Method of Using Dihydro-Resveratrol for Treating Acute Pancreatitis and Associated Pulmonary Injury
US-2016367498-A1 · Dec 22, 2016 · US
US2016016872A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016016872-A1 |
| Application number | US-201514792968-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 7, 2015 |
| Priority date | Jul 15, 2014 |
| Publication date | Jan 21, 2016 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Polymeric reaction products of certain substituted tetraarylmethane monomers are useful as underlayers in semiconductor manufacturing processes.
Opening claim text (preview).
What is claimed is: 1 . A polymeric reaction product comprising polymerized units of one or more tetraaryl monomers of formula (1) wherein AG represents an activating group chosen from OR, NR 2 , and SR; Ar 1 , Ar 2 , Ar 3 and Ar 4 independently represent an aryl moiety; R is independently chosen from H, an optionally substituted C 1-30 alkyl, an optionally substituted C 2-30 alkenyl moiety, an optionally substituted C 2-30 alkynyl moiety, an optionally substituted C 7-30 aralkyl moiety, or an optionally substituted C 6-20 aryl moiety; R 1 , R 2 , R 3 , and R 4 are independently chosen from an optionally substituted C 1-30 alkyl, an optionally substituted C 2-30 alkenyl moiety, an optionally substituted C 2-30 alkynyl moiety, an optionally substituted C 7-30 aralkyl moiety, or an optionally substituted C 6-20 aryl moiety; any 2 of Ar 1 , Ar 2 , Ar 3 and Ar 4 may be taken together along with the carbon to which they are attached to form a 5 or 6-membered fused alicyclic ring; a is an integer from 0 to 4; and b, c, and d are independently integers from 0 to 5. 2 . The polymeric reaction product of claim 1 wherein AG is OR. 3 . The polymeric reaction product of claim 1 wherein the tetraaryl monomer has the general formula (1-1) or (1-2): wherein AG, Ar 1 , Ar 2 Ar 3 , Ar 4 , R 1 , R 2 , R 3 , R 4 , a, and b are as defined above; a′ is an integer from 0 to 3; and c′ and d′ are independently integers from 0 to 4. 4 . The polymeric reaction product of claim 1 wherein the tetraaryl monomer has the general formula (1-2): wherein AG, Ar 1 , Ar 2 , Ar 3 , Ar 4 , R 1 , R 2 , R 3 , R 4 , a, and b are as defined above; and c″ and d″ are independently integers from 0 to 4. 5 . The polymeric reaction product of claim 1 wherein Ar 1 , Ar 2 , Ar 3 and Ar 4 are independently chosen from phenyl, biphenyl, naphthalenyl, anthracenyl, phenanthrenyl, pyrenyl, tetracenyl, triphenylenyl, tetraphenyl, benzo[f]tetraphenyl, benzo[m]tetraphenyl, benzo[k]tetraphenyl, pentacenyl, perylenyl, benzo[a]pyrenyl, benzo[e]pyrenyl, benzo[ghi]perylenyl, coronenyl, quinolonyl, 7,8-benzoquinolinyl, fluorenyl, chrysenyl, triphenylenyl, and 12H-dibenzo[b,h]fluorenyl. 6 . A composition comprising the polymeric reaction product of claim 1 , an organic solvent, and optionally one or more additives chosen from curing agents and surfactants. 7 . The composition of claim 6 wherein the curing agent is an acid or a thermal acid generator. 8 . A method of forming a patterned layer comprising disposing a layer of the composition of claim 6 on a substrate; removing organic solvent to form a polymeric underlayer; disposing a layer of a photoresist on the polymeric underlayer; exposing the photoresist layer to actinic radiation through a mask; developing the exposed photoresist layer to form a resist pattern; and transferring the pattern to the polymeric underlayer to expose portions of the substrate. 9 . A tetraaryl methane monomer having the formula (1) wherein AG represents an activating group chosen from OR, NR 2 , and SR; Ar 1 , Ar 2 , Ar 3 and Ar 4 independently represent an aryl moiety; R is independently chosen from H, an optionally substituted C 1-30 alkyl, an optionally substituted C 2-30 alkenyl moiety, an optionally substituted C 2-30 alkynyl moiety, an optionally substituted C 7-30 aralkyl moiety, or an optionally substituted C 6-20 aryl moiety; R 1 , R 2 , R 3 , and R 4 are independently chosen from an optionally substituted C 1-30 alkyl, an optionally substituted C 2-30 alkenyl moiety, an optionally substituted C 2-30 alkynyl moiety, an optionally substituted C 7-30 aralkyl moiety, or an optionally substituted C 6-20 aryl moiety; any 2 of Ar 1 , Ar 2 , Ar 3 and Ar 4 may be taken together along with the carbon to which they are attached to form a 5 or 6-membered fused alicyclic ring; a is an integer from 0 to 4; and b, c, and d are independently integers from 0 to 5; wherein at least one of Ar 1 , Ar 2 , Ar 3 and Ar 4 is an aryl moiety having 2 or more fused aromatic rings when none of Ar 1 , Ar 2 , Ar 3 and Ar 4 are joined to form a 5 or 6-membered fused alicyclic ring.
Exposure; Apparatus therefor (photographic printing apparatus for making copies G03B27/00) · CPC title
Chemistry & Metallurgy · mapped topic
of aldehydes with phenols · CPC title
Chemistry & Metallurgy · mapped topic
Liquid compositions therefor, e.g. developers · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.