pubmed-article:11917112 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11917112 | lifeskim:mentions | umls-concept:C0025663 | lld:lifeskim |
pubmed-article:11917112 | lifeskim:mentions | umls-concept:C0524637 | lld:lifeskim |
pubmed-article:11917112 | lifeskim:mentions | umls-concept:C0003075 | lld:lifeskim |
pubmed-article:11917112 | lifeskim:mentions | umls-concept:C1522492 | lld:lifeskim |
pubmed-article:11917112 | pubmed:issue | 8 | lld:pubmed |
pubmed-article:11917112 | pubmed:dateCreated | 2002-4-17 | lld:pubmed |
pubmed-article:11917112 | pubmed:abstractText | Two thread-shaped cations, pyridinium nicotinamide and imidazolium, as their chloride and hexafluorophosphate salts, were studied with regards to complexation with hydrogen-bond-donating acyclic and macrocyclic ligands. In the latter case, the cations form pseudorotaxanes templated by the chloride anion but not hexafluorophosphate. This formation is a function of the coupling of ion-pairing between the cation and chloride anion and subsequent recognition of the anion by the macrocyclic diamide, which provides the driving force for interpenetration. We propose that this anion template principle is a general method for the construction of pseudorotaxanes and could be applied to other cationic threads, anions, and macrocyclic species. | lld:pubmed |
pubmed-article:11917112 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:language | eng | lld:pubmed |
pubmed-article:11917112 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:11917112 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11917112 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11917112 | pubmed:month | Apr | lld:pubmed |
pubmed-article:11917112 | pubmed:issn | 0027-8424 | lld:pubmed |
pubmed-article:11917112 | pubmed:author | pubmed-author:BeerPaul DPD | lld:pubmed |
pubmed-article:11917112 | pubmed:author | pubmed-author:WisnerJames... | lld:pubmed |
pubmed-article:11917112 | pubmed:author | pubmed-author:BerryNeil GNG | lld:pubmed |
pubmed-article:11917112 | pubmed:author | pubmed-author:Tomapatanaget... | lld:pubmed |
pubmed-article:11917112 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11917112 | pubmed:day | 16 | lld:pubmed |
pubmed-article:11917112 | pubmed:volume | 99 | lld:pubmed |
pubmed-article:11917112 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11917112 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11917112 | pubmed:pagination | 4983-6 | lld:pubmed |
pubmed-article:11917112 | pubmed:dateRevised | 2010-9-14 | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:meshHeading | pubmed-meshheading:11917112... | lld:pubmed |
pubmed-article:11917112 | pubmed:year | 2002 | lld:pubmed |
pubmed-article:11917112 | pubmed:articleTitle | Anion recognition as a method for templating pseudorotaxane formation. | lld:pubmed |
pubmed-article:11917112 | pubmed:affiliation | Department of Chemistry, Inorganic Chemistry Laboratory, University of Oxford, Oxford OX1 3QR, United Kingdom. | lld:pubmed |
pubmed-article:11917112 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11917112 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |