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

^*Corresponding author for this work

Research output: Indexed journal article › Article › peer-review

17 Citations (Scopus)

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.

Original language	English
Pages (from-to)	2122-2124
Number of pages	3
Journal	Chemical Communications
Issue number	16
DOIs	https://doi.org/10.1039/b500735f
Publication status	Published - 28 Apr 2005
Externally published	Yes

Keywords

Extrusion
Porphyrin
Chemistry

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10.1039/b500735f

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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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day = "28",

doi = "10.1039/b500735f",

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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

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JO - Chemical Communications

JF - Chemical Communications

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ER -

Straightforward synthesis of sulfur bridged oligopyrrolic macrocycles

Abstract

Keywords

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