2B2: The ground state of the hexamethyl(Dewar benzene) radical cation. Time-resolved fluorescence detected magnetic resonance

1990 ◽  
Vol 112 (5) ◽  
pp. 2026-2027 ◽  
Author(s):  
X. Z. Qin ◽  
D. W. Werst ◽  
A. D. Trifunac
2010 ◽  
Vol 8 (3) ◽  
pp. 674-686 ◽  
Author(s):  
Magda Milewska ◽  
Katarzyna Guzow ◽  
Wiesław Wiczk

AbstractThe ability of new chelate ligands, benzoxazol-5-yl-alanine derivatives substituted in position 2 by heteroaromatic substituent, to form complexes with selected metal ions in acetonitrile are studied by means of absorption and steady-state and time-resolved fluorescence spectroscopy. Among the ligands studied, only azaaromatic derivatives form stable complexes with transition metal ions in the ground state. Their absorption bands are bathochromically shifted enabling to use those ligands as ratiometric sensors. The fluorescence of each ligand is quenched by metal ions, however, in the presence of Cd(II) and Zn(II) ions a new red shifted emission band is observed.


2004 ◽  
Vol 69 (4) ◽  
pp. 748-758 ◽  
Author(s):  
Israel V. Muthu Vijayan Enoch ◽  
Meenakshisundaram Swaminathan

The photophysical and photoprototropic behaviour of 4-aminobiphenyl (4ABP) in aqueous β-cyclodextrin (β-CDx) solution has been investigated using steady-state and time-resolved fluorescence spectroscopy. Fluorescence of the neutral form of 4ABP is enhanced due to the formation of a 1:1 complex with β-CDx. The formation of this complex has been confirmed by time-resolved spectroscopy. In the presence of β-CDx, no change was observed in the ground state pKa value but the excited state pKa value changed. Based on its photophysical and photoprototropic characteristics in β-CDx, the structure of the 1:1 inclusion complex is proposed.


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