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5-ethynylacenaphthylene

中文名称
——
中文别名
——
英文名称
5-ethynylacenaphthylene
英文别名
——
5-ethynylacenaphthylene化学式
CAS
——
化学式
C14H8
mdl
——
分子量
176.218
InChiKey
AEJWGRDUACFYBQ-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):
    3.9
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 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

  • 作为产物:
    描述:
    5-乙酰-1,2-二氢苊烯五氯化磷 作用下, 以 二氯甲烷 为溶剂, 1000.0 ℃ 、1.33 Pa 条件下, 反应 5.0h, 生成 5-ethynylacenaphthylene
    参考文献:
    名称:
    Sarobe, Martin; Flink, Simon; Jenneskens, Leonardus W., Journal of the Chemical Society. Perkin transactions II, 1996, # 10, p. 2125 - 2132
    摘要:
    DOI:
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文献信息

  • Origin of Pyrene under High Temperature Conditions in the Gas Phase. The Pivotal Role of Phenanthrene
    作者:Martin Sarobe、Leonardus W. Jenneskens、Ralph G. B. Steggink、Tom Visser
    DOI:10.1021/jo982030e
    日期:1999.5.1
    4-Ethynylphenanthrene (15), and the latent precursors for 2-ethynyl- (18) and 3-ethynylphenanthrene (19), viz., 2-(1-chloroethenyl)- (16) and 3-(1-chloroethenyl)phenanthrene (17), respectively, have been subjected to flash vacuum thermolysis (FVT). Whereas at 800 degrees C 15 is quantitatively converted into pyrene (1), 16 and 17 only give 18 and 19, respectively. Both 18 and 19 contain redundant ethynyl substituents, i.e., after ethynyl-ethylidene carbene equilibration neither five- nor six-membered ring formation can occur by carbene C-H insertion. At T greater than or equal to 1000 degrees C 16 and 17 gave pyrolysates containing the same set of 11 (non)-alternant polycyclic aromatic hydrocarbons (PAH), albeit in a different ratio. The different product ratio suggests that redundant ethynyl substituents migrate along the phenanthrene periphery presumably via transient cyclobuta-PAH intermediates toward positions suitable for either five- or six-membered ring formation by carbene C-H insertion. The results provide an explanation for the ubiquitous formation of pyrene (1), acephenanthrylene (9), and fluoranthene (3) during (incomplete) combustion. Phenanthrene (2) appears to be a point of divergence in PAH growth by C-2 addition.
  • Sarobe, Martin; Flink, Simon; Jenneskens, Leonardus W., Journal of the Chemical Society. Perkin transactions II, 1996, # 10, p. 2125 - 2132
    作者:Sarobe, Martin、Flink, Simon、Jenneskens, Leonardus W.、Zwikker, Jan W.、Wesseling, Jolanda
    DOI:——
    日期:——
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同类化合物

苊烯八醇 苊烯-1-甲醛 苊烯 苊并[3,4-d][1,3]噻唑 氘代二氢萘 全氟苊 乙酮,1-[2-(1-吡咯烷基)-1-苊烯基]- 7H-苊并[4,5-d]咪唑 5-溴苊烯 5-氟苊烯 5,6-二溴苊烯 2-氯苊烯-1-甲醛 2-偶氮基苊烯-1-醇 1-氰基苊 1-(4-甲氧基苯基)苊 1-(1-萘基)苊 1-(4-Pentenyl)acenaphthylene 1-Allylacenaphthylene 1-Methylsulfanyl-2-(prop-1-ynylsulfanyl)acenaphthylene 1,2-di(2-thienyl)acenaphthylene 1-(2-cyanophenyl)acenaphthylene 3235-acenaphthylene)Ru3(CO)7 5-hydroxymethylacenaphthylene 4-Vinylacenaphtylen 1-Chloroacenaphtho[1,2-d]-2,1,5-oxatellurazole 5-acenaphthylene boronic acid 1,1'-biacenaphthylene Pd-PEPPSI-IPrAn (dpp-BIAN)Mg(THF)3 5-ethynylacenaphthylene 4-Methyl-acenaphthylen Heptafluor-3-methoxy-acenaphthylen Acenaphthylen-5-OL 4-Chlor-acenaphthylen 4-Acenaphthylenamine diethyl (3S,4R,9S,10R)-21-oxohexacyclo[10.7.1.13,10.14,9.02,11.016,20]docosa-1(19),2(11),5,7,12,14,16(20),17-octaene-3,10-dicarboxylate 5-Acenaphthylenecarbonitrile trans-7,8-Dihydroxy-7,8-dihydrofluoranthene 5-Acenaphthylenamine anti-8,17-dimethylacenaphthyleno[1,2-a]-10-thia[2,3]metacyclophan-1-ene anti-8,16-dimethylacenaphthyleno[1,2-a][2,3]metacyclophan-1-ene 1,2-dibromo-4,7-dichloro-5,6-bis(dimethylamino)acenaphthylene 1,2,4-tribromo-6-dimethylamino-5-methylamino-acenaphthylene 1,2-dibromo-5,6-bis(dimethylamino)acenaphthylene 5,6-dimethylacenaphthylene 1-phenyl-2-propylacenaphthylene [1,2-2H]-acenaphthylene 5-Benzolsulfonylamino-acenaphthylen 1,3-bis(2,6-diisopropylphenyl)acenaphthoimidazol-2-ylidene 7,9-dihydrocyclopentacenaphthylen-8-one