高分子同质性和协调网络中的结构灵活性,由杆构建块维持
Yassin H Andaloussi1, Andrey A Bezrukov1, Debobroto Sensharma1
1Department of Chemical Sciences, Bernal Institute, University of Limerick Limerick V94 T9PX Republic of Ireland xtal@ul.ie.
概括
研究人员开发了一种新的链接器,PyImPr,创建2D和3D协调网络Cd的异构体 (PyImPr) 2. 这些同位素在去除溶剂后表现出不可逆转的结构转变,为晶体工程提供了洞察力.
科学领域:
- 协调化学 协调化学
- 超分子化学 超分子化学
- 材料科学 材料科学 材料科学
背景情况:
- 双功能N-捐赠体碳酸盐链接器是形成协调网络与dia和sql拓学的关键.
- 这些网络基于MN2(CO2) 2分子构建块 (MBB).
研究的目的:
- 为了引入一种新的N-捐赠者碳酸盐链接剂,β-(3,4-pyridinedicarboximido) propionate (PyImPr).
- 使用PyImPr和研究协调网络异构体的形成.
- 探索由此产生的协调化合物的结构灵活性和转变.
主要方法:
- 使用PyImPr和酸合成 ((II) 协调复合物.
- 通过分层和溶热方法制备2D和3D超分子异构体.
- 单晶X射线衍射用于结构分析.
- 剑桥结构数据库 (CSD) 调查用于拓分析.
主要成果:
- 新的链接器PyImPr形成了Cd(PyImPr) 2,根据制备方法产生了不同的2D和3D超分子异构体.
- 这两种异构体共享相同的碳酸盐桥梁杆构建块 (RBB).
- 在去除溶剂后观察到不可逆转的开放到闭合的结构转变.
结论:
- 在PyImPr中的乙烯部分有助于结构灵活性,导致可逆转变.
- 该研究通过分析相关协调网络中的RBB拓,提供了对晶体工程的见解.
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