奇拉结合珊瑚
Melissa Ball1, Brandon Fowler1, Panpan Li2,1
1†Department of Chemistry, Columbia University, New York, New York 10027, United States.
Journal of the American Chemical Society
|July 31, 2015
概括
研究人员开发了具有交替电子捐赠者 (bithiophene) 和受体 (perylene diimide) 的新型紧张的结合型宏循环. 这些分子表现出独特的立体同位素和"分子内逆转"机制.
科学领域:
- 有机化学
- 超分子化学
- 材料科学
背景情况:
- 结合的宏循环在超分子化学中至关重要.
- 设计具有特定空腔和电子特性的宏循环仍然是一个挑战.
研究的目的:
- 引入一个新的设计动机,应力,结合的宏循环.
- 用交替的电子捐赠和接受单位创建宏循环.
- 研究这些新型宏观循环的立体化学和动力学.
主要方法:
- 使用比西奥芬 (捐赠者) 和二胺衍生物 (接受者) 合成具有A-B-A-B模式的宏循环.
- 用于分离立体同位素的状高性能液体染色学 (HPLC).
- 光谱分析和密度函数理论 (DFT) 的计算.
主要成果:
- 形成由硫原子和二胺 π 面成的持续圆形腔.
- 存在性和无性形式,其中有三个立体同位素成功分离.
- 对立体同位素相互转换的"分子内翻转"机制的观察.
- 广泛的可见吸收光谱和由光诱导的电子转移从比西奥芬到二胺.
结论:
- 新的设计模式使复杂的,紧张的,结合的宏观循环可以构建.
- 已发现的"分子内翻身"机制为宏观周期动态提供了洞察力.
- 这些宏观循环由于分子内电子转移而具有有趣的光物理性质.
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