M
M. Fátima C. Guedes da Silva
Researcher at Instituto Superior Técnico
Publications - 353
Citations - 11287
M. Fátima C. Guedes da Silva is an academic researcher from Instituto Superior Técnico. The author has contributed to research in topics: Catalysis & Ligand. The author has an hindex of 54, co-authored 339 publications receiving 9820 citations. Previous affiliations of M. Fátima C. Guedes da Silva include Saint Petersburg State University & University of Lisbon.
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Journal ArticleDOI
Chalcogen bonding in synthesis, catalysis and design of materials
Kamran T. Mahmudov,Kamran T. Mahmudov,Maximilian N. Kopylovich,M. Fátima C. Guedes da Silva,Armando J. L. Pombeiro +4 more
TL;DR: This Perspective presents some demonstrative experimental observations in which chalcogen bonding is crucial for synthetic transformations, crystal engineering, catalysis and design of materials as synthons/tectons.
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Multinuclear Copper Triethanolamine Complexes as Selective Catalysts for the Peroxidative Oxidation of Alkanes under Mild Conditions
Alexander M. Kirillov,Maximilian N. Kopylovich,Marina V. Kirillova,Matti Haukka,M. Fátima C. Guedes da Silva,Armando J. L. Pombeiro +5 more
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Non-covalent interactions in the synthesis of coordination compounds: Recent advances
Kamran T. Mahmudov,Kamran T. Mahmudov,Maximilian N. Kopylovich,M. Fátima C. Guedes da Silva,Armando J. L. Pombeiro +4 more
TL;DR: In this paper, a review describes how non-covalent interactions, such as hydrogen (inter-and intramolecular, resonance-and charge-assisted hydrogen bonding), halogen, chalcogen and pnicogen bonds, π-interactions, as well as other types of weak forces can influence and control the reactions in the synthesis, providing a class of highly directional stabilizing contacts that can be exploited in the design of coordination compounds.
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Vanadium complexes: Recent progress in oxidation catalysis
Manas Sutradhar,Luísa M. D. R. S. Martins,M. Fátima C. Guedes da Silva,Armando J. L. Pombeiro +3 more
TL;DR: In this article, the main types of both homogeneous and supported vanadium catalysts and the most efficient catalytic systems in different reactions are presented and compared, and the proposed mechanisms of various catalytic oxidation processes are also outlined.
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Aminocarbene complexes derived from nucleophilic addition to isocyanide ligands
TL;DR: Isocyanides ligating medium to high-valent electron-poor metal centers can undergo activation toward α-nucleophilic addition to afford a variety of aminocarbene complexes with either heterocyclic or acyclic ligands.