15834473

Source:http://linkedlifedata.com/resource/pubmed/id/15834473

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007447, umls-concept:C0013850, umls-concept:C0054666, umls-concept:C0220781, umls-concept:C0596040, umls-concept:C0678594, umls-concept:C1883254
pubmed:issue	15
pubmed:dateCreated	2005-4-18
pubmed:abstractText	Two different syntheses of N-heterocyclic carbene complexes of P(I) cations are presented; the structural features of these phosphamethine cyanine salts, in conjunction with the results of computational investigations, provide insight into the nature of the bonding of these heavy allene analogues.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Apr
pubmed:issn	1359-7345
pubmed:author	pubmed-author:DeckenAndreasA, pubmed-author:DykerC AdamCA, pubmed-author:EllisBobby DBD, pubmed-author:MacdonaldCharles L BCL
pubmed:issnType	Print
pubmed:day	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1965-7
pubmed:year	2005
pubmed:articleTitle	The synthesis, characterisation and electronic structure of N-heterocyclic carbene adducts of P(I) cations.
pubmed:affiliation	Department of Chemistry and Biochemistry, University of Windsor, Windsor, Ontario N9B 3P4, Canada.
pubmed:publicationType	Journal Article