Composites derived from coordination polymers have been gathering great attention due to their singular properties and applications, especially catalysis and adsorption. In this work, seven new composites based on activated carbon (AC) and lanthanide-succinates (LnSuc; Ln = Pr, Nd, Sm, Gd, Dy, Er and Tm, and Suc = succinate) 3D-coordination polymers were obtained using hydrothermal reactions. Coordination polymers in LnSuc@AC composites (Ln = Pr, Nd, Sm, Gd) crystallize in monoclinic system and C2/c space group. However, the LnSuc in composites with Dy, Er and Tm have different crystal structures, due to the influence of the carbon matrix in the reaction. The systems were also characterized by Fourier transform infrared (FTIR) and thermogravimetric (TGA) analysis, and the results are in agreement with the X-ray powder diffraction (XRPD) data. The scanning electron microscopy (SEM) images confirm the crystallization of the compounds inside the pores of the carbon material. Photophysical properties of the NdSuc@AC and DySuc@AC were also investigated.

The accumulation of antibiotics in wastewater has led to the development and spreading of antibiotic resistance in the environment. Amoxicillin (Amox), a beta-lactamic antibiotic, is one of the most frequently consumed antibiotics in the world. We have applied two metal-organic frameworks (MOFs) containing zinc(II) as platforms to degrade Amox. We have predicted the adsorption of this antibiotic via molecular docking calculations which have been further corroborated by means of Fourier transform infrared and UV-Vis spectroscopies, thermogravimetric analysis, X-ray diffraction and scanning microscopy measurements. We have subsequently performed mass spectrometry analysis of Amox@zeolitic imidazolate framework-8 (ZIF-8) and Amox@Zn(1,4-benzenedicarboxylate) (ZnBDC) to demonstrate the degradation of Amox upon contact with the Zn-containing frameworks. We propose a possible pathway for the degradation of Amox involving the cleavage of the four-membered β-lactam ring. These Zn-containing frameworks provide a biocompatible platform for the degradation in solution of Amox, which should also be suitable to degrade other β-lactam antibiotics.

Filmes fluorescentes baseados em derivados de dansila foram preparados a partir de duas metodologias diferentes. Em uma delas, a superfície de um eletrodo de óxido de índio dopado com estanho (ITO) foi coberta com um filme de quitosana e o polímero foi posteriormente derivatizado com cloreto de dansila, enquanto que na outra metodologia, um filme de dansilglicina foi depositado eletroquimicamente sobre ITO. A técnica de microscopia de força atômica (AFM) foi usada para mapear a superfície dos filmes. A comparação das propriedades eletroquímicas, fotoquímicas e morfológicas destes filmes indicou que o filme de dansilglicina depositado eletroquimicamente sobre ITO apresentou resposta eletroquímica, nível de fluorescência mais intenso, maior rugosidade superficial e maior área superficial relativa em comparação com o seu homólogo quitosana-cloreto de dansila. Esse comportamento pode ser atribuído ao maior número de sítios ativos presentes na estrutura bem organizada do filme eletrodepositado em comparação com os filmes produzidos quimicamente

Dansyl-based fluorescent films were prepared by two different methods. In one of them, the surface of an indium tin oxide (ITO) electrode was coated with a film of chitosan and the polymer subsequently derivatized with dansyl chloride, whilst in the second method a film of dansylglycine was electrochemically deposited on the ITO surface. Atomic force microscopy (AFM) was employed to map the surfaces of the films. Comparison of the morphological, photochemical and electrochemical properties of these films indicated that the dansylglycine film electrodeposited on ITO exhibited electrochemical response, emitted a higher level of fluorescence, presented greater surface roughness and larger relative surface area in comparison with its dansyl chloride-chitosan counterpart. This behavior can be attributed to the higher number of active sites present in the well-organized and rough structure of the electrodeposited film in comparison with the chemically produced films

Um novo composto fluorescente de microcistina-LR marcado com criptato de térbio foi obtido pela conjugação inicial da microcistina-LR com aminoetanotiol, seguido pela reação com o grupo éster do criptato de térbio. A formação do produto foi acompanhada por cromatografia líquida de alta eficiência (CLAE) em 238 nm e 310 nm. A presença de microcistina-LR na molécula marcada foi confirmada através de ensaio com enzima ligada a imunoabsorvente (ELISA) e por reação protéica com ácido bicincônico. O espectro de luminescência do criptato e da molécula conjugada também foram confirmados.

A new fluorescent labeled compound of microcystin-LR with terbium cryptate was obtained by initial conjugation of microcystins-LR with aminoethanethiol followed by the reaction with the ester group of terbium cryptate. The product formation was followed by high performance liquid chromatography (HPLC) at 238 nm and 310 nm. The presence of microcystin-LR in the labeled molecule was confirmed by enzyme linked immunosorbent assay ELISA and by protein reaction with bicinhonic acid. Luminescence spectra of cryptate and the conjugated molecule were carried through as well.