子分类：
- C08G73/0605： ..{含未与其它环稠合的五元环的缩聚物,氮原子作为唯一的杂环原子}
- C08G73/0622： ..{含未与其它环稠合的六元环的缩聚物,氮原子作为唯一的杂环原子}
- C08G73/0666： ..{含与其它环稠合的五元环的缩聚物,氮原子作为唯一的杂环原子}
- C08G73/0683： ..{含与其它环稠合的六元环的缩聚物,氮原子作为唯一的杂环原子}
- C08G73/08： ..聚酰肼;聚三唑;聚氨基三唑;聚噁二唑
- C08G73/10： ..聚酰亚胺;聚酯-酰亚胺;聚酰胺-酰亚胺;聚酰胺酸或类似的聚酰亚胺的母体
- C08G73/18： ..聚苯并咪唑
- C08G73/20： ..吡酮类
- C08G73/22： ..聚苯并噁唑
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 141 | CARBAZOLE COMPOUNDS AND USE OF SUCH COMPOUNDS IN ORGANIC ELECTROLUMINESCENT DEVICES | PCT/IB2004050049 | 2004-01-23 | WO2004072205A3 | 2004-09-16 | BRUNNER KLEMENS; DE KOK-VAN BREEMEN MARGARETHA; LANGEVELD BEA M W; KIGGEN NICOLE M M; BASTIAANSEN JOLANDA J A M; HOFSTRAAT JOHANNES W; BOERNER HERBERT F; SCHOO HERMANNUS F M |
| A carbazole compound, polymeric or of low molecular weight, comprises a carbazole multimer unit of formula (I), wherein each carbazole unit may be unsubstituted or substituted with one or more substituents and n is larger than or equal to 2 for use in organic electroluminescent devices. The carbazole compounds provide facile hole-injection from a hole-injecting electrode and have a relatively triplet level enabling highly efficient electroluminescent devices to be obtained if combined with triplet emitter compounds. | ||||||
| 142 | BIODEGRADABLE POLY(BETA-AMINO ESTERS) AND USES THEREOF | PCT/US0131270 | 2001-10-05 | WO0231025A9 | 2003-05-30 | LANGER ROBERT S; LYNN DAVID M; PUTNAM DAVID; AMIJI MANSOOR M; ANDERSON DANIEL G |
| Poly( beta amino esters)prepared from the conjugate addition of bis(secondary amines) or primary amines to a bis (acylate ester) are described. Methods of preparing these polymers from commercially available starting materials are also provided. These tertiary amine-containing polymers are preferably biodegradable and biocompatible and may be used in a variety of drug delivery systems. Given the poly(amine) nature of these polymers, they are particularly suited for the delivery of polynucleotides. Nanoparticles containing polymer/polynucleotide complexes have been prepared. The inventive polymers may also be used to encapsulate other agents to be delivered. They are particularly useful in delivering labile agents given their ability to buffer the pH of their surroundings. | ||||||
| 143 | REDUCED BYPRODUCT HIGH SOLIDS POLYAMINE-EPIHALOHYDRIN COMPOSITIONS | PCT/US0147033 | 2001-12-07 | WO0250163A3 | 2003-01-03 | RIEHLE RICHARD J; BUSINK RONALD; BERRI MASSIMO; STEVELS WIM |
| Processes for rendering a polyamine-epihalohydrin resin storage stable, including processes that prepare a storage stable resin and/or processes that treat resins. A composition containing a polyamine-epihalohydrin resin with a solids content of at least 15 wt% treated with at least one enzymatic agent under conditions to at least one of inhibit, reduce and remove the CPD-forming species. A paper product containing the storage stable polyamine-epihalohydrin resin, when corrected for adding at about a 1 wt% addition level of the resin, contains less than about 250 ppb of CPD. | ||||||
| 144 | PHTHALONITRILE PREPOLYMER INTERMEDIATE | PCT/US2014058229 | 2014-09-30 | WO2015076934A3 | 2015-08-06 | KELLER TEDDY M; LASKOSKI MATTHEW |
| A compound having: one or more of the below repeat units, one or more terminating Ar-NH- groups bound to carbon radicals, and one or more terminating -H groups bound to nitrogen radicals. Each R is an organic group and each Ar is an aromatic group. The compound is not a thermoset. A method of: mixing an aromatic amine having the formula Ar-NH2 with a phthalonitrile compound, heating the mixture to form the compound described above (Eq. 1), and cooling the mixture before the onset of gelation. | ||||||
| 145 | MAIN-CHAIN BENZOXAZINE OLIGOMER COMPOSITIONS, AND METHOD FOR THE PREPARATION THEREOF | PCT/US2011028883 | 2011-03-17 | WO2011116232A1 | 2011-09-22 | ISHIDA HATSUO; AGAG TAREK |
| Disclosed are benzoxazine compositions where oxazine rings are part of the polymer main-chain. The benzoxazine oligomers are prepared by the reaction of a bisphenol and an aldehyde, such as formaldehyde or paraformaldehyde, with one or more diamines or polyamines, and optionally with one or more monofunctional amines or monofunctional phenols. Also disclosed are benzoxazine monomers prepared from a bisphenol, an aldehyde, such as formaldehyde or paraformaldehyde, and a monofunctional amine, which benzoxazine monomers may be optionally used as reactive diluents. Further disclosed are benzoxazine monomers are prepared from a diamine, and aldehyde, such as formaldehyde or paraformaldehyde, and a monofunctional phenol, which benzoxazine monomers may also be optionally used as reactive diluents. | ||||||
| 146 | VECTOR DIRECTIONAL POLYMER SYSTEMS AND METHODS OF NANO-STRUCTURAL SELF ASSEMBLY | PCT/US2006039262 | 2006-10-06 | WO2007044587A3 | 2007-07-12 | FOWKES STEVEN W |
| Vector-directional polymers and polymer systems are disclosed. In accordance with the embodiments of the invention, the polymer has aromatic moieties that are restrained or fixed through conformational linkage units bonding nearest neighbor aromatic moieties together to form the polymer backbone. The conformational linkage units preferably include conformational ring structures which exhibit hydrogen bonding or other Lewis acid-Lewis base type of interactions. The conformational ring structures can include hetero-atoms and cationic metal atoms. The chemical groups and bonding features of the polymer backbone constrain bond movement and bond rotation along the polymer backbone. Accordingly, the vector-directional polymers of the present invention can assemble into or form extended three dimensional structures or arrays. | ||||||
| 147 | SYNTHETIC BINDING PAIRS COMPRISING CUCURBITURIL DERIVATIVES AND POLYAMMONIUM COMPOUDS AND USES THEREOF | PCT/IL2004000796 | 2004-09-05 | WO2005023816A3 | 2005-07-14 | KEINAN EHUD |
| Derivatized cucurbiturils can be efficiently prepared and utilized for forming cucurbituril assemblies. These cucurbituril assemblies, in turn, can form affinity binding pairs with polyamines structures that are designed capable of binding to these assemblies. The resulting affinity pairs are, highly advantageous over the presently known affinity pairs and therefore can be efficiently utilized in a myriad of application. Thus, according to one aspect of the present invention there is provided a cucurbituril comprising at least one functional group covalently attached thereto, whereby the at least one functional group being for forming an assembly of at least two cucurbiturils. According to further features in preferred embodiments of the invention described below, the cucurbituril is selected from thé group consisting of CB[5], CB[6], CB[7], CB[8] and CB[n], wherein n is an integer that equals to or is lower' than 20. Preferably the cucurbituril is selected from the group consisting of CB[5J, CB[6], CB[7] and CB[8]. According to still further features in the described preferred embodiments the assembly is, selected from 'the group consisting of a dimer, a trimer, a polymer, an oligómer, a dendrimer and a cluster of the cucurbituril. | ||||||
| 148 | BIODEGRADABLE POLY(BETA-AMINO ESTERS) AND USES THEREOF | PCT/US2004016521 | 2004-05-26 | WO2004106411A3 | 2005-01-20 | LANGER ROBERT; LYNN DAVID M; ANDERSON DANIEL G; AKINC AKIN |
| Poly(beta-amino esters) prepared from the conjugate addition of bis(secondary amines) or primary amines to a bis(acrylate ester) are described. Methods of preparing these polymers from commercially available starting materials are also provided. These tertiary amine-containing polymers are preferably biodegradable and biocompatible and may be used in a variety of drug delivery systems. Given the poly(amine) nature of these polymers, they are particularly suited for the delivery of polynucleotides. Nanoparticles containing polymer/polynucleotide complexes have been prepared. The inventive polymers may also be used to encapsulate other agents to be delivered. They are particularly useful in delivering labile agents given their ability to buffer the pH of their surroundings. A system for preparing and screening polymers in parallel using semi-automated robotic fluid delivery systems is also provided. | ||||||
| 149 | ORGANIC ELECTROLUMINESCENT COMPONENT WITH TRIPLET EMITTER COMPLEX | PCT/IB0305744 | 2003-12-05 | WO2004055921A2 | 2004-07-01 | BOERNER HERBERT FRIEDRICH |
| An organic electroluminescent component having a layer composite, which comprisesa) a substrate layerb) a first transparent electrode layer,c) a mixing layer havingc.1) a matrix of a conductive organic material with one or more singlet states and one or more triplet states, selected from the group: p-conductive and n-conductive materials,c.2) in this matrix, a light-emitting material which contains a metallo-organic complex compound with an emissive triplet state, andd) a second electrode,the lowest-energy triplet state of the conductive organic material being higher than the emissive triplet state of the metallo-organic complex compound by an energy difference Et. | ||||||
| 150 | CASCADE POLYMERS WITH IODINE AROMATIC COMPOUNDS | PCT/EP9404245 | 1994-12-21 | WO9517448A3 | 1995-07-27 | KRAUSE WERNER; MAIER FRANZ-KARL; BAUER MICHAEL; SCHUHMANN-GIAMPIERI GABRIELE; PRESS WOLF-RUEDIGER |
| Iodine-containing dendrimeric polymers of general formula IA-(X)b(I),in which A stands for a nitrogen-containing nucleus of basic multiplicity b, and b stands for the numbers 1 to 8 and X stands for a radical composed of |
||||||
| 151 | AMINO-POLYESTERS FOR DRUG DELIVERY | US16179714 | 2018-11-02 | US20190194390A1 | 2019-06-27 | Umberto Capasso Palmiero; Piotr S. Kowalski; Davide Moscatelli; Daniel Griffith Anderson |
| Disclosed are methods, compositions, reagents, systems, and kits to prepare and utilize amino-polyesters (APEs). The APEs are shown to be effective biodegradable carriers for drug delivery applications. | ||||||
| 152 | POLYMERIZABLE COMPOSITION | US15779991 | 2016-12-02 | US20180346646A1 | 2018-12-06 | Sang Woo Kim; Seung Hee Lee; Ki Ho Ahn |
| The present application relates to a polymerizable composition, a prepolymer, a phthalonitrile resin, a composite, a process for preparing the same, and a use thereof. The present application can provide a polymerizable composition comprising a curing agent which has excellent heat resistance and does not cause defects such as voids that may adversely affect physical properties. In addition, the present application allows for the polymerizable composition to exhibit appropriate curing properties, processing temperatures and process windows and to be capable of forming a composite of excellent physical properties. The present application can provide a resin having both advantages of a phthalonitrile resin and a polyimide by curing a phthalonitrile compound as a raw material monomer with a curing agent having a polyimide structure. | ||||||
| 153 | POLYMER CONTAINING TRIAZINE RING AND COMPOSITION CONTAINING SAME | US15503330 | 2015-08-12 | US20180215870A1 | 2018-08-02 | Naoya NISHIMURA; Takahiro KASEYAMA; Kei YASUI; Daisuke MAEDA |
| It is possible to obtain a thin film that can form a minute pattern and that has a high index of refraction by using a polymer containing a triazine ring and containing a repeating unit structure represented for example by formula (22) or (26). | ||||||
| 154 | RESIN COMPOSITION, PREPREG, METAL FOIL-CLAD LAMINATE, AND PRINTED CIRCUIT BOARD | US15737490 | 2016-07-04 | US20180186933A1 | 2018-07-05 | Naoki KASHIMA; Katsuya TOMIZAWA; Meguru ITO; Tomoki HAMAJIMA; Eisuke SHIGA; Kentaro TAKANO; Shota KOGA |
| The present invention provides a resin composition containing an allyl group-containing compound (A) and a maleimide compound (B), in which the allyl group-containing compound (A) has a reactive functional group other than an allyl group. | ||||||
| 155 | CYANATE ESTER COMPOUND, CURABLE RESIN COMPOSITION CONTAINING THE COMPOUND, AND HARDENED PRODUCT THEREOF | US15560708 | 2016-02-19 | US20180105488A1 | 2018-04-19 | Masayuki KATAGIRI; Tatsuya SHIMA; Keita TOKUZUMI |
| The present invention provides a novel cyanate ester compound which has excellent solvent solubility and from which a hardened product having a low coefficiency of thermal expansion and excellent flame retardancy and heat resistance is obtained. The present invention is a cyanate ester compound obtained by cyanating a naphthol-dihydroxynaphthalene aralkyl resin or a dihydroxynaphthalene aralkyl resin. | ||||||
| 156 | MATERIAL FOR FORMING UNDERLAYER FILM FOR LITHOGRAPHY, COMPOSITION FOR FORMING UNDERLAYER FILM FOR LITHOGRAPHY, UNDERLAYER FILM FOR LITHOGRAPHY AND PATTERN FORMING METHOD | US15565064 | 2016-04-07 | US20180101097A1 | 2018-04-12 | Kana OKADA; Takashi MAKINOSHIMA; Masatoshi ECHIGO; Go HIGASHIHARA; Atsushi OKOSHI |
| A material for forming an underlayer film for lithography, including a cyanic acid ester compound obtained by cyanation of a modified xylene formaldehyde resin, a composition including the material, and a pattern forming method using the composition. | ||||||
| 157 | POLYMER AND ORGANIC LIGHT-EMITTING DEVICE | US15100106 | 2014-11-28 | US20170309837A1 | 2017-10-26 | Florence Bourcet; Annette Steudel; Richard J Wilson |
| A composition comprising a phosphorescent compound of formula (I) and a polymer comprising a repeat unit of formula (II) Ar1 is an aryl or heteroaryl group. R2 is a substituent. A is independently in each occurrence N or CR3 wherein R3 is H or a substituent. M is a transition metal or metal ion. x is a positive integer of at least 1. y is 0 or a positive integer. L1 is a mono- or polydentate ligand. R1 is a substituent. z is 0 or a positive integer. X is O or S. The phosphorescent compound of formula (I) may be mixed with the polymer or may be covalently bound thereto. The composition may be used in the light-emitting layer of an organic light-emitting device. | ||||||
| 158 | Polymeric benzoxazine resin structure with adamantane-containing main chain | US15207521 | 2016-07-12 | US09631053B1 | 2017-04-25 | Wen-Chiung Su; Ching-Hsuan Lin; Han-Ya Lin; Zi-Jun Chen |
| A polymeric benzoxazine resin structure with an adamantane-containing main chain produces materials of low dielectric characteristics when cured. | ||||||
| 159 | Thermosetting resin composition | US14778164 | 2014-03-18 | US09567435B2 | 2017-02-14 | Mamoru Tamura; Takuya Ohashi; Tomoyuki Enomoto |
| There is provided novel thermosetting resin composition. A thermosetting resin composition comprising a polymer having at least one structural unit of the following Formula (1): {wherein each of R1 and R2 is independently a hydrogen atom or a C1-4 alkyl group, X is a single bond or a divalent organic group, and Y is an arylene group of the following Formula (2): (wherein Z1 is a carbonyl group or a —CONH— group, Z2 is a C1-5 alkylene group or a 5- or 6-membered divalent saturated heterocyclic group containing at least one nitrogen atom, and Z3 is a 5- or 6-membered aromatic heterocyclic group containing two nitrogen atoms in which at least one of hydrogen atoms may be substituted by a C1-5 alkyl group)}. | ||||||
| 160 | Oxazolidone ring containing adducts | US14538281 | 2014-11-11 | US09481757B2 | 2016-11-01 | Joseph Gan; Emile C. Trottier |
| Embodiments include oxazolidone ring containing adducts obtainable by combining an aliphatic epoxy compound, an aromatic epoxy compound, and a diisocyanate. Embodiments further include a curable powder coating composition including a resin component and a hardener component, where the resin component includes the oxazolidone ring containing adduct. | ||||||
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