Oxidations and reductions of substituent side chains and non-aromatic ring systems (without altering chain length)

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1789
Author(s):  
Dmitry Tolmachev ◽  
George Mamistvalov ◽  
Natalia Lukasheva ◽  
Sergey Larin ◽  
Mikko Karttunen

We used atomistic molecular dynamics (MD) simulations to study polyelectrolyte brushes based on anionic α,L-glutamic acid and α,L-aspartic acid grafted on cellulose in the presence of divalent CaCl2 salt at different concentrations. The motivation is to search for ways to control properties such as sorption capacity and the structural response of the brush to multivalent salts. For this detailed understanding of the role of side-chain length, the chemical structure and their interplay are required. It was found that in the case of glutamic acid oligomers, the longer side chains facilitate attractive interactions with the cellulose surface, which forces the grafted chains to lie down on the surface. The additional methylene group in the side chain enables side-chain rotation, enhancing this effect. On the other hand, the shorter and more restricted side chains of aspartic acid oligomers prevent attractive interactions to a large degree and push the grafted chains away from the surface. The difference in side-chain length also leads to differences in other properties of the brush in divalent salt solutions. At a low grafting density, the longer side chains of glutamic acid allow the adsorbed cations to be spatially distributed inside the brush resulting in a charge inversion. With an increase in grafting density, the difference in the total charge of the aspartic and glutamine brushes disappears, but new structural features appear. The longer sides allow for ion bridging between the grafted chains and the cellulose surface without a significant change in main-chain conformation. This leads to the brush structure being less sensitive to changes in salt concentration.


2003 ◽  
Vol 13 (21) ◽  
pp. 3817-3820 ◽  
Author(s):  
Yujia Dai ◽  
Yan Guo ◽  
Michael L. Curtin ◽  
Junling Li ◽  
Lori J. Pease ◽  
...  

2006 ◽  
Vol 12 (6) ◽  
pp. 1610-1617 ◽  
Author(s):  
Masanori Sakamoto ◽  
Xichen Cai ◽  
Mamoru Fujitsuka ◽  
Tetsuro Majima

ChemInform ◽  
2003 ◽  
Vol 34 (44) ◽  
Author(s):  
Ali Khalafi-Nezhad ◽  
Mohammad Navid Soltani Rad ◽  
Gholam Hossein Hakimelahi

2006 ◽  
Vol 8 (6) ◽  
pp. 1241-1244 ◽  
Author(s):  
Yan-Guang Wang ◽  
Sun-Liang Cui ◽  
Xu-Feng Lin

2016 ◽  
Vol 22 (41) ◽  
pp. 14730-14738 ◽  
Author(s):  
Tetsuo Okujima ◽  
John Mack ◽  
Jun Nakamura ◽  
Gugu Kubheka ◽  
Tebello Nyokong ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Shen Li ◽  
Yanting Wang

Abstract Due to their complex molecular structures and interactions, phase behaviors of complex fluids are quite often difficult to be identified by common phase transition analysis methods. Percolation phase transition, on the other hand, only monitors the degree of connection among particles without strict geometric requirements such as translational or orientational order, and thus suitable for pinpointing phase transitions of complex fluids. As typical complex fluids, ionic liquids (ILs) exhibit phases beyond the description of simple liquid theories. In particular, with an intermediate cationic side-chain length, ILs can form the nanoscale segregated liquid (NSL) state, which will eventually transform into the ionic liquid crystal (ILC) structure when the side chains are adequately long. However, the microscopic mechanism of this transformation is still unclear. In this work, by means of coarse-grained molecular dynamics simulation, we show that, with increasing cationic side-chain length, some local pieces of non-polar domains are gradually formed by side chains aligned in parallel inside the NSL phase, before an abrupt percolation phase transition happens when the system transforms into the ILC phase. This work not only identifies that the NSL to ILC phase transition is a critical phenomenon, but also demonstrates the importance of percolation theory to complex fluids.


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