dc.contributor.author | SENGE, MATHIAS | en |
dc.date.accessioned | 2015-05-06T10:17:14Z | |
dc.date.available | 2015-05-06T10:17:14Z | |
dc.date.issued | 2014 | en |
dc.date.submitted | 2014 | en |
dc.identifier.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, 4283-4294 | en |
dc.identifier.issn | 1434-193X | en |
dc.identifier.other | Y | en |
dc.description | PUBLISHED | en |
dc.description.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. | en |
dc.description.sponsorship | This work was supported by a grant from Science Foundation Ireland (P.I.
09/IN.1/B2650). | en |
dc.format.extent | 4283-4294 | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY | en |
dc.relation.ispartofseries | 20 | en |
dc.rights | Y | en |
dc.subject | porphyrinoids • nucleophilic substitution • tetrapyrroles • macrocycles • photodynamic therapy | en |
dc.subject.lcsh | porphyrinoids • nucleophilic substitution • tetrapyrroles • macrocycles • photodynamic therapy | en |
dc.title | Simple Porphyrin Desymmetrization: 5,10,15,20-Tetrakis(3-hydroxyphenyl)porphyrin (mTHPP) as a Gateway Molecule for Peripheral Functionalization | en |
dc.type | Journal Article | en |
dc.type.supercollection | scholarly_publications | en |
dc.type.supercollection | refereed_publications | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/abdallm | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/sengem | en |
dc.identifier.rssinternalid | 99860 | en |
dc.identifier.doi | http://dx.doi.org/10.1002/ejoc.201402433 | en |
dc.rights.ecaccessrights | openAccess | |
dc.contributor.sponsor | Science Foundation Ireland (SFI) | en |
dc.identifier.uri | http://hdl.handle.net/2262/73839 | |