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(N,N-dimethylbenzylamine(-1H))Pd(II)(N,N'-dineopentyl-2-amino-5-alcoholate-1,4-benzoquinonemonoimine) | 797816-74-1

分子结构分类

中文名称
——
中文别名
——
英文名称
(N,N-dimethylbenzylamine(-1H))Pd(II)(N,N'-dineopentyl-2-amino-5-alcoholate-1,4-benzoquinonemonoimine)
英文别名
——
(N,N-dimethylbenzylamine(-1H))Pd(II)(N,N'-dineopentyl-2-amino-5-alcoholate-1,4-benzoquinonemonoimine)化学式
CAS
797816-74-1
化学式
C25H37N3O2Pd
mdl
——
分子量
518.008
InChiKey
OWVZMXNQBKAEKH-JKXROLASSA-M
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

反应信息

  • 作为产物:
    描述:
    bis[(benzyldimethylamino)chloropalladium(II)] 、 N,N'-dineopentyl-2-amino-5-sodium alcoholate-1,4-benzoquinonemonoimine 以 四氢呋喃 为溶剂, 以65%的产率得到(N,N-dimethylbenzylamine(-1H))Pd(II)(N,N'-dineopentyl-2-amino-5-alcoholate-1,4-benzoquinonemonoimine)
    参考文献:
    名称:
    Stepwise Synthesis, Structures, and Reactivity of Mono-, Di-, and Trimetallic Metal Complexes with a 6π + 6π Quinonoid Zwitterion
    摘要:
    The benzoquinonemonoimine N, N'-dineopentyl-2-amino-5-alcoholate-1,4-benzoquinonemonoiminium [C6H2( -NHCH(2)tBu)(2)( -O)(2)] 6, which is a rare example of an organic zwitterion being more stable than its canonical form, is best described as constituted of two chemically connected but electronically not conjugated 6pi electron subunits. The two successive acidities of 6 allow the preparation of mono-, di-, and trimetallic complexes in which the control of the pi-system delocalization becomes possible. Reaction of 6 with NaOt-Bu results in monodeprotonation of one N-H function, and the isolated sodium salt 9, which is stable under N-2, reacts with chloride-bridged Pd(II) homodimetallic complexes, [AuCl(PPh3)] or trans-[NiCl(Ph)(PPh3)(2)], to afford the monometallic complexes 10-15 in which the pi-system is localized. A second in situ deprotonation of the remaining N-H amino function of 10 with NaH followed by reaction with [Pd(8-mq)(mu-Cl)](2) (8-mq = orthometalated 8-methylquinoline) affords the homodimetallic complex 17 in which the pi-system of the quinonoid ligand is delocalized between the two metal centers. Deprotonation of both N-H amino functions of the square-planar complex trans-[Ni(N,O)(2)] 15 with NaH and reaction with [Pd(8-mq)(mu-Cl)]2 affords the heterotrimetallic (Pd, Ni, Pd) complex 18 in which the pi-system of the two quinonoid ligands is delocalized between the three metal centers. The crystal structures of the monometallic complexes 10 and 13 and of the dipalladium complex 17 are reported and consequences of metal coordination discussed. Complex 15 was tested in catalytic ethylene oligomerization with AlEtCl2 as cocatalyst.
    DOI:
    10.1021/ic049263a
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