Straightforward synthesis of sulfur bridged oligopyrrolic macrocycles

David Sanchez-Garcia; Thomas Köhler; Daniel Seidel; Vincent Lynch; Jonathan L. Sessler

doi:10.1039/b500735f

Straightforward synthesis of sulfur bridged oligopyrrolic macrocycles

David Sanchez-Garcia^*, Thomas Köhler, Daniel Seidel, Vincent Lynch, Jonathan L. Sessler

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Producció científica: Article en revista indexada › Article › Avaluat per experts

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Resum

Di- and trisulfide linked oligopyrrolic macrocycles are obtained when appropriate α,α′-free pyrrolic precursors are reacted with sulfur dichloride; these systems represent the first examples of what might be a general new class of porphyrin analogues.

Idioma original	Anglès
Pàgines (de-a)	2122-2124
Nombre de pàgines	3
Revista	Chemical Communications
Número	16
DOIs	https://doi.org/10.1039/b500735f
Estat de la publicació	Publicada - 28 d’abr. 2005
Publicat externament	Sí

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title = "Straightforward synthesis of sulfur bridged oligopyrrolic macrocycles",

abstract = "Di- and trisulfide linked oligopyrrolic macrocycles are obtained when appropriate α,α′-free pyrrolic precursors are reacted with sulfur dichloride; these systems represent the first examples of what might be a general new class of porphyrin analogues.",

keywords = "Extrusion, Porphyrin, Chemistry",

author = "David Sanchez-Garcia and Thomas K{\"o}hler and Daniel Seidel and Vincent Lynch and Sessler, \{Jonathan L.\}",

year = "2005",

month = apr,

day = "28",

doi = "10.1039/b500735f",

language = "English",

pages = "2122--2124",

journal = "Chemical Communications",

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publisher = "Royal Society of Chemistry",

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T1 - Straightforward synthesis of sulfur bridged oligopyrrolic macrocycles

AU - Sanchez-Garcia, David

AU - Köhler, Thomas

AU - Seidel, Daniel

AU - Lynch, Vincent

AU - Sessler, Jonathan L.

PY - 2005/4/28

Y1 - 2005/4/28

N2 - Di- and trisulfide linked oligopyrrolic macrocycles are obtained when appropriate α,α′-free pyrrolic precursors are reacted with sulfur dichloride; these systems represent the first examples of what might be a general new class of porphyrin analogues.

AB - Di- and trisulfide linked oligopyrrolic macrocycles are obtained when appropriate α,α′-free pyrrolic precursors are reacted with sulfur dichloride; these systems represent the first examples of what might be a general new class of porphyrin analogues.

KW - Extrusion

KW - Porphyrin

KW - Chemistry

UR - https://www.scopus.com/pages/publications/18544369030

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:000228559200016&DestLinkType=FullRecord&DestApp=WOS_CPL

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DO - 10.1039/b500735f

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JO - Chemical Communications

JF - Chemical Communications

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ER -

Straightforward synthesis of sulfur bridged oligopyrrolic macrocycles

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