Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonates

Alkylated Zn(salpyr) complexes (salpyr = N,N ́-bis[salicylidene]-3,4-pyridinediamine) have been prepared and used as catalyst precursors for the formation of cyclic carbonates from a range of (functional) epoxides and CO2. Reaction conditions were optimized to achieve good isolated yields of the tar...

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Autores: Martín, C., Whiteoak, C. J., Martin, E., Martínez Belmonte, M., Escudero- Adán, E. C., Kleij, A. W.
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2014
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2072/356068
Acceso en línea:http://hdl.handle.net/2072/356068
https://doi.org/10.1039/C3CY01043K
Access Level:acceso abierto
Palabra clave:54
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spelling Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonatesMartín, C.Whiteoak, C. J.Martin, E.Martínez Belmonte, M.Escudero- Adán, E. C.Kleij, A. W.54Alkylated Zn(salpyr) complexes (salpyr = N,N ́-bis[salicylidene]-3,4-pyridinediamine) have been prepared and used as catalyst precursors for the formation of cyclic carbonates from a range of (functional) epoxides and CO2. Reaction conditions were optimized to achieve good isolated yields of the targeted products. The molecular structure for the most active bifunctional Zn(salpyr) derivative has also been resolved using X-ray diffraction studies.2014info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersion1615 p.application/pdfhttp://hdl.handle.net/2072/356068https://doi.org/10.1039/C3CY01043KRECERCAT (Dipòsit de la Recerca de Catalunya)reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésL'accés als continguts d'aquest document queda condicionat a l'acceptació de les condicions d'ús establertes per la següent llicència Creative Commons:http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:recercat.cat:2072/3560682026-05-29T05:05:01Z
dc.title.none.fl_str_mv Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonates
title Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonates
spellingShingle Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonates
Martín, C.
54
title_short Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonates
title_full Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonates
title_fullStr Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonates
title_full_unstemmed Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonates
title_sort Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonates
dc.creator.none.fl_str_mv Martín, C.
Whiteoak, C. J.
Martin, E.
Martínez Belmonte, M.
Escudero- Adán, E. C.
Kleij, A. W.
author Martín, C.
author_facet Martín, C.
Whiteoak, C. J.
Martin, E.
Martínez Belmonte, M.
Escudero- Adán, E. C.
Kleij, A. W.
author_role author
author2 Whiteoak, C. J.
Martin, E.
Martínez Belmonte, M.
Escudero- Adán, E. C.
Kleij, A. W.
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv 54
topic 54
description Alkylated Zn(salpyr) complexes (salpyr = N,N ́-bis[salicylidene]-3,4-pyridinediamine) have been prepared and used as catalyst precursors for the formation of cyclic carbonates from a range of (functional) epoxides and CO2. Reaction conditions were optimized to achieve good isolated yields of the targeted products. The molecular structure for the most active bifunctional Zn(salpyr) derivative has also been resolved using X-ray diffraction studies.
publishDate 2014
dc.date.none.fl_str_mv 2014
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/acceptedVersion
format article
status_str acceptedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/2072/356068
https://doi.org/10.1039/C3CY01043K
url http://hdl.handle.net/2072/356068
https://doi.org/10.1039/C3CY01043K
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1615 p.
application/pdf
dc.source.none.fl_str_mv RECERCAT (Dipòsit de la Recerca de Catalunya)
reponame:Recercat. Dipósit de la Recerca de Catalunya
instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
instname_str Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
reponame_str Recercat. Dipósit de la Recerca de Catalunya
collection Recercat. Dipósit de la Recerca de Catalunya
repository.name.fl_str_mv
repository.mail.fl_str_mv
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score 15,811543

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