WAVELENGTH AND LIGAND PERIPHERAL GROUPS EFFECTS IN PHOTOREDOX CHEMISTRY OF [FE(R-SALEN)(BR-KOJI)] COMPLEXES (SALEN = N,N’-ETHYLENEBIS(R-SALICYLIDENEIMINATO); KOJI = 5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE)

Photoredox reactions occurring in irradiated methanolic solutions of the complexes [Fe(R-salen)(Br-koji)], (where R-salen²~ are N,N’-ethylenebis(R-salicylideneiminato) ligands (R = H, 5-F, 5-C1, 5-Br, 3-OCH3, 4-OCH3 or 5-OCH3); Br-kojr is the anión of 5-hydroxy-2-(bromomethyl)-4H-pyran-4-one) have b...

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Autor principal: ŠIMA,JOZEF
Lenguaje:English
Publicado: Sociedad Chilena de Química 2007
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000100016
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spelling oai:scielo:S0717-970720070001000162007-05-07WAVELENGTH AND LIGAND PERIPHERAL GROUPS EFFECTS IN PHOTOREDOX CHEMISTRY OF [FE(R-SALEN)(BR-KOJI)] COMPLEXES (SALEN = N,N’-ETHYLENEBIS(R-SALICYLIDENEIMINATO); KOJI = 5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE)ŠIMA,JOZEF complexes salen-type ligands bromokojato ligand photoredox reactions mechanism Photoredox reactions occurring in irradiated methanolic solutions of the complexes [Fe(R-salen)(Br-koji)], (where R-salen²~ are N,N’-ethylenebis(R-salicylideneiminato) ligands (R = H, 5-F, 5-C1, 5-Br, 3-OCH3, 4-OCH3 or 5-OCH3); Br-kojr is the anión of 5-hydroxy-2-(bromomethyl)-4H-pyran-4-one) have been investigated and their mechanism proposed. The complexes are redox stable in the dark. Continuous irradiation of such solutions in the región of intraligand (IL) and/or ligand-to-metal charge transfer (LMCT) transitions causes a series of photophysical and photochemical deactivations leading to the photoreduction of Fe(III) to Fe(II) and formation of formaldehyde CH(2)0 as final producís. Using EPR spin trapping technique -CH2OH radicáis were identified in the irradiated solutions. Both the tetradentate R-salen²~ and bidentate bromokojato Br-kojr ligands behave as innocent moieties virtually not participating in the redox processes of the complexes. The efficiency of the photoredox processes, expressed through the integral quantum yield of Fe(II) formation, <l>(Fe n) substantially decreases with increasing wavelength of the incident radiation, and is slightly influenced by the peripheral groups R of the R-salen²~ ligands. A mechanism of the primary photochemical and subsequent thermal reactions is proposedinfo:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.52 n.1 20072007-03-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000100016en10.4067/S0717-97072007000100016
institution Scielo Chile
collection Scielo Chile
language English
topic complexes
salen-type ligands
bromokojato ligand
photoredox reactions
mechanism
spellingShingle complexes
salen-type ligands
bromokojato ligand
photoredox reactions
mechanism
ŠIMA,JOZEF
WAVELENGTH AND LIGAND PERIPHERAL GROUPS EFFECTS IN PHOTOREDOX CHEMISTRY OF [FE(R-SALEN)(BR-KOJI)] COMPLEXES (SALEN = N,N’-ETHYLENEBIS(R-SALICYLIDENEIMINATO); KOJI = 5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE)
description Photoredox reactions occurring in irradiated methanolic solutions of the complexes [Fe(R-salen)(Br-koji)], (where R-salen²~ are N,N’-ethylenebis(R-salicylideneiminato) ligands (R = H, 5-F, 5-C1, 5-Br, 3-OCH3, 4-OCH3 or 5-OCH3); Br-kojr is the anión of 5-hydroxy-2-(bromomethyl)-4H-pyran-4-one) have been investigated and their mechanism proposed. The complexes are redox stable in the dark. Continuous irradiation of such solutions in the región of intraligand (IL) and/or ligand-to-metal charge transfer (LMCT) transitions causes a series of photophysical and photochemical deactivations leading to the photoreduction of Fe(III) to Fe(II) and formation of formaldehyde CH(2)0 as final producís. Using EPR spin trapping technique -CH2OH radicáis were identified in the irradiated solutions. Both the tetradentate R-salen²~ and bidentate bromokojato Br-kojr ligands behave as innocent moieties virtually not participating in the redox processes of the complexes. The efficiency of the photoredox processes, expressed through the integral quantum yield of Fe(II) formation, <l>(Fe n) substantially decreases with increasing wavelength of the incident radiation, and is slightly influenced by the peripheral groups R of the R-salen²~ ligands. A mechanism of the primary photochemical and subsequent thermal reactions is proposed
author ŠIMA,JOZEF
author_facet ŠIMA,JOZEF
author_sort ŠIMA,JOZEF
title WAVELENGTH AND LIGAND PERIPHERAL GROUPS EFFECTS IN PHOTOREDOX CHEMISTRY OF [FE(R-SALEN)(BR-KOJI)] COMPLEXES (SALEN = N,N’-ETHYLENEBIS(R-SALICYLIDENEIMINATO); KOJI = 5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE)
title_short WAVELENGTH AND LIGAND PERIPHERAL GROUPS EFFECTS IN PHOTOREDOX CHEMISTRY OF [FE(R-SALEN)(BR-KOJI)] COMPLEXES (SALEN = N,N’-ETHYLENEBIS(R-SALICYLIDENEIMINATO); KOJI = 5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE)
title_full WAVELENGTH AND LIGAND PERIPHERAL GROUPS EFFECTS IN PHOTOREDOX CHEMISTRY OF [FE(R-SALEN)(BR-KOJI)] COMPLEXES (SALEN = N,N’-ETHYLENEBIS(R-SALICYLIDENEIMINATO); KOJI = 5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE)
title_fullStr WAVELENGTH AND LIGAND PERIPHERAL GROUPS EFFECTS IN PHOTOREDOX CHEMISTRY OF [FE(R-SALEN)(BR-KOJI)] COMPLEXES (SALEN = N,N’-ETHYLENEBIS(R-SALICYLIDENEIMINATO); KOJI = 5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE)
title_full_unstemmed WAVELENGTH AND LIGAND PERIPHERAL GROUPS EFFECTS IN PHOTOREDOX CHEMISTRY OF [FE(R-SALEN)(BR-KOJI)] COMPLEXES (SALEN = N,N’-ETHYLENEBIS(R-SALICYLIDENEIMINATO); KOJI = 5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE)
title_sort wavelength and ligand peripheral groups effects in photoredox chemistry of [fe(r-salen)(br-koji)] complexes (salen = n,n’-ethylenebis(r-salicylideneiminato); koji = 5-hydroxy-2-(hydroxymethyl)-4h-pyran-4-one)
publisher Sociedad Chilena de Química
publishDate 2007
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000100016
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