Adsorption of polymer chains at surfaces. II. Amplitude ratios for end‐to‐end distance distribution at the critical point of adsorption

1985 ◽  
Vol 82 (2) ◽  
pp. 1032-1041 ◽  
Author(s):  
E. Eisenriegler
2004 ◽  
Vol 18 (17n19) ◽  
pp. 2365-2375
Author(s):  
LURU DAI ◽  
FEI LIU ◽  
ZHONG-CAN OU-YANG

Using the maximum-entropy method, the end-to-end distance distribution of the force stretched chain is calculated from the moments of the distribution, which can be obtained from the extension-force curves recorded in single-molecule experiments. If one knows force expansion of the extension through the (n-1)th power of force, it is enough information to calculate the n moments of the distribution. The method is examined with force stretched chain models, Gaussian chain and excluded-volume chain on two-dimension lattice. The method reconstructs all distributions precisely. The method also is applied to force stretched complex chain molecules: the hairpin and secondary structure conformations. We find that the distributions of homogeneous chains of two conformations are very different: there are two independent peaks in hairpin distribution; while only one peak is observed in the distribution of secondary structure conformations. Our discussion also shows that the end-to-end distance distribution may discover more critical physical information than the simpler extension-force curves can give.


ChemPhysChem ◽  
2005 ◽  
Vol 6 (11) ◽  
pp. 2286-2294 ◽  
Author(s):  
Benoît Muls ◽  
Hiroshi Uji-i ◽  
Sergey Melnikov ◽  
Alain Moussa ◽  
Wendy Verheijen ◽  
...  

1991 ◽  
Vol 24 (18) ◽  
pp. 5167-5170 ◽  
Author(s):  
Ana M. Rubio ◽  
Juan J. Freire ◽  
Arturo Horta ◽  
Ines Fernandez de Pierola

2020 ◽  
Vol 153 (16) ◽  
pp. 164903 ◽  
Author(s):  
Mohammadhasan Dinpajooh ◽  
Abraham Nitzan

1992 ◽  
Vol 278 ◽  
Author(s):  
Vassilios Galiatsatos

AbstractA recently developed computational methodology allows the quantitative study of the correlation between the end-to-end distance of a polymer chain and its dipole moment. This paper focuses on the further analysis of this correlation and aims in identifying the structural characteristics of the polymer chain that are responsible for the observed behavior of the correlation. We study chains in the independent rotation approximation with symmetric rotational potentials. We focus on two different orientations of the bond dipole moment vector : 010 and 001 (the bond length vector's orientation is [100]).


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