fij
SOCIEDADE PORTUGUESA
DE
QUfMICA
9-
11th
May
Faculdade de CiE?ncias
Universidade do Porta
Ano lnternacional da QUfMICA 20113PVCheM
3rd
Portuguese
Young
Chemists
Meeting
2012
Book of Abstracts of the 3rd Portuguese Young Chemists Meeting Editors Juliana Oliveira
Joana Reis
Cover Joao Martins
Montage Organizing committee
ISBN 978-989-97667-2-3
This book is a compilation of the abstracts submitted by the authors for
presentation at the meeting. There were introduced only minor editing alterations that do not change the scientific content.
The scientific content is sole the responsibility of the authors.
P12 Pressure waves generated by light-absorbing thin films
A. P. Marques. G. F. F. Sa, C. Serpa and L. G. Arnaut
Universidade de Coimbra, Portugal
71
P13 Thermodynamic study of phase transitions in methyl esters of ortho-, meta- 72 and para-aminobenzoic acids
Ana R. R. P. Almeida and M. J. S. Monte
Faculdade de Ciencias, Universidade do Porta, Portugal
P14 Monovacant polyoxometalates @ Mll-101: synthesis and heterogeneous 73
catalytic studies
Andre D. S. Barbosa. Filipe A. Almeida Paz, Baltazar de Castro, Salete S. Balula and Lufs Cunha-Silva
Faculdade de Ciencias, Universidade do Porta, Portugal
P15 Isolation and quantification of labdanolic acid from Cistus ladaniferus
Andre N. C. Martins. L. M. T. Frija, S. Simeonov and C. A. M. Afonso
Faculdade de Farmcicia, Universidade de Lisboa I lnstituto Superior Tecnico, Portugal
P16 Application of geochemistry software to corrosion studies
A. B. Oliveira. A. C. Bastos, 0. V. Karavai, A. A. Ferreira, M. L. Zheludkevich and M. G. S.
Ferreira
Universidode de Aveiro, Portugal
P17 Micro-electrochemical techniques to study localised corrosion
A. B. Oliveira, A. C. Bastos, 0. V. Karavai, M. L. Zheludkevich and M. G. S. Ferreira
Universidade de Aveiro, Portugal
74
75
76
P18 Approach to the synthesis of nucleoside inhibitors of butyrylcholinesterase 77
Andreia Almeida, Vasco Cachatra and Amelia P. Rauter
Facu/dade de Ciencias, Universidade de Lisboa, Portugal
P19 A green integrated biocatalytic system for the conversion of C02 and
vegetable oils into biodiesel
Andreia Pi menta, Pedro Vidinha and Susana Barreiros
Faculdade de Ciencias e Tecnologia, Universidade Nova de Lisboa, Portugal
P20 Development of ionic liquids based on biological compounds
Andreia Forte, Lufs C. Branco and Cesar Laia
Faculdade de Ciencias e Tecnologia, Universidade Nova de Lisboa, Portugal
78
79
P21 Topical drug delivery of lidocaine and diclofenac gels: Viscoelastic properties 80 and in vitro skin distribution studies
Angela Correia. Gon~alo F. F. Sa, Carlos Serpa and Luls G. Arnaut
Universidade de Coimbra, Portugal
P22 Computational studies of Binol based phosphites and respective metal 81
complexes at PM6 and DFT levels. Application in asymmetric hydrogenation of olefins.
Angela C. B. Neves, Rui M. B. Carrilho, Andreia F. Peixoto, Ana R. Almeida, Paulo E. Abreu, M. Calvete and Mariette M. Pereira
Universidade de Coimbra, Portugal
P23 Gamma irradiation protects oleic acid from oxidation: an experiment in 82
Lactarius de/iciosus wild mushroom
Angela Fernandes, M. Beatriz P. P. Oliveira, Amilcar L. Antonio, Anabela Martins and lsabel
c.
F. R. Ferreiralnstituto Politfknico de Bragan~a I Faculdade de Farmacia, Universidade do Porta, Portugal
Posters
Gamma irradiation protects oleic acid from oxidation: an
experiment
in
Lactarius deliciosus wild
mushroom
Angela Fernandes1•2, M. Beatriz P. P. Oliveira2, Amilcar L. Antonio1•3•4, Anabela Martins1
and Isabel C. F. R. Ferreira1·* -·
1
CIMO/ESA, Instituto Politecnico de Braganya, Portugal
2REQUIMTE/Dt. Ciencias Quimicas, Faculdade de Farmacia, Universidade do Porto, Portugal
3GTRPP/Unidade de Fisica e Aceleradores, Instituto Tecnologico e Nuclear, Portugal
4
Departamento de Fisica Fundamental, Universidade de Salamanca, Spain
*iferreira@ipb.pt
The short shelf-life of mushrooms is an obstacle to the distribution and marketing of the fresh product. Thus, prolonging postharvest storage, while preserving their quality, would benefit the mushroom industry as well as consumers (1]. There has been extensive research on finding the most appropriate technology for mushrooms preservation and a particular interest arises for wild species. Treatment by irradiation emerges as a possible conservation technique that has been tested successfully in several food products and is regulated in the European Union by the Directive
1999/2/EC.
In the present work, the influence of gamma irradiation dose (0.5 and 1 kGy) over the fatty acids profile of Lactarius deliciosus L. wild mushroom, collected in the Northeast of Portugal (November 2011), was evaluated by gas-chromatography coupled to flame ionization detection (GC-FID). The analyses were performed after 0, 4 and 8 days of storage at 4
oc
in irradiated and non-irradiated samples (control). The control and the irradiated samples revealed an identical profile, with C18:0 (stearic acid), Cl8:2n6c (linoleic acid), Cl8:ln9c (oleic acid) and Cl6:0 (palmitic acid) as main fatty acids. These results are in agreement to the reported by our research group in a previous study with nutritional characterization of this species [2]. Nevertheless, some differences were found in the percentage of some fatty acids in the different samples, mainly in oleic acid. Control sample (non-irradiated) after 8 days of storage, showed a lower C18:1n9c percentage (decreased from 8 to 4.4%) contributing to a decrease in monounsaturated fatty acids (MUF A) levels. Otherwise, in the sample irradiated with 0.5 kGy the percentage of the mentioned fatty acid did not changed until day 8.Overall, irradiation could be an alternative to ensure the quality and extend the life of mushrooms, protecting their fatty acids from oxidation, as is was demonstrated herein for oleic acid. In fact, food irradiation is now being commonly used in many countries, as people are becoming more aware of the role of food irradiation in regards to food safety and product shelf-life extension.
Acknowledgements: The authors are grateful to the Foundation for Science and Technology (FCT, Portugal)
for financial support to the research center CIMO (PEst-OE/AGRIUI0690/2011) and REQUIMTE (PEst-C/EQB/LA0006/2011). A. Femandes thanks to FCT, POPH-QREN and FSE for her grant (SFRH/BD/76019/2011).
[1] Akram, K.; Kwon, J. H., J. Korean Soc. Appl. Bioi. Chem. 2010, 53,257-265.
[2] Barros, L.; Baptista, P.; Correia, D. M.; Morais, J. S.; Ferreira, I. C. F. R., J. Agric. Food Chem.
2007, 55, 4781-4788.
3PYCheM
3rd Portuguese Young Chemists Meeting
9 - 11th May 2012
Departamento de Quimica e Bioqufmica
Faculdade de Ciencias da Universidade do Porto
Book of Highlights
100
Ano lntrro.Koon.JI d.J
QUIMICA
Editores 3PYCheM tuguese Voung :hemists .eting ' .. 2
Book of Highlights of the 3rd Portuguese Young Chemists Meeting
Ana Rodrigues Joao Martins
lnes Rocha Marisa Rocha
Montagem Organizing committee
This book is a compilation of the highlights submitted by the authors for presentation at the meeting. There were
introduced only minor editing alterations that do not change the scientific content. The scientific content is sole the responsibility of the authors.
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Gamma irradiation protects oleic acid from oxidation: an experiment in Lactarius de/iciosus wild mushroom
Angela Fernandes, M. Beatriz P. P. Oliveira, Amilcar L. Antonio, Anabela Martins and Isabel C. F. R. Ferreira·
lnstituto Politecnico de Braganr;al Faculdade de Farmcicia da Universidade do Por/o, Portugal.
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Control and irradiated L. deliciosus samples revealed identical fatty acid profiles.
Control sample showed a lower C18:ln9c content after 8 days of storage .
Sample irradiated with 0.5 kGy maintained Cl8:1n9c content until day 8 .
Irradiation protected fatty acids from oxidation .
Irradiation could be an alternative to extend the life of mushrooms .
1,3-Dipolar Cycloaddition of (2R,4aR,8aS)-2-phenyl-4,4a-dihyd ropyrano [3,2-d] [ 1,3 ]dioxin-6(8aH)-one
with Aromatic Diazomethyl Compounds
Ant6nio Ribeiro. Cristina E. A. Sousa, M. Jose Alves and A. Gil Fortes
Universidade do Minho, Portugal •antonio.manuel.p.ribeiro@gmail.com
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cycloaddition.
• Reactions with alkyl azides and diazomethyl compounds were totally
regio-and stereo-selective.
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