Synthesis and radical polymerization of pyrocarbonate-functionalized monomers: application to positive-tone photoresists

Citation
S. Vansteenkiste et al., Synthesis and radical polymerization of pyrocarbonate-functionalized monomers: application to positive-tone photoresists, MACRO RAPID, 20(6), 1999, pp. 333-336
Citations number
12
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
MACROMOLECULAR RAPID COMMUNICATIONS
ISSN journal
10221336 → ACNP
Volume
20
Issue
6
Year of publication
1999
Pages
333 - 336
Database
ISI
SICI code
1022-1336(199906)20:6<333:SARPOP>2.0.ZU;2-0
Abstract
The synthesis of two new tert-butyl carbonic anhydride monomers, 4-vinylben zoic and methacrylic tert-butylcarbonic anhydride was achieved successfully . Radical polymerization at 45 degrees C yielded tert-butyl pyrocarbonate p rotected materials. Thermographic analysis showed that both polymers decomp ose cleanly at 135 degrees C. The lithographic performance of both material s was evaluated in the presence of 2,4,6-tris-(trichloromethyl)-s-triazine as photoacid generating species. It was demonstrated that the large polarit y change results in a positively working chemically amplified photoresist s ystem.