2009
DOI: 10.1016/j.dyepig.2009.03.010
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The synthesis of bi- and trichromophoric dyes bearing an s-triazinyl ring spacer

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Cited by 9 publications
(3 citation statements)
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“…Previously, we have described the synthesis and photo-physical properties of similar bichromophores. 3-Aminobenzanthrone or 3-aminoperylene as acceptor moieties and 2-aminoanthracene donor [7] as well as 3-aminobenzanthrone and 1-aminopyrene acceptor/ donor of the excitation energy [8] were used. For D-T-A bichromophore where D is 1-aminopyrene and A is 3-aminobenzanthrone, very efficient EET was found which takes place on the subpicosecond time scale, i.e.…”
Section: Introductionmentioning
confidence: 99%
“…Previously, we have described the synthesis and photo-physical properties of similar bichromophores. 3-Aminobenzanthrone or 3-aminoperylene as acceptor moieties and 2-aminoanthracene donor [7] as well as 3-aminobenzanthrone and 1-aminopyrene acceptor/ donor of the excitation energy [8] were used. For D-T-A bichromophore where D is 1-aminopyrene and A is 3-aminobenzanthrone, very efficient EET was found which takes place on the subpicosecond time scale, i.e.…”
Section: Introductionmentioning
confidence: 99%
“…The 1 H chemical shifts were referenced to the solvent peak DMSO- d 6 (2.49 ppm) and the 13 C chemical shifts were referenced to the solvent peak DMSO d 6 (39.5 ppm). 2,4,6-Tri(1-pyrenylamino)-1,3,5-triazine Tz-Py was synthesized according to a procedure previously reported . The initiators are yellow powders for Tz_An , Tz_BP and Tz_Py .…”
Section: Experimental Partmentioning
confidence: 99%
“…2,4,6-Tri(1pyrenylamino)-1,3,5-triazine Tz-Py was synthesized according to a procedure previously reported. 5 The initiators are yellow powders for Tz_An, Tz_BP and Tz_Py. All the synthesized compounds were prepared with analytical purity up to accepted standards for new organic compounds (>98%) which was checked by high field NMR analysis.…”
Section: ■ Introductionmentioning
confidence: 99%