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[Ir(N,N-dimethyl-N',N''-di-p-tolylguanidinato)(cis-cyclooctene)2] | 1171249-80-1

中文名称
——
中文别名
——
英文名称
[Ir(N,N-dimethyl-N',N''-di-p-tolylguanidinato)(cis-cyclooctene)2]
英文别名
——
[Ir(N,N-dimethyl-N',N''-di-p-tolylguanidinato)(cis-cyclooctene)2]化学式
CAS
1171249-80-1
化学式
C33H48IrN3
mdl
——
分子量
678.984
InChiKey
MKXNPJYGWVCVIC-VIBDZMCESA-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

反应信息

  • 作为反应物:
    描述:
    lithium N,N-dimethyl-N′,N″-bis(4-methylphenyl)guanidinate 、 [Ir(N,N-dimethyl-N',N''-di-p-tolylguanidinato)(cis-cyclooctene)2]氧气 作用下, 生成 [Ir(N,N-dimethyl-N',N''-di-p-tolylguanidinato)3]
    参考文献:
    名称:
    Stabilization of Iridium(IV) by Monoanionic Dialkyldiarylguanidinato Ligands
    摘要:
    Etectron-rich tris(guanidinato) complexes of Ir-III, [Ir{ArNC(NR2)NAr}(3)] (where R = Me or Et; Ar = Ph or 4-Me6CH4),were synthesized from the respective [Ir{ArNC(NR2)NAr}(C8H14)(2)] precursors (C8H14 = cis-cyclooctene), are air-sensitive, and can be electrochemically oxidized in two one-electron transfer steps. The first electron transfer is reversible and occurs at much lower potentials than typical for Ir-III. Chemical oxidation by [FeCp2]PF6 afforded isolable, paramagnetic Ir-IV compounds, [Ir{ArNC(NR2)NAr}(3)]PF6, which were characterized by analytical and spectroscopic methods and a single-crystal structure determination, demonstrating that Ir-IV is accessible in a nitrogen-donor ligand environment.
    DOI:
    10.1021/ja9033445
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