Abstract
A furan-containing polymer turned to a gel and then solidified in 1,1,2,2-tetrachloroethane solution in the presence of fullerene C60 under visible light irradiation. The reaction mechanism involved the polycondensation of furan units via singlet oxygen generated from the excited triplet state of C60. This photo-crosslinking process was applied to a photoresist having sensitivity in the visible region. The first example was demonstrated for the micron size photolithographic patterning using the furan-containing polymer/fullerene system.
Similar content being viewed by others
Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
References
E. T. Samulski, J. M. DeSimone, M. O. Hunt, Y. Z. Menceloglu, R. C. Jarnagin, G. A. York, K.B. Labat, and H. Wang, Chem. Mater., 4, 1153 (1992).
K. E. Geckeler and A. Hirsch, J. Am. Chem. Soc., 115, 3850 (1993).
N. Manalova, I. Rashkov, F. Beguin, and H. V. Damme, J. Chem. Soc., Chem. Commun., 1725 (1993).
A. O. Patil, G. W. Schriver, B. Carstensen, and R. D. Lundberg, Polym. Bull., 30, 187 (1993).
C. J. Hawker, Macromolecules, 27, 4836 (1994).
K. I. Guhr, M. D. Greaves, and V. M. Rotello, J. Am. Chem. Soc., 116, 5997 (1994).
Y. Wang, Nature, 356, 585 (1992).
S. M. Silence, C. A. Walsh, J. C. Scott, and W. E. Moerner, Appl. Phys. Lett., 61, 2967 (1992).
Y. Tajima, Y. Tezuka, H. Yajima, T. Ishii, and K. Takeuchi, Polym. Commun., in press.
E. Fukuda and M. Kaibara, Thrombosis Res., 8 (Suppl. II), 49, (1976).
Y. Tajima, H. Arai, Y. Tezuka, T. Ishii, and K. Takeuchi, Fullerene Sci. Tech., in press.
H.-J. Schumacher and J. Stauff, Chemie, 55, 341 (1942).
N. Galego and A. Gandini, J. Polym. Sci., Polym. Chem. Ed., 15, 1027 (1977).
Y. Tajima, H. Masuko, and N. Bessho, Japan Print Associate, 118, 32 (1994).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Tajima, Y., Tezuka, Y., Ishii, T. et al. Application of a Furan-Containing Polymer/Fullerene System to Photolithography. Polym J 29, 1016–1019 (1997). https://doi.org/10.1295/polymj.29.1016
Issue date:
DOI: https://doi.org/10.1295/polymj.29.1016
Keywords
This article is cited by
-
Visible light-curable polymers for biomedical applications
Science China Chemistry (2014)
-
Photocurable O-carboxymethyl chitosan derivatives for biomedical applications: Synthesis, in vitro biocompatibility, and their wound healing effects
Macromolecular Research (2012)
-
Synthesis of visible light-induced cross-linkable chitosan as an anti-adhesive agent
Macromolecular Research (2011)


