Photooxidation of nickel(II) macrocyclic complexes on excitation in the charge-transfer-to-solvent band in aqueous solution and in the presence of oxygen

Dhanasekaran Thirunavukkarasu, H. Prakash, P. Natarajan

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10 Citations (Scopus)

Abstract

Photooxidation of the well known nickel(II)-macrocyclic complexes [Ni(tet-a)] (ClO4)2, 1, and [Ni(AT)] ClO4, 2, (where tet-a=-meso-5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane and AT=11,13-dimethyl-1,4,7,10-tetraazacyclotetradeca-10,12-dienato) has been observed for the first time on excitation in the charge transfer to solvent band. The adduct formed in the primary photochemical process with the complex 1 is efficiently scavenged in presence of H+ and O2 to produce HO2· radical. This radical further oxidizes the nickel(II) macrocyclic complex to produce nickel(III) complex in the secondary thermal reaction as seen by the growth in absorbance at 370nm in the conventional flash photolysis setup. Rate constants for the formation of nickel(III) by the reaction of HO2· radical with 1 was determined as a function of the concentration of the complex and hydrogen ion. Conventional flash photolysis of the complex 2 in presence of N2O produces a transient which shows maximum at 610nm. Stable nickel(III) complex is isolated on continuous photolysis of the complex 1 and characterized by electronic, IR, ESR spectroscopy and CHN analysis. In deaerated acidic aqueous solution containing alcohols, photolysis of 1 produced hydrogen gas as evidenced by gas chromatographic analysis. Quantum yield for the photooxidation of 1 to give the nickel(III) complex is found to be 0.03±0.005.

Original languageEnglish
Pages (from-to)17-24
Number of pages8
JournalJournal of Photochemistry and Photobiology A: Chemistry
Volume141
Issue number1
Publication statusPublished - 15 Jun 2001
Externally publishedYes

Fingerprint

Photooxidation
photooxidation
Nickel
Charge transfer
charge transfer
Photolysis
nickel
Oxygen
aqueous solutions
photolysis
oxygen
excitation
flash
Hydrogen
gas analysis
Quantum yield
hydrogen ions
Gas chromatography
adducts
Paramagnetic resonance

Keywords

  • Charge transfer processes
  • Ni(II) macrocyclic complexes
  • Ni(III) macrocyclic complexes
  • Photooxidation

ASJC Scopus subject areas

  • Bioengineering
  • Physical and Theoretical Chemistry

Cite this

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title = "Photooxidation of nickel(II) macrocyclic complexes on excitation in the charge-transfer-to-solvent band in aqueous solution and in the presence of oxygen",
abstract = "Photooxidation of the well known nickel(II)-macrocyclic complexes [Ni(tet-a)] (ClO4)2, 1, and [Ni(AT)] ClO4, 2, (where tet-a=-meso-5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane and AT=11,13-dimethyl-1,4,7,10-tetraazacyclotetradeca-10,12-dienato) has been observed for the first time on excitation in the charge transfer to solvent band. The adduct formed in the primary photochemical process with the complex 1 is efficiently scavenged in presence of H+ and O2 to produce HO2· radical. This radical further oxidizes the nickel(II) macrocyclic complex to produce nickel(III) complex in the secondary thermal reaction as seen by the growth in absorbance at 370nm in the conventional flash photolysis setup. Rate constants for the formation of nickel(III) by the reaction of HO2· radical with 1 was determined as a function of the concentration of the complex and hydrogen ion. Conventional flash photolysis of the complex 2 in presence of N2O produces a transient which shows maximum at 610nm. Stable nickel(III) complex is isolated on continuous photolysis of the complex 1 and characterized by electronic, IR, ESR spectroscopy and CHN analysis. In deaerated acidic aqueous solution containing alcohols, photolysis of 1 produced hydrogen gas as evidenced by gas chromatographic analysis. Quantum yield for the photooxidation of 1 to give the nickel(III) complex is found to be 0.03±0.005.",
keywords = "Charge transfer processes, Ni(II) macrocyclic complexes, Ni(III) macrocyclic complexes, Photooxidation",
author = "Dhanasekaran Thirunavukkarasu and H. Prakash and P. Natarajan",
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T1 - Photooxidation of nickel(II) macrocyclic complexes on excitation in the charge-transfer-to-solvent band in aqueous solution and in the presence of oxygen

AU - Thirunavukkarasu, Dhanasekaran

AU - Prakash, H.

AU - Natarajan, P.

PY - 2001/6/15

Y1 - 2001/6/15

N2 - Photooxidation of the well known nickel(II)-macrocyclic complexes [Ni(tet-a)] (ClO4)2, 1, and [Ni(AT)] ClO4, 2, (where tet-a=-meso-5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane and AT=11,13-dimethyl-1,4,7,10-tetraazacyclotetradeca-10,12-dienato) has been observed for the first time on excitation in the charge transfer to solvent band. The adduct formed in the primary photochemical process with the complex 1 is efficiently scavenged in presence of H+ and O2 to produce HO2· radical. This radical further oxidizes the nickel(II) macrocyclic complex to produce nickel(III) complex in the secondary thermal reaction as seen by the growth in absorbance at 370nm in the conventional flash photolysis setup. Rate constants for the formation of nickel(III) by the reaction of HO2· radical with 1 was determined as a function of the concentration of the complex and hydrogen ion. Conventional flash photolysis of the complex 2 in presence of N2O produces a transient which shows maximum at 610nm. Stable nickel(III) complex is isolated on continuous photolysis of the complex 1 and characterized by electronic, IR, ESR spectroscopy and CHN analysis. In deaerated acidic aqueous solution containing alcohols, photolysis of 1 produced hydrogen gas as evidenced by gas chromatographic analysis. Quantum yield for the photooxidation of 1 to give the nickel(III) complex is found to be 0.03±0.005.

AB - Photooxidation of the well known nickel(II)-macrocyclic complexes [Ni(tet-a)] (ClO4)2, 1, and [Ni(AT)] ClO4, 2, (where tet-a=-meso-5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane and AT=11,13-dimethyl-1,4,7,10-tetraazacyclotetradeca-10,12-dienato) has been observed for the first time on excitation in the charge transfer to solvent band. The adduct formed in the primary photochemical process with the complex 1 is efficiently scavenged in presence of H+ and O2 to produce HO2· radical. This radical further oxidizes the nickel(II) macrocyclic complex to produce nickel(III) complex in the secondary thermal reaction as seen by the growth in absorbance at 370nm in the conventional flash photolysis setup. Rate constants for the formation of nickel(III) by the reaction of HO2· radical with 1 was determined as a function of the concentration of the complex and hydrogen ion. Conventional flash photolysis of the complex 2 in presence of N2O produces a transient which shows maximum at 610nm. Stable nickel(III) complex is isolated on continuous photolysis of the complex 1 and characterized by electronic, IR, ESR spectroscopy and CHN analysis. In deaerated acidic aqueous solution containing alcohols, photolysis of 1 produced hydrogen gas as evidenced by gas chromatographic analysis. Quantum yield for the photooxidation of 1 to give the nickel(III) complex is found to be 0.03±0.005.

KW - Charge transfer processes

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KW - Ni(III) macrocyclic complexes

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