2013
DOI: 10.1016/j.dyepig.2012.11.001
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Novel luminescent phenothiazine-based Schiff bases with tuned morphology. Synthesis, structure, photophysical and thermotropic characterization

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Cited by 47 publications
(30 citation statements)
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“…As we reported before, the thin film DPF azomethine dye presents an absorption maximum around 392 nm -attributed to the chromophoric unit formed by an extended conjugation of the azomethine linkage with both fluorene and phenothiazine units [16]. Compared to the DPF pure film, the DPF/polymer composites absorbtion spectra show significant changes, indicating the influence of the matrix polymer on the DPF optical behavior.…”
Section: Photophysical Propertiesmentioning
confidence: 76%
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“…As we reported before, the thin film DPF azomethine dye presents an absorption maximum around 392 nm -attributed to the chromophoric unit formed by an extended conjugation of the azomethine linkage with both fluorene and phenothiazine units [16]. Compared to the DPF pure film, the DPF/polymer composites absorbtion spectra show significant changes, indicating the influence of the matrix polymer on the DPF optical behavior.…”
Section: Photophysical Propertiesmentioning
confidence: 76%
“…2b). No crystalline state appears from the melting state [16]. The structures of the DPF and the used polymers are presented in Scheme 1.…”
Section: Methodsmentioning
confidence: 99%
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