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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 
 
 
 

Phosphorescent organogels via "metallophilic" interactions for reversible RGB-color switching.

A trinuclear Au(I) pyrazolate complex bearing long alkyl chains (1) in hexane self-assembles via a Au(I)-Au(I) metallophilic interaction, to form a red-luminescent organogel (lambda(em) = 640 nm, lambda(ext) = 284 nm). Scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis of an air-dried gel with 1 show the presence of heavily entangled fibers, each consisting of a rectangularly packed columnar assembly of 1. Doping of the organogel with a small amount of Ag(+) results in a blue luminescence (lambda(em) = 458 nm, lambda(ext) = 370 nm) without disruption of the gel, while removal of doped Ag(+) with cetyltrimethylammonium chloride results in complete recovery of the original red-luminescent gel. Upon heating, these organogels undergo gel-to-sol transition due to the destabilization of the metallophilic interactions, where the red luminescence of the nondoped system becomes hardly visible, while the blue luminescence of the Ag(+)-doped system turns green (lambda(em) = 501 nm, lambda(ext) = 370 nm). On cooling, these solutions undergo gelation and synchronously recover the original luminescences. The observed RGB (red-green-blue) luminescences are all long-lived (3-6 micros) and assigned to electronic transitions from triplet-excited states.[1]

References

  1. Phosphorescent organogels via "metallophilic" interactions for reversible RGB-color switching. Kishimura, A., Yamashita, T., Aida, T. J. Am. Chem. Soc. (2005) [Pubmed]
 
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