Research Article

Palladium(II) Complexes Containing Mixed Nitrogen-Sulphur Donor Ligands: Interaction of [Pd(Methionine Methyl Ester)(H2O)2]2+ with Biorelevant Ligands

Table 1

Formation constants for complexes of [Pd(MME)(H2O)2]2+ with amino acids at 25°C and 0.1 M ionic strength.

SystemMLHa

Pd(MME)-OH10−1−5.29 (0.01)5.29
10−2−12.96 (0.05)7.67
20−1−2.46 (0.07)

Glycine0119.60 (0.01)9.60
01211.93 (0.02)2.33
11010.40 (0.03)

Alanine0119.69 (0.01)9.69
01211.89 (0.02)2.20
11010.33 (0.05)

Proline01110.52 (0.01)10.52
01212.03 (0.04)1.51
11010.79 (0.02)

-Phenyl alanine0119.12 (0.01)9.12
01211.01 (0.02)1.89
1109.87 (0.04)

Imidazole0117.04 (0.01)7.04
1108.41 (0.04)
12015.93 (0.06)

Lysine01110.51 (0.00)10.51
01219.71 (0.01)9.20
11011.15 (0.01)10.17
11120.29 (0.07)9.14

Methionine0118.76 (0.00)8.76
1109.05 (0.04)

Histamine0119.88 (0.01)9.88
01215.30 (0.01)5.42
11012.54 (0.04)3.43
11115.97 (0.1)3.43

Histidine0119.52 (0.01)9.52
01215.81 (0.02)6.29
11014.26 (0.07)
11118.30 (0.09)4.0

aM, L, and H are the stoichiometric coefficients corresponding to Pd(MME), amino acid, and H+, respectively; the coefficient −1 refers to a proton loss; b of Pd(MME)-amino acids complexes, standard deviations are given in parentheses; sum of square of residuals is less than ; cthe p of the ligands and the protonated complexes.