[Hg3(m-C6F4)3]. Naphthalene p-acid/p-base adduct - PowerPoint PPT Presentation

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[Hg3(m-C6F4)3]. Naphthalene p-acid/p-base adduct

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[Hg3(m-C6F4)3].Pyrene adduct. p-acid. p-base. p-acid/p-base adduct ... Unlike naphthalene, solid pyrene gives excimer not monomer emission. ... – PowerPoint PPT presentation

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Title: [Hg3(m-C6F4)3]. Naphthalene p-acid/p-base adduct


1
Hg3(m-C6F4)3. Naphthalene p-acid/p-base adduct
p-base
p-acid
p-acid/p-base adduct
2
Luminescence spectra of naphtahlene.Hg3(m-C6F4)3
at ambient temperature, resulting in 100
phosphorescence!
CONTROL Emission spectrum of solid napthalene
without the mercury trimer. Emission is due to
monomer fluorescence.
Average vibronic spacing 1434 80 cm-1
3
Hg3(m-C6F4)3.Pyrene adduct
p-base
p-acid
p-acid/p-base adduct
4
Emission spectra of pyrene.Hg3(m-C6F4)3
CONTROL Emission spectrum of solid pyrene
  • Science here has two important technological
    implications on the EL device industry
  • Phosphorescence enhancement (100)
  • Unlike naphthalene, solid pyrene gives excimer
    not monomer emission. Excimer emissions are not
    desired for organic fluorophores in EL
    applications. Solid-state interaction of pyrene
    with Hg3 units (see X-ray data) prevents pyrene
    from association.

5
Luminescence spectra of p-acid/p-base adducts
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