KR100909575B1 - 경화성 오가노폴리실록산 조성물, 당해 조성물의 경화생성물의 용도 및 반도체 장치 - Google Patents
경화성 오가노폴리실록산 조성물, 당해 조성물의 경화생성물의 용도 및 반도체 장치 Download PDFInfo
- Publication number
- KR100909575B1 KR100909575B1 KR1020047005795A KR20047005795A KR100909575B1 KR 100909575 B1 KR100909575 B1 KR 100909575B1 KR 1020047005795 A KR1020047005795 A KR 1020047005795A KR 20047005795 A KR20047005795 A KR 20047005795A KR 100909575 B1 KR100909575 B1 KR 100909575B1
- Authority
- KR
- South Korea
- Prior art keywords
- silicon
- bonded
- curable organopolysiloxane
- groups
- organopolysiloxane composition
- 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.)
- Expired - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 107
- 229920001296 polysiloxane Polymers 0.000 title claims abstract description 80
- 239000004065 semiconductor Substances 0.000 title claims abstract description 78
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims abstract description 36
- 238000002834 transmittance Methods 0.000 claims abstract description 28
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 24
- 125000003118 aryl group Chemical group 0.000 claims abstract description 21
- 125000005375 organosiloxane group Chemical group 0.000 claims abstract description 16
- 229910052697 platinum Inorganic materials 0.000 claims abstract description 16
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 14
- 125000000962 organic group Chemical group 0.000 claims abstract description 12
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910052710 silicon Inorganic materials 0.000 claims description 6
- 239000010703 silicon Substances 0.000 claims description 6
- KPWVUBSQUODFPP-UHFFFAOYSA-N ethenyl-(ethenyl-methyl-phenylsilyl)oxy-methyl-phenylsilane Chemical compound C=1C=CC=CC=1[Si](C)(C=C)O[Si](C)(C=C)C1=CC=CC=C1 KPWVUBSQUODFPP-UHFFFAOYSA-N 0.000 claims description 5
- 239000011253 protective coating Substances 0.000 claims description 5
- 239000000853 adhesive Substances 0.000 claims description 3
- 230000001070 adhesive effect Effects 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 238000004382 potting Methods 0.000 claims description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
- 238000010438 heat treatment Methods 0.000 abstract description 18
- 238000004383 yellowing Methods 0.000 abstract description 6
- -1 3-chloropropyl Chemical group 0.000 description 38
- 238000000034 method Methods 0.000 description 13
- 238000011156 evaluation Methods 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 8
- 150000003961 organosilicon compounds Chemical class 0.000 description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 6
- 125000003545 alkoxy group Chemical group 0.000 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 description 4
- 125000003710 aryl alkyl group Chemical group 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 150000002430 hydrocarbons Chemical group 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- 125000003944 tolyl group Chemical group 0.000 description 4
- 125000005023 xylyl group Chemical group 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- BITPLIXHRASDQB-UHFFFAOYSA-N ethenyl-[ethenyl(dimethyl)silyl]oxy-dimethylsilane Chemical compound C=C[Si](C)(C)O[Si](C)(C)C=C BITPLIXHRASDQB-UHFFFAOYSA-N 0.000 description 3
- 125000006038 hexenyl group Chemical group 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 3
- 239000002683 reaction inhibitor Substances 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 150000004756 silanes Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- HMVBQEAJQVQOTI-SOFGYWHQSA-N (e)-3,5-dimethylhex-3-en-1-yne Chemical compound CC(C)\C=C(/C)C#C HMVBQEAJQVQOTI-SOFGYWHQSA-N 0.000 description 1
- GRGVQLWQXHFRHO-AATRIKPKSA-N (e)-3-methylpent-3-en-1-yne Chemical compound C\C=C(/C)C#C GRGVQLWQXHFRHO-AATRIKPKSA-N 0.000 description 1
- CEBKHWWANWSNTI-UHFFFAOYSA-N 2-methylbut-3-yn-2-ol Chemical compound CC(C)(O)C#C CEBKHWWANWSNTI-UHFFFAOYSA-N 0.000 description 1
- KSLSOBUAIFEGLT-UHFFFAOYSA-N 2-phenylbut-3-yn-2-ol Chemical compound C#CC(O)(C)C1=CC=CC=C1 KSLSOBUAIFEGLT-UHFFFAOYSA-N 0.000 description 1
- NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 description 1
- MQSZOZMNAJHVML-UHFFFAOYSA-N 3-phenylbut-1-yn-1-ol Chemical compound OC#CC(C)C1=CC=CC=C1 MQSZOZMNAJHVML-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000002238 attenuated effect Effects 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000005417 glycidoxyalkyl group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- NYMPGSQKHIOWIO-UHFFFAOYSA-N hydroxy(diphenyl)silicon Chemical class C=1C=CC=CC=1[Si](O)C1=CC=CC=C1 NYMPGSQKHIOWIO-UHFFFAOYSA-N 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 230000005693 optoelectronics Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 150000003057 platinum Chemical class 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001843 polymethylhydrosiloxane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
- C08K5/56—Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
-
- 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
- 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
- C08G77/045—Polysiloxanes containing less than 25 silicon atoms
-
- 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
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
-
- 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
- C08G77/70—Siloxanes defined by use of the MDTQ nomenclature
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2224/00—Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
- H01L2224/01—Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
- H01L2224/42—Wire connectors; Manufacturing methods related thereto
- H01L2224/47—Structure, shape, material or disposition of the wire connectors after the connecting process
- H01L2224/48—Structure, shape, material or disposition of the wire connectors after the connecting process of an individual wire connector
- H01L2224/4805—Shape
- H01L2224/4809—Loop shape
- H01L2224/48091—Arched
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2224/00—Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
- H01L2224/01—Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
- H01L2224/42—Wire connectors; Manufacturing methods related thereto
- H01L2224/47—Structure, shape, material or disposition of the wire connectors after the connecting process
- H01L2224/48—Structure, shape, material or disposition of the wire connectors after the connecting process of an individual wire connector
- H01L2224/481—Disposition
- H01L2224/48151—Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive
- H01L2224/48221—Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked
- H01L2224/48245—Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked the item being metallic
- H01L2224/48247—Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked the item being metallic connecting the wire to a bond pad of the item
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2224/00—Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
- H01L2224/80—Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected
- H01L2224/85—Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected using a wire connector
- H01L2224/85909—Post-treatment of the connector or wire bonding area
- H01L2224/8592—Applying permanent coating, e.g. protective coating
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/10—Details of semiconductor or other solid state devices to be connected
- H01L2924/11—Device type
- H01L2924/13—Discrete devices, e.g. 3 terminal devices
- H01L2924/1301—Thyristor
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/15—Details of package parts other than the semiconductor or other solid state devices to be connected
- H01L2924/181—Encapsulation
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
실시예 형태 | 실시예 | 비교 실시예 | |||
1 | 2 | 1 | 2 | 3 | |
항목 | |||||
경화성 오가노폴리실록산 조성물 굴절률(%) | 1.54 | 1.53 | 1.41 | 1.54 | 1.54 |
광투과율(%) | 100 | 100 | 100 | 100 | 76 |
경화 생성물 굴절률(%) | 1.54 | 1.53 | 1.41 | 1.54 | 1.54 |
광투과율(%) | 100 | 100 | 97 | 92 | 69 |
UV 투과율(%) | 0 | 0 | 21 | 0 | 0 |
반도체 장치 신뢰도 평가(방법 1) 발광출력 상대치(%) | 100 | 100 | 99 | 98 | 95 |
평가(방법 2) 발광출력 상대치(%) | 100 | 100 | 98 | 97 | 93 |
Claims (9)
- (A) 분자당 두개 이상의 규소 결합된 알케닐 그룹을 갖고 규소 결합된 아릴 그룹을 갖는 오가노폴리실록산, (B) 분자당 두개 이상의 규소 결합된 수소원자를 갖는 오가노폴리실록산 및 (C) 백금의 오가노실록산 올리고머 착체를 포함하는 경화성 오가노폴리실록산 조성물로서,i) 성분(A) 중의 규소 결합된 유기 그룹 전체에 대한 규소 결합된 아릴 그룹의 함량이 40mol% 이상이고,ii) 성분(C)의 오가노실록산 올리고머가a) 분자당 규소원자수가 8개 이하이고,b) 규소 결합된 알케닐 그룹 및c) 규소 결합된 아릴 그룹을 갖는 것을 특징으로 하는, 경화성 오가노폴리실록산 조성물.
- 제1항에 있어서, 성분(C)의 오가노실록산 올리고머가 1,3-디메틸-1,3-디페닐-1,3-디비닐디실록산임을 특징으로 하는, 경화성 오가노폴리실록산 조성물.
- 제1항 내지 제4항 중의 어느 한 항에 있어서, 가시광의 귤절률이 1.5 이상이고, 광투과율이 80% 이상임을 특징으로 하는, 경화성 오가노폴리실록산 조성물.
- 제1항 내지 제4항 중의 어느 한 항에 있어서, 자외선 투과율이 10% 이하임을 특징으로 하는, 경화성 오가노폴리실록산 조성물.
- 제1항 내지 제4항 중의 어느 한 항에 따르는 조성물의 경화 생성물에 의해 반도체 소자가 피복되어 있음을 특징으로 하는 반도체 장치.
- 제7항에 있어서, 다이오드, 발광 다이오드, 트랜지스터, 다이리스터, 포토커플러, 전하 결합 장치, 모놀리틱 집적 회로(monolithic integrated circuits), 혼성 집적 회로, 대규모 집적 장치 및 초대규모 집적 장치로부터 선택된, 반도체 장치.
- 전기 또는 전자 부품용 접착제, 포팅 제제(potting agent), 보호 피복제 또는 언더필러(underfiller)에서 사용되는, 제1항 내지 제4항 중의 어느 한 항에 따르는 조성물의 경화 생성물.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001322138A JP4040858B2 (ja) | 2001-10-19 | 2001-10-19 | 硬化性オルガノポリシロキサン組成物および半導体装置 |
JPJP-P-2001-00322138 | 2001-10-19 | ||
PCT/JP2002/010499 WO2003035763A1 (en) | 2001-10-19 | 2002-10-09 | Curable organopolysiloxane composition, use of the cured product of the composition, and semiconductor device |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20040048423A KR20040048423A (ko) | 2004-06-09 |
KR100909575B1 true KR100909575B1 (ko) | 2009-07-29 |
Family
ID=19139232
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020047005795A Expired - Fee Related KR100909575B1 (ko) | 2001-10-19 | 2002-10-09 | 경화성 오가노폴리실록산 조성물, 당해 조성물의 경화생성물의 용도 및 반도체 장치 |
Country Status (7)
Country | Link |
---|---|
US (2) | US7271232B2 (ko) |
EP (1) | EP1442081B1 (ko) |
JP (1) | JP4040858B2 (ko) |
KR (1) | KR100909575B1 (ko) |
DE (1) | DE60223832T2 (ko) |
TW (1) | TWI253460B (ko) |
WO (1) | WO2003035763A1 (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101507006B1 (ko) | 2010-08-18 | 2015-03-30 | 제일모직주식회사 | 폴리오가노실록산 조성물, 상기 폴리오가노실록산 조성물로부터 형성된 봉지재 및 상기 봉지재를 포함하는 전자 소자 |
Families Citing this family (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4040858B2 (ja) * | 2001-10-19 | 2008-01-30 | 東レ・ダウコーニング株式会社 | 硬化性オルガノポリシロキサン組成物および半導体装置 |
TW200427111A (en) * | 2003-03-12 | 2004-12-01 | Shinetsu Chemical Co | Material for coating/protecting light-emitting semiconductor and the light-emitting semiconductor device |
AU2003261279A1 (en) * | 2003-07-28 | 2005-03-07 | Dow Corning Corporation | Method for etching a patterned silicone layyer |
JP4908736B2 (ja) * | 2003-10-01 | 2012-04-04 | 東レ・ダウコーニング株式会社 | 硬化性オルガノポリシロキサン組成物および半導体装置 |
JP2006073950A (ja) | 2004-09-06 | 2006-03-16 | Kansai Electric Power Co Inc:The | 高耐熱半導体装置 |
JP5392805B2 (ja) * | 2005-06-28 | 2014-01-22 | 東レ・ダウコーニング株式会社 | 硬化性オルガノポリシロキサン樹脂組成物および光学部材 |
JP2007258317A (ja) * | 2006-03-22 | 2007-10-04 | Shin Etsu Chem Co Ltd | 半導体装置の製造方法 |
JP5060074B2 (ja) * | 2006-05-11 | 2012-10-31 | 東レ・ダウコーニング株式会社 | 接着促進剤、硬化性オルガノポリシロキサン組成物、および半導体装置 |
JP5202822B2 (ja) | 2006-06-23 | 2013-06-05 | 東レ・ダウコーニング株式会社 | 硬化性オルガノポリシロキサン組成物および半導体装置 |
WO2008023746A1 (fr) | 2006-08-22 | 2008-02-28 | Mitsubishi Chemical Corporation | ÉLÉMENT DE DISPOSITIF SEMI-CONDUCTEUR, LIQUIDE POUR FORMER UN ÉLÉMENT DE DISPOSITIF SEMI-CONDUCTEUR, PROCÉDÉ DE FABRICATION D'UN ÉLÉMENT DE DISPOSITIF SEMI-CONDUCTEUR ET LIQUIDE POUR FORMER UN ÉLÉMENT DE DISPOSITIF SEMI-CONDUCTEUR UTILISANT LE PROCÉ |
JP5148088B2 (ja) * | 2006-08-25 | 2013-02-20 | 東レ・ダウコーニング株式会社 | 硬化性オルガノポリシロキサン組成物および半導体装置 |
KR101022994B1 (ko) * | 2006-09-29 | 2011-03-22 | 아사히 가세이 일렉트로닉스 가부시끼가이샤 | 폴리오르가노실록산 조성물 |
TWI361205B (en) * | 2006-10-16 | 2012-04-01 | Rohm & Haas | Heat stable aryl polysiloxane compositions |
US8029904B2 (en) * | 2006-12-01 | 2011-10-04 | Rohm And Haas Company | Aryl (thio)ether aryl polysiloxane composition and methods for making and using same |
US20080160317A1 (en) * | 2006-12-29 | 2008-07-03 | Deborah Ann Haitko | Optoelectronic device |
US8017246B2 (en) * | 2007-11-08 | 2011-09-13 | Philips Lumileds Lighting Company, Llc | Silicone resin for protecting a light transmitting surface of an optoelectronic device |
WO2009119841A1 (ja) | 2008-03-28 | 2009-10-01 | 三菱化学株式会社 | 硬化性ポリシロキサン組成物、並びに、それを用いたポリシロキサン硬化物、光学部材、航空宇宙産業用部材、半導体発光装置、照明装置、及び画像表示装置 |
JP2009284618A (ja) * | 2008-05-21 | 2009-12-03 | Sharp Corp | フォトカプラ及びスイッチング電源回路 |
JP5469874B2 (ja) | 2008-09-05 | 2014-04-16 | 東レ・ダウコーニング株式会社 | 硬化性オルガノポリシロキサン組成物、光半導体素子封止剤および光半導体装置 |
KR101632593B1 (ko) | 2008-10-31 | 2016-06-22 | 다우 코닝 도레이 캄파니 리미티드 | 경화성 오가노폴리실록산 조성물, 광 반도체 소자 밀봉제 및 광 반도체 장치 |
JP4862032B2 (ja) * | 2008-12-05 | 2012-01-25 | 信越化学工業株式会社 | 高屈折率を有する硬化物を与える付加硬化型シリコーン組成物、及び該組成物からなる光学素子封止材 |
KR101030019B1 (ko) | 2009-12-31 | 2011-04-20 | 제일모직주식회사 | 봉지재용 투광성 수지 및 이를 포함하는 전자 소자 |
JP2011219597A (ja) * | 2010-04-08 | 2011-11-04 | Nitto Denko Corp | シリコーン樹脂シート |
EP2586832B1 (en) * | 2010-06-24 | 2014-10-29 | Sekisui Chemical Co., Ltd. | Encapsulant for optical semiconductor device and optical semiconductor device using same |
TWI435914B (zh) | 2010-12-31 | 2014-05-01 | Eternal Chemical Co Ltd | 可固化之有機聚矽氧烷組合物及其製法 |
US8895662B2 (en) | 2010-12-31 | 2014-11-25 | Eternal Chemical Co., Ltd. | Curable composition and method for manufacturing the same |
US9045639B2 (en) | 2010-12-31 | 2015-06-02 | Eternal Materials Co., Ltd. | Curable composition and method for manufacturing the same |
JP5522111B2 (ja) | 2011-04-08 | 2014-06-18 | 信越化学工業株式会社 | シリコーン樹脂組成物及び当該組成物を使用した光半導体装置 |
EP2706095B1 (en) * | 2011-05-04 | 2021-03-03 | LG Chem, Ltd. | Curable composition |
WO2012157330A1 (ja) * | 2011-05-17 | 2012-11-22 | 積水化学工業株式会社 | 光半導体装置用封止剤及び光半導体装置 |
WO2013077707A1 (ko) * | 2011-11-25 | 2013-05-30 | 주식회사 엘지화학 | 경화성 조성물 |
KR101460863B1 (ko) * | 2011-11-25 | 2014-12-04 | 주식회사 엘지화학 | 오가노폴리실록산의 제조 방법 |
JP5805883B2 (ja) * | 2011-11-25 | 2015-11-10 | エルジー・ケム・リミテッド | 硬化性組成物 |
KR101493131B1 (ko) * | 2011-11-25 | 2015-02-13 | 주식회사 엘지화학 | 오가노폴리실록산 |
TWI473839B (zh) * | 2011-11-25 | 2015-02-21 | Lg Chemical Ltd | 可固化組成物 |
KR101409537B1 (ko) * | 2011-11-25 | 2014-06-19 | 주식회사 엘지화학 | 경화성 조성물 |
TWI558741B (zh) * | 2012-07-27 | 2016-11-21 | Lg化學股份有限公司 | 可固化組成物 |
JP5779155B2 (ja) * | 2012-08-28 | 2015-09-16 | 株式会社東芝 | 半導体装置 |
US9470395B2 (en) | 2013-03-15 | 2016-10-18 | Abl Ip Holding Llc | Optic for a light source |
EP3081365B1 (en) | 2013-05-10 | 2021-02-17 | ABL IP Holding LLC | Method and apparatus for manufacturing silicone optics |
KR101611009B1 (ko) | 2013-11-07 | 2016-04-08 | 제일모직주식회사 | 코어-쉘 미립자, 그 제조방법 및 이를 이용한 확산필름 |
DE102015101748A1 (de) | 2015-02-06 | 2016-08-11 | Osram Opto Semiconductors Gmbh | Elektronisches Bauelement mit einem Werkstoff umfassend Epoxysilan-modifiziertes Polyorganosiloxan |
US9416273B1 (en) | 2015-04-30 | 2016-08-16 | Eternal Materials Co., Ltd. | Curable composition and method for manufacturing the same |
JP6445947B2 (ja) * | 2015-09-04 | 2018-12-26 | 株式会社東芝 | 光結合装置 |
KR200485988Y1 (ko) | 2016-04-18 | 2018-03-20 | 우성화학(주) | 김 양식용 부구 |
JP6512181B2 (ja) * | 2016-06-23 | 2019-05-15 | 信越化学工業株式会社 | フォトカプラー一次封止用熱硬化性シリコーン樹脂組成物、該組成物で封止されたフォトカプラー及び該フォトカプラーを有する光半導体装置 |
EP3505569A4 (en) * | 2016-08-26 | 2020-03-25 | Shin-Etsu Chemical Co., Ltd. | AMBIENT TEMPERATURE CURABLE ORGANOPOLYSILOXANE COMPOSITION FOR DECOOLING, AND ARTICLE SEALED BY THE CURED PRODUCT THEREOF |
WO2020082359A1 (en) * | 2018-10-26 | 2020-04-30 | Elkem Silicones Shanghai Co., Ltd. | Silicone composition and method for additive manufacturing silicone elastomer article |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5616632A (en) * | 1994-05-09 | 1997-04-01 | Shin-Etsu Chemical Co., Ltd. | Silicone compositions |
WO2001017570A1 (en) * | 1999-09-08 | 2001-03-15 | Medennium, Inc. | High refractive index silicone for use in intraocular lenses |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4040858B2 (ja) | 2001-10-19 | 2008-01-30 | 東レ・ダウコーニング株式会社 | 硬化性オルガノポリシロキサン組成物および半導体装置 |
-
2001
- 2001-10-19 JP JP2001322138A patent/JP4040858B2/ja not_active Expired - Fee Related
-
2002
- 2002-10-09 DE DE60223832T patent/DE60223832T2/de not_active Expired - Lifetime
- 2002-10-09 WO PCT/JP2002/010499 patent/WO2003035763A1/en active IP Right Grant
- 2002-10-09 EP EP02802006A patent/EP1442081B1/en not_active Expired - Lifetime
- 2002-10-09 KR KR1020047005795A patent/KR100909575B1/ko not_active Expired - Fee Related
- 2002-10-09 US US10/492,569 patent/US7271232B2/en not_active Expired - Fee Related
- 2002-10-11 TW TW091123453A patent/TWI253460B/zh not_active IP Right Cessation
-
2007
- 2007-08-02 US US11/832,984 patent/US7763697B2/en active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5616632A (en) * | 1994-05-09 | 1997-04-01 | Shin-Etsu Chemical Co., Ltd. | Silicone compositions |
WO2001017570A1 (en) * | 1999-09-08 | 2001-03-15 | Medennium, Inc. | High refractive index silicone for use in intraocular lenses |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101507006B1 (ko) | 2010-08-18 | 2015-03-30 | 제일모직주식회사 | 폴리오가노실록산 조성물, 상기 폴리오가노실록산 조성물로부터 형성된 봉지재 및 상기 봉지재를 포함하는 전자 소자 |
Also Published As
Publication number | Publication date |
---|---|
EP1442081B1 (en) | 2007-11-28 |
JP2003128922A (ja) | 2003-05-08 |
US20070273051A1 (en) | 2007-11-29 |
DE60223832D1 (de) | 2008-01-10 |
US20040241927A1 (en) | 2004-12-02 |
WO2003035763A1 (en) | 2003-05-01 |
EP1442081A1 (en) | 2004-08-04 |
KR20040048423A (ko) | 2004-06-09 |
DE60223832T2 (de) | 2008-10-30 |
TWI253460B (en) | 2006-04-21 |
JP4040858B2 (ja) | 2008-01-30 |
US7271232B2 (en) | 2007-09-18 |
US7763697B2 (en) | 2010-07-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100909575B1 (ko) | 경화성 오가노폴리실록산 조성물, 당해 조성물의 경화생성물의 용도 및 반도체 장치 | |
KR101699383B1 (ko) | 경화성 오가노폴리실록산 조성물 및 반도체 장치 | |
JP4409160B2 (ja) | 硬化性オルガノポリシロキサン組成物および半導体装置 | |
JP5667740B2 (ja) | 硬化性オルガノポリシロキサン組成物及び半導体装置 | |
KR101730840B1 (ko) | 경화성 오가노폴리실록산 조성물 및 반도체 장치 | |
US8080614B2 (en) | Curable organopolysiloxane composition and semiconductor device | |
KR102165826B1 (ko) | 경화성 오르가노폴리실록산 조성물, 캡슐화제 및 반도체 장치 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0105 | International application |
Patent event date: 20040419 Patent event code: PA01051R01D Comment text: International Patent Application |
|
PG1501 | Laying open of application | ||
A201 | Request for examination | ||
PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20071002 Comment text: Request for Examination of Application |
|
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20090429 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20090721 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20090722 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
PR1001 | Payment of annual fee |
Payment date: 20120628 Start annual number: 4 End annual number: 4 |
|
FPAY | Annual fee payment |
Payment date: 20130701 Year of fee payment: 5 |
|
PR1001 | Payment of annual fee |
Payment date: 20130701 Start annual number: 5 End annual number: 5 |
|
FPAY | Annual fee payment |
Payment date: 20140703 Year of fee payment: 6 |
|
PR1001 | Payment of annual fee |
Payment date: 20140703 Start annual number: 6 End annual number: 6 |
|
FPAY | Annual fee payment |
Payment date: 20150619 Year of fee payment: 7 |
|
PR1001 | Payment of annual fee |
Payment date: 20150619 Start annual number: 7 End annual number: 7 |
|
FPAY | Annual fee payment |
Payment date: 20160616 Year of fee payment: 8 |
|
PR1001 | Payment of annual fee |
Payment date: 20160616 Start annual number: 8 End annual number: 8 |
|
FPAY | Annual fee payment |
Payment date: 20170616 Year of fee payment: 9 |
|
PR1001 | Payment of annual fee |
Payment date: 20170616 Start annual number: 9 End annual number: 9 |
|
FPAY | Annual fee payment |
Payment date: 20190617 Year of fee payment: 11 |
|
PR1001 | Payment of annual fee |
Payment date: 20190617 Start annual number: 11 End annual number: 11 |
|
PC1903 | Unpaid annual fee |
Termination category: Default of registration fee Termination date: 20210501 |