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rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
15
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|
pubmed:dateCreated |
2008-7-25
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|
pubmed:abstractText |
Acyclic anion receptors (BF 2 complexes of dipyrrolyldiketones) with heteroaryl moieties synthesized by using cross-coupling reactions have unique electronic states, as observed in UV/vis absorption spectra. Among heteroaryl-substituted derivatives, a pyrrolyl-substituted receptor exhibits an extremely high affinity for anions in solution.
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pubmed:language |
eng
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pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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|
pubmed:month |
Aug
|
|
pubmed:issn |
1523-7060
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|
pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:day |
7
|
|
pubmed:volume |
10
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
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pubmed:pagination |
3179-82
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pubmed:meshHeading |
pubmed-meshheading:18576661-Anions,
pubmed-meshheading:18576661-Boranes,
pubmed-meshheading:18576661-Crystallography, X-Ray,
pubmed-meshheading:18576661-Ketones,
pubmed-meshheading:18576661-Models, Molecular,
pubmed-meshheading:18576661-Pyrroles,
pubmed-meshheading:18576661-Spectrometry, Fluorescence,
pubmed-meshheading:18576661-Spectrophotometry, Ultraviolet
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|
pubmed:year |
2008
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|
pubmed:articleTitle |
Heteroaryl-substituted C3-bridged oligopyrroles: potential building subunits of anion-responsive pi-conjugated oligomers.
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|
pubmed:affiliation |
College of Pharmaceutical Sciences, Institute of Science and Engineering, Ritsumeikan University, Kusatsu 525-8577, Japan. maedahir@ph.ritsumei.ac.jp
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|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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