Polyphotolysis, namely the behavior of polyfunctional photoactive component
s (PACs), is an important aspect of dissolution inhibition resists. Polyfun
ctional PACs produce higher lithographic contrast and lead to higher line r
esolution. The effect is so important that trifunctional diazonaphthoquinon
e PACs have become the industry standard, virtually eliminating the use of
the corresponding monofunctional inhibitors. We believe that polyphotolysis
depends on an interaction between phenolic strings emanating from the acce
ptor groups of PACs located on the same backbone molecule. In the coating s
olution the strings of the PACs meet and connect with each other, and these
connections survive into the solid resist film. After partial exposure som
e of the strings are severed from their anchors and would lose their inhibi
ting power, were it not for an unexpected effect that allows the severed st
rings to be reconnected to still polarized, "living" strings. In this proce
ss of reconnection the living strings increase in length, and the final res
ult of exposure is the replacement of two shorter polarized strings by a si
ngle longer one. Inhibition depends on the overall number of phenolic units
taking part in polarized strings. If there is only a small change in the o
verall length of the phenolic strings in the system, there will be only a s
mall change in dissolution rate. That is precisely what Trefonas and Daniel
s observed.