Self-assembly Behavior of Interlocked Helical Supramolecule of Cyclodextrin Modified by 2-Furanmethanethiol

doi:10.6023/A12121070

Abstract

The mono-modified β-cyclodextrin, mono-[6-S-6-(2-methylfuran)]-β-cyclodextrin, was synthesized by the substituting 2-furanmethanethiol for toluenesulfonyl group at the primary rim of β-cyclodextrin. Its self-assembly behavior was measured in both solution and the solid state by X-ray crystallography and ¹H NMR spectroscopy. In the crystal structure, the complex, C₄₇H₁₀₆O₅₁S, crystallizes in the orthorhombic space group P212121. The furan group is located above the primary rim of β-cyclodextrin and stretches slantwise along the side wall of β-cyclodextrin with the dihedral angle of 104.4° between furan ring and the plane of glycosidic oxygen atoms O(4) of β-cyclodextrin. The furan group is inserted deeply into the hydrophobic cavity of the adjacent β-cyclodextrin from the second hydroxyl rim and makes an angle of 67.6° with the O(4) atoms plane of the adjacent β-cyclodextrin. The dihedral angle of the O(4) atoms plane between the adjacent β-cyclodextrin is 38.4°. The consequence is the formation of an interlocked helical columnar superstructure formed by the self-assembly of the complex molecules in which the modified cyclodextrins are stacked along a two-fold screw axis parallel to the a crystal axis. Thus each molecule behaves both a host and a guest molecule. And the position and orientation of the furan ring within the cyclodextrin cavity is determined by host guest interactions which include the van der Waals contacts and hydrogen bonds between the furan ring and cyclodextrin. The interlocked helical column is stabilized by the hydrogen bonds formed between the primary and secondary hydroxyl groups of the adjacent cyclodextrin or through intervening water molecules. Furthermore, ROESY data indicate that the furan ring is included in the cyclodextrin cavity, which is in accordance with the conformation of the solid state structure. ¹H NMR concentration dependent studies show that the complex molecule forms a dimer at concentrations of >10^-4 mol·L^-1. And the effective binding constant K and the aggregation number n were calculated to be 450 mol^-1·L and 1.9, respectively.

Key words: modified cyclodextrin, 2-furanmethanethiol, self-assembly, crystal structure, supramolecule

Cite this article

Han Cong, Xu Zhe, Diao Chunhua, Chen Xin, Liu Jing, Guo Minjie, Fan Zhi. Self-assembly Behavior of Interlocked Helical Supramolecule of Cyclodextrin Modified by 2-Furanmethanethiol[J]. Acta Chimica Sinica, 2013, 71(03): 439-442.

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