Lanthanide(III) complexes have been prepared with [L-1](-) [the tetradentate chelating ligand bis(3-(2-pyridyl)pyrazolyl)dihydroborate], [L-2](-) [the tetradentate chelating ligand bis{3-(2-pyrazinyl)pyrazolyl}dihydroborate], [L-3](-) [the hexadentate chelating ligand bis[3-{6'-(2,2'-bipyridyl)}pyrazol-1-yl]dihydroborate], and [L-4](2-) [the 12-dentate compartmental ligand hexakis{3-(2-pyridyl)pyrazol-1-yl}diboran(IV)ate, which has two hexadentate tris(pyrazolyl)borate-based cavities linked "back-to-back" by a B-B bond]. [Ln(L-1)(2)(NO)(3)] are 10-coordinate with two tetradentate N-donor ligands and one bidentate nitrate. [Ln(L-2)(2)(NO)(3)] have 10-coordinate structures similar to those of the [L-1](-) complexes except that the coordinated N-1 of the pyrazine rings is not such a good donor as the pyridine rings in the [L-1](-) complexes, leading to marked lengthening of these Ln-N bonds. [Ln(L-3)(NO3)(2)] are also 10-coordinate from one hexadentate chelating ligand which has a pseudoequatorial coordination mode and two pseudoaxial bidentate nitrate ligands; the hexadentate ligand has a shallow helical twist to prevent steric interference between its ends. Finally [{Ln(NO3)(2)(L-4)] are dinuclear, with each metal center being 10-coordinate from a tripodal hexadentate ligand cavity and two bidentate nitrates. Five complexes were structurally characterized: [Tb(L-2)(2)(NO3)].dmf is monoclinic (P2(1)/c) with a = 14.881(3) Angstrom, b = 15.5199(12) Angstrom, c = 15.845(2) Angstrom, beta = 92.387(12)degrees, and Z = 4. [Gd(L-2)(2)(NO3)].dmf is monoclinic (P2(1)/c) with a = 14.926(2) Angstrom, b = 15.465(2) Angstrom, c 15.878(2) Angstrom, beta = 92.698(11)degrees, and Z = 4. [Eu(L-3)(NO3)(2)].dmf.0.5Et(2)O is triclinic (P (1) over bar) with a 10.020(3) Angstrom, b = 13.036(3) Angstrom, c = 14.740(3) Angstrom, alpha = 70.114(14)degrees, beta = 71.55(2)degrees, gamma = 79.66(2)degrees, and Z = 2. [{La(NO3)(dmf)(2)}(2)(L-4)](NO3)(2).dmf is orthorhombic (Pbca) with a = 18.813(2) Angstrom, b = 15.241(2) Angstrom, c = 27.322(2), and Z = 4. [{Gd(NO3)(2)}(2)(L-4)].2.4dmf is tetragonal (P4(2)/n) with a = 16.622(6), c = 24.19(5) Angstrom, and Z = 4. Detailed photophysical studies have been performed on the free ligands and their complexes with Gd(III), Eu(III), and Tb(III) in several solvents. The results show a wide range in the emission properties of the complexes which can be rationalized in terms of subtle variations in the steric and electronic properties of the ligands. In particular the dinuclear Tb(III) complex of [L-4](2-) has an emission quantum yield of ca. 0.5 in D2O and MeOD.