Simple Porphyrin Desymmetrization: 5,10,15,20-Tetrakis(3-hydroxyphenyl)porphyrin (mTHPP) as a Gateway Molecule for Peripheral Functionalization
Citation:
Rogers, L, Burke-Murphy, E, Senge, MO, Simple Porphyrin Desymmetrization: 5,10,15,20-Tetrakis(3-hydroxyphenyl)porphyrin (mTHPP) as a Gateway Molecule for Peripheral Functionalization, EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 20, 2014, 4283-4294Download Item:
Abstract:
Abstract: The rise in the demand
towards unsymmetric porphyrin
systems for use in applications such as
photodynamic therapy and non-linear
optics mandates a concomitant
development of simple and practical
syntheses thereof. A new methodology
for the rapid generation of
unsymmetrical porphyrins synthesized
from the same common and easily
accessible symmetric porphyrin starting
material is discussed herein. A library
of unsymmetric mTHPP [5,10,15,20-
tetrakis(3-hydroxyphenyl)porphyrin]
derivatives was synthesized in good
yields through simple nucleophilic
substitution, esterification and metal
catalyzed cross-coupling reactions. The
methodology was optimized to quickly
generate a library of tailored
unsymmetrical porphyrins for use in a
variety of applications. Use of a
common meso-aryl substituted
porphyrin as starting material allowed
an updating of the synthetic toolkit
using a mixture of classical and modern
chemistry. This approach was tested as
a method for the synthesis of picketfence
porphyrin mimics and gave such
compounds in good yields and few
synthetic steps. Likewise, employing
simple nucleophilic substitution
chemistry co-facial, ‘caged’
bisporphyrin systems were accessible in
two synthetic steps.
Sponsor
Grant Number
Science Foundation Ireland (SFI)
Author's Homepage:
http://people.tcd.ie/abdallmhttp://people.tcd.ie/sengem
Description:
PUBLISHED
Author: SENGE, MATHIAS
Type of material:
Journal ArticleCollections
Series/Report no:
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY20
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Full text availableKeywords:
porphyrinoids • nucleophilic substitution • tetrapyrroles • macrocycles • photodynamic therapyDOI:
http://dx.doi.org/10.1002/ejoc.201402433ISSN:
1434-193XMetadata
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