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(pentamethylcyclopentadienyl)(η(3)-2-methylpropenyl)dibromoosmium(IV) | 243468-18-0

中文名称
——
中文别名
——
英文名称
(pentamethylcyclopentadienyl)(η(3)-2-methylpropenyl)dibromoosmium(IV)
英文别名
(C5Me5)Os(η3-CH2CMeCH2)Br2
(pentamethylcyclopentadienyl)(η(3)-2-methylpropenyl)dibromoosmium(IV)化学式
CAS
243468-18-0;160211-12-1
化学式
C14H22Br2Os
mdl
——
分子量
540.337
InChiKey
ZFEKZBVSLZFBRR-UHFFFAOYSA-L
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:
    (pentamethylcyclopentadienyl)(η(3)-2-methylpropenyl)dibromoosmium(IV)二甲基镁乙醚 为溶剂, 以32%的产率得到(pentamethylcyclopentadienyl)(η(3)-2-methylpropenyl)(methyl)dibromoosmium(IV)
    参考文献:
    名称:
    Synthesis of Hydride and Alkyl Compounds Containing the Cp*Os(η3-allyl) Fragment. Crystal Structures of Cp*Os(η3-C8H13)Br2 and [Cp*Os(η3-C4H7)Me(H2O)][BF4]
    摘要:
    Treatment of Gp*(2)Os(2)B(r)4 with 3-bromo-2-methylpropene or 1,3-cycloactadiene affords the 2-methylpropenyl and cyclooctenyl products Cp*Os(eta(3)-C4H7)Br-2 and Cp*Os(eta(3)-C8H13)Br-2, respectively. The monoalkyl complexes Cp*Os(eta(3)-C4H7)MeBr and Cp*Os(eta(3)-C4H7)(CH2SiMe3)-Br can be generated by treating Cp*Os(eta(3)-C4H7)Br-2 with MgMe2 or LiCE2SiMe3. The dimethyl complex Cp*Os(eta(3)-C4H7)Me-2 can be synthesized from CP*Os(eta(3)-C(4)H7())Br(2) by addition of methyllithium. In contrast, addition of ethyllithium to Cp*Os(eta(3)-C4H7)Br-2 yields the ethylene complex Cp*Os(eta(3)-C4H7)(eta(2)-C2H4) and a small amount of Cp*Os(eta(3)-C4H7)H-2. The latter dihydride can be synthesized in better yield by treating CP*Os(eta(3)-C4H7)Br-2 With LiAlH4. When the dimethyl complex Cp*Os(eta(3)-C4H7)Me-2 is protonated with HBF4 in the presence of H2O, the aqua complex [Cp*Os(eta(3)-C4H7)Me(H2O)][BF4] is formed.
    DOI:
    10.1021/om990150m
  • 作为产物:
    描述:
    3-溴-2-甲基丙烯dibromo(pentamethylcyclopentadienyl)osmium(III) dimer乙醇二氯甲烷 为溶剂, 以56%的产率得到(pentamethylcyclopentadienyl)(η(3)-2-methylpropenyl)dibromoosmium(IV)
    参考文献:
    名称:
    Synthesis of Hydride and Alkyl Compounds Containing the Cp*Os(η3-allyl) Fragment. Crystal Structures of Cp*Os(η3-C8H13)Br2 and [Cp*Os(η3-C4H7)Me(H2O)][BF4]
    摘要:
    Treatment of Gp*(2)Os(2)B(r)4 with 3-bromo-2-methylpropene or 1,3-cycloactadiene affords the 2-methylpropenyl and cyclooctenyl products Cp*Os(eta(3)-C4H7)Br-2 and Cp*Os(eta(3)-C8H13)Br-2, respectively. The monoalkyl complexes Cp*Os(eta(3)-C4H7)MeBr and Cp*Os(eta(3)-C4H7)(CH2SiMe3)-Br can be generated by treating Cp*Os(eta(3)-C4H7)Br-2 with MgMe2 or LiCE2SiMe3. The dimethyl complex Cp*Os(eta(3)-C4H7)Me-2 can be synthesized from CP*Os(eta(3)-C(4)H7())Br(2) by addition of methyllithium. In contrast, addition of ethyllithium to Cp*Os(eta(3)-C4H7)Br-2 yields the ethylene complex Cp*Os(eta(3)-C4H7)(eta(2)-C2H4) and a small amount of Cp*Os(eta(3)-C4H7)H-2. The latter dihydride can be synthesized in better yield by treating CP*Os(eta(3)-C4H7)Br-2 With LiAlH4. When the dimethyl complex Cp*Os(eta(3)-C4H7)Me-2 is protonated with HBF4 in the presence of H2O, the aqua complex [Cp*Os(eta(3)-C4H7)Me(H2O)][BF4] is formed.
    DOI:
    10.1021/om990150m
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文献信息

  • Synthesis and Reactivity of the Osmium(III) Pentamethylcyclopentadienyl Complex (C<sub>5</sub>Me<sub>5</sub>)<sub>2</sub>Os<sub>2</sub>Br<sub>4</sub>. X-ray Crystal Structures of (C<sub>5</sub>Me<sub>5</sub>)<sub>2</sub>Os<sub>2</sub>Br<sub>4</sub>, (C<sub>5</sub>Me<sub>5</sub>)<sub>2</sub>Os<sub>2</sub>(μ-O)Br<sub>4</sub>, and (C<sub>5</sub>Me<sub>5</sub>)<sub>2</sub>Os<sub>2</sub>(μ-NPh)<sub>2</sub>Br<sub>2</sub>
    作者:Christopher L. Gross、Julia L. Brumaghim、Gregory S. Girolami
    DOI:10.1021/om060983u
    日期:2007.4.1
    singlet−triplet splitting of >800 cm-1. The reactions of (C5Me5)2Os2Br4 with oxygen, bromine, lithium anilide, acetonitrile, and norbornadiene (NBD) are described, affording the compounds (C5Me5)2Os2(μ-O)Br4, (C5Me5)OsBr4, (C5Me5)2Os2(μ-NPh)2Br2, [(C5Me5)Os(MeCN)3][BPh4], and (C5Me5)Os(NBD)Br; the crystal structures of the bridging oxo and bridging imido complexes are given.
    叔丁醇中用C 5 Me 5 H处理H 2 OsBr 6得到双核(C 5 Me 5)2 Os 2 Br 4,一种单(五甲基环戊二烯基)配合物,是各种synthetic的“半三明治”配合物的关键合成入口。X射线晶体结构显示它包含两个桥接和两个末端化物配体,桥接化物配体的Os-Br键距离短于末端化物配体。2.970(1)Å的Os-Os距离表示单个-os键。该化合物在溶液和固态中呈弱顺磁性,在4-300 K范围内测定的磁化率给出了> 800 cm -1的单重态-三重态分裂。(C 5 Me 5)2 Os 2 Br 4的反应描述了用氧,苯胺乙腈和降冰片二烯(NBD)制备化合物(C 5 Me 5)2 Os 2(μ-O)Br 4,(C 5 Me 5)OsBr 4,(C 5 Me 5)2 Os 2(μ-NPh)2 Br 2,[(C 5 Me 5)Os(MeCN)3 ] [BPh 4 ]和(C
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