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Cover Picture: The Bis(ferrocenyl)phosphenium Ion Revisited (Angew. Chem. Int. Ed. 4/2020)
Author(s) -
Olaru Marian,
Mischin Alexandra,
Malaspina Lorraine A.,
Mebs Stefan,
Beckmann Jens
Publication year - 2020
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201915939
Subject(s) - chemistry , divalent , ion , lewis acids and bases , metal , carbene , stereochemistry , photochemistry , crystallography , catalysis , organic chemistry
Divalent phosphenium ions [R 2 P] + are highly reactive, Lewis superacidic carbene analogues requiring electronic stabilization, which is usually provided by donor atoms. In A. H. Cowley's bis(ferrocenyl)phosphenium ion (a species lacking any obvious donors), significant Fe ⋅⋅⋅ P interactions were found to have a stabilizing effect on the [Fc 2 P] + ion. S. Mebs, J. Beckmann, and co‐workers came to this conclusion in their Communication on page 1581 in which they examined the molecular and electronic structure of this species.

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