Transient Excited-State Absorption and Gain Spectroscopy of a Two-Photon Absorbing Probe with Efficient Superfluorescent Properties

被引:26
作者
Belfield, Kevin D. [1 ,2 ]
Bondar, Mykhailo V. [3 ]
Morales, Alma R. [1 ]
Yue, Xiling [1 ]
Luchita, Gheorghe [1 ]
Przhonska, Olga V. [3 ]
机构
[1] Univ Cent Florida, Coll Opt & Photon, Dept Chem, Orlando, FL 32816 USA
[2] Univ Cent Florida, Coll Opt & Photon, CREOL, Orlando, FL 32816 USA
[3] Inst Phys, UA-03028 Kiev 28, Ukraine
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
STIMULATED-EMISSION-DEPLETION; OPTICAL-DATA STORAGE; CHARGE-TRANSFER; SINGLET OXYGEN; FEMTOSECOND; DYNAMICS; CHROMOPHORES; PICOSECOND; RESOLUTION; BREAKING;
D O I
10.1021/jp302274v
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The synthesis, linear photophysical properties, two-photon absorption (2PA), excited-state transient absorption, and gain spectroscopy of a new fluorene derivative tertbutyl 4,4'-(4,4' (1E,1'E)-2,2'-(9,9-bis(2-(2-ethoxyethoxy)ethyl)-9H-fluorene-2,7-diyl)bis(ethene-2,1-diyl)bis(4,1 phenylene)]dipiperazine-1-carboxylate (1) are reported. The steady-state linear absorption and fluorescence spectra along with excitation anisotropy, fluorescence lifetimes, and photochemical stability of 1 were investigated in a number of organic solvents at room temperature. The 2PA spectra of 1 with a maximum cross section of 300 GM were obtained with a 1-kHz femtosecond laser system using open-aperture Z-scan and two-photon-induced fluorescence methods. The transient excited-state absorption (ESA) and gain kinetics of 1 were investigated by a femtosecond pump probe methodology. Fast relaxation processes (similar to 1-2 ps) in the gain and ESA spectra of 1 were revealed in ACN solution, attributable to symmetry-breaking effects in the first excited state. Efficient superfluorescence properties of 1 were observed in a nonpolar solvent under femtosecond excitation. One- and two-photon fluorescence microscopy imaging of HCT 116 cells incubated with probe 1 was accomplished, suggesting the potential of this new probe in two-photon fluorescence microscopy bioimaging.
引用
收藏
页码:11261 / 11271
页数:11
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