Journal
DALTON TRANSACTIONS
Volume 45, Issue 26, Pages 10836-10841Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6dt01161f
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Funding
- 973 Program of China [2014CB845600]
- NSFC [21301100]
- Education Department Fund of Henan [13A150819]
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A polydentate pyridyl derivative, 2,3,6,7,10,11-hexa(2-pyridy0-dipyrazino (2,3-f:2',3'-h]quinoxaline (HPDQ), exhibits a high-performance fluorescence response to La3+ with an similar to 65 nm redshifted emission wavelength and 38 fold enhanced intensity, in contrast to its weakened emission for other lanthanide ions. The final La3+ coordination complex in solution has a stoichiometric ratio of 1: 3 of ligand-to-metal, as testified by the Job's plot and single crystal structure analyses. The red shift of the luminescence emission as well as UV-vis absorption was rationalized in terms of the change of the electron structure as indicated by nuclear magnetic titration, electrochemical experiment and density functional theoretical calculation, while the significant enhancement of emission was attributed to the enhanced pi conjugated extent of HPDQ caused by La3+ coordination.
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