al., 4,6-BIS-(N,N-DIALKYLAMINO)-S-TRIAZINES AND 2,4,6-TRIS-(N,N-DIALKYLAMINO)-S-TRIAZINES - SYNTHESIS, NMR-SPECTRA AND RESTRICTED ROTATIONS, Perkin transactions. 2, (4), 1995, pp. 785-792
Citations number
14
Categorie Soggetti
Chemistry Physical","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
03009580
Issue
4
Year of publication
1995
Pages
785 - 792
Database
ISI
SICI code
0300-9580(1995):4<785:4A2>2.0.ZU;2-9
Abstract
Syntheses of various symmetrically and non-symmetrically trisubstitute d triazines are reported. Dynamic NMR (H-1 and C-13) experiments demon strate that 2,4,6-tris(dialkylamino)-s-triazines show correlated rotat ions of the alkyl groups in the dialkylamino moieties. Unsymmetrical 2 -chloro-, 2-alkoxy- and 2-aryloxy-4,6-bis(di-n-alkylamino)-s-triazines display two non-equivalent n-alkyl groups, due to the restricted rota tion around the Ar-N bonds.