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In silico studies of 1,3(R):2,4(S)‐dibenzylidene‐D‐sorbitol as a gelator for polypropylene
Author(s) -
Alperstein David,
Knani Dafna
Publication year - 2013
Publication title -
polymers for advanced technologies
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.61
H-Index - 90
eISSN - 1099-1581
pISSN - 1042-7147
DOI - 10.1002/pat.3093
Subject(s) - intramolecular force , intermolecular force , molecule , materials science , dimer , molecular dynamics , polypropylene , crystallography , computational chemistry , chemical physics , chemistry , stereochemistry , organic chemistry , composite material
The organic gelator 1,3(R):2,4(S)‐dibenzylidene‐D‐sorbitol (DBS) self‐organizes to form a 3‐D network at relatively low concentrations in a variety of nonpolar organic solvents and polymer melt. In this work, we have investigated the interactions between DBS molecules in polypropylene (PP) by molecular modeling. We have used quantum mechanics to elucidate the preferred geometry of one molecule and a dimer of DBS, and molecular mechanics and molecular dynamics to simulate pure DBS, pure PP, and mixture of DBS and PP as condensed phases, at various temperatures. It was found that inter‐ and intramolecular H‐bonds between DBS molecules are formed in PP in a much more pronounced manner than those formed in pure DBS. The most significant intermolecular H‐bonds are formed between the terminal hydroxyl groups. The most significant intramolecular H‐bonds are formed between O5 /H‐O6 groups. Due to the H‐bonds, DBS molecules form a rigid structure similar to liquid crystal forming molecules, which might explain their tendency to create nanofibrils. It seems that the aromatic rings do not contribute significantly to the intermolecular interactions. Their main role is probably to stiff the molecular structure. Temperature dependences of inter‐ and intramolecular interactions are different. Whereas intermolecular interactions peak heights decrease when temperature increases for pure DBS, the intramolecular interaction almost does not change. Copyright © 2012 John Wiley & Sons, Ltd.