The solution chemistry and solid state structures of the Co­(II), Fe­(II), and Ni­(II) complexes of N,N′-bis­(imidazole-2-ylmethyl)-4,10-diaza-15-crown-5 (HINO) are reported. The Co­(II) and Ni­(II) complexes of HINO are the first examples of paraCEST agents (paramagnetic chemical exchange saturation transfer) that feature exchangeable imidazole NH protons. The crystal structures of Co­(HINO)­CoCl4·H2O and Fe­(HINO)­(CF3SO3)2 have the metal ions coordinated to four nitrogen and three oxygen donor atoms of the macrocyclic ligand in a distorted pentagonal bipyramidal geometry. In Ni­(HINO)­(CF3SO3)2, the nickel ion is bound to only two of the three ether oxygens and three nitrogens to produce a complex with a distorted octahedral geometry. The 1H NMR spectra of the three paramagnetic complexes show resonances characteristic of effective C 2 symmetry in solution. CEST peaks attributed to the imidazole NH proton of the pendent group are observed at 32 and 55 ppm away from bulk water for Co­(HINO)2+ and Ni­(HINO)2+, respectively, on a 11.7 or 9.4 T NMR spectrometer. For both complexes, an optimal CEST effect was observed at pH 7.2, and the rate constant for proton exchange under these conditions was 1.0 × 103 s–1. Fe­(HINO)2+ did not produce a CEST peak due to oxidation of the complex in water at neutral pH. The CEST peak of Co­(HINO)2+ or Ni­(HINO)2+ is observed in the presence of human serum albumin (HSA). These complexes show enhanced kinetic inertness toward dissociation in acid or in the presence of HSA in comparison to analogous complexes with amide pendent groups.