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Vine‐twining polymerization: A new preparation method for well‐defined supramolecules composed of amylose and synthetic polymers
Author(s) -
Kaneko Yoshiro,
Kadokawa Junichi
Publication year - 2005
Publication title -
the chemical record
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.61
H-Index - 78
eISSN - 1528-0691
pISSN - 1527-8999
DOI - 10.1002/tcr.20031
Subject(s) - polymerization , polymer , polymer chemistry , chemistry , copolymer , amylose , materials science , organic chemistry , starch
Abstract In this article we describe a new method of polymerization called “vine‐twining polymerization” for preparation of well‐defined supramolecules, which are amylose–polymer inclusion complexes. The method was achieved by enzymatic polymerization of α‐D‐glucose‐1‐phosphate catalyzed by phosphorylase in the presence of various synthetic polymers such as polyethers, polyesters, poly(ester–ether), and amphiphilic block copolymer. Powder X‐ray diffraction (XRD) and 1 H‐NMR measurements determined the structures of the products to be inclusion complexes. The XRD patterns were completely different from those of amylose and guest polymers. The 1 H‐NMR spectra of the products indicated that the structures were composed of amylose and guest polymers. The formation process of the inclusion complexes during the enzymatic polymerization was also evaluated. In addition, we revealed that the bulkiness of the end groups and the hydrophobicity of the guest polymers strongly affected the formation of the inclusion complexes. By means of this method of polymerization, a graft polymer having inclusion complexes as side chains was prepared. Furthermore, as an evolution of the “vine‐twining polymerization,” we attempted a system of parallel polymerization to form an inclusion complex of amylose with a strongly hydrophobic guest polymer. © 2005 The Japan Chemical Journal Forum and Wiley Periodicals, Inc. Chem Rec 5: 36–46; 2005: Published online in Wiley InterScience ( www.interscience.wiley.com ) DOI 10.1002/tcr.20031

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