Polycycloolefin monomers and catalyst activated by compound capable of generating photoacid as 3d printing materials
US-2020002466-A1 · Jan 2, 2020 · US
US11299573B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11299573-B2 |
| Application number | US-202117145491-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 11, 2021 |
| Priority date | Jan 9, 2020 |
| Publication date | Apr 12, 2022 |
| Grant date | Apr 12, 2022 |
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.
Embodiments in accordance with the present invention encompass compositions encompassing a latent organo-ruthenium compound, a pyridine compound, a photosensitizer and an ultra violet light blocking compound along with one or more monomers which undergo ring open metathesis polymerization (ROMP) when said composition is exposed to suitable actinic radiation to form a substantially transparent film or a three dimensional object. Surprisingly, the compositions are very stable at ambient conditions to temperatures up to 80° C. for several days and undergo mass polymerization only when subjected to actinic radiation under inert atmosphere such as for example a blanket of nitrogen. Accordingly, compositions of this invention are useful in various opto-electronic applications, including as 3D printing materials, coatings, encapsulants, fillers, leveling agents, among others.
Opening claim text (preview).
What is claimed is: 1. A composition comprising: a) one or more monomers of formula (I): wherein: m is an integer 0, 1 or 2; R 1 , R 2 , R 3 and R 4 are the same or different and each independently selected from the group consisting of hydrogen, halogen, methyl, ethyl, linear or branched (C 3 -C 16 )alkyl, perfluoro(C 1 -C 12 )alkyl, hydroxy(C 1 -C 16 )alkyl, (C 3 -C 12 )cycloalkyl, (C 6 -C 12 )bicycloalkyl, (C 7 -C 14 )tricycloalkyl, (C 6 -C 10 )aryl, (C 6 -C 10 )aryl(C 1 -C 6 )alkyl, perfluoro(C 6 -C 10 )aryl, perfluoro(C 6 -C 10 )aryl(C 1 -C 6 )alkyl, tri(C 1 -C 6 )alkoxysilyl and a group of formula (A): —Z-Aryl (A) wherein: Z is a bond or a group selected from the group consisting of: (CR 5 R 6 ) a , O(CR 5 R 6 ) a , (CR 5 R 6 ) a O, (CR 5 R 6 ) a —O—(CR 5 R 6 ) b , (CR 5 R 6 ) a —O—(SiR 5 R 6 ) b , (CR 5 R 6 ) a —(CO)O—(CR 5 R 6 ) b , (CR 5 R 6 ) a —O(CO)—(CR 5 R 6 ) b , (CR 5 R 6 ) a —(CO)—(CR 5 R 6 ) b , where a and b are integers which may be the same or different and each independently is 1 to 12; R 5 and R 6 are the same or different and each independently selected from the group consisting of hydrogen, methyl, ethyl, linear or branched (C 3 -C 6 )alkyl, hydroxy, methoxy, ethoxy, linear or branched (C 3 -C 6 )alkyloxy, acetoxy, (C 2 -C 6 )acyl, hydroxymethyl, hydroxyethyl, linear or branched hydroxy(C 3 -C 6 )alkyl, phenyl and phenoxy; Aryl is phenyl or phenyl substituted with one or more of groups selected from the group consisting of methyl, ethyl, linear or branched (C 3 -C 6 )alkyl, hydroxy, methoxy, ethoxy, linear or branched (C 3 -C 6 )alkyloxy, acetoxy, (C 2 -C 6 )acyl, hydroxymethyl, hydroxyethyl, linear or branched hydroxy(C 3 -C 6 )alkyl, phenyl and phenoxy; b) an organo-ruthenium compound selected from the group consisting of a compound of formula (II) and a compound of formula (III): wherein L is P(R) 3 , wherein each R is independently selected from the group consisting of methyl, ethyl, linear or branched (C 3 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl and (C 6 -C 10 )aryl; R 7 and R 8 are the same or different and each independently selected from the group consisting of methyl, ethyl, linear or branched (C 3 -C 6 )alkyl, methoxy, ethoxy and linear or branched (C 3 -C 6 )alkyloxy; R 9 is selected from the group consisting of methyl, ethyl, linear or branched (C 3 -C 6 )alkyl, (C 6 -C 10 )aryl and (C 6 -C 10 )aryl(C 1 -C 6 )alkyl; Ar 1 , Ar 2 and Ar 3 are the same or different and each independently selected from the group consisting of substituted or unsubstituted phenyl, substituted or unsubstituted biphenyl and substituted or unsubstituted naphthyl, wherein each of said substituents are independently selected from the group consisting of methyl, ethyl and linear or branched (C 3 -C 6 )alkyl; c) a compound of formula (IV) or a compound of formula (V): wherein n is an integer from 0 to 4; each R 10 is independently selected from the group consisting of hydrogen, methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl and tert-butyl; R 11 is selected from the group consisting of methyl, ethyl, linear or branched (C 3 -C 6 )alkyl, (C 6 -C 10 )aryl, methoxy, ethoxy, linear or branched (C 3 -C 6 )alkoxy, (C 6 -C 10 )aryloxy and halogen; d) a photoactive compound of formula (VI): wherein Y is halogen; and R 30 and R 31 are the same or different and independently of each other selected from the group consisting of hydrogen, methyl, ethyl, linear or branched (C 3 -C 12 )alkyl, (C 3 -C 12 )cycloalkyl, (C 6 -C 12 )bicycloalkyl, (C 7 -C 14 )tricycloalkyl, (C 6 -C 10 )aryl, (C 6 -C 10 )aryl(C 1 -C 3 )alkyl, (C 1 -C 12 )alkoxy, (C 3 -C 12 )cycloalkoxy, (C 6 -C 12 )bicycloalkoxy, (C 7 -C 14 )tricycloalkoxy, (C 6 -C 10 )aryloxy(C 1 -C 3 )alkyl and (C 6 -C 10 )aryloxy; and e) a compound of formula (VII): wherein n is an integer from 0 to 4; each R 32 is independently selected from the group consisting of hydrogen, methyl, ethyl, linear or branched (C 3 -C 12 )alkyl, (C 3 -C 12 )cycloalkyl, (C 6 -C 12 )bicycloalkyl, (C 7 -C 14 )tricycloalkyl, (C 6 -C 10 )aryl, (C 6 -C 10 )aryl(C 1 -C 3 )alkyl, (C 1 -C 12 )alkoxy, (C 3 -C 12 )cycloalkoxy, (C 6 -C 12 )bicycloalkoxy, (C 7 -C 14 )tricycloalkoxy, (C 6 -C 10 )aryloxy(C 1 -C 3 )alkyl and (C 6 -C 10 )aryloxy; and said composition is in a clear liquid form at room temperature. 2. The composition according to claim 1 , wherein said composition comprises first and second monomer of formula (I) distinct from each other and one of said first and second monomers having a refractive index of at least 1.5 and viscosity below 100 centipoise, and wherein said first monomer is completely miscible with said second monomer to form a clear solution. 3. The composition according to claim 1 , wherein the monomer of formula (I) is selected from the group consisting of: 4. The composition according to claim 1 , wherein: L is selected from the group consisting of P(iPr) 3 , P(tert-Bu) 3 , PCy 3 and PPh 3 ; R 7 and R 8 are the same or different and each independently selected from the group consisting of hydrogen, methyl, ethyl and isopropyl; R 9 is selected from the group consisting of hydrogen, methyl, ethyl and isopropyl; Ar 1 , Ar 2 and Ar 3 are the same or different and each independently selected from the group consisting of phenyl, 2,6-dimethylphenyl, 2,6-diethylphenyl, 2,6-di(isopropyl)phenyl and 2,4,6-trimethylphenyl. 5. The composition according to claim 4 , wherein the organo-ruthenium compound of formula (II) or organo-ruthenium compound of formula (III) is selected from the group consisting of: 6. The composition according to claim 1 , wherein: n is an integer from 0 to 2; each R 10 is independently selected from the group consisting of methyl, ethyl, iso-propyl and tert-butyl; and R 11 is selected from the group consisting of methyl, ethyl, iso-propyl, tert-butyl, phenyl, methoxy, ethoxy, phenoxy, fluorine and chlorine. 7. The composition according to claim 1 , wherein the compound of formula (IV) is selected from the group consisting of: N,N-dimethylpyridin-4-amine; N,N-diethylpyridin-4-amine; N,N-diisopropylpyridin-4-amine; N,N-di-tert-butylpyridin-4-amine; N,N-dimethyl-2-methylpyridin-4-amine; N,N-di-tert-butyl-2-methylpyridin-4-amine; 2-methoxy-N,N-dimethylpyridin-4-amine; 2-fluoro-N,N-dimethylpyridin-4-amine;
Ruthenium compounds · CPC title
Heterocyclic compounds having sulfur in the ring · CPC title
Five-membered rings · CPC title
condensed with carbocyclic rings · CPC title
Six-membered rings · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.