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Updated: Mar 12, 2026

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
Published on: July 27, 2022
Silver(I) and rhenium(I) metal complexes of a 2,2'-bipyridine-functionalized third-generation tris(pyrazolyl)methane
Radu F Semeniuc1, Daniel L Reger2, Mark D Smith2
1Department of Chemistry, Eastern Illinois University, Charleston, Illinois 61920, USA.
Abstract:
Heterotopic ligands offer the possibility of preparing polynuclear bimetallic complexes. Recent studies of heteroditopic ligands and their metal complexes have focused on novel supramolecular systems, biological activity, and the development of MRI contrast agents. The heteroditopic ligand Bipy-CH2-O-CH2-C(pz)3 (Bipy-L; Bipy is 2,2'-bipyridine and pz is pyrazolyl) reacts with AgBF4 to produce the coordination polymer catena-poly[[silver(I)-(μ-5-{[tris(pyrazol-1-yl)methoxy]methyl-κ2N,N'}-2,2'-bipyridine-κ2N,N')] diethyl ether hemisolvate], {[Ag(C22H20N8O)]BF4·0.5C4H10O}n, and with Re(CO)5Br to form the discrete compound bromidotricarbonyl(5-{[tris(pyrazol-1-yl)methoxy]methyl}-2,2'-bipyridine-κ2N,N')rhenium(I), [ReBr(C22H20N8O)(CO)3]. The silver(I) compound is a one-dimensional coordination polymer, built up by a κ2 coordination mode of the bipyridine group and a κ2-κ0 coordination mode of the -C(pz)3 donor set. In [ReBr(Bipy-L)(CO)3], the ligand coordinates only via the bipyridine end, leaving the -C(pz)3 donor set free for further coordination interactions.
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