The synthesis and characterization of the two new oxa-aza macrocycles 10,13,16-trimethyl-1,4-dioxa-7,10,13,16,19-pentaazacyclohenicosane (Me3[21]aneN5O2) and 13,16,19-trimethyl-1,4,7-trioxa-10,13,16,19,22-pentaazacyclotetracosane (Me3[24]aneN5O3) are reported. Their basicity behavior in aqueous solution was investigated by means of potentiometric (298.1 +/- 0.1 K, I = 0. 1 5 mol dm-3) and NMR (H-1 and C-13) techniques. H-1-H-1 and H-1-C-13 two-dimensional NMR experiments permitted the unequivocal assignment of all H-1 and C-13 resonances. Both of them behave as tetraprotic bases under the experimental conditions used. The protonation mechanism of these macrocyclic ligands was determined by means of H-1 and C-13 NMR spectra at various pH values. The thermodynamic parameters for the formation of 1:1 copper(II) complexes of both macrocycles were determined by potentiometry and microcalorimetry at 298.1 +/- 0.1 K in 0. 1 5 mol dm-3 NaClO4. The involvement of all nitrogen donor atoms of the macrocycles in the coordination of the metal ion can be deduced, while the oxygens remain unbound. Furthermore mono- and diprotonated species are present at low pH. Crystal and molecular structures of the complexes [Cu(Me3[24]ancN5O3)] (ClO4)2 and [Cu(H2Me3[21]aneN5O2)Cl2] (ClO4)2.2H2O were determined by single-crystal X-ray analysis. In[Cu(Me3[24]ancN5O3)](ClO4)2 (space group P2(1), a = 8.371(2) angstrom, b = 11.781-(2) angstrom, c = 14.390(3) angstrom, beta = 96.90(2)-degrees, V = 1408.8(5) angstrom3, Z = 2, R = 0.047, R(w) = 0.045) the metal ion is bound by the five nitrogens of the macrocyclic ligand, in a distorted square-pyramidal coordination geometry. In [Cu-(H2Me3[21]aneN5O2)Cl2](ClO4)2.2H2O (space group P1BAR, a = 10.999(6) angstrom, b = 11.066(8) angstrom, c = 14.71(1) angstrom, a = 81.77(6), beta = 80.46(5), gamma = 61.68(5)-degrees, V = 1550(2) angstrom3, Z = 2, R = 0.052, R(w) = 0.047) the copper(II) ion is coordinated by the three methylated nitrogen atoms of the ligand and two chloride anions, while the uncoordinated nitrogens are protonated. The resulting coordination polyhedron can be described as a trigonal bipyramid distorted toward a square pyramid with elongated axial distances. The latter crystal structure can give information on the topological features of protonated complexes of polyaza macrocyclic ligands.