JBCS

18:14, Thu Nov 21

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vol. 23, No. 8, 2012, p. 1409-1576

 

There Is No Future without Good Primary Education

"Water dropping day by day wears the hardest rock away". This popular saying should enlighten and guide the actions of all those committed to improving the educational level and reducing truancy in Brazilian schools.
Sometimes, we seem to forget that from 100 students who start primary school, 44 make it to high school and only 12 go to college. Still worse is the fact that from those 12, not all manage to graduate and many exceed the regular periods of their courses.

(Read more at Editorial)


Cover Article
J. Braz. Chem. Soc. 2012, 23(8), 1411-1420

Iron(III) Porphyrin Covalently Supported onto Magnetic Amino-Functionalized Nanospheres as Catalyst for Hydrocarbon and Herbicide Oxidations

Joicy S. dos Santos; André L. Faria; Patrícia M. da Silva Amorin; Franco M. La Luna; Kely L. Caiado; Débora O. C. e Silva; Patrícia P. C. Sartoratto; Marilda D. Assis

How to cite this article

This work describes a new magnetic catalyst composed of an ironporphyrin, 5,10,15,20-tetrakis(pentafluorophenyl) porphyrin iron(III) chloride, FeTFPP, covalently immobilized onto magnetic maghemite nanospheres covered with aminofunctionalized silica. The catalyst can be easily recovered and washed after reaction through application of an external magnetic field, which favors its reuse. This catalytic system proved to be efficient and selective for hydrocarbon oxidation, specially R(+)-limonene, a compound present in orange peels and in the herbicide simazine, frequently used on sugar cane crops. Details are discussed on page 1411.

https://dx.doi.org/10.1590/S0103-50532012005000005

Published online: July 3, 2012
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Editorial J. Braz. Chem. Soc. 2012, 23(8), 1409-1410

There Is No Future without Good Primary Education

Angelo C. Pinto

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https://dx.doi.org/10.1590/S0103-50532012000800001

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Articles J. Braz. Chem. Soc. 2012, 23(8), 1411-1420

Iron(III) Porphyrin Covalently Supported onto Magnetic Amino-Functionalized Nanospheres as Catalyst for Hydrocarbon and Herbicide Oxidations

Joicy S. dos Santos; André L. Faria; Patrícia M. da Silva Amorin; Franco M. La Luna; Kely L. Caiado; Débora O. C. e Silva; Patrícia P. C. Sartoratto; Marilda D. Assis

How to cite this article

 

This work describes the covalent immobilization of an ironporphyrin, 5,10,15,20-tetrakis(pentafluorophenyl)porphyrin iron(III) chloride (FeTFPP), onto maghemite/silica magnetic nanospheres covered with aminofunctionalized silica and its use as catalyst for hydrocarbon and herbicide (simazine) oxidations

https://dx.doi.org/10.1590/S0103-50532012005000005

Published online: July 3, 2012

 

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Total access: 1274


J. Braz. Chem. Soc. 2012, 23(8), 1421-1428

Comparison of Different Pre-treatment Procedures for the Determination of Chromium in Crude Oil Samples by GF AAS

Helen M. Pessoa; Fernanda H. Lyra; Eustáquio Vinicius R. de Castro; Reinaldo C. de Campos; Maria Tereza W. D. Carneiro; Geisamanda P. Brandão

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Cr absorption signal obtained by DS-GF AAS of 0.760 mg of crude oil sample without pre-treatement (red - Cr atomic absorption signal; blue - background signal)

https://dx.doi.org/10.1590/S0103-50532012005000004

Published online: July 3, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1429-1436

PAHs in Cultured Mussels Perna perna from a Southeastern Brazilian Bay

Renato V. Yoshimine; Renato S. Carreira

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The occurrence of polycyclic aromatic hydrocarbons (PAHs) in mussels (Perna perna) cultured in farms from Ilha Grande Bay (Rio de Janeiro State, Brazil) was evaluated for the first time. The levels of PAHs were generally low and below the threshold concentrations recommended for human consumption of shellfish. The results also revealed reasonable good local environmental conditions

https://dx.doi.org/10.1590/S0103-50532012005000003

Published online: July 5, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1437-1440

Lanthanide Nitrates as Lewis Acids in the One-Pot Synthesis of 1,2,4-Oxadiazole Derivatives

Juliana A. Vale; Wagner M. Faustino; Davila de S. Zampieri; Paulo J. S. Moran; José A. R. Rodrigues; Gilberto F. de Sá

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Lanthanide nitrates [Ln(NO3)3] acting as catalyst in direct one-pot synthesis of 3-benzoyl- and 3-acetyl-1,2,4-oxadiazoles derivatives from aromatic ketones with electron-donating (EDG) and electron-withdrawing groups (EWG)

https://dx.doi.org/10.1590/S0103-50532012005000002

Published online: July 5, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1441-1449

Simultaneous Quantification of Lycopene, β-Carotene, Retinol and α-Tocopherol in Plasma after a Simple Extraction Procedure: Stability Study and Application to Human Volunteers

Mariele F. Charão; Angela M. Moro; Natália Brucker; Rachel P. Bulcão; Marília Baierle; Fernando Freitas; Juliano Durgante; Sabrina Nascimento; Guilherme B. Bubols; Paulo H. Saldiva; Denise Bohrer; Solange C. Garcia

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The described method consists of a rapid and simple liquid-liquid extraction procedure and posterior quantification by high-performance liquid chromatography (HPLC) with Vis/fluorescence detection. It was shown to be a sensitive method for the simultaneous determination of lycopene, β-carotene, retinol and α-tocopherol in human plasma and can be utilized in routines of clinical laboratories

https://dx.doi.org/10.1590/S0103-50532012005000001

Published online: July 10, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1450-1459

Kinetic Analytical Method for Determination of Uric Acid in Human Urine using Analyte Pulse Perturbation Technique

Nataša D. Pejić; Jelena P. Maksimović; Slavica M. Blagojević; Slobodan R. Anić; Željko D. Čupić; Ljiljana Z. Kolar-Anić

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The kinetic methods based on the potentiometric monitoring of the concentration perturbations of the both the Bray-Liebhafsky oscillatory reaction in a stable non-equilibrium stationary state and Dushman reaction in a steady state, are described. The methods are utilized for determination of uric acid in human urine samples

https://dx.doi.org/10.1590/S0103-50532012005000006

Published online: July 12, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1460-1468

Optimization of an Analytical Protocol for the Extraction, Fractionation and Determination of Aromatic and Aliphatic Hydrocarbons in Sediments

Vânia R. Ferreira; Cindy D. Gouveia; Cesar A. da Silva; Andreia N. Fernandes; Marco T. Grassi

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PAH concentrations recovered from certified reference sediment (NWRI EC-3). Vertical bars represent the standard deviation (n = 3) for the recovered and for the certified values (n = 3)

https://dx.doi.org/10.1590/S0103-50532012005000010

Published online: July 12, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1469-1475

Spectrophotometric Evaluation of the Behavior of Disperse Red 1 Dye in Aqueous Media and its Interaction with Calf Thymus ds-DNA

Carolina V. Uliana; Gustavo S. Garbellini; Hideko Yamanaka

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Studies of the solubility of the model dye disperse red 1 (DR1) in aqueous solutions, its determination in water samples and the interaction of the dye with calf thymus ds-DNA were performed using UV-Vis spectrophotometry

https://dx.doi.org/10.1590/S0103-50532012005000009

Published online: July 12, 2012

 

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Total access: 1459


J. Braz. Chem. Soc. 2012, 23(8), 1476-1487

Currently Used Pesticides in Water Matrices in Central-Western Brazil

Elisângela N. Nogueira; Eliana F. G. C. Dores; Alício A. Pinto; Ricardo S. S. Amorim; Maria L. Ribeiro; Carolina Lourencetti

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Currently used pesticides in water matrices in Central-Western Brazil reveal a higher diversity of compounds and frequency of detection in rain water than in surface and groundwater samples and point to the risk of pesticide contamination in important headwater streams in the study areas

https://dx.doi.org/10.1590/S0103-50532012005000008

Published online: July 12, 2012

 

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Total access: 2132


J. Braz. Chem. Soc. 2012, 23(8), 1488-1500

Anionic Chromogenic Chemosensors Highly Selective for Fluoride or Cyanide Based on 4-(4-Nitrobenzylideneamine)phenol

Celso R. Nicoleti; Vanderléia G. Marini; Lizandra M. Zimmermann; Vanderlei G. Machado

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4-(4-Nitrobenzylideneamine)phenol is used in the study of anionic chromogenic chemosensors in acetonitrile allowing the highly selective detection of F- and CN-. These chemosensors are based on acid-base and on indicator displacement strategies

https://dx.doi.org/10.1590/S0103-50532012005000007

Published online: July 12, 2012

 

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Total access: 2101


J. Braz. Chem. Soc. 2012, 23(8), 1501-1505

Comparison of the n-Alkanes and Polycyclic Aromatic Hydrocarbons Concentrations in the Atmosphere during the Preparation of Warm and Hot Mixtures Asphalt for Pavements

Rosângela Motta; Pérola C. Vasconcellos; Liedi Bernucci; Simone G. Avila; Talita Cornetti

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Warm mix asphalt (WMA) is a new paving technology produced with temperature around 30 °C lower than conventional hot mix asphalt (HMA). Due to the reduction of temperature, less n-alkanes and polycyclic aromatic hydrocarbons (PAH) are generated during the production of WMA than HMA

https://dx.doi.org/10.1590/S0103-50532012005000011

Published online: July 19, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1506-1514

Quantitative Chemical Profile and Multivariate Statistical Analysis of Alembic Distilled Sugarcane Spirit Fractions

Felipe A. T. Serafim; Carlos A. Galinaro; Alexandre A. da Silva; Silmara F. Buchviser; Eduardo S. P. do Nascimento; Fernando V. Novaes; Douglas W. Franco

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During the alembic distillation process, the sugarcane spirit is separated into three different fractions which presented differences among their quantitative chemical profile. In this work was suggested a quantitative chemical model for it in order to support the standardization of this production step

https://dx.doi.org/10.1590/S0103-50532012005000015

Published online: July 19, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1515-1522

A LED Based Photometer for Solid Phase Photometry: Zinc Determination in Pharmaceutical Preparation Employing a Multicommuted Flow Analysis Approach

Tuanne R. Dias; Boaventura F. Reis

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A LED (light emitting diode) based photometer for solid phase photometry coupled to a multicommuted flow analysis approach forming a downsized setup that is designed for zinc determination in pharmaceutical products

https://dx.doi.org/10.1590/S0103-50532012005000014

Published online: July 19, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1523-1535

Synthesis, Electrochemical, Spectrophotometric and Potentiometric Studies of Two Azo-Compounds Derived from 4-Amino-2-Methylquinoline in Ethanolic-Aqueous Buffered Solutions

Mona A. El-Attar; Iqbal M. Ismail; Mohamed M. Ghoneim

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Two azo-compounds derived from 4-amino-2-methylquinoline were synthesized and characterized. Their electrode reaction pathways were elucidated and discussed. Dissociation and stability constants of the examined azo-derivatives and stoichiometry of their complexes with some transition metal ions were determined

https://dx.doi.org/10.1590/S0103-50532012005000013

Published online: July 31, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1536-1542

A Peroxotungstate-Ionic Liquid Brush Assembly: an Efficient and Reusable Catalyst for Selectively Oxidizing Sulfides with Aqueous H2O2 Solution in Neat Water

Xianying Shi; Wenjuan Ma; Hui Ou; Xiaoyan Han; Congmin Lu; Yan Chen; Junfa Wei

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An environmentally-friendly procedure was developed for selective oxidation of sulfides at room temperature using 30 wt.% hydrogen peroxide as terminal oxidant and water as sole solvent. The catalyst is easily recovered post-reaction (via simple filtration) and reused at least eight times without a noticeable loss of activity

https://dx.doi.org/10.1590/S0103-50532012005000012

Published online: July 31, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1543-1550

Kinetics and Mechanism of Chlorate-Chloride Reaction

Rafaela T. P. Sant'Anna; Cristina M. P. Santos; Guilherme P. Silva; Ricardo J. R. Ferreira; André P. Oliveira; Carlos E. S. Côrtes; Roberto B. Faria

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A saturation profile for chloride concentration was found in a kinetic study for the chlorate-chloride reaction, suggesting the formation of Cl2O32- intermediate. The proposed mechanism was able to reproduce the experimental behavior

https://dx.doi.org/10.1590/S0103-50532012005000017

Published online: July 31, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1551-1557

Evaluation of Herbicidal Potential of Depsides from Cladosporium uredinicola, an Endophytic Fungus Found in Guava Fruit

Lívia S. de Medeiros; Olívia M. Sampaio; Maria Fátima das G. F. da Silva; Edson Rodrigues Filho; Thiago André M. Veiga

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Two natural depsides, 2,4-dihydroxy-3,6-dimethylbenzoate (1) and 3-hydroxy-2,5-dimethylphenyl 4-[(2,4-dihydroxy-3,6-dimethylbenzoyl) oxy]-2-hydroxy-3,6-dimethylbenzoate (2), were isolated from Cladosporium uredinicola and their effects on various steps of photosynthesis were investigated

https://dx.doi.org/10.1590/S0103-50532012005000018

Published online: August 2, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1558-1562

Cytotoxic Cordiaquinones from the Roots of Cordia polycephala

Hozana Patrícia S. Freitas; Ana Isabel V. Maia; Edilberto R. Silveira; José Delano B. Marinho Filho; Manoel O. Moraes; Cláudia Pessoa; Letícia V. Costa Lotufo; Otília Deusdênia L. Pessoa

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The chemical investigation of the roots of Cordia polycephala resulted in the isolation of two new terpenoid naphtoquinones, named as cordiaquinones N and O. Both compounds showed cytotoxic effects with IC50 values in the range of 1.2 to 3.4 μmol L-1

https://dx.doi.org/10.1590/S0103-50532012005000019

Published online: August 7, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1563-1569

Photocatalytic Degradation of Camphor by Suspended and Immobilized Photocatalysts

Carla Sirtori; Adriane M. de Freitas; Sérgio Toshio Fujiwara; Patricio Peralta-Zamora

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Immobilized forms of TiO2 permit almost total photocatalytic degradation of camphor in aqueous solution, including high mineralization degrees

https://dx.doi.org/10.1590/S0103-50532012005000020

Published online: August 7, 2012

 

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J. Braz. Chem. Soc. 2012, 23(8), 1570-1576

A Quantitative Method using Near Infrared Imaging Spectroscopy for Determination of Surface Composition of Tablet Dosage Forms: an Example of Spirolactone Tablets

Renato L. Carneiro; Ronei J. Poppi

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The homogeneity of the components of a tablet was investigated using near infrared (NIR) imaging spectroscopy. Left side of the graphical abstract presents the chemometric technique used to find concentration maps of excipients and active pharmaceutical ingredient. Right side of the figure shows a tablet and the distribution of compounds in the tablet surface

https://dx.doi.org/10.1590/S0103-50532012005000022

Published online: August 9, 2012

 

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Online version ISSN 1678-4790 Printed version ISSN 0103-5053
Journal of the Brazilian Chemical Society
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