Source:http://linkedlifedata.com/resource/pubmed/id/15176783
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2004-6-4
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pubmed:abstractText |
[reaction: see text] Titration of porphyrin-fullerene rotaxanes with DABCO or 4,4'-bipyridine led to photo- and redoxactive catenanic architectures, which upon photoexcitation undergo a sequence of short-range energy and electron transfer events to give a long-lived charge-separated radical-pair state.
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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 |
Jun
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pubmed:issn |
1523-7060
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
10
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1919-22
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15176783-Catenanes,
pubmed-meshheading:15176783-Fullerenes,
pubmed-meshheading:15176783-Models, Molecular,
pubmed-meshheading:15176783-Molecular Structure,
pubmed-meshheading:15176783-Oxidation-Reduction,
pubmed-meshheading:15176783-Photochemistry,
pubmed-meshheading:15176783-Porphyrins,
pubmed-meshheading:15176783-Rotaxanes
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pubmed:year |
2004
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pubmed:articleTitle |
Novel porphyrin-fullerene assemblies: from rotaxanes to catenanes.
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pubmed:affiliation |
Chemistry Department, New York University, New York City, New York 10003, USA. david.schuster@nyu.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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