posted on 2014-12-22, 00:00authored byAsif Noor, Gregory
S. Huff, Sreedhar V. Kumar, James
E. M. Lewis, Brett M. Paterson, Christine Schieber, Paul S. Donnelly, Heather J. L. Brooks, Keith C. Gordon, Stephen C. Moratti, James D. Crowley
There is considerable interest in
the development of bifunctional ligand scaffolds for the group 7 metals
due to potential biological applications. Building on our recent work
in the development of “click” ligands and macrocycles,
we show that a CuAAC “click” approach can be exploited
for the synthesis of a small family of bioconjugated tridentate pyridyl-1,2,3-triazole
macrocycles. These bioconjugated tridentate macrocycles form stable
[Re(CO)3]+ complexes, and this could facilitate
the development of [M(CO)3]+ (M = Mn, Tc, Re)
targeted agents. The parent macrocycle, bioconjugates, and [Re(CO)3]+ complexes were characterized by elemental analysis
and HR-ESI-MS, 1H and 13C NMR, and IR spectroscopy,
and the molecular structures of the alcohol-functionalized macrocycle
and two of the Re(I) complexes were confirmed by X-ray crystallography.
The electronic structure of the parent [Re(CO)3]+ macrocycle complex was examined using UV–vis, Raman, and
emission spectroscopy and density functional theory calculations.
The complex exhibited intense absorptions in the UV region which were
modeled using time-dependent density functional theory (TD-DFT). The
calculations suggest that the lower energy part of the absorption
band is MLCT in nature and additional higher energy π–π*
transitions are present. The complex was weakly emissive at room temperature
in methanol with a quantum yield of 5.1 × 10–3 and correspondingly short excited state lifetime (τ ≈
20 ns). The family of macrocycles and the corresponding Re(I) complexes
were tested for antimicrobial activity in vitro against
both Gram positive (Staphylococcus aureus) and Gram negative (Escherichia coli) microorganisms. Agar-based disk diffusion assays indicated that
two of the Re(I) complexes displayed antimicrobial activity but the
minimum inhibitory concentrations (MIC) for these compounds proved
to be extremely modest (MIC > 256 μg/mL).