Mukhopadhyay Joy, Bhagat Srikant, Sahoo Subash C, Bharatam Prasad V
Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), Sector 67, S. A. S., Nagar, Punjab, 160062, India.
Department of Chemistry, Panjab University, Sector 14, Chandigarh, 160014, India.
Chempluschem. 2024 Aug;89(8):e202400150. doi: 10.1002/cplu.202400150. Epub 2024 Apr 24.
(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. A 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 C 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.
已知存在(NHC)→E配位相互作用,其中NHC为N-杂环卡宾,E为主族元素(B、C、N、Si、P)。最近有人提出,具有(NHC)→S配位化学的化合物也是可能的。这项工作报道了以苯并噻唑-2-亚基为配体的(NHC)→S-R配合物的量子化学分析和合成。密度泛函研究表明,(NHC)→S相互作用最好描述为配位相互作用。最初进行了合成尝试,以生成含有苯并噻唑取代基的二价硫化合物。使用三氟甲磺酸甲酯对这些硫化物中的杂环进行N-烷基化,导致生成具有(NHC)→S配位化学的所需产物,这涉及原位生成NHC环配体。甲基化前后观察到的碳核磁共振谱变化证实了C-S键的电子性质从共价性质转变为配位性质。