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Article: Synthesis of aryl-substituted 2-pyridyl-1,10-phenanthrolines; A series of oriented terpyridine analogues

TitleSynthesis of aryl-substituted 2-pyridyl-1,10-phenanthrolines; A series of oriented terpyridine analogues
Authors
Klosterman, Jeremy K.Linden, AnthonySiegel, Jay S.
Issue Date2008
Citation
Organic and Biomolecular Chemistry, 2008, v. 6, n. 15, p. 2755-2764 How to Cite?
DOI: http://dx.doi.org/10.1039/b804106g
AbstractA 3 × 3 matrix of manisyl (4-methoxy-2,6-dimethylphenyl) substituted pyridyl-1,10-phenanthrolines has been synthesized by utilizing a general palladium catalyzed cross-coupling procedure. The directionality of these terdentate ligands will generate chiral octahedral ML2 complexes, potentially useful for the metal templated synthesis of topologically chiral structures. © The Royal Society of Chemistry.
Persistent Identifierhttp://hdl.handle.net/10722/341105
ISSN
1477-0520
2023 Impact Factor: 2.9
2023 SCImago Journal Rankings: 0.607
ISI Accession Number ID
WOS:000257737300015

 

DC FieldValueLanguage
dc.contributor.authorKlosterman, Jeremy K.-
dc.contributor.authorLinden, Anthony-
dc.contributor.authorSiegel, Jay S.-
dc.date.accessioned2024-03-13T08:40:11Z-
dc.date.available2024-03-13T08:40:11Z-
dc.date.issued2008-
dc.identifier.citationOrganic and Biomolecular Chemistry, 2008, v. 6, n. 15, p. 2755-2764-
dc.identifier.issn1477-0520-
dc.identifier.urihttp://hdl.handle.net/10722/341105-
dc.description.abstractA 3 × 3 matrix of manisyl (4-methoxy-2,6-dimethylphenyl) substituted pyridyl-1,10-phenanthrolines has been synthesized by utilizing a general palladium catalyzed cross-coupling procedure. The directionality of these terdentate ligands will generate chiral octahedral ML2 complexes, potentially useful for the metal templated synthesis of topologically chiral structures. © The Royal Society of Chemistry.-
dc.languageeng-
dc.relation.ispartofOrganic and Biomolecular Chemistry-
dc.titleSynthesis of aryl-substituted 2-pyridyl-1,10-phenanthrolines; A series of oriented terpyridine analogues-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/b804106g-
dc.identifier.scopuseid_2-s2.0-47849107520-
dc.identifier.volume6-
dc.identifier.issue15-
dc.identifier.spage2755-
dc.identifier.epage2764-
dc.identifier.isiWOS:000257737300015-

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