A new bifunctional amino acid chelator targeting the glucose transporter

The coupling reactions of D-glucosamine, 1,3,4,6-tetra-O-acetylglucosamine, and 4-aminophenyl-galactopyranosine with N,N-bis(quinolinoyl) aminovaleric acid (L1) provided a series of conjugates containing a potentially tridentate donor group terminus linked to a sugar moiety, L2', L2 and L3, respectively. Reactions of the ligands with [NEt4](2)[Re(CO)(3)Br-3] in refluxing methanol provided the rhenium complexes [Re(CO3)(L1)]Br (ReL1), [Re(CO)(3)(L2)]Br (ReL2), [Re(CO)(3)(L2')]Br (ReL2') and [Re(CO)(3)(L3)]Br (ReL3). The ligands and complexes were characterized by elemental analyses, H-1 and C-13 NMR, mass spectroscopy and, in the case of L1 and ReL1, by X-ray crystallography. The rhenium complexes exhibit fluorescence emissions with long lifetimes, large Stokes shifts, and moderate quantum yields. (c) 2005 Elsevier B.V. All rights reserved.