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

^*Autor/a de correspondencia de este trabajo

Producción científica: Artículo en revista indizada › Artículo › revisión exhaustiva

17 Citas (Scopus)

Resumen

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	Inglés
Páginas (desde-hasta)	2122-2124
Número de páginas	3
Publicación	Chemical Communications
N.º	16
DOI	https://doi.org/10.1039/b500735f
Estado	Publicada - 28 abr 2005
Publicado de forma externa	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.\}",

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AU - Sanchez-Garcia, David

AU - Köhler, Thomas

AU - Seidel, Daniel

AU - Lynch, Vincent

AU - Sessler, Jonathan L.

PY - 2005/4/28

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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

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Straightforward synthesis of sulfur bridged oligopyrrolic macrocycles

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