由内在平面压缩驱动的二维金属有机协调网络的结构转换
Jun Liu1, Tao Lin, Ziliang Shi
1Shanghai Key Laboratory of Functional Materials Chemistry and Institute of Fine Chemicals, East China University of Science and Technology, Meilong Road 130, Shanghai, China.
Journal of the American Chemical Society
|October 12, 2011
概括
研究人员探索了1,3,5-三二和铜如何在黄金表面形成网络. 增加分子密度驱动结构变化和改变协调,揭示基于压缩压力的相位图.
科学领域:
- 表面科学是一门学科.
- 材料化学 材料化学
- 纳米技术纳米技术
背景情况:
- 金属有机框架 (MOF) 的自组装对于先进材料至关重要.
- 了解表面的协调行为,为分子设计提供了信息.
- 黄金表面是研究表面现象的常见平台.
研究的目的:
- 调查1,3,5-三二二与铜在Au111表面上的协调组合.
- 描述因分子密度增加而引起的结构转变.
- 确定机内压缩压力在自组装中的作用.
主要方法:
- 在超高真空 (UHV) 条件下扫描道显微镜 (STM).
- 分子自我组装和网络形成的分析.
- 不同阶段的定量结构分析.
主要成果:
- 形成一个二维蜂巢金属有机网络.
- 多步骤,不可逆转的结构转变为五角形,形,形和三角形网络,分子密度增加.
- 在Cu-pyridyl协调中从双重结合转变为三重结合.
- 结构和协调变化归因于平面内压缩压力.
结论:
- 平面内压缩压力决定了自组装路径和由此产生的网络结构.
- 构建了一个相位图,说明网络结构与平面内压缩的对比.
- 这项研究提供了通过外部刺激来控制MOF结构的见解.
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