Source:http://linkedlifedata.com/resource/pubmed/id/19928176
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2009-11-20
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pubmed:abstractText |
We have newly synthesized unsymmetrical D-sugar-based hydrogelators, which have either D-alanine (1) or L-alanine (2) moieties and their chiral molecular arrangements were characterized by TEM, powder-XRD, CD and FT-IR spectroscope. The D-sugar-based hydrogelator, which contained D-alanine, showed remarkably slow chiral molecular packing by intermolecular hydrogen bonding interaction in gel formation. Hydrogelator 1 possesses the orthorhombic perpendicular (O(perpendicular)) subcell type according to the wide-angle region of the XRD pattern and the CH2 scissoring band delta(CH2) in the IR spectrum. On the other hand, hydrogel 2, which contained the D-sugar, but L-alanine, did not undergo the chiral molecular arrangement.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1533-4880
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4981-4
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pubmed:year |
2009
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pubmed:articleTitle |
Chiral molecular arrangement behaviour of unsymmetrical sugar-based gelators by introduction of steroisomeric alanine moiety.
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pubmed:affiliation |
Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University, Jinju 660-701, Korea.
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pubmed:publicationType |
Journal Article
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