The 7-azaindole chromophore in water is studied by means of picosecond absorption and fluorescence spectroscopy in order to determine its nonradiative decay pathways. It is concluded that a small population of 7-azaindole molecules (-20%) undergo excited-state tautomerization in about 70 ps. Intersystem crossing and photoionization are also identified as nonradiative decay channels. Photoionization occurs largely from an electronic state lying slightly in energy above the fluorescent state. This new understanding of the photophysics of the 7-azaindole chromophore in water will be essential in interpreting its behavior when it is used as an optical probe of protein structure and dynamics
Author Institution: Physical Chemistry Department, Indian Association for the Cultivation of Science...
Author Institution: Physical Chemistry Department, Indian Association for the Cultivation of Science...
$^{a}$ J.A. Hageman, R. Wehrens, R. de Gelder, W.L. Meerts and L.M.C. Buydens. J. Chem. Phys. 113 (2...
7-Azaindole is the chromophoric side chain of the nonnatural amino acid 7-azatryptopha11, which we h...
Time-resolved and steady-state fluorescence study of the biological optical probe, 7-azatryptophan, ...
The nonradiative pathways of 7-azaindole are extremely sensitive to solvent. In alcohols, 7-azaindol...
A study of the fluorescence lifetimes and quantum yields of 7-azaindole and its methylated derivativ...
7-Azaindole is the chromophoric moiety of 7-azatryptophan, which is an alternative to tryptophan as ...
The excited-state photophysics of the biological probe, 7-azaindole, are examined in water and metha...
The proton inventory technique is used for the first time to investigate excited-state proton-transf...
The fluorescence decay of an optical probe, the nonnatural amino acid 7-azatryptophan, is measured a...
7-Azaindole undergoes monophotonic ionization just as its counterpart, indole. This result suggests ...
Multireference wave functions, augmented by second-order perturbation theory, are used to examine th...
Ab initio calculations are reported on 7-azaindole and the 1:1 complexes between 7-azaindole and wat...
The nonradiative pathways of 7-azaindole are extremely sensitive to solvent. In alcohols, 7-azaindol...
Author Institution: Physical Chemistry Department, Indian Association for the Cultivation of Science...
Author Institution: Physical Chemistry Department, Indian Association for the Cultivation of Science...
$^{a}$ J.A. Hageman, R. Wehrens, R. de Gelder, W.L. Meerts and L.M.C. Buydens. J. Chem. Phys. 113 (2...
7-Azaindole is the chromophoric side chain of the nonnatural amino acid 7-azatryptopha11, which we h...
Time-resolved and steady-state fluorescence study of the biological optical probe, 7-azatryptophan, ...
The nonradiative pathways of 7-azaindole are extremely sensitive to solvent. In alcohols, 7-azaindol...
A study of the fluorescence lifetimes and quantum yields of 7-azaindole and its methylated derivativ...
7-Azaindole is the chromophoric moiety of 7-azatryptophan, which is an alternative to tryptophan as ...
The excited-state photophysics of the biological probe, 7-azaindole, are examined in water and metha...
The proton inventory technique is used for the first time to investigate excited-state proton-transf...
The fluorescence decay of an optical probe, the nonnatural amino acid 7-azatryptophan, is measured a...
7-Azaindole undergoes monophotonic ionization just as its counterpart, indole. This result suggests ...
Multireference wave functions, augmented by second-order perturbation theory, are used to examine th...
Ab initio calculations are reported on 7-azaindole and the 1:1 complexes between 7-azaindole and wat...
The nonradiative pathways of 7-azaindole are extremely sensitive to solvent. In alcohols, 7-azaindol...
Author Institution: Physical Chemistry Department, Indian Association for the Cultivation of Science...
Author Institution: Physical Chemistry Department, Indian Association for the Cultivation of Science...
$^{a}$ J.A. Hageman, R. Wehrens, R. de Gelder, W.L. Meerts and L.M.C. Buydens. J. Chem. Phys. 113 (2...