Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, 1-1 Minami-Osawa, Hachioji, Tokyo, 192-0397, Japan.
Chem Asian J. 2022 Mar 1;17(5):e202101329. doi: 10.1002/asia.202101329. Epub 2022 Jan 14.
Thiacrown ethers have attracted much attention in host-guest chemistry. Herein, we present the polymethylation reactions of unsaturated thiacrown ethers. Unsaturated thiacrown ethers having sulfonium groups were synthesized by the reaction of corresponding unsaturated thiacrown ethers with methyl triflate. The obtained methylated unsaturated thiacrown ethers were characterized by single-crystal X-ray diffraction analysis, UV absorption measurement, and cyclic voltammetry. The occupied and unoccupied molecular orbitals of the obtained methylated unsaturated thiacrown ethers are essentially localized respectively around the sulfide groups and the sulfonium groups. Furthermore, the results of electrostatic potential maps indicated that positive charges were distributed throughout the entire unsaturated thiacrown ether moieties.
硫代冠醚在主客体化学中引起了广泛关注。在此,我们介绍了不饱和硫代冠醚的聚合甲基化反应。通过相应的不饱和硫代冠醚与甲基三氟甲磺酸酯反应合成了带有𬭩基团的不饱和硫代冠醚。通过单晶 X 射线衍射分析、紫外吸收测量和循环伏安法对得到的甲基化不饱和硫代冠醚进行了表征。所得甲基化不饱和硫代冠醚的占据和非占据分子轨道分别基本上定域在硫醚基团和𬭩基团周围。此外,静电势图的结果表明,正电荷分布在整个不饱和硫代冠醚部分。