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cyclonona-1,5-diyne | 118620-69-2

中文名称
——
中文别名
——
英文名称
cyclonona-1,5-diyne
英文别名
——
cyclonona-1,5-diyne化学式
CAS
118620-69-2
化学式
C9H10
mdl
——
分子量
118.178
InChiKey
IOBMXAHSUDFCIA-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):
    2.5
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    bis(η2-ethylene)(η5-pentamethylcyclopentadienyl)cobalt(I)cyclonona-1,5-diyne 以 not given 为溶剂, 以3%的产率得到
    参考文献:
    名称:
    环状二炔的三倍和四倍[2 + 2]环加成反应作为立体效应的结果:在通往聚合物的过程中。
    摘要:
    CpCo介导的环状二炔的[2 + 2]环加成的微调具有三键(C 2 H 4,Si 2 Me 4)之间的小桥,产生纳米带状环芳基1和2。2 ; R = H(1),CO 2 Me(1、2)。
    DOI:
    10.1002/(sici)1521-3773(19981231)37:24<3376::aid-anie3376>3.0.co;2-x
  • 作为产物:
    描述:
    nona-2,7-diyne-1,9-diol联苯三溴化磷lithium 作用下, 以 四氢呋喃 为溶剂, 生成 cyclonona-1,5-diyne
    参考文献:
    名称:
    A convenient synthesis of ethano-bridged cyclic diynes — Preparation of 1,1,2,2-tetramethyl-1,2-disilacycloocta-3,7-diyne
    摘要:
    Cyclic diynes bridged by an ethano moiety on one side are formed in the reaction of alpha,omega-dihalogen precursors with lithium in presence of biphenyl. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4039(97)10329-x
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文献信息

  • Syntheses and properties of medium sized carbocyclic diacetylenes
    作者:Rolf Gleiter、Detlef Kratz、Volker Schehlmann
    DOI:10.1016/0040-4039(88)85217-1
    日期:1988.1
    The syntheses and properties of cyclonona-1,5-diyne (1), cyclodeca-1,5-diyne (3), cycloundeca-1,5-diyne (4) and cycloundeca-1,6-diyne(5) are reported.
    报道了Cyclonona-1,5-diyne(1),cyclodeca-1,5-diyne(3),cycloundeca-1,5-diyne(4)和cycloundeca-1,6-diyne(5)的合成和性质。
  • Synthesis and properties of medium-sized (C9-C12) carbocyclic diacetylenes
    作者:R. Gleiter、D. Kratz、W. Schaefer、V. Schehlmann
    DOI:10.1021/ja00024a035
    日期:1991.11
    The syntheses of 1,5-cyclononadiyne (3), 1,5-cyclodecadiyne (4), 1,5-cycloundecadiyne (5), 1,6-cycloundecadiyne (6), 1,6-cyclododecadiyne (7), and 1,7-cyclododecadiyne (8) have been carried out. Diacetylenes 3 and 4 are prepared from 5-cyclononynone and 5-cyclodecynone, respectively. Compounds 5-8 are synthesized from cyclic diones by thermolysis of the corresponding bisselenadiazoles. The obtained cyclic diacetylenes are further characterized by their bis(hexacarbonyldicobalt) complexes. The geometrical parameters of 3-8 were calculated with force field and semiempirical methods. From the structural data, a correlation between the C-13 resonance of the sp-hybridized carbon atoms adjacent to the ethano bridge in 3-5 and the corresponding resonance of the symmetric dialkynes 1,5-cyclooctadiyne (1), 1,6-cyclodecadiyne (2), and 1,7-cyclododecadiyne (8) with the bending angle at this center can be verified. The PE spectra of 3-8 have been recorded, and an interpretation of the bands in the low-energy region is presented. It is found that the splitting of the PE bands that are assigned to the in-plane pi-MO's (pi-i) strongly depends on the size of the methylene bridge. In the case of a propano bridge (e.g., in 3, 6, and 7), the splitting between pi-i- and pi=i+ is relatively large. The splitting of the bands that are assigned to the out-of-plane pi-MO's (pi-o) decreases with increasing transannular distance.
  • GLEITER, ROLF;KRATZ, DETLEF;SCHEHLMANN, VOLKER, TETRAHEDRON LETT., 29,(1988) N 23, C. 2813-2816
    作者:GLEITER, ROLF、KRATZ, DETLEF、SCHEHLMANN, VOLKER
    DOI:——
    日期:——
  • A convenient synthesis of ethano-bridged cyclic diynes — Preparation of 1,1,2,2-tetramethyl-1,2-disilacycloocta-3,7-diyne
    作者:Gebhard Haberhauer、Rolf Roers、Rolf Gleiter
    DOI:10.1016/s0040-4039(97)10329-x
    日期:1997.12
    Cyclic diynes bridged by an ethano moiety on one side are formed in the reaction of alpha,omega-dihalogen precursors with lithium in presence of biphenyl. (C) 1997 Elsevier Science Ltd.
  • Threefold and Fourfold [2+2] Cycloadditions of Cyclic Diynes as a Consequence of Steric Effects: En Route to Polymers
    作者:Gebhard Haberhauer、Frank Rominger、Rolf Gleiter
    DOI:10.1002/(sici)1521-3773(19981231)37:24<3376::aid-anie3376>3.0.co;2-x
    日期:1998.12.31
    The fine-tuning of the CpCo-mediated [2+2] cycloaddition of cyclic diynes with small bridges between the triple bonds (C2 H4 , Si2 Me4 ) yields nanosized beltlike cyclophanes 1 and 2. =SiMe2 ; R = H (1), CO2 Me (1, 2).
    CpCo介导的环状二炔的[2 + 2]环加成的微调具有三键(C 2 H 4,Si 2 Me 4)之间的小桥,产生纳米带状环芳基1和2。2 ; R = H(1),CO 2 Me(1、2)。
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