| 1329428-81-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• CAS: 1329428-81-0
• 化学式: C₄H₆O
• 分子量: 71.0831
• InChiKey: JEZQVLUHIIQXMF-UICOGKGYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  5
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  以 氩 为溶剂， 生成
  参考文献：
  名称：

  Cyclopropylhydroxycarbene

  摘要：

  Cyclopropylhydroxycarbene was generated by high-vacuum flash pyrolysis of cyclopropylglyoxylic acid at 960 degrees C. The pyrolysis products were matrix-isolated in solid Ar at 11 K and characterized by means of IR spectroscopy. Upon photolysis, the carbene undergoes ring expansion, thereby paralleling the reactivity of other known cyclopropylcarbenes. The ring expansion product, cyclobut-1-en-1-ol, was characterized for the first time. Matrix-isolated cyclopropylhydroxycarbene undergoes [1,2]H-tunneling through a barrier of approximately 30 kcal . mol(-1), yielding cyclopropylcarboxaldehyde. The cyclopropyl moiety acts as a pi-donor and increases the half-life by almost a factor of 10 compared to parent hydroxymethylene, resulting in a temperature-independent half-life of tau = 17.8 h at both 11 and 20 K. Hence, cyclopropylhydroxycarbene is the first hydroxycarbene that differs from other members of its family by a significantly prolonged half-life. As expected, the O-deuterated analogue does not show tunneling. Our findings are rationalized by accurate CCSD(T)/cc-pVnZ (n = D, T)//M06-2X/6-311++G(d,p) computations. The half-life of cyclopropylhydroxycarbene was verified by tunneling computations employing the Wentzel-Kramers-Brillouin formalism. By comparison with other experimentally known hydroxycarbenes, we determine the electronic donor capabilities of the carbenes' substituents to be a dominant factor governing their half-lives.

  DOI：

  10.1021/ja204507j
• 作为产物：
  描述：

  O-d-cyclopropylglyoxylic acid 960.0 ℃ 、0.0 Pa 条件下， 生成 、
  参考文献：
  名称：

  Cyclopropylhydroxycarbene

  摘要：

  Cyclopropylhydroxycarbene was generated by high-vacuum flash pyrolysis of cyclopropylglyoxylic acid at 960 degrees C. The pyrolysis products were matrix-isolated in solid Ar at 11 K and characterized by means of IR spectroscopy. Upon photolysis, the carbene undergoes ring expansion, thereby paralleling the reactivity of other known cyclopropylcarbenes. The ring expansion product, cyclobut-1-en-1-ol, was characterized for the first time. Matrix-isolated cyclopropylhydroxycarbene undergoes [1,2]H-tunneling through a barrier of approximately 30 kcal . mol(-1), yielding cyclopropylcarboxaldehyde. The cyclopropyl moiety acts as a pi-donor and increases the half-life by almost a factor of 10 compared to parent hydroxymethylene, resulting in a temperature-independent half-life of tau = 17.8 h at both 11 and 20 K. Hence, cyclopropylhydroxycarbene is the first hydroxycarbene that differs from other members of its family by a significantly prolonged half-life. As expected, the O-deuterated analogue does not show tunneling. Our findings are rationalized by accurate CCSD(T)/cc-pVnZ (n = D, T)//M06-2X/6-311++G(d,p) computations. The half-life of cyclopropylhydroxycarbene was verified by tunneling computations employing the Wentzel-Kramers-Brillouin formalism. By comparison with other experimentally known hydroxycarbenes, we determine the electronic donor capabilities of the carbenes' substituents to be a dominant factor governing their half-lives.

  DOI：

  10.1021/ja204507j