| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | Fire retardant compounds | US512303 | 1974-10-04 | US4049726A | 1977-09-20 | Hendrik Harm Jannes Oosterwijk; Ulfert Elle Wiersum; Eduard Pieter Magre; Johannes Hendrinus VAN Dijk |
| Novel brominated polydiisopropylarylene compounds which can be used for imparting fire retardance properties to polymers such as polystyrene and polypropylene contain bromine as a substituent on the aliphatic radicals and have the following formula: ##STR1## A is a thienylene group or an arylene group such as a substituted or unsubstituted phenylene, biphenylene, napthylene, or anthracylene group, R.sub.1 through R.sub.4 a methyl group substituted or not with bromine, R.sub.5 and R.sub.6 a bromine atom or a hydrogen atom, and n a whole number in the range of 2 to 10, the number of bromine atoms per molecule in the aliphatic groups being at least 2 and the total bromine content being not more than 70 per cent by weight. | ||||||
| 2 | Method of treating carbon black and carbon black so treated | US343805 | 1994-11-22 | US5500201A | 1996-03-19 | Michael Binder; Robert J. Mammone |
| The physical and chemical properties of carbon blacks are modified by expng them to a room temperature gas plasma. | ||||||
| 3 | Fluoroalkylaryliodonuim compounds | US245940 | 1988-09-19 | US4873027A | 1989-10-10 | Teruo Umemoto; Yoshihiko Gotoh |
| Fluoroalkylaryliodonium compounds having the formula (I): ##STR1## wherein AR, A and Rf are as defined above, are disclosed. The fluoroalkylaryliodonium compounds of the present invention are useful as intermediates for producing N-fluoroalkylanilines or derivatives thereof which are important precursors for fluorine-containing disperse azo dyes having an excellent resistance to light. | ||||||
| 4 | 新規オニウム塩化合物及びそれを用いたレジスト組成物並びにパターン形成方法 | JP2014226553 | 2014-11-07 | JP6323302B2 | 2018-05-16 | 福島 将大; 大橋 正樹; 畠山 潤 |
| 5 | JPH02504633A - | JP50711488 | 1988-08-03 | JPH02504633A | 1990-12-27 | |
| 6 | JPS4940703B1 - | JP3623269 | 1969-05-13 | JPS4940703B1 | 1974-11-05 | |
| 7 | 신규 오늄염 화합물 및 그것을 이용한 레지스트 조성물 및 패턴 형성 방법 | KR1020150155219 | 2015-11-05 | KR1020160055074A | 2016-05-17 | 후쿠시마마사히로; 오하시마사키; 하타케야마준 |
| [해결수단] 일반식(1)로표시되는오늄염화합물.(R, R, R, R, R및 R은수소원자또는 1가탄화수소기를나타내고, j는 0 또는 1이다. Z는일반식(a)로표시되는술포늄양이온또는일반식(b)로표시되는요오도늄양이온을나타낸다.)(R, R및 R은 1가탄화수소기를나타낸다. R및 R은 1가탄화수소기를나타낸다.) [효과] 본발명의레지스트조성물에포함되는오늄염화합물은, 산확산제어제로서양호하게기능하고, 결과적으로 MEF 및 LWR이작으며, 초점심도가우수하여고해상인패턴프로파일을구축할수 있다. | ||||||
| 8 | Production method of iodinated aromatic compounds | JP50318788 | 1988-03-16 | JP2559484B2 | 1996-12-04 | RUURU MAAKU; TASUTEIN JERARUDO CHAARUZU |
| 9 | Liquid phase isomerization of iodine aromatic compounds | JP50280388 | 1988-03-16 | JP2559483B2 | 1996-12-04 | RUURU MAAKU; TASUTEIN JERARUDO CHAARUZU |
| 10 | JPH01503067A - | JP50318788 | 1988-03-16 | JPH01503067A | 1989-10-19 | |
| 11 | JPH01502825A - | JP50280388 | 1988-03-16 | JPH01502825A | 1989-09-28 | |
| 12 | Fluoroalkylaryliodonium compound | JP14244984 | 1984-07-11 | JPS6124529A | 1986-02-03 | UMEMOTO TERUO; GOTO YOSHIHIKO |
| NEW MATERIAL:A fluoroalkylaryliodonium compound expressed by formula I [Rf represents polyfluoroalkyl or formula II (n is an integer 1W20); Ar represents substituted- or nonsubstituted-phenyl; A represents alkyl, alkoxyl, aryl, halogen atom, OH or high molecular chain]. EXAMPLE: 2,2,2-Trifluoroethylphenyliodonium trifluoromethanesulfonate. USE: An intermediate allowing to produce easily N-fluoroalkylanilines useful as an intermediate for fluorine-containing disperse azo dyes with superior light resistance. PREPARATION: A fluoroalkyliodoso compound expressed by formula III (Rf' represents polyfluoroalkyl or formula IV is reacted with an aromatic compound expressed by the formula ArH and a sulfonic acid expressed by the formula ASO 3H to obtain the compound expressed by formula I. COPYRIGHT: (C)1986,JPO&Japio | ||||||
| 13 | Refinement of side chain chlorinated alkyl aromatics by rectification | JP20631081 | 1981-12-22 | JPS57130931A | 1982-08-13 | HANSUUYOAHIMU HERUMAN; GIYUNTAA MAIYAA; KURAUSUUDEIITAA SHIYUTETSUFUEN |
| 14 | 신규 오늄염 화합물 및 그것을 이용한 레지스트 조성물 및 패턴 형성 방법 | KR1020150155219 | 2015-11-05 | KR101920112B1 | 2018-11-19 | 후쿠시마마사히로; 오하시마사키; 하타케야마준 |
| [해결수단] 일반식(1)로표시되는오늄염화합물.(R, R, R, R, R및 R은수소원자또는 1가탄화수소기를나타내고, j는 0 또는 1이다. Z는일반식(a)로표시되는술포늄양이온또는일반식(b)로표시되는요오도늄양이온을나타낸다.)(R, R및 R은 1가탄화수소기를나타낸다. R및 R은 1가탄화수소기를나타낸다.) [효과] 본발명의레지스트조성물에포함되는오늄염화합물은, 산확산제어제로서양호하게기능하고, 결과적으로 MEF 및 LWR이작으며, 초점심도가우수하여고해상인패턴프로파일을구축할수 있다. | ||||||
| 15 | 요오드 방향족 화합물에 대한 액상 불균화 반응의 선택적인 촉매 | KR1019880701543 | 1988-03-16 | KR1019960001688B1 | 1996-02-03 | 룰,마크; 터스틴,제럴드찰스 |
| 내용 없음. | ||||||
| 16 | 新規オニウム塩化合物及びそれを用いたレジスト組成物並びにパターン形成方法 | JP2014226553 | 2014-11-07 | JP2016088898A | 2016-05-23 | 福島 将大; 大橋 正樹; 畠山 潤 |
| 【課題】レジスト組成物で、酸拡散制御剤として機能し、MEF及びLWRの小さく、焦点深度に優れ高解像なパターンプロファイルを構築できるオニウム塩化合物の提供。 【解決手段】トリフェニルスルホニウム=4−モルホリン−4−イル−ベンゾエートなどの一般式(1)で示されるオニウム塩化合物。 (R11〜R55及びR01は各々独立にH又は一価炭化水素基;R11とR22、R33とR01は相互に結合して炭素環を形成しても良く;R44とR4は互いに結合してNと共に環を形成、更にO、S、NH基等が介在しても良い;jは0又は1;j=0の場合0≦k≦1、j=1の場合0≦k≦3;Z+はスルホニウムカチオン又はヨードニウムカチオン) 【選択図】なし |
||||||
| 17 | Production method of iodinated aromatic compounds | JP50269388 | 1988-03-16 | JP2634217B2 | 1997-07-23 | RUURU MAAKU; REEN DONARUDO UEIN; RAAKINSU TOOMASU HASURU JUNIA; TASUTEIN JERARUDO CHAARUZU |
| 18 | Process for decreasing halogen content of polyhalogenated aromatic compound | JP5805293 | 1993-02-24 | JPH0665119A | 1994-03-08 | HAINRIHI SHIYURAGE; HERUMUUTO FUIIGE |
| PURPOSE: To decrease halogen content by reacting a polyhalogenated aromatic compound with a mono- and/or non-halogenated aromatic compound in the presence of a catalyst and a hydrogen halide in gaseous phase. CONSTITUTION: (A) A polyhalogenated aromatic compound is allowed to react with (B) a monohalogenated aromatic compound and/or a non-halogenated aromatic compound in gaseous phase in the presence of a catalyst contg. at least one element selected from platinum group metals as a simple substance form or a compd. form and in the presence of a hydrogen halide to transfer the halogen atom from the compd. A to the compd. B, and at the same time, to transfer the hydrogen atom from the compd. B to the compd. A and to decrease the halogen content of the compd. A. As the catalyst, single substance palladium and palladium compds. (for example, palladium dichlorides) are especially preferable and 0.005-10 wt.% palladium and its compds. are used to the compds. A. The 10-100 wt.% hydrogen halide is used based on the amount of the aromatic compounds. COPYRIGHT: (C)1994,JPO | ||||||
| 19 | Reaction method of aromatic compound | JP2584392 | 1992-01-17 | JPH04312539A | 1992-11-04 | FURANTSUUYOZEFU MAISU; HERUMUUTO FUIIGE |
| PURPOSE: To accelerate the reaction by using a ruthenium-contg. catalyst at the time of migrating a halogen from a polyhalogenated arom. compd. to a monohalogenated or nonhalogenated arom. compd. CONSTITUTION: (A) The polyhalogenated arom. compd. and (B) the monohalogenated or nonhalogenated arom. compd. are brought into reaction in the presence of the catalyst contg. (C) the ruthenium in the form of an element or compd. and if desired, further, contg. (D) ≥1 kinds of the metals (for example, copper, silver, gold, zinc, mercury or cadmium) of groups I and II of periodic table or their compds. and more particularly the salts of the copper and silver, by which the halogen is migrated from A to B. The component C in the catalyst exhibits good activity at the time of the migration of the halogen from A to B and the addition of the component D greatly improves its activity. COPYRIGHT: (C)1992,JPO | ||||||
| 20 | JPH0358332B2 - | JP14244984 | 1984-07-11 | JPH0358332B2 | 1991-09-05 | UMEMOTO TERUO; GOTO YOSHIHIKO |
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