We study the orientational properties of labeled segments in semiflexible dendrimers making use of the viscoelastic approach of Dolgushev and Blumen [J. Chem. Phys. 131, 044905 (2009)]. We focus on the segmental orientational autocorrelation functions (ACFs), which are fundamental for the frequency-dependent spin-lattice relaxation times T1(ω). We show that semiflexibility leads to an increase of the contribution of large-scale motions to the ACF. This fact influences the position of the maxima of the [1/T1]-functions. Thus, going from outer to inner segments, the maxima shift to lower frequencies. Remarkably, this feature is not obtained in the classical bead-spring model of flexible dendrimers, although many experiments on dendrimers manifest such a behavior.
We study the dynamics of general treelike networks, which are semiflexible due to restrictions on the orientations of their bonds. For this we extend the generalized Gaussian structure model, in which the dynamics obeys Langevin equations coupled through a dynamical matrix. We succeed in formulating analytically this matrix for arbitrary treelike networks and stiffness coefficients. This allows the straightforward determination of dynamical characteristics relevant to mechanical and dielectric relaxation. We show that our approach also follows from the maximum entropy principle; this principle was previously implemented for linear polymers and we extend it here to arbitrary treelike architectures.
Focusing on mechanical and dielectric relaxation, we study the dynamics of semiflexible linear chains, stars, and dendrimers. For this, we use an extension of the Rouse-model in which we include, in the spirit of Bixon and Zwanzig ( J. Chem. Phys. 1978, 68, 1896 and of von Ferber and Blumen ( J. Chem. Phys. 2002, 116, 8616), restrictions on the bonds' orientations. In every case the dynamical matrix in the bonds' representation turns out to be a sparse matrix, a fact which simplifies its diagonalization and may pave the way for further analytical treatments.
We study the dynamics of semiflexible dendritic polymers following the method of Dolgushev and Blumen [J. Chem. Phys. 131, 044905 (2009)]. The scheme allows to formulate in analytical form the corresponding Langevin equations. We determine the eigenvalues by first block-diagonalizing the problem, which allows to treat even very large dendritic objects. A basic ingredient of the procedure is the observation that a set of eigenmodes in the semiflexible case is similar to that chosen by Cai and Chen [Macromolecules 30, 5104 (1997)] for fully flexible dendritic structures. Varying the flexibility of the macromolecules allows us to better understand their mechanical loss moduli G"(ω) based on their eigenvalue spectra. We present the G"(ω) for a series of stiffness parameters and for different functionalities of the branching points.
We study the dynamics of semiflexible Vicsek fractals (SVF) following the framework established by Dolgushev and Blumen [J. Chem. Phys. 131, 044905 (2009)], a scheme which allows to model semiflexible treelike polymers of arbitrary architecture. We show, extending the methods used in the treatment of semiflexible dendrimers by Fürstenberg et al. [J. Chem. Phys. 136, 154904 (2012)], that in this way the Langevin-dynamics of SVF can be treated to a large part analytically. For this we show for arbitrary Vicsek fractals (VF) how to construct complete sets of eigenvectors; these reduce considerably the diagonalization problem of the corresponding equations of motion. In fact, such eigenvector sets arise naturally from a hierarchical procedure which follows the iterative construction of the VF. We use the obtained eigenvalues to calculate the loss moduli G(")(ω) of SVF for different degrees of stiffness of the junctions. Finally, we compare the results for SVF to those found for semiflexible dendrimers.
Recent approaches for taking stiffness effects into account when modeling multifunctional polymer structures are reported. The theoretical part is focused on arbitrary tree‐like polymers, modeled through extensions of the GGS scheme that allows the inclusion of local constraints. The theoretical findings are compared to the results of numerical simulations in which stiffness is included into the bond fluctuation model with the help of additional bending potentials. The procedure is illustrated by evaluating the static properties of semiflexible linear chains, stars, cospectral polymers and rings. The dynamical properties are exemplified by the mechanical relaxation of semiflexible polymers, including situations in which the local conditions at different sites are the same or different.magnified image
We consider polymer structures which are known in the mathematical literature as "cospectral." Their graphs have (in spite of the different architectures) exactly the same Laplacian spectra. Now, these spectra determine in Gaussian (Rouse-type) approaches many static as well as dynamical polymer characteristics. Hence, in such approaches for cospectral graphs many mesoscopic quantities are predicted to be indistinguishable. Here we show that the introduction of semiflexibility into the generalized Gaussian structure scheme leads to different spectra and hence to distinct macroscopic patterns. Moreover, particular semiflexible situations allow us to distinguish well between cospectral structures. We confirm our theoretical results through Monte Carlo simulations.
The internally functionalized dendrimers are novel polymers that differ from conventional dendrimers by having additional functional units which do not branch out further. We investigate the dynamics of these structures with the inclusion of local semiflexibility and analyze their eigenmodes. The functionalized units clearly manifest themselves leading to a group of eigenvalues which are not present for homogeneous dendrimers. This part of the spectrum reveals itself in the local relaxation, leading to a corresponding process in the imaginary part of the complex dielectric susceptibility.
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