Thioxanthone aromatic amine compound and organic light emitting device using the same
US-2016351831-A1 · Dec 1, 2016 · US
US9399633B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9399633-B2 |
| Application number | US-201514938896-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 12, 2015 |
| Priority date | Nov 12, 2010 |
| Publication date | Jul 26, 2016 |
| Grant date | Jul 26, 2016 |
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The present invention provides novel photoinitiators for polyurethane formation, in which a photoinitiator moiety and a tertiary amine are incorporated into the photoinitiator structure, and thus the polyurethane polymer.
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The invention claimed is: 1. A photoinitiator of the formula (I): in which: Pi is With Za attached in para position to the chlorine atom; Za and Zb together form a single bond, or a linker in which Za is selected from optionally substituted —(O—(C 1 -C 12 alkylene)) n -, optionally substituted —(NR 1 —(C 1 -C 12 alkylene)) n wherein R 1 is H or optionally substituted C 1 -C 12 alkyl and optionally substituted —(S—(C 1 -C 12 alkylene)) n -; wherein n is 1; wherein Za is joined to Pi via the O, N or S atom in Za; and Zb is a single bond; X 1 and X 2 are independently selected from optionally substituted C 1 -C 12 alkylene, optionally substituted C 1 -C 12 alkenylene, optionally substituted heterocyclyl, —O—, —S—, —NR 2 —, —C(═O)—, —C(═NR 2 )—, —Si(R 2 ) 2 —O—, optionally substituted aryl, and combinations thereof, wherein R 2 is H or optionally substituted C 1 -C 12 alkyl; wherein X 1 and X 2 may be linked to one another or to Za to form one or more ring structures; wherein Za, X 1 and X 2 are selected such that N is a tertiary amine; W 1 and W 2 are independently selected from the group consisting of —OH, —NH 2 , —NHR 3 and —SH, wherein R 3 is an optionally substituted C 1 -C 12 alkyl. 2. A photoinitiator according to claim 1 , wherein W 1 and W 2 are the same. 3. A photoinitiator according to claim 1 , wherein X 1 and X 2 are independently selected from optionally substituted C 1 -C 12 alkylene, —O—, —S—, —NR 2 —, wherein R 2 is H or optionally substituted C 1 -C 12 alkyl, and combinations thereof. 4. A photoinitiator according to claim 1 , wherein X 1 and X 2 may be linked to one another to form one or more ring structures. 5. A photoinitiator according to claim 1 , wherein X 1 and X 2 are independently selected from optionally substituted C 1 -C 12 alkylene, or optionally substituted C 1 -C 6 alkylene. 6. A photoinitiator according to claim 1 , wherein X 1 and X 2 are the same. 7. A photoinitiator according to claim 1 , wherein Za is selected from optionally substituted —O—(C 1 -C 12 alkylene)-, or optionally substituted —O—(C 1 -C 6 alkylene)-. 8. A photoinitiator according to claim 1 , wherein X 1 and X 2 are independently selected from optionally substituted C 1 -C 12 alkylene, and W 1 and W 2 are —OH. 9. A photoinitiator according to claim 1 , being 4-{3-[bis(2-hydroxyethyl)amino]propoxy}-1-chloro-9H-thioxanthen-9-one.
containing primary and/or secondary amino groups · CPC title
Crosslinking, e.g. vulcanising, of macromolecules (mechanical aspects B29C35/00; crosslinking agents C08K) · CPC title
containing two hydroxy groups · CPC title
Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers · CPC title
containing two or more cycloaliphatic rings · CPC title
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