Dennis A. Barnes
University of Akron
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SPIE's 27th Annual International Symposium on Microlithography | 2002
Ralph R. Dammel; Raj Sakamuri; Sang-Ho Lee; Dalil Rahman; Takanori Kudo; Andrew R. Romano; Larry F. Rhodes; John-Henry Lipian; Cheryl Hacker; Dennis A. Barnes
The copolymerization reaction between methyl cyanoacrylate (MCA) and a variety of cycloolefins (CO) was investigated. Cycololefin/cyanoacrylate (COCA) copolymers were obtained in good yields and with lithographically interesting molecular weights for all cycoolefins studied. Anionic MCA homopolymerization could be largely suppressed using acetic acid. Based on NMR data, the copolymerization may tend to a 1:1 CO:MCA incorporation ratio but further work with better suppression of the anionic component is needed to confirm this. Lithographic tests on copolymers of appropriately substituted norbornenes and MCA showed semi-dense and isolated line performance down to 90 nm.
Advances in resist technology and processing. Conference | 2005
Larry F. Rhodes; Chun Chang; Cheryl Burns; Dennis A. Barnes; Brian Bennett; Larry Seger; Xiaoming Wu; Andy Sobek; Mike Mishak; Craig Peterson; Leah J. Langsdorf; Hideo Hada; Hiroaki Shimizu; Kazuhito Sasaki
Of all candidate 193 nm photoresist binder resins, transition metal catalyzed vinyl addition cyclic olefin (i.e., norbornene) polymers (PCO) hold the promise of high transparency and excellent etch resistance. In order to access lower molecular weight polymers, which are typically used in photoresists, α-olefin chain transfer agents (CTAs) are used in synthesizing vinyl addition poly(norbornenes). For example, HFANB (α,α-bis(trifluoromethyl)bicyclo [2.2.1]hept-5-ene-2-ethanol) homopolymers (p(HFANB)) with molecular weights (Mn) less than 5000 have been synthesized using such chain transfer agents. However, the optical density (OD) at 193 nm of these materials was found to rise as their molecular weights decreased consistent with a polymer end group effect. Extensive NMR and MS analysis of these polymers revealed that olefinic end groups derived from the chain transfer agent were responsible for the deleterious rise in OD. Chemical modification of these end groups by epoxidation, hydrogenation, hydrosilation, etc. lowers the OD of the polymer by removing the olefinic chromophore, however, it does require a second synthetic step. Thus a new class of non-olefinic chain transfer agents has been developed at Promerus that allow for excellent control of vinyl addition cyclic olefin polymer molecular weight and low optical density without the need of a post-polymerization chemical modification. Low molecular weight homopolymers of HFANB have been synthesized using these chain transfer agents that exhibit ODs ≤ 0.07 absorbance units per micron. This molecular weight control technology has been applied to both positive tone and negative tone vinyl addition cyclic olefin binder resins. Lithographic and etch performance of positive tone photoresists based on these binder resins will be presented.
Macromolecules | 2003
Dennis A. Barnes; George M. Benedikt; Brian L. Goodall; Shyhchang S. Huang; Heather A. Kalamarides; Susan Lenhard; Lester H. McIntosh; K. T. Selvy; Robert A. Shick; Larry F. Rhodes
Archive | 1994
Brian L. Goodall; George M. Benedikt; Lester H. McIntosh; Dennis A. Barnes; Larry Funderburk Rhodes
Archive | 1993
Brian L. Goodall; George M. Benedikt; Lester H. McIntosh; Dennis A. Barnes
Archive | 1996
Brian L. Goodall; Lester H. McIntosh; Dennis A. Barnes
Archive | 2004
Larry F. Rhodes; Dennis A. Barnes; Andrew Simon Bell; Brian K. Bennet; Chung Chang; John-Henry Lipian; Xiaoming Wu
Archive | 1989
Lindwood P. Tenney; David John Smith; Dennis Joseph Janda; Dennis A. Barnes
Archive | 2006
Larry F. Rhodes; Dennis A. Barnes; Andrew Simon Bell; Brian K. Bennett; Chun Chang; John-Henry Lipian; Xiaoming Wu
Macromolecular Chemistry and Physics | 2005
Chun Chang; John Lipian; Dennis A. Barnes; Larry Seger; Cheryl Burns; Brian Bennett; Laura Bonney; Larry F. Rhodes; George M. Benedikt; Robert P. Lattimer; Shyhchang S. Huang; Victor W. Day