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Volumn 11, Issue 12, 2005, Pages 3643-3658

Synthesis, spectroscopic and nonlinear optical properties of multiple [60]fullerene-oligo(p-phenylene ethynylene) hybrids

Author keywords

Conjugation; Electrochemistry; Fullerenes; NMR spectroscopy; Nonlinear optics

Indexed keywords

CHARGE TRANSFER; ELECTRONIC PROPERTIES; NONLINEAR OPTICS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OLIGOMERS; OPTICAL PROPERTIES; SYNTHESIS (CHEMICAL);

EID: 20644467266     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200401198     Document Type: Article
Times cited : (101)

References (146)
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    • and references cited in these papers to other relevant papers
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    • (Ed.: J. E. Midwinter), Academic Press, San Diego
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    • note
    • 2, some undissolved residue was observed. The quantity of this paniculate was extremely small and should not impact the concentration. If, however, the concentration were lower than reported, the molecular nonlinearities reported herein for 31 would only be greater than reported.
  • 138
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    • note
    • Nonlinear absorption measurements conducted with ns pulses often show signals that are orders of magnitude higher than those conducted with fs pulses. This is mainly due to signals from excited-state absorption mixing with pure TPA signals. However, comparisons of the same "AFX" compounds' TPA cross-sections have been done by the same group at both pulse duration regimes. We have also studied an "AFX" compound (not discussed herein) that allows for scaling of our fs results for comparisons with ns results. See: ref. [82] and [97].


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