JP2017530973A5 - - Google Patents
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- Publication number
- JP2017530973A5 JP2017530973A5 JP2017515763A JP2017515763A JP2017530973A5 JP 2017530973 A5 JP2017530973 A5 JP 2017530973A5 JP 2017515763 A JP2017515763 A JP 2017515763A JP 2017515763 A JP2017515763 A JP 2017515763A JP 2017530973 A5 JP2017530973 A5 JP 2017530973A5
- Authority
- JP
- Japan
- Prior art keywords
- trifluoromethyl
- diazilin
- alkyl
- bis
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 135
- 125000000217 alkyl group Chemical group 0.000 claims description 58
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 43
- 125000003118 aryl group Chemical group 0.000 claims description 41
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 40
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 35
- -1 n- butyl Chemical group 0.000 claims description 35
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 33
- 239000000203 mixture Substances 0.000 claims description 33
- 150000001875 compounds Chemical class 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 19
- 229920000642 polymer Polymers 0.000 claims description 19
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 19
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 125000003545 alkoxy group Chemical group 0.000 claims description 17
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 16
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 16
- OTTZHAVKAVGASB-UHFFFAOYSA-N hept-2-ene Chemical group CCCCC=CC OTTZHAVKAVGASB-UHFFFAOYSA-N 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 150000002367 halogens Chemical class 0.000 claims description 15
- 125000001624 naphthyl group Chemical group 0.000 claims description 15
- 125000004104 aryloxy group Chemical group 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 14
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 12
- 229910052731 fluorine Inorganic materials 0.000 claims description 11
- 239000011737 fluorine Substances 0.000 claims description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims description 11
- 125000005647 linker group Chemical group 0.000 claims description 10
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 10
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 9
- 125000003944 tolyl group Chemical group 0.000 claims description 9
- SQQNYSQLBYICBP-UHFFFAOYSA-N 3-(trifluoromethyl)-3h-diazirine Chemical compound FC(F)(F)C1N=N1 SQQNYSQLBYICBP-UHFFFAOYSA-N 0.000 claims description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 8
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 125000001072 heteroaryl group Chemical group 0.000 claims description 8
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 8
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 8
- 125000005004 perfluoroethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims description 8
- 229910052710 silicon Inorganic materials 0.000 claims description 8
- 239000010703 silicon Substances 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 8
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 8
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 claims description 8
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 6
- 125000001153 fluoro group Chemical group F* 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical group C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- CFJYNSNXFXLKNS-UHFFFAOYSA-N p-menthane Chemical compound CC(C)C1CCC(C)CC1 CFJYNSNXFXLKNS-UHFFFAOYSA-N 0.000 claims description 6
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 6
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 6
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 claims description 5
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 5
- HHBBIOLEJRWIGU-UHFFFAOYSA-N 4-ethoxy-1,1,1,2,2,3,3,4,5,6,6,6-dodecafluoro-5-(trifluoromethyl)hexane Chemical compound CCOC(F)(C(F)(C(F)(F)F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)F HHBBIOLEJRWIGU-UHFFFAOYSA-N 0.000 claims description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 5
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 5
- RGSWQNIDTMEOAA-UHFFFAOYSA-N O(CC1=CC=C(C=C1)C1(N=N1)C(F)(F)F)CC1=CC=C(C=C1)C1(N=N1)C(F)(F)F Chemical compound O(CC1=CC=C(C=C1)C1(N=N1)C(F)(F)F)CC1=CC=C(C=C1)C1(N=N1)C(F)(F)F RGSWQNIDTMEOAA-UHFFFAOYSA-N 0.000 claims description 5
- SHGIMXAUOMYSGB-UHFFFAOYSA-N O(CCC1=CC=C(C=C1)C1(N=N1)C(F)(F)F)CCC1=CC=C(C=C1)C1(N=N1)C(F)(F)F Chemical compound O(CCC1=CC=C(C=C1)C1(N=N1)C(F)(F)F)CCC1=CC=C(C=C1)C1(N=N1)C(F)(F)F SHGIMXAUOMYSGB-UHFFFAOYSA-N 0.000 claims description 5
- 229940022663 acetate Drugs 0.000 claims description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 125000004423 acyloxy group Chemical group 0.000 claims description 4
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000000732 arylene group Chemical group 0.000 claims description 4
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 claims description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 4
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 claims description 4
- 125000005549 heteroarylene group Chemical group 0.000 claims description 4
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims description 4
- 238000004377 microelectronic Methods 0.000 claims description 4
- 239000000178 monomer Substances 0.000 claims description 4
- 230000005693 optoelectronics Effects 0.000 claims description 4
- 125000000466 oxiranyl group Chemical group 0.000 claims description 4
- 229920003050 poly-cycloolefin Polymers 0.000 claims description 4
- UFUASNAHBMBJIX-UHFFFAOYSA-N propan-1-one Chemical compound CC[C]=O UFUASNAHBMBJIX-UHFFFAOYSA-N 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 4
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 claims description 3
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 claims description 3
- ZVQPLXXHYUUJRX-UHFFFAOYSA-N 5-but-3-enylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CCC=C)CC1C=C2 ZVQPLXXHYUUJRX-UHFFFAOYSA-N 0.000 claims description 3
- WMWDGZLDLRCDRG-UHFFFAOYSA-N 5-hexylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CCCCCC)CC1C=C2 WMWDGZLDLRCDRG-UHFFFAOYSA-N 0.000 claims description 3
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 3
- 125000006343 heptafluoro propyl group Chemical group 0.000 claims description 3
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 3
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims description 3
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 claims description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 3
- QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 claims description 2
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 claims description 2
- 239000001856 Ethyl cellulose Substances 0.000 claims description 2
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 claims description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 229940007550 benzyl acetate Drugs 0.000 claims description 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 2
- DIOQZVSQGTUSAI-NJFSPNSNSA-N decane Chemical group CCCCCCCCC[14CH3] DIOQZVSQGTUSAI-NJFSPNSNSA-N 0.000 claims description 2
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 claims description 2
- 229920001249 ethyl cellulose Polymers 0.000 claims description 2
- 235000019325 ethyl cellulose Nutrition 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 238000003780 insertion Methods 0.000 claims description 2
- 230000037431 insertion Effects 0.000 claims description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 claims description 2
- BDJSOPWXYLFTNW-UHFFFAOYSA-N methyl 3-methoxypropanoate Chemical compound COCCC(=O)OC BDJSOPWXYLFTNW-UHFFFAOYSA-N 0.000 claims description 2
- 238000000059 patterning Methods 0.000 claims description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 claims description 2
- 229920000058 polyacrylate Polymers 0.000 claims description 2
- 230000005855 radiation Effects 0.000 claims description 2
- 238000004528 spin coating Methods 0.000 claims description 2
- 229920006132 styrene block copolymer Polymers 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 5
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 3
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 claims 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 125000006663 (C1-C6) perfluoroalkyl group Chemical group 0.000 claims 1
- OKIYQFLILPKULA-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4-nonafluoro-4-methoxybutane Chemical compound COC(F)(F)C(F)(F)C(F)(F)C(F)(F)F OKIYQFLILPKULA-UHFFFAOYSA-N 0.000 claims 1
- CVIUJSXIENVAGJ-UHFFFAOYSA-N 1-methyl-2H-pyrrol-2-ide Chemical compound CN1C=CC=[C-]1 CVIUJSXIENVAGJ-UHFFFAOYSA-N 0.000 claims 1
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims 1
- 239000001273 butane Substances 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 239000010979 ruby Substances 0.000 claims 1
- 229910001750 ruby Inorganic materials 0.000 claims 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical group C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 0 *C1([*+]I*C2(N)N=N2)N=N1 Chemical compound *C1([*+]I*C2(N)N=N2)N=N1 0.000 description 2
- NIQLOLNJWXWZHX-UHFFFAOYSA-N 2-(5-bicyclo[2.2.1]hept-2-enylmethyl)-1,1,1,3,3,3-hexafluoropropan-2-ol Chemical compound C1C2C(CC(O)(C(F)(F)F)C(F)(F)F)CC1C=C2 NIQLOLNJWXWZHX-UHFFFAOYSA-N 0.000 description 2
- BEHBBKCBARHMJQ-UHFFFAOYSA-N 5-(2-phenylethyl)bicyclo[2.2.1]hept-2-ene Chemical compound C1C(C=C2)CC2C1CCC1=CC=CC=C1 BEHBBKCBARHMJQ-UHFFFAOYSA-N 0.000 description 2
- OTNQPIGKYBCGDX-UHFFFAOYSA-N 5-bicyclo[2.2.1]hept-2-enyl-ethoxy-dimethylsilane Chemical compound C1C2C([Si](C)(C)OCC)CC1C=C2 OTNQPIGKYBCGDX-UHFFFAOYSA-N 0.000 description 2
- LUMNWCHHXDUKFI-UHFFFAOYSA-N 5-bicyclo[2.2.1]hept-2-enylmethanol Chemical compound C1C2C(CO)CC1C=C2 LUMNWCHHXDUKFI-UHFFFAOYSA-N 0.000 description 2
- 229930004008 p-menthane Natural products 0.000 description 2
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- AUVBRDFPYKVSTD-UHFFFAOYSA-N 1,1,1,2,2,3,4,4,4-nonafluoro-3-methoxybutane Chemical compound COC(F)(C(F)(F)F)C(F)(F)C(F)(F)F AUVBRDFPYKVSTD-UHFFFAOYSA-N 0.000 description 1
- GEWWCWZGHNIUBW-UHFFFAOYSA-N 1-(4-nitrophenyl)propan-2-one Chemical compound CC(=O)CC1=CC=C([N+]([O-])=O)C=C1 GEWWCWZGHNIUBW-UHFFFAOYSA-N 0.000 description 1
- DYXMZCGEXNLOMT-UHFFFAOYSA-N 1-[3-(5-bicyclo[2.2.1]hept-2-enyl)propyl]-3,4-dimethylpyrrole-2,5-dione Chemical compound O=C1C(C)=C(C)C(=O)N1CCCC1C(C=C2)CC2C1 DYXMZCGEXNLOMT-UHFFFAOYSA-N 0.000 description 1
- PEALEMBUUUVDRP-UHFFFAOYSA-N 1-[4-(5-bicyclo[2.2.1]hept-2-enyl)butyl]-3,4-dimethylpyrrole-2,5-dione Chemical compound O=C1C(C)=C(C)C(=O)N1CCCCC1C(C=C2)CC2C1 PEALEMBUUUVDRP-UHFFFAOYSA-N 0.000 description 1
- IJWCNIZYIKMAET-UHFFFAOYSA-N 1-[6-(5-bicyclo[2.2.1]hept-2-enyl)hexyl]-3,4-dimethylpyrrole-2,5-dione Chemical compound O=C1C(C)=C(C)C(=O)N1CCCCCCC1C(C=C2)CC2C1 IJWCNIZYIKMAET-UHFFFAOYSA-N 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
- VCOXSVQMANZZDY-UHFFFAOYSA-N 5-[2-(2-methoxyethoxy)ethoxymethyl]bicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(COCCOCCOC)CC1C=C2 VCOXSVQMANZZDY-UHFFFAOYSA-N 0.000 description 1
- JHPLUQZQEHCSIP-UHFFFAOYSA-N 5-bicyclo[2.2.1]hept-2-enylmethyl acetate Chemical compound C1C2C(COC(=O)C)CC1C=C2 JHPLUQZQEHCSIP-UHFFFAOYSA-N 0.000 description 1
- YHESWXAODSYVCO-UHFFFAOYSA-N 5-but-1-enylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=CCC)CC1C=C2 YHESWXAODSYVCO-UHFFFAOYSA-N 0.000 description 1
- LWIJXSCVOXHMMF-UHFFFAOYSA-N 5-but-2-enylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CC=CC)CC1C=C2 LWIJXSCVOXHMMF-UHFFFAOYSA-N 0.000 description 1
- YSWATWCBYRBYBO-UHFFFAOYSA-N 5-butylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CCCC)CC1C=C2 YSWATWCBYRBYBO-UHFFFAOYSA-N 0.000 description 1
- GOLQZWYZZWIBCA-UHFFFAOYSA-N 5-octylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CCCCCCCC)CC1C=C2 GOLQZWYZZWIBCA-UHFFFAOYSA-N 0.000 description 1
- 125000005293 bicycloalkoxy group Chemical group 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462053921P | 2014-09-23 | 2014-09-23 | |
| US62/053,921 | 2014-09-23 | ||
| PCT/US2015/051619 WO2016049123A1 (en) | 2014-09-23 | 2015-09-23 | Diazirine compounds as photocrosslinkers and photoimageable compositions comprising them |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017530973A JP2017530973A (ja) | 2017-10-19 |
| JP2017530973A5 true JP2017530973A5 (enExample) | 2018-07-26 |
| JP6479171B2 JP6479171B2 (ja) | 2019-03-06 |
Family
ID=54249657
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017515763A Active JP6479171B2 (ja) | 2014-09-23 | 2015-09-23 | 光架橋剤としてのジアジリン化合物およびそれを含む光現像性組成物 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US9938241B2 (enExample) |
| EP (1) | EP3197881B1 (enExample) |
| JP (1) | JP6479171B2 (enExample) |
| KR (1) | KR102172938B1 (enExample) |
| CN (1) | CN106715399B (enExample) |
| TW (1) | TWI648271B (enExample) |
| WO (1) | WO2016049123A1 (enExample) |
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| EP3433884B1 (en) | 2016-03-22 | 2023-01-11 | Promerus, LLC | Diazirine containing organic electronic compositions and device thereof |
| JP6758070B2 (ja) * | 2016-03-31 | 2020-09-23 | 日鉄ケミカル＆マテリアル株式会社 | 遮光膜用感光性樹脂組成物、これを硬化させた遮光膜を備えたディスプレイ用基板、及びディスプレイ用基板の製造方法 |
| US11406731B2 (en) | 2017-09-06 | 2022-08-09 | Nanyang Technological University | Hygroscopic, crosslinking coatings and bioadhesives |
| US11084897B2 (en) * | 2017-12-12 | 2021-08-10 | International Business Machines Corporation | Chemical compounds with perfluoroaryl groups that can facilitate post-synthesis functionalization |
| US10738153B2 (en) | 2018-07-06 | 2020-08-11 | International Business Machines Corporation | Ring-opening polymerizations using a flow reactor |
| US10815335B2 (en) | 2018-07-06 | 2020-10-27 | International Business Machines Corporation | Ring-opening polymerizations using a flow reactor |
| US11118008B2 (en) | 2018-07-06 | 2021-09-14 | International Business Machines Corporation | Ring-opening polymerizations using a flow reactor |
| FR3088322A1 (fr) | 2018-11-14 | 2020-05-15 | Universite De Rouen Normandie | Nouvelle voie de synthese de diazirines, enrichies ou non en azote-15 |
| CN109628042A (zh) * | 2018-12-26 | 2019-04-16 | 深圳日高胶带新材料有限公司 | 一种光交联胶黏剂 |
| MX2021008821A (es) | 2019-01-25 | 2021-08-24 | Avedro Inc | Derivados de bis (diazirina) como foto-reticulante para el tratamiento de trastornos ectasicos de cornea. |
| CN111416088B (zh) * | 2020-03-26 | 2021-11-09 | 江苏厚生新能源科技有限公司 | 一种锂电陶瓷隔膜的制备方法 |
| KR20230092950A (ko) * | 2020-11-05 | 2023-06-26 | 내셔널 유니버시티 코포레이션 이와테 유니버시티 | 반응성 부여 화합물, 반응성 부여 화합물의 제조 방법, 및 적층체 |
| KR102612236B1 (ko) * | 2020-12-11 | 2023-12-08 | 삼성에스디아이 주식회사 | 편광판용 점착제 조성물, 이를 포함하는 편광판 및 이를 포함하는 광학표시장치 |
| CN114790171A (zh) * | 2021-01-26 | 2022-07-26 | 中国科学院化学研究所 | 一类双吖丙啶交联剂及其制备方法与应用 |
| WO2022187932A1 (en) * | 2021-03-09 | 2022-09-15 | Xlynx Materials Inc. | Aryl ether diazirines for use in polymer crosslinking and adhesion |
| US20220298399A1 (en) * | 2021-03-19 | 2022-09-22 | Facebook Technologies, Llc | Synthesis and use of multi-functional diazirine adhesives for elastomer bonding |
| CN114839835B (zh) * | 2022-03-18 | 2025-12-09 | 清华大学 | 量子点的无损光刻图案化方法和设备 |
| CN115312971A (zh) * | 2022-08-18 | 2022-11-08 | 江阴纳力新材料科技有限公司 | 聚合物膜及其制备方法、复合集流体 |
| WO2024113041A1 (en) * | 2022-12-02 | 2024-06-06 | Xlynx Materials Inc. | Selectively activated diazirine-containing molecules and polymers |
| CN118421316A (zh) * | 2023-01-31 | 2024-08-02 | 华为技术有限公司 | 一种纳米晶复合材料及其应用方法 |
| CN119497548B (zh) * | 2023-08-15 | 2025-10-21 | 清华大学 | 一种量子点薄膜图案化方法与应用 |
| CN117924964A (zh) * | 2023-12-22 | 2024-04-26 | 山东中康国创先进印染技术研究院有限公司 | 一种含有二氮丙啶结构的卡宾染料及其制备方法 |
| CN119977887A (zh) * | 2025-02-11 | 2025-05-13 | 四川大学 | 用于有机小分子半导体光图案化的化合物及其制备方法 |
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| US4571375A (en) * | 1983-10-24 | 1986-02-18 | Benedikt George M | Ring-opened polynorbornene negative photoresist with bisazide |
| US6156478A (en) * | 1998-10-30 | 2000-12-05 | 3M Innovative Properties Company | Photocurable and photopatternable hydrogel matrix based on azlactone copolymers |
| WO2005056582A1 (en) * | 2003-12-12 | 2005-06-23 | Merck Frosst Canada Ltd. | Ptp1b photoprobes |
| US7799883B2 (en) | 2005-02-22 | 2010-09-21 | Promerus Llc | Norbornene-type polymers, compositions thereof and lithographic process using such compositions |
| JP4122446B2 (ja) * | 2005-05-09 | 2008-07-23 | 国立大学法人富山大学 | フェニルジアジリン付加核酸誘導体とその製造方法、フェニルジアジリン付加ヌクレオチド誘導体とその製造方法、並びにタンパク質の分析方法および調製方法 |
| GB0616724D0 (en) | 2006-08-23 | 2006-10-04 | Isis Innovation | Surface adhesion using arylcarbene reactive intermediates |
| JP2010101661A (ja) * | 2008-10-21 | 2010-05-06 | Girasol Bio Kk | 物質固定化法 |
| WO2011109326A2 (en) * | 2010-03-02 | 2011-09-09 | Yumei Huang | Crosslinking reagents, methods, and compositions for studying protein-protein interactions |
| JP5728790B2 (ja) | 2011-07-14 | 2015-06-03 | 住友ベークライト株式会社 | 自己現像層形成ポリマーおよびその組成物 |
| US9511150B2 (en) * | 2011-07-19 | 2016-12-06 | CellMosaic, Inc. | Crosslinking reagents, macromolecules, therapeutic bioconjugates, and synthetic methods thereof |
| WO2013012961A2 (en) * | 2011-07-19 | 2013-01-24 | Cellmosaic, Llc | Novel crosslinking reagents, macromolecules, therapeutic conjugates, and synthetic methods thereof |
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- 2015-09-23 KR KR1020177007930A patent/KR102172938B1/ko active Active
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