TRIFLUORO-6,8-DIMETHYL-3-TRIFLUOROMETHYLPHENAZINE, C15H8F6N2, PRODUCED VIA THERMOLYSIS OF PERFLUORO-4-AZIDOTOLUENE IN THE PRESENCE OF 2,4,6-TRIMETHYLANILINE
Re. Banks et al., TRIFLUORO-6,8-DIMETHYL-3-TRIFLUOROMETHYLPHENAZINE, C15H8F6N2, PRODUCED VIA THERMOLYSIS OF PERFLUORO-4-AZIDOTOLUENE IN THE PRESENCE OF 2,4,6-TRIMETHYLANILINE, Acta crystallographica. Section C, Crystal structure communications, 49, 1993, pp. 1988-1990
Despite extensive substitution, the dimensions of the planar phenazine
rings remain very close to those of the unsubstituted molecule [Wozni
ak, Kariuki and Jones (1991). Acta Cryst. C47, 1113-1114]. Typically,
the molecules form stacks in which fluorinated rings overlap methylate
d rings of adjacent molecules.