10.1021/la304628d.s001
Shaohua Chen
Shaohua
Chen
Jean Duhamel
Jean
Duhamel
Probing the Hydrophobic
Interactions of a Series of
Pyrene End-Labeled Poly(ethylene oxide)s in Aqueous Solution Using
Time-Resolved Fluorescence
American Chemical Society
2013
pyrene pendants subject
pyrene excimer formation
CP
SM
polymer concentrations
PEO chain length
pyrene excimer
intramolecular pyrene excimer formation
IE
2013-03-05 00:00:00
Journal contribution
https://acs.figshare.com/articles/journal_contribution/Probing_the_Hydrophobic_Interactions_of_a_Series_of_Pyrene_End_Labeled_Poly_ethylene_oxide_s_in_Aqueous_Solution_Using_Time_Resolved_Fluorescence/2437708
The hydrophobic association of a series of poly(ethylene
oxide)s
covalently labeled at both ends with pyrene (PEO(<i>X</i>)-Py<sub>2</sub> where <i>X</i> represents the number average
molecular weight (<i>M</i><sub>n</sub>) of the PEO chains
equal to 2, 5, 10, and 16.5 kDa) in aqueous solutions was investigated
at different polymer concentrations (<i>C</i><sub>P</sub>) using steady-state and time-resolved fluorescence measurements.
Phase separation was observed with PEO(2 kDa)-Py<sub>2</sub> and PEO(5
kDa)-Py<sub>2</sub> samples at high <i>C</i><sub>P</sub>. The steady-state fluorescence spectra showed that the ratios of
excimer-to-monomer fluorescence intensities (<i>I</i><sub>E</sub>/<i>I</i><sub>M</sub>) of all PEO samples remained
constant when <i>C</i><sub>P</sub> was below 4 × 10<sup>–5</sup> M and decreased dramatically with increasing PEO
chain length due to a decrease in intramolecular pyrene excimer formation.
The <i>I</i><sub>E</sub>/<i>I</i><sub>M</sub> ratio
in this regime was found to scale as <i>M</i><sub>n</sub><sup>–2.3±0.2</sup>. For <i>C</i><sub>P</sub> > 4 × 10<sup>–5</sup> M, pyrene excimer is formed
by
both intra- and intermolecular interactions and the <i>I</i><sub>E</sub>/<i>I</i><sub>M</sub> ratio increases linearly
with increasing <i>C</i><sub>P</sub> except for PEO(2 kDa)-Py<sub>2</sub> which undergoes phase separation. The decays obtained at
various polymer concentrations were fitted according to a “sequential
model” (SM) which assumes that the pyrene excimer is formed
in a sequential manner. The molar fractions of all excited pyrene
species and the rate constants for pyrene excimer formation were determined
from the global analysis of the monomer and excimer fluorescence decays.
The fraction of pyrenes that formed excimer from ground-state pyrene
aggregates (<i>f</i><sub>E0</sub>) was found to increase
with <i>C</i><sub>P</sub> in the regime where the pyrene
excimer is formed both intra- and intermolecularly and decrease with <i>M</i><sub>n</sub> in the regime where the pyrene excimer is
formed only intramolecularly. The fraction of pyrene pendants subject
to hydrophobic interactions were used to determine the hydrophobic
capture radius (<i>R</i><sub>c</sub>) of pyrene in water
from the distribution of PEO end-to-end distances. <i>R</i><sub>c</sub> was found to equal 2.2 ± 0.2 nm using <i>f</i><sub>E0</sub>.