Cycloadditions of diazoalkenes with P4 and tBuCP: access to diazaphospholes
dc.contributor.author | Hauer, Sebastian | |
dc.contributor.author | Reitz, Justus | |
dc.contributor.author | Koike, Taichi | |
dc.contributor.author | Hansmann, Max M. | |
dc.contributor.author | Wolf, Robert | |
dc.date.accessioned | 2025-04-25T14:12:00Z | |
dc.date.available | 2025-04-25T14:12:00Z | |
dc.date.issued | 2024-07-01 | |
dc.description.abstract | Diazoalkenes 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. | en |
dc.identifier.uri | http://hdl.handle.net/2003/43684 | |
dc.identifier.uri | http://dx.doi.org/10.17877/DE290R-25457 | |
dc.language.iso | en | |
dc.relation.ispartofseries | Angewandte Chemie. International edition; 63(38) | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Diazoalkenes | en |
dc.subject | main-group chemistry | en |
dc.subject | azaphospholes | en |
dc.subject | transition-metal chemistry | en |
dc.subject | nitrogen heterocycles | en |
dc.subject.ddc | 540 | |
dc.title | Cycloadditions of diazoalkenes with P4 and tBuCP: access to diazaphospholes | en |
dc.type | Text | |
dc.type.publicationtype | Article | |
dcterms.accessRights | open access | |
eldorado.openaire.projectidentifier | info:eu-repo/grantAgreement/EC/HE/101077332/EU/NAME/CC-CHARGED | |
eldorado.secondarypublication | true | |
eldorado.secondarypublication.primarycitation | S. Hauer, J. Reitz, T. Koike, M. M. Hansmann, R. Wolf, Angew. Chem. Int. Ed. 2024, 63, e202410107. https://doi.org/10.1002/anie.202410107 | |
eldorado.secondarypublication.primaryidentifier | https://doi.org/10.1002/anie.202410107 |
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