Copper is an important micronutrient, and it is present in some protein structures, as well as participate in several important biological processes. Due to its importance, some ligands are used and studied like carriers of copper in the biological systems. This work has investigated the affinity of CuII by three ligands of biological interest: N, N, N, N’-tetrakis (2-pyridilmethyl) ethylenediamine (TPEN), triethylenetetramine (TRIEN), and diethyldithiocarbamate (Et2DTC), used for this purpose. The studies were performed by evaluating the CuII d-d band when complexed with these three ligands. The CuII d-d band in aqueous solution appears around 800 nm; when in the presence of TRIEN, this band displaces to 576 nm. TRIEN ligand is substituted by TPEN ligand (d-d band at 689 nm), and finally, in the presence of the Et2DTC ligand, the d-d band displaces to 665 nm. Theoretical calculations were used to obtain the binding energy and the values obtained were −481.85 kcal mol−1 for the CuII-TPEN, −417.80 kcal mol−1 for CuII-TRIEN and −726.72 kcal mol−1 for CuII-Et2DTC. Electrochemical studies showed an oxidation peak at 0.008 V to CuII-TRIEN complex, −0.135 V to CuII-TPEN and 0.150 V to CuII-Et2DTC. These results showed that CuII has a higher affinity by the Et2DTC ligand compared to the other ligands studied.

A afinidade de dois pesticidas muito utilizados com diversas especificidades, isto é, o fungicida Thiram e o herbicida Picloram, por íons chumbo foi estudado por medidas eletroquímicas. O perfil voltamétrico de redissolução anódica para o íon metálico estudado foi significativamente afetado pela natureza química dos pesticidas (ligantes) e uma nova interpretação foi feita sobre a natureza, força e possível estequiometria dos complexos formados. Thiram causou um pronunciado efeito no sinal de redissolução do Pb. Algoritmos de linearização dos dados de titulação permitiram calcular a constante de estabilidade condicional para o Thiram (log K'= 6,8) e Picloram (log K' = 6,0). Foi encontrado que ambos os pesticidas contribuíram para a formação dos respectivos complexos 1:1 com Pb em uma alta porcentagem (aproximadamente 83%).

The affinity of two widely used pesticides of diverse specificities, i.e., the fungicide Thiram and the herbicide Picloram, for lead ions has been studied by an electrochemical approach. The anodic stripping voltammetric profile of the studied metallic ion was significantly affected by the chemical nature of pesticide (ligand) used and new light has been shed on the nature, strength and possible stoichiometry of formed complexes. Thiram caused a pronounced effect on the stripping signals of Pb. Linearization algorithms of titration data with the metal allowed the conditional stability constant to be calculated for Thiram (log K' = 6.8) and Picloram (log K' = 6.0). It was found that both pesticides contribute to the formation of the respective 1:1 complexes with Pb in a high percentage (ca. 83%).

As reações de substituição [RuCl2(P-P)(N-N)] + L → [RuCl(L)(P-P)(N-N)]+ + Cl-, onde P-P = 1,4-bis(difenilfosfino)butano e N-N = 2,2´-bipiridina, 4,4´-dimetóxi-2,2´-bipiridina, 4,4´-dimetil-2,2´-bipiridina e 4,4´-dicloro-2,2´-bipiridina, L = piridina (py) ou 4-metilpiridina (4-pic), foram estudadas sob condições de pseudo-primeira ordem. As reações ocorrem por um mecanismo dissociativo e as constantes de velocidade nas reações de substituição aumentam com o aumento do pKa dos ligantes N-heterocíclicos e com a diminuição dos potenciais de oxidação do centro metálico. Quanto mais alta é a porcentagem de participação dos orbitais atômicos d do metal na formação do HOMO, conforme calculado pelo método DFT, mais fácil é a dissociação do cloreto da esfera de coordenação do complexo. Nos espectros de 31P{¹H} RMN da série de complexos de fórmula geral [RuCl(L)(P-P)(N-N)]PF6, há dois dubletos com Δσ < 1, o que é consistente com produtos formados pela dissociação do cloreto trans ao átomo de fósforo nos precursores.

The substitution reactions [RuCl2(P-P)(N-N)] + L → [RuCl(L)(P-P)(N-N)]+ + Cl-, where P-P = 1,4-bis(diphenylphosphino)butane and N-N = 2,2´-bipyridine, 4,4´-dimethoxy-2,2´-bipyridine, 4,4´-dimethylpyridine-2,2´-bipyridine and 4,4´-dichloro-2,2´-bipyridine, L = pyridine (py) or 4-methylpyridine (4-pic), were studied under pseudo-first order conditions. The reactions proceeded by means of a dissociative mechanism. The rate constants of the substitution reactions increased as the pKa of the N-heterocyclic ligands increased and as the oxidation potential of the metal center decreased. The greater the participation of the atomic d orbitals of the metal in the HOMO, according to DFT calculations, the easier is the dissociation of the chloride from the coordination sphere of the complex. In the 31P{¹H} NMR spectra of the series of complexes of general formula [RuCl(L)(P-P)(N-N)]PF6, there are two doublets with Δσ < 1. This is consistent with products formed by dissociation of the chloride trans to one of the phosphorus atoms in the precursors.