CN110982053B - Organic nonmetal catalyst for preparing poly (p-dioxanone) - Google Patents
Organic nonmetal catalyst for preparing poly (p-dioxanone) Download PDFInfo
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- 229920002463 poly(p-dioxanone) polymer Polymers 0.000 title claims abstract description 53
- 239000003054 catalyst Substances 0.000 title claims abstract description 39
- 229910052755 nonmetal Inorganic materials 0.000 title claims abstract description 24
- 238000006243 chemical reaction Methods 0.000 claims abstract description 41
- 239000000622 polydioxanone Substances 0.000 claims abstract description 27
- 238000007151 ring opening polymerisation reaction Methods 0.000 claims abstract description 25
- 239000003999 initiator Substances 0.000 claims abstract description 8
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 6
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 15
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- 239000002904 solvent Substances 0.000 claims description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 8
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 6
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 6
- 235000019445 benzyl alcohol Nutrition 0.000 claims description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 3
- -1 3, 5-bistrifluoromethylphenyl Chemical group 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 239000003863 metallic catalyst Substances 0.000 claims 2
- SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 claims 1
- 239000000178 monomer Substances 0.000 abstract description 7
- 238000006116 polymerization reaction Methods 0.000 abstract description 7
- 230000000694 effects Effects 0.000 abstract description 5
- 230000003213 activating effect Effects 0.000 abstract description 3
- 125000000524 functional group Chemical group 0.000 abstract description 3
- 229920000117 poly(dioxanone) Polymers 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 description 19
- 229920000642 polymer Polymers 0.000 description 15
- 230000035484 reaction time Effects 0.000 description 5
- OEBXWWBYZJNKRK-UHFFFAOYSA-N 1-methyl-2,3,4,6,7,8-hexahydropyrimido[1,2-a]pyrimidine Chemical compound C1CCN=C2N(C)CCCN21 OEBXWWBYZJNKRK-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 238000005227 gel permeation chromatography Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 229920000954 Polyglycolide Polymers 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 229920003232 aliphatic polyester Polymers 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 229920001610 polycaprolactone Polymers 0.000 description 2
- 239000004632 polycaprolactone Substances 0.000 description 2
- 239000004633 polyglycolic acid Substances 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- VPVXHAANQNHFSF-UHFFFAOYSA-N 1,4-dioxan-2-one Chemical compound O=C1COCCO1 VPVXHAANQNHFSF-UHFFFAOYSA-N 0.000 description 1
- VSTXCZGEEVFJES-UHFFFAOYSA-N 1-cycloundecyl-1,5-diazacycloundec-5-ene Chemical compound C1CCCCCC(CCCC1)N1CCCCCC=NCCC1 VSTXCZGEEVFJES-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000004626 polylactic acid Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
- C08G63/82—Preparation processes characterised by the catalyst used
- C08G63/87—Non-metals or inter-compounds thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/06—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
- C08G63/08—Lactones or lactides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
- C08G63/82—Preparation processes characterised by the catalyst used
- C08G63/823—Preparation processes characterised by the catalyst used for the preparation of polylactones or polylactides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2230/00—Compositions for preparing biodegradable polymers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
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- Chemical & Material Sciences (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyethers (AREA)
Abstract
The invention discloses an organic non-metal catalyst for preparing poly (p-dioxanone), which is prepared by reacting poly (p-dioxanone) with an organic non-metal catalystCarrying out ring-opening polymerization reaction under the action of an initiator with a hydroxyl structure to obtain the polydioxanone, wherein the structural formula of the organic nonmetal catalyst is selected from one or more of the following:wherein R is 1 、R 2 Each group is independently an aliphatic group or a cyclic group. The organic nonmetal catalyst provided by the invention realizes efficient ring-opening polymerization of monomers by activating functional groups in PDO, and the polymerization reaction has the advantages of high activity, easiness in adjustment and mild reaction.
Description
Technical Field
The invention belongs to the technical field of organic catalytic systems, and particularly relates to an organic nonmetal catalyst for preparing poly (p-dioxanone).
Background
Since the last century, aliphatic polyesters have been used as biomedical and environmentally friendly materials because of their good biocompatibility, absorbability and biodegradability. As a typical aliphatic polyester, polydioxanone (PPDO) is similar to Polycaprolactone (PCL), polylactic acid (PLA) and polyglycolic acid (PGA), and ester bonds in molecular chains endow the polyester with good biocompatibility, biodegradability and absorbability; the PPDO molecular chain has unique ether bond, and the PPDO molecular chain has excellent flexibility and tensile strength, compared with natural polymer materials (such as chitin, chitosan, gelatin and the like), the PPDO molecular chain overcomes the defect that the mechanical property is reduced due to the influence of a pore structure, so that PPDO is distinguished in the field of biomedicine and is favored by clinical medical treatment.
Generally, aliphatic polydioxanones are prepared by ring opening polymerization of a dioxanone monomer (PDO) (formula I). The choice of catalyst is critical to the ring-opening polymerization, and commonly used catalysts include tin, aluminum, zinc, and enzyme catalysis, among others.
Kricheldo realizes ring-opening polymerization of PDO by using zinc acetate as a catalyst, and the reaction is carried out under the high-temperature condition, although the obtained polymer has higher molecular weight, the conversion rate is low.Tokiwa professor of Tokyo university in Japan realizes reversible polymerization of PDO for the first time by using stannous octoate and triethylaluminum as catalysts at 60-180 ℃, the monomer conversion rate can reach more than 95%, the number average molecular weight can reach 30 ten thousand at most, and polymers with higher quality can be obtained. AlEt utilized by Wangyouzhong team and the like 3 -H 2 O-H 3 PO 4 The catalytic system realizes the high-efficiency ring-opening polymerization of PDO under the reaction condition of 80 ℃, the molecular weight is more than one hundred thousand, but the catalytic system mainly comprising metal generally has the defects of long reaction time, low conversion rate and difficult control of side reaction. Although the above-mentioned catalytic system realizes the ring-opening polymerization of PDO, the catalytic system used is mostly a metal catalyst, and lacks modulation factors, resulting in less activity control factors of PDO ring-opening polymerization, and although the regulation can be performed by raising the polymerization temperature and prolonging the reaction time, the side reactions are increased by raising the temperature and prolonging the time, resulting in the phenomena of wider distribution of the polymerization material and decomposition of the product, which are very unfavorable for the subsequent material processing. In recent years, organic catalysts such as phosphorus, nitrile, alkali, carbene and the like, organic non-metal catalysts, can also be used for synthesizing PPDO, alcohol or aniline is used as an initiator in the reaction, the reaction activity is higher, and the organic catalyst has more possibility as an efficient catalytic system to carry out ring-opening polymerization on cyclic compounds.
Disclosure of Invention
The invention aims to provide an organic nonmetal catalyst for preparing polydioxanone, which realizes efficient ring-opening polymerization of monomers by activating functional groups in PDO, and has the advantages of high activity, easiness in adjustment and mild reaction in polymerization reaction.
The technical scheme provided by the invention is as follows:
an organic nonmetal catalyst for preparing polydioxanone, wherein the polydioxanone is subjected to ring opening polymerization reaction under the action of the organic nonmetal catalyst and an initiator carrying a hydroxyl structure to obtain the polydioxanone, and the structural formula of the organic nonmetal catalyst is selected from one or more of the following:
wherein R is 1 、R 2 Each group is independently an aliphatic group or a cyclic group.
The structural formulas are respectively as follows: thiourea, urea, 7-methyl-1, 5, 7-triazabicyclo [4.4.0] dec-5-ene (MTBD) and 1, 8-diazabicycloundec-7-ene (DBU).
Preferably, the aliphatic group is selected from methyl, ethyl, isopropyl or n-butyl and the cyclic group is selected from phenyl or cycloalkyl.
Preferably, R is 1 The group is 3, 5-bistrifluoromethylphenyl, R 2 The group is cycloalkyl or N, N-dimethyl cyclohexylamino, and the structural formula of the organic nonmetal catalyst A is shown as follows:
preferably, the organic nonmetal catalyst has a structural formula selected from one or more of:
the organic nonmetal catalyst has the advantages of high conversion rate and mild reaction conditions for preparing the polydioxanone, and the prepared polydioxanone has narrow molecular weight distribution.
The initiator is selected from one or more of benzyl alcohol BA, ethylene glycol EG, diethylene glycol DEG and 1, 4-butanediol BDO.
Preferably, the initiator is selected from benzyl alcohol or ethylene glycol.
The ring-opening polymerization reaction is carried out under the condition of no solvent, and the temperature of the ring-opening polymerization reaction is 100-160 ℃.
The ring-opening polymerization reaction is carried out in the presence of a solvent, wherein the solvent is one or more selected from toluene, dichloromethane, chloroform or tetrahydrofuran. The temperature of the ring-opening polymerization reaction is-40-150 ℃.
Preferably, the ring-opening polymerization reaction is carried out in the presence or absence of a solvent, the temperature of the ring-opening polymerization reaction is 25-100 ℃, and the reaction time is 1-4 h.
Preferably, the ring-opening polymerization reaction is carried out in the presence of a solvent, the temperature of the ring-opening polymerization reaction is 25 ℃, and the reaction time is 1-4 h.
The number average molecular weight of the poly (p-dioxanone) is 500-150000, and the molecular weight distribution is 1.01-15.00.
Preferably, the number average molecular weight of the polydioxanone is 52000-87000, and the molecular weight distribution is 1.02-1.32. Preferably, the molecular weight distribution of the polydioxanone is 1.09-1.25.
The invention realizes the high-efficiency ring-opening polymerization of the PDO monomer by selecting different types of organic nonmetal catalysts and regulating and controlling the structure of the initiator.
Compared with the prior art, the invention has the beneficial effects that:
the organic nonmetal catalyst provided by the invention realizes the high-efficiency ring-opening polymerization of the monomer by activating the functional group in the PDO, and the polymerization reaction has the advantages of high activity, easy regulation and mild reaction. The organic nonmetal catalyst provided by the invention overcomes the defects of long reaction time, low conversion rate and low molecular weight of the traditional metal catalytic system, and the obtained PPDO material has the advantages of high molecular weight and narrow distribution.
Drawings
FIG. 1 is a nuclear magnetic spectrum of polydioxanone prepared in example 1;
FIG. 2 is a gel permeation chromatogram of polydioxanone prepared in example 1;
FIG. 3 is a gel permeation chromatogram of polydioxanone prepared in example 13.
Detailed Description
In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention will be further described in detail with reference to the accompanying drawings and examples. It should be understood that the detailed description and specific examples, while indicating the scope of the invention, are intended for purposes of illustration only and are not intended to limit the scope of the invention.
The organometalloid catalysts used in the following examples are of the formula 1-4:
example 1
The operation process is carried out in a glove box under anhydrous and oxygen-free environment, organic nonmetal catalyst 1(0.0250g, 0.05mmol), benzyl alcohol (0.0060g, 0.05mmol), PDO (1.02g, 10mmol) and 1mL toluene are added into a glass reaction bottle with an effective volume of 25mL, and the reaction is carried out for 4 hours at 25 ℃. When the system is completely solidified, adding benzoic acid to quench, adding hot chloroform to dissolve the product, sampling and utilizing 1 H NMR gave monomer conversion and settling in methanol gave PPDO polymer as a white powder. The catalytic results are shown in table 1, and the nuclear magnetic spectrum and the gel permeation chromatogram are shown in fig. 1 and fig. 2 (abscissa is time, ordinate is detector signal), respectively.
Example 2
As shown in example 1, a PPDO polymer was obtained after 4 hours of reaction under the same conditions using organometalloid catalyst 2, and the catalytic results are shown in Table 1.
Example 3
As shown in example 1, PPDO polymer was obtained after 1 hour of reaction under the same conditions using the organometalloid catalyst 3, and the catalytic results are shown in Table 1.
Example 4
As shown in example 1, PPDO polymer was obtained after 4 hours of reaction under the same conditions using organometalloid catalyst 4, and the catalytic results are shown in Table 1.
Example 5
As shown in example 4, the benzyl alcohol was changed to ethylene glycol under the same conditions, and after 4 hours of reaction, PPDO polymer was obtained, and the catalytic results are shown in Table 1.
Example 6
As shown in example 4, PPDO polymer was obtained after 2 hours of reaction under the same conditions, and the catalytic results are shown in Table 1.
Example 7
As shown in example 6, under the same conditions, the temperature was increased to 60 degrees, and after 2 hours of reaction, PPDO polymer was obtained, and the catalytic results are shown in Table 1.
Example 8
As shown in example 6, under the same conditions, the temperature was increased to 80 degrees, and after 2 hours of reaction, PPDO polymer was obtained, and the catalytic results are shown in Table 1.
Example 9
As shown in example 6, under the same conditions, the temperature was increased to 100 degrees, and after 2 hours of reaction, a PPDO polymer was obtained, and the catalytic results are shown in Table 1.
Example 10
As shown in example 6, under the same conditions, the temperature was increased to 130 degrees, and after 2 hours of reaction, PPDO polymer was obtained, and the catalytic results are shown in Table 1.
Example 11
As shown in example 6, the solvent was changed to methylene chloride under the same conditions, and after 2 hours of reaction, a PPDO polymer was obtained, and the catalytic results are shown in Table 1.
Example 12
As shown in example 6, the solvent was changed to tetrahydrofuran under the same conditions, and after 2 hours of reaction, a PPDO polymer was obtained, and the catalytic results are shown in Table 1.
Example 13
Under the same conditions, as shown in example 9, without any addition of solvent, the amount of PDO was increased to 2.55 g, and after 4 hours of reaction, a PPDO polymer was obtained, the catalysis results of which are shown in Table 1 and the GPC characterization is shown in FIG. 3.
TABLE 1 test results of polymerization reactions of examples 1 to 13
a M n Number average molecular weight, as determined by gel permeation chromatography; b molecular weight distribution (PDI) as determined by gel permeation chromatography.
The above-mentioned embodiments are intended to illustrate the technical solutions and advantages of the present invention, and it should be understood that the above-mentioned embodiments are only the most preferred embodiments of the present invention, and are not intended to limit the present invention, and any modifications, additions, equivalents, etc. made within the scope of the principles of the present invention should be included in the scope of the present invention.
Claims (9)
1. The application of the organic non-metal catalyst in preparing the polydioxanone is characterized in that the polydioxanone is subjected to ring opening polymerization reaction under the action of the organic non-metal catalyst and an initiator carrying a hydroxyl structure to obtain the polydioxanone, and the structural formula of the organic non-metal catalyst is selected from one or more of the following:
wherein R is 1 、R 2 Each group is independently an aliphatic group or a cyclic group.
2. Use of an organometalloid catalyst for the preparation of polydioxanone according to claim 1, wherein the aliphatic group is selected from methyl, ethyl, isopropyl or n-butyl and the cyclic group is selected from phenyl or cycloalkyl.
4. use of an organic non-metallic catalyst for the preparation of polydioxanone according to claim 1, wherein the initiator is selected from one or more of benzyl alcohol BA, ethylene glycol EG, diethylene glycol DEG, 1, 4-butanediol BDO.
5. The use of the organometalloid catalyst for preparing polydioxanone according to claim 1, wherein the ring-opening polymerization is carried out in the absence of a solvent at a temperature of 100-160 ℃.
6. The use of an organic non-metallic catalyst for the preparation of polydioxanone according to claim 1, wherein the ring opening polymerization reaction is carried out in the presence of a solvent selected from one or more of toluene, dichloromethane, chloroform or tetrahydrofuran.
7. Use of the organometalloid catalyst for preparing polydioxanone according to claim 6, wherein the temperature of the ring-opening polymerization reaction is-40-150 ℃.
8. The use of the organometalloid catalyst for the preparation of polydioxanone according to claim 1, wherein the polydioxanone has a number average molecular weight of between 500 and 150000 and a molecular weight distribution of between 1.01 and 15.00.
9. The application of the organic nonmetal catalyst for preparing polydioxanone according to claim 1, wherein the polydioxanone has a number average molecular weight of 52000 to 87000 and a molecular weight distribution of 1.02 to 1.32.
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CN103288788B (en) * | 2013-05-09 | 2015-02-11 | 北京师范大学 | Delta-valerolactone compounds, preparation method and application |
CN103497314B (en) * | 2013-10-10 | 2016-05-11 | 大连理工大学 | Linear pectination polycaprolactone of one class and preparation method thereof |
CN105037702B (en) * | 2015-07-23 | 2017-01-04 | 浙江大学 | The application process of plasticity shape-memory polymer based on ester exchange |
CN107022069A (en) * | 2017-04-27 | 2017-08-08 | 南京工业大学 | A kind of method that utilization bionic catalyst is catalyzed γ valerolactone ring-opening polymerisations |
CN107915832B (en) * | 2017-10-19 | 2020-07-28 | 复旦大学 | X-ray developed iodine-containing polycarbonate/polyester material and preparation method and application thereof |
CN110305303B (en) * | 2019-07-24 | 2021-07-30 | 青岛科技大学 | Preparation method of degradable bio-based polyester with side chain containing double-bond functional group |
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