Talita Martins Lacerda

Dr. Talita Martins Lacerda

Department of Biotechnology, Engineering School of Lorena, University of São Paulo, Lorena 12.602-810, Brazil
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Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 August 2015 in Chemical Reviews
Verified
Journal Article
Closed access
AGAlessandro Gandini
Alessandro Gandini
TLTalita Martins Lacerda
Talita Martins Lacerda
ACAntonio José Felix de Carvalho
Antonio José Felix de Carvalho
ETEliane Trovatti
Eliane Trovatti

1 September 2015 in Progress in Polymer Science
Verified
Journal Article
Closed access
AGAlessandro Gandini
Alessandro Gandini
TLTalita Martins Lacerda
Talita Martins Lacerda

16 February 2015 in Advanced Materials
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Journal Article
Closed access
PDF file
ETEliane Trovatti
Eliane Trovatti
TLTalita Martins Lacerda
Talita Martins Lacerda
ACAntonio José Felix de Carvalho
Antonio José Felix de Carvalho
Alessandro GandiniAlessandro Gandini
Alessandro Gandini

20 February 2015 in Macromolecules
Verified
Journal Article
Closed access
MWMatthias Winkler
Matthias Winkler
TLTalita Martins Lacerda
Talita Martins Lacerda
FMFelix Mack
Felix Mack
MMMichael Meier
Michael Meier

11 January 2022 in Macromolecular Materials and Engineering
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Journal Article
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Alessandro GandiniAlessandro Gandini
Alessandro Gandini
TLTalita Martins Lacerda
Talita Martins Lacerda

9 June 2014 in RSC Advances
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Journal Article
Closed access
PDF file
TLTalita Martins Lacerda
Talita Martins Lacerda
ACAntonio José Felix de Carvalho
Antonio José Felix de Carvalho
AGAlessandro Gandini
Alessandro Gandini
Novel linear and crosslinked polymers from non-modified and modified tung oil are reported. These materials are based on the exploitation of the Diels–Alder reaction using, on the one hand, the dienic character of the three conjugated double bonds of tung oil and their susceptibility to react with a dienophile, and, on the other hand, the bulk reaction of furfuryl amine at the ester moieties of tung oil to produce three fatty acid furan amides, still bearing the three conjugated double bonds, and their linear polymerization with bismaleimides.