The photochemistry of a series of bis(sulfonyl)diazomethanes was investigat
ed in solution and in low temperature matrices. These diazo compounds are o
f interest as photoacid generators in photoresists for deep UV lithography.
Triplet carbenes could be trapped in solution, but attempts to isolate the
carbenes in argon matrices at 10 K were unsuccessful, the corresponding su
lfenes and other rearranged products being observed under these conditions
instead. This is in line with DFT and ab initio calculations, which predict
the singlet carbenes to be transition states on the pathway to oxathiirene
oxides, which can be looked upon as intramolecularly stabilized carbenes.
The triplet carbenes lie energetically above the singlet transition states
and so are not expected to have a prolonged lifetime even in low-temperatur
e matrices.