配位复合体
卡宾
配体(生物化学)
化学
三氟甲磺酸
戒指(化学)
化学位移
烷基化
苯并噻唑
组合化学
量子化学
立体化学
有机化学
超分子化学
晶体结构
催化作用
金属
物理化学
生物化学
受体
作者
Jayanta Mukhopadhyay,Sunita Bhagat,Subash Chandra Sahoo,Prasad V. Bharatam
标识
DOI:10.1002/cplu.202400150
摘要
(NHC)→E coordination interactions were known where NHC is an N‐heterocyclic carbene, and E is a main group element (B, C, N, Si, P). Recently, it was suggested that compounds with (NHC)→S coordination chemistry are also possible. This work reports quantum chemical analysis and synthesis of (NHC)→S‐R(+) complexes in which benzothiazol‐2‐ylidene acts as a ligand. Density functional study established that (NHC)→S interaction can best be described as a coordination interaction. Synthetic efforts were made, initially, to generate divalent sulfur compounds containing benzothiazole substituents. N‐alkylation of the heterocyclic ring in these sulfides using methyl triflate led to the generation of the desired products with (NHC)→S coordination chemistry, which involves the in situ generation of NHC ring ligands. The observed changes in the 13C NMR spectra, before and after methylation, confirmed the change in the electronic character of the C‐S bond from a covalent character to a coordination character.
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