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pubmed-article:16316210pubmed:dateCreated2005-11-30lld:pubmed
pubmed-article:16316210pubmed:abstractTextA cobalt(III)-salen complex (3) with an axial substituent on the diamine backbone has been synthesized. Crystal structure reveals that the axial substituent (p-nitrophenyl group) is positioned in close proximity to the metal binding site. The stereoselectivity of the cobalt complex for binding amino alcohols increases with increasing steric bulk of the amino alcohol from alaninol (2.9) to valinol (6.2) and t-leucinol (36.0).lld:pubmed
pubmed-article:16316210pubmed:languageenglld:pubmed
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pubmed-article:16316210pubmed:statusPubMed-not-MEDLINElld:pubmed
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pubmed-article:16316210pubmed:issn0002-7863lld:pubmed
pubmed-article:16316210pubmed:authorpubmed-author:LoughAlan JAJlld:pubmed
pubmed-article:16316210pubmed:authorpubmed-author:KimB MoonBMlld:pubmed
pubmed-article:16316210pubmed:authorpubmed-author:ChinJikJlld:pubmed
pubmed-article:16316210pubmed:authorpubmed-author:KimHae-JoHJlld:pubmed
pubmed-article:16316210pubmed:authorpubmed-author:KimWoosungWlld:pubmed
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pubmed-article:16316210pubmed:volume127lld:pubmed
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pubmed-article:16316210pubmed:pagination16776-7lld:pubmed
pubmed-article:16316210pubmed:dateRevised2008-1-17lld:pubmed
pubmed-article:16316210pubmed:year2005lld:pubmed
pubmed-article:16316210pubmed:articleTitleA cobalt(III)-salen complex with an axial substituent in the diamine backbone: stereoselective recognition of amino alcohols.lld:pubmed
pubmed-article:16316210pubmed:affiliationDepartment of Chemistry, University of Toronto, Canada.lld:pubmed
pubmed-article:16316210pubmed:publicationTypeJournal Articlelld:pubmed
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