2014
DOI: 10.1039/c3tc32048k
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A degradable polycyclic cross-linker for UV-curing nanoimprint lithography

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Cited by 20 publications
(13 citation statements)
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“…However, the vast majority of these cross-linkers are labile to acidic hydrolysis conditions, with only one example of cross-linker being readily amenable to cleavage under basic conditions. Regarding the former type of cross-linkers, these include several acetal di(meth)acrylates or diacrylamides, [3][4][5][6][7][8][9][10][11][12][13][14][15] hemiacetal ester dimethacrylates, 16,17 ketal di(meth)acrylates, diacrylamides, or di(N-vinylformamides), [18][19][20][21][22][23][24][25][26] silyl ether di(meth)acrylates, 27,28 and tertiary ester di(meth)acrylates. [29][30][31][32][33] Regarding the latter type, the only example of cross-linker spontaneously degradable under alkaline hydrolysis conditions is, to the best of our knowledge, tetrafluorophenylene diacrylate, 34 which is very costly to prepare because of its perfluorinated ring.…”
mentioning
confidence: 99%
“…However, the vast majority of these cross-linkers are labile to acidic hydrolysis conditions, with only one example of cross-linker being readily amenable to cleavage under basic conditions. Regarding the former type of cross-linkers, these include several acetal di(meth)acrylates or diacrylamides, [3][4][5][6][7][8][9][10][11][12][13][14][15] hemiacetal ester dimethacrylates, 16,17 ketal di(meth)acrylates, diacrylamides, or di(N-vinylformamides), [18][19][20][21][22][23][24][25][26] silyl ether di(meth)acrylates, 27,28 and tertiary ester di(meth)acrylates. [29][30][31][32][33] Regarding the latter type, the only example of cross-linker spontaneously degradable under alkaline hydrolysis conditions is, to the best of our knowledge, tetrafluorophenylene diacrylate, 34 which is very costly to prepare because of its perfluorinated ring.…”
mentioning
confidence: 99%
“…Z‐shrinkage was calculated by measuring the difference in thicknesses of the UV‐curable material spin‐coated on silicon wafer before and after the UV‐curing process. In our previous study, compared with the lateral shrinkage, the Z‐shrinkage of the UV‐curable film contributed mostly to volume shrinkage . Figure e shows the experimental shrinkages of film thicknesses of DP resist and other three UV‐curable acrylated materials after the UV‐curing process (DP resist, 1.35%; DAMTT, 2.48%; pentaerythritol triacrylate, 4.17%; CN975, 7.08%; CN996, 6.17%).…”
Section: Resultsmentioning
confidence: 84%
“…2,10‐Diacryloyloxymethyl‐1,4,9,12‐tetraoxaspiro[4.2.4.2] tetradecane was made in our laboratory . Pentaerythritol tetra (3‐mercaptopropionate) (PETMP) was purchased from Sigma–Aldrich.…”
Section: Methodsmentioning
confidence: 99%
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“…UV‐curing soft nanoimprint lithography using soft polymeric stamps has been widely used to fabricate nanopatterns on both planar and curved surfaces . Adhesion between mould and the imprinted resist is greatly improved due to the high density of the nanoscale structure.…”
mentioning
confidence: 99%