. . "N-Triazinyl Derivatives of 1-and 9-aminoanthracene: Synthesis and Photo-Physical Properties" . . "N-Triazinyl Derivatives of 1-and 9-aminoanthracene: Synthesis and Photo-Physical Properties"@en . "Journal of Fluorescence" . "RIV/68407700:21340/13:00218818" . "http://link.springer.com/article/10.1007%2Fs10895-013-1156-3" . "10.1007/s10895-013-1156-3" . "23" . "Burgert, L." . "N-Triazinyl Derivatives of 1-and 9-aminoanthracene: Synthesis and Photo-Physical Properties" . "3" . . . . "[C7AB9D16808C]" . "Michl, Martin" . "8"^^ . . "Nepra\u0161, M." . "21340" . "\u010Cerm\u00E1k, J." . . . "1053-0509" . "RIV/68407700:21340/13:00218818!RIV15-GA0-21340___" . . "quenching; quantum yield; fluorescence spectra; synthesis; N-Triazinyl aminoanthracenes"@en . . . "2"^^ . "New N-triazinyl derivatives were synthesized by reaction of cyanuric chloride with 1- and 9-aminoanthracenes and subsequent nucleophilic substitution of chlorine atoms on triazinyl ring with methoxy and/or phenylamino groups. The compounds were characterized by H-1 and C-13 NMR and mass spectra. The influence of the chemical structure and solvent polarity on the UV/Vis absorption and fluorescence spectra and fluorescence quantum yields were investigated. Semi-empirical computations revealed highly polar CT states in singlet excited state manifold connected with charge-transfer from the hydrocarbon moiety to the triazinyl ring. The relationships between the CT-to-emitting state energy gap, solvent polarity and fluorescence quantum yield were discussed."@en . "P\u0159ichystalov\u00E1, H." . "13"^^ . "I, P(GAP208/10/0941)" . "Almonasy, N." . . . "Bure\u0161, F." . . . "000319079400010" . "Dvo\u0159\u00E1k, Miroslav" . "US - Spojen\u00E9 st\u00E1ty americk\u00E9" . . . . "New N-triazinyl derivatives were synthesized by reaction of cyanuric chloride with 1- and 9-aminoanthracenes and subsequent nucleophilic substitution of chlorine atoms on triazinyl ring with methoxy and/or phenylamino groups. The compounds were characterized by H-1 and C-13 NMR and mass spectra. The influence of the chemical structure and solvent polarity on the UV/Vis absorption and fluorescence spectra and fluorescence quantum yields were investigated. Semi-empirical computations revealed highly polar CT states in singlet excited state manifold connected with charge-transfer from the hydrocarbon moiety to the triazinyl ring. The relationships between the CT-to-emitting state energy gap, solvent polarity and fluorescence quantum yield were discussed." . "92480" . "N-Triazinyl Derivatives of 1-and 9-aminoanthracene: Synthesis and Photo-Physical Properties"@en .