Transition metal-catalyzed processes for the preparation of N-allyl compounds and use thereof
US-9499557-B2 · Nov 22, 2016 · US
US10246405B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10246405-B2 |
| Application number | US-201615008167-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 27, 2016 |
| Priority date | Jun 7, 2011 |
| Publication date | Apr 2, 2019 |
| Grant date | Apr 2, 2019 |
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Provided are a radial porous diacetylene particle, which is synthesized by ion-bonding a diacetylene-containing dicarboxylic acid or diamine monomer represented by Formula 1 with a diamine or dicarboxylic acid monomer represented by Formula 2, and a method of manufacturing the same.
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What is claimed is: 1. A method of manufacturing a radial porous diacetylene particle, comprising the steps of: (a) respectively dissolving a diacetylene-containing dicarboxylic acid monomer represented by Formula 1 below and a diamine monomer represented by Formula 2 below in a solvent to prepare a solution including the diacetylene-containing dicarboxylic acid monomer and a solution including the diamine monomer: G-(A) x -C≡C—C≡C—(B) y -G [Formula 1] wherein A and B are each independently selected from the group consisting of a substituted or unsubstituted alkyl group of two or more carbon atoms, an ethylene oxide group, an amide group and an ester group, G is COOH, and x and y are each independently an integer of 1 to 20, Q-(D) m -Z-(E) n -Q [Formula 2] wherein Z is selected from the group consisting of a benzene group, a pyridine group, a pyrimidine group and a naphthalene group, D and E are each independently a substituted or unsubstituted alkyl group of one or more carbon atoms Q, NH 2 , and m and n are each independently an integer of 0 to 20; (b) ultrasonically treating each of the solutions; (c) maintaining each of the ultrasonically-treated solutions at room temperature; and (d) mixing the solution including the diacetylene-containing dicarboxylic acid monomer represented by Formula 1 above with the solution including the diamine monomer represented by Formula 2 above to form a radial porous diacetylene particle and then growing the radial porous acetylene particle. 2. The method according to claim 1 , wherein the solvent is at least one selected from the group consisting of tetrahydrofuran (THF), chloroform, toluene, ethanol, isopropanol, and n-hexane. 3. The method according to claim 1 , wherein each of the solution including the diacetylene-containing dicarboxylic acid monomer represented by Formula 1 above and the solution including the diamine monomer represented by Formula 2 above has a concentration of 10 mM˜50 mM. 4. The method according to claim 1 , wherein each of the solution including the diacetylene-containing dicarboxylic acid monomer represented by Formula 1 above and the solution including the diamine monomer represented by Formula 2 above has a concentration of 10 mM˜20 mM. 5. The method according to claim 1 , wherein a mixing temperature of the step (d) is maintained at a temperature of 5˜30° C. for 10 minutes˜1 hour. 6. The method according to claim 1 , wherein a mixing temperature of the step (d) is maintained at a temperature of 10˜25° C. for 10 minutes˜1 hour. 7. The method according to claim 1 , wherein the solution including the diacetylene-containing dicarboxylic acid monomer represented by Formula 1 above and the solution including the diamine monomer represented by Formula 2 above are mixed in a volume ratio of 1:0.2˜5. 8. The method according to claim 1 , wherein the ultrasonic treatment is carried out for 30 minutes by a power of 5˜20 W.
Manufacture or treatment of nanostructures · CPC title
by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part · CPC title
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Particulate matter [e.g., sphere, flake, etc.] · CPC title
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