Stimulated emission spectroscopy of the ground state of Na3

1989 ◽  
Vol 90 (8) ◽  
pp. 4620-4622 ◽  
Author(s):  
M. Broyer ◽  
G. Delacrétaz ◽  
G.‐Q. Ni ◽  
R. L. Whetten ◽  
J.‐P. Wolf ◽  
...  
Keyword(s):  
Ground State ◽  
Emission Spectroscopy ◽  
Stimulated Emission

Tuning the Electrochemical and Photophysical Properties of Osmium-Based Photoredox Catalysts

Synlett ◽  
2022 ◽  
Author(s):  
Eva Bednářová ◽  
Logan R. Beck ◽  
Tomislav Rovis ◽  
Samantha L. Goldschmid ◽  
Katherine Xie ◽  
...  
Keyword(s):  
Ground State ◽  
Emission Spectroscopy ◽  
Near Infrared ◽  
Photophysical Properties ◽  
Low Energy ◽  
Redox Potentials ◽  
Nir Light ◽  
Osmium Complexes ◽  
Absorption And Emission Spectroscopy

AbstractThe use of low-energy deep-red (DR) and near-infrared (NIR) light to excite chromophores enables catalysis to ensue across barriers such as materials and tissues. Herein, we report the detailed photophysical characterization of a library of OsII polypyridyl photosensitizers that absorb low-energy light. By tuning ligand scaffold and electron density, we access a range of synthetically useful excited state energies and redox potentials.1 Introduction1.1 Scope1.2 Measuring Ground-State Redox Potentials1.3 Measuring Photophysical Properties1.4 Synthesis of Osmium Complexes2 Properties of Osmium Complexes2.1 Redox Potentials of Os(L)2-Type Complexes2.2 Redox Potentials of Os(L)3-Type Complexes2.3 UV/Vis Absorption and Emission Spectroscopy3 Conclusions

Growth and stimulated emission spectroscopy of Ca3Ga2Ge3O12Nd3+ garnet crystals

1983 ◽  
Vol 78 (2) ◽  
pp. 723-732 ◽  
Author(s):  
A. A. Kaminskii ◽  
B. V. Mill ◽  
A. V. Butashin
Keyword(s):  
Emission Spectroscopy ◽  
Stimulated Emission

scholarly journals Dynamic solvatochromism in solvent mixtures

2001 ◽  
Vol 73 (3) ◽  
pp. 405-409 ◽  
Author(s):  
Diana E. Wetzler ◽  
Carlos Chesta ◽  
Roberto Fernández-Prini ◽  
Pedro F. Aramendía
Keyword(s):  
Excited State ◽  
Ground State ◽  
Emission Spectroscopy ◽  
Characteristic Time ◽  
Polar Solvent ◽  
Emission Spectra ◽  
Spectral Shift ◽  
Solvent Mixtures ◽  
Time Resolved ◽  
Different Temperatures

Solvatochromism and thermochromism of 4-aminophthalimide and 4-amino-N-methylphthalimide were studied by absorption and steady-state and time-resolved emission spectroscopy in solvent mixtures of toluene­ethanol and toluene­acetonitrile at different temperatures. Emission spectra shift to the red upon addition of a polar solvent (PS) to toluene. Solvent mixtures show a much greater thermochromic shift to the blue in emission than the neat solvents. This is explained by the decrease in temperature of the exothermic association of the polar solvent to the excited state. Emission spectra are time dependent in solvent mixtures in the ns timescale. The time evolution of this emission is interpreted on the basis of the different solvation of the ground state and the emitting excited state. Stern­Volmer plots are obtained for the dependence of the spectral-shift characteristic time with [PS].

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