TY - JOUR
T1 - New two-photon-absorbing probe with efficient superfluorescent properties
AU - Belfield, Kevin D.
AU - Andrade, Carolina D.
AU - Yanez, Ciceron O.
AU - Bondar, Mykhailo V.
AU - Hernandez, Florencio E.
AU - Przhonska, Olga V.
N1 - Funding Information:
We thank Marı́a del Carmen Plaza for excellent technical support. Also, we thank Dr. A. Colige for the generous gift of type I and III procollagens and ADAMTS2, Dr. R. Heljasvaara, for the generous gift of type XVIII collagen, and Dr. H. Sage, for type VIII collagen. This work was supported by the Margaret Early Foundation and an NIH Grant CA 77420 to MLIA, by an award from the American Heart Association to JW, and the Shriners of North America and the Arthritis Foundation to JDS.
PY - 2010/11/11
Y1 - 2010/11/11
N2 - The synthesis, linear photophysical, and photochemical parameters, two-photon absorption (2PA), and superfluorescence properties of 2,2'-(5,5'-(9,9-didecyl-9H-fluorene-2,7-diyl)bis(ethyne-2,1-diyl) bis(thiophene-5,2-diyl))dibenzo[d]thiazole (1) were investigated, suggesting its potential as an efficient fluorescent probe for bioimaging applications. The steady-state absorption, fluorescence, and excitation anisotropy spectra of 1 were measured in several organic solvents and aqueous media. Probe 1 exhibited high fluorescence quantum yield (∼0.7-0.8) and photochemical stability (photobleaching quantum yield ∼(3-7) × 10-6). The 2PA spectra were determined over a broad spectral range (640-920 nm) using a standard two-photon induced fluorescence method under femtosecond excitation. A well-defined two-photon allowed absorption band at 680-720 nm with corresponding 2PA cross sections δ2PA ≈ 800-900 GM was observed. The use of probe 1 in bioimaging was shown via one- and two-photon fluorescence imaging of HCT-116 cells. An amplification of the stimulated emission of 1 was demonstrated in organic solvents and thin polystyrene films, which potentially can be used for the development of new fluorescent labels with increased spectral brightness.
AB - The synthesis, linear photophysical, and photochemical parameters, two-photon absorption (2PA), and superfluorescence properties of 2,2'-(5,5'-(9,9-didecyl-9H-fluorene-2,7-diyl)bis(ethyne-2,1-diyl) bis(thiophene-5,2-diyl))dibenzo[d]thiazole (1) were investigated, suggesting its potential as an efficient fluorescent probe for bioimaging applications. The steady-state absorption, fluorescence, and excitation anisotropy spectra of 1 were measured in several organic solvents and aqueous media. Probe 1 exhibited high fluorescence quantum yield (∼0.7-0.8) and photochemical stability (photobleaching quantum yield ∼(3-7) × 10-6). The 2PA spectra were determined over a broad spectral range (640-920 nm) using a standard two-photon induced fluorescence method under femtosecond excitation. A well-defined two-photon allowed absorption band at 680-720 nm with corresponding 2PA cross sections δ2PA ≈ 800-900 GM was observed. The use of probe 1 in bioimaging was shown via one- and two-photon fluorescence imaging of HCT-116 cells. An amplification of the stimulated emission of 1 was demonstrated in organic solvents and thin polystyrene films, which potentially can be used for the development of new fluorescent labels with increased spectral brightness.
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U2 - 10.1021/jp107343k
DO - 10.1021/jp107343k
M3 - Article
C2 - 20949957
AN - SCOPUS:78149241385
SN - 1520-6106
VL - 114
SP - 14087
EP - 14095
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 44
ER -