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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Investigation of the correlation between chemical structure and morphology in oligoaniline microspheres produced in buffered conditions

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Author(s):
dos Santos, Isabela F. S. [1] ; Temperini, Marcia L. A. [1]
Total Authors: 2
Affiliation:
[1] Univ Sao Paulo, Inst Chem, Dept Fundamental Chem, Av Prof Lineu Prestes 748, BR-05508000 Sao Paulo, SP - Brazil
Total Affiliations: 1
Document type: Journal article
Source: EUROPEAN POLYMER JOURNAL; v. 122, JAN 5 2020.
Web of Science Citations: 0
Abstract

Although the mainly intermolecular forces involved in the self-assembly of oligoaniline molecules have been consistently discussed (hydrogen bonds and pi-pi stacking interactions) the correlation between the driving forces and the large variations of morphology that can be obtained is still open in discussion, mostly because a detailed chemical characterization of such products is usually difficult to achieve. In this work, 3-D fluorescence spectroscopy is presented as a powerful technique in the identification and differentiation of phenazinic segments, with Raman spectroscopy being crucial for identification of 1,4-Michael-type segments and the verification of non-hydrolyzed imine groups in oligoaniline microspheres produced under pH 4.5 buffered conditions and employing different reagent concentrations. The results suggested that the self-assembly must occur by hydrogen bonds related to the non-hydrolyzed iminic groups and pi-pi stacking interactions between non-substituted phenazinic segments. Moreover, obtaining specific morphologies (flower-like structures, porous microspheres and hollow microspheres) showed dependence with the increase of the relative reagent concentrations. (AU)

FAPESP's process: 16/21070-5 - Vibrational spectroscopy with spatial resolution
Grantee:Mauro Carlos Costa Ribeiro
Support Opportunities: Research Projects - Thematic Grants