144393-34-0Relevant articles and documents
Two-photon fluorescent holographic rewritable micropatterning
Ishow, Elena,Brosseau, Arnaud,Clavier, Gilles,Nakatani, Keitaro,Pansu, Robert B.,Vachon, Jean-Jacques,Tauc, Patrick,Chauvat, Dominique,Mendonca, Cleber R.,Piovesan, Erick
, p. 8970 - 8971 (2007)
Monomeric amorphous systems involving an upper azo-based layer and a lower fluorophore layer have been carefully designed to enable holographic formation of micrometric emissive photopatterns through reversible photoinduced mass migration of azoderivatives. The fluorescent patterns evidenced by NIR biphotonic excitation match the micrometric surface relief. After successful erasure by using a circularly polarized visible light, new patterns can be written again. Copyright
Erratum: Construction of electrocatalytic electrodes bearing the triphenylamine nucleus covalently bound to carbon. A halogen dance in protonated aminotriphenylamines (Organic Letters (2006) 8 (412-414))
Mayers, Brian T.,Fry, Albert J.
, p. 1253 - 1253 (2007/10/03)
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Electrophilic nitration of triphenylamines as a route to high oxidation potential electrocatalysts. Polynitration, nitrodebromination, and bromine dance
Wu, Xin,Dube, Mufaro A.,Fry, Albert J.
, p. 7667 - 7669 (2007/10/03)
The nitration of triphenylamine derivatives is facile, readily leading to an introduction of up to three nitro groups at room temperature. The nitration of 4,4′,4″-tribromotriphenylamine results in nitrodebromination on one or more rings and bromination a
