Methods for determining relative binding energy of monomers and methods of using the same
US-2015338423-A1 · Nov 26, 2015 · US
US2016145379A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016145379-A1 |
| Application number | US-201514886121-A |
| Country | US |
| Kind code | A1 |
| Filing date | Oct 19, 2015 |
| Priority date | Nov 24, 2014 |
| Publication date | May 26, 2016 |
| Grant date | — |
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A monomer, a polymer, an organic layer composition, an organic layer and associated methods, the monomer being represented by Chemical Formula 1:
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What is claimed is: 1 . A monomer represented by Chemical Formula 1: wherein, in Chemical Formula 1, A 1 , A 2 , A 3 , A 4 , and A 5 are each independently a substituted or unsubstituted aromatic ring group, X 1 , X 2 , X 3 , and X 4 are each independently a hydroxy group, a substituted or unsubstituted amino group, a halogen atom, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C3 to C30 cycloalkenyl group, a substituted or unsubstituted C1 to C20 alkylamine group, a substituted or unsubstituted C7 to C20 arylalkyl group, a substituted or unsubstituted C1 to C20 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 heteroaryl group, a substituted or unsubstituted C1 to C4 alkyl ether group, a substituted or unsubstituted C7 to C20 arylalkylene ether group, a substituted or unsubstituted C1 to C30 haloalkyl group, or a combination thereof, C 1 , C 2 , C 3 , C 4 , D 1 , D 2 , D 3 , D 4 , E 1 , E 2 , E 3 , and E 4 are each independently hydrogen atom, hydroxy group, a substituted or unsubstituted amino group, a halogen atom, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C3 to C30 cycloalkenyl group, a substituted or unsubstituted C1 to C20 alkylamine group, a substituted or unsubstituted C7 to C20 arylalkyl group, a substituted or unsubstituted C1 to C20 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 heteroaryl group, a substituted or unsubstituted C1 to C4 alkyl ether group, a substituted or unsubstituted C7 to C20 arylalkylene ether group, a substituted or unsubstituted C1 to C30 haloalkyl group, or a combination thereof, and a, b, and c are each independently 0 or 1. 2 . The monomer as claimed in claim 1 , wherein A 1 , A 2 , A 3 , A 4 and A 5 are each independently a substituted or unsubstituted aromatic ring group below: wherein, in the groups above, Z 1 is a single bond, a substituted or unsubstituted C1 to C20 alkylene group, a substituted or unsubstituted C3 to C20 cycloalkylene group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C2 to C20 heteroarylene group, a substituted or unsubstituted C2 to C20 alkenylene group, a substituted or unsubstituted C2 to C20 alkynylene group, C═O, NR a , oxygen (O), sulfur (S), or a combination thereof, wherein R a is hydrogen, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C2 to C20 heteroarylene group, a halogen atom, or a combination thereof, Z 3 to Z 18 are each independently C═O, NR a , oxygen (O), sulfur (S), CR b R c or a combination thereof, in which R a to R c are each independently hydrogen, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C2 to C20 heteroarylene group, a halogen atom, a halogen-containing group, or a combination thereof. 3 . The monomer as claimed in claim 1 , wherein at least one of X 1 and X 2 is a hydroxy group. 4 . The monomer as claimed in claim 3 , wherein: a, b, and c are 1, and at least one of X 3 and X 4 is a hydroxy group. 5 . The monomer as claimed in claim 3 , wherein: a is 0, b and c are 1, and at least one of X 3 and X 4 is a hydroxy group. 6 . The monomer as claimed in claim 1 , wherein: at least one of C 1 , D 1 and E 1 is a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof, and at least one of C 2 , D 2 and E 2 is a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof. 7 . The monomer as claimed in claim 1 , wherein: a, b, and c are 1, at least one of C 3 , D 3 and E 3 is a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof, and at least one of C 4 , D 4 and E 4 is a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof. 8 . The monomer as claimed in claim 1 , wherein: c is 1, and at least one of A 1 , A 2 and A 3 is an aromatic ring group independently substituted with 1 or more methoxy groups or ethoxy groups. 9 . The monomer as claimed in claim 8 , wherein: a, b, and c are 1, and at least one of A 4 and A 5 is an aromatic ring group independently substituted with 1 or more methoxy groups or ethoxy groups. 10 . The monomer as claimed in claim 1 , wherein the monomer has a molecular weight of about 800 to about 5,000. 11 . A polymer including a moiety represented by Chemical Formula 2: wherein, in Chemical Formula 2, A 1 , A 2 , A 3 , A 4 , and A 5 are each independently a substituted or unsubstituted aromatic ring group, X 1 , X 2 , X 3 , and X 4 are each independently a hydroxy group, a substituted or unsubstituted amino group, a halogen atom, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C3 to C30 cycloalkenyl group, a substituted or unsubstituted C1 to C20 alkylamine group, a substituted or unsubstituted C7 to C20 arylalkyl group, a substituted or unsubstituted C1 to C20 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 heteroaryl group, a substituted or unsubstituted C1 to C4 alkyl ether group, a substituted or unsubstituted C7 to C20 arylalkylene ether group, a substituted or unsubstituted C1 to C30 haloalkyl group, or a combination thereof, C 1 , C 2 , C 3 , C 4 , D 1 , D 2 , D 3 , D 4 , E 1 , E 2 , E 3 , and E 4 are each independently hydrogen atom, hydroxy group, a substituted or unsubstituted amino group, a halogen atom, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C3 to C30 cycloalkenyl group, a substituted or unsubstituted C1 to C20 alkylamine group, a substituted or unsubstituted C7 to C20 arylalkyl group, a substituted or unsubstituted C1 to C20 heteroalkyl group, a substituted or unsubstituted C2 to C30 heterocycloalkyl group, a substituted or unsubstituted C2 to C30 heteroaryl group, a substituted or unsubstituted C1 to C4 alkyl ether group, a substituted or unsubstituted C7 to C20 arylalkylene ether group, a substituted or unsubstituted C1 to C30 haloalkyl group, or a combination thereof, a, b, and c are each independently 0 or 1, and n is an integer of 1 to 500. 12 . The polymer as claimed in claim 11 , wherein A 1 , A 2 , A 3 , A 4 , and A 5 are each independent
containing hydroxy or O-metal groups · CPC title
Coating compositions based on macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain (C09D107/00 - C09D157/00, C09D161/00 take precedence); Coating compositions based on derivatives of such polymers · CPC title
Derivatisation · CPC title
Friedel-Crafts-type · CPC title
containing only carbon atoms · CPC title
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