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[Co(η4-tetramethylcyclobutadiene)(η5-indenyl)] | 813420-36-9

中文名称
——
中文别名
——
英文名称
[Co(η4-tetramethylcyclobutadiene)(η5-indenyl)]
英文别名
[(tetramethylcyclobutadiene)Co(η5-indenyl)];[(η4-C4Me4)Co(η5-indenyl)]
[Co(η4-tetramethylcyclobutadiene)(η5-indenyl)]化学式
CAS
813420-36-9
化学式
C17H19Co
mdl
——
分子量
282.331
InChiKey
MXXOHBFCMXBUJS-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):
    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

点击查看最新优质反应信息

文献信息

  • (Tetramethylcyclobutadiene)cobalt Complexes with Five-Electron Carbo- and Heterocyclic Ligands
    作者:Elena V. Mutseneck、Dmitry A. Loginov、Dmitry S. Perekalin、Zoya A. Starikova、Denis G. Golovanov、Pavel V. Petrovskii、Piero Zanello、Maddalena Corsini、Franco Laschi、Alexander R. Kudinov
    DOI:10.1021/om0495832
    日期:2004.12.1
    g with NaBH4/AlCl3 or LiAlH4 affords the alkyl derivatives 5b and 5h (R = Et) or the alcohols 5i (R = CH2OH) and 5j (R = CH(OH)Me), respectively. The reaction of 1 with fluorene/AlCl3 yields complex [Cb*Co(η6-fluorene)]+ (8), which was deprotonated by KOBut to give Cb*Co(η6-fluorenyl) (9). Visible light irradiation of 9 induces η6→η5 haptotropic rearrangement to afford Cb*Co(η5-fluorenyl) (7). The pyrrolyl
    Tetramethylcyclobutadiene(环戊二烯基)络合物的Cb *(C 5 H ^ 4 R)(CB * =η 4 -C 4我4 ; R = H(图5a)中,Me(图5b),森达3(图5d),C(O) H(5f)和C(O)Me(5g))是通过环戊二烯阴离子与(羰基)化物络合物Cb * Co(CO)2 I(1)(方法A)或更高反应性的反应获得的乙腈络合物[Cb * Co(MeCN)3 ] +(2)(方法B)。类似化合物Cb * CoCp *(5c),Cb * Co(1,3-C5 ħ 3(森达3)2)(图5e),和Cb *(η 5 -基)(6)可以仅通过的方法B.处理来制备图5f,克用NaBH 4 /的AlCl 3或的LiAlH 4,得到烷基衍生物5b和5h(R = Et)或醇5i(R = CH 2 OH)和5j(R = CH(OH)Me)。的反应1与/的AlCl 3倍的产率络合物[*的Cb的Co(η
  • Slipped μ‐Indenyl Triple‐Decker Complexes Containing (C <sub>4</sub> Me <sub>4</sub> )Co and (C <sub>5</sub> R <sub>5</sub> )Ru Fragments
    作者:Elena V. Mutseneck、Zoya A. Starikova、Konstantin A. Lyssenko、Pavel V. Petrovskii、Piero Zanello、Maddalena Corsini、Alexander R. Kudinov
    DOI:10.1002/ejic.200600264
    日期:2006.11
    AbstractSlipped triple‐decker complexes with a bridging indenyl ligand, namely [Cb*Co(μ:η56‐C9H7)CoCb*]+ (2, Cb* = C4Me4) and [Cb*Co(μ:η56‐C9H7)Ru(C5R5)]+ (R = H, 5a; Me, 5b), have been synthesised by electrophilic stacking of [Cb*Co(η5‐C9H7)] (1) with [Cb*Co(MeCN)3]+ or [(C5R5)Ru(MeCN)3]+ (R = H, Me), respectively. A similar reaction of [(C5R5)Ru(η5‐C9H7)] (R = H, 3a; Me, 3b) with [Cb*Co(MeCN)3]+ affords the cations [(C5R5)Ru(μ:η56‐C9H7)CoCb*]+ (R = H, 4a; Me, 4b), which are isomeric with 5a,b. Stacking of [Ru(η5‐C9H7)2] (7) with [Cb*Co(MeCN)3]+ or [Cb*CoI]x/TlBF4 gives the triple‐decker complex [(η5‐C9H7)Ru(μ:η56‐C9H7)CoCb*]+ (8). Further reaction of 8 with [Cp*RuCl]4/TlBF4 unexpectedly affords the slipped tetra‐decker ruthenium complex [Cp*Ru(μ:η56‐C9H7)Ru(μ:η56‐C9H7)RuCp*]2+ (11). The structures of [4b][Co(η‐7,8‐C2B9H11)2] and [Cp*Ru(η6‐C9H7)] (6) have been determined by X‐ray diffraction, and the electrochemical behaviour of the complexes prepared has been studied. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
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