| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 101 | ニトロフェニルボロン酸組成物によって安定化したナノ粒子 | JP2015560153 | 2013-03-01 | JP2016517393A | 2016-06-16 | マーク イー． デイヴィス; ハン ハン |
| ボロン酸含有ポリマーにカップリングしたポリオール含有ポリマーを含むナノ粒子が本明細書中で記載され、このナノ粒子は、ボロン酸含有ポリマーがこのナノ粒子の外部の環境に提示されるように構成される。記載のナノ粒子の標的化バージョンもまた、関連の組成物、方法およびシステムと共に記載される。【選択図】図16 | ||||||
| 102 | The multi-arm polymer alkanoate conjugates | JP2011522993 | 2009-08-11 | JP5588983B2 | 2014-09-10 | アントニ コズロウスキー，; サムエル ピー． マクマヌス，; ジェニファー リッグス−ソーシアー，; シャオミン シェン，; ウェン チャン， |
| Among other aspects, provided herein are multi-armed polymer conjugates comprising an alkanoate-linker, compositions comprising such conjugates, and related methods of making and administering the same. Methods of treatment employing such conjugates and related uses are also provided. The conjugates are prepared with high drug loading efficiencies. | ||||||
| 103 | Ferroelectric polymer | JP2009131382 | 2009-05-29 | JP2010016360A | 2010-01-21 | ISHIDA TAKEHISA; BHANGALE SUNIL MADHUKAR; HAN HONG; CHAI LI LIN CHRISTINA |
| PROBLEM TO BE SOLVED: To provide a ferroelectric film that can be manufactured by a simple method and also has satisfactorily residual magnetism, and to provide a method of manufacturing the ferroelectric film. SOLUTION: The ferroelectric film includes polyaminodifluoroborane (PADFB) as ferroelectric. Furthermore, the ferroelectric film is a ferroelectric polymer film mixed with the PADFB, and the ferroelectric polymer is selected from a group of polyvinylidenefluoride (PVDF), a copolymer of polyvinylidenefluoride and trifluoroethylene (P(VDF/TrFE)), and polyundecaneamide (Nylon 11). Also, a storage using the ferroelectric film, a method of manufacturing a ferroelectric polymer, and a ferroelectric solution are provided. COPYRIGHT: (C)2010,JPO&INPIT | ||||||
| 104 | Organic electroluminescence device | JP2008509318 | 2006-04-06 | JP2008541417A | 2008-11-20 | ストエッセル、フィリップ; ハイル、ホルガー; パルハム、アミル; ブエシンク、アルネ; フェストベーバー、ホルスト; ブロイニンク、エステル |
| 本発明は、有機電子デバイス、特にエレクトロルミネセンス素子における、芳香族ボロン酸若しくはボリン酸誘導体応用に関する。 | ||||||
| 105 | Perarylated borane non-conjugated polymers, their use as an organic semiconductor light-emitting material and / or transport material, its preparation and use thereof | JP2006505399 | 2004-05-07 | JP2006525395A | 2006-11-09 | カニッツ アンドレアス; ログラー ヴォルフガング; ヴェールレ ヤスミーン |
| 本発明は、半導体特性を有する非共役の発光体化合物並びにその製造及び有機発光ダイオード（ＯＬＥＤＳ）、有機太陽電池、有機受光器及び有機電界効果トランジスタ中での使用に関する。 これは、タイプＫのコポリアリールボランであり、これは最初に適当な電場の印加により及び／又はアリール置換基Ｒのドナー置換により、記号について請求項１記載の意味を有する共役ポリマーと同様に挙動する構造タイプに移行する。 | ||||||
| 106 | Aryl boronate functionalized polymer for the treatment of obesity | JP2003508952 | 2002-07-01 | JP2004534887A | 2004-11-18 | ダール，プラディープ，ケイ．; フーバル，チャド，コリ; ホームズ−ファーレイ，スティーブン，ランダル; ポロモスキャニック，スティーブン，シー．; サード マンデヴィル，ハリー，ダブリュ．，ザ; リー，シンフア |
| 構造式（I）：により表されるフェニルボロン酸化合物が開示される。 Arは置換または非置換のアリール基である。 ＺおよびZ'は独立して、-O-、-NH-または-S-である。 Ｘは電子吸引基である。 Ｒは、１つ以上のアミン、アンモニウム、エステル、チオエーテルまたはフェニレン結合基を任意に含む置換または非置換の直鎖ヒドロカルビル基であり、Ｙは-H、アミン、-[NH-(NH 2 ) q ]-NH 2 、ハロゲン、-CF 3 、チオール、アンモニウム、アルコール、-COOH、-SO 3 H、-OSO 3 HまたはＲの末端位に共有結合したホスホニウム基である。 -[NH-(NH 2 ) q ]-NH 2の各-NH-は任意にN-アルキル化またはN,N-ジアルキル化されており、-[NH-(NH 2 ) q ]-NH 2の-NH 2は、任意に、N-アルキル化、N,N-ジアルキル化またはN,N,N-トリアルキル化されている。 ｑは２〜約10の整数であり、ｒは１〜約５の整数である。 R 1およびR 1 'は、独立して、-H、脂肪族基、置換脂肪族基、アリール基または置換アリール基、または一緒になって、アミン結合基-[N + (R 1a )-]を任意に含むNH 2 C2-C5置換または非置換のアルキレン基である。 構造式（I）の各R 1は、好ましくは、-Hである。 R 1aは-H、アルキル、置換アルキル、フェニルまたは置換フェニルである。 構造式（I）により表される化合物ならびに該化合物および薬学的に許容されうる担体または希釈剤を含む医薬組成物の有効量を投与することにより被験体の肥満症を処置する方法もまた開示される。 | ||||||
| 107 | For a lithium battery conductive polymer composition | JP2002510578 | 2001-06-16 | JP2004511879A | 2004-04-15 | アンゲル， チャールズ エイ．; スー， ウー |
| 弱塩基性のアニオン部分を含む新しい鎖ポリマーは、制御可能にアニオン分離において、ポリエーテルのバックボーン中に化学的に結合される。 好適なポリマーは、二塩基酸残基でキャップされたオルトボラートアニオンを含む。 これらポリマーの伝導度は、大部分の従来のポリマー中の塩による電解質の伝導度に高い関連性があることが発見される。 高温における伝導度および広い電気化学的手段における伝導度は、これらの材料を再充電可能なリチウム電池用の電解質として適したものにする。 | ||||||
| 108 | Borazine condensate calcined product and a method for manufacturing | JP12266488 | 1988-05-19 | JP2572813B2 | 1997-01-16 | KIMURA YOSHIHARU |
| 109 | Synthesis and novel materials obtained from that of the iodine and nitrogen should be boron nitride Motono precursor based on a polymer | JP25895989 | 1989-10-05 | JPH0725893B2 | 1995-03-22 | ジェラール・ミニャニ; ピエール・アルドー; モーリス・シャルプネル |
| 110 | JPH0478653B2 - | JP19477187 | 1987-08-04 | JPH0478653B2 | 1992-12-11 | KOBAYASHI TAKASHI; URABE TAKASHI |
| 111 | Crosslinked polysilazane and its preparation | JP33522291 | 1991-12-18 | JPH04335033A | 1992-11-24 | PIERETSUTO PONSU; MARIIBERUNAARU BEJIERU; KURISUTEIAN KORONBIE |
| PURPOSE: To obtain the subject polysilazanes being useful as ceramic precursors by selecting specified crosslinked polysilazanes. CONSTITUTION: Crosslinked polysilazanes comprizing a plurality of patterns of formula I and wherein these patterns are bonded with at least one bridge of =AlX [wherein X is a group-NHZ (wherein Z is H, a metal or a metalloid, especially Si) or Si≡] and each of the available valencies of the Si or nitrogen atoms can bear H, a 1-6C alkyl, vinyl, allyl, cyclohexyl, an at most 18C aryl, an alkylaryl or an aralkyl, are selected. COPYRIGHT: (C)1992,JPO | ||||||
| 112 | Crosslinking of polymer based on boron and nitrogen for especially producing ceramic fiber | JP11215891 | 1991-04-18 | JPH04227637A | 1992-08-17 | PIEERU ARUDOO; JIYATSUKU DESUREIOO; JIERAARU MINIYANI |
| PURPOSE: To easily obtain a polymer bringing about a ceramic material in a high weight yield especially after pyrolysis based on boron, nitrogen and, voluntarily, silicon and sufficiently stable against hydrolysis. CONSTITUTION: A polymer (A) based on boron and nitrogen containing at least one unit selected from formulae = N-SiR 1 3 (1) and -NH-2 (2) (wherein R 1 is a hydrocarbon group) per one molecule is brought into contact with an effective amt. of a compd. (B) selected from the compd. having at least one boron atom having at least two halogen atoms directly bonded thereto per one molecule and a compd. represented by the general formula (BX-NR) n (3) (wherein n is an integer of 3-10, R is a hydrogen atom, a hydrocarbon group or an organosilyl or hydrogenoorganosilyl group and X is a halogen atom) to be crosslinked. COPYRIGHT: (C)1992,JPO | ||||||
| 113 | Ceramic coating of carbon-containing article | JP7033291 | 1991-03-12 | JPH04219380A | 1992-08-10 | PIEERU ARUDOO; EBURIINU SHIYASANIYUU; JIERAARU MINIYANI |
| PURPOSE: To form a protective coating for preventing oxidizing denaturation at a temperature near 800°C concerning an article containing a carbon such as a graphite or carbon fiber. CONSTITUTION: The carbon-containing article is coated with a ceramic precursor mixture composed of 10 to 95 wt.% polyborazane and 90 to 5 wt.% polysilazane (a) and pyrolytic treatment is performed to this coated article in an inert or reduced atmosphere or under vacuum (b) so that this mixture can be changed into ceramic, in a ceramic coating method for carbon-containing article. COPYRIGHT: (C)1992,JPO | ||||||
| 114 | JPH0363576B2 - | JP23034683 | 1983-12-05 | JPH0363576B2 | 1991-10-01 | TAKAMIZAWA MINORU; KOBAYASHI YASUSHI; HAYASHIDA AKIRA; TAKEDA YOSHIFUMI |
| 115 | Organometallic ceramic precursor having boron, nitrogen, and silica as basis | JP20260790 | 1990-08-01 | JPH0384035A | 1991-04-09 | PASUKARU BARUTERUMI; SHIYARURU BOBISHIYON; JIYANJIYATSUKU RUBURAN |
| PURPOSE: To obtain the subject precursor controlled in physicochemical properties, and having a low silicon content during pyrolysis by reacting a mixture of trihaloborane A, silazne B, and B-trichloroborazined. CONSTITUTION: The objective preceramic polymer is obtained by reacting a mixture of (A) at least one kind of trihaloborane A corresponding to BX (X is halogen selected from Cl, Br, I, F), (B) at least one kind of disilazane corresponding to formula I (R is H, a hydrocarbon, the number of H bonded directly to Si is not more than 1), (C) B-trichloroborazine corresponding to formula II (R 1, is H, 1-6C alkyl). It is preferable that the mole ratio of the components A-C meets 0.5 < component A/C < 2.5 < component B/(A+C) < 8. COPYRIGHT: (C)1991,JPO | ||||||
| 116 | Boron-and nitrogen-based polymer, its production and its use as boron nitride precursor | JP25896089 | 1989-10-05 | JPH02155931A | 1990-06-15 | PIEERU ARUDOO; JIERAARU MINIYANI |
| PURPOSE: To provide efficiently, economically and easily a boron- and nitrogen- based polymer by reacting a respectively specified cyclic compound with a compound having a halogen atom and boron and a compound having NH 2. CONSTITUTION: A boron- and nitrogen-based polymer having repeating units of formulas II, III is provided by reacting (a) a cyclic compound comprising a repeating unit of formula I (A is a halogen atom; R is H, a hydrocarbon group, an organosilyl group or a hydrogen organosilyl group) with (b) a compound having one or more boron atoms to which two halogen atoms are directly bonded and (c) a compound containing one or more NH 2 groups. In formulas II, III, X is N-R 3; Y is N(R 1)(R 2); Z is NR; R, R 1, R 2, R 3 are H, a hydrocarbon group, an organosilyl group, a hydrogeno organosilyl group, respectively. COPYRIGHT: (C)1990,JPO | ||||||
| 117 | Synthesis of polymer based on boron and nitrogen which are precursor material of boron nitride, and novel material obtained therefrom | JP25895989 | 1989-10-05 | JPH02142833A | 1990-05-31 | PIEERU ARUDOO; MOORISU SHIYARUPUNERU; JIERAARU MINIYANI |
| PURPOSE: To obtain a polymer useful for providing a ceramic product based on BN in a satisfactory weight yield when thermally decomposed, by reacting a trihalogenoborane with a silazane compound having ≡Si-NH-Si≡ group under a specified condition. CONSTITUTION: While one or more trihalogenoboranes (e.g.: BCl 3) and one or more silazane compounds having one or more ≡Si-NH-Si≡ group (e.g.: hexamethyldisilazane) are held at a temperature between about -100 and 0°C, the silazane compounds are gradually introduced and reacted so that the ratio of the gram equivalent of ≡Si-NH-Si≡ group to mole number of trihalogenoborane is 1 or more, and the resulting reaction product is recovered. COPYRIGHT: (C)1990,JPO | ||||||
| 118 | JPH02500848A - | JP50596688 | 1988-06-17 | JPH02500848A | 1990-03-22 | |
| 119 | Organoborosilazane polymer | JP1011289 | 1989-01-20 | JPH01252638A | 1989-10-09 | RENAADO MAACHIN NIIBIRUSUKI |
| PURPOSE: To provide polymers useful as a composition for protecting materials in liable to oxidative oxidation at elevated temperatures by reacting a poly- silazane and a trialkyl-, trialkoxy- or triaryloxyboroxine on specified conditions. CONSTITUTION: An anmonolysis product provided by reacting an organodihalosilane (such as a methyldichlorosilane) with NH 3, for example, is treated by a basic catalyst (such as KH, for example), for deprotonizing an NH group adjacent to an SiH group and the resulting product is further quenched by an electrophilic quenching tester (such as dimethylchlorosilane, for example), so that the poly-silazane can be provided. This poly-silazane in 1 wt.% and 0.25-20 wt.% of C 1-6 trialkyl-, trialcoxy- or triaryloxyboroxine are reacted in an organic solvent (such as xylene). COPYRIGHT: (C)1989,JPO | ||||||
| 120 | Polymer with boron and nitrogen as base, its manufacture, ceramic material with boron nitride as base and use to manufacture | JP22489088 | 1988-09-09 | JPH01129034A | 1989-05-22 | JIERAARU MINIYANI; JIYANJIYATSUKU RUBURAN |
| PURPOSE: To manufacture the polymers of various forms by a method which gives a material with BN as a base high weight yield at the time of thermal decomposition and which can easily be executed, by reacting the mixture of trihalogenoborane and compound containing specified halogen and B with compound containing an NH 2 group. CONSTITUTION: Polymers with B and N as the base are manufactured by allowing (A) trihalogenoborane (example: trichloroborane and the like) and (B) compound [example: the compound of a formula I (A is halogen; Y is a formula II, R 1 and R 2 are each H, hydrocarbon group, olganosilyl or hydrogenoorganosilyl) having at least one B atom to which two halogen atoms are directly connected to react with (C) the compound (example: such as ammonia) containing at least one NH 2 group. With the method, the polymers where the material with BN as the base at the time of thermal decomposition are obtained with high weight yield can easily and efficiently be manufactured in the various forms (thread, fiber, moldings, sheet and the like) so that it can easily be executed. COPYRIGHT: (C)1989,JPO | ||||||
QQ群二维码
意见反馈
意见反馈