CN108503661A - Asymmetric aluminum complex of the base containing o-phenylenediamine and its preparation method and application - Google Patents
Asymmetric aluminum complex of the base containing o-phenylenediamine and its preparation method and application Download PDFInfo
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- CN108503661A CN108503661A CN201711314942.7A CN201711314942A CN108503661A CN 108503661 A CN108503661 A CN 108503661A CN 201711314942 A CN201711314942 A CN 201711314942A CN 108503661 A CN108503661 A CN 108503661A
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- Prior art keywords
- reaction
- ligand
- phenylenediamine
- aluminum complex
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- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 75
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 75
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 title claims abstract description 50
- 238000002360 preparation method Methods 0.000 title claims abstract description 25
- 238000006243 chemical reaction Methods 0.000 claims abstract description 141
- 239000003446 ligand Substances 0.000 claims abstract description 91
- 239000003054 catalyst Substances 0.000 claims abstract description 67
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 claims abstract description 26
- 238000007151 ring opening polymerisation reaction Methods 0.000 claims abstract description 25
- -1 cyclic lactone Chemical group 0.000 claims abstract description 24
- 239000001257 hydrogen Substances 0.000 claims abstract description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 24
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 9
- 239000004411 aluminium Substances 0.000 claims abstract description 8
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 8
- 150000002367 halogens Chemical class 0.000 claims abstract description 8
- 150000001335 aliphatic alkanes Chemical class 0.000 claims abstract description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 65
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 65
- 238000005406 washing Methods 0.000 claims description 40
- 238000001035 drying Methods 0.000 claims description 28
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 25
- 229910052794 bromium Chemical group 0.000 claims description 25
- 239000011261 inert gas Substances 0.000 claims description 23
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 22
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 claims description 18
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 17
- 239000002904 solvent Substances 0.000 claims description 17
- 239000003960 organic solvent Substances 0.000 claims description 10
- RKDVKSZUMVYZHH-UHFFFAOYSA-N 1,4-dioxane-2,5-dione Chemical compound O=C1COC(=O)CO1 RKDVKSZUMVYZHH-UHFFFAOYSA-N 0.000 claims description 8
- 239000002994 raw material Substances 0.000 claims description 7
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims description 5
- JJTUDXZGHPGLLC-ZXZARUISSA-N (3r,6s)-3,6-dimethyl-1,4-dioxane-2,5-dione Chemical compound C[C@H]1OC(=O)[C@H](C)OC1=O JJTUDXZGHPGLLC-ZXZARUISSA-N 0.000 claims description 4
- 150000001875 compounds Chemical group 0.000 abstract description 16
- 229920000642 polymer Polymers 0.000 abstract description 11
- 230000003197 catalytic effect Effects 0.000 abstract description 9
- 229910052751 metal Inorganic materials 0.000 abstract description 6
- 229910052760 oxygen Inorganic materials 0.000 abstract description 6
- 230000008859 change Effects 0.000 abstract description 3
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000047 product Substances 0.000 description 74
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 48
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 30
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 24
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 21
- 235000019445 benzyl alcohol Nutrition 0.000 description 21
- 239000007787 solid Substances 0.000 description 21
- 239000003708 ampul Substances 0.000 description 19
- 150000003938 benzyl alcohols Chemical class 0.000 description 19
- 229910001873 dinitrogen Inorganic materials 0.000 description 19
- 238000000034 method Methods 0.000 description 18
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 17
- 229920000747 poly(lactic acid) Polymers 0.000 description 15
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 14
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 14
- 238000010438 heat treatment Methods 0.000 description 14
- 239000012299 nitrogen atmosphere Substances 0.000 description 14
- 238000005160 1H NMR spectroscopy Methods 0.000 description 12
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 238000001914 filtration Methods 0.000 description 11
- 238000012869 ethanol precipitation Methods 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 238000012512 characterization method Methods 0.000 description 9
- 238000000926 separation method Methods 0.000 description 9
- 125000001246 bromo group Chemical group Br* 0.000 description 8
- 239000012043 crude product Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 238000003808 methanol extraction Methods 0.000 description 8
- 239000012074 organic phase Substances 0.000 description 8
- 238000010992 reflux Methods 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 7
- 235000019441 ethanol Nutrition 0.000 description 7
- 230000005311 nuclear magnetism Effects 0.000 description 7
- 150000003613 toluenes Chemical class 0.000 description 7
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical group OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 5
- 238000007259 addition reaction Methods 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Polymers OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 4
- 229920000954 Polyglycolide Polymers 0.000 description 4
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical group [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 4
- JBFHTYHTHYHCDJ-UHFFFAOYSA-N gamma-caprolactone Chemical compound CCC1CCC(=O)O1 JBFHTYHTHYHCDJ-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229920001610 polycaprolactone Polymers 0.000 description 4
- 238000001291 vacuum drying Methods 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- 239000007868 Raney catalyst Substances 0.000 description 3
- 229910000564 Raney nickel Inorganic materials 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003426 co-catalyst Substances 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000004632 polycaprolactone Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229960004217 benzyl alcohol Drugs 0.000 description 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000002685 polymerization catalyst Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- ILIJTAOTQJBETA-UHFFFAOYSA-N (2-formylphenyl) hypobromite Chemical compound BrOC1=CC=CC=C1C=O ILIJTAOTQJBETA-UHFFFAOYSA-N 0.000 description 1
- IOTXSIGGFRQYKW-UHFFFAOYSA-N 4,4',4''-(4-propylpyrazole-1,3,5-triyl)trisphenol Chemical compound CCCC=1C(C=2C=CC(O)=CC=2)=NN(C=2C=CC(O)=CC=2)C=1C1=CC=C(O)C=C1 IOTXSIGGFRQYKW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 206010013786 Dry skin Diseases 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 241000219000 Populus Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- MQRWBMAEBQOWAF-UHFFFAOYSA-N acetic acid;nickel Chemical compound [Ni].CC(O)=O.CC(O)=O MQRWBMAEBQOWAF-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001399 aluminium compounds Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 238000010668 complexation reaction Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000013270 controlled release Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000005909 ethyl alcohol group Chemical group 0.000 description 1
- 230000005713 exacerbation Effects 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- BSRBMSCLMKFQGE-UHFFFAOYSA-N n-[2-(2-benzoyl-4-bromoanilino)-2-oxoethyl]-2-bromobenzamide Chemical compound C=1C=CC=CC=1C(=O)C1=CC(Br)=CC=C1NC(=O)CNC(=O)C1=CC=CC=C1Br BSRBMSCLMKFQGE-UHFFFAOYSA-N 0.000 description 1
- 229940078494 nickel acetate Drugs 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 230000037048 polymerization activity Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- GGHDAUPFEBTORZ-UHFFFAOYSA-N propane-1,1-diamine Chemical compound CCC(N)N GGHDAUPFEBTORZ-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/061—Aluminium compounds with C-aluminium linkage
- C07F5/066—Aluminium compounds with C-aluminium linkage compounds with Al linked to an element other than Al, C, H or halogen (this includes Al-cyanide linkage)
-
- 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
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Toxicology (AREA)
Abstract
The invention discloses asymmetric aluminum complexes of a kind of base containing o-phenylenediamine and its preparation method and application, with the structural formula described in formula I, wherein R is the alkane or halogen of hydrogen, C1 C4.The asymmetric aluminum complex catalyst of present invention base containing o-phenylenediamine is reacted by ligand and trimethyl aluminium and is obtained, preparation method is simple, it is at low cost, product yield is high, the compound structure is special, structure change is various, the divalent N of metal center aluminium and ligand, N, O, O is coordinated, it can be used as the catalyst of cyclic lactone ring-opening polymerization, catalytic activity is high, stereoselectivity is good, reaction rate is fast, polymerisation is easy to operate, obtained polymer molecular weight narrowly distributing, molecular weight is controllable, yield is high, it can be widely applied to cyclic lactone ring-opening polymerisation, it is a kind of very ideal catalyst.
Description
Technical field
The present invention relates to a kind of asymmetric aluminum complexes of base containing o-phenylenediamine, further relate to the non-right of the base containing o-phenylenediamine
Claim the application of aluminum complex and preparation method thereof and the catalyst as cyclic lactone ring-opening polymerization.
Background technology
It is the conventional polymer plastics of raw material while offering convenience to the production and life of people using oil, also there is two
A fatal disadvantage：Non-renewable and non-biodegradable.Because oil is non-renewable resources, petroleum is relied on
The fast development of high molecule plastic material is by severely restricts, and high molecule plastic material is difficult to degrade, a large amount of macromolecule
Plastic material waste accumulates in for a long time pollutes also gradually exacerbation caused by environment for human survival in actual life.It finds and replaces
The renewable resource of oil, development environment friendly, biodegradation type new material become the following high molecule plastic material hair
The trend of exhibition.
Polyester is the high molecular material of the environmental type of biodegradable, and the substitute as oil product is more next
More it is concerned by people.In natural living environment, discarded polylactone material can thoroughly be divided by the microorganism in soil
Xie Chengshui and carbon dioxide, it is environmentally friendly and renewable.Because polyester is nontoxic, nonirritant, and has good biocompatibility,
It is therefore widely used in medicine and field of environment protection, such as operation suture thread, packaging, drug controlled release and tissue engineering bracket
Deng.The performance that the excellent biocompatibility of polylactone, biological degradability and sustainable development utilize, makes it have become 21 generation
The most promising high molecular material of discipline.
The advantages of easily method of synthesizing polyester is the ring-opening polymerisation method of cyclic lactone, this synthetic method be：Polymerization
Controllability, relatively narrow molecular weight distribution.Currently used catalyst is mostly the complex that ligand and metal are formed, in catalyst
Metal includes magnesium, calcium, germanium, tin, aluminium, zinc, iron, titanium, zirconium, group of the lanthanides etc..The selection of catalyst for ring-opening polymerization speed,
The three-dimensional regularity of resulting polymers and the performance of molecular weight products obtained therefrom all have a great influence, and the ligand of catalyst and match
The selection of position metal is all very crucial for the speed of ring-opening polymerization, the three-dimensional regularity of polymer and molecular weight, therefore
It studies the good catalyst ligand of new performance and composition catalyst is very necessary.
Invention content
The present invention provides a kind of asymmetric aluminum complex of base containing o-phenylenediamine, which can be used as cyclic lactone
The catalyst of ring-opening polymerization, catalytic activity is high, stereoselectivity is good, and resulting polymers molecular weight controllability is good, has
Good application prospect.
It is opened the present invention also provides the preparation method of the asymmetric aluminum complex of the base containing o-phenylenediamine and as cyclic lactone
The application of the catalyst of cyclopolymerization reaction.
The present invention is in the young project of National Nature fund committee（No 21104026）Subsidy under complete, skill of the present invention
Art scheme is as follows：
The asymmetric aluminum complex of present invention base containing o-phenylenediamine has the structural formula described in formula I：
。
The asymmetric aluminum complex of present invention base containing o-phenylenediamine is complex, by selection to ligand structure and with gold
The coordination for belonging to aluminium has excellent performance, and ligand structure of the present invention is special, and the selection of substituent group is for the aluminum complex in ligand
Catalytic performance as cyclic lactone ring-opening polymerization catalyst has larger impact.Wherein, R is the alkane or halogen of hydrogen, C1-C4
Element, the halogen are fluorine, chlorine, bromine or iodine.Further, stereoselectivity is best when R is tertiary butyl, catalytic activity when R is bromine
Most preferably.
The asymmetric aluminum complex of present invention base containing o-phenylenediamine is obtained by the reaction by ligand and trimethyl aluminium, preparation side
Method includes the following steps：Ligand A is added in organic solvent, -10~0 oTrimethyl aluminium is added under C, reaction temperature is made after adding
Degree nature is warmed to room temperature, and temperature is then risen to 30~110oC is reacted, and vacuum drains solvent, washing, filtering after reaction,
Obtain the asymmetric aluminum complex of the base containing o-phenylenediamine described in formula I.
The equation that ligand A is reacted with trimethyl aluminium is as follows, and the structural formula of wherein ligand A is shown below, and R is hydrogen, C1-
The alkane or halogen of C4, the halogen are fluorine, chlorine, bromine, iodine；R is preferably tertiary butyl or bromine；
In above-mentioned preparation method, the preparation method of ligand A includes the following steps：P-methyl benzenesulfonic acid is dissolved into dimethylbenzene, first
It is slowly added into the o-phenylenediamine of p-methyl benzenesulfonic acid equimolar amounts, adds the phthalic anhydride of p-methyl benzenesulfonic acid equimolar amounts,
Then heating carries out back flow reaction, is cooled to room temperature after reaction, filters, and obtains p-methyl benzenesulfonic acid and phthalic anhydride protection
O-phenylenediamine；The o-phenylenediamine that p-methyl benzenesulfonic acid and phthalic anhydride are protected is dissolved into dichloromethane, is slowly added dropwise
Saturated sodium bicarbonate aqueous solution is reacted to slough p-methyl benzenesulfonic acid, liquid separation after reaction, by gained organic phase with anhydrous
Magnesium sulfate is dried, and solvent is then spin-dried for, and obtains the o-phenylenediamine of unilateral phthalic anhydride protection；
Salicylide of o-phenylenediamine and equimolar amounts that unilateral phthalic anhydride is protected or derivatives thereof dissolves in methyl alcohol,
Heating carries out back flow reaction, and cooling after reaction, filtering, obtained solid is washed with cold methanol, is dry, obtains ligand A；The water
For the structural formula of poplar aldehyde derivatives as shown in following formula B, wherein R is the alkane or halogen of hydrogen, C1-C4, preferably tertiary butyl or bromine；
。
In above-mentioned preparation method, addition reaction occurs for ligand A and trimethyl aluminium, and the alkyl of trimethyl aluminium adds to ligand A
In C=O double bonds on, C=O double bonds become C-O singly-bounds.It is found by nuclear-magnetism characterizationδ=1.5-2.0 nearby has one group of CH3's
Characteristic peak, this characteristic peak are exactly NC (O) (Ar) CH 3Middle CH3Characteristic peak.
In above-mentioned preparation method, the molar ratio 1 of ligand A and trimethyl aluminium：1~1.3, preferably 1：1~1.05.
In above-mentioned preparation method, the organic solvent is one or both of hexane, toluene and the hexamethylene of drying, excellent
It is selected as dry hexane or toluene.
In above-mentioned preparation method, consumption of organic solvent is reaction raw materials（Ligand A and trimethyl aluminium）The 5~40 of gross mass
Times.
In above-mentioned preparation method, reaction carries out under gas shield, and the gas is inert gas or nitrogen.
In above-mentioned preparation method, reaction nature rises to 30~110 again after being raised to room temperatureoC is reacted, such as 30oC、
40oC、50oC、60oC、70oC、80oC、90oC、100oC、110oC, preferably 40~60oC.30~110oC（It is preferred that 40~60oC）
The time reacted is 1~12 hour, preferably 3~6 hours.After reaction, precipitation is washed with n-hexane.
The asymmetric aluminum complex of the base of the present invention containing o-phenylenediamine is the centre of the compound described in formula II
The asymmetric aluminum complex of product, the base containing o-phenylenediamine is more sensitive to water, the reaction solution after ligand A is reacted with trimethyl aluminium
Middle addition water is sufficiently stirred and aluminum complex can be made to hydrolyze, and through liquid separation, collects organic phase, the processing of organic phase recycling design, gained is surplus
Excess is through the compound that recrystallization is described in formula II.Therefore, preparing aluminum complex will be in the case of anhydrous and proton solvent
It carries out.In addition, using the compound described in formula II as raw material, ligand A is replaced with into the compound described in formula II, according to above-mentioned containing neighbour
The preparation method of the asymmetric aluminum complex of phenylenediamine base can also obtain the asymmetric aluminum complex of I base containing o-phenylenediamine of formula again.
When preparing the asymmetric aluminum complex of the base containing o-phenylenediamine with the compound described in formula II, organic solvent is dry
One or both of hexane, toluene and hexamethylene, preferably hexane or toluene.Consumption of organic solvent is reaction raw materials（Formula II
The compound and trimethyl aluminium）5~40 times of gross mass.Reaction is recrystallized after terminating with dry hexane, is obtained
The asymmetric aluminum complex of high I base containing o-phenylenediamine of formula of purity.
The asymmetric aluminum complex of present invention base containing o-phenylenediamine is complex, and N, N, O, O and aluminium of ligand are coordinated,
The structure of complex and classical cyclic lactone catalyst（salenAl）Structure it is very similar, excellent catalytic effect, have it is higher
Stereoselectivity.Asymmetric aluminum complex urging as cyclic lactone ring-opening polymerization of the present invention for the base containing o-phenylenediamine
The application of agent is also protected.
It, can when catalyst of the asymmetric aluminum complex of present invention base containing o-phenylenediamine as cyclic lactone ring-opening polymerization
To be catalyzed the ring-opening polymerisation of a variety of cyclic lactones, a series of polylactone is obtained.The cyclic lactone can beεCaprolactone, lactide
One or both of with glycolide, lactide can be levorotatory lactide, Study of Meso-Lactide, rac-lactide again.This
It is obtained by the reaction when the asymmetric aluminum complex of invention base containing o-phenylenediamine carries out cyclic lactone ring-opening polymerization as catalyst
Polymer molecule Mass Distribution is narrow, molecular weight is controllable, yield is high, especially when being catalyzed rac-lactide polymerization, obtains
The isotaxy polylactide high to fusing point, shows higher stereoselectivity, stereoselectivity reaches as high asP m= 0.80。
When the asymmetric aluminum complex of present invention base containing o-phenylenediamine is used as the catalyst of cyclic lactone ring-opening polymerization, when
Stereoselectivity is best when R is tertiary butyl, and catalytic activity is best when R is bromine.
When the asymmetric aluminum complex of present invention base containing o-phenylenediamine is as catalyst, cyclic lactone ring-opening polymerization tool
Body includes the following steps：It will be in the asymmetric aluminum complex catalyst of the base containing o-phenylenediamine, organic solvent, alcohol co-catalyst and ring
Ester mixes, and ring-opening polymerization is carried out under anhydrous and oxygen-free and inert gas shielding, handles reactant after reaction, is obtained poly-
Lactone.
In above-mentioned ring-opening polymerization, the molar ratio of cyclic lactone and the asymmetric aluminum complex catalyst of the base containing o-phenylenediamine
It is 50~1500：1, such as 50:1、100：1、150:1、200:1、300:1、400:1、500:1、600：1、800:1、1000:1、
1200:1、1500：1.
In above-mentioned ring-opening polymerization, it is toluene or tetrahydrofuran, preferably toluene to react organic solvent used.
In above-mentioned ring-opening polymerization, alcohol co-catalyst is benzylalcohol.Benzylalcohol co-catalyst is non-right with the base containing o-phenylenediamine
The molar ratio of aluminum complex catalyst is referred to as 1~3：1.
In above-mentioned ring-opening polymerization, polymeric reaction temperature be 20~110 DEG C, such as 20 DEG C, 30 DEG C, 40 DEG C, 50 DEG C, 60
℃、70℃、80℃、90℃、100℃、110℃.With the raising of polymeric reaction temperature, the stereoselectivity of catalyst has reduction
Trend, catalytic activity has raised trend, when reaction temperature is at 80 DEG C, solid when being catalyzed to rac-lactide
Selectivity is reachableP m =0.60, when reaction temperature is at 20 DEG C, stereoselectivity when being catalyzed to rac-lactide can
It reachesP m = 0.80。
In above-mentioned ring-opening polymerization, polymerization reaction time be 1-1440 minutes, such as 1 minute, 10 minutes, 30 minutes,
40 minutes, 60 minutes, 120 minutes, 240 minutes, 600 minutes, 900 minutes, 1200 minutes, 1440 minutes etc..
In above-mentioned ring-opening polymerization, cold methanol or ethanol purification polylactone are added after reaction, obtains polylactone after purification.
Catalytic activity when the asymmetric aluminum complex of present invention base containing o-phenylenediamine is as ring-opening polymerization catalyst
Height is catalyzed cyclic lactone open loop in the presence of benzylalcohol, since the structure of catalyst metals center aluminium is the chiral knot of NNOO coordinations
Structure, obtains fusing point high isotaxy polylactide when being catalyzed lactide polymerization, and obtained polymer is benzyloxy envelope
The polymer at end.When being catalyzed caprolactone and glycolide, obtained polymer is also the polymer of benzyloxy sealing end.
The asymmetric aluminum complex catalyst of present invention base containing o-phenylenediamine is reacted by ligand and trimethyl aluminium and is obtained, and is prepared
Method is simple, at low cost, and product yield is high, and the compound structure is special, and structure change is various, and the two of metal center aluminium and ligand
Valence N, N, O, O coordinations can be used as the catalyst of cyclic lactone ring-opening polymerization, and catalytic activity is high, stereoselectivity is good, reaction is fast
Rate is fast, and polymerisation is easy to operate, and obtained polymer molecular weight narrowly distributing, molecular weight is controllable, yield is high, can use extensively
It is a kind of very ideal catalyst in cyclic lactone ring-opening polymerisation.
Specific implementation mode
It is further illustrated the present invention below by specific embodiment, but the present invention is not limited thereto, specific protection domain is shown in
Claim.
In following embodiments, the stereoselectivity of isotaxy polylactide is carried out using nuclear magnetic resonance same core decoupling hydrogen spectrum
Test.
Prepare the o-phenylenediamine (a) of unilateral phthalic anhydride protection
0.60 g p-methyl benzenesulfonic acid is dissolved into dimethylbenzene, the o-phenylenediamine of p-methyl benzenesulfonic acid equimolar amounts is first slowly added into,
The phthalic anhydride of p-methyl benzenesulfonic acid equimolar amounts, heating reflux reaction 6h are added, reaction is cooled to room temperature after terminating
Solid is filtered, is washed, the o-phenylenediamine of p-methyl benzenesulfonic acid and phthalic anhydride protection is dried to obtain.By p-methyl benzenesulfonic acid and
The o-phenylenediamine of phthalic anhydride protection is dissolved into dichloromethane, and it is water-soluble that excessive sodium bicarbonate saturation is slowly added dropwise in room temperature
Liquid is reacted, and to slough p-methyl benzenesulfonic acid, liquid separation after reaction is dried with anhydrous magnesium sulfate, is spin-dried for solvent, obtains unilateral
0.74 g of o-phenylenediamine of phthalic anhydride protection, yield 89.2%.
Prepare the unsymmetric ligand of the base containing o-phenylenediamine（A）
The ligand of the base containing o-phenylenediamine is obtained by condensation reaction by the o-phenylenediamine of unilateral protection and salicylide or derivatives thereof
It arrives, illustrates below to synthesizing different ligand A.
Embodiment 1
Synthesized ligand structure formula such as above formula（A）, wherein R is hydrogen, and reaction process is：By the o-phenylenediamine of unilateral protection（a）
The salicylide of 0.40 g and equimolar amounts is added in 20 mL methanol, heating reflux reaction 12 hours, and reaction is cooled after terminating
It filters and is washed with cold methanol, filtered, collect and drying is weighed, obtain 0.50 g solids, yield 87.7%.
Products obtained therefrom is characterized, it is as a result as follows：
1H NMR (400 MHz, CDCl3) δ12.86 (s, 1H, OH), 8.42 (s, 1H, ArHC=N), 7.85 (m,
2H, Ar–H), 7.64 (d, J = 7.0 Hz, 1H, Ar–H), 7.56 (m, 1H, Ar–H), 7.44 (m, 3H,
Ar–H), 7.32 (m, 2H, Ar–H), 6.96 (m, 4H, Ar–H).
HRESI-MS: m/z cacld. C21H14N2O3 [M-H]-; 341.0926, found: 341.0924.
Can be seen that products obtained therefrom from the above characterization result is above formula（A）Middle R is the ligand of hydrogen.
Embodiment 2
Synthesized ligand structure formula such as above formula（A）, wherein R is methyl, and reaction process is：By the o-phenylenediamine of unilateral protection（a）
3, the 5- dimethyl salicylides of 0.30 g and equimolar amounts are added in 20 mL methanol, and heating reflux reaction 12 hours, reaction terminates
Later cold filtration is simultaneously washed with cold methanol, is filtered, and collects and drying is weighed, obtain 0.40 g solids, yield 85.1%.
Products obtained therefrom is characterized, it is as a result as follows：
1H NMR (400 MHz, CDCl3) δ12.72 (s, 1H, OH), 8.40 (s, 1H, ArHC=N), 7.80 (m,
2H, Ar–H), 7.66 (m, 2H, Ar–H), 7.15 (m, 3H, Ar–H), 6.92 (s, 1H, Ar–H), 2.15
(s, 3H, ArCH 3), 2.04 (s, 3H, ArCH 3). HRESI-MS: m/z cacld. C23H18N2O3 [M-H]-;
369.1238, found: 369.1238.
Can be seen that products obtained therefrom from the above characterization result is above formula（A）Middle R is the ligand of methyl.
Embodiment 3
Synthesized ligand structure formula such as above formula（A）, wherein R is bromine, and reaction process is：By the o-phenylenediamine of unilateral protection（a）
3, the 5- Dibromosalicylaldehydes of 0.35 g and equimolar amounts be added 20 mL methanol in, heating reflux reaction 12 hours, reaction terminate with
Postcooling is filtered and is washed with cold methanol, filtering, collects and drying is weighed, obtain 0.66 g solids, yield 90.4%.
Products obtained therefrom is characterized, it is as a result as follows：
1H NMR (400 MHz, CDCl3) δ12.64 (s, 1H, OH), 8.344 (s, 1H, ArHC=N), 7.86
(d, J = 7.2 Hz, 1H, Ar–H), 7.68 (m, 3H, Ar–H), 7.42 (m, 2H, Ar–H), 7.36 (m,
1H, Ar–H), 7.10 (m, 3H, Ar–H).
HRESI-MS: m/z cacld. C21H12Br2N2O3 [M-H]-; 496.9134, found: 496.9136.
Can be seen that products obtained therefrom from the above characterization result is above formula（A）Middle R is the ligand of bromine.
Embodiment 4
Synthesized ligand structure formula such as above formula（A）, wherein R is tertiary butyl, and reaction process is：By the o-phenylenediamine of unilateral protection
（a）3, the 5- di-tert-butyl salicylaldehydes of 0.40 g and equimolar amounts are added in 20 mL methanol, heating reflux reaction 12 hours, instead
It should terminate later cold filtration and be washed with cold methanol, be filtered, collect and drying is weighed, obtain 0.66 g solids, yield
86.8%。
Products obtained therefrom is characterized, it is as a result as follows：
1H NMR (400 MHz, CDCl3) δ12.80 (s, 1H, OH), 8.37 (s, 1H, ArHC=N), 7.82 (d,
J = 6.8 Hz, 1H, Ar–H), 7.70 (m, 3H, Ar–H), 7.64 (m, 2H, Ar–H), 7.38 (m, 1H,
Ar–H), 7.12 (m, 3H, Ar–H), 1.31 (s, 9H, CH 3), 1.24 (s, 9H, CH 3).
HRESI-MS: m/z cacld. C29H30N2O3 [M-H]-; 453.2176, found: 453.2177.
Can be seen that products obtained therefrom from the above characterization result is above formula（A）Middle R is the ligand of tertiary butyl.
Aluminum complex is prepared using ligand A as raw material（I）
Formula（I）Shown aluminum complex is eliminated by alkyl by ligand A and trimethyl aluminium and alkyl addition reaction generates, and reaction equation is such as
Under.
Embodiment 5
Ligand structure formula such as above formula used（A）, wherein R is hydrogen, and reaction process is：In a nitrogen atmosphere, by 0.35 g of ligand A
It is dissolved in 12 mL dry toluenes, the trimethyl aluminium of ligand 1.0 times of moles of A is added at -10 DEG C, waits for that reaction temperature rises naturally
It to after room temperature, is heated to 100 DEG C and reacts 1 hour, vacuum drains solvent after reaction terminates, and dry n-hexane filtering is added simultaneously
It is washed, is filtered with dry n-hexane, collected and drying is weighed, obtain 0.33 g solids, yield 80.5%.
Products therefrom nuclear-magnetism information is as follows, can be seen that the compound that R is hydrogen from nuclear-magnetism information（I）It synthesizes successfully.
1H NMR (400 MHz, CDCl3) δ 8.34 (s, 1H, ArHC=N), 7.63 (m, 2H, Ar–H),
7.51 (d, J = 6.2 Hz, 1H, Ar–H), 7.43 (m, 1H, Ar–H), 7.30 (m, 3H, Ar–H), 7.05
(m, 2H, Ar–H), 6.74 (m, 4H, Ar–H), 1.70 (s, 3H, CH 3), –0.53(s, 3H, AlCH 3).
Anal. Calcd for C23H19AlN2O3: C 69.34, H 4.81, N 7.03. Found: C 69.36, H 4.89,
N 7.00.
Embodiment 6
Ligand structure formula such as above formula used（A）, wherein R is methyl, and reaction process is：Under nitrogen atmosphere, by 0.30 g of ligand A
It is dissolved in 10 mL drying hexamethylenes, the trimethyl aluminium of ligand 1.05 times of moles of A is added at 0 DEG C, wait for reaction temperature nature
After being raised to room temperature, heating reaction temperature to 60 DEG C react 5 hours, reaction terminate after vacuum drain solvent, be added it is dry just
Hexane is filtered and is washed with dry n-hexane, is filtered, and collects and drying is weighed, obtain 0.29g solids, yield 82.9%.
Products therefrom nuclear-magnetism information is as follows, can be seen that the compound that R is methyl from nuclear-magnetism information（I）It synthesizes successfully.
1H NMR (400 MHz, CDCl3) δ 8.35 (s, 1H, ArHC=N), 7.62 (m, 2H, Ar–H),
7.52 (m, 2H, Ar–H), 7.18 (m, 3H, Ar–H), 6.83 (s, 1H, Ar–H), 2.12 (s, 3H,
ArCH 3), 2.06 (s, 3H, ArCH 3), 1.65 (s, 3H, CCH 3), –0.52 (s, 3H, AlCH 3). Anal.
Calcd for C25H23AlN2O3: C 70.41, H 5.44, N 6.57. Found: C 70.44, H 5.49, N
6.64.
Embodiment 7
Ligand structure formula such as above formula used（A）, wherein R is bromine, and reaction process is：Under nitrogen atmosphere, 0.40 g of ligand A is molten
In 12 mL dry toluenes, the trimethyl aluminium of ligand 1.1 times of moles of A is added at -5 DEG C, waits for that reaction temperature is raised to naturally
It after room temperature, is heated to 50 DEG C and reacts 7 hours, vacuum drains solvent after reaction terminates, and dry n-hexane is added filters and be used in combination
Dry n-hexane washing, filtering, is collected and drying is weighed, and obtains 0.37 g solids, yield 84.1%.
The nuclear-magnetism information of products obtained therefrom is as follows, it can be seen that R is the compound of bromine（I）It synthesizes successfully.
1H NMR (400 MHz, CDCl3) δ 8.40 (s, 1H, ArHC=N), 7.89 (d, J = 7.2 Hz,
1H, Ar–H), 7.63 (m, 3H, Ar–H), 7.48 (m, 2H, Ar–H), 7.37 (m, 1H, Ar–H), 7.16
(m, 3H, Ar–H), 1.74 (s, 1H, CCH 3), –0.48 (s, 3H, AlCH 3). Anal. Calcd for
C23H17AlBr2N2O3: C 49.67, H 3.08, N 5.04. Found: C 49.72, H 3.12, N 5.08.
Embodiment 8
Ligand structure formula such as above formula used（A）, wherein R is tertiary butyl, and reaction process is：Under nitrogen atmosphere, by ligand A 0.30
G is dissolved in 12 mL drying n-hexanes, and the trimethyl aluminium of ligand 1.0 times of moles of A is added at -10 DEG C, waits for reaction temperature certainly
It after being so raised to room temperature, is heated to 40 DEG C and reacts 8 hours, filter and weighed with dry n-hexane filter wash cake, collection and drying, obtained
0.27 g solids, yield 79.4%.
The nuclear-magnetism information of products therefrom is as follows, it can be seen that R is the compound of tertiary butyl（I）It synthesizes successfully.
1H NMR (400 MHz, CDCl3) δ 8.34 (s, 1H, ArHC=N), 7.84 (d, J = 7.0 Hz,
1H, Ar–H), 7.64 (m, 3H, Ar–H), 7.55 (m, 2H, Ar–H), 7.34 (m, 1H, Ar–H), 7.13
(m, 3H, Ar–H), 1.65 (s, 3H, CCH 3), 1.34 (s, 9H, CH 3), 1.26(s, 9H, CH 3), –0.48
(s, 3H, AlCH 3). Anal. Calcd for C31H35AlN2O3: C 72.92, H 6.91, N 5.49. Found: C
72.98, H 6.97, N 5.53.
It is that raw material prepares aluminum complex with ligand II（I）
Embodiment 9
R is that the ligand II of hydrogen synthesizes：In a nitrogen atmosphere, by ligand A（R is hydrogen）0.25 g is dissolved in 10 mL dry toluenes,
The trimethyl aluminium that ligand 1.0 times of moles of A are added at -10 DEG C is heated to 50 DEG C after reaction temperature is raised to room temperature naturally
Reaction 4 hours after reaction terminates, is added 39 microlitres of water and stops reaction, organic phase, anhydrous sodium sulfate drying, rotation are collected in liquid separation
Dry solvent, obtains crude product, by crude product through recrystallizing methanol, obtains 0.21 g of net product, 80.8 % of yield.
Products obtained therefrom is characterized, it is as a result as follows：
1H NMR (400 MHz, CDCl3) δ12.42 (s, 1H, OH), 8.36 (s, 1H, ArHC=N), 7.69 (m,
2H, Ar–H), 7.56 (d, J = 6.2 Hz, 1H, Ar–H), 7.48 (m, 1H, Ar–H), 7.33 (m, 3H,
Ar–H), 7.2 (m, 2H, Ar–H), 6.82 (m, 4H, Ar–H), 1.74 (s, 3H, CH 3).
HRESI-MS: m/z cacld. C22H18N2O3 [M-H]-; 357.1237, found: 357.1239.
Can be seen that products obtained therefrom from the above characterization result is above formula（Ⅱ）Middle R is the ligand of hydrogen.
Ligand structure formula such as above formula used（II）, wherein R is hydrogen, and reaction process is：In a nitrogen atmosphere, by ligand i I
0.40 g is dissolved in 10 mL drying hexamethylenes, and the trimethyl aluminium of ligand i 1.0 times of moles of I is added at -10 DEG C, waits reacting
After temperature is raised to room temperature naturally, it is heated to 40 DEG C and reacts 6 hours, reaction is filtered after terminating and is washed with dry n-hexane,
Filtering, is collected and drying is weighed, and obtains 0.36 g solids, yield 81.8%.For product structure formula as shown in formula I, R is hydrogen.
Embodiment 10
R is that the ligand II of methyl synthesizes：Under nitrogen atmosphere, by ligand A（R is methyl）0.35 g is dissolved in 10 mL drying hexamethylenes
In, the trimethyl aluminium of ligand 1.05 times of moles of A is added at 0 DEG C, after reaction temperature is raised to room temperature naturally, heating reaction
Temperature is reacted 3 hours to 70 DEG C, and 51 microlitres of water are added after reaction and stop reacting, liquid separation collection organic phase, anhydrous sodium sulfate drying,
It is spin-dried for solvent, obtains crude product, by crude product through recrystallizing methanol, obtains 0.30 g of net product, yield 81.1%.
Products obtained therefrom is characterized, it is as a result as follows：
1H NMR (400 MHz, CDCl3) δ12.60 (s, 1H, OH), 8.24 (s, 1H, ArHC=N), 7.60 (m,
2H, Ar–H), 7.46 (m, 2H, Ar–H), 7.12 (m, 3H, Ar–H), 6.80 (s, 1H, Ar–H), 2.10
(s, 3H, ArCH 3), 2.02 (s, 3H, ArCH 3), 1.67 (s, 3H, CCH 3). HRESI-MS: m/z cacld.
C24H22N2O3 [M-H]-; 386.1554, found: 386.1556.
Can be seen that products obtained therefrom from the above characterization result is above formula（Ⅱ）Middle R is the ligand of methyl.
Ligand structure formula such as above formula used（II）, wherein R is methyl, and reaction process is：Under nitrogen atmosphere, by ligand i I
0.30 g is dissolved in 10 mL dry toluenes, and the trimethyl aluminium of ligand i 1.05 times of moles of I is added at 0 DEG C, waits for reaction temperature
Naturally after being raised to room temperature, heating reaction temperature is reacted 1 hour to 110 DEG C, and vacuum drains solvent after reaction terminates, and is added dry
Dry n-hexane is filtered and is washed with dry n-hexane, is filtered, and collects and drying is weighed, obtain 0.26 g solids, yield
78.8%.For product structure formula as shown in formula I, R is methyl.
Embodiment 11
R is that the ligand II of bromine synthesizes：Under nitrogen atmosphere, by ligand A（R is bromine）0.35 g is dissolved in 12 mL dry toluenes ,-
The trimethyl aluminium of ligand 1.1 times of moles of A is added at 5 DEG C, after reaction temperature is raised to room temperature naturally, is heated to 50 DEG C of reactions 6
Hour, reaction is added 38 microlitres of water and stops reaction after terminating, organic phase is collected in liquid separation, and anhydrous sodium sulfate drying is spin-dried for molten
Agent obtains crude product, by crude product through ethyl alcohol recrystallization, obtains 0.30 g of net product, yield 83.3%.
Products obtained therefrom is characterized, it is as a result as follows：
1H NMR (400 MHz, CDCl3) δ12.43 (s, 1H, OH), 8.34 (s, 1H, ArHC=N), 7.64 (d,
J = 7.0 Hz, 1H, Ar–H), 7.54 (m, 3H, Ar–H), 7.37 (m, 2H, Ar–H), 7.30 (m, 1H,
Ar–H), 7.08 (m, 3H, Ar–H), 1.67 (s, 1H, CCH 3).
HRESI-MS: m/z cacld. C22H16Br2N2O3 [M-H]-; 512.9449, found: 512.9447.
Can be seen that products obtained therefrom from the above characterization result is above formula（Ⅱ）Middle R is the ligand of bromine.
Ligand structure formula such as above formula used（II）, wherein R is bromine, and reaction process is：Under nitrogen atmosphere, by ligand i I
0.40 g is dissolved in 15 mL drying hexanes, and the trimethyl aluminium of ligand i 1.0 times of moles of I is added at -5 DEG C, waits for reaction temperature
Naturally after being raised to room temperature, 60 DEG C is heated to and is reacted 2 hours, reaction is filtered and washed with dry n-hexane, mistake after terminating
Filter, is collected and drying is weighed, and obtains 0.39 g solids, yield 90.7%.For product structure formula as shown in formula I, R is bromine.
Embodiment 12
R is that the ligand II of tertiary butyl synthesizes：Under nitrogen atmosphere, by ligand A（R is tertiary butyl）0.25 g is being dissolved in 10 mL dryings just
In hexane, the trimethyl aluminium of ligand 1.3 times of moles of A is added at -5 DEG C, after reaction temperature is raised to room temperature naturally, heating
It is reacted 9 hours to 30 DEG C, 30 microlitres of water is added after reaction and stop reaction, organic phase is collected in liquid separation, and anhydrous sodium sulfate drying is spin-dried for
Solvent obtains crude product, by crude product through recrystallizing methanol, obtains 0.21 g of net product, yield 80.8%.
Products obtained therefrom is characterized, it is as a result as follows：
1H NMR (400 MHz, CDCl3) δ12.67 (s, 1H, OH), 8.30 (s, 1H, ArHC=N), 7.74 (d,
J = 6.6 Hz, 1H, Ar–H), 7.62 (m, 3H, Ar–H), 7.52 (m, 2H, Ar–H), 7.30 (m, 1H,
Ar–H), 7.08 (m, 3H, Ar–H), 1.67 (s, 3H, CCH 3), 1.30 (s, 9H, CH 3), 1.22(s, 9H,
CH 3).
HRESI-MS: m/z cacld. C30H34N2O3 [M-H]-; 469.2491, found: 469.2493.
Can be seen that products obtained therefrom from the above characterization result is above formula（Ⅱ）Middle R is the ligand of tertiary butyl.
Ligand structure formula such as above formula used（II）, wherein R is tertiary butyl, and reaction process is：Under nitrogen atmosphere, by ligand i I
0.30 g is dissolved in 10 mL dry toluenes, and the trimethyl aluminium of ligand i 1.2 times of moles of I is added at 0 DEG C, waits for reaction temperature
Naturally after being raised to room temperature, 50 DEG C is heated to and is reacted 4 hours, reaction is filtered and washed with dry n-hexane, mistake after terminating
Filter, is collected and drying is weighed, and obtains 0.29 g solids, yield 87.9%.For product structure formula as shown in formula I, R is tertiary butyl.
Prepare polyglycolide
Embodiment 13
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
100 μm of ol catalyst are added（Aluminum complex shown in formula I, R are hydrogen）, 100 μm of ol benzylalcohols, 20 mL toluene and 10 mmol
Glycolide, be subsequently placed in 110oIn the oil bath of C, reaction is added a small amount of water and terminates reaction after 14 minutes, with ethanol precipitation, washing
For several times, it is dried in vacuo at room temperature, obtains 1.10 g products, yield 94.8%, molecular weight 2.3 ten thousand.
Embodiment 14
Polyglycolide is prepared according to the method for embodiment 13, unlike：Catalyst used is aluminum complex shown in formula I, R
For methyl.The quality of products obtained therefrom is 1.08 g after reaction 15 minutes, and yield 93.1%, molecular weight is 2.1 ten thousand.
Embodiment 15
Polyglycolide is prepared according to the method for embodiment 13, unlike：Catalyst used is aluminum complex shown in formula I, R
For bromine.The quality of products obtained therefrom is 1.12 g after reaction 8 minutes, and yield 96.6%, molecular weight is 2.1 ten thousand.
Embodiment 16
Polyglycolide is prepared according to the method for embodiment 13, unlike：Catalyst used is aluminum complex shown in formula I, R
For tertiary butyl.The quality of products obtained therefrom is 1.11 g after reaction 18 minutes, and yield 95.7%, molecular weight is 2.2 ten thousand.
Embodiment 17
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
100 μm of ol catalyst are added（Aluminum complex shown in formula I, R are bromine）, 100 μm of ol benzylalcohols, 20 mL toluene and 10 mmol
Glycolide, then respectively 20oC、40oC、60oC、80oC and 100oIt is reacted under C, a small amount of water is added after reaction and terminates instead
It answers, for several times with methanol extraction, washing, is dried in vacuo at room temperature.
Wherein, it is reacted 20 hours at 20 DEG C, obtains 1.10 g products, yield 94.8%, molecular weight 2.2 ten thousand.
It is reacted 11 hours at 40 DEG C, obtains 1.10 g products, yield 94.8%, molecular weight 2.1 ten thousand.
It is reacted 6 hours at 60 DEG C, obtains 1.11 g products, yield 95.7%, molecular weight 2.3 ten thousand.
It is reacted 45 minutes at 80 DEG C, obtains 1.11 g products, yield 95.7%, molecular weight 2.1 ten thousand.
It is reacted 16 minutes at 100 DEG C, obtains 1.12 g products, yield 96.6%, molecular weight 2.2 ten thousand.
Embodiment 18
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
10 μm of ol catalyst are added（Aluminum complex shown in formula I, R are hydrogen）, 30 μm of ol benzylalcohols, 10 mL tetrahydrofurans and 15
The glycolide of mmol, then 30oC is added a small amount of water and terminates reaction after reacting 18 hours, for several times with methanol extraction, washing, room temperature
Lower vacuum drying obtains 1.65 g products, yield 94.8%, molecular weight 14.2 ten thousand.
Embodiment 19
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
10 μm of ol catalyst are added（Aluminum complex shown in formula I, R methyl）, 20 μm of ol benzylalcohols, 20 mL tetrahydrofurans and 10
The glycolide of mmol, is subsequently placed in 50oIn the oil bath of C, reaction is added a small amount of water and terminates reaction after 9 hours, with ethanol precipitation, wash
It washs for several times, is dried in vacuo at room temperature, obtain 1.11 g products, yield 95.7%, molecular weight 14.8 ten thousand.
Embodiment 20
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
200 μm of ol catalyst are added（Aluminum complex shown in formula I, R are tertiary butyl）, 200 μm of ol benzylalcohols, 10 mL toluene and 10
The glycolide of mmol, is subsequently placed in 70oIn the oil bath of C, reaction is added a small amount of water and terminates reaction after 6 hours, with methanol extraction, wash
It washs for several times, is dried in vacuo at room temperature, obtain 1.11 g products, yield 95.7%, molecular weight 1.2 ten thousand.
Embodiment 21
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
10 μm of ol catalyst are added（Aluminum complex shown in formula I, R are hydrogen）, 20 μm of ol benzylalcohols, 15 mL toluene and 5 mmol second
Lactide, then 90oC is added a small amount of water and terminates reaction after reacting 6 hours, for several times with methanol extraction, washing, vacuum is dry at room temperature
It is dry, obtain 0.55 g products, yield 94.8%, molecular weight 7.4 ten thousand.
Prepare poly-epsilon-caprolactone
Embodiment 22
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
100 μm of ol catalyst are added（Aluminum complex shown in formula I, R are hydrogen）, 100 μm of ol benzylalcohols, 10 mL toluene and 10 mmol
Caprolactone, be subsequently placed in 110oIn the oil bath of C, reaction is added a small amount of water and terminates reaction after 6 minutes, with ethanol precipitation, washing
For several times, it is dried in vacuo at room temperature, obtains 1.10 g products, yield 96.5%, molecular weight 2.3 ten thousand.
Embodiment 23
Polycaprolactone is prepared according to the method for embodiment 22, unlike：Catalyst used is aluminum complex shown in formula I, R
For methyl.The quality of products obtained therefrom is 1.11 g after reaction 8 minutes, and yield 97.4%, molecular weight is 2.1 ten thousand.
Embodiment 24
Polycaprolactone is prepared according to the method for embodiment 22, unlike：Catalyst used is aluminum complex shown in formula I, R
For bromine.The quality of products obtained therefrom is 1.12 g after reaction 2 minutes, and yield 98.2%, molecular weight is 2.4 ten thousand.
Embodiment 25
Polycaprolactone is prepared according to the method for embodiment 22, unlike：Catalyst used is aluminum complex shown in formula I, R
For tertiary butyl.The quality of products obtained therefrom is 1.11 g after reaction 9 minutes, and yield 97.4%, molecular weight is 2.2 ten thousand.
Embodiment 26
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
100 μm of ol catalyst are added（Aluminum complex shown in formula I, R are bromine）, 100 μm of ol benzylalcohols, 10 mL toluene and 10 mmol
Caprolactone, then respectively 20oC、40oC、60oC、80oC and 100oIt is reacted under C, a small amount of water is added after reaction and terminates instead
It answers, for several times with methanol extraction, washing, is dried in vacuo at room temperature.
Wherein, it is reacted 40 minutes at 20 DEG C, obtains 1.10 g products, yield 96.5%, molecular weight 2.2 ten thousand.
It is reacted 20 minutes at 40 DEG C, obtains 1.10 g products, yield 96.5%, molecular weight 2.1 ten thousand.
It is reacted 14 minutes at 60 DEG C, obtains 1.11 g products, yield 97.4%, molecular weight 2.2 ten thousand.
It is reacted 11 minutes at 80 DEG C, obtains 1.11 g products, yield 97.4%, molecular weight 2.3 ten thousand.
It is reacted 4 minutes at 100 DEG C, obtains 1.12 g products, yield 98.2%, molecular weight 2.1 ten thousand.
Embodiment 27
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
10 μm of ol catalyst are added（Aluminum complex shown in formula I, R are hydrogen）, 30 μm of ol benzylalcohols, 10 mL tetrahydrofurans and 5 mmol
6-caprolactone, then 30oC reactions are added a small amount of water and terminate reaction after sixty minutes, for several times with ethanol precipitation, washing, at room temperature
Vacuum drying, obtains 0.55 g products, yield 96.5%, molecular weight 6.4 ten thousand.
Embodiment 28
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
10 μm of ol catalyst are added（Aluminum complex shown in formula I, R are methyl）, 30 μm of ol benzylalcohols, 10 mL toluene and 10 mmol
6-caprolactone, then 50oC is added a small amount of water and terminates reaction after reacting 30 minutes, for several times with ethanol precipitation, washing, at room temperature
Vacuum drying, obtains 1.10 g products, yield 96.5%, molecular weight 7.8 ten thousand.
Embodiment 29
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
10 μm of ol catalyst are added（Aluminum complex shown in formula I, R are tertiary butyl）, 20 μm of ol benzylalcohols, 15 mL toluene and 15
The 6-caprolactone of mmol, is subsequently placed in 90oIn the oil bath of C, reaction is added a small amount of water and terminates reaction after 11 minutes, heavy with ethyl alcohol
It forms sediment, wash for several times, be dried in vacuo at room temperature, obtain 1.65 g products, yield 96.5%, molecular weight 16.3 ten thousand.
Embodiment 30
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
100 μm of ol catalyst are added（Aluminum complex shown in formula I, R are hydrogen）, 100 μm of ol benzylalcohols, 10 mL toluene and 5 mmol
6-caprolactone, be subsequently placed in 70oIn the oil bath of C, reaction is added a small amount of water and terminates reaction after 16 minutes, with ethanol precipitation, wash
It washs for several times, is dried in vacuo at room temperature, obtain 0.54 gram of product, yield 94.7%, molecular weight 1.1 ten thousand.
Prepare polylactide
Embodiment 31
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
100 μm of ol catalyst are added（Aluminum complex shown in formula I, R are hydrogen）, 100 μm of ol benzylalcohols, 20 mL toluene and 10 mmol
Rac-lactide, then 20oC is added a small amount of water and terminates reaction after reacting 22 hours, for several times with ethanol precipitation, washing, room
The lower vacuum drying of temperature, obtains 1.35 g products, yield 93.8%.Products therefrom be isotaxy polylactide, molecular weight 2.9 ten thousand,
Isotaxy stereoselectivityP m= 0.75。
Embodiment 32
Polylactide is prepared according to the method for embodiment 31, unlike：Catalyst used is aluminum complex shown in formula I, R
For methyl.The quality of products obtained therefrom is 1.3 3 g after reaction 23 hours, and yield 92.4%, molecular weight is 2.7 ten thousand, Quan Tongli
Structure stereoselectivityP m= 0.78。
Embodiment 33
Polylactide is prepared according to the method for embodiment 31, unlike：Catalyst used is aluminum complex shown in formula I, R
For bromine.The quality of products obtained therefrom is 1.37 g after reaction 21 hours, and yield 95.1%, molecular weight is 2.7 ten thousand, isotaxy
StereoselectivityP m= 0.77。
Embodiment 34
Polylactide is prepared according to the method for embodiment 31, unlike：Catalyst used is aluminum complex shown in formula I, R
For tertiary butyl.The quality of products obtained therefrom is 1.36 g after reaction 24 hours, and yield 94.4%, molecular weight is 2.8 ten thousand, Quan Tong
Vertical structure stereoselectivityP m= 0.80。
Embodiment 35
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
100 μm of ol catalyst are added（Aluminum complex shown in formula I, R are tertiary butyl）, 100 μm of ol benzylalcohols, 10 mL toluene and 10
The rac-lactide of mmol, then respectively 40oC、60oC and 80oIt is reacted under C, a small amount of water is added after reaction and terminates instead
It answers, for several times with methanol extraction, washing, is dried in vacuo at room temperature.
Wherein, it is reacted 22 hours at 40 DEG C, obtains 1.38 g products, yield 95.8%, molecular weight 2.9 ten thousand,P m = 0.76。
It is reacted 19 hours at 60 DEG C, obtains 1.40 g products, yield 97.2%, molecular weight 2.6 ten thousand,P m = 0.68。
It is reacted 16 hours at 80 DEG C, obtains 1.38 g products, yield 95.8%, molecular weight 2.8 ten thousand,P m = 0.60。
Embodiment 36
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
200 μm of ol catalyst are added（Aluminum complex shown in formula I, R are hydrogen）, 200 μm of ol benzylalcohols, 20 mL tetrahydrofurans and 10
The levorotatory lactide of mmol, then 30oC is added a small amount of water and terminates reaction after reacting 21 hours, for several times with ethanol precipitation, washing,
It is dried in vacuo at room temperature, obtains 1.41 g products, yield 97.9%, molecular weight 1.2 ten thousand.
Embodiment 37
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
10 μm of ol catalyst are added（Aluminum complex shown in formula I, R are methyl）, 10 μm of ol benzylalcohols, 10 mL tetrahydrofurans and 5
The Study of Meso-Lactide of mmol, is subsequently placed in 50oIn the oil bath of C, reaction is added a small amount of water and terminates reaction after 18 hours, use ethyl alcohol
Precipitation, washing for several times, are dried in vacuo, obtain 0.68 g products, yield 94.4%, molecular weight 12.1 ten thousand at room temperature.
Embodiment 38
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
10 μm of ol catalyst are added（Aluminum complex shown in formula I, R are bromine）, 30 μm of ol benzylalcohols, 20 mL toluene and 10 mmol
Levorotatory lactide, then 90oC is added a small amount of water and terminates reaction after reacting 3 hours, for several times with ethanol precipitation, washing, at room temperature very
Sky is dry, obtains 1.41 g products, yield 97.9%, molecular weight 7.4 ten thousand.
Embodiment 39
It is reacted under anhydrous and oxygen-free and inert gas shielding, the sequence first in the ampulla after being toasted with high pure nitrogen gas washing
10 μm of ol catalyst are added（Aluminum complex shown in formula I, R are bromine）, 20 μm of ol benzylalcohols, 20 mL toluene and 15 mmol
Levorotatory lactide is subsequently placed in 110oIn the oil bath of C, reaction is added a small amount of water and terminates reaction after 1.5 hours, with ethanol precipitation,
Washing for several times, is dried in vacuo, obtains 2.10 grams of products, yield 97.2%, molecular weight 17.8 ten thousand at room temperature.
Comparative example 1
The preparation of Raney nickel：Ligand structure formula such as above formula used（II）, R is bromine, and reaction process is：0.30 g of ligand is dissolved in
In 20 mL absolute ethyl alcohols, the nickel acetate of 1.0 times of ligand moles is added at room temperature, heating reflux reaction 12 hours, reaction terminates
It is concentrated in vacuo solvent later, dichloromethane is added, solid is precipitated, filter and simultaneously washed with hexane, dry Raney nickel, structure
Formula is as follows.
Polylactide is prepared according to the method for embodiment 39, unlike：Catalyst used is above-mentioned Raney nickel.Instead
A small amount of water is added after answering 24 hours and terminates reaction, for several times with methanol extraction, washing, is dried in vacuo at room temperature, obtains 0.43 g, yield
19.9 %, molecular weight 1.9 ten thousand.The Raney nickel is too low to the polymerization activity of lactide, is not worth.
Comparative example 2
The preparation of Al catalysts：Ligand structure formula such as following formula used（LH2）, reaction process is：In anhydrous and oxygen-free and inert gas
Under protection, 0.20 g of ligand is dissolved in 10 mL toluene, the trimethyl aluminium of 1.0 times of ligand moles is added at -5 DEG C, is delayed
Slowly it is heated to 80 DEG C after being warmed to room temperature to react 12 hours, reaction is concentrated in vacuo solvent after terminating, addition drying hexane is precipitated solid
Body is filtered and is simultaneously washed with hexane, dry Al catalysts, structural formula LAlMe as follows.
Polylactide is prepared according to the method for embodiment 35, unlike：Catalyst used is the Al catalysts.In nothing
It is reacted under water anaerobic and inert gas shielding, is sequentially added 100 in the ampulla after being toasted with high pure nitrogen gas washing first
μm ol catalyst（Aluminum complex shown in formula I, R are tertiary butyl）, 100 μm of ol benzylalcohols, 10 mL toluene and 10 mmol it is outer
Meso-lactide, then respectively 20oC and 80oReacted under C, a small amount of water be added after reaction and terminates reaction, with methanol extraction,
Washing for several times, is dried in vacuo at room temperature.
Wherein, it reacts at 20 DEG C 36 hours and is generated without product, illustrate that the catalyst can not be catalyzed third at a lower temperature
The polymerization of lactide.
1.15 g products, 79.9 % of yield, molecular weight 1.4 ten thousand, the selection of isotaxy solid are reacted 24 hours to obtain at 80 DEG C
PropertyP m = 0.53.It compares with the Al catalysts of embodiment 35, stereoselectivity and activity are all relatively low.
Comparative example 3
Polylactide is prepared according to the method for embodiment 31, unlike：Catalyst used is patent 201410609375.8
Catalyst used in middle embodiment 10.Gained polylactide is heterotactic polylactide, quality 1.33 after reaction
G, yield 92.4%, molecular weight are 1.7 ten thousand, heterotactic stereoselectivityP r It is 0.71.
Comparative example 4
Under nitrogen atmosphere, by ligand A（R is methyl）0.35 g is dissolved in 10 mL drying hexamethylenes, and ligand A is added at 0 DEG C
The triisopropylaluminiuand of 1.05 times of moles, after reaction temperature is raised to room temperature naturally, heating reaction temperature is small to 70 DEG C of reactions 12
When, 51 microlitres of water are added after reaction and stop reaction, organic phase is collected in liquid separation, and anhydrous sodium sulfate drying is spin-dried for solvent, finds to obtain
Compound does not change（Isopropyl does not carry out C=O addition reactions）.Triisopropylaluminiuand can not carry out addition reaction.
Comparative example 5
Polylactide is prepared according to the method for embodiment 31, unlike：Catalyst used is aluminum complex shown in formula I, R
For methoxyl group.The quality of products obtained therefrom is 0.99 g after reaction 36 hours, and yield 68.8%, molecular weight is 1.3 ten thousand, Quan Tong
Vertical structure stereoselectivityP m= 0.67。
Comparative example 6
P-methyl benzenesulfonic acid is dissolved into dimethylbenzene, is first slowly added into 1, the 3- propane diamine of p-methyl benzenesulfonic acid equimolar amounts, then add
Enter the phthalic anhydride of p-methyl benzenesulfonic acid equimolar amounts, heating reflux reaction, reaction is cooled to room temperature by solid after terminating
Filtering is washed, dry, obtains 1, the 3- propane diamine of p-methyl benzenesulfonic acid and phthalic anhydride protection.By p-methyl benzenesulfonic acid and neighbour
1, the 3- propane diamine of phthalate anhydride protection is dissolved into dichloromethane, and excessive sodium bicarbonate saturated water is slowly added dropwise at room temperature
Solution is reacted, and to slough p-methyl benzenesulfonic acid, liquid separation after reaction is dried with anhydrous magnesium sulfate, is spin-dried for solvent, obtains list
1, the 3- propane diamine of side phthalic anhydride protection.3, the 5- bis- of the propane diamine and equimolar amounts of unilateral phthalic anhydride protection
Bromosalicylaldehyde is heated to reflux in methyl alcohol, and reaction is put into cooling in refrigerator, precipitation solid, filtering, with cold methanol after terminating
Washing, it is dry, obtain compound L D.
The preparation of Al catalysts：Under nitrogen atmosphere, 0.20 g of compound L D are dissolved in 10 mL dry toluenes, -10
The trimethyl aluminium of 1.0 times of compound L D moles is added at DEG C, after reaction temperature is raised to room temperature naturally, is heated to 110 DEG C instead
It answers 1 hour, vacuum drains solvent after reaction terminates, and dry n-hexane washing, filtering, drying is added, it is solid to obtain 0.18 g
Body, yield 81.8%, the aluminium compound through hydrolysis after do mass spectral characteristi find such ligand can only unilateral generation addition reaction obtain
To LDAlMe2（HRESI-MS: m/z cacld. C18H14Br2N2O3 [M-H]-; 462.9294, found: 462.9292）.
Polylactide is prepared according to the method for embodiment 31, unlike：Catalyst used is the Al catalysts.Reaction
The quality of products obtained therefrom is 0.60 g afterwards, and yield 41.7%, molecular weight is 1.2 ten thousand, no stereoselectivity.
Claims (9)
1. a kind of asymmetric aluminum complex of base containing o-phenylenediamine, it is characterized in that：It is with the structural formula described in formula I, wherein R
For hydrogen, the alkane or halogen of C1-C4；
。
2. asymmetric aluminum complex according to claim 1, it is characterized in that：R is preferably tertiary butyl or bromine.
3. the preparation method of the asymmetric aluminum complex of a kind of base described in claim 1 containing o-phenylenediamine, it is characterized in that including
Following steps：Ligand A or ligand II are added in organic solvent, -10~0 oTrimethyl aluminium is added under C, makes reaction after adding
Temperature is warmed to room temperature naturally, and temperature is then risen to 30~110oC is reacted, and vacuum drains solvent, washing, mistake after reaction
Filter, obtains the asymmetric aluminum complex of the base containing o-phenylenediamine described in formula I；Ligand A and II structural formula of ligand are as follows, wherein R is
The alkane or halogen of hydrogen, C1-C4, preferably tertiary butyl or bromine；
。
4. preparation method according to claim 3, it is characterized in that：The molar ratio 1 of ligand A or ligand II and trimethyl aluminium：1
~1.3, preferably 1：1~1.05.
5. preparation method according to claim 3, it is characterized in that：The organic solvent is hexane, toluene and the ring of drying
One or both of hexane.
6. preparation method according to claim 3, it is characterized in that：Consumption of organic solvent be reaction raw materials gross mass 5~
40 times.
7. preparation method according to claim 3, it is characterized in that：It is raised to room temperature and temperature is risen to 30~110 again lateroC
（It is preferred that 40~60oC）Reaction 1~12 hour is preferably reacted 3~6 hours.
8. preparation method according to claim 3, it is characterized in that：Reaction carries out under inert gas protection.
9. the asymmetric aluminum complex of the base as claimed in claim 1 or 2 containing o-phenylenediamine is as cyclic lactone ring-opening polymerization
The application of catalyst, it is preferred that the cyclic lactone be levorotatory lactide, Study of Meso-Lactide, rac-lactide, caprolactone or
Glycolide.
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Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103421034A (en) * | 2013-08-09 | 2013-12-04 | 中国科学院长春应用化学研究所 | Chiral aluminum compound and preparation method thereof and preparation method of polylactic acid |
| CN104370951A (en) * | 2014-11-04 | 2015-02-25 | 济南大学 | Methyl aluminum complex of tetradentate nitrogen-oxygen ligand and application thereof |
| CN108503576A (en) * | 2017-12-12 | 2018-09-07 | 济南大学 | Unsymmetric ligand of the base containing o-phenylenediamine and its preparation method and application |
-
2017
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103421034A (en) * | 2013-08-09 | 2013-12-04 | 中国科学院长春应用化学研究所 | Chiral aluminum compound and preparation method thereof and preparation method of polylactic acid |
| CN104370951A (en) * | 2014-11-04 | 2015-02-25 | 济南大学 | Methyl aluminum complex of tetradentate nitrogen-oxygen ligand and application thereof |
| CN108503576A (en) * | 2017-12-12 | 2018-09-07 | 济南大学 | Unsymmetric ligand of the base containing o-phenylenediamine and its preparation method and application |
Non-Patent Citations (1)
| Title |
|---|
| STUART L. HANCOCK ET AL: "Aluminium salalen complexes based on 1,2-diaminocyclohexane and their exploitation for the polymerisation of rac-lactide", 《DALTON TRANSACTIONS》 * |
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| CN108503576B (en) * | 2017-12-12 | 2020-08-21 | 济南大学 | Asymmetric ligand containing o-phenylenediamine group, preparation method and application thereof |
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