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Decacyclo[24.4.3.36,11.316,21.01,26.02,25.05,12.06,11.015,22.016,21]nonatriaconta-2(25),5(12),7,9,15(22),17,19,27,29-nonaen-3,13,23-triyne | 183152-49-0

中文名称
——
中文别名
——
英文名称
Decacyclo[24.4.3.36,11.316,21.01,26.02,25.05,12.06,11.015,22.016,21]nonatriaconta-2(25),5(12),7,9,15(22),17,19,27,29-nonaen-3,13,23-triyne
英文别名
decacyclo[24.4.3.36,11.316,21.01,26.02,25.05,12.06,11.015,22.016,21]nonatriaconta-2(25),5(12),7,9,15(22),17,19,27,29-nonaen-3,13,23-triyne
Decacyclo[24.4.3.36,11.316,21.01,26.02,25.05,12.06,11.015,22.016,21]nonatriaconta-2(25),5(12),7,9,15(22),17,19,27,29-nonaen-3,13,23-triyne化学式
CAS
183152-49-0
化学式
C39H30
mdl
——
分子量
498.667
InChiKey
DQGCNOASPBVWBQ-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):
    8.8
  • 重原子数:
    39
  • 可旋转键数:
    0
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.38
  • 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

点击查看最新优质反应信息

文献信息

  • [2 + 2] Cycloreversion of [4.3.2]Propella-1,3,11-trienes:  An Approach to Cyclo[<i>n</i>]carbons from Propellane-Annelated Dehydro[<i>n</i>]annulenes
    作者:Yoshito Tobe、Toshihiko Fujii、Hideki Matsumoto、Kunihiro Tsumuraya、Daisuke Noguchi、Nobuko Nakagawa、Motohiro Sonoda、Koichiro Naemura、Yohji Achiba、Tomonari Wakabayashi
    DOI:10.1021/ja993314z
    日期:2000.3.1
    Next, dehydro[12]-, [16]-, [18]-, [20]-, and [24]annulene derivatives annelated by the [4.3.2]propellatriene units were prepared as precursors to the corresponding cyclo[n]carbons, a monocyclic form of carbon clusters. Laser-desorption mass spectra of the dehydroannulenes exhibited, in the negative mode, peaks due to the corresponding cyclo[n]carbon anions (n = 12, 16, 18, 20, and 24) formed by successive
    作为一种从稳定的前体生成具有高反应性聚炔单元的全碳分子的方法,开发了 [4.3.2]propella-1,3,11-triene 衍生物的 [2 + 2] 环回复。为了测试该方法的效率,该反应首先应用于简单的二乙炔基和二丁二炔基取代的丙炔三烯,它们分别在紫外线照射下产生线性己三炔和十戊炔衍生物。接下来,制备了由 [4.3.2] 丙炔三烯单元退火的脱氢 [12]-、[16]-、[18]-、[20]- 和 [24] 环烯衍生物作为相应环 [n] 的前体碳,碳簇的单环形式。脱氢环烯的激光解吸质谱在负模式下表现出由于相应的环 [n] 碳阴离子(n = 12, 16, 18, 20, 和 24) 由芳香族茚满碎片的连续损失形成。脱氢[16]环烯和脱氢[18]环烯衍生物的溶液光解通过[2+2]环还原反应形成反应性聚炔中间体...
  • Tobe, Yoshito; Matsumoto, Hideki; Naemura, Koichiro, Angewandte Chemie, 1996, vol. 108, # 16, p. 1924 - 1926
    作者:Tobe, Yoshito、Matsumoto, Hideki、Naemura, Koichiro、Achiba, Yohji、Wakabayashi, Tomonari
    DOI:——
    日期:——
  • Photoelectron spectroscopy of Cn− produced from laser ablated dehydroannulene derivatives having carbon ring size of n=12, 16, 18, 20, and 24
    作者:Tomonari Wakabayashi、Masamichi Kohno、Yohji Achiba、Haruo Shiromaru、Takamasa Momose、Tadamasa Shida、Koichiro Naemura、Yoshito Tobe
    DOI:10.1063/1.474841
    日期:1997.10
    n -Dehydroannulenes with the ring size of n=12, 16, 18, 20, and 24 and with three to five indanyl substituents are laser ablated by 355 nm photons. The indanyl unit is lost stepwise up to the complete deletion to leave the bare annulenyl skeleton. The monoanions of these products are mass analyzed first, and then subjected to a second laser pulse of 266 nm to obtain photoelectron spectra for Cn− with n=12, 16, 18, 20, and 24. The spectra are compared with those obtained by using graphite as a target of the laser ablation. The comparison of the two spectra provides useful information on the structure of neutral carbon clusters.
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