scholarly journals Competition Between Steric Hindrance and Hydrogen Bonding in the Formation of Supramolecular Bottle Brush Polymers

2013 ◽  
Vol 46 (19) ◽  
pp. 7911-7919 ◽  
Author(s):  
Sylvain Catrouillet ◽  
Cécile Fonteneau ◽  
Laurent Bouteiller ◽  
Nicolas Delorme ◽  
Erwan Nicol ◽  
...  
RSC Advances ◽  
2021 ◽  
Vol 11 (18) ◽  
pp. 10929-10934
Author(s):  
Chuangui Cao ◽  
Zhihui Zhao ◽  
Yong Qi ◽  
Hui Peng ◽  
Kuanjun Fang ◽  
...  

The solvent, DEA, reduces the dye aggregation that may be caused by the weak hydrogen bonding and relatively smaller steric hindrance effect.


2016 ◽  
Vol 49 (5) ◽  
pp. 1950-1960 ◽  
Author(s):  
Gary M. Leuty ◽  
Mesfin Tsige ◽  
Gary S. Grest ◽  
Michael Rubinstein
Keyword(s):  

2011 ◽  
Vol 135 (16) ◽  
pp. 164903 ◽  
Author(s):  
Panagiotis E. Theodorakis ◽  
Hsiao-Ping Hsu ◽  
Wolfgang Paul ◽  
Kurt Binder

2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Anca Aldea ◽  
Ana-Maria Albu ◽  
Alina Nicolescu ◽  
Victorita Tecuceanu

Two N-substituted amides (N-acryloyl morpholine and N-methyl-N-vinylacetamide) were polymerized in different solvents using radical initiator. The tacticity of obtained polymers was determined by 400 MHz1H-NMR and13C-NMR. At a given temperature, the syndiotacticity increased with increasing the solvent polarity. This solvent effect may be related to the hydrogen bonding interaction among solvent, monomer, and/or growing species. A peculiar aspect regards the steric hindrance at the nitrogen atom.


1998 ◽  
Vol 63 (4) ◽  
pp. 1079-1085 ◽  
Author(s):  
J. Oriol Magrans ◽  
Ana M. Rincón ◽  
Félix Cuevas ◽  
Javier López-Prados ◽  
Pedro M. Nieto ◽  
...  

2011 ◽  
Vol 133 (3) ◽  
pp. 559-566 ◽  
Author(s):  
Jeremiah A. Johnson ◽  
Ying Y. Lu ◽  
Alan O. Burts ◽  
Yeon-Hee Lim ◽  
M. G. Finn ◽  
...  

1972 ◽  
Vol 25 (3) ◽  
pp. 639 ◽  
Author(s):  
BD Andrews ◽  
AJ Poynton ◽  
ID Rae

A series of 2-substituted 3,5-dimethylanilines and their N-acetyl derivatives have been synthesized, and their proton magnetic resonance spectra recorded. Intramolecular hydrogen bonding between the amide N-H and the 2-substituent is disturbed by steric hindrance of the 2-substituent only in the case of the 2-nitro, 2-acetyl, and 2-methoxycarbonyl substituents.


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