Metal-organic framework (MOF) derivatives, such as porous metal oxides with controlled morphology have received great attention for applications in various fields. In this paper, the experimental results show that porous CeO2 with high specific surface area (90.5 m2 g-1) and nanorod morphology can be obtained by calcining a Ce-MOF template at optimized temperature (300-500 °C). The formation mechanism of this porous structure as well as the influence of the calcination temperature are well explained by taking into account thermal behavior and intrinsic structural features of the Ce-MOF precursor. We employed the oxides formed as heterogeneous catalysts to reduce the soot originating from the incomplete combustion of diesel or diesel/biodiesel blends. The CeO2 materials exhibit outstanding catalytic activity, lowering the temperature of soot combustion from 610 to 370 °C. Compared with similar work, our catalyst exhibits enhanced soot oxidation activity, making it highly promising for diesel particulate filter applications. Such outstanding catalytic performance of the porous CeO2 nanorods benefits from their large specific surface area, and morphological and structural characteristics. Metalorganic Metal organic MOF (MOF derivatives fields paper CeO 90.5 905 90 5 (90. m g1 g 1 g-1 CeMOF Ce 300500 300 500 (300-50 C °C . °C) precursor dieselbiodiesel biodiesel blends activity 61 37 work characteristics 90. 9 (90 g- 30050 30 50 (300-5 6 3 (9 3005 (300- ( (300 (30 (3

Abstract Degradation of the dentin-resin interface can occur due to hydrolysis of exposed collagen, resulting in reduced bond strength. This study assessed the effect of dentin treatment with chitosan combined with an etch-and-rinse or self-etch adhesive system on improvement of bond strength and preservation of the interface durability. Methodology Enamel was removed from 80 molars and the teeth were divided into two groups: without chitosan (control) or with 2.5% chitosan gel (1 min). They were further subdivided into two subgroups according to the adhesive system: etch-and-rinse or self-etch. Dentin was restored using a composite resin. Half of the specimens from each restored group were subjected to interface aging and the remaining specimens were used for immediate analysis. The specimens were sectioned and subjected to microtensile bond strength (µTBS) test (n=10), chemical composition testing using Fourier-transform infrared (FTIR) spectroscopy (n=4) and energy-dispersive spectroscopy (EDS) (n=5), and morphological analysis of the adhesive interface using scanning electron microscopy (SEM) (n=5). Data were analyzed using three-way ANOVA. Results Chitosan improved the µTBS of the adhesive interface when compared with the control group (p=0.004). No significant differences were observed in dentin adhesion between the adhesive systems (p=0.652). Immediate µTBS was not significantly different from that after 6 months (p=0.274). EDS and SEM did not show significant differences in the chemical and structural composition of the specimens. FTIR showed a decrease in the intensity of phosphate and carbonate bands after using chitosan. Conclusions Dentin treatment with chitosan combined with an etch-and-rinse or self-etch adhesive system improved the immediate and preserved the 6-month bond strength of the adhesive interface.

[RE(czb)3(H2O)2] complexes (where RE = Eu3+, Tb3+, Gd3+; and czb = 4-(9H-carbazol-9-yl)benzoato) have been synthesized and characterized. The Gd3+ complex was used to determine the triplet state energy of the czb ligand. Photoluminescence measurements of the complexes have been carried out under UV excitation. The Tb3+ complex exhibited a strong green luminescence indicating an efficient antenna effect, whereas the Eu3+ complex showed low red luminescence and the Gd3+ complex a blue-green luminescence from the ligand. The luminescence lifetimes and quantum yields have also been measured for the evaluation of the spectroscopic behavior of the complexes.

This work describes a simple and economical experiment for the extraction and purification of chlorophyll a from Spirulina maxima. Extraction and purification of natural compounds can be considered one of the most illustrative experiments that can be performed in Organic Chemistry courses. Particularly, the chromatography of dyes and pigments allows students to have a better comprehension of the chromatography separations. These compounds represent an important class of organic pigments applied in pharmaceutical, cosmetic, detergent compositions, and various other fields and can be extracted from plants and algae. To extract, separate and purify chlorophyll a from associated pigments such as xanthophylls, carotenes, and pheophytins, very costly processes are reported. The present approach is perfectly adequate for use in Chemistry experiments for undergraduate students.

The sol-gel process is a methodology used to obtain organic-inorganic hybrid solids, which open new possibilities in the field of material science. The sol-gel technique offers a low temperature attractive approach for introducing organic molecules into amorphous materials. In order to introduce tetrakis (2-hydroxy-5-nitrophenyl)porphyrin covalently bounded to a silicate matrix, the inorganic precursor 3-isocyanatopropyltriethoxysilane was added (molar ratio 2:1) to the porphyrin solution in anhydrous dimethylformamide and triethylamine. The isolated porphyrin and the hybrid porphyrinosilica have excitation maximum centred at 400 nm and 424 nm, respectively and the emission spectra for both materials has bands centred at 650 nm and 713 nm. The formation of hybrid matrix was investigated by FTIR.

Muitos compostos modelo contendo porfirinas têm sido preparados num esforço para entender o sistema de fotossíntese e os processos de aproveitamento de energia solar. Sistemas doadores-receptores contendo porfirinas têm sido freqüentemente estudados para testar várias descrições teóricas sobre transferência de elétrons. O estudo de parâmetros fotoquímicos e fotofísicos como a distância para transferência de energia, geometria molecular e a diferença de potencial eletrônico, tem se mostrado importante para a definição da transferência eletrônica em porfirinas. Neste trabalho apresentamos a síntese, purificação e caracterização por espectroscopia UV/Vis, ¹H e 19F RMN, luminescência e tempos de vida de novos modelos moleculares de porfirinas, que permitam investigar esses parâmetros. Utilizou-se o dímero Zn,Mn(TPPF4)2pip e seus monômeros ZnTPPF4pipH e MnF5TPP. A caracterização do ZnMn(TPPF4)2pip, foi dificultada devido a presença de Mn+3, devido ao forte acoplamento dos orbitais dpi do manganês e o sistema pi da porfirina, que aumenta a interação manganês-porfirina mudando o espectro eletrônico UV/Vis e distorcendo os sinais de ¹H e 19F RMN do dímero. A presença de Mn+3 desloca E1/2 do anel porfirínico para valores mais negativos, o que resulta em reduções mais difíceis, impedindo a transferência de energia da Znporfirina para a Mnporfirina.

Porphyrins have revealed that factors as the energy transfer distance, molecular geometry and the difference of electronic potential, are important in a well defined electronic transfer. Porphyrin- containing donor-acceptor systems have been usefully employed to test various theoretical descriptions of electron transfer. The objective of this paper consists on the synthesis, purification and characterization by UV/Vis spectroscopy, ¹H and 19F NMR, luminescence and lifetime of new molecular models, allowing the investigation of energy transfer parameters. This study was accomplished using the dimer Zn,Mn(TPPF4)2pip and its monomers ZnTPPF4pipH and MnF5TPP. The dimer characterization, Zn,Mn(TPPF4)2pip, was difficult due to the presence of Mn3+. The strong overlap between dpi orbitals of manganese and the porphyrin pi system increases the interaction manganese-porphyrin in changing the UV/Vis electronic spectrum and distorting the ¹H and 19F NMR signals of dimer. The presence of Mn3+ shifts the reduction potential of E1/2 of the porphyrin ring to more negatives values, what results in more difficult reductions, disabling the transfer of energy from Zincporphyrin to Manganeseporphyrin.