Tough, healable composites displaying stress relaxation at the resin-filler interface
The present invention relates in part to compositions displaying stress relaxation at the polymer-filler interface. The adaptive interface (AI) formed by coupling moieties capable of dynamic covalent chemistry (DCC) within the polymer-filler interface promotes stress relaxation and yields tough, and healable composites.
1. A composition comprising:
a polymer comprising at least one selected from at least one multifunctional thiol monomer, a thiol-ene polymer, and a combination thereof; and
a filler, wherein the filler comprises at least one nanoparticle (NP) functionalized with a chemical moiety capable of engaging in dynamic covalent chemistry (DCC) with the polymer at the polymer-filler interface;
wherein the composition displays stress relaxation at the interface between the polymer and the filler; and
wherein the at least one nanoparticle (NP) is functionalized with a linker comprising at least one of the following groups:
(a) at least one allylic terminal thiol (—SH) group;
or
(b) at least one multifunctional thioester of formula (I),
wherein:
A 1 and A 2 are each independently selected from the group consisting of optionally substituted C 1 -C 15 alkylene, optionally substituted C 2 -C 15 alkenylene, optionally substituted C 2 -C 15 alkynylene, optionally substituted C 2 -C 15 heteroalkylene, optionally substituted C 2 -C 15 heteroalkenylene and optionally substituted C 2 -C 15 heteroalkynylene;
E 2 is selected from the group consisting of:
each instance of Y 1 is independently selected from the group consisting of O and N(R 1 );
each instance of R 1 being independently selected from the group consisting of H and C 1 -C 6 alkyl;
m1 is 0 or 1;
m2 is 0 or 1;
X 1 is
wherein:
bond a is to A 1 ,
Q is CH 2 or
n is 0, 1, 2, 3, 4, 5 or 6;
X 2 is
wherein:
bond a is to A 2 ,
bond b is to E 2 ,
Q is CH 2 or
n is 0, 1, 2, 3, 4, 5 or 6;
each instance of Y 2 is independently selected from the group consisting of C(R 1 ) 2 , O, and N(R 1 );
each instance of Y 3 is independently selected from the group consisting of C(R 1 ) 2 , O, and N(R 1 ); and
each instance of R 1 is independently selected from the group consisting of H and C 1 -C 6 alkyl.
2. The composition of claim 1 , wherein the at least one multifunctional thiol monomer is selected from the group consisting of:
wherein each instance of n is independently an integer from 0 to 500; or
wherein the at least one multifunctional thiol monomer is selected from the group consisting of: pentaerythritol tetramercaptopropionate (PETMP), ethylene glycol bis(3-mercaptopropionate) (EGBMP); trimethylolpropane tris(3-mercaptopropionate)(TMPMP), 2,4,6-trioxo-1,3,5-triazina-triy (triethyl-tris (3-mercapto propionate); 1,2-ethanedithiol, 1,3-propanedithiol, 1,4-butanedithiol; 1,5-pentanedithiol; 1,6-hexanedithiol, 1,8-octanedithiol, 1,9-nonanedithiol, 1,11-undecanedithiol; 1,16-hexadecanedithiol, 2,5-dimercaptomethyl-1,4-dithiane, pentaerythritol tetramercaptoacetate; trimethylolpropane trimercaptoacetate; glycol dimercaptoacetate, 2,3-dimercapto-1-propanol; DL-dithiothreitol; 2-mercaptoethylsulfide, 2,3-(dimercaptoethylthio)-1-mercaptopropane, 1,2,3-trimercaptopropane, toluenedithiol; benzenedithiol, biphenyldithiol, benzenedimethanethiol; xylylenedithiol, 4,4′-dimercaptostilbene, glycol dimercaptopropionate, and combinations thereof; or
wherein the thiol-ene polymer comprises an ene monomer selected from a group consisting of ethylene glycoldi(meth)acrylate, ethoxylated bisphenol-A dimethacrylate (EBPADMA), tetraethyleneglycoldi(meth)acrylate (TEGDMA), poly(ethylene glycol) dimethacrylates, the condensation product of bisphenol A and glycidyl methacrylate, 2,2′-bis-[4-(3-methacryloxy-2-hydroxy propoxy)-phenyl]propane (BisGMA), hexanediol di(meth)acrylate, tripropylene glycol di(meth)acrylate, butanediol di(meth) acrylate, neopentyl glycol di(meth) acrylate, diethylene glycol di(meth)acrylate, triethylene glycol di(meth) acrylate, dipropylene glycol di(meth)acrylate, trimethylolpropane triacrylate (TMPTA), di(trimethylolpropane) tetraacrylate (DTPTA), divinyl sulfone (DVS), propargyl acrylate, 6-azidohexyl acrylate, [2-(acryloyloxy)ethyl]trimethylammonium chloride, acrylic acid, 2-(4-benzoyl-3-hydroxyphenoxy)ethyl acrylate, 3-sulfopropyl acrylate potassium salt, 2-hydroxyethyl acrylate and 2-(dimethylamino)ethyl acrylate, 1,1′-(methylenedi-4,1-phenylene)bismaleimide, 1,4-di(maleimido)butane, N,N′-phenylenedimaleimide, N,N′-methylenebisacrylamide, triallyl-1,3,5-triazine-2,4,6-trione (TATATO), triethyleneglycol divinyl ether (TEGDVE), trimethylolpropane diallyl ether, dodecyl vinyl ether (DDVE), 1,6-heptadiyne, 1,7-octadiyne, bis-2,2-[4-(2-[norborn-2-ene-5-carboxylate]ethoxy) phenyl]propane (BPAEDN), 1,6-hexanediol di-(endo,exo-norborn-2-ene-5-carboxylate) (HDDN), trimethylolpropane tri-(norborn-2-ene-5-carboxylate) (TMPTN), pentaerythritoltri-(norborn-2-ene-5-carboxylate) (PTN3), pentaerythritol tetra-(norborn-2-ene-5-carboxylate) (PTN4), tricyclodecane dimethanol di-(endo, exo-norborn-2-ene-5-carboxylate) (TCDMDN), di(trimethylolpropane) tetra-(norborn-2-ene-5-carboxylate) (DTMPTN), and combinations thereof.
3. The composition of claim 1 ,
wherein group (a) comprises —SCH 2 C(═CH 2 )CH 2 SH;
or
wherein the linker comprises group (b) and the polymer comprises at least one free thiol from the at least one multifunctional thiol monomer;
or
wherein group (b) comprises a linker of formula (Ia):
or
wherein group (b) comprises a linker selected from the group consisting of:
wherein each occurrence of m is independently selected from the group consisting of 0, 1, 2, 3, 4, 5, and 6.
4. The composition of claim 1 , wherein the linker comprises group (b) and the polymer comprises at least one free thiol from the at least one multifunctional thiol monomer.
5. The composition of claim 1 , further comprising at least one polymerization initiator selected from the group consisting of a photoinitiator, a thermal initiator, and a redox initiator.
6. The composition of claim 5 , wherein the at least one photoinitiator is selected from the group consisting of: acetophenone, benzophenone, 2-phenylacetophenone, 2,2-dimethoxy-2-phenylacetophenone, bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide, 2-hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone, 2-methyl-(4-methylthienyl)-2-morpholinyl-1-propan-1-one, Diphenyl diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide, ethyl (2,4,6-trimethylbenzoyl) phenyl phosphinate, lithium phenyl-2,4,6-trimethylbenzoylphosphinate,
7. The composition of claim 5 , wherein the at least one thermal initiator is a compound selected from the group consisting of tert-amyl peroxybenzoate, 4,4-azobis(4-cyanovaleric acid), 1,1′-azobis(cyclohexanecarbonitrile), 2,2′-azobisisobutyronitrile (AIBN), benzoyl peroxide, 2,2-bis(tert-butylperoxy)butane, 1,1-bis(tert-butylperoxy)cyclohexane, 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane, 2,5-bis(tert-butylperoxy)-2,5-dimethyl-3-hexyne, bis(1-(tert-butylperoxy)-1-methylethyl)benzene, 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane, tert-butyl hydroperoxide, tert-butyl peracetate, tert-butyl peroxide, tert-butyl peroxybenzoate, tert-butylperoxy isopropyl carbonate, cumene hydroperoxide, cyclohexanone peroxide, dicumyl peroxide, lauroyl peroxide, 2,4-pentanedione peroxide, peracetic acid, and potassium persulfate.
8. The composition of claim 5 , wherein the at least one redox initiator is selected from the group consisting of: sodium iodide/hydrogen peroxide, potassium iodide/hydrogen peroxide, benzoyl peroxide/dimethyaniline, benzoyl peroxide/N,N-dimethyl p-toluidine, benzoyl peroxide/4-N,N-dimethylaminophenethyl alcohol, benzoyl peroxide/ethyl 4-dimethylamino benzoate, glucose oxidase/oxygen/iron(II) sulfate; and copper(II) sulfate/sodium ascorbate.
9. The composition of claim 1 , further comprising a catalyst selected from the group consisting of a nucleophile and a base.
10. The composition of claim 9 , wherein the nucleophile is selected from the group consisting of quinuclidine, 1,4-diazabicyclo[2.2.2]octane (DABCO), 4-dimethylaminopyridine (DMAP), IMes (1,3-bis(2,4,6-trimethylphenyl)-1,3-dihydro-2H-imidazol-2-ylidene), IPr (1,3-bis(2,6-diisopropylphenyl)-1,3-dihydro-2H-imidazol-2-ylidene), Ender's carbene, PPh 3 , P(nBu) 3 , P(tBu) 3 , PCy 3 , and PMe 3 .
11. The composition of claim 9 , wherein the base deprotonates at least about 10% of the thiol groups in the composition.
12. The composition of claim 9 , wherein the base is selected from the group consisting of an alkylthiolate salt, tetramethylguanidine (TMG), 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU), N,N-diisopropylethylamine (DIPEA or Hunig's base), 4-tert-butyl pyridine, triethylamine (TEA), and N,N,N′,N″,N″-pentamethyldiethylenetriamine (PMDETA).
13. A method of forming a polymer-filler composite, the method comprising:
combining at least one nanoparticle (NP), at least one multifunctional thiol monomer, at least one ene monomer, and at least one polymerization initiator to form an uncured polymer-filler composite; and
activating the at least one polymerization initiator to form the polymer-filler composite,
wherein the at least one nanoparticle is functionalized with a linker comprising at least one of the following groups:
(a) at least one allylic terminal thiol (—SH) group;
or
(b) at least one multifunctional thioester of formula (I),
wherein:
A 1 and A 2 are each independently selected from the group consisting of optionally substituted C 1 -C 15 alkylene, optionally substituted C 2 -C 15 alkenylene, optionally substituted C 2 -C 15 alkynylene, optionally substituted C 2 -C 15 heteroalkylene, optionally substituted C 2 -C 15 heteroalkenylene and optionally substituted C 2 -C 15 heteroalkynylene;
E 2 is selected from the group consisting of:
each instance of Y 1 is independently selected from the group consisting of O and N(R 1 ); and
each instance of R 1 being independently selected from the group consisting of H and C 1 -C 6 alkyl;
m1 is 0 or 1;
m2 is 0 or 1;
X 1 is
wherein:
bond a is to A 1 ,
Q is CH 2 or
n is 0, 1, 2, 3, 4, 5 or 6;
X 2 is
wherein:
bond a is to A 2 ,
bond b is to E 2 ,
Q is CH 2 or
n is 0, 1, 2, 3, 4, 5 or 6;
each instance of Y 2 is independently selected from the group consisting of C(R 1 ) 2 , O, and NR 1 ; and
each instance of Y 3 is independently selected from the group consisting of C(R 1 ) 2 , O, and NR 1 ; and
each instance of R 1 is independently selected from the group consisting of H and C 1 -C 6 alkyl.
14. The method of claim 13 , wherein the at least one polymerization initiator is selected from the group consisting of a photoinitiator, a thermal initiator, and a redox initiator.
15. The method of claim 14 , wherein the at least one photoinitiator is selected from the group consisting of: acetophenone, benzophenone, 2-phenylacetophenone, 2,2-dimethoxy-2-phenylacetophenone, bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide, 2-hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone, 2-methyl-(4-methylthienyl)-2-morpholinyl-1-propan-1-one, diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide, ethyl (2,4,6-trimethylbenzoyl) phenyl phosphinate, lithium phenyl-2,4,6-trimethylbenzoylphosphinate,
16. The method of claim 14 , wherein the at least one thermal initiator is a compound selected from the group consisting of tert-amyl peroxybenzoate, 4,4-azobis(4-cyanovaleric acid), 1,1′-azobis(cyclohexanecarbonitrile), 2,2′-azobisisobutyronitrile (AIBN), benzoyl peroxide, 2,2-bis(tert-butylperoxy)butane, 1,1-bis(tert-butylperoxy)cyclohexane, 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane, 2,5-bis(tert-butylperoxy)-2,5-dimethyl-3-hexyne, bis(1-(tert-butylperoxy)-1-methylethyl)benzene, 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane, tert-butyl hydroperoxide, tert-butyl peracetate, tert-butyl peroxide, tert-butyl peroxybenzoate, tert-butylperoxy isopropyl carbonate, cumene hydroperoxide, cyclohexanone peroxide, dicumyl peroxide, lauroyl peroxide, 2,4-pentanedione peroxide, peracetic acid, and potassium persulfate.
17. The method of claim 13 , wherein the at least one multifunctional thiol monomer is selected from the group consisting of:
wherein each instance of n is independently an integer from 0 to 500; or
wherein the at least one multifunctional thiol monomer is selected from the group consisting of: pentaerythritol tetramercaptopropionate (PETMP), ethylene glycol bis(3-mercaptopropionate) (EGBMP); trimethylolpropane tris(3-mercaptopropionate)(TMPMP), 2,4,6-trioxo-1,3,5-triazina-triy (triethyl-tris (3-mercapto propionate); 1,2-ethanedithiol, 1,3-propanedithiol, 1,4-butanedithiol; 1,5-pentanedithiol; 1,6-hexanedithiol, 1,8-octanedithiol, 1,9-nonanedithiol, 1,11-undecanedithiol; 1,16-hexadecanedithiol, 2,5-dimercaptomethyl-1,4-dithiane, pentaerythritol tetramercaptoacetate; trimethylolpropane trimercaptoacetate; glycol dimercaptoacetate, 2,3-dimercapto-1-propanol; DL-dithiothreitol; 2-mercaptoethylsulfide, 2,3-(dimercaptoethylthio)-1-mercaptopropane, 1,2,3-trimercaptopropane, toluenedithiol; benzenedithiol, biphenyldithiol, benzenedimethanethiol; xylylenedithiol, 4,4′-dimercaptostilbene, glycol dimercaptopropionate, and combinations thereof, or
wherein the thiol-ene polymer comprises an ene monomer selected from a group consisting of ethylene glycoldi(meth)acrylate, ethoxylated bisphenol-A dimethacrylate (EBPADMA), tetraethyleneglycoldi(meth)acrylate (TEGDMA), poly(ethylene glycol) dimethacrylates, the condensation product of bisphenol A and glycidyl methacrylate, 2,2′-bis-[4-(3-methacryloxy-2-hydroxy propoxy)-phenyl]propane (BisGMA), hexanediol di(meth)acrylate, tripropylene glycol di(meth)acrylate, butanediol di(meth) acrylate, neopentyl glycol di(meth) acrylate, diethylene glycol di(meth)acrylate, triethylene glycol di(meth) acrylate, dipropylene glycol di(meth)acrylate, trimethylolpropane triacrylate (TMPTA), di(trimethylolpropane) tetraacrylate (DTPTA), divinyl sulfone (DVS), propargyl acrylate, 6-azidohexyl acrylate, [2-(acryloyloxy)ethyl]trimethylammonium chloride, acrylic acid, 2-(4-benzoyl-3-hydroxyphenoxy)ethyl acrylate, 3-sulfopropyl acrylate potassium salt, 2-hydroxyethyl acrylate and 2-(dimethylamino)ethyl acrylate, 1,1′-(methylenedi-4,1-phenylene)bismaleimide, 1,4-di(maleimido)butane, N,N′-phenylenedimaleimide, N,N′-methylenebisacrylamide, triallyl-1,3,5-triazine-2,4,6-trione (TATATO), triethyleneglycol divinyl ether (TEGDVE), trimethylolpropane diallyl ether, dodecyl vinyl ether (DDVE), 1,6-heptadiyne, 1,7-octadiyne, bis-2,2-[4-(2-[norborn-2-ene-5-carboxylate]ethoxy) phenyl]propane (BPAEDN), 1,6-hexanediol di-(endo,exo-norborn-2-ene-5-carboxylate) (HDDN), trimethylolpropane tri-(norborn-2-ene-5-carboxylate) (TMPTN), pentaerythritoltri-(norborn-2-ene-5-carboxylate) (PTN3), pentaerythritol tetra-(norborn-2-ene-5-carboxylate) (PTN4), tricyclodecane dimethanol di-(endo, exo-norborn-2-ene-5-carboxylate) (TCDMDN), di(trimethylolpropane) tetra-(norborn-2-ene-5-carboxylate) (DTMPTN), and combinations thereof.
18. The method of claim 13 ,
wherein group (a) comprises —SCH 2 C(═CH 2 )CH 2 SH;
or
wherein the linker comprise group (b) and the polymer comprises at least one free thiol from the at least one multifunctional thiol monomer;
or
wherein group (b) comprises a linker of formula (Ia):
or
wherein group (b) comprises a linker selected from the group consisting of:
wherein each occurrence of m is independently selected from the group consisting of 0, 1, 2, 3, 4, 5, and 6.