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									<identifier>oai:www.peertechzpublications.org:10.17352/abse.000015</identifier>
									<datestamp>2020-03-02</datestamp>
									<setSpec>PTZ.ABSE:VOL6</setSpec>
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										<dc:title>
										Differential Analysis of O-(2- hydroxypropyl) cellulose by Using Two-Dimensional 1H-NMR Spectroscopy
										</dc:title><dc:creator>Naotaka Sakamoto</dc:creator><dc:creator> Edmont Stoyanov</dc:creator><dc:description>&lt;p&gt;Two-dimensional 1H-NMR is used to determine the intra-molecular interactions of O-(2-hydroxypropyl) cellulose (HPC) in aqueous (D2O), DMF and DMSO solutions. Four grades HPC with different molecular weights are analyzed by using NOESY (Nuclear Overhauser Effect Spectroscopy) for proton-proton cross-interactions. A strong dependence of the polymer chain structure on the HPC Molecular Weight (MW) is overserved. The lower MW HPCs exist in solutions as a more linear chain showing less proton-proton interactions whereas the higher MW HPCs are more twisted and bended and form a tangled molecule mess with very intensive interactions between the -CH3, -CH2- and -C-H protons. From all the grades, the ultra-low molecular weight HPC-UL (MW 20,000) revealed the weakest proton-proton cross-relaxations and exists in solutions probably only as an almost linear chain polymer.&lt;/p&gt;</dc:description>
										<dc:publisher>Archive of Biomedical Science and Engineering - Peertechz Publications</dc:publisher>
										<dc:date>2020-03-02</dc:date>
										<dc:type>Research Article</dc:type>
										<dc:identifier>https://doi.org/10.17352/abse.000015</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Naotaka Sakamoto et al.</dc:rights>
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