High resolution 13C-n.m.r. spectroscopy of 'mixed linkage' xylans

Three xylan fractions, obtained by stepwise precipitation with ethanol, were analysed by 75-MHz 13C-n.m.r. spectroscopy. Diad frequencies, determined from the C-2 resonances, show that the (1 → 3)-linkages are interspersed throughout the chain rather than grouped contiguously. This type of distribut...

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Autores principales: Matulewicz, M.C., Cerezo, A.S., Jarret, R.M., Syn, N.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_01418130_v14_n1_p29_Matulewicz
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spelling todo:paper_01418130_v14_n1_p29_Matulewicz2023-10-03T14:58:42Z High resolution 13C-n.m.r. spectroscopy of 'mixed linkage' xylans Matulewicz, M.C. Cerezo, A.S. Jarret, R.M. Syn, N. 13C-n.m.r. diad frequencies Xylans carbon xylan xylan article chemistry comparative study conformation isolation and purification methodology nuclear magnetic resonance spectroscopy optical rotation seaweed carbon nuclear magnetic resonance chemical bond chemical structure nonhuman Carbohydrate Conformation Carbon Isotopes Comparative Study Magnetic Resonance Spectroscopy Optical Rotation Seaweed Support, Non-U.S. Gov't Xylans Three xylan fractions, obtained by stepwise precipitation with ethanol, were analysed by 75-MHz 13C-n.m.r. spectroscopy. Diad frequencies, determined from the C-2 resonances, show that the (1 → 3)-linkages are interspersed throughout the chain rather than grouped contiguously. This type of distribution is in agreement with a random coil conformation and with the constancy of the optical rotation in solvents of different ionic strength and chaotropic power. These diad frequencies were compared with the theoretical values calculated for a random distribution from the ratio of (1 → 4)-:(1 → 3)-linkages in the 1H-n.m.r. spectra, and from the methylation analysis for one of the fractions. © 1992 Butterworth-Heinemann Limited. Fil:Matulewicz, M.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Cerezo, A.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01418130_v14_n1_p29_Matulewicz
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 13C-n.m.r.
diad frequencies
Xylans
carbon
xylan
xylan
article
chemistry
comparative study
conformation
isolation and purification
methodology
nuclear magnetic resonance spectroscopy
optical rotation
seaweed
carbon nuclear magnetic resonance
chemical bond
chemical structure
nonhuman
Carbohydrate Conformation
Carbon Isotopes
Comparative Study
Magnetic Resonance Spectroscopy
Optical Rotation
Seaweed
Support, Non-U.S. Gov't
Xylans
spellingShingle 13C-n.m.r.
diad frequencies
Xylans
carbon
xylan
xylan
article
chemistry
comparative study
conformation
isolation and purification
methodology
nuclear magnetic resonance spectroscopy
optical rotation
seaweed
carbon nuclear magnetic resonance
chemical bond
chemical structure
nonhuman
Carbohydrate Conformation
Carbon Isotopes
Comparative Study
Magnetic Resonance Spectroscopy
Optical Rotation
Seaweed
Support, Non-U.S. Gov't
Xylans
Matulewicz, M.C.
Cerezo, A.S.
Jarret, R.M.
Syn, N.
High resolution 13C-n.m.r. spectroscopy of 'mixed linkage' xylans
topic_facet 13C-n.m.r.
diad frequencies
Xylans
carbon
xylan
xylan
article
chemistry
comparative study
conformation
isolation and purification
methodology
nuclear magnetic resonance spectroscopy
optical rotation
seaweed
carbon nuclear magnetic resonance
chemical bond
chemical structure
nonhuman
Carbohydrate Conformation
Carbon Isotopes
Comparative Study
Magnetic Resonance Spectroscopy
Optical Rotation
Seaweed
Support, Non-U.S. Gov't
Xylans
description Three xylan fractions, obtained by stepwise precipitation with ethanol, were analysed by 75-MHz 13C-n.m.r. spectroscopy. Diad frequencies, determined from the C-2 resonances, show that the (1 → 3)-linkages are interspersed throughout the chain rather than grouped contiguously. This type of distribution is in agreement with a random coil conformation and with the constancy of the optical rotation in solvents of different ionic strength and chaotropic power. These diad frequencies were compared with the theoretical values calculated for a random distribution from the ratio of (1 → 4)-:(1 → 3)-linkages in the 1H-n.m.r. spectra, and from the methylation analysis for one of the fractions. © 1992 Butterworth-Heinemann Limited.
format JOUR
author Matulewicz, M.C.
Cerezo, A.S.
Jarret, R.M.
Syn, N.
author_facet Matulewicz, M.C.
Cerezo, A.S.
Jarret, R.M.
Syn, N.
author_sort Matulewicz, M.C.
title High resolution 13C-n.m.r. spectroscopy of 'mixed linkage' xylans
title_short High resolution 13C-n.m.r. spectroscopy of 'mixed linkage' xylans
title_full High resolution 13C-n.m.r. spectroscopy of 'mixed linkage' xylans
title_fullStr High resolution 13C-n.m.r. spectroscopy of 'mixed linkage' xylans
title_full_unstemmed High resolution 13C-n.m.r. spectroscopy of 'mixed linkage' xylans
title_sort high resolution 13c-n.m.r. spectroscopy of 'mixed linkage' xylans
url http://hdl.handle.net/20.500.12110/paper_01418130_v14_n1_p29_Matulewicz
work_keys_str_mv AT matulewiczmc highresolution13cnmrspectroscopyofmixedlinkagexylans
AT cerezoas highresolution13cnmrspectroscopyofmixedlinkagexylans
AT jarretrm highresolution13cnmrspectroscopyofmixedlinkagexylans
AT synn highresolution13cnmrspectroscopyofmixedlinkagexylans
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