The structure of the solvated bismuth(III) ion in aqueous, dimethyl sulfoxide, N, N'-dimethylpropylene urea, and N,N-dimethylthioformamide solution has been studied by means of EXAFS and large-angle X-ray scattering (LAXS). The crystal structures of the solid compounds octakis(dimethyl sulfoxide)bismuth(III) perchlorate, [Bi(OS(CH3)(2))(8)](ClO4)(3), hexakis(N,N'-dimethylpropyleneurea)bismuth(III) perchlorate, [Bi(OCN2(CH2)(3)(CH3)(2))(6)]-(ClO4)(3), and nonaaquabismuth(III) trifluoromethanesulfonate, [Bi(H2O)(9)](CF3SO3)(3) (redetermination), have been determined. The aqueous solutions must be strongly acidic, since the hydrated bismuth(III) ion starts to hydrolyze into Bi6O4(OH)(4)(6+) complexes already at an excess of strong acid at 1.0 mol.dm(-3). For very acidic aqueous perchlorate solutions, the LAXS and EXAFS data gave a satisfactory fit for eight-coordination of the bismuth-(III) ion, with a mean Bi-O bond distance of 2.41(1) Angstrom. The crystal structure of octakis(dimethyl sulfoxide)bismuth(III) perchlorate shows that the bismuth(III) ion coordinates eight dimethyl sulfoxide molecules via the oxygen atoms in a distorted square antiprismatic configuration. The mean Bi-O bond distance is 2.43 Angstrom and the mean Bi ... S distance 3.56 Angstrom. For the dimethyl sulfoxide solution, the corresponding mean distances were found to be 2.411(6) and 3.535(12) Angstrom. The N,N'-dimethylpropyleneurea-solvated bismuth(III) ion is octahedrally coordinated in both solid state and solution with the Bi-O bond distances of 2.324(5) and 2.322(3) Angstrom, respectively. The bismuth(III) ion is six-coordinated in the sulfur donor solvent N,N-dimethylthioformamide with a mean Bi-S bond distance of 2.794(8) Angstrom. A comparison with the structure of the solvated lanthanum(III) ion shows that the bismuth(III) ion is smaller for all coordination numbers. New effective ionic radii for the bismuth(III) ion in different coordination numbers are proposed, based on results in this study and in the literature.