The dimer and the excimer formation mechanisms of anthracene in NaY zeolitic nanocavities have been studied by using various spectroscopic techniques of 129Xe NMR, diffuse reflectance, and emission as well as time-resolved fluorescence. Two anthracene molecules adsorb concertedly into a zeolitic supercage to form a ground-state stable dimer. An excited monomer in a singly occupied supercage gives birth to an excimer if another monomer exists in a tetrahedrally connected nearest supercage. An excited monomer forms a nonluminescent ion pair with a monomer in a nearest supercage by transferring an electron within 100 ps. The dark intermediate rearranges to transform into an excimer on the time scale of 400 ps.close161
The spectroscopy and dynamics of the lowest excited states of the jet formed anthracene clusters (n<...
Excimer formation in a new class of terthiophene-based fluorophores covalently bonded to a cyclotetr...
Work presented in this thesis is the consolidation of our experiments aimed at achieving selectivity...
The photo-physical properties of dicyanoanthracene (DCA) molecules adsorbed on the external surface ...
Photolyses of acenaphthylene included in M+ Y zeolites gave the corresponding cis and trans dimers. ...
Solid-state excimer emission of anthracene and its derivatives is a rare case at ambient conditions....
The photophysical properties of dicyanoanthracene (DCA) molecules adsorbed on the external surface o...
The understanding of excimer formation in organic materials is of fundamental importance, since exci...
We present an experimental study investigating the solvent-dependent dynamics of a 9,10-bis(phenylet...
Cyclodextrin cavities have been intercalated in a layered metal hydroxide to create hydrophobic nano...
Cyclodextrin cavities have been intercalated in a layered metal hydroxide to create hydrophobic nano...
We report on steady-state absorption and emission and time-resolved emission studies of (<i>E</i>)-2...
*S Supporting Information ABSTRACT: Nonadiabatic excited-state molecular dynamics (NA-ESMD) simulati...
The appearence of the new fluorescence peak at about 570 nm demonstrates exciplex formation between ...
The excited-state deprotonation and ground-state reprotonation of a 2-naphthol molecule encapsulated...
The spectroscopy and dynamics of the lowest excited states of the jet formed anthracene clusters (n<...
Excimer formation in a new class of terthiophene-based fluorophores covalently bonded to a cyclotetr...
Work presented in this thesis is the consolidation of our experiments aimed at achieving selectivity...
The photo-physical properties of dicyanoanthracene (DCA) molecules adsorbed on the external surface ...
Photolyses of acenaphthylene included in M+ Y zeolites gave the corresponding cis and trans dimers. ...
Solid-state excimer emission of anthracene and its derivatives is a rare case at ambient conditions....
The photophysical properties of dicyanoanthracene (DCA) molecules adsorbed on the external surface o...
The understanding of excimer formation in organic materials is of fundamental importance, since exci...
We present an experimental study investigating the solvent-dependent dynamics of a 9,10-bis(phenylet...
Cyclodextrin cavities have been intercalated in a layered metal hydroxide to create hydrophobic nano...
Cyclodextrin cavities have been intercalated in a layered metal hydroxide to create hydrophobic nano...
We report on steady-state absorption and emission and time-resolved emission studies of (<i>E</i>)-2...
*S Supporting Information ABSTRACT: Nonadiabatic excited-state molecular dynamics (NA-ESMD) simulati...
The appearence of the new fluorescence peak at about 570 nm demonstrates exciplex formation between ...
The excited-state deprotonation and ground-state reprotonation of a 2-naphthol molecule encapsulated...
The spectroscopy and dynamics of the lowest excited states of the jet formed anthracene clusters (n<...
Excimer formation in a new class of terthiophene-based fluorophores covalently bonded to a cyclotetr...
Work presented in this thesis is the consolidation of our experiments aimed at achieving selectivity...