1991
DOI: 10.1007/bf00544683
|View full text |Cite
|
Sign up to set email alerts
|

Structural determination of a semiconductive tetramer of aniline by IR, UV-visible, ESR, XPS and mass spectroscopy techniques

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

1
14
0

Year Published

2005
2005
2012
2012

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 14 publications
(15 citation statements)
references
References 38 publications
1
14
0
Order By: Relevance
“…In UV–Vis spectra (Figure 3a), the solution of MASA in distilled water did not have any adsorption above 300 nm. Similar to TA in N , N ‐dimethyl formamide, all solutions of MASA‐TA in double distilled water had two absorptions around 301 nm (π–π * transition in benzene ring) and 562 nm (π B‐ ‐π Q exciton transition from benzenoid ring to quinoid ring) 11, 20, 23. Altogether, the above characterization of MASA‐TA confirmed the successful introduction of TA to MASA.…”
Section: Resultssupporting
confidence: 59%
“…In UV–Vis spectra (Figure 3a), the solution of MASA in distilled water did not have any adsorption above 300 nm. Similar to TA in N , N ‐dimethyl formamide, all solutions of MASA‐TA in double distilled water had two absorptions around 301 nm (π–π * transition in benzene ring) and 562 nm (π B‐ ‐π Q exciton transition from benzenoid ring to quinoid ring) 11, 20, 23. Altogether, the above characterization of MASA‐TA confirmed the successful introduction of TA to MASA.…”
Section: Resultssupporting
confidence: 59%
“…Due to the transient nature of the intermediates, it is also possible that different pathways are involved at high vs. low proton concentrations. Many different reaction pathways and possible oligoaniline structures have been proposed in literature for aniline polymerization, ranging from N-phenylquinonediimine, [55,57,64] to linear tetramer, [65,66] to azane, [44] to phenazine constitutional units, [43] to a series of macromolecules based on 1,4-Michael-type addition on benzoquinoimine. [67] The work of Stejskal and Sapurina [43] suggests that aniline polymerization under any conditions goes through the same initial reaction sequences involving the same N-phenylphenazine-type trimer or tetramer formation.…”
Section: Resultsmentioning
confidence: 99%
“…[29][30][31] Alternative reaction pathways and Self-Assembled Polyaniline Nanotubes with Rectangular Cross-Sections many possible chemical structures of the oligoanilines formed at high pH have also been proposed in recent years. [3,[32][33][34] These vary from linear tetramer, [32] to phenazine constitutional units, [3] to azane, [33] to a series of macromolecules from 1,4-Michael type reaction. [34] The work of Stejskal and coworkers [3,12] suggest that different nanostructures (NFs, granulars, microspheres, and NTs etc.)…”
Section: Resultsmentioning
confidence: 99%