JPH0567645B2 - - Google Patents
Info
- Publication number
- JPH0567645B2 JPH0567645B2 JP21173382A JP21173382A JPH0567645B2 JP H0567645 B2 JPH0567645 B2 JP H0567645B2 JP 21173382 A JP21173382 A JP 21173382A JP 21173382 A JP21173382 A JP 21173382A JP H0567645 B2 JPH0567645 B2 JP H0567645B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- polymer
- resist
- product
- molecular weight
- 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 - Lifetime
Links
- 239000004641 Diallyl-phthalate Substances 0.000 claims description 17
- 229920000642 polymer Polymers 0.000 claims description 17
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 10
- 229910052710 silicon Inorganic materials 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 14
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000004342 Benzoyl peroxide Substances 0.000 description 5
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 5
- 235000019400 benzoyl peroxide Nutrition 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000001312 dry etching Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000010703 silicon Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- ZDNFTNPFYCKVTB-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,4-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C=C1 ZDNFTNPFYCKVTB-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- -1 polydimethylsiloxane Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- HYWCXWRMUZYRPH-UHFFFAOYSA-N trimethyl(prop-2-enyl)silane Chemical compound C[Si](C)(C)CC=C HYWCXWRMUZYRPH-UHFFFAOYSA-N 0.000 description 2
- ROLAGNYPWIVYTG-UHFFFAOYSA-N 1,2-bis(4-methoxyphenyl)ethanamine;hydrochloride Chemical compound Cl.C1=CC(OC)=CC=C1CC(N)C1=CC=C(OC)C=C1 ROLAGNYPWIVYTG-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2,2'-azo-bis-isobutyronitrile Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- CSDQQAQKBAQLLE-UHFFFAOYSA-N 4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Chemical compound C1=CC(Cl)=CC=C1C1C(C=CS2)=C2CCN1 CSDQQAQKBAQLLE-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- WORJEOGGNQDSOE-UHFFFAOYSA-N chloroform;methanol Chemical compound OC.ClC(Cl)Cl WORJEOGGNQDSOE-UHFFFAOYSA-N 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000004452 microanalysis Methods 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000001039 wet etching Methods 0.000 description 1
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21173382A JPS59102911A (ja) | 1982-12-02 | 1982-12-02 | シリコン原子を有するジアリルフタレ−ト系共重合体 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21173382A JPS59102911A (ja) | 1982-12-02 | 1982-12-02 | シリコン原子を有するジアリルフタレ−ト系共重合体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59102911A JPS59102911A (ja) | 1984-06-14 |
| JPH0567645B2 true JPH0567645B2 (enExample) | 1993-09-27 |
Family
ID=16610687
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP21173382A Granted JPS59102911A (ja) | 1982-12-02 | 1982-12-02 | シリコン原子を有するジアリルフタレ−ト系共重合体 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59102911A (enExample) |
-
1982
- 1982-12-02 JP JP21173382A patent/JPS59102911A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59102911A (ja) | 1984-06-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH0567645B2 (enExample) | ||
| US20120187045A1 (en) | Method for separating substance mixtures by means of multiphase polymer films | |
| JPH0397735A (ja) | シロキサンイニファーター化合物 | |
| JPS6084310A (ja) | けい素原子含有有機高分子化合物の製造方法 | |
| JPS6127537A (ja) | レジスト剤 | |
| JPS62256804A (ja) | レジスト材料 | |
| JPH02279706A (ja) | 珪素を含有する重合体 | |
| JPS62215608A (ja) | アルケニルシリル基含有高分子化合物の製法 | |
| JP3290461B2 (ja) | ジフェニルアセチレン系ポリマー | |
| JPH0734113B2 (ja) | レジスト材料 | |
| Abe et al. | Preparation of polysiloxanes from silicic acid. X. Preparation and properties of allyldimethylsilylated silicic acids | |
| JPS60196750A (ja) | ケイ素原子を有するスチレン系重合体 | |
| JPS59219313A (ja) | トリアリルシラン系重合体 | |
| JPH0565527B2 (enExample) | ||
| JPS63258909A (ja) | ケイ素原子とアリル基を含むスチレン系重合体 | |
| JPS6238381B2 (enExample) | ||
| JPH055345B2 (enExample) | ||
| JPS6088015A (ja) | けい素原子含有有機高分子化合物の製造方法 | |
| JPH0535865B2 (enExample) | ||
| JPH0551391A (ja) | 3−(ビニルフエニルオキシ)プロピルシラン化合物 | |
| Kwak et al. | Synthesis and stable high oxygen permeability of poly (diphenylacetylene) s with two or three trimethylsilyl groups | |
| JPS62209528A (ja) | 新規なるレジスト材料 | |
| JPH0551417A (ja) | フツ素含有共重合体 | |
| JPS635337A (ja) | 感光性樹脂組成物 | |
| JP2655580B2 (ja) | ポリオルガノシルセスキオキサン及びその製法ならびにパターン形成材料 |