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pubmed-article:17001609rdf:typepubmed:Citationlld:pubmed
pubmed-article:17001609lifeskim:mentionsumls-concept:C0034325lld:lifeskim
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pubmed-article:17001609lifeskim:mentionsumls-concept:C1883254lld:lifeskim
pubmed-article:17001609lifeskim:mentionsumls-concept:C0678594lld:lifeskim
pubmed-article:17001609lifeskim:mentionsumls-concept:C0679622lld:lifeskim
pubmed-article:17001609lifeskim:mentionsumls-concept:C0205314lld:lifeskim
pubmed-article:17001609lifeskim:mentionsumls-concept:C0871161lld:lifeskim
pubmed-article:17001609pubmed:issue2lld:pubmed
pubmed-article:17001609pubmed:dateCreated2007-1-1lld:pubmed
pubmed-article:17001609pubmed:abstractTextCalix[2]benzo[4]pyrrole m-6 and p-6, each containing two dipyrromethane moieties and two m-phenylene or p-phenylene units, respectively, were readily synthesised from pyrrole, 1,3- and 1,4-bis(1,1'-dimethylhydroxymethyl)benzene, (m-4 and p-4, respectively) and acetone. Macrocycles m-6 and p-6 were tested as receptors for a selection of anions, such as acetate, dihydrogenphosphate and fluoride. The X-ray structures of m-6 and p-6 and those of the complexes m-6F(-), m-6Cl(-) and m-6CH(3)COO(-) (with an nBu(4)N(+) counterion) were also determined.lld:pubmed
pubmed-article:17001609pubmed:languageenglld:pubmed
pubmed-article:17001609pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17001609pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:17001609pubmed:issn0947-6539lld:pubmed
pubmed-article:17001609pubmed:authorpubmed-author:WhiteAndrew...lld:pubmed
pubmed-article:17001609pubmed:authorpubmed-author:GarozzoDomeni...lld:pubmed
pubmed-article:17001609pubmed:authorpubmed-author:MessinaAngela...lld:pubmed
pubmed-article:17001609pubmed:authorpubmed-author:CafeoGraziaGlld:pubmed
pubmed-article:17001609pubmed:authorpubmed-author:KohnkeFranz...lld:pubmed
pubmed-article:17001609pubmed:issnTypePrintlld:pubmed
pubmed-article:17001609pubmed:volume13lld:pubmed
pubmed-article:17001609pubmed:ownerNLMlld:pubmed
pubmed-article:17001609pubmed:authorsCompleteYlld:pubmed
pubmed-article:17001609pubmed:pagination649-56lld:pubmed
pubmed-article:17001609pubmed:dateRevised2009-8-4lld:pubmed
pubmed-article:17001609pubmed:year2007lld:pubmed
pubmed-article:17001609pubmed:articleTitleSyntheses, structures, and anion-binding properties of two novel calix[2]benzo[4]pyrroles.lld:pubmed
pubmed-article:17001609pubmed:affiliationDipartimento di Chimica Organica e Biologica, Università di Messina, Salita Sperone 31, 98166 Messina, Italy. ella@isengard.umime.itlld:pubmed
pubmed-article:17001609pubmed:publicationTypeJournal Articlelld:pubmed