A positive-working alkaline developable photoresist based on partially tert-Boc-protected calix[4]resorcinarene and a photoacid generator

A positive working low-molecular-weight photoresist based on partially t-Boc protected tetra-C-methylcalix[4]resorcinarene (t-Boc C-4-R) and a photoacid generator (PAG), diphenyliodonium 9,10-dimethoxyanthracene-2-sulfonate (DIAS) has been developed. t-Boc C-4-Rs were prepared by the reaction of C-4-R with di-tert-butyl dicarbonate in the presence of 4-dimethylaminopyridine (DMAP). A clear film cast from a 20 wt% t-Boc C-4-R solution in cyclohexanone showed high transparency to UV above 300 nm. The appropriate t-Boc protecting ratio was about 60 mol% in view of adhesion, deprotection temperature and dissolution rate. The photoresist consisting of 60 mol% t-Boc C-4-R (95 wt%) and DIAS (5 wt%) showed a sensitivity of 13 mJ cm−2 and a contrast of 12.6 when it was exposed to 365 nm light and postbaked at 105 °C for 90 s, followed by developing with a 2.38 wt% aqueous tetramethylammonium hydroxide (TMAH) solution at room temperature. A fine positive image featuring 1.5 µm of minimum line and space patterns was observed on the film of the photoresist exposed to 40 mJ cm−2 of UV-light at 365 nm by the contact mode.

[1]  T. Fujigaya,et al.  A New Photoresist Based on Poly(propyleneimine) Dendrimer. , 2000 .

[2]  C. Quate,et al.  Synthesis and Preparation of Ionically Bound Dendrimer Monolayers and Application toward Scanning Probe Lithography , 1999 .

[3]  Lewis W. Flanagin,et al.  Surface roughness development during photoresist dissolution , 1999 .

[4]  Osamu Haba,et al.  A New Photoresist Based on Calix[4]resorcinarene Dendrimer , 1999 .

[5]  G. Gonzalez,et al.  Clusters of C60 Molecules , 1999 .

[6]  M. Ueda,et al.  A New Three-Component Photoresist Based on Calix[4]resorcinarene Derivative, a Cross-linker, and a Photo-acid Generator , 1998 .

[7]  Osamu Haba,et al.  Three-Component Negative-Type Photoresist Based on Calix[4]resorcinarene, a Cross-linker, and a Photoacid Generator , 1998 .

[8]  Hiroshi Ito,et al.  The “Living” Free Radical Synthesis of Poly(4-hydroxystyrene): Physical Properties and Dissolution Behavior , 1998 .

[9]  Lewis W. Flanagin,et al.  The Mechanism of Phenolic Polymer Dissolution: A New Perspective , 1997 .

[10]  A. Reiser,et al.  Percolation View of Novolak Dissolution. 5. The Dissolution of Exposed Resist Films , 1996 .

[11]  Y. Kawai,et al.  Characteristics of a Monodisperse PHS-Based Positive Resist (MDPR) in KrF Excimer Laser Lithography , 1992 .

[12]  Enrico Dalcanale,et al.  Host-guest complexation. 48. Octol building blocks for cavitands and carcerands , 1989 .

[13]  Jean M. J. Fréchet,et al.  Phase transfer catalysis in the tert-butyloxycarbonylation of alcohols, phenols, enols, and thiols with di-tert-butyl dicarbonate , 1985 .

[14]  Hiroshi Ito,et al.  Poly(p-tert-butoxycarbonyloxystyrene): a convenient precursor to p-hydroxystyrene resins , 1983 .

[15]  D. K. Owens,et al.  Estimation of the surface free energy of polymers , 1969 .