Hierlmeier G, Coburger P, Scott DJ, Maier TM, Pelties S, Wolf R, Pividori DM, Meyer K, van Leest NP, de Bruin B (2021)
Publication Type: Journal article
Publication year: 2021
Reactions of di-tert-butyldiphosphatetrahedrane (1) with cycloocta-1,5-diene- or anthracene-stabilised metalate anions of iron and cobalt consistently afford complexes of the rarely encountered 1,2-diphosphacyclobutadiene ligand, which have previously been very challenging synthetic targets. The subsequent reactivity of 1,2-diphosphacyclobutadiene cobaltates toward various electrophiles has also been investigated and is compared to reactions of related 1,3-diphosphacyclobutadiene complexes. The results highlight the distinct reactivity of such isomeric species, showing that the 1,2-isomers can act as precursors for previously unknown triphospholium ligands. The electronic structures of the new complexes were investigated by several methods, including NMR, EPR and Mößbauer spectroscopies as well as quantum chemical calculations.
APA:
Hierlmeier, G., Coburger, P., Scott, D.J., Maier, T.M., Pelties, S., Wolf, R.,... de Bruin, B. (2021). Di-tert-butyldiphosphatetrahedrane as a Source of 1,2-Diphosphacyclobutadiene Ligands. Chemistry - A European Journal. https://doi.org/10.1002/chem.202102335
MLA:
Hierlmeier, Gabriele, et al. "Di-tert-butyldiphosphatetrahedrane as a Source of 1,2-Diphosphacyclobutadiene Ligands." Chemistry - A European Journal (2021).
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