RESUMEN
To investigate the interplay between on-chain keto defect and interchain interaction and its consequence on the blue emission of polyfluorene (PF), first- to third-generation dendronized PFs as well as single-fluorenone-unit doped PF (PFN), synthesized by Suzuki polycondensation, were used as model compounds for steady-state and picosecond time-resolved photoluminescence (PL) spectroscopic studies. For PF film, the broad-band green emission did not appear, although severe interchain interaction was observed. For PFN film, the green emission that peaked at approximately 540 nm decayed in a multiphasic manner, suggesting significant heterogeneity in the excitation migration toward the keto center. To further examine the interplay effect, a series of novel dendronized-PF/PFN blend films in a molar ratio of 40:1 fluorene-to-fluorenone unit were studied. With reference to pure PFN film, those of the green emission of the blends showed strong dependence on the order of dendronization, that is, a higher generation resulted in a shorter-lived green emission. These observations are discussed in terms of interchain and/or intersegment interactions between the fluorene segments and the keto defect. It is concluded that the keto unit and the keto-centered, interchain aggregation lead to severe color degradation in a synergistic manner, and that dendronization can effectively minimize the undesirable green emission.
RESUMEN
This communication provides a facile method for distributing and dispersing molecules within a molecular template. Using the self-assembled template of oligo(phenylene-ethynylene) (OPE), organic molecules such as coronene (COR) and biomolecules such as tripeptide are controllably distributed and dispersed within this molecular template on highly oriented pyrolytic graphite (HOPG) surfaces. COR molecules were controllably distributed into various regular arrays by simply adjusting the molecular molar ratio, while tripeptide molecules were uniformly positioned at the vacancies of the OPE template.