Complexation Of Amino Acid With Cadmium And Its Application To Remove Cadmium From Contaminated Soil

Low molecular organic acids, such as amino acid, play an important role in cadmium (Cd) mobility. However, its complexation ability with Cd was not well studied. The complexation structure of amino and cadmium was investigated by theory calculation based on B3ly/SDD and detecting by FTIR spectrum. The conformers were found to be [COc, COc] for fatty amino-cadmium and PheCd2+, [COc, COc, COs] for GluCd2+and ThrCd2+, respectively. The complex energy of these conformers was calculated in water phase by SMD model and the order of chelation energy was; PheCd2+> AlaCd2+ > LeuCd2+ > GluCd2+ > GlyCd2+ > ThrCd2+. All the dissolving energy of complexes was below zero, indicating these complexes was easily dissolved in water. In aqueous solution experiment, the Cd2+ concentration decreased with increasing amino acid concentration. The order of logβ (Complex stability constant) was: PheCd2+> AlaCd2+ > LeuCd2+ > GluCd2+ > GlyCd2+ > ThrCd2+, consisting with the order of calculated chelation energy. The Cd removal efficiency by Thr, Glu, Gly, Ala, Leu and Phe were 38.88%, 37.47%, 35.5%, 34.72%, 34.04% and 31.99%, respectively. From soil batch experiment, the total Cd in soil was decreased in present of amino acid with the concentration of Cd in water increased from 231.97 µg/L to 652.94-793.51 µg/L. The results of BCR sequential extraction showed that the Cd in acid soluble and reducible fraction sharply decreased. From all the results, the amino acid has potential to be used as a chelation to remedy the Cd contaminated soil.

Dendrimers Functionalized with Palladium Complexes of N-, N,N-, and N,N,N-Ligands

Pyridine, pyridine imine, and bipyridine imine ligands functionalized by a phenol have been synthesized and characterized, in many cases by X-ray diffraction. Several of these N-, N,N-, and N,N,N,-ligands have been grafted onto the surface of phosphorhydrazone dendrimers, from generation 1 to generation 3. The complexation ability of these monomers and dendrimers towards palladium(II) has been assayed. The corresponding complexes have been either isolated or prepared in situ. In both cases, the monomeric and dendritic complexes have been tested as catalysts in Heck couplings and in Sonogashira couplings. In some cases, a positive dendritic effect has been observed, that is, an increase of the catalytic efficiency proportional to the dendrimer generation.

Spectral properties and biological activity of La(III) and Nd(III) Monensinates

The present research is focused on evaluation of complexation ability of Monensic acid (MonH) towards La3+ and Nd3+ ions.Changes in the SRCD spectrum of Monensinate anion were monitored upon addition of lanthanide(III) ions. The antibiotic undergoes formation of one neutral ([Ln(Mon)3(H2O)3]) and two positively charged complex species of composition [Ln(Mon)2(H2O)2]+ and [Ln(Mon) (H2O)]2+, respectively (Ln = La3+, Nd3+). Neutral complexes were isolated as fine powders and were characterized by IR, FAB-MS and ESI-MS. It is assumed that Monensin acts in bidentate coordination mode via monodentate carboxylate moiety and hydroxyl group, both located at the opposite ends of antibiotic molecule.Activity of Monensic acid and [Ln(Mon)3(H2O)3] to decrease visible bacteria growth of B. subtilis, S. Lutea and B. mycoides was evaluated by agar hole diffusion method. Results showed that complexation of lanthanide(III) ions to Monensin enhances the activity of non-coordinated ligand.Antitumor efficacy of compounds was assayed on human triple negative breast cancer and transplantable sarcoma in rat. The cytotoxicity was accessed by MTT test, NR uptake, CV assay and double AO/PI staining. Experimental data revealed that Monensic acid and [Ln(Mon)3(H2O)3] possess concentration- and time-dependent activity, and express promising cytotoxic properties against human and rat permanent cancer cell lines.

Mass Spectrometry Reveals Complexing Properties of Modified PNP-Lariat Ether Containing Benzyl Derivative of (S)–Prolinamine

In the investigation presented here the synthesis of new lariat ether derivative obtained from the modification of tetrapyrrolidinyl-PNP-crown ether macrocycle is described. The polyheterotopic molecular coreceptor consisted of the replacement of chlorine atoms with an optically active (S)-(1-benzylpyrrolidin-2-yl) methanamine. The structure was confirmed by using elemental analysis, mass spectrometry, and NMR spectroscopy. This work covers results concerning the complexing properties of the new ligand towards Ag+, Cu2+, Co2+, Ni2+, and Zn2+ ions. The formation of non-covalent complexes of 1:1 stoichiometry with the Cu2+, Co2+, Ni2+, and Zn2+ ions have been confirmed by mass spectrometry. Due to the previous work and application possibilities, a large emphasis was put on the investigation of the complexation ability of lariat ether with silver (I) cation to determine stability constants by direct potentiometric method. In this case, the formation of four different forms of complexes AgL, Ag2L, Ag3L, and Ag4L has been proved. The observed unusual binding through the nitrogen atoms from the exocyclic substituents may provide the structural unit to build a new coordination polymers.