scholarly journals The Structure of Dipolar Polymer Brushes and Their Interaction in the Melt. Impact of Chain Stiffness

Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 2887
Author(s):  
Ivan V. Mikhailov ◽  
Victor M. Amoskov ◽  
Anatoly A. Darinskii ◽  
Tatiana M. Birshtein

By using the numerical lattice Scheutjens–Fleer self-consistent field (SF-SCF) method we have studied the effect of the restricted flexibility of grafted chains on the structure and mutual interaction of two opposing planar conventional and A-type dipolar brushes. Brushes are immersed in the solvent consisting of chains similar to the grafted ones. The increase of the chain rigidity enhances the segregation of grafted chains in a A-type dipolar brush into two populations: backfolded chains with terminal monomers near the grafting surface and chains with the ends at the brush periphery. The fraction of backfolded chains grows by an increase of the Kuhn segment length. It is shown that two opposite A-type dipolar brushes from semi-rigid chains are attracted to each other at short distances. The attraction becomes more pronounced and begins at larger distances for more rigid chains with the same brush characteristics: polymerization degree, grafting density, and dipole moments of monomer units. This attraction is connected with the dipole-dipole interactions between chains of oncoming brushes with oppositely directed dipoles penetrating deeply into each other upon contact. This effect of the chain rigidity is opposite to that for conventional brushes without dipoles in the chains. For such brushes, an increase in the chain rigidity leads to the enhanced repulsion between them.

2011 ◽  
Vol 45 (1) ◽  
pp. 510-524 ◽  
Author(s):  
Andrew D. Price ◽  
Su-Mi Hur ◽  
Glenn H. Fredrickson ◽  
Amalie L. Frischknecht ◽  
Dale L. Huber

Soft Matter ◽  
2018 ◽  
Vol 14 (10) ◽  
pp. 1887-1896 ◽  
Author(s):  
Wenjuan Qiu ◽  
Baohui Li ◽  
Qiang Wang

Ring brushes are slightly less stretched than, thus nearly but not completely identical to, the “equivalent” linear brushes having half the chain length and double the grafting density.


Author(s):  
Gaohang Chen ◽  
Hui Zhang ◽  
Teng Lu ◽  
Ying Jiang

A self-consistent field theory formalism based on the wormlike chain model is developed to investigate the stress–strain relation for mesostructures in diblock copolymers under the influence of chain rigidity.


Soft Matter ◽  
2014 ◽  
Vol 10 (32) ◽  
pp. 5974-5990 ◽  
Author(s):  
Andrey Milchev ◽  
Sergei A. Egorov ◽  
Kurt Binder

The adsorption of long flexible macromolecules by polymer brush-coated surfaces is studied by molecular dynamics simulations and by calculations using density functional and self-consistent field theories.


2010 ◽  
Vol 43 (22) ◽  
pp. 9555-9566 ◽  
Author(s):  
Alexey A. Polotsky ◽  
Torben Gillich ◽  
Oleg V. Borisov ◽  
Frans A. M. Leermakers ◽  
Marcus Textor ◽  
...  

2013 ◽  
Vol 46 (11) ◽  
pp. 4651-4662 ◽  
Author(s):  
Oleg V. Rud ◽  
Alexey A. Polotsky ◽  
Torben Gillich ◽  
Oleg V. Borisov ◽  
Frans A. M. Leermakers ◽  
...  

Some recent calculations by the self-consistent field molecular orbital method are generalized to allow for electron correlation. Correlations between the motions of the valence electrons are introduced explicitly by means of configuration interaction, whilst the effects of intra-atomic electron correlation are estimated semi-empirically. Both forms of correlation, but especially the latter, are found to have a profound effect on the calculated properties of the hydrides. The total electronic energies obtained in the final calculations fall consistently above the experimental values by an almost constant amount (0.5 to 0.7 eV). The wave functions and dipole moments of the molecules are analyzed in the frameworks of both the valence-bond and molecular orbital theories.


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