CN101346419A - 绝缘或半导体表面的改性方法和如此获得的产品 - Google Patents
绝缘或半导体表面的改性方法和如此获得的产品 Download PDFInfo
- Publication number
- CN101346419A CN101346419A CNA2006800491558A CN200680049155A CN101346419A CN 101346419 A CN101346419 A CN 101346419A CN A2006800491558 A CNA2006800491558 A CN A2006800491558A CN 200680049155 A CN200680049155 A CN 200680049155A CN 101346419 A CN101346419 A CN 101346419A
- Authority
- CN
- China
- Prior art keywords
- diazonium salt
- diazonium
- group
- grafted
- charge
- 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
Links
- 238000000034 method Methods 0.000 title claims description 94
- 239000012954 diazonium Substances 0.000 claims abstract description 148
- 150000001989 diazonium salts Chemical class 0.000 claims abstract description 118
- 125000003118 aryl group Chemical group 0.000 claims abstract description 74
- 150000001875 compounds Chemical class 0.000 claims abstract description 39
- 239000000463 material Substances 0.000 claims abstract description 25
- 239000004065 semiconductor Substances 0.000 claims abstract description 25
- -1 sulfate radical Chemical class 0.000 claims description 81
- 239000000126 substance Substances 0.000 claims description 57
- 230000002829 reductive effect Effects 0.000 claims description 40
- 238000012546 transfer Methods 0.000 claims description 40
- 239000003795 chemical substances by application Substances 0.000 claims description 34
- OKKJLVBELUTLKV-UHFFFAOYSA-N methyl alcohol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 34
- 230000005855 radiation Effects 0.000 claims description 32
- 239000002253 acid Substances 0.000 claims description 31
- 230000004048 modification Effects 0.000 claims description 30
- 238000012986 modification Methods 0.000 claims description 30
- 230000009467 reduction Effects 0.000 claims description 18
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 claims description 18
- 125000000524 functional group Chemical group 0.000 claims description 16
- 239000011159 matrix material Substances 0.000 claims description 15
- 230000015572 biosynthetic process Effects 0.000 claims description 12
- 229920005989 resin Polymers 0.000 claims description 12
- 239000011347 resin Substances 0.000 claims description 12
- 238000009413 insulation Methods 0.000 claims description 10
- 230000008569 process Effects 0.000 claims description 10
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 claims description 8
- 239000011810 insulating material Substances 0.000 claims description 8
- 238000005406 washing Methods 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 6
- 235000009518 sodium iodide Nutrition 0.000 claims description 6
- 150000002500 ions Chemical class 0.000 claims description 5
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 3
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- RXROENJMSSTMHH-UHFFFAOYSA-N 2H-chromene-5-diazonium Chemical compound O1CC=CC=2C(=CC=CC1=2)[N+]#N RXROENJMSSTMHH-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 229910000085 borane Inorganic materials 0.000 claims description 2
- QZHPTGXQGDFGEN-UHFFFAOYSA-N chromene Chemical compound C1=CC=C2C=C[CH]OC2=C1 QZHPTGXQGDFGEN-UHFFFAOYSA-N 0.000 claims description 2
- GPRSOIDYHMXAGW-UHFFFAOYSA-N cyclopenta-1,3-diene cyclopentanecarboxylic acid iron Chemical compound [CH-]1[CH-][CH-][C-]([CH-]1)C(=O)O.[CH-]1C=CC=C1.[Fe] GPRSOIDYHMXAGW-UHFFFAOYSA-N 0.000 claims description 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 229960004889 salicylic acid Drugs 0.000 claims description 2
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 2
- 239000012279 sodium borohydride Substances 0.000 claims description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N trihydridoboron Substances B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 claims description 2
- BRDWIEOJOWJCLU-LTGWCKQJSA-N GS-441524 Chemical compound C=1C=C2C(N)=NC=NN2C=1[C@]1(C#N)O[C@H](CO)[C@@H](O)[C@H]1O BRDWIEOJOWJCLU-LTGWCKQJSA-N 0.000 claims 1
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical group CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 108
- 239000000523 sample Substances 0.000 description 60
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 57
- 238000001228 spectrum Methods 0.000 description 47
- 239000004698 Polyethylene Substances 0.000 description 46
- 229920000573 polyethylene Polymers 0.000 description 45
- 238000006243 chemical reaction Methods 0.000 description 43
- 239000000243 solution Substances 0.000 description 42
- 239000004696 Poly ether ether ketone Substances 0.000 description 37
- 229920002530 polyetherether ketone Polymers 0.000 description 37
- 239000004743 Polypropylene Substances 0.000 description 34
- 229920001155 polypropylene Polymers 0.000 description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 28
- 229920000642 polymer Polymers 0.000 description 28
- 238000002042 time-of-flight secondary ion mass spectrometry Methods 0.000 description 27
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 23
- 150000003254 radicals Chemical class 0.000 description 20
- 239000000203 mixture Substances 0.000 description 19
- 235000019441 ethanol Nutrition 0.000 description 17
- UPQQTAIBAVTEGV-UHFFFAOYSA-N 4-bromobenzenediazonium Chemical compound BrC1=CC=C([N+]#N)C=C1 UPQQTAIBAVTEGV-UHFFFAOYSA-N 0.000 description 16
- 238000012360 testing method Methods 0.000 description 16
- 229910052799 carbon Inorganic materials 0.000 description 15
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 13
- 150000001412 amines Chemical class 0.000 description 13
- 230000000903 blocking effect Effects 0.000 description 13
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 12
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 11
- 125000004799 bromophenyl group Chemical group 0.000 description 11
- 150000001721 carbon Chemical group 0.000 description 11
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 10
- 239000012153 distilled water Substances 0.000 description 10
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 239000004809 Teflon Substances 0.000 description 9
- 229920006362 Teflon® Polymers 0.000 description 9
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 9
- 125000004093 cyano group Chemical group *C#N 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 229920002554 vinyl polymer Polymers 0.000 description 9
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 8
- 229910004298 SiO 2 Inorganic materials 0.000 description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 8
- 229910052794 bromium Inorganic materials 0.000 description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 8
- 238000004377 microelectronic Methods 0.000 description 8
- 230000002269 spontaneous effect Effects 0.000 description 8
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 8
- WLDHEUZGFKACJH-UHFFFAOYSA-K amaranth Chemical compound [Na+].[Na+].[Na+].C12=CC=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(O)=C1N=NC1=CC=C(S([O-])(=O)=O)C2=CC=CC=C12 WLDHEUZGFKACJH-UHFFFAOYSA-K 0.000 description 7
- 150000001408 amides Chemical class 0.000 description 7
- 125000004429 atom Chemical group 0.000 description 7
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 description 7
- 239000005020 polyethylene terephthalate Substances 0.000 description 7
- 239000002243 precursor Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 230000004913 activation Effects 0.000 description 6
- 125000003636 chemical group Chemical group 0.000 description 6
- 230000005518 electrochemistry Effects 0.000 description 6
- 238000002329 infrared spectrum Methods 0.000 description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 6
- 238000012545 processing Methods 0.000 description 6
- 239000012047 saturated solution Substances 0.000 description 6
- 229910052710 silicon Inorganic materials 0.000 description 6
- 239000010703 silicon Substances 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
- IKLQCZFWTGJMFM-UHFFFAOYSA-N 4-(trifluoromethyl)benzenediazonium Chemical compound FC(F)(F)C1=CC=C([N+]#N)C=C1 IKLQCZFWTGJMFM-UHFFFAOYSA-N 0.000 description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 5
- 239000012346 acetyl chloride Substances 0.000 description 5
- 150000008065 acid anhydrides Chemical class 0.000 description 5
- 150000001266 acyl halides Chemical class 0.000 description 5
- 125000000746 allylic group Chemical group 0.000 description 5
- 125000006242 amine protecting group Chemical group 0.000 description 5
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 5
- 238000000151 deposition Methods 0.000 description 5
- 230000008021 deposition Effects 0.000 description 5
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 5
- 239000012634 fragment Substances 0.000 description 5
- 238000006897 homolysis reaction Methods 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 150000002825 nitriles Chemical class 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 229920000620 organic polymer Polymers 0.000 description 5
- 150000003008 phosphonic acid esters Chemical class 0.000 description 5
- 150000003009 phosphonic acids Chemical class 0.000 description 5
- 230000035484 reaction time Effects 0.000 description 5
- 238000006557 surface reaction Methods 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- 239000004697 Polyetherimide Substances 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- 239000004734 Polyphenylene sulfide Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 238000006193 diazotization reaction Methods 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 230000002349 favourable effect Effects 0.000 description 4
- 239000011888 foil Substances 0.000 description 4
- 229920001601 polyetherimide Polymers 0.000 description 4
- 229920006380 polyphenylene oxide Polymers 0.000 description 4
- 229920000069 polyphenylene sulfide Polymers 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- AYWYBCRYWKVVBR-UHFFFAOYSA-N 9,10-dioxoanthracene-1-diazonium Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1[N+]#N AYWYBCRYWKVVBR-UHFFFAOYSA-N 0.000 description 3
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 206010018910 Haemolysis Diseases 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 3
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 description 3
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 3
- 229910052785 arsenic Inorganic materials 0.000 description 3
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 3
- 229910052796 boron Inorganic materials 0.000 description 3
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 239000010432 diamond Substances 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 230000008588 hemolysis Effects 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000008399 tap water Substances 0.000 description 3
- 235000020679 tap water Nutrition 0.000 description 3
- 238000009736 wetting Methods 0.000 description 3
- OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- JHXVRRJXCDAINK-UHFFFAOYSA-N NC(=O)N.N#CC#N Chemical compound NC(=O)N.N#CC#N JHXVRRJXCDAINK-UHFFFAOYSA-N 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 229920012266 Poly(ether sulfone) PES Polymers 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 210000001367 artery Anatomy 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 description 2
- 230000031709 bromination Effects 0.000 description 2
- 238000005893 bromination reaction Methods 0.000 description 2
- 125000001246 bromo group Chemical group Br* 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 230000005281 excited state Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000004992 fission Effects 0.000 description 2
- 238000007306 functionalization reaction Methods 0.000 description 2
- 229920000578 graft copolymer Polymers 0.000 description 2
- 239000012456 homogeneous solution Substances 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 238000005240 physical vapour deposition Methods 0.000 description 2
- 229920000885 poly(2-vinylpyridine) Polymers 0.000 description 2
- 229920001627 poly(4-methyl styrene) Polymers 0.000 description 2
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 2
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920002312 polyamide-imide Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920006324 polyoxymethylene Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229960001866 silicon dioxide Drugs 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
- 238000013022 venting Methods 0.000 description 2
- AJKNNUJQFALRIK-UHFFFAOYSA-N 1,2,3-trifluorobenzene Chemical compound FC1=CC=CC(F)=C1F AJKNNUJQFALRIK-UHFFFAOYSA-N 0.000 description 1
- QZYDOKBVZJLQCK-UHFFFAOYSA-N 1,2-diethoxybenzene Chemical compound CCOC1=CC=CC=C1OCC QZYDOKBVZJLQCK-UHFFFAOYSA-N 0.000 description 1
- AUHZEENZYGFFBQ-UHFFFAOYSA-N 1,3,5-trimethylbenzene Chemical compound CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
- DGZQEAKNZXNTNL-UHFFFAOYSA-N 1-bromo-4-butan-2-ylbenzene Polymers CCC(C)C1=CC=C(Br)C=C1 DGZQEAKNZXNTNL-UHFFFAOYSA-N 0.000 description 1
- LURCTYNFDPTMMM-UHFFFAOYSA-N 2,3,4,5,6-pentafluorobenzenediazonium Chemical compound FC1=C(F)C(F)=C([N+]#N)C(F)=C1F LURCTYNFDPTMMM-UHFFFAOYSA-N 0.000 description 1
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 1
- MJABAEJQHKYEKL-UHFFFAOYSA-N 2-(trifluoromethyl)benzenediazonium Chemical compound FC(F)(F)C1=CC=CC=C1[N+]#N MJABAEJQHKYEKL-UHFFFAOYSA-N 0.000 description 1
- OLCKRGCUQOKQCM-UHFFFAOYSA-N 2-fluoro-1,3,5-triazine Chemical class FC1=NC=NC=N1 OLCKRGCUQOKQCM-UHFFFAOYSA-N 0.000 description 1
- VJPQZOXMOAGWHE-UHFFFAOYSA-N 2-fluorobenzenediazonium Chemical compound FC1=CC=CC=C1[N+]#N VJPQZOXMOAGWHE-UHFFFAOYSA-N 0.000 description 1
- AUFVJZSDSXXFOI-UHFFFAOYSA-N 2.2.2-cryptand Chemical compound C1COCCOCCN2CCOCCOCCN1CCOCCOCC2 AUFVJZSDSXXFOI-UHFFFAOYSA-N 0.000 description 1
- WREVVZMUNPAPOV-UHFFFAOYSA-N 8-aminoquinoline Chemical compound C1=CN=C2C(N)=CC=CC2=C1 WREVVZMUNPAPOV-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 1
- 229910017214 AsGa Inorganic materials 0.000 description 1
- DPUHDRPFXHCBES-UHFFFAOYSA-N C(=O)O.[N+](=[N-])=C1CC=CC=C1 Chemical compound C(=O)O.[N+](=[N-])=C1CC=CC=C1 DPUHDRPFXHCBES-UHFFFAOYSA-N 0.000 description 1
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 1
- JOZYBUSXAGFNKN-UHFFFAOYSA-N N-pyridin-2-ylpyridin-2-amine Chemical class N(c1ccccn1)c1ccccn1.N(c1ccccn1)c1ccccn1 JOZYBUSXAGFNKN-UHFFFAOYSA-N 0.000 description 1
- 240000002853 Nelumbo nucifera Species 0.000 description 1
- 235000006508 Nelumbo nucifera Nutrition 0.000 description 1
- 235000006510 Nelumbo pentapetala Nutrition 0.000 description 1
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical compound CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical group OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229920000265 Polyparaphenylene Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000003875 Wang resin Substances 0.000 description 1
- NERFNHBZJXXFGY-UHFFFAOYSA-N [4-[(4-methylphenyl)methoxy]phenyl]methanol Chemical compound C1=CC(C)=CC=C1COC1=CC=C(CO)C=C1 NERFNHBZJXXFGY-UHFFFAOYSA-N 0.000 description 1
- KFDLHDGFDLHFRW-UHFFFAOYSA-N [O-][N+](Br)=O Chemical compound [O-][N+](Br)=O KFDLHDGFDLHFRW-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 1
- 229940121363 anti-inflammatory agent Drugs 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 239000000427 antigen Substances 0.000 description 1
- 102000036639 antigens Human genes 0.000 description 1
- 108091007433 antigens Proteins 0.000 description 1
- 239000003080 antimitotic agent Substances 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000012062 aqueous buffer Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-N benzene-dicarboxylic acid Natural products OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 125000005997 bromomethyl group Chemical group 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000013626 chemical specie Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 150000003983 crown ethers Chemical class 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
- MYRTYDVEIRVNKP-UHFFFAOYSA-N divinylbenzene Substances C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
- JMANVNJQNLATNU-UHFFFAOYSA-N glycolonitrile Natural products N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- ICIWUVCWSCSTAQ-UHFFFAOYSA-M iodate Chemical compound [O-]I(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-M 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- SNHMUERNLJLMHN-UHFFFAOYSA-N iodobenzene Chemical compound IC1=CC=CC=C1 SNHMUERNLJLMHN-UHFFFAOYSA-N 0.000 description 1
- 125000006303 iodophenyl group Chemical group 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000033116 oxidation-reduction process Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000013319 spin trapping Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 238000001149 thermolysis Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 125000004360 trifluorophenyl group Chemical group 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 238000002371 ultraviolet--visible spectrum Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/302—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to change their surface-physical characteristics or shape, e.g. etching, polishing, cutting
- H01L21/306—Chemical or electrical treatment, e.g. electrolytic etching
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/10—Homopolymers or copolymers of propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2371/00—Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
- C08J2371/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
- C08J2371/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Power Engineering (AREA)
- General Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Computer Hardware Design (AREA)
- Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Formation Of Insulating Films (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
表面 | 峰(强度*) | 归属 |
PP | 79-81(0.3 104)127((2 103) | Br-I- |
PET | 79-81(1 104)139-141(0.5 104)167-169(2 103)213 | Br-[OCH2CH2O+Br]-[O=COCH2CH2O+Br]-[O=COCH2CH2O+I]- |
PEEK | 79-81(1.5 104)127(0.4 104) | Br-I- |
TiN | 79-81(2 104)127(6 104) | Br-I- |
SiC | 79-81(2 104)127(3.5 104) | Br-I- |
SiOC | 79-81(0.3 103)127(1 102) | Br-I- |
SiO2 | 79-81(0.8 103)127(1 103) | Br-I- |
样品 | 峰(强度*) | 归属 |
PP | 79-81(0.6 104) | Br- |
PET | 79-81(1 104)93-95(3 103)125-127(3 103)l39-141(56 103)153-155(1 103) | Br-CH2Br[BrCOOH2]-[BrCH2COOH2]-[BrCH2CH2COOH2]- |
PEEK | 79-81(1.5 104) | Br- |
TiN | 79-81(3 105) | Br- |
SiC | 79-81(0.6 104) | Br- |
SiOC | 79-81(2 103) | Br- |
SiO2 | 79-81(0.5 104) | Br- |
样品 | IR谱带1)cm-1 | 归属 | 4-氨基苯甲酸2)cm-1 |
PP | 16871617 | C=O环振动 | 16581599 |
PET | 16813) | C=O | 1658 |
PEEK | /4) | / |
样品 | 处理前的接触角 | 处理后的接触角 |
PPa) | 124 | 11472(10分钟后)69(20分钟后) |
PET | 90 | 62 |
PEEK | 87 | 55(10’后) |
样品 | IR谱带1)cm-1 | 归属 | 4-碘代苯重氮 |
PP | 1541812 | 环振动在平面外的CH | 1548825757 |
PET | 1532845 | 环振动在平面外的CH | |
PEEK | 1562825 | 环振动在平面外的CH |
样品 | 峰(强度*) | 归属 |
PP | 127(2.5 103)205(6 101)231(1 101) | I-[C6H5I+H]-[CH2CH2C6H4I]- |
PET | 127(4 103)214(2 102)228(0.5 102)242(0.5 102)256(0.5 102)351(2 101) | I-C-C6H3-I-214+CH2 -228+CH2 -242+CH2 -C6H5(C=O)OCH2CHC6H4I- |
PEEK | 127(3.5 103)254(3.5 101) | I-I2 - |
样品 | IR谱带1)cm-1 | 归属 | 4-碘代苯重氮 |
PE | 1555843763 | 环振动在平面外的CHid | 1555826764 |
Teflon | 1548852758 | 环振动在平面外的CHid | |
ABS | 1584824744 | 环振动在平面外的CHid |
样品 | 峰(强度*) | 归属 |
PE | 79-81104-106179-181197-199225-227264-266290-292183-185265-267 | Br-,Br+CH3-CH2Br-C2C6H4Br-(CH2)3C6H4Br-(CH2)5C6H4Br-non attribuénon attribué(CH2)2C6H4Br+(CH2)6-CH=CH-C6H4Br+ |
Teflon | 79-81 | Br-(faible) |
ABS | 79-81191-193 | Br-,Br+C3-C6H4Br+ |
样品 | 峰(强度*) | 归属 |
PP | 79-81(1,5 105)91-93(1 103)103-105(0,5 103) | Br-CBr-CH2CH2Br |
PET | 79-81(1 104)93-95(0,8 104) | Br-[CH2Br]- |
PEEK | 79-81(1 105) | Br- |
TiN | 79-81(0,5 104) | Br- |
SiC | 79-81(7 104) | Br- |
SiOC | 79-81(1,5 103) | Br- |
SiO2 | 79-81(0,2 103) | Br- |
样品 | IR谱带1)cm-1 | 归属 | 4-氨基苯甲酸2)cm-1 |
PP | 1686 | C=O | 1658 |
PET | ≈16813) | C=O | 1658 |
PEEK | /4) | / |
样品 | 处理前的接触角 | 处理后的接触角 |
PPa) | 124 | 12372(10分钟后)70(20分钟后) |
PET | 90 | 79 |
PEEK | 87 | 58 |
表面 | 峰(强度*) | 归属 |
PP | 79-81(3 103) | Br- |
PET | 79-81(1 104)93-95(0.5 104) | Br-CH2Br |
PEEK | 79-81(3 104) | Br- |
TiN | 79-81(6 105) | Br- |
SiC | 79-81(0.8 105) | Br- |
SiOC | 79-81(2 103) | Br- |
SiO2 | 79-81(4 105) | Br- |
样品 | IR谱带1)cm-1 | 归属 | 4-溴代苯重氮 |
PET | 1551(投影)837758 | 环振动在平面外的CH振动 | 15551460826756 |
PEEK | 15531465830759 | 环振动在平面外的CH振动 | |
PE | 1551852739 | 环振动在平面外的CH振动 | |
Teflon | 1551810756 | 环振动在平面外的CH振动 | |
ABS | 1550sh824 | 环振动在平面外的CH振动 |
样品 | IR谱带1)cm-1 | 归属 | 4-氨基苯甲酸2)cm-1 |
PP | 16871612 | C=O环振动 | 16581599 |
PET | 16803) | C=O | 1658 |
PEEK | /4) | / |
样品 | 处理前的接触角 | 处理后的接触角 |
PP | 124 | 12582(10’后)b)82(20’后)b) |
PET | 90 | 75 |
PEEK | 87 | 55 |
样品 | IR带1)cm-1 | 归属 |
PP | 1749vw≈1367vw≈1219vw | C=O 1749,对于Fast Red1367,对于Fast Red1219,对于Fast Red |
PET | ≈1749vw | C=O 1749,对于Fast Red |
PEEK | 1749vw1371vw≈1167vw | C=O 1749,对于Fast Red1367,对于Fast Red1164,对于Fast Red |
2HN-C6H4-CF3 | + 2N-C6H4CF3BF4 -a) | PPc) | PET | PEEK | 归属 |
3052 | 3055 | d) | 芳族C-H伸长 | ||
1626 | 1636 | d) | 芳环的振动 | ||
1527 | 1559 | d) | 芳环的振动 | ||
1441 | 1426 | 1452 | d) | 芳环的振动 | |
1319 | 1320 | 1340 | CF3 | ||
1185 | 1180 | 1222 | CF3 | ||
1157 | 1138 | 1160 | CF3 | ||
1061 | b) | 1070 | CF3 | ||
829 | 852 | 844 | 在平面外的CH振动1,4-二取代 |
2HNC6H4COOH | + 2NC6H4COOH | -C6H4COOH | -C6H4COF* | |
COOH | 3400-2200 | 3242 | 3139 | |
C=O | 1660 | 1719 | 1843 | |
CH aromatique(hors du plan) | 841769698 | 866763702 | 853777719**692 |
m/z | 归属 |
19 | F- |
111 | C6H4FO- |
123 | C6H4COF+ |
143 | C7H5F2O+ |
m/z | 归属 |
19 | F- |
69 | CF3 - |
145 | C6H4CF3 - |
159 | CH2C6H4CF3 + |
160 | NHC6H4CF3 - |
m/z | 归属 |
77 | C6H5 + |
105 | C6H5C=O+ |
119 | CH3C6H4C=O+ |
133 | CH3CH2C6H4C=O+ |
Claims (15)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0510914A FR2892325B1 (fr) | 2005-10-26 | 2005-10-26 | Procede de modification de surfaces isolantes, semi-conductrices ou metalliques, et produits tels qu'obtenus |
FR0510914 | 2005-10-26 | ||
PCT/FR2006/002260 WO2007048894A1 (fr) | 2005-10-26 | 2006-10-09 | Procede de modification de surfaces isolantes ou semi- conductrices, et produits tels qu'obtenus |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101346419A true CN101346419A (zh) | 2009-01-14 |
CN101346419B CN101346419B (zh) | 2012-05-09 |
Family
ID=36603677
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2006800491558A Active CN101346419B (zh) | 2005-10-26 | 2006-10-09 | 绝缘或半导体表面的改性方法和如此获得的产品 |
Country Status (12)
Country | Link |
---|---|
US (1) | US8133549B2 (zh) |
EP (1) | EP1948720B1 (zh) |
JP (1) | JP5210170B2 (zh) |
KR (1) | KR101367781B1 (zh) |
CN (1) | CN101346419B (zh) |
AT (1) | ATE503794T1 (zh) |
CA (1) | CA2627222C (zh) |
DE (1) | DE602006021049D1 (zh) |
ES (1) | ES2373299T3 (zh) |
FR (1) | FR2892325B1 (zh) |
IL (1) | IL191022A (zh) |
WO (1) | WO2007048894A1 (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109401360A (zh) * | 2017-08-18 | 2019-03-01 | 中国科学院化学研究所 | 一种对高温结构陶瓷材料进行表面改性的方法 |
CN110945298A (zh) * | 2017-06-16 | 2020-03-31 | 开利公司 | 电热元件、包含电热元件的传热***及它们的制备方法 |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2910007B1 (fr) | 2006-12-19 | 2009-03-06 | Commissariat Energie Atomique | Procede de preparation d'un film organique a la surface d'un support solide dans des conditions non-electrochimiques, support solide ainsi obtenu et kit de preparation |
FR2910010B1 (fr) | 2006-12-19 | 2009-03-06 | Commissariat Energie Atomique | Procede de preparation d'un film organique a la surface d'un support solide dans des conditions non-electrochimiques, support solide ainsi obtenu et kit de preparation |
FR2910006B1 (fr) | 2006-12-19 | 2009-03-06 | Commissariat Energie Atomique | Procede de preparation d'un film organique a la surface d'un support solide dans des conditions non-electrochimiques, support solide ainsi obtenu et kit de preparation |
US9725602B2 (en) | 2006-12-19 | 2017-08-08 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Method for preparing an organic film at the surface of a solid support under non-electrochemical conditions, solid support thus obtained and preparation kit |
FR2929618B1 (fr) * | 2008-04-03 | 2011-03-18 | Commissariat Energie Atomique | Procede pour assembler deux surfaces ou une surface avec une molecule d'interet |
KR101096031B1 (ko) | 2009-03-31 | 2011-12-19 | 한양대학교 산학협력단 | 자기조립단분자막 형성방법과 이를 이용한 반도체 소자의 구리배선 및 그의 형성방법 |
FR2943930B1 (fr) * | 2009-04-02 | 2011-09-30 | Commissariat Energie Atomique | Procede pour modifier l'energie de surface d'un solide |
US8287699B2 (en) * | 2009-07-27 | 2012-10-16 | Nanotek Instruments, Inc. | Production of chemically functionalized nano graphene materials |
FR2969628B1 (fr) * | 2010-12-22 | 2013-09-27 | Pegastech | Procede de revetement par greffage chimique electrocatalyse d'une surface d'un substrat par une couche polymere. |
WO2013152967A1 (en) | 2012-04-13 | 2013-10-17 | Universite Libre De Bruxelles (Ulb) | Materials coated with calixarenes |
FR3019477B1 (fr) | 2014-04-03 | 2023-03-17 | Commissariat Energie Atomique | Procede de fonctionnalisation de surface |
WO2015188261A1 (en) * | 2014-06-11 | 2015-12-17 | The Royal Institution For The Advancement Of Learning/Mcgill University | Surface modification methods for biomedical scaffolds |
RU2640768C1 (ru) * | 2016-12-29 | 2018-01-11 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Российский экономический университет имени Г.В. Плеханова" (ФГБОУ ВО "РЭУ им. Г.В. Плеханова") | Способ модификации поверхности эластомера |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3311889A1 (de) * | 1983-03-31 | 1984-10-11 | Byk-Mallinckrodt Chemische Produkte Gmbh, 6057 Dietzenbach | Verfahren zur irreversiblen bindung von protein an polystyroloberflaechen unter erhaltung der biologischen aktivitaet, so erhaltene polystyroloberflaechen und ihre verwendung |
DE3425328A1 (de) * | 1984-07-10 | 1986-01-16 | Hoechst Ag, 6230 Frankfurt | Lichtempfindliches gemisch und damit hergestelltes lichtempfindliches aufzeichnungsmaterial |
FR2672307B1 (fr) * | 1991-02-01 | 1993-06-04 | Centre Nat Rech Scient | Procede de modification de la surface de materiaux carbones par reduction electrochimique de sels de diazonium, notamment de fibres de carbone pour materiaux composites, materiaux carbones ainsi modifies. |
FR2761377B1 (fr) * | 1997-03-27 | 1999-05-07 | Centre Nat Rech Scient | Procede de realisation par voie electrochimique d'un materiau carbone dont la surface est modifiee par des groupes organiques, utilisation du materiau modifie |
US6458458B1 (en) * | 1998-10-13 | 2002-10-01 | Cabot Corporation | Polymer coated carbon products and other pigments and methods of making same by aqueous media polymerizations or solvent coating methods |
FR2804973B1 (fr) * | 2000-02-11 | 2002-09-20 | Univ Paris 7 Denis Diderot | Materiau metallique dont la surface est modifiee, son procede de preparation et utilisation du materiau modifie |
US7250147B2 (en) * | 2001-01-29 | 2007-07-31 | Tour James M | Process for derivatizing carbon nanotubes with diazonium species |
US6555175B2 (en) * | 2001-02-20 | 2003-04-29 | Joseph E. Johnson | Process for the surface modification of a polymeric substrate |
FR2829046B1 (fr) * | 2001-08-28 | 2005-01-14 | Commissariat Energie Atomique | Procede de greffage et de croissance d'un film organique conducteur sur une surface |
US7176146B2 (en) * | 2002-02-01 | 2007-02-13 | William Marsh Rice University | Method of making a molecule-surface interface |
FR2838048B1 (fr) * | 2002-04-03 | 2005-05-27 | Prod Dentaires Pierre Rolland | Produit dentaire reticulable/dereticulable |
JP2007500669A (ja) * | 2003-07-29 | 2007-01-18 | ウィリアム・マーシュ・ライス・ユニバーシティ | カーボンナノチューブの選択的官能化 |
FR2871162B1 (fr) * | 2004-06-02 | 2007-06-29 | Univ Paris 7 Denis Diderot | Materiau de surface modifiee, son procede de preparation et ses utilisations |
ES2533764T3 (es) * | 2006-02-28 | 2015-04-15 | Alchimer | Formación de películas orgánicas electroinjertadas sobre la superficie de superficies conductoras o semiconductoras eléctricamente |
FR2904319B1 (fr) * | 2006-07-27 | 2009-10-30 | Commissariat Energie Atomique | Sels de diazonium polymerisables, procede de fabrication et utilisations de ceux-ci |
-
2005
- 2005-10-26 FR FR0510914A patent/FR2892325B1/fr active Active
-
2006
- 2006-10-09 AT AT06820167T patent/ATE503794T1/de not_active IP Right Cessation
- 2006-10-09 CN CN2006800491558A patent/CN101346419B/zh active Active
- 2006-10-09 EP EP06820167A patent/EP1948720B1/fr active Active
- 2006-10-09 JP JP2008537128A patent/JP5210170B2/ja active Active
- 2006-10-09 DE DE602006021049T patent/DE602006021049D1/de active Active
- 2006-10-09 CA CA2627222A patent/CA2627222C/fr not_active Expired - Fee Related
- 2006-10-09 ES ES06820167T patent/ES2373299T3/es active Active
- 2006-10-09 WO PCT/FR2006/002260 patent/WO2007048894A1/fr active Application Filing
- 2006-10-09 US US12/091,894 patent/US8133549B2/en active Active - Reinstated
- 2006-10-09 KR KR1020087012553A patent/KR101367781B1/ko active IP Right Grant
-
2008
- 2008-04-27 IL IL191022A patent/IL191022A/en active IP Right Grant
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110945298A (zh) * | 2017-06-16 | 2020-03-31 | 开利公司 | 电热元件、包含电热元件的传热***及它们的制备方法 |
CN110945298B (zh) * | 2017-06-16 | 2022-06-10 | 开利公司 | 电热元件、包含电热元件的传热***及它们的制备方法 |
CN109401360A (zh) * | 2017-08-18 | 2019-03-01 | 中国科学院化学研究所 | 一种对高温结构陶瓷材料进行表面改性的方法 |
CN109401360B (zh) * | 2017-08-18 | 2020-08-21 | 中国科学院化学研究所 | 一种对高温结构陶瓷材料进行表面改性的方法 |
Also Published As
Publication number | Publication date |
---|---|
DE602006021049D1 (de) | 2011-05-12 |
JP5210170B2 (ja) | 2013-06-12 |
FR2892325A1 (fr) | 2007-04-27 |
WO2007048894A1 (fr) | 2007-05-03 |
KR20080072003A (ko) | 2008-08-05 |
FR2892325B1 (fr) | 2008-01-18 |
EP1948720A1 (fr) | 2008-07-30 |
CA2627222C (fr) | 2014-08-05 |
ES2373299T3 (es) | 2012-02-02 |
US20090301862A1 (en) | 2009-12-10 |
EP1948720B1 (fr) | 2011-03-30 |
US8133549B2 (en) | 2012-03-13 |
IL191022A (en) | 2013-08-29 |
JP2009518459A (ja) | 2009-05-07 |
ATE503794T1 (de) | 2011-04-15 |
KR101367781B1 (ko) | 2014-02-27 |
CA2627222A1 (fr) | 2007-05-03 |
CN101346419B (zh) | 2012-05-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101346419B (zh) | 绝缘或半导体表面的改性方法和如此获得的产品 | |
Xu et al. | Vinylene-linked two-dimensional covalent organic frameworks: synthesis and functions | |
Chen et al. | Central unit fluorination of non‐fullerene acceptors enables highly efficient organic solar cells with over 18% efficiency | |
TWI338702B (en) | Aromatic polymer, film, electrolyte film and separator | |
TW201000532A (en) | Low-k dielectrics obtainable by twin polymerization | |
JP2008156636A (ja) | ポリマーのドーピング方法 | |
JP3184642B2 (ja) | 導電性複合材料およびその製造方法 | |
TW201231529A (en) | An ionic gelator, a gel, a process for preparation of the gel and a cross-linker | |
US7273918B2 (en) | Thermally stable self-doped functionalized polyanilines | |
Cho et al. | Role of simultaneous thermodynamic and kinetic variables in optimizing blade-coated organic solar cells | |
Chen et al. | Oxidative graft polymerization of aniline on modified Si (100) surface | |
Le et al. | New Chemical Dopant and Counterion Mechanism for Organic Electrochemical Transistors and Organic Mixed Ionic–Electronic Conductors | |
Lin et al. | Minimalist Design for Solar Energy Conversion: Revamping the π-Grid of an Organic Framework into Open-Shell Superabsorbers | |
JP2006265478A (ja) | 電解質材料及びその製造方法 | |
JPS61235427A (ja) | アリレン基を繰り返し単位として有する芳香族ポリマ−を基板表面に形成する方法 | |
TW390895B (en) | Cross-linked electrically conductive polymers, precursors thereof, methods of fabrication thereof and applications thereof | |
Cheng et al. | Diketopyrrolopyrrole-based conjugated polymers containing planar benzo [c] cinnoline and tetraazapyrene structures for high-performance and long-term stable triboelectric nanogenerators | |
Sangthumchai et al. | Polyacrylonitrile‐based proton conducting membranes containing sulfonic acid and tetrazole moieties | |
KR102353552B1 (ko) | 고투과도 유기 전도성 박막의 제조방법 및 이에 의해 제조된 고투과도 유기 전도성 박막 및 소자 | |
TW201107419A (en) | New polyelectrolyte complexes and the use thereof | |
TW492981B (en) | Oligomer, uncured polymer or cured polymer, a process for forming an uncured polymer or a cured polymer, and an integrated circuit article | |
Lim et al. | Lamination of conductive polypyrrole films to poly (tetrafluoroethylene) films via interfacial graft copolymerization | |
JP2007035611A (ja) | 燃料電池用電解質組成物及び燃料電池 | |
Briers et al. | Moessbauer Spectroscopy of FeCl3-Doped Poly (p-Phenylenevinylene) and of I2-Doped Poly (2, 5-Thienylenevinylene) | |
Idris | Synthesis of oligomers, polymers and cucurbituril-based polyrotaxanes towards polymer light emitting diode and photodynamic therapy application |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
ASS | Succession or assignment of patent right |
Owner name: SAINUO MEDICAL SICIENCE AND TECHNOLOGY CO,. LTD. Free format text: FORMER OWNER: ALSHI MEDICAL CORP. Effective date: 20140620 Owner name: ALSHI MEDICAL CORP. Effective date: 20140620 |
|
C41 | Transfer of patent application or patent right or utility model | ||
C56 | Change in the name or address of the patentee |
Owner name: ALCHIMER Free format text: FORMER NAME: ALCHIMER SA |
|
CP01 | Change in the name or title of a patent holder |
Address after: French horse Patentee after: ALCHIMER Address before: French horse Patentee before: Alchimer |
|
TR01 | Transfer of patent right |
Effective date of registration: 20140620 Address after: French horse Patentee after: ALCHIMER Patentee after: Sino Medical Sciences Technology Inc. Address before: French horse Patentee before: Alchimer Patentee before: Arsh Pharmaceuticals Effective date of registration: 20140620 Address after: French horse Patentee after: ALCHIMER Patentee after: Arsh Pharmaceuticals Address before: French horse Patentee before: Alchimer |
|
CP01 | Change in the name or title of a patent holder |
Address after: French horse Co-patentee after: SINO MEDICAL SCIENCES TECHNOLOGY Inc. Patentee after: ALCHIMER Address before: French horse Co-patentee before: Sino Medical Sciences Technology Inc. Patentee before: Alchimer |
|
CP01 | Change in the name or title of a patent holder |