1,2,3,3a,4,5,6,6a,10b,10c-decahydrofluoranthene

• 分子结构分类: 有机化合物 - 苯类化合物 - 芴
• 英文名称: 1,2,3,3a,4,5,6,6a,10b,10c-decahydrofluoranthene
• 英文别名: Fluoranthene, 1,2,3,3a,4,5,6,6a,10b,10c-decahydro-
• 化学式: C₁₆H₂₀
• 分子量: 212.335
• InChiKey: KGAWXQOQEZMKII-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  16
• 可旋转键数：
  0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为产物：
  描述：

  荧蒽 生成 1,2,3,3a,4,5,6,6a,10b,10c-decahydrofluoranthene
  参考文献：
  名称：

  INUKAI YOSHINARI; ADACHI YOSHIO; SHIBATA MASAO; ARITA SEIJI, J. FUEL. SOC. JAP., 65,(1986) N 8, 643-652

  摘要：

  DOI：

文献信息

• Relative Reactivities of Some Polycyclic Aromatic Hydrocarbons in Catalytic Hydrogenation over Raney Nickel
  作者：Masahiro Minabe、Shuuichi Urushibara、Fumihiko Mishina、Takao Kimura、Motohiro Tsubota

  DOI：10.1246/bcsj.66.670

  日期：1993.2

  Catalytic hydrogenation of 9H-fluorene (1), phenanthrene (2), 4H-cyclopenta[def ]phenanthrene (3), pyrene (4), and fluoranthene (5) was carried out over Raney nickel (W-7) at 323 K under 608 kPa of hydrogen. The order of the reaction rate was 5 > 4 > 3 > 2 > 1. The adsorption equilibrium constant of the substrates decreased in the order 4 ≥ 5 >> 2 > 3 >> 1.

  9H-芴 (1)、菲 (2)、4H-环戊 [def ]菲 (3)、芘 (4) 和荧蒽 (5) 在 323 K 雷尼镍 (W-7) 上进行催化氢化在 608 kPa 的氢气下。反应速率顺序为 5 > 4 > 3 > 2 > 1。底物的吸附平衡常数依次为 4 ≥ 5 >> 2 > 3 >> 1。
• The Reactivities of Polyaromatic Hydrocarbons in Catalytic Hydrogenation over Supported Noble Metals
  作者：Kinya Sakanishi、Masato Ohira、Isao Mochida、Hiroshi Okazaki、Mahito Soeda

  DOI：10.1246/bcsj.62.3994

  日期：1989.12

  The reactivities of several polyaromatic hydrocarbons (pyrene: P, fluoranthene: FL, anthracene: An, fluorene: F, acridine: Ac, and carbazole: C) in the catalytic hydrogenation were studied and compared over supported noble metals (Pt, Pd, Rh, and Ru on a carbon or alumina support). The specific reactivity and selectivity were found to be strongly dependent upon the combination of the catalyst species and the substrate. The catalysts exhibited the activity order of Rh > Pd >> Pt > Ru for tricyclic aromatics of An, F, Ac, and C, although the catalysts provided very variable selectivities of the partially hydrogenated products which were produced via both consecutive and competitive routes, apparently according to the type of ring-skeleton and the presence of a nitrogen atom. The reactivity of the starting substrates and intermediates are compared to the quantum chemical reactivity indices, calculated based on MNDO (modified neglect of diatomic overlap). The values of the LUMO electron density, the π-bond order, and the stability of the product appear to govern the reactivity and selectivity of the hydrogenation, depending upon the combination of the catalyst species and the substrate. No hydrogenation of a substrate proceeds when its reactivity indices are less than the threshold value, which is subject to the activity of the catalyst and the reaction conditions defining product selectivity via both competitive and consecutive schemes.

  几种多芳烃（芘：P、氟蒽：FL、蒽：H）的反应活性P、荧蒽：FL、蒽：An、芴：Fluorene）的反应活性：An、芴F、吖啶Ac 和咔唑：在催化氢化过程中，研究并比较了支撑贵金属（碳或氧化铝支撑的铂、钯、铑和钌）的催化氢化作用。）研究发现，特定反应活性和选择性与催化剂种类和底物的组合密切相关。催化剂对 An、F、Ac 和 C 三环芳烃的活性顺序为 Rh > Pd >> Pt > Ru，但催化剂对通过连续和竞争路线产生的部分氢化产物的选择性差异很大，这显然与环骨架类型和氮原子的存在有关。起始底物和中间产物的反应性与量子化学反应性指数进行了比较，量子化学反应性指数是根据 MNDO（修正的二原子重叠忽略）计算得出的。LUMO 电子密度值、π 键顺序和产物的稳定性似乎决定了氢化反应的反应性和选择性，这取决于催化剂种类和底物的组合。当底物的反应性指数小于阈值时，底物不会发生氢化反应，而阈值则取决于催化剂的活性以及通过竞争和连续方案确定产物选择性的反应条件。
• INUKAI YOSHINARI; ADACHI YOSHIO; SHIBATA MASAO; ARITA SEIJI, J. FUEL. SOC. JAP., 65,(1986) N 8, 643-652
  作者：INUKAI YOSHINARI、 ADACHI YOSHIO、 SHIBATA MASAO、 ARITA SEIJI

  DOI：——

  日期：——