Hauer, SebastianReitz, JustusKoike, TaichiHansmann, Max M.Wolf, Robert2025-04-252025-04-252024-07-01http://hdl.handle.net/2003/4368410.17877/DE290R-25457Diazoalkenes readily react with tert-butylphosphaalkyne (tBuCP) and white phosphorus (P4) to afford novel phosphorus heterocycles, 3H-1,2,4-diazamonophospholes and 1,2,3,4-diazadiphospholes. Both species represent rare examples of neutral heterophospholes. The mechanism of formation and the electronic structures of these formal (3+2) cycloaddition products were analyzed computationally. The new phospholes form structurally diverse coordination compounds with transition metal and main group elements. Given the growing number of stable diazoalkenes, this work offers a straightforward route to neutral aza(di-)phospholes as a new ligand class.enAngewandte Chemie. International edition; 63(38)https://creativecommons.org/licenses/by/4.0/Diazoalkenesmain-group chemistryazaphospholestransition-metal chemistrynitrogen heterocycles540Cycloadditions of diazoalkenes with P4 and tBuCP: access to diazaphospholesArticle