Abstract

The model-free analysis (MFA) was applied to measure the average rate constant (<k>) for pyrene excimer formation (PEF) in a series of pyrene-labeled dendrons referred to as Pyx-G(N), where x (= 2N) is the number of pyrenyl labels born by a dendron of generation N ranging from 1 to 6. <k> was measured in four different solvents, namely tetrahydrofuran (THF), toluene, N,N-dimethylformamide (DMF), and dimethylsulfoxide (DMSO). <k> was found to increase linearly with increasing local pyrene concentration ([Py]loc), where [Py]loc had been determined mathematically for the Pyx-G(N) dendrons. The slope of each straight line changed with the nature of the solvent and represented kdiff, the bimolecular rate constant for PEF. kdiff depended on the solvent viscosity (η) and the probability (p) for PEF upon encounter between an excited and a ground-state pyrene. In a same solvent, kdiff for the Pyx-G(N) dendrons was about 360 ± 30 times smaller than kdiff obtained for ethyl 4-(1-pyrene)butyrate (PyBE), a pyrene model compound similar to the pyrene derivative used to label the dendrons. The massive decrease in kdiff observed for the Pyx-G(N) samples reflected the massive loss in mobility experienced by the pyrenyl labels after being covalently attached onto a macromolecule compared to freely diffusing PyBE. Interestingly, the kdiff values obtained for the Pyx-G(N) dendrons and the PyBE model compound followed similar trends as a function of solvent, indicating that the difference in behavior between the kdiff values obtained in different solvents were merely due to the changes in the η and p values between the solvents. Normalizing the <k> values obtained with the Pyx-G(N) dendrons by the kdiff values obtained for PyBE in the same solvents accounted for changes in η and p, resulting in a master curve upon plotting <k>/(fdiff × kdiff) as a function of [Py]loc, where fdiff was introduced to account for some pyrene aggregation in the higher generation dendron (Py64-G(6)). This result demonstrates that <k> represents a direct measure of [Py]loc in pyrene-labeled macromolecules.

Highlights

  • Techniques such as viscometry, light scattering (LS), and small angle X-ray (SAXS) or neutron (SANS) scattering have traditionally played a critical role in the characterization of macromolecules due to their ability to determine the internal density of macromolecules in solution

  • Fluorescence is better known for its ability to probe fast photochemical processes, which has led to the implementation of many fluorescence-based applications to characterize the internal dynamics of macromolecules in solution [2]

  • The multiexponential fluorescence decays acquired with macromolecules labeled with more than two pyrenes can be satisfyingly fit according to the model-free analysis (MFA), which yields the average rate constant of pyrene excimer formation (PEF) [3,6]

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Summary

Introduction

Techniques such as viscometry, light scattering (LS), and small angle X-ray (SAXS) or neutron (SANS) scattering have traditionally played a critical role in the characterization of macromolecules due to their ability to determine the internal density of macromolecules in solution. The multiexponential fluorescence decays acquired with macromolecules labeled with more than two pyrenes can be satisfyingly fit according to the model-free analysis (MFA), which yields the average rate constant of pyrene excimer formation (PEF) [3,6] In this case, the ground-state pyrenes act as quenchers, and is related to the local pyrene concentration ([Py]loc ) experienced by an excited pyrene according to Equation (1). The MFA of the fluorescence decays acquired with the Pyx -G(N) dendrons yielded , which was found to increase linearly with increasing [Py]loc as predicted by Equation (1) This original study is extended to the three additional solvents toluene, N,N-dimethylformamide (DMF), and dimethylsulfoxide (DMSO), which provide, after including THF, a series of four solvents with a broad range of polarity and viscosity. After accounting for the changes in kdiff due to solvent polarity and viscosity, all vs. [Py]loc plots obtained for the Pyx -G(N) samples in the different solvents merged into a single master curve, demonstrating the validity and generality of Equation (1)

Materials
Synthesis of
UV–Vis
Steady-State Fluorometer
A FluoroHub
Birks Scheme Analysis of the Fluorescence Decays
Results and Discussion
Plot of the
Figure 3 between
Figure2 loc
Plot of for
Conclusions a χ
Full Text
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