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2-(4-trifluoromethylphenyl)indene | 2729-93-3

中文名称
——
中文别名
——
英文名称
2-(4-trifluoromethylphenyl)indene
英文别名
2--inden;2-(p-Trifluormethyl-phenyl)-inden;2-[4-(trifluoromethyl)phenyl]-1H-indene
2-(4-trifluoromethylphenyl)indene化学式
CAS
2729-93-3
化学式
C16H11F3
mdl
——
分子量
260.259
InChiKey
FGDKINIWCWEWLN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.8
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

点击查看最新优质反应信息

文献信息

  • Catalysts for thermoplastic elastomeric olefin polymers
    申请人:The Board of Trustees of the Leland Stanford Jr. University
    公开号:US06566544B1
    公开(公告)日:2003-05-20
    This invention is directed to novel catalysts the structure and activity of which can be controlled to produce a wide range of alpha olefin polymers and co-polymers, and preferably for the production of stereoblock poly alpha olefins comprising a wide range of preselected amorphous and crystalline segments for precise control of the physical properties thereof, principally elastomeric thermoplastic properties. More specifically, this invention is directed to novel catalysts and catalysts systems for producing stereoblock polypropylene comprising alternating isotactic and atactic diastereosequences, which result in a wide range of elastomeric properties. The amount and numbers of crystalline sections, the isotactic pentad content, the number and length of intermediate atactic chains and overall molecular weight are all controllable by the steric structure of the catalysts and the process conditions. The novel catalysts provided by the present invention are ligand-bearing non-rigid metallocenes the geometry of which can be controlled on a time scale that is slower than the rate of olefin insertion, but faster than the average time to construct (polymerize) a single polymer chain, in order to obtain a stereoblock structure in the produced polyolefins. The symmetry of the catalyst structure is such that upon isomerization the catalyst symmetry alternates between a chiral and an achiral geometry. This geometry alteration can be controlled by selecting ligand type and structure, and through control of polymerization conditions to precisely control the physical properties of the resulting polymers.
    该发明涉及一种新型催化剂,其结构和活性可被控制,以生产广泛范围的α烯烃聚合物和共聚物,最好用于生产包含广泛范围预选的无定形和结晶片段以精确控制其物理性质,主要是弹性热塑性性质的立体块状聚α烯烃。更具体地说,该发明涉及一种新型催化剂和催化剂系统,用于生产包含交替等同构和非等构二对映序列的立体块状聚丙烯,这些序列导致广泛范围的弹性性能。结晶部分的数量和数量、等同构五聚体含量、中间非等构链的数量和长度以及总分子量都可通过催化剂的立体结构和工艺条件来控制。本发明提供的新型催化剂是带有配体的非刚性茂金属烯,其几何形状可以在比烯烃插入速率慢但比构建(聚合)单个聚合物链的平均时间快的时间尺度上进行控制,以获得所生产聚烯烃中的立体块状结构。催化剂结构的对称性使得在异构化时,催化剂的对称性在手性和非手性几何形状之间交替。这种几何形状的改变可以通过选择配体类型和结构以及通过控制聚合条件来精确控制所得聚合物的物理性质。
  • Catalyst systems for high melting thermoplastic elastomeric alpha-olefin polymers and plastomers
    申请人:The Board of Trustees of the Leland Stanford Junior University
    公开号:US20030195308A1
    公开(公告)日:2003-10-16
    This invention relates generally to low ethylene insertions into &agr;-olefin polymers and processes for production of such polymers using unbridged fluxional metallocenes, primarily substituted aryl indenyl metallocenes, and more particularly to use of unbridged, fluxional, cyclopentadienyl or indenyl metallocene catalyst systems in methods of production of high melting point &agr;-olefin homo- and co-polymers, particularly elastomeric crystalline and amorphous block homo- and co-polymers of &agr;-olefins. The activity of fluxional unbridged metallocene polymerization catalysts containing at least one 2-arylindene ligand is increased 10× or more by the addition of small (typically 0.1-10 wt. %) amounts of ethylene to the polymerization system, which increase is termed the Polymerization Rate-Enhancement effect (PRE), which is measured in terms of an Ethylene Enhancement Factor (EEF) as a dimensionless ratio in the range of from about 1.1 to about 10 or above. The amount of ethylene included in the reaction system can be selected and controlled to be so small as to result in essentially minimal (<2 mole %) incorporation of ethylene units into the resulting elastomeric polymer and the molecular weight may be increased. Amounts of ethylene to generate the PRE effect may be greater than 0.1 wt. % and preferably range up to about 2 wt. %. However, if a polymer with more ethylene is desired, additional ethylene may be incorporated into the polymerization feed, including up to 10 to about 50 mole % based on olefin units. A second important aspect of this invention is the ability to use a PRE activity-enhancing amount of ethylene in an olefin polymerization without substantially affecting the physical properties of the elastomer. In a third important aspect of this invention, &agr;-olefin elastomers are produced through incorporation of ethylene using unbridged fluxional catalyst systems which may not otherwise produce acceptable elastomeric homopolymers. This effect is termed the EPE effect, for Elastomeric Property-Enhancing effect. The EPE amount of ethylene required to produce such elastomers typically overlaps the PRE activity-enhancing amount. Incorporation of up to about 5 mole % or more of ethylene typically will produce an elastomeric polymer using such catalyst systems. Typical useful amounts of incorporated ethylene include about 1 to 3 mole %. Preferred polymers of this invention retain sufficient crystallinity to provide a high melting point (by DSC) of about 80° C., preferably above 100° C., including in the range of from about 120° C. to about 140° C. and above. Novel flexible &agr;-olefin homo and copolymers having elongation in excess of 600% and substantially no retained force are disclosed.
    本发明涉及低乙烯插入到α-烯烃聚合物中以及使用未桥联流动金属芳基茚基金属烯催化剂,尤其是取代芳基茚基金属烯催化剂的方法生产这种聚合物的过程,更特别地,使用未桥联、流动的环戊二烯基或茚基金属烯催化剂体系在生产高熔点α-烯烃均聚物和共聚物的方法中,特别是α-烯烃弹性结晶和非晶块状均聚物和共聚物的方法。至少含有一个2-芳基茚烯配体的流动未桥联金属烯聚合催化剂的活性通过向聚合体系中添加少量(通常为0.1-10重量%)乙烯而增加10倍或更多,这种增加被称为聚合速率增强效应(PRE),以无量纲比例的乙烯增强因子(EEF)的形式进行测量,范围为约1.1至约10或以上。可以选择和控制反应系统中包含的乙烯量非常小,以致于在所得到的弹性聚合物中几乎不包含(<2摩尔%)乙烯单元,分子量可以增加。产生PRE效应的乙烯量可能大于0.1重量%,并且最好在约2重量%范围内。但是,如果需要含更多乙烯的聚合物,可以将额外的乙烯并入聚合物化反馈中,包括基于烯烃单位的10至约50摩尔%。本发明的第二个重要方面是,在α-烯烃聚合中使用PRE活性增强量的乙烯而几乎不影响弹性体的物理性质。在本发明的第三个重要方面中,通过使用未桥联流动催化剂体系并将乙烯并入其中,可以生产α-烯烃弹性体,而该催化剂体系可能不会产生可接受的弹性体均聚物。这种效应称为EPE效应,用于弹性物性增强效应。通常需要并入约5摩尔%或更多的乙烯来使用这种催化剂体系生产弹性聚合物。通常有用的并入乙烯量包括约1至3摩尔%。本发明的优选聚合物保持足够的结晶性,以提供高熔点(通过DSC)约80℃,优选高于100℃,包括约120℃至约140℃以上的范围。还公开了具有超过600%的延伸率和基本无保留力的新型柔性α-烯烃均聚物和共聚物。
  • THERMOPLASTIC ELASTOMERIC STEREOBLOCK OLEFIN POLYMERS METHODS AND METALLOCENE CATALYSTS
    申请人:THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
    公开号:EP0802935A1
    公开(公告)日:1997-10-29
  • EP0802935A4
    申请人:——
    公开号:EP0802935A4
    公开(公告)日:1998-09-30
  • PROCESS FOR PREPARING 2-ARYL-SUBSTITUTED INDENES
    申请人:Montell Technology Company bv
    公开号:EP0910560A1
    公开(公告)日:1999-04-28
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