Amidinium⋯phosphonate charge assisted hydrogen-bonded organic frameworks: influence of diverse intermolecular interactions

被引:2
作者
Almuhana, Asia R. Y. [1 ,2 ]
Griffin, Sarah L. [2 ]
Champness, Neil R. [2 ]
机构
[1] King Faisal Univ, PO 380, Al Hasa 31982, Saudi Arabia
[2] Univ Birmingham, Sch Chem, Birmingham, England
基金
英国工程与自然科学研究理事会;
关键词
NAPHTHALENE DIIMIDE; MOLECULAR NETWORKS; PHOSPHONATE; STABILITY; CHEMISTRY; PHOSPHATE;
D O I
10.1039/d4ce00479e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis of charge assisted amidinium & ctdot;phosphonate hydrogen-bonded organic frameworks (HOFs) is reported. Two tectons, with either a biphenyl or naphthalene diimide backbone, were combined with bis-amidinium salts to afford HOF1 and HOF2, respectively. Whereas HOF1 formed rapidly, typically within two days of mixing, HOF2 proved more challenging to synthesise. Interestingly, the presence of sunlight facilitated the rapid formation of HOF2 within a few hours. Although crystals of tectons 1H4 or 2Et4 exhibited densely packed structures, combination of the corresponding phosphonate bases with bis-amidinium cations, through amidinium & ctdot;phosphonate interactions, gave open framework materials. The HOFs formed through this approach exhibited notable stability limitations, including a propensity for phase transformations or structural collapse upon solvent removal. Charge assisted amidinium & ctdot;phosphonate hydrogen-bonded organic frameworks (HOFs) are reported displaying a complex array of intermolecular interactions.
引用
收藏
页码:4643 / 4648
页数:6
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