dc.citation.conferencePlace |
US |
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dc.citation.conferencePlace |
Santa Clara, California |
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dc.citation.title |
SPIE Conference on Advances in Resist Technology and Processing XV |
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dc.citation.volume |
3678 |
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dc.contributor.author |
Kim, Jin-Baek |
- |
dc.contributor.author |
Park, Jong Jin |
- |
dc.contributor.author |
Jang, Ji-Hyun |
- |
dc.contributor.author |
Kim, Jae-Young |
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dc.date.accessioned |
2023-12-20T06:38:41Z |
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dc.date.available |
2023-12-20T06:38:41Z |
- |
dc.date.created |
2014-12-23 |
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dc.date.issued |
1999-03-01 |
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dc.description.abstract |
We have examined a novel class of ketal based deep UV photoresist. 1,4-Dioxaspiro(4,4)nonane-2-methyl methacrylate was synthesized and polymerized. A ketal group of poly(1,4- dioxaspiro(4,4)nonane-2-methyl methacrylate) hydrolyzes under acid catalysis to give two alcohol functionalities and a cyclopentanone molecule. The ketal polymer is insoluble in an aqueous developer, while the hydrolyzed products are soluble.It was found the cyclopentanone product affects diffusion of acid in the resist. As a result, the generated cyclopentanone increases mobility of the acid significantly. |
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dc.identifier.bibliographicCitation |
SPIE Conference on Advances in Resist Technology and Processing XV, v.3678 |
- |
dc.identifier.doi |
10.1117/12.350247 |
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dc.identifier.uri |
https://scholarworks.unist.ac.kr/handle/201301/52331 |
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dc.publisher |
SPIE |
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dc.title |
Chemically amplifed resists based on acrylate polymers containing ketal groups in the side chains |
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dc.type |
Conference Paper |
- |
dc.date.conferenceDate |
1999-03-01 |
- |