bis-(2-methoxy-1-naphthyl)cyclopropenone | 65891-52-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: bis-(2-methoxy-1-naphthyl)cyclopropenone
• 英文别名: bis(2-methoxynaphthyl)cyclopropenone；Bis(2-methoxynaphth-1-yl)cyclopropenone；2,3-bis(2-methoxynaphthalen-1-yl)cycloprop-2-en-1-one
• CAS: 65891-52-3
• 化学式: C₂₅H₁₈O₃
• 分子量: 366.416
• InChiKey: WODBNBNNCMLHFW-UHFFFAOYSA-N

物化性质

• 熔点：
  162 °C(Solv: dichloromethane (75-09-2); hexane (110-54-3))
• 沸点：
  636.9±55.0 °C(Predicted)
• 密度：
  1.291±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  28
• 可旋转键数：
  4
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  bis-(2-methoxy-1-naphthyl)cyclopropenone 生成 bis(2-methoxy-1-naphthyl-1)acetylene
  参考文献：
  名称：

  双光子诱导的环丙烯酮的光脱羰反应。

  摘要：

  用800 nm脉冲的超快激光辐照环丙烯酮（1a-c）会通过光的非共振双光子吸收导致光脱羰反应。

  DOI：

  10.1039/b513248g
• 作为产物：
  描述：

  四氯环丙烯 、 2-萘甲醚 在 三氯化铝 、 水 作用下， 生成 bis-(2-methoxy-1-naphthyl)cyclopropenone
  参考文献：
  名称：

  Preparation of Diarylacetylenes via Cyclopropenones

  摘要：

  DOI：

  10.1055/s-1981-29417

文献信息

• Two-photon induced photodecarbonylation reaction of cyclopropenones
  作者：Nurtay K. Urdabayev、Andrei Poloukhtine、Vladimir V. Popik

  DOI：10.1039/b513248g

  日期：——

  Irradiation of cyclopropenones (1a-c) with 800 nm pulses of ultrafast laser results in a photodecarbonylation reaction via nonresonant two-photon absorption of light.

  用800 nm脉冲的超快激光辐照环丙烯酮（1a-c）会通过光的非共振双光子吸收导致光脱羰反应。
• Preparation of Diarylacetylenes via Cyclopropenones
  作者：D. H. Wadsworth、B. A. Donatelli

  DOI：10.1055/s-1981-29417

  日期：——
• WADSWORTH D. H.; DONATELLI B. A., SYNTHESIS, 1981, NO 4, 285-286
  作者：WADSWORTH D. H.、 DONATELLI B. A.

  DOI：——

  日期：——
• Photonic Amplification by a Singlet-State Quantum Chain Reaction in the Photodecarbonylation of Crystalline Diarylcyclopropenones
  作者：Gregory Kuzmanich、Matthew N. Gard、Miguel A. Garcia-Garibay

  DOI：10.1021/ja9043449

  日期：2009.8.19

  The photochemical decarbonylation of diphenylcyclopropenone (DPCP) to diphenylacetylene (DPA) proceeds with remarkable efficiency both in solution and in the crystalline solid state. It had been previously shown that excitation to the second electronic excited state (S-2) of DPCP in solution proceeds within ca. 200 fs by an adiabatic ring-opening pathway to yield the S-2 state of DPA, which has a lifetime of ca. 8 ps before undergoing internal conversion to S-1(Takeuchi, S.; Tahara, T. J. Chem. Phys. 2004, 120, 4768). More recently, we showed that reactions by excitation to S-2 in crystalline solids proceed by a quantum chain process where the excited photoproducts transfer energy to neighboring molecules of unreacted starting material, which are able to propagate the chain. Quantum yields in crystalline suspensions revealed values of Phi(DPCP) = 3.3 +/- 0.3. To explore the generality of this reaction, and recognizing its potential as a photonic amplification system, we have synthesized nine crystalline diarylcyclopropenone derivatives with phenyl, biphenyl, naphthyl, and anthryl substituents. To quantity the efficiency of the quantum chain in the crystalline state, we determined the quantum yields of reaction for all of these compounds both in solution and in nanocrystalline suspensions. While the quantum yields of decarbonylation in solution vary from Phi = 0.0 to 1.0, seven of the nine new structures display quantum yields of reaction in the solid that are above 1. The chemical amplification that results from efficient energy transfer in the solid state, analyzed in terms of the quantum yields determined in the solid state and in solution (Phi(cryst)/Phi(soln)), reveals quantum chain amplification factors that range from 3.2 to 11.0. The remarkable mechanical response of the solid-to-solid reaction previously documented with macroscopic crystals, where large single-crystalline specimens turn into fine powders, was investigated at the nanometer scale. Experiments with dry crystals of DPCP analyzed by atomic force microscopy showed the formation of DPA in the form of isolated crystalline specimens ca. 35 nm in size.