A distinct tetradentate N2O2-type ligand: (o-Carboranyl)bis(2-hydroxymethyl)pyridine

A new chiral racemic ligand (o-carboranyl)bis(2-hydroxymethyl)pyridine oCB(hmpH)2, that is composed of a central o-carborane unit where two arms radiate out of the cluster carbons each one containing a 2-pyridylmethylalcohol chelating arms, provides two potentially bidentate {NO} or one tetradentate...

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Autores principales: Di Salvo, F., Teixidor, F., Viñas, C., Giner Planas, J.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00442313_v639_n7_p1194_DiSalvo
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spelling todo:paper_00442313_v639_n7_p1194_DiSalvo2023-10-03T14:51:38Z A distinct tetradentate N2O2-type ligand: (o-Carboranyl)bis(2-hydroxymethyl)pyridine Di Salvo, F. Teixidor, F. Viñas, C. Giner Planas, J. Boron clusters Carboranylalcohols Chiral ligands Cobalt Self-assembly A new chiral racemic ligand (o-carboranyl)bis(2-hydroxymethyl)pyridine oCB(hmpH)2, that is composed of a central o-carborane unit where two arms radiate out of the cluster carbons each one containing a 2-pyridylmethylalcohol chelating arms, provides two potentially bidentate {NO} or one tetradentate {N2O2} binding pockets. An unprecedented octahedral CoII complex [CoCl2(anti- oCB(hmpH)2] was obtained under aerobic conditions and characterized by X-ray crystallography as well as IR and NMR spectroscopy. anti-oCB(hmpH) 2 acts as a tetradentate N2O2-ligand affording the complex as a racemic mixture of cis-α Δ-[CoCl2( RRanti-oCB(hmpH)2)] and Λ-[CoCl2( SSanti-oCB(hmpH)2)]. The new ligand oCB(hmpH)2 appears to be suitable for producing a variety of new chiral-at-metal complexes. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Fil:Di Salvo, F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00442313_v639_n7_p1194_DiSalvo
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Boron clusters
Carboranylalcohols
Chiral ligands
Cobalt
Self-assembly
spellingShingle Boron clusters
Carboranylalcohols
Chiral ligands
Cobalt
Self-assembly
Di Salvo, F.
Teixidor, F.
Viñas, C.
Giner Planas, J.
A distinct tetradentate N2O2-type ligand: (o-Carboranyl)bis(2-hydroxymethyl)pyridine
topic_facet Boron clusters
Carboranylalcohols
Chiral ligands
Cobalt
Self-assembly
description A new chiral racemic ligand (o-carboranyl)bis(2-hydroxymethyl)pyridine oCB(hmpH)2, that is composed of a central o-carborane unit where two arms radiate out of the cluster carbons each one containing a 2-pyridylmethylalcohol chelating arms, provides two potentially bidentate {NO} or one tetradentate {N2O2} binding pockets. An unprecedented octahedral CoII complex [CoCl2(anti- oCB(hmpH)2] was obtained under aerobic conditions and characterized by X-ray crystallography as well as IR and NMR spectroscopy. anti-oCB(hmpH) 2 acts as a tetradentate N2O2-ligand affording the complex as a racemic mixture of cis-α Δ-[CoCl2( RRanti-oCB(hmpH)2)] and Λ-[CoCl2( SSanti-oCB(hmpH)2)]. The new ligand oCB(hmpH)2 appears to be suitable for producing a variety of new chiral-at-metal complexes. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
format JOUR
author Di Salvo, F.
Teixidor, F.
Viñas, C.
Giner Planas, J.
author_facet Di Salvo, F.
Teixidor, F.
Viñas, C.
Giner Planas, J.
author_sort Di Salvo, F.
title A distinct tetradentate N2O2-type ligand: (o-Carboranyl)bis(2-hydroxymethyl)pyridine
title_short A distinct tetradentate N2O2-type ligand: (o-Carboranyl)bis(2-hydroxymethyl)pyridine
title_full A distinct tetradentate N2O2-type ligand: (o-Carboranyl)bis(2-hydroxymethyl)pyridine
title_fullStr A distinct tetradentate N2O2-type ligand: (o-Carboranyl)bis(2-hydroxymethyl)pyridine
title_full_unstemmed A distinct tetradentate N2O2-type ligand: (o-Carboranyl)bis(2-hydroxymethyl)pyridine
title_sort distinct tetradentate n2o2-type ligand: (o-carboranyl)bis(2-hydroxymethyl)pyridine
url http://hdl.handle.net/20.500.12110/paper_00442313_v639_n7_p1194_DiSalvo
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