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19 条记录 (耗时 0.018 秒)

    Process for the manufacture of in situ polymer alloys and microcompounds, and use thereof
    6.
    发明授权
    Process for the manufacture of in situ polymer alloys and microcompounds, and use thereof 失效
    原位聚合物合金和微型化合物的制造方法及其用途

    公开(公告)号：US5312875A

    公开(公告)日：1994-05-17

    申请号：US109711

    申请日：1993-08-20

    申请人： Rolf Mulhaupt ,  Joachim Rosch ,  Siegfried Hopperdietzel ,  Ekkehard Weinberg ,  Herbert Klein

    发明人： Rolf Mulhaupt ,  Joachim Rosch ,  Siegfried Hopperdietzel ,  Ekkehard Weinberg ,  Herbert Klein

    IPC分类号： C08G69/14 ,  C08G69/04 ,  C08L23/02 ,  C08L23/26 ,  C08L77/00 ,  C08L77/02 ,  C08L101/00 ,  C09D177/00 ,  C09D177/02 ,  C09J123/26 ,  C09J177/00 ,  C09J177/02 ,  D01F6/46 ,  C08L77/10

    CPC分类号： C08L77/02 ,  C08L101/00 ,  C08L23/02

    摘要： A polymer mixture reinforced by an in situ, melt-polymerized microphase whereby the rigidity of the base material is increased, a process for manufacturing same, and use thereof for providing reinforced compositions and articles in which the polymer mixture is prepared by polymerizing a component B in a melt of a component A composed of at least one thermoplastic polymer. Component B is composed of at least one compound having the structure ##STR1## The reaction of component B in a melt of component A results in linear, branched or cross-linked, high or low molecular weight polymers constituting a microphase. Preferably, the microphases have the form of microfibers. In the structure of component B, X is NH.sub.2, NHR.sup.3, OH or an N-substituted, Y-activated lactam of the ##STR2## type which is activated with an electrophilic substituent Y, where Y is CO, SO.sub.2, or R.sup.5 P=O; R.sup.1, R.sup.2 and R.sup.4 are bivalent or multivalent aliphatic-, aromatic-, heterocyclic- or heteroatom-containing segments, with R.sup.2 and R.sup.4 preferably being bivalent aliphatic or aromatic radicals (CH.sub.2).sub.z in which 1

    摘要翻译： 通过原位，熔融聚合的微相增强的聚合物混合物，由此增加基材的刚性，其制备方法及其用于提供增强组合物和制品的用途，其中通过聚合组分B制备聚合物混合物 在由至少一种热塑性聚合物组成的组分A的熔体中。 组分B由至少一种具有结构的化合物组成。组分B在组分A的熔体中的反应产生构成微相的直链，支链或交联的高分子量或低分子量聚合物。 优选地，微细管具有微纤维的形式。 在组分B的结构中，X是NH 2，NHR 3，OH或N-取代的Y活化的具有亲电取代基Y活化的Y型活化的内酰胺，其中Y是CO，SO2或R5P = O ; R 1，R 2和R 4是二价或多价的脂族 - ，芳族 - ，杂环或含杂原子的链段，其中R 2和R 4优选是二价脂族或芳族基团（CH 2）z，其中1

    Synthesis of Polynaphthalenes and Their Use
    7.
    发明申请
    Synthesis of Polynaphthalenes and Their Use 审中-公开
    聚萘的合成及其用途

    公开(公告)号：US20070287821A1

    公开(公告)日：2007-12-13

    申请号：US11574546

    申请日：2005-09-05

    申请人： Florian Doetz ,  Simon Nord ,  Horst Weiss ,  Joachim Rosch

    发明人： Florian Doetz ,  Simon Nord ,  Horst Weiss ,  Joachim Rosch

    IPC分类号： C08G61/10 ,  H01B1/12

    CPC分类号： H01B1/128 ,  C08G61/02 ,  C08G61/10

    摘要： The present invention relates to a process for preparing polynaphthalene derivatives comprising repeating units of the general formula Ia and/or Ib where R1, R2, R1′, R2′ are as defined in the description. The present invention further relates to polynaphthalene derivatives which can be prepared by the process of the invention, films comprising or consisting of at least one polynaphthalene derivative according to the invention, organic light-emitting diodes (OLEDs) comprising at least one polynaphthalene derivative according to the invention, a light-emitting layer comprising or consisting of at least one polynaphthalene derivative according to the invention, an OLED comprising the light-emitting layer of the invention, devices comprising an OLED according to the invention and the use of the polynaphthalene derivatives of the invention as emitter substances in OLEDs.

    摘要翻译： 本发明涉及一种制备聚萘衍生物的方法，其包含通式Ia和/或Ib的重复单元，其中R 1，R 2，R 1， ，R“2”如说明书中所定义。 本发明还涉及可以通过本发明的方法制备的聚萘衍生物，包含或由至少一种根据本发明的聚萘衍生物的膜组成的有机发光二极管（OLED）包含至少一种根据本发明的聚萘衍生物 本发明包括由至少一种根据本发明的聚萘衍生物或由本发明的至少一种聚萘衍生物构成的发光层，包含本发明的发光层的OLED，包含根据本发明的OLED的器件和使用 本发明作为OLED中的发射物质。

    Synthesis of phenyl-substituted fluoranthenes by a diesel-alder reaction and the use thereof
    8.
    发明申请
    Synthesis of phenyl-substituted fluoranthenes by a diesel-alder reaction and the use thereof 有权
    苯基取代的荧蒽通过狄尔斯 - 阿尔德反应合成及其应用

    公开(公告)号：US20070069198A1

    公开(公告)日：2007-03-29

    申请号：US10573803

    申请日：2004-09-28

    申请人： Florian Dotz ,  Reinhold Schwalm ,  Joachim Rosch

    发明人： Florian Dotz ,  Reinhold Schwalm ,  Joachim Rosch

    IPC分类号： H01L51/00 ,  C07C69/52 ,  C07D213/84

    CPC分类号： C07C13/66 ,  C07C2/867 ,  C07C2603/48 ,  C09K11/06 ,  C09K2211/1011 ,  H01L51/0054 ,  H01L51/0058 ,  H01L51/5012 ,  H05B33/14 ,  Y10S428/917

    摘要： Fluoranthene derivatives of the general formula I where the symbols have the following meanings: R1, R2, R3, R4, R5 are each hydrogen, alkyl, an aromatic radical, a fused aromatic ring system, a heteroaromatic radical or —CH═CH2, (E)- or (Z)-CH═CH—C6H5, acryloyl, methacryloyl, methylstyryl, —O—CH═CH2 or glycidyl; where at least one of the radicals R1, R2 and/or R3 is not hydrogen; X is an alkyl radical, an aromatic radical, a fused aromatic ring system, a heteroaromatic radical or a radical of the formula (I′) or an oligophenyl group; n is from 1 to 10 or, in the case of X=oligophenyl group, 1-20; with the proviso that R1, R2, R3 and X are not at the same time phenyl when R4 and R5 are hydrogen. Furthermore, the invention relates to a process for preparing them and the use of fluoranthene derivatives as emitter molecule in organic light-emitting diodes (OLEDs), a light-emitting layer comprising the fluoranthene derivatives of the invention as emitter molecules, an OLED comprising the light-emitting layer of the invention and devices comprising the OLED of the invention.

    摘要翻译： 其中符号具有以下含义的通式I的荧蒽衍生物：R 1，R 2，R 3，R 4， R 5各自为氢，烷基，芳族基，稠合芳环系，杂芳族基或-CH-CH 2，（E） - 或（Z）-CH-CH-C 6 H 5，丙烯酰基，甲基丙烯酰基，甲基苯乙烯基，-O-CH-CH 2或 缩水甘油基 其中基团R 1，R 2和/或R 3中的至少一个不是氢; X是烷基，芳族基团，稠合芳族环系统，杂芳族基团或式（I'）的基团或低级苯基; n为1至10，或在X =低聚苯基的情况下为1-20; 条件是R 4，R 2，R 3和X不在同时为R 4时的苯基， SUP>和R 5是氢。 此外，本发明涉及其制备方法以及在有机发光二极管（OLED）中使用荧蒽衍生物作为发射体分子的方法，包含本发明的荧蒽衍生物作为发射体分子的发光层，包含 本发明的发光层和包含本发明的OLED的器件。

    Highly flowable propylene block copolymers
    10.
    发明申请
    Highly flowable propylene block copolymers 有权
    高流动性丙烯嵌段共聚物

    公开(公告)号：US20050038208A1

    公开(公告)日：2005-02-17

    申请号：US10296256

    申请日：2001-05-23

    申请人： Ulrich Dahn ,  Wolfgang Bidell ,  Hans-Jurgen Zimmermann ,  Roland Hingmann ,  Joachim Rosch ,  Gunther Schweier ,  Jurgen Oelze

    发明人： Ulrich Dahn ,  Wolfgang Bidell ,  Hans-Jurgen Zimmermann ,  Roland Hingmann ,  Joachim Rosch ,  Gunther Schweier ,  Jurgen Oelze

    IPC分类号： C08J5/00 ,  C08F2/00 ,  C08F4/642 ,  C08F10/06 ,  C08F110/06 ,  C08F210/06 ,  C08F297/08 ,  C08L53/00 ,  D01F6/30

    CPC分类号： C08F297/08 ,  C08F10/06 ,  C08F110/06 ,  C08F210/06 ,  C08L53/00 ,  C08F2/001 ,  C08F2/34 ,  C08L2666/02 ,  C08F2500/12 ,  C08F2500/17 ,  C08F210/16

    摘要： The invention relates to highly flowable propylene block copolymers that comprise 50 to 80 wt.-% of a propylene homopolymer and 10 to 70 wt.-% of a propylene copolymer having 5 to 50 wt.-% of a C2-C8 alk-1-ene polymerized into it that is different from propylene, and that are obtainable from the gaseous phase by a two-step polymerization by means of a Ziegler-Natta catalyst system. In a first polymerization step, the propylene is polymerized at a pressure of 10 to 50 bar, a temperature of 50 to 100° C. and an average dwelling time of the reaction mixture of 0.3 to 5 hours in the presence of at least 2.0% by volume, based on the total volume, of hydrogen. The propylene homopolymer obtained in said first polymerization step is transferred together with the Ziegler-Natta catalyst system into an intermediate container, expanded for 0.01 to 5 minutes to less than 5 bar and maintained at a temperature of 10 to 80° C. The pressure in the intermediate container is then increased by 5 to 60 bar by introducing under pressure a gaseous mixture, and the propylene homopolymer is then transferred to a second polymerization step together with the Ziegler-Natta catalyst system. In said second polymerization step, a mixture from propylene and a C2-C8 alkylene is polymerized into the propylene homopolymer at a pressure of 10 to 50 bar, a temperature of 50 to 100° C. and an average dwelling time of 0.5 to 5 hours. The weight ratio between the monomers reacted in the first and those reacted in the second polymerization step are adjusted to be in the range of from 4:1 to 1:1.

    摘要翻译： 本发明涉及高流动性丙烯嵌段共聚物，其包含50至80重量％的丙烯均聚物和10至70重量％的丙烯共聚物，其具有5至50重量％的C 2 -C 8烷基-1 其与丙烯不同，并且可通过采用齐格勒 - 纳塔催化剂体系的两步聚合由气相获得。 在第一聚合步骤中，丙烯在10至50巴的压力，50至100℃的温度和在至少2.0％的存在下反应混合物的平均停留时间为0.3至5小时的聚合反应， ，基于总体积的氢气。 将所述第一聚合步骤中获得的丙烯均聚物与齐格勒 - 纳塔催化剂体系一起转移到中间容器中，膨胀0.01至5分钟至小于5巴，并保持在10至80℃的温度。 然后通过在压力下引入气体混合物将中间容器增加5至60巴，然后将丙烯均聚物与齐格勒 - 纳塔催化剂体系一起转移到第二聚合步骤。 在所述第二聚合步骤中，将丙烯和C 2 -C 8亚烷基的混合物在10至50巴的压力，50至100℃的温度和0.5至5小时的平均停留时间内聚合成丙烯均聚物 。 在第一聚合步骤中反应的单体和在第二聚合步骤中反应的单体之间的重量比被调节至4:1至1:1的范围内。