1989
DOI: 10.1021/bk-1989-0412.ch003
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Chemically Amplified Resists

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Cited by 6 publications
(3 citation statements)
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“…Consequently, 193 nm resists could be designed using the same PAGs as those that are in use with 248 nm resists. In addition to absorption, the considerations in designing a PAG are solubility, volatility of both the PAG and its photoproducts, acid strength, cost, and toxicity 5c. For tert- butyl-substituted materials, high acid strength (often superacids are required) and high postexposure bake (PEB) temperatures are required for complete removal of the ester appendage.…”
Section: Alicyclic Polymers For 193 Nm Imagingmentioning
confidence: 99%
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“…Consequently, 193 nm resists could be designed using the same PAGs as those that are in use with 248 nm resists. In addition to absorption, the considerations in designing a PAG are solubility, volatility of both the PAG and its photoproducts, acid strength, cost, and toxicity 5c. For tert- butyl-substituted materials, high acid strength (often superacids are required) and high postexposure bake (PEB) temperatures are required for complete removal of the ester appendage.…”
Section: Alicyclic Polymers For 193 Nm Imagingmentioning
confidence: 99%
“…Additionally, high glass transition temperature ( T g ) polymers based on N-blocked maleimide/styrene resins and substituted styrene-sulfone copolymers have been explored . Notably, the first commercially available positive 248 nm resist was introduced in 1990 after almost 10 years of research, and was based on the copolymer derived from tert -butoxycarbonyloxystyrene and sulfur dioxide used in conjunction with a nitrobenzyl tosylate photoacid generator material …”
Section: Introduction and Historical Perspectivementioning
confidence: 99%
“…Examp les include poly(hy droxystyrene) (109), poly(vinyl benzoate) (157), poly(methacrylic acid) (153), N-blocked malei mide/styrene resins (158,159), and poly(hy droxyphenyl methacrylat e) (160). A matrix polymer that combines the advantages of chemically amplified deprotection with conventional chain scission processes is poly( 4-t-butoxy carb onyloxystyrene-sulfone) (PTBSS) (161,162). As in the case of PTBS, the t-butoxycarbonyl moiety is used as the acid-labile protective group.…”
Section: Deprotection Chemistrymentioning
confidence: 99%