Source:http://linkedlifedata.com/resource/pubmed/id/11971690
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
17
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pubmed:dateCreated |
2002-4-24
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pubmed:abstractText |
A family of chiral molecular squares based on fac-Re(CO)3Cl metallocorners and enantiopure atropisomeric bipyridine bridging ligands (L1-4) have been synthesized in high yields by refluxing ClRe(CO)5 and L1-4 in 1:1 molar ratio. These novel chiral metallocycles have been characterized by 1H and 13C{1H} NMR, UV-vis, luminescence, and circular dichroism (CD) spectroscopies, FAB mass spectrometry, and microanalysis. Molecular square 4 which contains four 1,1'-bi-2-naphthol functionalities exhibits interesting enantioselective luminescence quenching by 2-amino-1-propanol. This research illustrates the potential of generating novel functional materials based on supramolecular chemistry.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0002-7863
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
124
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4554-5
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pubmed:dateRevised |
2008-1-17
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pubmed:meshHeading | |
pubmed:year |
2002
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pubmed:articleTitle |
A chiral molecular square with metallo-corners for enantioselective sensing.
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pubmed:affiliation |
Department of Chemistry, CB # 3290, University of North Carolina, Chapel Hill, North Carolina 27599, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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