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
supporting information, 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
-
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
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
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
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
-
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
