13C NMR assignments of regenerated cellulose from solid-state 2D NMR spectroscopy

被引:95
作者
Idstrom, Alexander [1 ]
Schantz, Staffan [2 ]
Sundberg, Johan [1 ,3 ]
Chmelka, Bradley F. [4 ]
Gatenholm, Paul [1 ,3 ]
Nordstierna, Lars [1 ]
机构
[1] Chalmers Univ Technol, Dept Chem & Chem Engn, SE-41296 Gothenburg, Sweden
[2] AstraZeneca R&D, SE-43150 Molndal, Sweden
[3] Chalmers Univ Technol, Wallenberg Wood Sci Ctr, SE-41296 Gothenburg, Sweden
[4] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
基金
美国国家科学基金会;
关键词
C-13 CP/MAS NMR; 2D correlation NMR; Regenerated cellulose; Mercerized cellulose; Assignment; Deconvolution; SUPRAMOLECULAR STRUCTURE; CRYSTALLINITY INDEX; DISSOLUTION; MERCERIZATION; SPECTRA; FIBERS; WATER;
D O I
10.1016/j.carbpol.2016.05.107
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
From the assignment of the solid-state C-13 NMR signals in the C4 region, distinct types of crystalline cellulose, cellulose at crystalline surfaces, and disordered cellulose can be identified and quantified. For regenerated cellulose, complete C-13 assignments of the other carbon regions have not previously been attainable, due to signal overlap. In this study, two-dimensional (2D) NMR correlation methods were used to resolve and assign C-13 signals for all carbon atoms in regenerated cellulose. C-13 -enriched bacterial nanocellulose was biosynthesized, dissolved, and coagulated as highly crystalline cellulose II. Specifically, four distinct C-13 signals were observed corresponding to conformationally different anhydroglucose units: two signals assigned to crystalline moieties and two signals assigned to non -crystalline species. The Cl, C4 and C6 regions for cellulose II were fully examined by global spectral deconvolution, which yielded qualitative trends of the relative populations of the different cellulose moieties, as a function of wetting and drying treatments. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:480 / 487
页数:8
相关论文
共 47 条
[1]   Comparison of sample crystallinity determination methods by X-ray diffraction for challenging cellulose I materials [J].
Ahvenainen, Patrik ;
Kontro, Inkeri ;
Svedstrom, Kirsi .
CELLULOSE, 2016, 23 (02) :1073-1086
[2]   The role of solid state 13C NMR spectroscopy in studies of the nature of native celluloses [J].
Atalla, RH ;
VanderHart, DL .
SOLID STATE NUCLEAR MAGNETIC RESONANCE, 1999, 15 (01) :1-19
[3]   Structural and dynamic studies of proteins by high-resolution solid-state NMR [J].
Böckmann, A .
COMPTES RENDUS CHIMIE, 2006, 9 (3-4) :381-392
[4]   Chemical shift correlations in disordered solids [J].
Cadars, S ;
Lesage, A ;
Emsley, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (12) :4466-4476
[5]   The refocused INADEQUATE MAS NMR experiment in multiple spin-systems: Interpreting observed correlation peaks and optimising lineshapes [J].
Cadars, Sylvian ;
Sein, Julien ;
Duma, Luminita ;
Lesage, Anne ;
Pham, Tran N. ;
Baltisberger, Jay H. ;
Brown, Steven P. ;
Emsley, Lyndon .
JOURNAL OF MAGNETIC RESONANCE, 2007, 188 (01) :24-34
[6]   A CP/MAS 13C-NMR study of cellulose fibril aggregation in eucalyptus dissolving pulps during drying and the correlation between aggregate dimensions and chemical reactivity [J].
Chunilall, Viren ;
Bush, Tamara ;
Larsson, Per Tomas ;
Iversen, Tommy ;
Kindness, Andrew .
HOLZFORSCHUNG, 2010, 64 (06) :693-698
[7]   Progress towards a greener textile industry [J].
Dawson, Tim .
COLORATION TECHNOLOGY, 2012, 128 (01) :1-8
[8]  
Ernst R. R., 1987, PRINCIPLES NUCL MAGN
[9]   Research progress on dissolution and functional modification of cellulose in ionic liquids [J].
Feng, Li ;
Chen, Zhong-Ian .
JOURNAL OF MOLECULAR LIQUIDS, 2008, 142 (1-3) :1-5
[10]   Advances in solid-state NMR of cellulose [J].
Foston, Marcus .
CURRENT OPINION IN BIOTECHNOLOGY, 2014, 27 :176-184