Pyrazolylpropanoate Complexes of Palladium(II) Chloride

Affiliation
Department of Chemistry and Biochemistry James Madison University MSC 4501 Harrisonburg Virginia 22807 United States
Johnson, Ryan;
GND
1276149425
ORCID
0000-0002-4660-1691
Affiliation
Institut für Anorganische und Analytische Chemie Friedrich-Schiller-Universität Jena Humboldtstr. 8 07743 Jena Germany
Liebing, Phil;
ORCID
0009-0000-4603-8977
Affiliation
Department of Chemistry and Biochemistry James Madison University MSC 4501 Harrisonburg Virginia 22807 United States
Musikanth, Daniel P.;
Affiliation
Department of Chemistry and Biochemistry James Madison University MSC 4501 Harrisonburg Virginia 22807 United States
Regitz, Stuart A.;
ORCID
0000-0003-3485-2941
Affiliation
Department of Chemistry and Biochemistry James Madison University MSC 4501 Harrisonburg Virginia 22807 United States
Amenta, Donna S.;
ORCID
0000-0001-8296-2331
Affiliation
Institut für Physik der Otto-von-Guericke-Universität Magdeburg Universitätsplatz 2 39106 Magdeburg Germany
Goldhahn, Rüdiger;
ORCID
0000-0001-5209-0018
Affiliation
Institut für Physik der Otto-von-Guericke-Universität Magdeburg Universitätsplatz 2 39106 Magdeburg Germany
Edelmann, Frank T.;
ORCID
0000-0002-1766-4298
Affiliation
Department of Chemistry and Biochemistry James Madison University MSC 4501 Harrisonburg Virginia 22807 United States
Gilje, John W.

Abstract The syntheses of the new ligands 3‐(pyrazol‐1‐yl)methylpropanoate (L1) and 3‐(2,4‐dimethylpyrazol‐1‐yl)methylpropanoate (L2) and their complexation with palladium(II) have been investigated. In our hands L1 is best prepared by a Michael addition catalyzed by Cs 2 CO 3 and L2 by a catalyst‐ and solvent‐free reaction. Both L1 and L2 react with PdCl 2 (COD) to produce trans‐ PdCl 2 (L1) 2 ( 3 ) and trans‐ PdCl 2 (L2) 2 ( 4 ) respectively. The crystal structures of both new complexes have been determined. An isomerization has been observed when complex 4 is dissolved in CDCl 3 or CD 3 CN. Kinetic data indicate that this is an equilibrium that is first order in both directions. We suggest this may be due to the isomerization of the trans‐ to the cis ‐isomer. Their ease of preparation in nearly quantitative yields make the new ligands L1 and L2 potentially useful for further studies.

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