Address to Convocation 1979
- Authors: Henderson, Derek Scott
- Subjects: Rhodes University -- Convocation
- Language: English
- Type: Text
- Identifier: vital:7381 , http://hdl.handle.net/10962/d1017270
- Full Text:
- Authors: Henderson, Derek Scott
- Subjects: Rhodes University -- Convocation
- Language: English
- Type: Text
- Identifier: vital:7381 , http://hdl.handle.net/10962/d1017270
- Full Text:
Effect of bovine serum albumin and single walled carbon nanotube on the photophysical properties of zinc octacarboxy phthalocyanine
- Ogbodu, Racheal O, Nyokong, Tebello
- Authors: Ogbodu, Racheal O , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7321 , http://hdl.handle.net/10962/d1020566
- Description: This work reports on the photophysical parameters of the conjugate between zinc octacarboxy phthalocyanine (ZnOCPc) and bovine serum albumin (BSA) represented as ZnOCPc–BSA (1) which was further adsorbed onto single walled carbon nanotubes (SWCNT) represented as (ZnOCPc–BSA–SWCNT 2). ZnOCPc (without BSA) was also adsorbed on SWCNT represented as ZnOCPc–SWCNT (3). The presence of BSA resulted in the increase in singlet oxygen quantum yield (ΦΔ) for 1 (at ΦΔ = 0.44) and 2 (at ΦΔ = 0.41) compared to ΦΔ = 0.21 for ZnOCPc alone. For complex 3 which did not contain BSA singlet oxygen quantum yield decreased. , Original publication is available at http://dx.doi.org/10.1016/j.saa.2013.10.064
- Full Text: false
- Authors: Ogbodu, Racheal O , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7321 , http://hdl.handle.net/10962/d1020566
- Description: This work reports on the photophysical parameters of the conjugate between zinc octacarboxy phthalocyanine (ZnOCPc) and bovine serum albumin (BSA) represented as ZnOCPc–BSA (1) which was further adsorbed onto single walled carbon nanotubes (SWCNT) represented as (ZnOCPc–BSA–SWCNT 2). ZnOCPc (without BSA) was also adsorbed on SWCNT represented as ZnOCPc–SWCNT (3). The presence of BSA resulted in the increase in singlet oxygen quantum yield (ΦΔ) for 1 (at ΦΔ = 0.44) and 2 (at ΦΔ = 0.41) compared to ΦΔ = 0.21 for ZnOCPc alone. For complex 3 which did not contain BSA singlet oxygen quantum yield decreased. , Original publication is available at http://dx.doi.org/10.1016/j.saa.2013.10.064
- Full Text: false
Effects of Redox Mediators on the Catalytic Activity of Iron Porphyrins towards Oxygen Reduction in Acidic Media
- He, Qinggang, Wu, Gang, Liu, Ke, Khene, M Samson, Li, Qing, Mugadza, Tawanda, Deunf, Elise, Nyokong, Tebello, Chen, Shaowei W
- Authors: He, Qinggang , Wu, Gang , Liu, Ke , Khene, M Samson , Li, Qing , Mugadza, Tawanda , Deunf, Elise , Nyokong, Tebello , Chen, Shaowei W
- Language: English
- Type: Article
- Identifier: vital:7291 , http://hdl.handle.net/10962/d1020354
- Description: The effects of different redox mediators on the oxygen reduction reaction (ORR) catalyzed by an iron porphyrin complex, iron(III) meso-tetra(N-methyl-4-pyridyl)porphine chloride [FeIIITMPyP], in 0.1 M triflic acid were investigated by cyclic voltammetry (CV) and spectroelectrochemistry in conjunction with density functional theory (DFT) calculations. The formal potentials of the FeIIITMPyP catalyst and the redox mediators, as well as the half-wave potentials for the ORR, were determined by CV in the absence and presence of oxygen in acidic solutions. UV/Vis spectroscopic and spectroelectrochemical studies confirmed that only the 2,2′-azino-bis(3-ethylbenzothiazioline-6-sulfonic acid)diammonium salt (C18H24N6O6S4) showed effective interactions with FeIIITMPyP during the ORR. DFT calculations suggested strong interaction between FeIIITMPyP and the C18H24N6O6S4 redox mediator. The redox mediator caused lengthening of the dioxygen iron bond, which thus suggested easier dioxygen reduction. Consistent results were observed in electrochemical impedance spectroscopic measurements for which the electron-transfer kinetics were also evaluated. , Original publication is available at http://dx.doi.org/10.1002/celc.201402054
- Full Text: false
- Authors: He, Qinggang , Wu, Gang , Liu, Ke , Khene, M Samson , Li, Qing , Mugadza, Tawanda , Deunf, Elise , Nyokong, Tebello , Chen, Shaowei W
- Language: English
- Type: Article
- Identifier: vital:7291 , http://hdl.handle.net/10962/d1020354
- Description: The effects of different redox mediators on the oxygen reduction reaction (ORR) catalyzed by an iron porphyrin complex, iron(III) meso-tetra(N-methyl-4-pyridyl)porphine chloride [FeIIITMPyP], in 0.1 M triflic acid were investigated by cyclic voltammetry (CV) and spectroelectrochemistry in conjunction with density functional theory (DFT) calculations. The formal potentials of the FeIIITMPyP catalyst and the redox mediators, as well as the half-wave potentials for the ORR, were determined by CV in the absence and presence of oxygen in acidic solutions. UV/Vis spectroscopic and spectroelectrochemical studies confirmed that only the 2,2′-azino-bis(3-ethylbenzothiazioline-6-sulfonic acid)diammonium salt (C18H24N6O6S4) showed effective interactions with FeIIITMPyP during the ORR. DFT calculations suggested strong interaction between FeIIITMPyP and the C18H24N6O6S4 redox mediator. The redox mediator caused lengthening of the dioxygen iron bond, which thus suggested easier dioxygen reduction. Consistent results were observed in electrochemical impedance spectroscopic measurements for which the electron-transfer kinetics were also evaluated. , Original publication is available at http://dx.doi.org/10.1002/celc.201402054
- Full Text: false
South Africa after Soweto
- Authors: Henderson, Derek Scott
- Subjects: South Africa -- Politics and government -- 1978-1989
- Language: English
- Type: Text
- Identifier: vital:7342 , http://hdl.handle.net/10962/d1017071
- Full Text:
- Authors: Henderson, Derek Scott
- Subjects: South Africa -- Politics and government -- 1978-1989
- Language: English
- Type: Text
- Identifier: vital:7342 , http://hdl.handle.net/10962/d1017071
- Full Text:
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