Premium
Singlet Energy Transfer as the Main Pathway in the Sensitization of Near‐Infrared Nd 3+ Luminescence by Dansyl and Lissamine Dyes
Author(s) -
Hebbink Gerald A.,
Klink Stephen I.,
Grave Lennart,
Oude Alink Patrick G. B.,
van Veggel Frank C. J. M.
Publication year - 2002
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.200290002
Subject(s) - photochemistry , fluorescence , chemistry , singlet state , lanthanide , singlet oxygen , excited state , luminescence , ion , energy transfer , triplet state , phosphorescence , materials science , molecule , chemical physics , atomic physics , optoelectronics , organic chemistry , optics , physics , oxygen
In general, sensitization of lanthanide( III ) ions by organic sensitizers is regarded to take place via the triplet state of the sensitizers. Herein, we show that in dansyl‐ and lissamine‐functionalized Nd 3+ complexes energy transfer occurs from the singlet state of the sensitizers to the Nd 3+ center. No sensitized emission was observed in the corresponding complexes with Er 3+ , Yb 3+ , and Gd 3+ ions. Furthermore, the fluorescence of the sensitizers was quenched only in the Nd 3+ complex and not in the complexes with the other ions. Only Nd 3+ centers can accept energy from the singlet state of the dyes, because the excited states of Nd 3+ have a high spectral overlap with the fluorescence of the dansyl and lissamine sensitizers, and because the selection rules allow a fast energy transfer, which apparently is competitive with the fluorescence.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom