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Diacetyl-bis(2,6-dimethylphenylimin) | 343633-43-2

中文名称
——
中文别名
——
英文名称
Diacetyl-bis(2,6-dimethylphenylimin)
英文别名
N,N'-bis(2,6-dimethylphenyl)-1,4-diaza-2,3-dimethyl-1,3-butadiene
Diacetyl-bis(2,6-dimethylphenylimin)化学式
CAS
343633-43-2
化学式
C20H24N2
mdl
——
分子量
292.424
InChiKey
XFRDTZDCMXJTNJ-KSTNYAOJSA-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):
    5.81
  • 重原子数:
    22.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    24.72
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    Diacetyl-bis(2,6-dimethylphenylimin)正丁基锂四丁基氟化铵二异丙胺 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 16.0h, 生成 8,9-bis[(E)-2,6-dimethylphenylimino]decal-1-ol
    参考文献:
    名称:
    Efficient Slurry-Phase Homopolymerization of Ethylene to Branched Polyethylenes Using α-Diimine Nickel(II) Catalysts Covalently Linked to Silica Supports
    摘要:
    alpha-Diimine nickel(II) complexes covalently linked to a silica support were obtained by the reaction of an amino- or hydroxy-functionalized alpha-diimine nickel complex with silica particles treated with trimethyl aluminum. These silica-supported aryl R-diimine nickel(II) precatalysts linked via an amino (1a) or hydroxy functionality (1b-c) at the p-aryl position, and precatalysts linked via one (2a) or two (2b) hydroxy functionalities in the alkyl backbone were used in slurry polymerizations of ethylene to produce branched polyethylenes. Activation of precatalysts with ethylaluminum sesquichloride was effective even at very low Al/Ni ratios of 48. Initial polymerizations, performed at 60 degrees C and 150 psig ethylene, showed excellent productivities of up to 10.8 kg PE per gram of 1b (3.0 wt % nickel loading). Low productivities at temperatures above 60 degrees C can in part be overcome by increase in ethylene pressure. For example, a productivity of 6.0 kg PE per gram of 1b (3.0 wt % nickel loading) was obtained at 80 degrees C and 700 psig ethylene. The best polymerization productivities were obtained with trimethylaluminum as a traceless silica-linker, however, tetrachlorosilane and trichloroborane are attractive alternatives. Branching densities can be controlled by choice of ortho-aryl substituents. No reactor fouling occurs with these supported catalysts.
    DOI:
    10.1021/ma061032v
  • 作为产物:
    描述:
    2,3-丁二酮2,6-二甲基苯胺盐酸 作用下, 以 乙醚 为溶剂, 反应 4.0h, 生成 Diacetyl-bis(2,6-dimethylphenylimin)
    参考文献:
    名称:
    Imino-amide catalyst compositions for the polymerization of olefins
    摘要:
    本发明提供了一个催化剂前驱体和催化剂系统,包括所述前驱体,前驱体的一个实施例选自以下结构:其中T是桥接基团;M选自元素周期表的3至7族元素和镧系元素;Z是配位配体;每个L是一价、二价或三价阴离子配体;X和Y各自独立选自氮、氧、硫和磷;R是一个与X相对具有相对较低的立体位阻的非臃肿取代基;R′是一个与Y相对具有立体位阻的臃肿取代基。
    公开号:
    US06919467B2
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文献信息

  • [EN] METHODS OF PRODUCING ALPHA, BETA-UNSATURATED CARBOXYLIC ACID SALTS FROM ALKANES AND CARBON DIOXIDE<br/>[FR] PROCÉDÉS DE PRODUCTION DE SELS D'ACIDE CARBOXYLIQUE ALPHA, BÊTA-INSATURÉS À PARTIR D'ALCANES ET DE DIOXYDE DE CARBONE
    申请人:SABIC GLOBAL TECHNOLOGIES BV
    公开号:WO2019053540A1
    公开(公告)日:2019-03-21
    Methods of producing α,β-unsaturated carboxylic acid salt are described. A method can include reacting an alkene and carbon dioxide with a composition that includes a carboxylation catalyst, an organic base that is solubilized in the composition, and an inorganic base that is not solubilized in the composition, under reaction conditions suitable to produce an inorganic base salt of an α,β-unsaturated carboxylic acid. The organic base can have a first pKa and the inorganic base has a second pKa that is greater than the first pKa.
    描述了生产α,β-不饱和羧酸盐的方法。一种方法可以包括在适合于产生α,β-不饱和羧酸的无机盐的条件下,将烯烃和二氧化碳与包括羧化催化剂、在组合物中溶解的有机碱和不在组合物中溶解的无机碱的组成反应。所述有机碱具有第一pKa值,所述无机碱具有大于第一pKa值的第二pKa值。
  • Contribution to the Reactivity of <i>N</i> , <i>N′</i> ‐Diaryl‐1,4‐diazabutadienes Aryl–N=CH–CH=N–Aryl (Aryl = 2,6‐Dimethylphenyl; 2,4,6‐Trimethylphenyl) Towards Boron Trichloride
    作者:Lothar Weber、Jan Förster、Hans‐Georg Stammler、Beate Neumann
    DOI:10.1002/ejic.200600728
    日期:2006.12
    The reaction of Aryl-N=CH-CH=N-Aryl (3a: Aryl = 2,6-Me2C6H3; 3b: Aryl=2,4,6-Me3C6H2) with 2 equiv. BCl3 in a toluene/hexane mixture at -50 degrees C led to an inseparable mixture of borolium salts [Aryl-N-a=CH-CH=N(Aryl)BCl2(N-a-B)]+BCl4- (4a: Aryl = 2,6-Me2C6H3; 9a: Aryl = 2,4,6-Me3C6H2) and (Aryl-N-a=CH-C(Cl)=N(Aryl)BCl2(N-a-B)+BCl4- (4b: Aryl = 2,6-Me2C6H3; 9b: Aryl = 2,4,6-Me3C6H2) and the bicyclic
    Aryl-N=CH-CH=N-Aryl(3a:Aryl = 2,6-Me2C6H3;3b:Aryl=2,4,6-Me3C6H2)与 2 当量的反应。BCl3 在 -50 摄氏度的甲苯/己烷混合物中形成不可分离的硼盐混合物 [Aryl-Na=CH-CH=N(Aryl)BCl2(NaB)]+BCl4- (4a: Aryl = 2,6- Me2C6H3; 9a: Aryl = 2,4,6-Me3C6H2) 和 (Aryl-Na=CH-C(Cl)=N(Aryl)BCl2(NaB)+BCl4- (4b: Aryl = 2,6-Me2C6H3; 9b) : Aryl = 2,4,6-Me3C6H2) 和双环类 [HCa=N(Aryl)BCl2N(Aryl)-Cb=(CaCb)](2) (5: Aryl = 2,6-Me2C6H3; 10: Aryl = 2,4,6-Me3C6H2。硼的钠汞齐还原。盐 4a
  • [EN] METHODS OF MAKING ALPHA, BETA-UNSATURATED CARBOXYLIC ACIDS OR SALTS<br/>[FR] PROCÉDÉS DE FABRICATION D'ACIDES CARBOXYLIQUES ALPHA,BÊTA-INSATURÉS OU DE LEURS SELS
    申请人:SABIC GLOBAL TECHNOLOGIES BV
    公开号:WO2017158469A1
    公开(公告)日:2017-09-21
    Methods of making an α,β-unsaturated carboxylic acid or a salt thereof is disclosed. The method can include reacting an alkene and carbon dioxide with a composition comprising a metal containing carboxylation catalyst and a coordinating ligand under conditions suitable to produce the α,β-unsaturated carboxylic acid or salt thereof. The coordinating ligand can include at least two coordinating atoms selected from nitrogen (N), oxygen (O), sulfur (S), and carbene that coordinate with the metal in the carboxylation catalyst.
    揭示了制备α,β-不饱和羧酸或其盐的方法。该方法可以包括在适宜条件下,将烯烃和二氧化碳与含有金属含有羧化催化剂和配位配体的组合物反应,以产生α,β-不饱和羧酸或其盐。配位配体可以包括至少两个与羧化催化剂中的金属配位的氮(N)、氧(O)、硫(S)和卡宾等配位原子。
  • Metal-Organic Framework Catalysts and Their Use in Hydrocarbon Transformation
    申请人:Lillerud Karl-Petter
    公开号:US20080306315A1
    公开(公告)日:2008-12-11
    The invention relates to a porous heterogeneous catalyst material comprising frameworks of inorganic cornerstones connected by organic bridges, characterized in that as organic bridges are used ligands having a complexed catalytically active metal. The metals are preferably palladium and platinum. The ligands preferably contain nitrogen donor groups for complexing the catalytically active metal and carboxylate groups connecting to the inorganic cornerstones.
    这项发明涉及一种多孔的异质催化剂材料,其包括由无机基石通过有机桥连接而成的框架,其特征在于作为有机桥的配体是具有络合催化活性金属的。金属优选为钯和铂。配体优选包含氮供体基团以络合催化活性金属,并且连接到无机基石的羧基团。
  • Method for selective hydrogenation of polyunsaturated compounds into monounsaturated compounds using a homogeneous catalyst
    申请人:Hillion Gerard
    公开号:US20060129010A1
    公开(公告)日:2006-06-15
    A process for the selective hydrogenation of diolefinic compounds to mono-olefinic compounds uses a catalyst composition comprising at least one salt of a transition metal from groups IB, IIB, VB, VIB, VIIB and VIII of the periodic table, at least one ligand and at least one organometallic reducing agent, optionally in the presence of a non-aqueous ionic liquid selected from the group formed by liquid salts with general formula Q + A − (in which Q + represents a quaternary ammonium and/or quaternary phosphonium and A − represents any anion which can form a liquid salt below 90° C.).
    一种用于选择性氢化二烯烃化合物为单烯烃化合物的方法使用催化剂组合物,该组合物包括周期表IB、IIB、VB、VIB、VIIB和VIII族过渡金属的至少一种盐,至少一种配体和至少一种有机金属还原剂,可选地在非水离子液体的存在下进行,所述非水离子液体从具有通式Q+A−的液态盐组成的组中选取(其中Q+代表季铵和/或季磷酸盐,A−代表可以在90°C以下形成液态盐的任何阴离子)。
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