在多孔晶体中的偏好光反应,金属宏循环框架:PdII-介导的氨酸迁移超过 [2+2] 循环添加
Hirotaka Yonezawa1, Shohei Tashiro1, Takafumi Shiraogawa2
1Department of Chemistry, Graduate School of Science , The University of Tokyo , 7-3-1 Hongo , Bunkyo-ku, Tokyo 113-0033 , Japan.
Journal of the American Chemical Society
|November 9, 2018
概括
在金属宏循环框架 (MMF) 中,1,6-二烯经历光诱导的烯迁移,而不是典型的 [2+2] 循环添加. 这种狭窄的空间控制了反应,抑制了不必要的反应,并使选择性转换成为可能.
科学领域:
- 超分子化学
- 摄影化学
- 催化剂
背景情况:
- 提供精确的化学反应控制.
- 1,6-二烯在光辐射下通常会形成分子内 [2+2] 循环载荷管.
- 在多孔材料中的光化学反应中控制选择性是一个重大挑战.
研究的目的:
- 在金属宏观循环框架 (MMF) 中研究1,6-dienes的光化学行为.
- 证明货币市场基金能够改变反应路径并增强选择性.
- 在封闭的环境中阐明光诱导的烯迁移机制.
主要方法:
- 金属宏观循环框架 (MMF) 的合成和表征.
- 在MMF中使用1,6-二烯基基底的光照射实验.
- 频谱分析包括紫外线与扩散反射光谱.
- 用X射线衍射 (XRD) 进行结构测定.
- 用CASPT2计算进行质谱测量以获得机械学见解.
主要成果:
- 在MMF中,1,6-二烯主要经过光诱导的烯迁移.
- 在狭窄的空间中,分子内 [2+2] 循环添加被完全抑制.
- 提出了一种涉及光诱导Pd-Cl键解离的反应机制.
- 使用替代的基衍生物成功检查了基迁移的基板范围.
结论:
- 金属宏循环框架可以有效地控制光化学反应途径.
- 在MMF中封闭使选择性烯迁移成为可能,抑制竞争性循环添加反应.
- 这项研究提供了对多孔晶体材料光诱导变化的机理理解.
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