P. Kirsch et al., Bis(4-nitrophenyl)tetrafluorosulfuranes: Synthesis, isomerization and structural characterization, J AM CHEM S, 121(49), 1999, pp. 11277-11280
Due to their octahedral symmetry, otherwise not available for carbon based
chemistry, hypervalent sulfur fluorides are very attractive as structural b
uilding blocks for functional organic materials. Direct fluorination offers
a convenient access to multigram quantities of highly stable bis(4-nitroph
enyl)tetrafluorosulfurane Guided by molecular modeling, a novel catalytic p
rocess was devised to isomerize the predominantly formed cis isomer to the
pure trans isomer.