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Capturing the portrait of isolated individual natural cellulose molecules
Author(s) -
Wan Zhenzhen,
Li Lu,
Cui Shuxun
Publication year - 2008
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.21070
Subject(s) - cellulose , preprint , chemistry , molecule , adsorption , polymer science , polymer , surface charge , chemical physics , chemical engineering , nanotechnology , organic chemistry , materials science , physics , quantum mechanics , engineering
Natural cellulose molecules have a strong tendency of being aggregated into larger structures. Thus, the imaging of isolated individual cellulose molecules is hampered for a long time. In this work, we manage to observe, for the first time, the isolated individual natural cellulose chains on a sample surface by means of atomic force microscope. The advantage of the ionic liquid, in which natural cellulose can be molecularly dispersed, is considered to be the key point for the successful imaging. Moreover, we find that the surface charge can influence the morphology of the single cellulose chains upon adsorption. That is, on the positively charged surface, individual cellulose chains adopt an extended conformation; whereas on the negatively charged surface, a compact globule conformation is observed. © 2008 Wiley Periodicals, Inc. Biopolymers 89: 1170–1173, 2008. This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at biopolymers@wiley.com