Phthalocyanines and related complexes as electrocatalysts for the detection of nitric oxide
- Nyokong, Tebello, Vilakazi, Sibulelo
- Authors: Nyokong, Tebello , Vilakazi, Sibulelo
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290346 , vital:56741 , xlink:href="https://doi.org/10.1016/S0039-9140(03)00356-4"
- Description: Metallophthalocyanine (MPc) and metalloporphyrin complexes as well as some metalloproteins including myoglobin, hemoglobin, cyanocobalamin and cytochrome c catalyse the detection of nitric oxide (NO). The catalytic process often involve changes in the oxidation state of the catalyst. These complexes catalyse both the reduction and oxidation of NO. MPc complexes containing electroactive central metals such as CoPc and FePc generally show better catalytic activity towards the detection of NO than complexes containing electroinacive central metals. However, the involvement of ring based redox processes was confirmed for the homogenous NO catalysis using CoPc.
- Full Text:
- Date Issued: 2003
- Authors: Nyokong, Tebello , Vilakazi, Sibulelo
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290346 , vital:56741 , xlink:href="https://doi.org/10.1016/S0039-9140(03)00356-4"
- Description: Metallophthalocyanine (MPc) and metalloporphyrin complexes as well as some metalloproteins including myoglobin, hemoglobin, cyanocobalamin and cytochrome c catalyse the detection of nitric oxide (NO). The catalytic process often involve changes in the oxidation state of the catalyst. These complexes catalyse both the reduction and oxidation of NO. MPc complexes containing electroactive central metals such as CoPc and FePc generally show better catalytic activity towards the detection of NO than complexes containing electroinacive central metals. However, the involvement of ring based redox processes was confirmed for the homogenous NO catalysis using CoPc.
- Full Text:
- Date Issued: 2003
Self-Assembled Monolayers of Cobalt and Iron Phthalocyanine Complexes on Gold Electrodes
- Ozoemena, Kenneth I, Nyokong, Tebello, Westbroek, Philippe
- Authors: Ozoemena, Kenneth I , Nyokong, Tebello , Westbroek, Philippe
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290363 , vital:56743 , xlink:href="https://doi.org/10.1002/elan.200302753"
- Description: The self-assembling of the octa(hydroxyethylthio)-metallophthalocyanine {MOHETPc (M=Co and Fe)} complexes and their similar analogues, octabutylthiometallophthalocyanine {MOBTPc (M=Co and Fe)} complexes on gold electrodes are investigated. Comparative surface voltammetric insights into their distinct self-assembling properties with respect to the passivation of Faradaic processes and surface coverages, including their solution electrochemistry, suggest different orientations and non-cleavage of their CS bonds. In the pH 2−9 range, the reversible [M(III)Pc(−2)]+ / [M(II)Pc(−2)] redox couples show potential shifts close to −59 mV / pH. The gold electrodes modified with the SAMs of these species show electrocatalytic activity towards the oxidation of thiols (L-cysteine, homocysteine and penicillamine) and thiocyanate in acidic media with detection limits in the region of 10−7–10−6 mol dm−3. These monolayers are stable and easily reproducible.
- Full Text:
- Date Issued: 2003
- Authors: Ozoemena, Kenneth I , Nyokong, Tebello , Westbroek, Philippe
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290363 , vital:56743 , xlink:href="https://doi.org/10.1002/elan.200302753"
- Description: The self-assembling of the octa(hydroxyethylthio)-metallophthalocyanine {MOHETPc (M=Co and Fe)} complexes and their similar analogues, octabutylthiometallophthalocyanine {MOBTPc (M=Co and Fe)} complexes on gold electrodes are investigated. Comparative surface voltammetric insights into their distinct self-assembling properties with respect to the passivation of Faradaic processes and surface coverages, including their solution electrochemistry, suggest different orientations and non-cleavage of their CS bonds. In the pH 2−9 range, the reversible [M(III)Pc(−2)]+ / [M(II)Pc(−2)] redox couples show potential shifts close to −59 mV / pH. The gold electrodes modified with the SAMs of these species show electrocatalytic activity towards the oxidation of thiols (L-cysteine, homocysteine and penicillamine) and thiocyanate in acidic media with detection limits in the region of 10−7–10−6 mol dm−3. These monolayers are stable and easily reproducible.
- Full Text:
- Date Issued: 2003
Solvent effects on the photochemical and fluorescence properties of zinc phthalocyanine derivatives
- Ogunsipe, Abimbola Olukayode, Maree, D, Nyokong, Tebello
- Authors: Ogunsipe, Abimbola Olukayode , Maree, D , Nyokong, Tebello
- Date: 2003
- Language: English
- Type: Article
- Identifier: vital:6586 , http://hdl.handle.net/10962/d1004162 , http://dx.doi.org/10.1016/S0022-2860(03)00155-8
- Description: The effects of solvents on the singlet oxygen, photobleaching and fluorescence quantum yields for zinc phthalocyanine (ZnPc) and its derivatives; (pyridino)zinc phthalocyanine ((py)ZnPc), zinc octaphenoxyphthalocyanine (ZnOPPc) and zinc octaestronephthalocyanine (ZnOEPc), is presented. The effects of the solvents on the ground state spectra are also discussed. The largest red shift of the Q band was observed in aromatic solvents, the highest shift being observed for 1-chloronaphthalene. Higher singlet fluorescence quantum yields were observed in THF for ZnPc and ZnOPPC. Also in the same solvent phototransformation rather than photobleaching was observed for ZnOPPc. Split Q band in the emission and excitation spectra of ZnOPPc was observed in some solvents and this is explained in terms of the lowering of symmetry following excitation.
- Full Text:
- Date Issued: 2003
- Authors: Ogunsipe, Abimbola Olukayode , Maree, D , Nyokong, Tebello
- Date: 2003
- Language: English
- Type: Article
- Identifier: vital:6586 , http://hdl.handle.net/10962/d1004162 , http://dx.doi.org/10.1016/S0022-2860(03)00155-8
- Description: The effects of solvents on the singlet oxygen, photobleaching and fluorescence quantum yields for zinc phthalocyanine (ZnPc) and its derivatives; (pyridino)zinc phthalocyanine ((py)ZnPc), zinc octaphenoxyphthalocyanine (ZnOPPc) and zinc octaestronephthalocyanine (ZnOEPc), is presented. The effects of the solvents on the ground state spectra are also discussed. The largest red shift of the Q band was observed in aromatic solvents, the highest shift being observed for 1-chloronaphthalene. Higher singlet fluorescence quantum yields were observed in THF for ZnPc and ZnOPPC. Also in the same solvent phototransformation rather than photobleaching was observed for ZnOPPc. Split Q band in the emission and excitation spectra of ZnOPPc was observed in some solvents and this is explained in terms of the lowering of symmetry following excitation.
- Full Text:
- Date Issued: 2003
Synthesis, spectral and electrochemical properties of a new family of pyrrole substituted cobalt, iron, manganese, nickel and zinc phthalocyanine complexes
- Obirai, Joe, Rodrigues, Nazaré Pereira, Bedioui, Fethi, Nyokong, Tebello
- Authors: Obirai, Joe , Rodrigues, Nazaré Pereira , Bedioui, Fethi , Nyokong, Tebello
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/304852 , vital:58496 , xlink:href="https://0-doi.org.wam.seals.ac.za/10.1142/S1088424603000641"
- Description: A new family of pyrrole substituted metallophthalocyanine complexes, namely cobalt(II), iron(II), manganese(III), nickel(II) and zinc(II) tetrakis-4-(pyrrol-1-yl)phenoxy phthalocyanines (noted as M(TPhPyrPc), where M is the metallic cation) have been synthesized and fully characterized. In particular, the UV-visible spectra of the iron and nickel complexes showed extensive aggregation even at low concentrations. The cyclic voltammetry of the cobalt, iron and manganese complexes showed three to four redox couples assigned to metal and ring based processes. Spectroelectrochemistry of the manganese derivative confirmed that the synthesized complex is MnIII(TPhPyrPc-2) and that the reduction of MnII(TPhPyrPc-2) to be centred on the ring and rather than on the metal, forming the MnII(TPhPyrPc-4) species. Also, the electrochemical polymerization of these newly synthesized pyrrole-substituted phthalocyanines has been demonstrated in the case of the cobalt complex and the electrocatalytic activity of the obtained film has been tested towards the oxidation of L-cysteine.
- Full Text:
- Date Issued: 2003
- Authors: Obirai, Joe , Rodrigues, Nazaré Pereira , Bedioui, Fethi , Nyokong, Tebello
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/304852 , vital:58496 , xlink:href="https://0-doi.org.wam.seals.ac.za/10.1142/S1088424603000641"
- Description: A new family of pyrrole substituted metallophthalocyanine complexes, namely cobalt(II), iron(II), manganese(III), nickel(II) and zinc(II) tetrakis-4-(pyrrol-1-yl)phenoxy phthalocyanines (noted as M(TPhPyrPc), where M is the metallic cation) have been synthesized and fully characterized. In particular, the UV-visible spectra of the iron and nickel complexes showed extensive aggregation even at low concentrations. The cyclic voltammetry of the cobalt, iron and manganese complexes showed three to four redox couples assigned to metal and ring based processes. Spectroelectrochemistry of the manganese derivative confirmed that the synthesized complex is MnIII(TPhPyrPc-2) and that the reduction of MnII(TPhPyrPc-2) to be centred on the ring and rather than on the metal, forming the MnII(TPhPyrPc-4) species. Also, the electrochemical polymerization of these newly synthesized pyrrole-substituted phthalocyanines has been demonstrated in the case of the cobalt complex and the electrocatalytic activity of the obtained film has been tested towards the oxidation of L-cysteine.
- Full Text:
- Date Issued: 2003
Synthesis, spectroscopy and photochemistry of octasubstituted thiol-derivatized phthalocyaninatozinc (II) complexes
- Ozoemena, Kenneth I, Nyokong, Tebello
- Authors: Ozoemena, Kenneth I , Nyokong, Tebello
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290401 , vital:56746 , xlink:href="https://doi.org/10.1016/S1387-7003(03)00218-1"
- Description: Synthesis, spectroscopic and photochemical characterization of phenylthiol-derivatized zinc phthalocyanine complex: 2,3,9,10,16,17,23,24-octa(4-methylphenylthio-)phthalocyaninatozinc(II) [ZnPc(SC6H4CH3)8] (3a) and its alkanethiol derivative, 2,3,9,10,16,17,23,24-octabutylthiophthalocyaninatozinc(II) [ZnPc(SC4H9)8] (3b) are described. Spectroscopic analyses show that 3a has a higher aggregation tendency than 3b in organic solvents. Photochemical studies indicate that 3b is more photostable and more efficient at singlet oxygen generation than 3a.
- Full Text:
- Date Issued: 2003
- Authors: Ozoemena, Kenneth I , Nyokong, Tebello
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290401 , vital:56746 , xlink:href="https://doi.org/10.1016/S1387-7003(03)00218-1"
- Description: Synthesis, spectroscopic and photochemical characterization of phenylthiol-derivatized zinc phthalocyanine complex: 2,3,9,10,16,17,23,24-octa(4-methylphenylthio-)phthalocyaninatozinc(II) [ZnPc(SC6H4CH3)8] (3a) and its alkanethiol derivative, 2,3,9,10,16,17,23,24-octabutylthiophthalocyaninatozinc(II) [ZnPc(SC4H9)8] (3b) are described. Spectroscopic analyses show that 3a has a higher aggregation tendency than 3b in organic solvents. Photochemical studies indicate that 3b is more photostable and more efficient at singlet oxygen generation than 3a.
- Full Text:
- Date Issued: 2003
Cyclic voltammetric studies of octabutylthiophthalo-cyaninato-cobalt (II) and its self-assembled monolayer (SAM) on gold electrode
- Ozoemena, Kenneth, Westbroek, Philippe, Nyokong, Tebello
- Authors: Ozoemena, Kenneth , Westbroek, Philippe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289567 , vital:56650 , xlink:href="https://doi.org/10.1142/S1088424602000130"
- Description: The synthesis of thiol-derivatized cobalt phthalocyanine complex, 2,3,9,10,16,17,23,24-octa (butylthiophthalocyaninatocobalt(II) (CoOBTPc) is described. Cyclic voltammetric data of this complex in DMF showed five quasi-reversible and reversible, diffusion-controlled redox couples, comprising both the phthalocyanine ring and central metal redox processes. The CoOBTPc complex forms a self-assembled monolayer (SAM) on gold electrode. The investigation of the integrity of this SAM, using the established cyclic voltammetric methods in aqueous alkaline solutions, gave evidence about the formation of a stable and easily reproducible monolayer. However, due to its susceptibility to destruction via oxidative and reductive desorptions, its potential application as an electrochemical sensor in alkaline pH is limited to a potential window of between −0.20 and +0.55 V vs Ag/AgCl.
- Full Text:
- Date Issued: 2002
- Authors: Ozoemena, Kenneth , Westbroek, Philippe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289567 , vital:56650 , xlink:href="https://doi.org/10.1142/S1088424602000130"
- Description: The synthesis of thiol-derivatized cobalt phthalocyanine complex, 2,3,9,10,16,17,23,24-octa (butylthiophthalocyaninatocobalt(II) (CoOBTPc) is described. Cyclic voltammetric data of this complex in DMF showed five quasi-reversible and reversible, diffusion-controlled redox couples, comprising both the phthalocyanine ring and central metal redox processes. The CoOBTPc complex forms a self-assembled monolayer (SAM) on gold electrode. The investigation of the integrity of this SAM, using the established cyclic voltammetric methods in aqueous alkaline solutions, gave evidence about the formation of a stable and easily reproducible monolayer. However, due to its susceptibility to destruction via oxidative and reductive desorptions, its potential application as an electrochemical sensor in alkaline pH is limited to a potential window of between −0.20 and +0.55 V vs Ag/AgCl.
- Full Text:
- Date Issued: 2002
Effects of axial ligands on the photophysical properties of silicon octaphenoxyphthalocyanine
- Maree, M David, Nyokong, Tebello, Suhling, Klaus, Phillips, David
- Authors: Maree, M David , Nyokong, Tebello , Suhling, Klaus , Phillips, David
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289582 , vital:56651 , xlink:href="https://doi.org/10.1142/S1088424602000452"
- Description: The photochemistry and photophysics of six axially substituted silicon phthalocyanines are reported and show the importance of the axial groups in the photochemistry of these compounds. The fluorescence quantum yields are especially affected by the axial ligand. A very good correlation was found for the experimentally determined fluorescence lifetimes and the theoretically determined lifetimes using the Strickler-Berg equation for the unaggregated molecules.
- Full Text:
- Date Issued: 2002
- Authors: Maree, M David , Nyokong, Tebello , Suhling, Klaus , Phillips, David
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289582 , vital:56651 , xlink:href="https://doi.org/10.1142/S1088424602000452"
- Description: The photochemistry and photophysics of six axially substituted silicon phthalocyanines are reported and show the importance of the axial groups in the photochemistry of these compounds. The fluorescence quantum yields are especially affected by the axial ligand. A very good correlation was found for the experimentally determined fluorescence lifetimes and the theoretically determined lifetimes using the Strickler-Berg equation for the unaggregated molecules.
- Full Text:
- Date Issued: 2002
Interaction of sulfur dioxide and cyanide with cobalt (II) tetrasulfophthalocyanine in aqueous media
- Thamae, Mamothibe, Nyokong, Tebello
- Authors: Thamae, Mamothibe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289595 , vital:56652 , xlink:href="https://doi.org/10.1016/S0277-5387(01)00968-8"
- Description: Kinetic and equilibrium studies for the coordination of cyanide or sulfur dioxide to the cobalt(II) tetrasulfophthalocyanine ([CoTSPc]4−) complex are reported. The equilibrium constant for the coordination of the cyanide under pH 11 conditions and an oxygen atmosphere, and the formation of [(CN−)2Co(III)TSPc]5− species, was found to be 2.1×101 dm3 mol−1 and the rate constant, kf was found to be 7.4 dm3 mol−1 s−1. Similarly, the coordination of SO2 to [CoTSPc]4− occurred with an equilibrium constant of 8.7×101 dm3 mol−1 and a rate constant of 2.1×102 dm3 mol−1 s−1, at pH 11. These rate and equilibrium constants represent the coordination of the second cyanide or sulfur dioxide ligands to the [CoTSPc]4− species. Coordination of the first ligand occurred faster than that of the second ligand in both cases. The coordination is accompanied by the oxidation of the central Co(II) metal with the formation of a Co(III) tetrasulfophthalocyanine species.
- Full Text:
- Date Issued: 2002
Interaction of sulfur dioxide and cyanide with cobalt (II) tetrasulfophthalocyanine in aqueous media
- Authors: Thamae, Mamothibe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289595 , vital:56652 , xlink:href="https://doi.org/10.1016/S0277-5387(01)00968-8"
- Description: Kinetic and equilibrium studies for the coordination of cyanide or sulfur dioxide to the cobalt(II) tetrasulfophthalocyanine ([CoTSPc]4−) complex are reported. The equilibrium constant for the coordination of the cyanide under pH 11 conditions and an oxygen atmosphere, and the formation of [(CN−)2Co(III)TSPc]5− species, was found to be 2.1×101 dm3 mol−1 and the rate constant, kf was found to be 7.4 dm3 mol−1 s−1. Similarly, the coordination of SO2 to [CoTSPc]4− occurred with an equilibrium constant of 8.7×101 dm3 mol−1 and a rate constant of 2.1×102 dm3 mol−1 s−1, at pH 11. These rate and equilibrium constants represent the coordination of the second cyanide or sulfur dioxide ligands to the [CoTSPc]4− species. Coordination of the first ligand occurred faster than that of the second ligand in both cases. The coordination is accompanied by the oxidation of the central Co(II) metal with the formation of a Co(III) tetrasulfophthalocyanine species.
- Full Text:
- Date Issued: 2002
Iron perchlorophthalocyanine and tetrasulfophthalocyanine catalyzed oxidation of cyclohexane using hydrogen peroxide, chloroperoxybenzoic acid and tert-butylhydroperoxide as oxidants
- Grootboom, Natasha, Nyokong, Tebello
- Authors: Grootboom, Natasha , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289606 , vital:56653 , xlink:href="https://doi.org/10.1016/S1381-1169(01)00404-6"
- Description: Polychlorophthalocyanine (Cl16PcFeII) and tetrasulfophthalocyanine ([FeIITSPc]4−) complexes of iron are employed as catalysts for the oxidation of cyclohexane using tert-butyl hydroperoxide (TBHP), m-chloroperoxybenzoic acid (m-CPBA) and hydrogen peroxide as oxidants. Catalysis using the Cl16PcFeII was performed in a dimethylformamide:dichloromethane (3:7) solvent mixture. For the [FeIITSPc]4−catalyst, a water:methanol (1:9) mixture was employed. The products of the catalysis are cyclohexanone, cyclohexanol and cyclohexanediol. The relative yields of the products depended on oxidant and the catalyst. TBHP was found to be the best oxidant since minimal destruction of the catalyst and higher selectivity in the products were observed when this oxidant was employed. The mechanism of the oxidation of cyclohexane in the presence of the Cl16PcFeII and [FeIITSPc]4− involves the oxidation of these catalysts, forming an Fe(III) phthalocyanine species as an intermediate. Higher yields were observed when [FeTSPc]4− was employed as a catalyst, which is more soluble than the perchlorinated iron phthalocyanine catalyst.
- Full Text:
- Date Issued: 2002
- Authors: Grootboom, Natasha , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289606 , vital:56653 , xlink:href="https://doi.org/10.1016/S1381-1169(01)00404-6"
- Description: Polychlorophthalocyanine (Cl16PcFeII) and tetrasulfophthalocyanine ([FeIITSPc]4−) complexes of iron are employed as catalysts for the oxidation of cyclohexane using tert-butyl hydroperoxide (TBHP), m-chloroperoxybenzoic acid (m-CPBA) and hydrogen peroxide as oxidants. Catalysis using the Cl16PcFeII was performed in a dimethylformamide:dichloromethane (3:7) solvent mixture. For the [FeIITSPc]4−catalyst, a water:methanol (1:9) mixture was employed. The products of the catalysis are cyclohexanone, cyclohexanol and cyclohexanediol. The relative yields of the products depended on oxidant and the catalyst. TBHP was found to be the best oxidant since minimal destruction of the catalyst and higher selectivity in the products were observed when this oxidant was employed. The mechanism of the oxidation of cyclohexane in the presence of the Cl16PcFeII and [FeIITSPc]4− involves the oxidation of these catalysts, forming an Fe(III) phthalocyanine species as an intermediate. Higher yields were observed when [FeTSPc]4− was employed as a catalyst, which is more soluble than the perchlorinated iron phthalocyanine catalyst.
- Full Text:
- Date Issued: 2002
Melatonin protects against copper‐mediated free radical damage
- Parmar, Paresh, Limson, Janice L, Nyokong, Tebello, Daya, Santy
- Authors: Parmar, Paresh , Limson, Janice L , Nyokong, Tebello , Daya, Santy
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289617 , vital:56654 , xlink:href=" https://doi.org/10.1034/j.1600-079X.2002.01859.x"
- Description: Copper is an essential trace element which forms an integral component of many enzymes. While trace amounts of copper are needed to sustain life, excess copper is extremely toxic. Copper has been implicated in various neurodegenerative disorders, such as Wilson's and Alzheimer's diseases. Previous studies showed that melatonin, the principle secretory product of the pineal gland, binds Cupric chloride (Cu2+) and that this may have implications in copper-induced neurodegenerative diseases. In the present study, in vitro copper-mediated lipid peroxidation was induced. Melatonin (5 mM) protected against copper-mediated lipid peroxidation in liver homogenates. Electron micrographs of in vivo administered Cu2+ and melatonin show that melatonin affords some protection to rat hepatocytes in the presence of copper. Electrochemical studies performed show that melatonin, in addition to binding Cu2+, may provide protection against copper-mediated free radical damage by binding Cu1+. The findings of these studies provide further evidence for the neuroprotective role of melatonin.
- Full Text:
- Date Issued: 2002
- Authors: Parmar, Paresh , Limson, Janice L , Nyokong, Tebello , Daya, Santy
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289617 , vital:56654 , xlink:href=" https://doi.org/10.1034/j.1600-079X.2002.01859.x"
- Description: Copper is an essential trace element which forms an integral component of many enzymes. While trace amounts of copper are needed to sustain life, excess copper is extremely toxic. Copper has been implicated in various neurodegenerative disorders, such as Wilson's and Alzheimer's diseases. Previous studies showed that melatonin, the principle secretory product of the pineal gland, binds Cupric chloride (Cu2+) and that this may have implications in copper-induced neurodegenerative diseases. In the present study, in vitro copper-mediated lipid peroxidation was induced. Melatonin (5 mM) protected against copper-mediated lipid peroxidation in liver homogenates. Electron micrographs of in vivo administered Cu2+ and melatonin show that melatonin affords some protection to rat hepatocytes in the presence of copper. Electrochemical studies performed show that melatonin, in addition to binding Cu2+, may provide protection against copper-mediated free radical damage by binding Cu1+. The findings of these studies provide further evidence for the neuroprotective role of melatonin.
- Full Text:
- Date Issued: 2002
pH study of the electrocatalytic SO2 detection at a glassy carbon electrode modified with iron (II) tetrasulfophthalocyanine
- Thamae, Mamothibe, Westbroek, Philippe, Nyokong, Tebello
- Authors: Thamae, Mamothibe , Westbroek, Philippe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/304786 , vital:58490 , xlink:href="https://doi.org/10.1007/s00604-002-0914-8"
- Description: The electrocatalytic determination of SO2 is studied as a function of pH at a glassy carbon electrode modified with iron(II)tetrasulfophthalocyanine ([Fe(II)TSPc]4−). It was found in the literature that depending on pH, SO2·xH2O, HSO3 − and/or SO3 2− are the main compounds in solution, that these compounds behave differently at the electrode surface, and that the condition of the electrode surface is stable over the entire pH-range. The use of SO2(g) or sodium sulfite as starting material did result in identical curves except in the pH range from 7.5–9.0. A possible explanation could be given by proposing that SO2·xH2O is very unstable in the presence of SO3 2−. In strongly acidic medium, SO2·xH2O is the main compound, which can be oxidized as well as reduced with exchange of two electrons. HSO3 − is the main compound at pH = 4 and can also be oxidized and reduced with exchange of, respectively, two and four electrons. In alkaline solution sulfite is the main compound and can only be oxidized, also under exchange of two electrons. Detection limits are in the range of 4.0 ± 0.1 × 10−5 and 7.5 ± 0.1 × 10−5 mol L−1, dependent of pH and of the type of reaction (oxidation or reduction) used.
- Full Text:
- Date Issued: 2002
- Authors: Thamae, Mamothibe , Westbroek, Philippe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/304786 , vital:58490 , xlink:href="https://doi.org/10.1007/s00604-002-0914-8"
- Description: The electrocatalytic determination of SO2 is studied as a function of pH at a glassy carbon electrode modified with iron(II)tetrasulfophthalocyanine ([Fe(II)TSPc]4−). It was found in the literature that depending on pH, SO2·xH2O, HSO3 − and/or SO3 2− are the main compounds in solution, that these compounds behave differently at the electrode surface, and that the condition of the electrode surface is stable over the entire pH-range. The use of SO2(g) or sodium sulfite as starting material did result in identical curves except in the pH range from 7.5–9.0. A possible explanation could be given by proposing that SO2·xH2O is very unstable in the presence of SO3 2−. In strongly acidic medium, SO2·xH2O is the main compound, which can be oxidized as well as reduced with exchange of two electrons. HSO3 − is the main compound at pH = 4 and can also be oxidized and reduced with exchange of, respectively, two and four electrons. In alkaline solution sulfite is the main compound and can only be oxidized, also under exchange of two electrons. Detection limits are in the range of 4.0 ± 0.1 × 10−5 and 7.5 ± 0.1 × 10−5 mol L−1, dependent of pH and of the type of reaction (oxidation or reduction) used.
- Full Text:
- Date Issued: 2002
Spectrophotometric and electrochemical studies of the interaction between iron (II) tetrasulfophthalocyanine and histamine
- Oni, Joshua, Nyokong, Tebello
- Authors: Oni, Joshua , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289629 , vital:56657 , xlink:href="https://doi.org/10.1142/S1088424602000233"
- Description: The interaction between iron(II) tetrasulfophthalocyanine ([FeIITSPc]4+) and histamine results in the oxidation of the central metal by oxygen in the former, with the formation of a complex denoted as [(His)FeIIITSPc]3− (where His = histamine). The rate constant for the formation of the complex is kf = 2.41 × 10−2dm3.mol−1.s−1 and an equilibrium constant of 6.3 dm3.mol-1 was obtained. The oxidation state of the central metal of [FeIITSPc]4− before and after the coordination of histamine is confirmed by spectroelectrochemistry. Further electrochemical oxidation of this [(His)FeIIITsPc]3− derivative results in a metal-based process proposed to involve an FeIV phthalocyanine species.
- Full Text:
- Date Issued: 2002
- Authors: Oni, Joshua , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289629 , vital:56657 , xlink:href="https://doi.org/10.1142/S1088424602000233"
- Description: The interaction between iron(II) tetrasulfophthalocyanine ([FeIITSPc]4+) and histamine results in the oxidation of the central metal by oxygen in the former, with the formation of a complex denoted as [(His)FeIIITSPc]3− (where His = histamine). The rate constant for the formation of the complex is kf = 2.41 × 10−2dm3.mol−1.s−1 and an equilibrium constant of 6.3 dm3.mol-1 was obtained. The oxidation state of the central metal of [FeIITSPc]4− before and after the coordination of histamine is confirmed by spectroelectrochemistry. Further electrochemical oxidation of this [(His)FeIIITsPc]3− derivative results in a metal-based process proposed to involve an FeIV phthalocyanine species.
- Full Text:
- Date Issued: 2002
Synthesis, electrochemical and photochemical properties of unsymmetrically substituted zinc phthalocyanine complexes
- Matlaba, Pulane M, Nyokong, Tebello
- Authors: Matlaba, Pulane M , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289650 , vital:56658 , xlink:href="https://doi.org/10.1016/S0277-5387(02)01226-3"
- Description: The synthesis of symmetrically and unsymmetrically substituted zinc phthalocyanine (ZnPc) derivatives are reported. The ZnPc derivatives are synthesized by ring expansion of subphthalocyanine complexes. Ring substitution is effected with tert-butyl phenol, naphthol and hydroxybenzoic acid. Comparison of the redox potentials for complexes substituted with varying numbers of tert-butyl phenol: 1 (complex 5), 2 (complex 6), 3 (complex 7), 6 (complex 8) and 8 (complex 9) shows that the complexes with the highest number of substituents are more difficult to oxidize and easier to reduce. All the reported complexes are relatively photostable, with photobleaching quantum yields of the order of 10−5. Singlet oxygen quantum yields for the complexes ranged from 0.22 to 0.68.
- Full Text:
- Date Issued: 2002
- Authors: Matlaba, Pulane M , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289650 , vital:56658 , xlink:href="https://doi.org/10.1016/S0277-5387(02)01226-3"
- Description: The synthesis of symmetrically and unsymmetrically substituted zinc phthalocyanine (ZnPc) derivatives are reported. The ZnPc derivatives are synthesized by ring expansion of subphthalocyanine complexes. Ring substitution is effected with tert-butyl phenol, naphthol and hydroxybenzoic acid. Comparison of the redox potentials for complexes substituted with varying numbers of tert-butyl phenol: 1 (complex 5), 2 (complex 6), 3 (complex 7), 6 (complex 8) and 8 (complex 9) shows that the complexes with the highest number of substituents are more difficult to oxidize and easier to reduce. All the reported complexes are relatively photostable, with photobleaching quantum yields of the order of 10−5. Singlet oxygen quantum yields for the complexes ranged from 0.22 to 0.68.
- Full Text:
- Date Issued: 2002
Synthesis, photophysical and photochemical studies of germanium and tin phthalocyanine complexes
- Maree, Suzanne, Phillips, David, Nyokong, Tebello
- Authors: Maree, Suzanne , Phillips, David , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289667 , vital:56661 , xlink:href="https://doi.org/10.1142/S108842460200004X"
- Description: This work reports on the synthesis of tin and germanium phthalocyanine complexes containing phenoxy and substituted phenoxy groups as phthalocyanine ring substituents. The compounds studied are: dichlorogermanium phthalocyanine complexes containing eight phenoxy (4a), o-methyl phenoxy (4b) or estrone (4c) groups on the ring. The corresponding dichlorotin complexes (5a, 5b and 5c) and diiodotin complex (6a) were also investigated, as well as diestrone phthalocyaninato tin (7). Germanium octaphenoxy phthalocyanine complexes undergo phototransformation rather than direct photobleaching, whereas tin octaphenoxy phthalocyanine complexes undergo a photobleaching process, which is mediated by photoreduction of the phthalocyanine ring. Tin octaphenoxy phthalocyanine complexes gave higher ΦΔ values than the corresponding germanium complexes. Also tin phthalocyanine complexes containing an unsubstituted ring gave higher ΦΔ values than the corresponding octaphenoxy substituted complexes. The triplet quantum yields increased with the increase in electron-donating power of the ring substituents.
- Full Text:
- Date Issued: 2002
- Authors: Maree, Suzanne , Phillips, David , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289667 , vital:56661 , xlink:href="https://doi.org/10.1142/S108842460200004X"
- Description: This work reports on the synthesis of tin and germanium phthalocyanine complexes containing phenoxy and substituted phenoxy groups as phthalocyanine ring substituents. The compounds studied are: dichlorogermanium phthalocyanine complexes containing eight phenoxy (4a), o-methyl phenoxy (4b) or estrone (4c) groups on the ring. The corresponding dichlorotin complexes (5a, 5b and 5c) and diiodotin complex (6a) were also investigated, as well as diestrone phthalocyaninato tin (7). Germanium octaphenoxy phthalocyanine complexes undergo phototransformation rather than direct photobleaching, whereas tin octaphenoxy phthalocyanine complexes undergo a photobleaching process, which is mediated by photoreduction of the phthalocyanine ring. Tin octaphenoxy phthalocyanine complexes gave higher ΦΔ values than the corresponding germanium complexes. Also tin phthalocyanine complexes containing an unsubstituted ring gave higher ΦΔ values than the corresponding octaphenoxy substituted complexes. The triplet quantum yields increased with the increase in electron-donating power of the ring substituents.
- Full Text:
- Date Issued: 2002
Voltammetric characterization of the self-assembled monolayer (SAM) of octabutylthiophthalocyaninatoiron (II)
- Ozoemena,Kenneth, Nyokong, Tebello
- Authors: Ozoemena,Kenneth , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290419 , vital:56748 , xlink:href="https://doi.org/10.1016/S0013-4686(02)00362-6"
- Description: The fabrication of a self-assembled monolayer (SAM) of 2,3,9,10,16,17,23,24-octa (butylthio)-phthalocyaninatoiron(II) [FePc(SBu)8] on gold electrode is described. The integrity of the SAM, with respect to its ability to block certain Faradaic processes, is interrogated using cyclic voltammetric experiments in aqueous solutions. The experiments show that this SAM provide an excellent blocking capability to the Faradaic processes emanating from gold surface oxidation, underpotential deposition (UPD) of copper and redox chemistry of Fe(NH4)(SO4)2 in HClO4. It is revealed by cyclic voltammetry that an ill-defined reversible couple of the SAM of FePc(SBu)8 can be greatly improved by a simple repetitive cycling of the modified electrode in a DMF solution containing TBAP within a short space of time (ca. 2 min). This ‘activation’ process provides good information concerning the surface coverage and orientation of the monolayer. The reversible redox wave shows a potential shift of about −57 mV per pH in the pH range of 2–9. A preliminary investigation indicates that FePc(SBu)8-SAM modified gold electrode shows electrocatalytic activity toward the oxidation of L-cysteine in acidic medium. The monolayer is stable and easily reproducible. However, due to its susceptibility to destruction via oxidative and reductive desorptions, its potential application as an electrochemical sensor would be much better in acidic and neutral than alkaline environments.
- Full Text:
- Date Issued: 2002
- Authors: Ozoemena,Kenneth , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290419 , vital:56748 , xlink:href="https://doi.org/10.1016/S0013-4686(02)00362-6"
- Description: The fabrication of a self-assembled monolayer (SAM) of 2,3,9,10,16,17,23,24-octa (butylthio)-phthalocyaninatoiron(II) [FePc(SBu)8] on gold electrode is described. The integrity of the SAM, with respect to its ability to block certain Faradaic processes, is interrogated using cyclic voltammetric experiments in aqueous solutions. The experiments show that this SAM provide an excellent blocking capability to the Faradaic processes emanating from gold surface oxidation, underpotential deposition (UPD) of copper and redox chemistry of Fe(NH4)(SO4)2 in HClO4. It is revealed by cyclic voltammetry that an ill-defined reversible couple of the SAM of FePc(SBu)8 can be greatly improved by a simple repetitive cycling of the modified electrode in a DMF solution containing TBAP within a short space of time (ca. 2 min). This ‘activation’ process provides good information concerning the surface coverage and orientation of the monolayer. The reversible redox wave shows a potential shift of about −57 mV per pH in the pH range of 2–9. A preliminary investigation indicates that FePc(SBu)8-SAM modified gold electrode shows electrocatalytic activity toward the oxidation of L-cysteine in acidic medium. The monolayer is stable and easily reproducible. However, due to its susceptibility to destruction via oxidative and reductive desorptions, its potential application as an electrochemical sensor would be much better in acidic and neutral than alkaline environments.
- Full Text:
- Date Issued: 2002
Voltammetric detection of vitamin B1 at carbon paste electrodes and its determination in tablets
- Oni, Joshua, Westbroek, Philippe, Nyokong, Tebello
- Authors: Oni, Joshua , Westbroek, Philippe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289692 , vital:56663 , xlink:href="https://doi.org/10.1002/1521-4109(200209)14"
- Description: The voltammetric behavior of vitamin B1 in alkaline medium at carbon paste electrode (CPE) is discussed. A method based on cyclic voltammetry for the determination of vitamin B1 at carbon paste electrode modified with manganese phthalocyanine (MnPc-CPE) is presented. In pH 10 buffer, the modified electrode showed catalytic activity towards the oxidation of vitamin B1 by considerably increasing the oxidation current of one of the observed waves compared to the oxidation current obtained at an unmodified electrode. The modified electrode was stable towards the determination of vitamin B1 compared to the unmodified electrode that is completely poisoned after a few scans. A linear relationship between the oxidation current and the concentration of vitamin B1 in solution was observed. The detection limit for vitamin B1 at the modified electrode was of the order of 10−5 mol dm−3. Commercial vitamin B1 tablets were analyzed using the modified electrodes.
- Full Text:
- Date Issued: 2002
- Authors: Oni, Joshua , Westbroek, Philippe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289692 , vital:56663 , xlink:href="https://doi.org/10.1002/1521-4109(200209)14"
- Description: The voltammetric behavior of vitamin B1 in alkaline medium at carbon paste electrode (CPE) is discussed. A method based on cyclic voltammetry for the determination of vitamin B1 at carbon paste electrode modified with manganese phthalocyanine (MnPc-CPE) is presented. In pH 10 buffer, the modified electrode showed catalytic activity towards the oxidation of vitamin B1 by considerably increasing the oxidation current of one of the observed waves compared to the oxidation current obtained at an unmodified electrode. The modified electrode was stable towards the determination of vitamin B1 compared to the unmodified electrode that is completely poisoned after a few scans. A linear relationship between the oxidation current and the concentration of vitamin B1 in solution was observed. The detection limit for vitamin B1 at the modified electrode was of the order of 10−5 mol dm−3. Commercial vitamin B1 tablets were analyzed using the modified electrodes.
- Full Text:
- Date Issued: 2002
Voltammetric detection of vitamin B1 at carbon paste electrodes and its determination in tablets
- Oni, Joshua, Westbroek, Philippe, Nyokong, Tebello
- Authors: Oni, Joshua , Westbroek, Philippe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289678 , vital:56662 , xlink:href="https://doi.org/10.1002/1521-4109(200209)14"
- Description: The voltammetric behavior of vitamin B1 in alkaline medium at carbon paste electrode (CPE) is discussed. A method based on cyclic voltammetry for the determination of vitamin B1 at carbon paste electrode modified with manganese phthalocyanine (MnPc-CPE) is presented. In pH 10 buffer, the modified electrode showed catalytic activity towards the oxidation of vitamin B1 by considerably increasing the oxidation current of one of the observed waves compared to the oxidation current obtained at an unmodified electrode. The modified electrode was stable towards the determination of vitamin B1 compared to the unmodified electrode that is completely poisoned after a few scans. A linear relationship between the oxidation current and the concentration of vitamin B1 in solution was observed. The detection limit for vitamin B1 at the modified electrode was of the order of 10−5 mol dm−3. Commercial vitamin B1 tablets were analyzed using the modified electrodes.
- Full Text:
- Date Issued: 2002
- Authors: Oni, Joshua , Westbroek, Philippe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289678 , vital:56662 , xlink:href="https://doi.org/10.1002/1521-4109(200209)14"
- Description: The voltammetric behavior of vitamin B1 in alkaline medium at carbon paste electrode (CPE) is discussed. A method based on cyclic voltammetry for the determination of vitamin B1 at carbon paste electrode modified with manganese phthalocyanine (MnPc-CPE) is presented. In pH 10 buffer, the modified electrode showed catalytic activity towards the oxidation of vitamin B1 by considerably increasing the oxidation current of one of the observed waves compared to the oxidation current obtained at an unmodified electrode. The modified electrode was stable towards the determination of vitamin B1 compared to the unmodified electrode that is completely poisoned after a few scans. A linear relationship between the oxidation current and the concentration of vitamin B1 in solution was observed. The detection limit for vitamin B1 at the modified electrode was of the order of 10−5 mol dm−3. Commercial vitamin B1 tablets were analyzed using the modified electrodes.
- Full Text:
- Date Issued: 2002
Comparative photosensitised transformation of polychlorophenols with different sulphonated metallophthalocyanine complexes in aqueous medium
- Ozoemena, Kenneth, Kuznetsova, Nina, Nyokong, Tebello
- Authors: Ozoemena, Kenneth , Kuznetsova, Nina , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291520 , vital:56883 , xlink:href="https://doi.org/10.1016/S1381-1169(01)00243-6"
- Description: The relative efficiencies for the oxidation of trichlorophenol (TCP) and pentachlorophenol (PCP), sensitised by sulphonated phthalocyanine complexes containing Zn, Al, Sn and Si as central metals, were studied in aqueous solutions. For the first time, sulphonated silicon and tin phthalocyanines were synthesised and their activity towards photosensitisation of singlet oxygen and photo-oxidation of polychlorophenols was examined. The efficiency of the sensitised photo-oxidative degradation of polychlorophenols depends not only on singlet oxygen quantum yield of sensitiser, but also on its stability. The influence of substrate structure and the pH of the solution on the photo-oxidation efficiency, as well as on the sensitiser photodegradation were studied. It was found that the contribution of the Type II (singlet oxygen-mediated) mechanism to the relative efficiency of the photosensitised photo-oxidation of the phenol, decreased from phenol to p-chlorophenol, TCP and PCP, whereas Type I radical pathway increased. The results obtained for PCP give evidence that electron transfer from the excited sensitiser to the substrate in its unionised form is responsible for enhanced sensitiser photodegradation.
- Full Text:
- Date Issued: 2001
- Authors: Ozoemena, Kenneth , Kuznetsova, Nina , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291520 , vital:56883 , xlink:href="https://doi.org/10.1016/S1381-1169(01)00243-6"
- Description: The relative efficiencies for the oxidation of trichlorophenol (TCP) and pentachlorophenol (PCP), sensitised by sulphonated phthalocyanine complexes containing Zn, Al, Sn and Si as central metals, were studied in aqueous solutions. For the first time, sulphonated silicon and tin phthalocyanines were synthesised and their activity towards photosensitisation of singlet oxygen and photo-oxidation of polychlorophenols was examined. The efficiency of the sensitised photo-oxidative degradation of polychlorophenols depends not only on singlet oxygen quantum yield of sensitiser, but also on its stability. The influence of substrate structure and the pH of the solution on the photo-oxidation efficiency, as well as on the sensitiser photodegradation were studied. It was found that the contribution of the Type II (singlet oxygen-mediated) mechanism to the relative efficiency of the photosensitised photo-oxidation of the phenol, decreased from phenol to p-chlorophenol, TCP and PCP, whereas Type I radical pathway increased. The results obtained for PCP give evidence that electron transfer from the excited sensitiser to the substrate in its unionised form is responsible for enhanced sensitiser photodegradation.
- Full Text:
- Date Issued: 2001
Construction and characterization of carbon paste ultra-microelectrodes
- Oni, Joshua, Westbroek, Philippe, Nyokong, Tebello
- Authors: Oni, Joshua , Westbroek, Philippe , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291531 , vital:56884 , xlink:href="https://doi.org/10.1016/S1388-2481(01)00212-0"
- Description: The construction and characterization of carbon paste ultra-microelectrodes is reported. Besides a disc-shaped electrode, a carbon paste band electrode is studied. It was found that for both electrode configurations steady-state currents were obtained but that with the type of electrode material used for the band electrode, the upper limit of ultra-microelectrode dimensions, which could be used was 100–150 μm. Smaller dimensions for the band electrodes resulted in a high resistance due to the limited conductivity of the carbon paste, when using the optimal paste composition. With cyclic voltammetry, the oxidation of [Fe(CN)6]4− was studied at individual constructed electrodes and at ensembles of individual electrodes. Detection limits of less than 10−6moll−1 were obtained. Using the data of the same curves it was possible to test if the electrodes have errors and about 20% of the constructed electrodes did not pass this test. Finally it was found that these electrodes show good stability.
- Full Text:
- Date Issued: 2001
- Authors: Oni, Joshua , Westbroek, Philippe , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291531 , vital:56884 , xlink:href="https://doi.org/10.1016/S1388-2481(01)00212-0"
- Description: The construction and characterization of carbon paste ultra-microelectrodes is reported. Besides a disc-shaped electrode, a carbon paste band electrode is studied. It was found that for both electrode configurations steady-state currents were obtained but that with the type of electrode material used for the band electrode, the upper limit of ultra-microelectrode dimensions, which could be used was 100–150 μm. Smaller dimensions for the band electrodes resulted in a high resistance due to the limited conductivity of the carbon paste, when using the optimal paste composition. With cyclic voltammetry, the oxidation of [Fe(CN)6]4− was studied at individual constructed electrodes and at ensembles of individual electrodes. Detection limits of less than 10−6moll−1 were obtained. Using the data of the same curves it was possible to test if the electrodes have errors and about 20% of the constructed electrodes did not pass this test. Finally it was found that these electrodes show good stability.
- Full Text:
- Date Issued: 2001
Effect of oligomerization on the photochemical properties of silicon octaphenoxyphthalocyanine
- Maree, M David, Nyokong, Tebello
- Authors: Maree, M David , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291542 , vital:56885 , xlink:href="https://doi.org/10.1016/S1010-6030(01)00485-3"
- Description: The photochemical properties of silicon octaphenoxyphthalocyanines (SiOPPc) oligomerized were studied in dimethylsulfoxide (DMSO) solutions. Oligomers containing 2–5 and 9 SiOPPc rings linked with terephthalate linkages were synthesized. Singlet oxygen quantum yields were found to be in the range 0.11–0.34, and increased with the number of rings up to five rings, a decrease in the quantum yield was observed for nine rings. This is explained in terms of the high aggregation of the oligomer containing nine rings.
- Full Text:
- Date Issued: 2001
- Authors: Maree, M David , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291542 , vital:56885 , xlink:href="https://doi.org/10.1016/S1010-6030(01)00485-3"
- Description: The photochemical properties of silicon octaphenoxyphthalocyanines (SiOPPc) oligomerized were studied in dimethylsulfoxide (DMSO) solutions. Oligomers containing 2–5 and 9 SiOPPc rings linked with terephthalate linkages were synthesized. Singlet oxygen quantum yields were found to be in the range 0.11–0.34, and increased with the number of rings up to five rings, a decrease in the quantum yield was observed for nine rings. This is explained in terms of the high aggregation of the oligomer containing nine rings.
- Full Text:
- Date Issued: 2001