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
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, 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
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