An Ag(I) metallacycle obtained unexpectedly during the preparation of Pd(II) complexes of the bifunctional ligand 5-([2,2'-bipyridin]-5-yl)pyrimidine-2-amine () has been characterized using X-ray structure determination as a binuclear, metallacyclic species [Ag](SbF), where both the bipyridine and pyrimidine-N donors of are involved in coordination to the metal. The full coordination environment of the Ag(I) defines a case of highly irregular 4-coordination. In the crystal, the Ag-metallacycles assemble into one-dimensional supramolecular metalladynamers linked together by hydrogen-bonding interactions.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465845 | PMC |
http://dx.doi.org/10.3390/molecules26185719 | DOI Listing |
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