期刊:Organometallics [American Chemical Society] 日期:2025-08-27卷期号:44 (17): 1876-1880
标识
DOI:10.1021/acs.organomet.5c00228
摘要
A Lewis/Brønsted acid-promoted intramolecular cyclization of diarylselenoethers bearing formyl groups afforded novel selenoxanthylium salts in good yield. The electronic structures of these selenoxanthylium salts were determined using NMR and UV–vis absorption spectroscopy techniques as well as DFT calculations. The obtained results clearly imply effective conjugation of the π-electrons throughout the entire fused selenium-containing heterocyclic framework.