1985
DOI: 10.1021/bk-1985-0282.ch006
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Thermally Stable Polymers for Electronic Applications

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Cited by 10 publications
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“…Quantitative XPS data shown in Table confirm this result by showing that no carbon atom from C⋮C is observed and 38.2% carbon atoms in the form of CC are detected on the surface of poly(1,8-dibutyl-1,3,5,7-octatetrayne) microbeads. Therefore, it can be surmised that the main reactions for the polymerization involve the conversion of sp 1 -hybridized carbon atoms in the molecule of 1,8-dibutyl-1,3,5,7-octatetrayne into sp 2 -hybridized carbon atoms by a variety of triple bond additions 21 (Scheme ) including [4+2] cycloaddition and any further cyclizations , to form graphite-like structures.
2 Triple Bond Additions and Cyclization in the Polymerization of 1,8-Dibutyl-1,3,5,7-octatetrayne
…”
Section: Resultsmentioning
confidence: 99%
“…Quantitative XPS data shown in Table confirm this result by showing that no carbon atom from C⋮C is observed and 38.2% carbon atoms in the form of CC are detected on the surface of poly(1,8-dibutyl-1,3,5,7-octatetrayne) microbeads. Therefore, it can be surmised that the main reactions for the polymerization involve the conversion of sp 1 -hybridized carbon atoms in the molecule of 1,8-dibutyl-1,3,5,7-octatetrayne into sp 2 -hybridized carbon atoms by a variety of triple bond additions 21 (Scheme ) including [4+2] cycloaddition and any further cyclizations , to form graphite-like structures.
2 Triple Bond Additions and Cyclization in the Polymerization of 1,8-Dibutyl-1,3,5,7-octatetrayne
…”
Section: Resultsmentioning
confidence: 99%
“…9 However, its low solubility and crystalline nature make it difficult to form a stable thin film. 10 Several studies have been carried out to solve this problem. Stille and Whitesides incorporated a solubilizing aliphatic side group.…”
Section: Introductionmentioning
confidence: 99%
“…Poly( m -diethynylbenzene), discovered initially in the early 1960s by Hay and co-workers, was chosen in this study as a starting material because of its high thermal stability, low moisture pickup, low dielectric constant, and possible lithographic sensitivity. , Moreover, it can form a highly condensed aromatic structure after curing, which would provide high Young's modulus and hardness . However, its low solubility and crystalline nature make it difficult to form a stable thin film . Several studies have been carried out to solve this problem.…”
Section: Introductionmentioning
confidence: 99%