766545-67-9Relevant academic research and scientific papers
Facile synthesis of fluorescent distyrylnaphthalene derivatives for bioapplications
?ukasik, Beata,Milczarek, Justyna,Pawlowska, Roza,Zurawiński, Remigiusz,Chworos, Arkadiusz
, p. 6977 - 6980 (2017/08/01)
A series of novel 2,6-bis(4-aminostyryl)naphthalene based derivatives were synthesized and their spectroscopic properties investigated. Due to their low cytotoxicity, suitable optical properties and potential affinity towards biological structures these d
Paracyclophane molecules for two-photon absorption applications
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Page/Page column 7-8, (2010/11/23)
Chromophores having two-photon or other multi-photon absorptivity. The chromophores are based on a structure of four stilbenoid groups attached to a paracyclophane core, where each stilbenoid group comprises a nitrogen-containing organic group attached by
Solvent effects on the two-photon absorption of distyrylbenzene chromophores
Woo, Han Young,Liu, Bin,Kohler, Bernhard,Korystov, Dmitry,Mikhailovsky, Alexander,Bazan, Guillermo C.
, p. 14721 - 14729 (2007/10/03)
A series of organic- and water-soluble distyrylbenzene-based two-photon absorption (TPA) fluorophores containing dialkylamino donor groups at the termini was designed, synthesized, and characterized. The central core was systematically substituted to modu
Solvatochromism of distyrylbenzene pairs bound together by [2.2]paracyclophane: Evidence for a polarizable "through-space" delocalized state
Hong, Janice W.,Woo, Han Young,Liu, Bin,Bazan, Guillermo C.
, p. 7435 - 7443 (2007/10/03)
A series of compounds were designed and synthesized to examine how through-space and through-bond electron delocalization respond to solvent effects. The general strategy involves the study of "dimers" of the distyrylbenzene chromophore held in close prox
Water-soluble [2.2]paracyclophane chromophores with large two-photon action cross sections
Woo, Han Young,Hong, Janice W.,Liu, Bin,Mikhailovsky, Alexander,Korystov, Dmitry,Bazan, Guillermo C.
, p. 820 - 821 (2007/10/03)
A series of α,ω-donor-substituted distyrylbenzene dimers held together by the [2.2]paracyclophane core were designed, synthesized, and characterized. Different substituents were chosen to modulate the strength of the donor nitrogen groups and to allow the
Water-soluble distyrylbenzene chromophores for applications in optoelectronic technologies
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Page 3, (2008/06/13)
Two-photon or multi-photon chromophores having a conjugated pi-electron system with donating groups at each end of the pi-electron system providing charge-transfer properties, and having quaternary amine groups that can enhance the solubility of the chrom
