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[Ni2Br4(N-(1-(pyridin-2-yl)ethylidene)-N'-((pyridin-2-yl)methylene)-2,3,5,6-tetramethylbenzene-1,4-diamine)] | 870641-87-5

中文名称
——
中文别名
——
英文名称
[Ni2Br4(N-(1-(pyridin-2-yl)ethylidene)-N'-((pyridin-2-yl)methylene)-2,3,5,6-tetramethylbenzene-1,4-diamine)]
英文别名
[2,3,5,6-tetramethyl-N-(pyridin-2-ylethylidene)-N-(pyridin-2-ylmethylene)benzene-1,4-diamine]dinickel tetrabromide
[Ni2Br4(N-(1-(pyridin-2-yl)ethylidene)-N'-((pyridin-2-yl)methylene)-2,3,5,6-tetramethylbenzene-1,4-diamine)]化学式
CAS
870641-87-5
化学式
C23H24Br4N4Ni2
mdl
——
分子量
793.466
InChiKey
SANRZOYADVEPAQ-XJKHDCAFSA-J
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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    [Ni2Br4(N-(1-(pyridin-2-yl)ethylidene)-N'-((pyridin-2-yl)methylene)-2,3,5,6-tetramethylbenzene-1,4-diamine)]N,N-二甲基甲酰胺N,N-二甲基甲酰胺 为溶剂, 以60%的产率得到[Ni2Br2(DMF)6(N-(1-(pyridin-2-yl)ethylidene)-N'-((pyridin-2-yl)methylene)-2,3,5,6-tetramethylbenzene-1,4-diamine)]Br2*0.75DMF
    参考文献:
    名称:
    From symmetrical to unsymmetrical bimetallic nickel complexes bearing aryl-linked iminopyridines; synthesis, structures and ethylene polymerisation studies
    摘要:
    Both symmetrical and unsymmetrical tetramethylphenyl-linked iminopyridines, 1,4-{(2-C5H4N)RC=N}(2)-2,3,5,6-Me4C6 [R = H (L1a), Me (L1b)] and 1-{(2-C5H4N)HC=N}-4-{(2-C5H4N)MeC=N}-2,3,5,6-Me4C6 (L1c), have been prepared in good yield using straightforward condensation strategies. The molecular structures of L1a and L1c reveal the adjacent imino and pyridyl nitrogen atoms to adopt transoid configurations. Interaction of L1x with two equivalents of NiX2 [NiX2 = (DME)NiBr2 (DME = 1,2-dimethoxyethane), NiCl2] in n-BuOH at elevated temperature affords the paramagnetic bimetallic complexes, [(L1x) Ni2X4] [L1x = L1a, X = Br (1a); L1x = L1b, X = Br (1b); L1x = L1c, X = Br (1c); L1x = L1a, X = Cl (1d)] in moderate to good yield. Adduct formation results on treatment of bromide-containing 1a-1c with DMF (dimethylformamide) to yield dicationic [(L1x) Ni2Br2(DMF)(6)]Br-2 [L1x = L1a (2a), L1b (2b), L1c (2c)], while with chloride-containing 1d the neutral species [(L1a)Ni2Cl4(DMF)(4)] (3) is obtained. Activation of 1a-1d and 2c with excess methylaluminoxane (MAO) generates active ethylene polymerisation catalysts (1b/MAO > 1c/MAO > 1a/MAO similar to 1d/MAO > 2c/MAO) affording mixtures of waxes and low molecular weight solid polyethylene. Multinuclear NMR and GC analysis of the waxy components reveal methyl branched materials that contain mostly internal unsaturation along with low levels of alpha-olefins. Broad molecular weight distributions are observed for all the polymers obtained, with that from 1b/MAO leading to the highest molecular weight. Single crystal X-ray diffraction studies have been performed on L1a, L1c, 2a-2c and 3. (c) 2008 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2008.05.020
  • 作为产物:
    描述:
    乙二醇二甲醚溴化镍N-(1-(pyridin-2-yl)ethylidene)-N'-((pyridin-2-yl)methylene)-2,3,5,6-tetramethylbenzene-1,4-diamine正丁醇 为溶剂, 反应 1.5h, 以56%的产率得到[Ni2Br4(N-(1-(pyridin-2-yl)ethylidene)-N'-((pyridin-2-yl)methylene)-2,3,5,6-tetramethylbenzene-1,4-diamine)]
    参考文献:
    名称:
    [EN] TRANSITION METAL COMPOUNDS FOR OLEFIN POLYMERIZATION AND OLIGOMERIZATION
    [FR] COMPOSES METALLIQUES DE TRANSITION POUR LA POLYMERISATION D'OLEFINES ET L'OLIGOMERISATION
    摘要:
    这项发明涉及由式(I)表示的新过渡金属催化剂化合物,其中:M和M'分别是8、9、10或11族过渡金属,优选为Ni、Co、Pd、Cu或Fe;每个R基分别是氢,或烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基,且可选地,相邻的R基可以结合在一起形成取代或未取代的饱和、部分不饱和或芳香环或多环取代基;R'是氢,或烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基,且可选地,相邻的R基可以与R'结合在一起形成取代或未取代的饱和、部分不饱和或芳香环或多环取代基;每个X基分别是氢,卤素,或烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基,且可选地,相邻的X基可以结合在一起形成取代或未取代的饱和、部分不饱和或芳香环或多环取代基;m和m'分别为0、1、2或3;z和z'分别为0、1、2或3;N为氮;Q为氢,或烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基;Q'为氢,或烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基;L为烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基。
    公开号:
    WO2005118605A1
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同类化合物

()-2-(5-甲基-2-氧代苯并呋喃-3(2)-亚乙基)乙酸乙酯 (双(2,2,2-三氯乙基)) (乙基N-(1H-吲唑-3-基羰基)ethanehydrazonoate) (Z)-3-[[[2,4-二甲基-3-(乙氧羰基)吡咯-5-基]亚甲基]吲哚-2--2- (S)-(-)-5'-苄氧基苯基卡维地洛 (S)-(-)-2-(α-(叔丁基)甲胺)-1H-苯并咪唑 (S)-(-)-2-(α-甲基甲胺)-1H-苯并咪唑 (S)-氨氯地平-d4 (S)-8-氟苯并二氢吡喃-4-胺 (S)-4-(叔丁基)-2-(喹啉-2-基)-4,5-二氢噁唑 (S)-4-氯-1,2-环氧丁烷 (S)-3-(2-(二氟甲基)吡啶-4-基)-7-氟-3-(3-(嘧啶-5-基)苯基)-3H-异吲哚-1-胺 (S)-2-(环丁基氨基)-N-(3-(3,4-二氢异喹啉-2(1H)-基)-2-羟丙基)异烟酰胺 (SP-4-1)-二氯双(喹啉)-钯 (SP-4-1)-二氯双(1-苯基-1H-咪唑-κN3)-钯 (R,S)-可替宁N-氧化物-甲基-d3 (R,S)-六氢-3H-1,2,3-苯并噻唑-2,2-二氧化物-3-羧酸叔丁酯 (R)-(+)-5'-苄氧基卡维地洛 (R)-(+)-2,2'',6,6''-四甲氧基-4,4''-双(二苯基膦基)-3,3''-联吡啶(1,5-环辛二烯)铑(I)四氟硼酸盐 (R)-卡洛芬 (R)-N'-亚硝基尼古丁 (R)-DRF053二盐酸盐 (R)-4-异丙基-2-恶唑烷硫酮 (R)-3-甲基哌啶盐酸盐; (R)-2-苄基哌啶-1-羧酸叔丁酯 (N-(Boc)-2-吲哚基)二甲基硅烷醇钠 (N-{4-[(6-溴-2-氧代-1,3-苯并恶唑-3(2H)-基)磺酰基]苯基}乙酰胺) (E)-2-氰基-3-(5-(2-辛基-7-(4-(对甲苯基)-1,2,3,3a,4,8b-六氢环戊[b]吲哚-7-基)-2H-苯并[d][1,2,3]三唑-4-基)噻吩-2-基)丙烯酸 (E)-2-氰基-3-[5-(2,5-二氯苯基)呋喃-2-基]-N-喹啉-8-基丙-2-烯酰胺 (8α,9S)-(+)-9-氨基-七氢呋喃-6''-醇,值90% (6R,7R)-7-苯基乙酰胺基-3-[(Z)-2-(4-甲基噻唑-5-基)乙烯基]-3-头孢唑啉-4-羧酸二苯甲基酯 (6-羟基嘧啶-4-基)乙酸 (6,7-二甲氧基-4-(3,4,5-三甲氧基苯基)喹啉) (6,6-二甲基-3-(甲硫基)-1,6-二氢-1,2,4-三嗪-5(2H)-硫酮) (5aS,6R,9S,9aR)-5a,6,7,8,9,9a-六氢-6,11,11-三甲基-2-(2,3,4,5,6-五氟苯基)-6,9-甲基-4H-[1,2,4]三唑[3,4-c][1,4]苯并恶嗪四氟硼酸酯 (5R,Z)-3-(羟基((1R,2S,6S,8aS)-1,3,6-三甲基-2-((E)-prop-1-en-1-yl)-1,2,4a,5,6,7,8,8a-八氢萘-1-基)亚甲基)-5-(羟甲基)-1-甲基吡咯烷-2,4-二酮 (5E)-5-[(2,5-二甲基-1-吡啶-3-基-吡咯-3-基)亚甲基]-2-亚磺酰基-1,3-噻唑烷-4-酮 (5-(4-乙氧基-3-甲基苄基)-1,3-苯并二恶茂) (5-溴-3-吡啶基)[4-(1-吡咯烷基)-1-哌啶基]甲酮 (5-氯-2,1,3-苯并噻二唑-4-基)-氨基甲氨基硫代甲酸甲酯一氢碘 (5-氨基-6-氰基-7-甲基[1,2]噻唑并[4,5-b]吡啶-3-甲酰胺) (5-氨基-1,3,4-噻二唑-2-基)甲醇 (4aS-反式)-八氢-1H-吡咯并[3,4-b]吡啶 (4aS,9bR)-6-溴-2,3,4,4a,5,9b-六氢-1H-吡啶并[4,3-B]吲哚 (4S,4''S)-2,2''-环亚丙基双[4-叔丁基-4,5-二氢恶唑] (4-(4-氯苯基)硫代)-10-甲基-7H-benzimidazo(2,1-A)奔驰(德)isoquinolin-7一 (4-苄基-2-甲基-4-nitrodecahydropyrido〔1,2-a][1,4]二氮杂) (4-甲基环戊-1-烯-1-基)(吗啉-4-基)甲酮 (4-己基-2-甲基-4-nitrodecahydropyrido〔1,2-a][1,4]二氮杂) (4,5-二甲氧基-1,2,3,6-四氢哒嗪)