| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 41 | 一种用于快速反应的装置 | CN201721193414.6 | 2017-09-18 | CN207307868U | 2018-05-04 | 张锋; 张志炳; 罗化勋; 张玲玲; 孟为民 |
| 本实用新型公开一种用于快速反应的装置，该装置强化了两股物料的快速混合及传热传质，且能及移除反应产生的热，调节反应温度，从而减少副反应，提高选择性，降低物耗。所述的装置包括：至少一个反应器和换热套；反应器包括反应腔和两个相对设置的喷射管；反应腔包括侧壁和两个相对的端面；侧壁上设置有反应液出口；两个喷射管分别穿过两个端面并与端面密封连接，喷头位于反应腔内；换热套设于反应器外并与反应器的外壁围成换热腔；换热套上还设置有换热介质进口和换热介质出口连通换热腔。该装置的喷射管使两股高速流相向流动撞击，解决了普通反应器相间传质效率低、反应效果差的问题，且同时通过换热套快速换热，及时带走反应产生的热量。(ESM)同样的发明创造已同日申请发明专利 | ||||||
| 42 | BIORESPONSIVE HYDROGELS | PCT/US2006020173 | 2006-05-24 | WO2006127865A3 | 2009-05-22 | LYON LOUIS ANDREW; KIM JONGSEONG |
| The invention is a structure capable of detecting a target molecule, the invention including a functionalized polymer matrix having chemically reactive groups and at least one biomolecule attached to the chemically reactive groups to form a surface-modified bioresponsive polymer matrix. | ||||||
| 43 | SYNTHETIC ROUTES TO CYCLOPENTANECARBOXYLIC ACID DERIVATIVES | PCT/EP8600678 | 1986-11-25 | WO8703278A3 | 1987-07-02 | NUMMY LAURENCE JOHN; CORKINS H GLENN; SCARANO LOUIS S; BYRNE DENNIS P |
| A ring contraction approach is applied to preparation of cyclopentane derivatives, especially 2,2,5,5-tetra-methylcyclopentanecarboxylic acid from cyclohexane compounds. In one aspect, a cyclohexane diazoketone is reacted with an amine (e.g., an alanine ester) to form the corresponding cyclopentane acid amide. | ||||||
| 44 | Plant ethylene response inhibition compound and complex | JP2005153914 | 2005-05-26 | JP2005314430A | 2005-11-10 | DALY JAMES; KOURELIS BOB |
| <P>PROBLEM TO BE SOLVED: To regulate the physiological functions of plants, and more particularly to provide a method for inhibiting the ethylene response of plants or of plant products. <P>SOLUTION: The method for minimizing impurities capable of reversibly binding to the ethylene receptor site of a plant is provided which comprises the step of forming a compound having the formula by reacting a metal amide salt with a halocarbene in an inert atmosphere and optionally in the presence of a non-reactive solvent. In the formula, n is a number of 1 to 4; and R is selected from the group consisting of hydrogen, a saturated or unsaturated 1 to 4C alkyl, a hydroxy, a halogen, a 1 to 4C alkoxy, an amino, and a carboxy. <P>COPYRIGHT: (C)2006,JPO&NCIPI | ||||||
| 45 | Production method of 1,2-naphthoquinone-2-diazide derivative | JP13192899 | 1999-05-12 | JP3481884B2 | 2003-12-22 | 邦彦 小島; 敏雄 板花; 信博 米山; 成重 飛嶋; 弘忠 飯田 |
| 46 | Plant ethylene response inhibitor compound and complex | JP2000565720 | 1999-06-30 | JP2002523337A | 2002-07-30 | コウレリス，ボブ; ダレー，ジェイムス |
| (57)【要約】 本発明は植物の生理機能を調節することに関し、特に、植物または植物産生物のエチレン応答を阻害する方法に関し、三実施態様を有する。 第一の実施態様は、シクロプロペンおよびメチルシクロプロペンのようなその誘導体の合成中に植物エチレン受容体部位に可逆的に結合できる不純物を可及的に少なくさせる方法に関する。 第二の実施態様は、シクロペンタジエンおよびジアゾシクロペンタジエンおよびそれらの誘導体に加えて、シクロデキストリンのような分子カプセル化剤と、シクロプロペンおよびメチルシクロプロペンのようなその誘導体とから形成された複合体に関し、当該複合体の形成により、植物のエチレン応答を阻害できるこれらの化合物を貯蔵したり輸送したりする都合のよい手段を与える。 これらの化合物は反応性のガスであり、酸化やその他の潜在的な反応のため高度に不安定である。 第三の実施態様は、植物の寿命を延ばすために植物のエチレン応答を阻害できるこれらの化合物を植物に送達する都合の良い方法に関する。 | ||||||
| 47 | Production of 1,2-naphthoquinone-2-diazide derivative | JP13192899 | 1999-05-12 | JP2000072740A | 2000-03-07 | IIDA HIROTADA; YONEYAMA NOBUHIRO; TOBISHIMA NARUSHIGE; ITAHANA TOSHIO; KOJIMA KUNIHIKO |
| PROBLEM TO BE SOLVED: To provide a method for efficiently producing a 1,2-naphthoquinone-2- diazide or its sulfo substitution product from a 2-diazo-1-naphthalenesulfonic acid or its sulfo substitution product. SOLUTION: A 2-diazo-1-naphthalenesulfonic acid derivative is treated in an alkaline aqueous solution containing iodine or an alkaline aqueous solution containing iodine dissolved in an organic solvent or treated in an alkaline aqueous solution containing the iodine or an iodine compound and an oxidizing agent added thereto to produce a 1,2-naphthoquinone-2-diazide derivative. COPYRIGHT: (C)2000,JPO | ||||||
| 48 | Method for producing a diazo and azo compounds | JP15700988 | 1988-06-27 | JP2538997B2 | 1996-10-02 | MANFUREETO RORENTSU |
| 49 | Preparation of substituted benzene, benzenesulfonic acid and its derivative, and preparation of n,n'-substituted urea | JP22525993 | 1993-08-18 | JPH06172294A | 1994-06-21 | PEETAA BAUMAISUTAA; GOTSUTOFURIITO ZAIFUERUTO; HAINTSU SHIYUTAINAA |
| PURPOSE: To efficiently obtain the compds. having a plant-growth regulating characteristic, by subjecting amino-benzenes to diazotization, after that subjecting it to homogeneous Pd-catalysed coupling with an olefin and then subjecting it to heterogeneous Pd-catalysed hydrogenation of the olefinic substituent. CONSTITUTION: Anilines (e.g. aniline-2-sulfonic acid, etc.), are treated with sodium nitrite in the presence of an acid to form diazonium salts represented by formula I [where Ar is 6-20C (substd.) aryl, 3-20C heteroaryl, etc.]. The compds. of 1 mole equiv. are reacted with olefins (e.g. 3,3,3-trifluoropropene, etc.), of ≥1 mole equiv., represented by formula II (Ra-Rc are each H or hydrogenation stable substitent), in an inert solvent and in the presence of a homogeneous palladium catalyst, alkali (alkaline earth) metal salt of carboxylic acids, etc., to form the compds. represented by formula III. The compds. are hydrogenated in an inert solvent and in the presence of a palladium hydrogenation catalyst to obtain the objective compds. (for example, trifluoropropyl benzenesulfonic acid, etc.), represented by formula IV. COPYRIGHT: (C)1994,JPO | ||||||
| 50 | Deep ultraviolet photoresist composition containing polycyclic cyclopentane-2-diazo-1,3-dione | JP17256090 | 1990-06-29 | JPH03213864A | 1991-09-19 | CHIENJIYU U; AN EMU MUURINGU; JIEEMUZU TEII YAADORII |
| PURPOSE: To ensure peak absorption in a deep UV region by mixing a specified resin binder soluble or swellable in an aq. alkali soln. and a specified compd. with a solvent compsn. CONSTITUTION: A photosensitive compsn. is obtd. by mixing a resin binder insoluble in water but soluble or swellable in an aq. alkali soln. and a compd. represented by formula I, II, etc., with an enough solvent compsn. to prepare a practically uniform mixture. The amt. of the resin binder and that of the compd. are about 65-98% and about 2-35% of the weight of the photosensitive compsn. except the solvent compsn., respectively. The photosensitive compsn. can be imagewise exposed with UV in the range of about 200-300nm. COPYRIGHT: (C)1991,JPO | ||||||
| 51 | JPS5934701B2 - | JP7784473 | 1973-07-10 | JPS5934701B2 | 1984-08-24 | JERAADO GAREIJAA; TEIRETSUKU UOOKAA; DEIBITSUDO TOOMASU IISUTORITSUKU |
| 52 | Novel cyclopentene-1,3-dione derivative | JP3953077 | 1977-04-08 | JPS53127496A | 1978-11-07 | ODA MASASHI; KASAI MASAJI |
| PURPOSE: 10-Oxa-exo-tricyclo[5.2.1.0 2, 6]-deca-8-ene-4-diazo-3, 5-dione I. COPYRIGHT: (C)1978,JPO&Japio | ||||||
| 53 | JPS4980002A - | JP7784473 | 1973-07-10 | JPS4980002A | 1974-08-02 | |
| 54 | 赤外線感光性発色組成物、平版印刷版原版、平版印刷版の製版方法、発色物形成方法、画像形成方法、及び、発色剤 | JP2014061482 | 2014-03-25 | JP2015186841A | 2015-10-29 | 野越 啓介; 鈴木 昭太 |
| 【課題】赤外線露光により高濃度で発色し、かつ経時による退色が少ない赤外線感光性発色組成物を提供すること。 【解決手段】(成分A)式(1)で表される化合物、及び、(成分B)赤外線吸収剤を含有することを特徴とする赤外線感光性発色組成物。式(1)中、R1及びR2はそれぞれ独立に、水素原子又は炭素数1〜8の炭化水素基を表し、R1及びR2の少なくとも一方は水素原子であり、R3〜R6はそれぞれ独立に、水素原子又は一価の置換基を表し、R3〜R6のうちの2〜4つが結合して環状構造を形成していてもよく、Xは、脱離してポリメチン色素、アゾベンゼン色素又はピラゾロトリアゾール色素を生成する基を表す。 【選択図】なし |
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| 55 | Gold cluster catalyst and production method thereof | JP2012133329 | 2012-06-12 | JP2013255887A | 2013-12-26 | HARUTA MASAKI; KAN ETSU; HUANG JIAHUI; TAKETOSHI AYAKO; ISHIDA TAMAO; AKITA TOMOKI; OGATA ATSUSHI; KIN KENKA |
| PROBLEM TO BE SOLVED: To provide a gold cluster catalyst which is capable of promoting and controlling the chemical reaction with high catalytic activity and selectivity, and to provide a production method thereof.SOLUTION: A gold cluster catalyst, in which a cluster produced by gathering a plurality of gold atoms is carried on a carrier, is produced by carrying a plurality of gold cluster compounds having a predetermined number of gold atoms stabilized by an organic ligand on a carrier, and thereafter conducting a treatment. The particle size of the cluster is 10 nm or less and the cluster comprises almost only of gold atoms. | ||||||
| 56 | Process for producing a substituted benzene and benzenesulfonic acid and its derivatives, and n, n'method for producing a substituted urea | JP22525993 | 1993-08-18 | JP3629591B2 | 2005-03-16 | ザイフェルト ゴットフリート; シュタイナー ハインツ; バウマイスター ペーター |
| 57 | Diazo compound | JP13549399 | 1999-05-17 | JP2000327648A | 2000-11-28 | KUNIDA KAZUTO |
| PROBLEM TO BE SOLVED: To obtain a new compound useful as a material for a positive type lithography for a heat mode recording having excellent sensitivity, an increased demand by a remarkable development of infrared laser. SOLUTION: This compound is shown by formula I [Z is an organic group of the formula SO2R1 or SO2R2 (R1 is a hydrocarbon; R2 is a hydrocarbon containing an electron attractive substituent group such as a halogen or the like) having <=14 pKa of dissociative H of Ph-NH-Z; Q1 and Q2 are each an organic group and may be bonded to form an aliphatic ring or an aromatic ring]. A method through the diazotization of a corresponding amine such as a formula II may be cited as its synthetic method. An infrared laser is useful as a recording light source in the direct make-up of printing plate. The high sensitivity of image recording material to such light source is required. | ||||||
| 58 | Polycyclic cyclopentane-2-diazo-1,3-dione the deep ultraviolet photoresist compositions containing | JP17256090 | 1990-06-29 | JP2986858B2 | 1999-12-06 | CHENJU U; AN EMU MUURINGU; JEEMUZU TEII YAADORII |
| 59 | 5-α- reductase useful diazo to inhibition - Fenansurenon compound | JP52710295 | 1995-04-13 | JPH09512017A | 1997-12-02 | アベル，アンドリュー・デイビッド; ホルト，デニス・アラン |
| (57)【要約】 本発明は、ジアゾ−フェナンスレノン化合物、これらの化合物を含有する医薬組成物、および５−α−レダクターゼを阻害するためのこれらの化合物の使用方法を提供する。 また、本発明はこれらの化合物の製造方法、およびこれらの化合物の使用方法を提供する。 | ||||||
| 60 | Methine dye | JP8147696 | 1996-04-03 | JPH08283591A | 1996-10-29 | ANDOREASU YOHAN SHIYUMITSUTO; RIYUUDEIGAA ZENSU |
| PROBLEM TO BE SOLVED: To improve heat stability, light fastness, tinting strength, and brightness in thermal transfer by using a specific methine dye. SOLUTION: A methine dye for use in thermal transfer, represented by the formula [wherein K represents a five- or six-membered carbocyclic or heterocyclic group; X represents N or C-Q 1; Q 1 to Q 3 represent H, a 1-6C alkyl, benzyl, a 3-8C cycloalkyl, (substd.) phenyl, a 1-4C fluoroalkyl, a 1-6C alkoxy, benzyloxy, (substd.) phenoxy, a 1-6C alkylthio, a halogen, cyanom formylamino, R 3, -CO-OR 1, -CO-NHR 1, -CP-NH-CO-R 1, -CO-NH-CO-R 4, -CO-NH-SO 2R 4, -NH-CO-R 1, -NH-CO- OR 1, -NH-CO-NR 1R 2, -NH-CS-OR 1, -NH-CS-NR 1R 2, -NH-CO-R 4, -NH-SO 2-R 1, -NH-SO 2-R 4, or -NH-SO 2-NR 1R 2; R 1 and R 2 represents a 1-13C alkyl, a 3-8C cycloalkyl, or (substd.) phenyl; and R 3 and R 4 represent a five- or six-membered heterocyclic group]. COPYRIGHT: (C)1996,JPO | ||||||
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