Journal article
Finding a soft spot for vanadium: a P-bound OCP ligand.
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Grant LN
Department of Chemistry, University of Pennsylvania, Philadelphia, PA 19104, USA. mindiola@sas.upenn.edu.
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Krzystek J
National High Magnetic Field Laboratory, Florida State University, Tallahassee, FL 32310, USA.
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Pinter B
Department of Chemistry, Universidad Técnica Federico Santa María, Valparaíso, 2390123, Chile.
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Telser J
Department of Biological, Physical and Health Sciences, Roosevelt University, Chicago, IL 60605, USA.
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Grützmacher H
Department of Chemistry and Applied Biosciences, ETH Zürich, Vladimir-Prelog Weg1, Hönggerberg, Zürich 8093, Switzerland.
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Mindiola DJ
Department of Chemistry, University of Pennsylvania, Philadelphia, PA 19104, USA. mindiola@sas.upenn.edu.
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Published in:
- Chemical communications (Cambridge, England). - 2019
English
Transmetallation studies with the phosphaethynolate ion, [OCP]-, have largely resulted in coordination according to classical Lewis acid-base theory. That is, for harder early transition metal ions, O-bound coordination has been observed, whereas in the case of softer late transition metal ions, P-bound coordination predominates. Herein, we report the use of a V(iii) complex, namely [(nacnac)VCl(OAr)] (1) (nacnac- = [ArNC(CH3)]2CH; Ar = 2,6-iPr2C6H3), to transmetallate [OCP]- and bind via the P-atom as [(nacnac)V(OAr)(PCO)] (2), the first example of a 3d early transition metal that binds [OCP]-via the P-atom. Full characterization studies of this molecule including HFEPR spectroscopy, SQuID measurements, and theoretical studies are presented.
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Language
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Open access status
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closed
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Identifiers
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Persistent URL
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https://sonar.ch/global/documents/278181
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