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Synthesis and Helical Structures of Poly(ω‐alkynamide)s Having Chiral Side Chains: Effect of Solvent on Their Screw‐Sense Inversion
Author(s) -
Suzuki Yuji,
Miyagi Yu,
Shiotsuki Masashi,
Inai Yoshihito,
Masuda Toshio,
Sanda Fumio
Publication year - 2014
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201402628
Subject(s) - random coil , intramolecular force , solvent , polymer chemistry , polymer , polymerization , chemistry , hydrogen bond , materials science , solvent effects , crystallography , circular dichroism , stereochemistry , molecule , organic chemistry
New ω‐alkynamides, ( S )‐HCCCH 2 CONHCH 2 CH(CH 3 )CH 2 CH 3 ( 1 ) and ( S )‐HCCCH 2 CH 2 CONHCH(CH 3 )CH 2 CH 2 CH 2 CH 2 CH 3 ( 2 ) were synthesized and polymerized with a rhodium catalyst in CHCl 3 to obtain cis ‐stereoregular poly(ω‐alkynamide)s (poly( 1 ) and poly( 2 )). Polarimetric, CD, and IR spectroscopic studies revealed that in solution the polymers adopted predominantly one‐handed helical structures stabilized by intramolecular hydrogen bonds between the pendent amide groups. This behavior was similar to that of the corresponding poly( N ‐alkynylamide) counterparts (poly( 3 ) and poly( 4 )) reported previously, whereas the helical senses were opposite to each other. The helical structures of the poly(ω‐alkynamide)s were stable upon heating similar to those of the poly( N ‐alkynylamide)s, but the solvent response was completely different. An increase in MeOH content in CHCl 3 /MeOH resulted in inversion of the predominant screw‐sense for poly( 1 ) and poly( 2 ). Conversely, poly( 3 ) was transformed into a random coil, and poly( 4 ) maintained the predominant screw‐sense irrespective of MeOH content. The solvent dependence of predominant screw‐sense for poly( 1 ) and poly( 2 ) was reasonably explained by molecular orbital studies using the conductor‐like screening model (COSMO).