JP2013532223A - オンデマンド型硬化性ポリシロキサンコーティング組成物 - Google Patents
オンデマンド型硬化性ポリシロキサンコーティング組成物 Download PDFInfo
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- JP2013532223A JP2013532223A JP2013518530A JP2013518530A JP2013532223A JP 2013532223 A JP2013532223 A JP 2013532223A JP 2013518530 A JP2013518530 A JP 2013518530A JP 2013518530 A JP2013518530 A JP 2013518530A JP 2013532223 A JP2013532223 A JP 2013532223A
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- combinations
- diazabicyclo
- alkyl
- nonane
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- -1 polysiloxane Polymers 0.000 title claims abstract description 171
- 229920001296 polysiloxane Polymers 0.000 title claims description 67
- 239000008199 coating composition Substances 0.000 title description 7
- 239000000203 mixture Substances 0.000 claims abstract description 193
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims abstract description 24
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 23
- 150000001409 amidines Chemical class 0.000 claims abstract description 20
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims abstract description 14
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims abstract description 14
- 206010073306 Exposure to radiation Diseases 0.000 claims abstract description 8
- GKTNLYAAZKKMTQ-UHFFFAOYSA-N n-[bis(dimethylamino)phosphinimyl]-n-methylmethanamine Chemical compound CN(C)P(=N)(N(C)C)N(C)C GKTNLYAAZKKMTQ-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000000576 coating method Methods 0.000 claims description 43
- 125000000217 alkyl group Chemical group 0.000 claims description 36
- 239000011248 coating agent Substances 0.000 claims description 33
- 239000000758 substrate Substances 0.000 claims description 33
- 239000003054 catalyst Substances 0.000 claims description 25
- 239000001257 hydrogen Substances 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 18
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 claims description 17
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 16
- 125000003709 fluoroalkyl group Chemical group 0.000 claims description 16
- 230000005855 radiation Effects 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 13
- 125000003118 aryl group Chemical group 0.000 claims description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 claims description 10
- BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- AMDNICFZCMZSPD-UHFFFAOYSA-N 1-benzyl-3,4,6,7,8,9,10,10a-octahydro-2h-pyrimido[1,2-a]azepine Chemical compound C1CCN2CCCCCC2N1CC1=CC=CC=C1 AMDNICFZCMZSPD-UHFFFAOYSA-N 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- 125000001188 haloalkyl group Chemical group 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 239000003504 photosensitizing agent Substances 0.000 claims description 6
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 claims description 5
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 5
- 125000001624 naphthyl group Chemical group 0.000 claims description 5
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 5
- SGUVLZREKBPKCE-UHFFFAOYSA-N 1,5-diazabicyclo[4.3.0]-non-5-ene Chemical compound C1CCN=C2CCCN21 SGUVLZREKBPKCE-UHFFFAOYSA-N 0.000 claims description 4
- PNZNKBFIWFBSAU-UHFFFAOYSA-N 1-benzyl-10-methyl-3,4,6,7,8,9,10,10a-octahydro-2h-pyrimido[1,2-a]azepine Chemical compound C12C(C)CCCCN2CCCN1CC1=CC=CC=C1 PNZNKBFIWFBSAU-UHFFFAOYSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- IIYFAKIEWZDVMP-UHFFFAOYSA-N tridecane Chemical compound CCCCCCCCCCCCC IIYFAKIEWZDVMP-UHFFFAOYSA-N 0.000 claims description 4
- WITKTULZSTXEPZ-UHFFFAOYSA-N 1-[(2,3-dichlorophenyl)methyl]-3,4,6,7,8,8a-hexahydro-2h-pyrrolo[1,2-a]pyrimidine Chemical compound ClC1=CC=CC(CN2C3CCCN3CCC2)=C1Cl WITKTULZSTXEPZ-UHFFFAOYSA-N 0.000 claims description 3
- DQYLOECNFGCJJO-UHFFFAOYSA-N 1-[(2-chlorophenyl)methyl]-3,4,6,7,8,8a-hexahydro-2h-pyrrolo[1,2-a]pyrimidine Chemical compound ClC1=CC=CC=C1CN1C2CCCN2CCC1 DQYLOECNFGCJJO-UHFFFAOYSA-N 0.000 claims description 3
- NZIKRXNQISEPFM-UHFFFAOYSA-N 1-[(2-nitrophenyl)methyl]-3,4,6,7,8,8a-hexahydro-2h-pyrrolo[1,2-a]pyrimidine Chemical compound [O-][N+](=O)C1=CC=CC=C1CN1C2CCCN2CCC1 NZIKRXNQISEPFM-UHFFFAOYSA-N 0.000 claims description 3
- BWHKKLIEWJAMGD-UHFFFAOYSA-N 1-[(4-ethenylphenyl)methyl]-3,4,6,7,8,8a-hexahydro-2h-pyrrolo[1,2-a]pyrimidine Chemical compound C1=CC(C=C)=CC=C1CN1C2CCCN2CCC1 BWHKKLIEWJAMGD-UHFFFAOYSA-N 0.000 claims description 3
- XSPRVEIZHHNLAJ-UHFFFAOYSA-N 1-[(4-phenylphenyl)methyl]-3,4,4a,5,6,7-hexahydro-2h-pyrrolo[1,2-b]pyridazine Chemical group C1CCC2CCCN2N1CC(C=C1)=CC=C1C1=CC=CC=C1 XSPRVEIZHHNLAJ-UHFFFAOYSA-N 0.000 claims description 3
- ZIONUNFGMHFISV-UHFFFAOYSA-N 1-benzyl-2,3,4,6,7,8,9,10,11,11a-decahydropyrimido[1,2-a]azocine Chemical compound C1CCN2CCCCCCC2N1CC1=CC=CC=C1 ZIONUNFGMHFISV-UHFFFAOYSA-N 0.000 claims description 3
- HYQWHUCTTYCIAU-UHFFFAOYSA-N 1-benzyl-3,4,6,7,8,8a-hexahydro-2h-pyrrolo[1,2-a]pyrimidine Chemical compound C1CCN2CCCC2N1CC1=CC=CC=C1 HYQWHUCTTYCIAU-UHFFFAOYSA-N 0.000 claims description 3
- VMVPYUCMIYVDTQ-UHFFFAOYSA-N 1-benzyl-4-methyl-3,4,6,7,8,8a-hexahydro-2h-pyrrolo[1,2-a]pyrimidine Chemical compound C12CCCN2C(C)CCN1CC1=CC=CC=C1 VMVPYUCMIYVDTQ-UHFFFAOYSA-N 0.000 claims description 3
- VTZJYWZPBKAHHE-UHFFFAOYSA-N 3-(3,4,6,7,8,8a-hexahydro-2h-pyrrolo[1,2-a]pyrimidin-1-ylmethyl)benzonitrile Chemical compound N#CC1=CC=CC(CN2C3CCCN3CCC2)=C1 VTZJYWZPBKAHHE-UHFFFAOYSA-N 0.000 claims description 3
- HCSNCZRWKWOCAS-UHFFFAOYSA-N 4-[[4-(1,2,3,4,6,7,8,8a-octahydropyrrolo[1,2-a]pyrimidin-4-ylmethyl)phenyl]methyl]-1,2,3,4,6,7,8,8a-octahydropyrrolo[1,2-a]pyrimidine Chemical compound C1CNC2CCCN2C1CC(C=C1)=CC=C1CC1N2CCCC2NCC1 HCSNCZRWKWOCAS-UHFFFAOYSA-N 0.000 claims description 3
- 150000008365 aromatic ketones Chemical group 0.000 claims description 3
- 125000000732 arylene group Chemical group 0.000 claims description 3
- 239000004305 biphenyl Substances 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 3
- 125000004407 fluoroaryl group Chemical group 0.000 claims description 3
- 125000005348 fluorocycloalkyl group Chemical group 0.000 claims description 3
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 3
- 125000001072 heteroaryl group Chemical group 0.000 claims description 3
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 3
- 125000005647 linker group Chemical group 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 3
- 125000001725 pyrenyl group Chemical group 0.000 claims description 3
- NYVSRILRAHOPTF-UHFFFAOYSA-N 1-[(2,6-dichlorophenyl)methyl]-3,4,6,7,8,9,10,10a-octahydro-2h-pyrimido[1,2-a]azepine Chemical compound ClC1=CC=CC(Cl)=C1CN1C2CCCCCN2CCC1 NYVSRILRAHOPTF-UHFFFAOYSA-N 0.000 claims description 2
- RQXFKBIKINJEBU-UHFFFAOYSA-N 1-benzyl-2,3,4,6,7,8,9,10,11,12,13,13a-dodecahydropyrimido[1,2-a]azecine Chemical compound C1CCN2CCCCCCCCC2N1CC1=CC=CC=C1 RQXFKBIKINJEBU-UHFFFAOYSA-N 0.000 claims description 2
- CSWWINREAHNZIC-UHFFFAOYSA-N 4-(3,4,6,7,8,8a-hexahydro-2h-pyrrolo[1,2-a]pyrimidin-1-ylmethyl)benzonitrile Chemical compound C1=CC(C#N)=CC=C1CN1C2CCCN2CCC1 CSWWINREAHNZIC-UHFFFAOYSA-N 0.000 claims description 2
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 125000004474 heteroalkylene group Chemical group 0.000 claims description 2
- 125000005549 heteroarylene group Chemical group 0.000 claims description 2
- 125000006588 heterocycloalkylene group Chemical group 0.000 claims description 2
- 125000002524 organometallic group Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 5
- LLTYSYWKRVZEDT-UHFFFAOYSA-N 1-[(2-chlorophenyl)methyl]-3,4,6,7,8,9,10,10a-octahydro-2h-pyrimido[1,2-a]azepine Chemical compound ClC1=CC=CC=C1CN1C2CCCCCN2CCC1 LLTYSYWKRVZEDT-UHFFFAOYSA-N 0.000 claims 1
- WJCDJUMRNUMRLR-UHFFFAOYSA-N 1-[(4-methylphenyl)methyl]-3,4,6,7,8,8a-hexahydro-2h-pyrrolo[1,2-a]pyrimidine Chemical compound C1=CC(C)=CC=C1CN1C2CCCN2CCC1 WJCDJUMRNUMRLR-UHFFFAOYSA-N 0.000 claims 1
- PKHFOFUUVQEVBA-UHFFFAOYSA-N C(C1=CC=CC=C1)N1C2C(CCCCN2CCC1)C.C(C1=CC=CC=C1)N1C2CCCCCN2CCC1 Chemical compound C(C1=CC=CC=C1)N1C2C(CCCCN2CCC1)C.C(C1=CC=CC=C1)N1C2CCCCCN2CCC1 PKHFOFUUVQEVBA-UHFFFAOYSA-N 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 description 29
- 238000001723 curing Methods 0.000 description 23
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 21
- 239000000463 material Substances 0.000 description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 14
- 229920000642 polymer Polymers 0.000 description 14
- 239000002904 solvent Substances 0.000 description 14
- 238000012360 testing method Methods 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- 229910052799 carbon Inorganic materials 0.000 description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 9
- 229910052760 oxygen Inorganic materials 0.000 description 9
- 239000001301 oxygen Substances 0.000 description 9
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- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
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- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
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- OEBXWWBYZJNKRK-UHFFFAOYSA-N 1-methyl-2,3,4,6,7,8-hexahydropyrimido[1,2-a]pyrimidine Chemical compound C1CCN=C2N(C)CCCN21 OEBXWWBYZJNKRK-UHFFFAOYSA-N 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
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- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 5
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- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 4
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- 239000012965 benzophenone Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 4
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- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 3
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- ZFDWWDZLRKHULH-UHFFFAOYSA-N 1,2-dimethyl-5,6-dihydro-4h-pyrimidine Chemical compound CN1CCCN=C1C ZFDWWDZLRKHULH-UHFFFAOYSA-N 0.000 description 2
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 2
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- 125000003373 pyrazinyl group Chemical group 0.000 description 1
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- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 238000006862 quantum yield reaction Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
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- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
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- 150000003384 small molecules Chemical class 0.000 description 1
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- 239000004575 stone Substances 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical compound [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- PVNUIRUAPVSSOK-UHFFFAOYSA-N tert-butylimino(tripyrrolidin-1-yl)-$l^{5}-phosphane Chemical compound C1CCCN1P(N1CCCC1)(=NC(C)(C)C)N1CCCC1 PVNUIRUAPVSSOK-UHFFFAOYSA-N 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
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- 125000004933 β-carbolinyl group Chemical group C1(=NC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
Classifications
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- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/062—Organo-phosphoranes without P-C bonds
- C07F9/065—Phosphoranes containing the structure P=N-
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/572—Five-membered rings
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6581—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms
- C07F9/6584—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms having one phosphorus atom as ring hetero atom
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6581—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms
- C07F9/6584—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms having one phosphorus atom as ring hetero atom
- C07F9/65842—Cyclic amide derivatives of acids of phosphorus, in which one nitrogen atom belongs to the ring
- C07F9/65846—Cyclic amide derivatives of acids of phosphorus, in which one nitrogen atom belongs to the ring the phosphorus atom being part of a six-membered ring which may be condensed with another ring system
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
- C09D183/06—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J183/00—Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Adhesives based on derivatives of such polymers
- C09J183/04—Polysiloxanes
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/12—Polysiloxanes containing silicon bound to hydrogen
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C08G77/16—Polysiloxanes containing silicon bound to oxygen-containing groups to hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/5399—Phosphorus bound to nitrogen
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2809—Web or sheet containing structurally defined element or component and having an adhesive outermost layer including irradiated or wave energy treated component
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Laminated Bodies (AREA)
Applications Claiming Priority (5)
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| US36000710P | 2010-06-30 | 2010-06-30 | |
| US36006810P | 2010-06-30 | 2010-06-30 | |
| US61/360,007 | 2010-06-30 | ||
| US61/360,068 | 2010-06-30 | ||
| PCT/US2011/042006 WO2012003153A1 (en) | 2010-06-30 | 2011-06-27 | Curable-on-demand polysiloxane coating composition |
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| JP2013532223A true JP2013532223A (ja) | 2013-08-15 |
| JP2013532223A5 JP2013532223A5 (enExample) | 2014-08-07 |
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| JP2013518530A Pending JP2013532223A (ja) | 2010-06-30 | 2011-06-27 | オンデマンド型硬化性ポリシロキサンコーティング組成物 |
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| EP (2) | EP2588536A1 (enExample) |
| JP (2) | JP5925201B2 (enExample) |
| CN (2) | CN102971381A (enExample) |
| WO (2) | WO2012003153A1 (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013532222A (ja) * | 2010-06-30 | 2013-08-15 | スリーエム イノベイティブ プロパティズ カンパニー | 硬化性ポリシロキサンコーティング組成物 |
| WO2015052859A1 (ja) * | 2013-10-10 | 2015-04-16 | 信越化学工業株式会社 | 室温硬化性樹脂組成物 |
| WO2016006252A1 (ja) * | 2014-07-10 | 2016-01-14 | 東レ・ダウコーニング株式会社 | 剥離コントロール剤、それを含むシリコーン剥離剤組成物、剥離シート、及び積層体 |
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| WO2012003160A1 (en) | 2010-06-30 | 2012-01-05 | 3M Innovative Properties Company | Curable composition comprising dual reactive silane functionality |
| WO2012003153A1 (en) | 2010-06-30 | 2012-01-05 | 3M Innovative Properties Company | Curable-on-demand polysiloxane coating composition |
| EP2797985B1 (en) | 2011-12-29 | 2015-09-23 | 3M Innovative Properties Company | Curable-on-demand polysiloxane coating composition |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2013532222A (ja) * | 2010-06-30 | 2013-08-15 | スリーエム イノベイティブ プロパティズ カンパニー | 硬化性ポリシロキサンコーティング組成物 |
| WO2015052859A1 (ja) * | 2013-10-10 | 2015-04-16 | 信越化学工業株式会社 | 室温硬化性樹脂組成物 |
| US9434817B2 (en) | 2013-10-10 | 2016-09-06 | Shin-Etsu Chemical Co., Ltd. | Room-temperature-curable resin composition |
| JPWO2015052859A1 (ja) * | 2013-10-10 | 2017-03-09 | 信越化学工業株式会社 | 室温硬化性樹脂組成物 |
| WO2016006252A1 (ja) * | 2014-07-10 | 2016-01-14 | 東レ・ダウコーニング株式会社 | 剥離コントロール剤、それを含むシリコーン剥離剤組成物、剥離シート、及び積層体 |
| JPWO2016006252A1 (ja) * | 2014-07-10 | 2017-04-27 | 東レ・ダウコーニング株式会社 | 剥離コントロール剤、それを含むシリコーン剥離剤組成物、剥離シート、及び積層体 |
| US10494484B2 (en) | 2014-07-10 | 2019-12-03 | Dow Toray Co., Ltd. | Release control agent, silicone release agent composition containing same, release sheet, and laminated body |
Also Published As
| Publication number | Publication date |
|---|---|
| US8968868B2 (en) | 2015-03-03 |
| CN102971380A (zh) | 2013-03-13 |
| US20130178553A1 (en) | 2013-07-11 |
| WO2012003153A1 (en) | 2012-01-05 |
| CN102971381A (zh) | 2013-03-13 |
| EP2588536A1 (en) | 2013-05-08 |
| US8968869B2 (en) | 2015-03-03 |
| CN102971380B (zh) | 2015-08-19 |
| WO2012003152A1 (en) | 2012-01-05 |
| EP2588537A1 (en) | 2013-05-08 |
| US20130101841A1 (en) | 2013-04-25 |
| JP5925201B2 (ja) | 2016-05-25 |
| JP2013529724A (ja) | 2013-07-22 |
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