Dimensional and hydrodynamic properties of cellulose tris(alkylcarbamate)s in solution: Side chain dependent conformation in tetrahydrofuran
Dimensional and hydrodynamic properties of cellulose tris(alkylcarbamate)s in solution: Side chain dependent conformation in tetrahydrofuran
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溶液中纤维素三(烷基氨基甲酸酯)的尺寸和流体动力学性质:四氢呋喃中的侧链依赖性构象
DOI:
10.1016/j.polymer.2017.02.012
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发表时间:
2017
期刊:
影响因子:
4.6
通讯作者:
K. Terao
中科院分区:
文献类型:
--
作者:
Xinyue Jiang;Akiyuki Ryoki;K. Terao
We prepared cellulosetris(ethylcarbamate) (CTEC), cellulosetris(n-butylcarbamate) (CTBC), and cellulosetris(n-octadecylcarbamate) (CTODC) samples with different molecular weight to determine their conformational properties in dilute solution. Weight average molar massesMw,z-average mean-square radii of gyration <S2>z, particle scattering functionsP(q), and intrinsic viscosities [η] of the CTEC, CTBC, and CTODC samples in tetrahydrofuran (THF) at 25 °C were determined by size exclusion chromatography equipped with multi-angle light scattering detectors (SEC-MALS), small angle X-ray scattering (SAXS), and viscometry. Infrared (IR) absorption measurements were also made to observe intramolecular hydrogen bonding between C=O and NH groups. The obtained <S2>z,P(q), and [η] data were analyzed in terms of the wormlike chain model to determine the Kuhn segment length (stiffness parameter, or twice of the persistence length)λ−1and the helix pitch (rise) per residueh.While CTBC has the highest chain stiffness in the three cellulose derivatives as in the case of the corresponding amylose derivatives, the difference in the wormlike chain parameters is less significant for the cellulose alkylcarbamate derivatives. Indeed, intramolecular hydrogen bonding of CTEC, CTBC, and CTODC is weaker and fewer than that for the corresponding amylose derivatives owing to the main chain linkage,αorβ.
影响因子:
5.5
作者:
NAKANISHI, Y;NORISUYE, T;KITAMURA, S
通讯作者:
KITAMURA, S
DOI:
--
发表时间:
2008
期刊:
Macromolecules 41
影响因子:
--
作者:
K. Terao;K. Mizuno;M. Murashima;Y. Kita;C. Hongo;K. Okuyama;T. Norisue;H.P. Bachinger
通讯作者:
H.P. Bachinger