Charge
Transfer Modulated Self-Assembly in Poly(aryl
ether) Dendron Derivatives with Improved Stability and Transport Characteristics
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Abstract
Alteration of native gelation properties
of anthracene and pyrene
cored first generation poly(aryl ether) dendrons, G1-An and G1-Py,
by introducing a common acceptor, 2,4,7-trinitro-9<i>H</i>-fluoren-9-one (TNF), results in forming charge transfer gels in
long chain alcoholic solvents. This strategy leads to significant
perturbation of optical and electronic properties within the gel matrix.
Consequently, a noticeable increase of their electrical conductivities
is observed, making these poly(aryl ether) dendron based gels potential
candidates for organic electronics. While the dc-conductivity (σ)
value for the native gel from G1-An is 2.8 × 10<sup>–4</sup> S m<sup>–1</sup>, the value increased 3 times (σ =
8.7 × 10<sup>–4</sup> S m<sup>–1</sup>) for its
corresponding charge transfer gel. Further, the dc-conductivity for
the native gel self-assembled from G1-Py dramatically enhanced by
approximately an order of magnitude from 4.9 × 10<sup>–4</sup> to 1.3 × 10<sup>–3</sup> S m<sup>–1</sup>, under
the influence of an acceptor. Apart from H-bonding and π···π
interactions, charge transfer results in the formation of a robust
3D network of fibers, with improved aspect ratio, providing high thermo-mechanical
stability to the gels compared to the native ones. The charge transfer
gels self-assembled from G1-An/TNF (1:1) and G1-Py/TNF exhibit a 7.3-
and 2.5-fold increase in their yield stress, respectively, compared
to their native assemblies. A similar trend follows in the case of
their thermal stabilities. This is attributed to the typical bilayer
self-assembly of the former which is not present in the case of G1-Py/TNF
charge transfer gel. Density functional calculations provide deeper
insights accounting for the role of charge transfer interactions in
the mode of self-assembly. The 1D potential energy surface for the
G1-An/TNF dimer and G1-Py/TNF dimer is found to be 11.8 and 1.9 kcal
mol<sup>–1</sup> more stable than their corresponding native
gel dimers, G1-An/G1-An and G1-Py/G1-Py, respectively