IP Library Granted Patent US 9,487,630
Granted Patent B2
US 9,487,630 · App. 14/428,917 · Granted Nov 8, 2016

Method for manufacturing polyrotaxane

Inventors: Tomoaki Yamasaki (Hyogo, JP); Akira Kimura (Hyogo, JP); Hiroki Okazaki (Hyogo, JP); Changming Zhao (Chiba, JP)
Assignees: Sumitomo Seika Chemicals Co., Ltd.; Advanced Softmaterials Inc.
C08G81/00C08B37/0015C08G65/332C08G65/33306C08G83/007C08L5/16
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Quick Facts
Patent No.
US 9,487,630
App. No.
14/428,917
Granted
Nov 8, 2016
Kind
B2
Abstract

The present invention aims to provide a method for producing a polyrotaxane which enables industrially advantageous production of a polyrotaxane with a high inclusion rate. The present invention relates to a method for producing a polyrotaxane that includes a cyclodextrin; a compound having a repeating structural unit represented by the following formula (1), and threading through a cavity of the cyclodextrin in a skewered manner to be included in the cyclodextrin; and capping groups individually placed at each end of a molecule of the compound having a repeating structural unit represented by the formula (1) to prevent the cyclodextrin from separating, the method comprising: a step 1 of mixing the compound having a repeating structural unit represented by the formula (1) and the cyclodextrin in an aqueous medium to prepare an aqueous dispersion of pseudopolyrotaxan particles in which the compound having a repeating structural unit represented by the formula (1) is included in a cavity of a cyclodextrin molecule in a skewered manner; and a step 2 of mixing a triazine compound represented by the formula (2), a compound having at least one tertiary amino group, the aqueous dispersion of pseudopolyrotaxane particles prepared in the step 1, and a capping agent to introduce capping groups individually at each end of a molecule of the compound having a repeating structural unit represented by the formula (1) in the pseudopolyrotaxane particles, wherein, in the formula (2), R 1 and R 2 are each independently a C1-C4 alkyl group or a C6-C8 aryl group, and X represents a halogen atom.

Claims (38)

1. A method for producing a polyrotaxane that includes a cyclodextrin; a compound having a repeating structural unit represented by the following formula (1), and threading through a cavity of the cyclodextrin in a skewered manner to be included in the cyclodextrin; and capping groups individually placed at each end of a molecule of the compound having a repeating structural unit represented by the formula (1) to prevent the cyclodextrin from separating, the method comprising:

a step 1 of mixing the compound having a repeating structural unit represented by the formula (1) and the cyclodextrin in an aqueous medium to prepare an aqueous dispersion of pseudopolyrotaxan particles in which the compound having a repeating structural unit represented by the formula (1) is included in a cavity of a cyclodextrin molecule in a skewered manner; and

a step 2 of mixing a triazine compound represented by the following formula (2), a compound having at least one tertiary amino group, the aqueous dispersion of pseudopolyrotaxane particles prepared in the step 1, and a capping agent to introduce capping groups individually at each end of a molecule of the compound having a repeating structural unit represented by the formula (1) in the pseudopolyrotaxane particles,

wherein, in the formula (2), R 1 and R 2 are each independently a C1-C4 alkyl group or a C6-C8 aryl group, and X represents a halogen atom.

2. The method for producing a polyrotaxane according to claim 1 ,

wherein the triazine compound represented by the formula (2) is 2-chloro-4,6-dimethoxy-1,3,5-triazine.

3. The method for producing a polyrotaxane according to claim 1 ,

wherein the triazine compound represented by the formula (2) is used in an amount of 0.7 to 50 times the number of moles of end groups of the compound having a repeating structural unit represented by the formula (1).

4. The method for producing a polyrotaxane according to claim 1 ,

wherein the compound having at least one tertiary amino group is a morpholine compound represented by the following formula (3):

wherein, in the formula (3), R 3 represents a C1-C4 alkyl group.

5. The method for producing a polyrotaxane according to claim 4 ,

wherein the morpholine compound represented by the formula (3) is N-methylmorpholine.

6. The method for producing a polyrotaxane according to claim 1 ,

wherein the compound having at least one tertiary amino group is used in an amount of 0.1 to 3 mol per mole of the triazine compound represented by the formula (2).

7. The method for producing a polyrotaxane according to claim 1 ,

wherein the step 2 includes a step 2-1 of preparing a quaternary ammonium salt represented by the following formula (4) by mixing and reacting the triazine compound represented by the formula (2) and the compound having at least one tertiary amino group; and

a step 2-2 of mixing the quaternary ammonium salt represented by the formula (4), the aqueous dispersion of pseudopolyrotaxane particles prepared in the step 1, and the capping agent,

wherein, in the formula (4), E is an organic group containing one or two tertiary amino groups, and a monovalent or divalent organic group attached to a triazine ring via a nitrogen atom of the one or two tertiary amino groups; n is 1 when E contains one tertiary amino group, or is 2 when E contains two tertiary amino groups; R 1 and R 2 each independently represent a C1-C4 alkyl group or a C6-C8 aryl group; a is 1 or 2, and is 1 when n is 1; and Z −(n/a) represents a counter anion having a valence of (n/a).

8. The method for producing a polyrotaxane according to claim 7 ,

wherein the quaternary ammonium salt represented by the formula (4) is a quaternary ammonium salt represented by the following formula (5):

wherein, in the formula (5), R 1 and R 2 are each independently a C1-C4 alkyl group or a C6-C8 aryl group, R 4 is a C1-C4 alkyl group, and X represents a halogen atom.

9. The method for producing a polyrotaxane according to claim 7 ,

wherein the quaternary ammonium salt represented by the formula (4) is used in an amount of 0.7 to 50 times the number of moles of end groups of the compound having a repeating structural unit represented by the formula (1).

10. The method for producing a polyrotaxane according to claim 7 ,

wherein, in the step 2-2, the morpholine compound represented by the following formula (3) is further added

11. The method for producing a polyrotaxane according to claim 1 ,

wherein the compound having a repeating structural unit represented by the formula (1) to be used in the step 1 has a mass average molecular weight of 1000 to 500000.

12. The method for producing a polyrotaxane according to claim 1 ,

wherein both the end groups of the compound having a repeating structural unit represented by the formula (1) to be used in the step 1 are the same and are hydroxyl groups, carboxyl groups, or amino groups.

13. The method for producing a polyrotaxane according to claim 1 ,

wherein a mass ratio of the compound having a repeating structural unit represented by the formula (1) to the cyclodextrin to be used in the step 1 is 1:2 to 1:5.

14. The method for producing a polyrotaxane according to claim 1 ,

wherein the aqueous medium to be used in the step 1 is water or a mixed solvent of an aqueous organic solvent and water.

15. The method for producing a polyrotaxane according to claim 1 ,

wherein the step 2 is performed in the presence of an inorganic salt.

16. The method for producing a polyrotaxane according to claim 1 ,

wherein the step 2 is performed in the presence of an aqueous organic solvent.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2025
From: SUMITOMO SEIKA CHEMICALS CO., LTD.
To: ASM INC.
Reel/Frame 070783/0755 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2015
From: YAMASAKI, TOMOAKI; KIMURA, AKIRA; OKAZAKI, HIROKI; ZHAO, CHANGMING
To: SUMITOMO SEIKA CHEMICALS CO., LTD.; ADVANCED SOFTMATERIALS INC.
Reel/Frame 035569/0195 →
Priority Claims (1)
JP 2012-205834 · Sep 19, 2012 · national
Continuity (1)
Related Publication 20150240036A1 · Aug 27, 2015