CdTe quantum dots functionalized with 4-amino-2, 2, 6, 6-tetramethylpiperidine-N-oxide as luminescent nanoprobe for the sensitive recognition of bromide ion
- Adegoke, Oluwasesan, Hosten, Eric, McCleland, Cedric, Nyokong, Tebello
- Authors: Adegoke, Oluwasesan , Hosten, Eric , McCleland, Cedric , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/244393 , vital:51253 , xlink:href="https://doi.org/10.1016/j.aca.2012.01.040"
- Description: A novel bromide ion-selective modified nanoprobe sensor based on 4-amino-2,2,6,6-tetramethylpiperidine-N-oxide (4AT)-functionalized CdTe quantum dots (QDs-4AT) has been developed. Fluorescence quenching of the QDs by 4AT was observed. The functionalized QDs-4AT nanoprobe allowed a highly sensitive determination of bromide ion via analyte-induced change in the photoluminescence (fluorescence recovery) of the modified QDs. A detection limit of 0.6 nM of bromide ion was obtained, while the interfering effect of other inorganic cations and anions was investigated to examine the selectivity of the nanoprobe. The linear range was between 0.01 and 0.13 μM. Combined fluorescence lifetime and electron paramagnetic resonance measurements confirmed electron transfer processes between bromide ion and QDs-4AT.
- Full Text:
- Date Issued: 2012
- Authors: Adegoke, Oluwasesan , Hosten, Eric , McCleland, Cedric , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/244393 , vital:51253 , xlink:href="https://doi.org/10.1016/j.aca.2012.01.040"
- Description: A novel bromide ion-selective modified nanoprobe sensor based on 4-amino-2,2,6,6-tetramethylpiperidine-N-oxide (4AT)-functionalized CdTe quantum dots (QDs-4AT) has been developed. Fluorescence quenching of the QDs by 4AT was observed. The functionalized QDs-4AT nanoprobe allowed a highly sensitive determination of bromide ion via analyte-induced change in the photoluminescence (fluorescence recovery) of the modified QDs. A detection limit of 0.6 nM of bromide ion was obtained, while the interfering effect of other inorganic cations and anions was investigated to examine the selectivity of the nanoprobe. The linear range was between 0.01 and 0.13 μM. Combined fluorescence lifetime and electron paramagnetic resonance measurements confirmed electron transfer processes between bromide ion and QDs-4AT.
- Full Text:
- Date Issued: 2012
Synthesis and photophysical properties of peripherally and non-peripherally mercaptopyridine substituted metal free, Mg (II) and Al (III) phthalocyanines
- Arslanoğlu, Yasin, Idowu, Mopelela, Nyokong, Tebello
- Authors: Arslanoğlu, Yasin , Idowu, Mopelela , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243248 , vital:51131 , xlink:href="https://doi.org/10.1016/j.saa.2012.04.004"
- Description: The syntheses and photophysical properties of metallophthalocyanines containing Mg2+ and Al3+ as central metal ions and their unmetallated derivative (complexes 3–8) tetra- substituted at the non-peripheral (α) and peripheral (β) positions with 2-mercaptopyridine are reported. The trends in triplet and fluorescence quantum yields are described for these compounds. The complexes exhibited relatively high triplet quantum yields (ΦT) ranging from 0.33 to 0.54 and fluorescence quantum yields (ΦF) ranging from 0.02 to 0.29. Triplet state lifetimes of the complexes were long ranging from 120 to 460 μs, indicating a potential use of these complexes as photosensitizers.
- Full Text:
- Date Issued: 2012
- Authors: Arslanoğlu, Yasin , Idowu, Mopelela , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243248 , vital:51131 , xlink:href="https://doi.org/10.1016/j.saa.2012.04.004"
- Description: The syntheses and photophysical properties of metallophthalocyanines containing Mg2+ and Al3+ as central metal ions and their unmetallated derivative (complexes 3–8) tetra- substituted at the non-peripheral (α) and peripheral (β) positions with 2-mercaptopyridine are reported. The trends in triplet and fluorescence quantum yields are described for these compounds. The complexes exhibited relatively high triplet quantum yields (ΦT) ranging from 0.33 to 0.54 and fluorescence quantum yields (ΦF) ranging from 0.02 to 0.29. Triplet state lifetimes of the complexes were long ranging from 120 to 460 μs, indicating a potential use of these complexes as photosensitizers.
- Full Text:
- Date Issued: 2012
The way forward with ecosystem-based management in tropical contexts: Reconciling with existing management systems
- Aswani, Shankar, Christie, Patrick, Muthiga, Nyawira A, Mahon, Robin, Primavera, Jurgenne H, Cramer, Lori A, Barbier, Edward B, Granek, Elise F, Kennedy, Chris J, Wolanski, Eric, Hacker, Sally
- Authors: Aswani, Shankar , Christie, Patrick , Muthiga, Nyawira A , Mahon, Robin , Primavera, Jurgenne H , Cramer, Lori A , Barbier, Edward B , Granek, Elise F , Kennedy, Chris J , Wolanski, Eric , Hacker, Sally
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/422693 , vital:71969 , xlink:href="https://doi.org/10.1016/j.marpol.2011.02.014"
- Description: This paper discusses some of the challenges and opportunities that can arise when implementing ecosystem-based management (EBM) in tropical nations. EBM creates a new series of challenges, problems, and opportunities that must be considered in light of existing governance and management frameworks in a local context. The paper presents five case studies from different parts of the tropical world, including Oceania, insular and continental Southeast Asia, East Africa, and the Caribbean, which illustrate that the implementation of EBM in watershed and marine ecosystems offers a new series of challenges and opportunities for its inclusion with existing forms of environmental governance and management. The paper suggests that EBM is best thought of as an expansion of customary management (CM) and integrated coastal management (ICM), rather than a paradigm shift, and that it has certain benefits that are worth integrating into existing systems when possible. The paper concludes that the cultural and institutional context of CM as well as the experience, technical skills, and legal basis that serve ICM programs are logical platforms from which to build EBM programs. Some guidelines for creating hybrid management regimes are suggested. In sum, declining marine species and ecosystems require urgent action, necessitating utilization of existing paradigms such as ICM and CM as a foundation for building EBM.
- Full Text:
- Date Issued: 2012
- Authors: Aswani, Shankar , Christie, Patrick , Muthiga, Nyawira A , Mahon, Robin , Primavera, Jurgenne H , Cramer, Lori A , Barbier, Edward B , Granek, Elise F , Kennedy, Chris J , Wolanski, Eric , Hacker, Sally
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/422693 , vital:71969 , xlink:href="https://doi.org/10.1016/j.marpol.2011.02.014"
- Description: This paper discusses some of the challenges and opportunities that can arise when implementing ecosystem-based management (EBM) in tropical nations. EBM creates a new series of challenges, problems, and opportunities that must be considered in light of existing governance and management frameworks in a local context. The paper presents five case studies from different parts of the tropical world, including Oceania, insular and continental Southeast Asia, East Africa, and the Caribbean, which illustrate that the implementation of EBM in watershed and marine ecosystems offers a new series of challenges and opportunities for its inclusion with existing forms of environmental governance and management. The paper suggests that EBM is best thought of as an expansion of customary management (CM) and integrated coastal management (ICM), rather than a paradigm shift, and that it has certain benefits that are worth integrating into existing systems when possible. The paper concludes that the cultural and institutional context of CM as well as the experience, technical skills, and legal basis that serve ICM programs are logical platforms from which to build EBM programs. Some guidelines for creating hybrid management regimes are suggested. In sum, declining marine species and ecosystems require urgent action, necessitating utilization of existing paradigms such as ICM and CM as a foundation for building EBM.
- Full Text:
- Date Issued: 2012
Spatial variation in the macrobenthic assemblages of intertidal seagrass along the long axis of an estuary
- Barnes, R S K, Ellwood, M D F
- Authors: Barnes, R S K , Ellwood, M D F
- Date: 2014-05-29
- Language: English
- Type: Article
- Identifier: vital:6870 , http://hdl.handle.net/10962/d1011513
- Description: Invertebrate macrofaunal biodiversity within intertidal seagrass meadows was investigated over a salinity gradient of <5–35 in the Knysna estuarine system (Garden Route National Park, South Africa). Rather than the classic gradual decline in species richness with distance from the mouth there were zones of considerable faunal stability separated by relatively sharp discontinuities. At the point upstream at which salinity regularly falls below 30, the rich, diverse and highly spatially variable downstream faunal assemblage changed to a less rich, less diverse and more uniform one that dominated the upstream stretch without any further upstream reduction in richness. Nevertheless, without loss of overall richness, assemblage composition changed, again rapidly, in the upper region of the upstream stretch to a zone dominated by the microgastropod Hydrobia, which otherwise occurs in the Knysna system only in highly sheltered regions of the downstream stretch where it is also dominant. The upstream faunal assemblage was a subset of that in the marine-influenced downstream region not a different replacing one. Position along the estuarine gradient accounted for 29% of total assemblage variation. Overall faunal abundance declined with distance upstream until the Hydrobia zone where it rose sharply, but there was no evidence of increase in density of those species remaining on putative release from competition.
- Full Text:
- Authors: Barnes, R S K , Ellwood, M D F
- Date: 2014-05-29
- Language: English
- Type: Article
- Identifier: vital:6870 , http://hdl.handle.net/10962/d1011513
- Description: Invertebrate macrofaunal biodiversity within intertidal seagrass meadows was investigated over a salinity gradient of <5–35 in the Knysna estuarine system (Garden Route National Park, South Africa). Rather than the classic gradual decline in species richness with distance from the mouth there were zones of considerable faunal stability separated by relatively sharp discontinuities. At the point upstream at which salinity regularly falls below 30, the rich, diverse and highly spatially variable downstream faunal assemblage changed to a less rich, less diverse and more uniform one that dominated the upstream stretch without any further upstream reduction in richness. Nevertheless, without loss of overall richness, assemblage composition changed, again rapidly, in the upper region of the upstream stretch to a zone dominated by the microgastropod Hydrobia, which otherwise occurs in the Knysna system only in highly sheltered regions of the downstream stretch where it is also dominant. The upstream faunal assemblage was a subset of that in the marine-influenced downstream region not a different replacing one. Position along the estuarine gradient accounted for 29% of total assemblage variation. Overall faunal abundance declined with distance upstream until the Hydrobia zone where it rose sharply, but there was no evidence of increase in density of those species remaining on putative release from competition.
- Full Text:
The syntheses and photophysical properties of 4, 4′-isopropylidendioxydiphenyl substituted ball-type dinuclear Mg (II) and Zn (II) phthalocyanines
- Canlıca, Mevlüde, Nyokong, Tebello
- Authors: Canlıca, Mevlüde , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243554 , vital:51163 , xlink:href="https://doi.org/10.1016/j.poly.2011.10.024"
- Description: The syntheses of ball-type dinuclear Zn(II) and Mg(II) phthalocyanines containing four 4,4′-isopropylidendioxydiphenyl substituents at the peripheral and non-peripheral positions are presented. The structures of the synthesized compounds were characterized using elemental analyses, and UV–Vis, FT-IR, 1H NMR and mass spectroscopies. The ΦF values were 0.14, 0.11, 0.22, 0.15 and ΦT values were 0.84, 0.88, 0.62, 0.74, for 6–9, respectively. The largest triplet yields were observed for the non-peripherally substituted complexes 6 and 7, showing that non-peripheral substitution favors increased population of the triplet state. All complexes showed reasonably long triplet lifetimes with τT 510, 310, 910 and 350 μs in DMSO, respectively.
- Full Text:
- Date Issued: 2012
- Authors: Canlıca, Mevlüde , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243554 , vital:51163 , xlink:href="https://doi.org/10.1016/j.poly.2011.10.024"
- Description: The syntheses of ball-type dinuclear Zn(II) and Mg(II) phthalocyanines containing four 4,4′-isopropylidendioxydiphenyl substituents at the peripheral and non-peripheral positions are presented. The structures of the synthesized compounds were characterized using elemental analyses, and UV–Vis, FT-IR, 1H NMR and mass spectroscopies. The ΦF values were 0.14, 0.11, 0.22, 0.15 and ΦT values were 0.84, 0.88, 0.62, 0.74, for 6–9, respectively. The largest triplet yields were observed for the non-peripherally substituted complexes 6 and 7, showing that non-peripheral substitution favors increased population of the triplet state. All complexes showed reasonably long triplet lifetimes with τT 510, 310, 910 and 350 μs in DMSO, respectively.
- Full Text:
- Date Issued: 2012
4-Azidoaniline-based electropolymer as a building block for functionalisation of conductive surfaces
- Coates, Megan, Elamari, Hichem, Girard, Christian, Griveau, Sophie, Nyokong, Tebello, Bedioui, Fethi
- Authors: Coates, Megan , Elamari, Hichem , Girard, Christian , Griveau, Sophie , Nyokong, Tebello , Bedioui, Fethi
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/244404 , vital:51254 , xlink:href="https://doi.org/10.1016/j.jelechem.2012.01.001"
- Description: We propose in this work to compare three approaches using 4-azidoaniline combined with “click” chemistry and electrochemistry to anchor ferrocene moieties at glassy carbon surfaces. The immobilisation of a newly synthesised molecule, 4-(4-ferrocenyl-1H-1,2,3-triazol-1-yl)aniline, through direct electropolymerisation or via in situ diazotization followed by electrografting is studied by analysing the samples by XPS and electrochemistry.
- Full Text:
- Date Issued: 2012
4-Azidoaniline-based electropolymer as a building block for functionalisation of conductive surfaces
- Authors: Coates, Megan , Elamari, Hichem , Girard, Christian , Griveau, Sophie , Nyokong, Tebello , Bedioui, Fethi
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/244404 , vital:51254 , xlink:href="https://doi.org/10.1016/j.jelechem.2012.01.001"
- Description: We propose in this work to compare three approaches using 4-azidoaniline combined with “click” chemistry and electrochemistry to anchor ferrocene moieties at glassy carbon surfaces. The immobilisation of a newly synthesised molecule, 4-(4-ferrocenyl-1H-1,2,3-triazol-1-yl)aniline, through direct electropolymerisation or via in situ diazotization followed by electrografting is studied by analysing the samples by XPS and electrochemistry.
- Full Text:
- Date Issued: 2012
The direct use value of municipal commonage goods and services to urban households in the Eastern Cape, South Africa
- Davenport, Nicholas A, Shackleton, Charlie M, Gambiza, James
- Authors: Davenport, Nicholas A , Shackleton, Charlie M , Gambiza, James
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181071 , vital:43696 , xlink:href="https://doi.org/10.1016/j.landusepol.2011.09.008"
- Description: To redress past racial discrepancies in ownership and tenure, the ANC government of South Africa initiated programmes to make land accessible to the previously disadvantaged. A key component of the national land reform programme was the provision of commonage lands to urban municipalities for use by the urban poor. However, there has been no assessment of the contribution that urban commonage makes to previously disadvantaged households. This study assessed the economic benefits of the commonage programme to local households, through an in-depth survey of 90 households across three small towns in the Eastern Cape of South Africa. We examined the marketed and non-marketed consumptive direct-use values of land-based livelihoods on commonage, calculated via the ‘own reported values’ approach. The results indicate that a proportion of South Africa's urban population rely to some degree on municipal commonage for part of their livelihoods. Commonage contributions to total livelihood incomes ranged between 14 and 20%. If the contributions from commonage were excluded, the incomes of over 10% of households in each study town would drop below the poverty line. Overall, the value of harvests from commonage was worth over R1 000 (US$ 142) per hectare per year and over R4.7 million (US$ 0.68 million) per commonage per year. However, the extent and nature of use and reliance was not uniform among households, so that we developed a typology of commonage users, with four types being identified. However, rapidly growing urban populations and high levels of poverty potentially threaten the sustainability of commonage resource use. Yet the national land reform programme focuses largely on the transfer of land to municipalities and not on sustainable management. Municipalities, in turn, invest relatively little in commonage management, and the little they do is focussed on livestock production. Non-timber forest products are not considered at all, even though this study shows that they are a vital resource for the urban poor, notably for energy and construction materials.
- Full Text:
- Date Issued: 2012
- Authors: Davenport, Nicholas A , Shackleton, Charlie M , Gambiza, James
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181071 , vital:43696 , xlink:href="https://doi.org/10.1016/j.landusepol.2011.09.008"
- Description: To redress past racial discrepancies in ownership and tenure, the ANC government of South Africa initiated programmes to make land accessible to the previously disadvantaged. A key component of the national land reform programme was the provision of commonage lands to urban municipalities for use by the urban poor. However, there has been no assessment of the contribution that urban commonage makes to previously disadvantaged households. This study assessed the economic benefits of the commonage programme to local households, through an in-depth survey of 90 households across three small towns in the Eastern Cape of South Africa. We examined the marketed and non-marketed consumptive direct-use values of land-based livelihoods on commonage, calculated via the ‘own reported values’ approach. The results indicate that a proportion of South Africa's urban population rely to some degree on municipal commonage for part of their livelihoods. Commonage contributions to total livelihood incomes ranged between 14 and 20%. If the contributions from commonage were excluded, the incomes of over 10% of households in each study town would drop below the poverty line. Overall, the value of harvests from commonage was worth over R1 000 (US$ 142) per hectare per year and over R4.7 million (US$ 0.68 million) per commonage per year. However, the extent and nature of use and reliance was not uniform among households, so that we developed a typology of commonage users, with four types being identified. However, rapidly growing urban populations and high levels of poverty potentially threaten the sustainability of commonage resource use. Yet the national land reform programme focuses largely on the transfer of land to municipalities and not on sustainable management. Municipalities, in turn, invest relatively little in commonage management, and the little they do is focussed on livestock production. Non-timber forest products are not considered at all, even though this study shows that they are a vital resource for the urban poor, notably for energy and construction materials.
- Full Text:
- Date Issued: 2012
Unquenched fluorescence lifetime for β-phenylthio substituted zinc phthalocyanine upon conjugation to gold nanoparticles
- Forteath, Shaun, Antunes, Edith M, Chidawanyika, Wadzanai J U, Nyokong, Tebello
- Authors: Forteath, Shaun , Antunes, Edith M , Chidawanyika, Wadzanai J U , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/245774 , vital:51404 , xlink:href="https://doi.org/10.1016/j.poly.2011.12.015"
- Description: Photoinduced processes in phthalocyanine-functionalized gold nanoparticles have been investigated by spectroscopic measurements. The zinc phthalocyanine used contained four phenylthio peripheral substituents (ZnPc(SPh)4). The conjugates formed are represented as ZnPc(SPh)4–AuNP. The absorption spectrum of the ZnPc(SPh)4–AuNP shows a broadening of the phthalocyanine Q-band absorption, probably due to a tight packing of the phthalocyanines on the gold nanoparticle surface. For the attached phthalocyanines, the two fluorescence lifetimes obtained by time-correlated single photon counting (TCSPC) were determined to be both longer and shorter than that of the free Pc. The fluorescence lifetimes were resolved using time resolved fluorescence spectroscopy (TRES).
- Full Text:
- Date Issued: 2012
- Authors: Forteath, Shaun , Antunes, Edith M , Chidawanyika, Wadzanai J U , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/245774 , vital:51404 , xlink:href="https://doi.org/10.1016/j.poly.2011.12.015"
- Description: Photoinduced processes in phthalocyanine-functionalized gold nanoparticles have been investigated by spectroscopic measurements. The zinc phthalocyanine used contained four phenylthio peripheral substituents (ZnPc(SPh)4). The conjugates formed are represented as ZnPc(SPh)4–AuNP. The absorption spectrum of the ZnPc(SPh)4–AuNP shows a broadening of the phthalocyanine Q-band absorption, probably due to a tight packing of the phthalocyanines on the gold nanoparticle surface. For the attached phthalocyanines, the two fluorescence lifetimes obtained by time-correlated single photon counting (TCSPC) were determined to be both longer and shorter than that of the free Pc. The fluorescence lifetimes were resolved using time resolved fluorescence spectroscopy (TRES).
- Full Text:
- Date Issued: 2012
Synthesis and photophysical behavior of a novel zinc phthalocyanine containing a single carboxylic acid and three phenylthio substituents
- Forteath, Shaun, Antunes, Edith M, Chidawanyika, Wadzanai J U, Nyokong, Tebello
- Authors: Forteath, Shaun , Antunes, Edith M , Chidawanyika, Wadzanai J U , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243207 , vital:51127 , xlink:href="https://doi.org/10.1016/j.jlumin.2012.03.050"
- Description: Zinc 2, (3)-tri-(phenylthio)-2, (3)-carboxy phthalocyanine (ZnPc(COOH)(SPh)3), zinc 2, (3)-tetra-(phenylthio) phthalocyanine (ZnPc(SPh)4) and 2, (3)-tetra-(phenylthio) phthalocyanine (H2Pc(SPh)4) were synthesized and their photophysical behavior were compared with those of a number of zinc phthalocyanine (ZnPc) derivatives. ZnPc(COOH)(SPh)3 and ZnPc(SPh)4 had similar fluorescence (ΦF=0.14) and triplet state (ΦT=0.65) quantum yields in dimethylsulfoxide, hence showing no effects of the replacement of one of the phenylthio groups with a carboxylic acid group. ZnPc(COOH)(SPh)3 displayed a slightly shorter triplet lifetime (τT=331 μs) than ZnPc (τT=350 μs) in DMSO, but within the range of ZnPc derivatives. The triplet lifetime for ZnPc(COOH)(SPh)3 is much longer than for the symmetrical derivative (ZnPc(SPh)4) with τT=149 μs in DMSO.
- Full Text:
- Date Issued: 2012
- Authors: Forteath, Shaun , Antunes, Edith M , Chidawanyika, Wadzanai J U , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243207 , vital:51127 , xlink:href="https://doi.org/10.1016/j.jlumin.2012.03.050"
- Description: Zinc 2, (3)-tri-(phenylthio)-2, (3)-carboxy phthalocyanine (ZnPc(COOH)(SPh)3), zinc 2, (3)-tetra-(phenylthio) phthalocyanine (ZnPc(SPh)4) and 2, (3)-tetra-(phenylthio) phthalocyanine (H2Pc(SPh)4) were synthesized and their photophysical behavior were compared with those of a number of zinc phthalocyanine (ZnPc) derivatives. ZnPc(COOH)(SPh)3 and ZnPc(SPh)4 had similar fluorescence (ΦF=0.14) and triplet state (ΦT=0.65) quantum yields in dimethylsulfoxide, hence showing no effects of the replacement of one of the phenylthio groups with a carboxylic acid group. ZnPc(COOH)(SPh)3 displayed a slightly shorter triplet lifetime (τT=331 μs) than ZnPc (τT=350 μs) in DMSO, but within the range of ZnPc derivatives. The triplet lifetime for ZnPc(COOH)(SPh)3 is much longer than for the symmetrical derivative (ZnPc(SPh)4) with τT=149 μs in DMSO.
- Full Text:
- Date Issued: 2012
Fishing in the dark-local knowledge, night spearfishing and spawning aggregations in the Western Solomon Islands
- Hamilton, R. J, Giningele, M, Aswani, Shankar, Ecochard, J. L
- Authors: Hamilton, R. J , Giningele, M , Aswani, Shankar , Ecochard, J. L
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/422673 , vital:71966 , xlink:href="https://doi.org/10.1016/j.biocon.2011.11.020"
- Description: Within the marine conservation community there is considerable interest in combining local knowledge and science to achieve management objectives. Yet there remain few studies which have examined the merits and caveats of local knowledge, or shown how combining both knowledge systems has resulted in better management outcomes. This study outlines collaborative efforts to conserve fish spawning aggregations (FSAs) in Roviana Lagoon, Western Solomon Islands. Baseline information on FSAs was obtained through local knowledge and spearfishing creel surveys. This information provided the starting point for establishing a 2-year community-based underwater monitoring program at the largest known FSA in Roviana Lagoon, where the brown-marbled grouper (Epinephelus fuscoguttatus), camouflage grouper (Epinephelus polyphekadion) and squaretail coralgrouper (Plectropomus areolatus) co-aggregate. This participatory research shows that local knowledge on FSAs is utilised to maximise returns from fishing, with spearfishermen targeting aggregations at night during the lunar periods when abundances peak. Because of its shallow distribution P. areolatus is the most vulnerable of the three groupers to nighttime spearfishing, with two fishermen capable of removing 15–30% of the total spawning biomass in two nights. Underwater monitoring demonstrates that while fishermen provided accurate information on many aspects of FSAs, their knowledge on spawning seasons was inaccurate for the FSA reported on here. Peak aggregations occurred from December to April each year, which differs from the traditionally recognised grouper season of October to January. A combination of local knowledge and science was used to develop appropriate management measures for this FSA, with the aggregation declared a community-based marine protected area (MPA) in 2006.
- Full Text:
- Date Issued: 2012
- Authors: Hamilton, R. J , Giningele, M , Aswani, Shankar , Ecochard, J. L
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/422673 , vital:71966 , xlink:href="https://doi.org/10.1016/j.biocon.2011.11.020"
- Description: Within the marine conservation community there is considerable interest in combining local knowledge and science to achieve management objectives. Yet there remain few studies which have examined the merits and caveats of local knowledge, or shown how combining both knowledge systems has resulted in better management outcomes. This study outlines collaborative efforts to conserve fish spawning aggregations (FSAs) in Roviana Lagoon, Western Solomon Islands. Baseline information on FSAs was obtained through local knowledge and spearfishing creel surveys. This information provided the starting point for establishing a 2-year community-based underwater monitoring program at the largest known FSA in Roviana Lagoon, where the brown-marbled grouper (Epinephelus fuscoguttatus), camouflage grouper (Epinephelus polyphekadion) and squaretail coralgrouper (Plectropomus areolatus) co-aggregate. This participatory research shows that local knowledge on FSAs is utilised to maximise returns from fishing, with spearfishermen targeting aggregations at night during the lunar periods when abundances peak. Because of its shallow distribution P. areolatus is the most vulnerable of the three groupers to nighttime spearfishing, with two fishermen capable of removing 15–30% of the total spawning biomass in two nights. Underwater monitoring demonstrates that while fishermen provided accurate information on many aspects of FSAs, their knowledge on spawning seasons was inaccurate for the FSA reported on here. Peak aggregations occurred from December to April each year, which differs from the traditionally recognised grouper season of October to January. A combination of local knowledge and science was used to develop appropriate management measures for this FSA, with the aggregation declared a community-based marine protected area (MPA) in 2006.
- Full Text:
- Date Issued: 2012
Molecular catalysis of the oxygen reduction reaction by iron porphyrin catalysts tethered into Nafion layers
- He, Qinggang, Mugadza, Tawanda, Kang, Xiongwu, Zhu, Xiaobing, Chen, Shaowei, Kerr, John, Nyokong, Tebello
- Authors: He, Qinggang , Mugadza, Tawanda , Kang, Xiongwu , Zhu, Xiaobing , Chen, Shaowei , Kerr, John , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243168 , vital:51123 , xlink:href="https://doi.org/10.1016/j.jpowsour.2012.05.043"
- Description: This study was motivated by the need for improved understanding of the kinetics and transport phenomena in a homogeneous catalyst system for the oxygen reduction reaction (ORR). Direct interaction between the sulfonic groups of Nafion and an Fe(III) meso-tetra(N-methyl-4-pyridyl) porphine chloride (Fe(III)TMPyP) compound was observed using FTIR and in situ UV–Vis spectroelectrochemical characterizations. A positive shift of the half wave potential value (E1/2) for ORR on the iron porphyrin catalyst (Fe(III)TMPyP) was observed upon addition of a specific quantity of Nafion ionomer on a glassy carbon working electrode, indicating not only a faster charge transfer rate but also the role of protonation in the oxygen reduction reaction (ORR) process. A membrane electrode assembly (MEA) was made as a sandwich of a Pt-coated anode, a Nafion® 212 membrane, and a Fe(III)TMPyP + Nafion ionomer-coated cathode. This three-dimensional catalysis system has been demonstrated to be working in a H2/O2 proton exchange membrane (PEM) fuel cell test.
- Full Text:
- Date Issued: 2012
- Authors: He, Qinggang , Mugadza, Tawanda , Kang, Xiongwu , Zhu, Xiaobing , Chen, Shaowei , Kerr, John , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243168 , vital:51123 , xlink:href="https://doi.org/10.1016/j.jpowsour.2012.05.043"
- Description: This study was motivated by the need for improved understanding of the kinetics and transport phenomena in a homogeneous catalyst system for the oxygen reduction reaction (ORR). Direct interaction between the sulfonic groups of Nafion and an Fe(III) meso-tetra(N-methyl-4-pyridyl) porphine chloride (Fe(III)TMPyP) compound was observed using FTIR and in situ UV–Vis spectroelectrochemical characterizations. A positive shift of the half wave potential value (E1/2) for ORR on the iron porphyrin catalyst (Fe(III)TMPyP) was observed upon addition of a specific quantity of Nafion ionomer on a glassy carbon working electrode, indicating not only a faster charge transfer rate but also the role of protonation in the oxygen reduction reaction (ORR) process. A membrane electrode assembly (MEA) was made as a sandwich of a Pt-coated anode, a Nafion® 212 membrane, and a Fe(III)TMPyP + Nafion ionomer-coated cathode. This three-dimensional catalysis system has been demonstrated to be working in a H2/O2 proton exchange membrane (PEM) fuel cell test.
- Full Text:
- Date Issued: 2012
In vitro photodynamic effect of aluminum tetrasulfophthalocyanines on melanoma skin cancer and healthy normal skin cells
- Maduray, Kaminee, Odhay, Bharti, Nyokong, Tebello
- Authors: Maduray, Kaminee , Odhay, Bharti , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/245762 , vital:51403 , xlink:href="https://doi.org/10.1016/j.pdpdt.2011.07.001"
- Description: Photodynamic therapy is a medical treatment that uses an inactive dye/drug and lasers as a light source to activate the dye/drug to produce a toxic form of oxygen that destroys the cancer cells. This study aimed at investigating the cytotoxic effects of different concentrations of aluminum tetrasulfophthalocyanines in its inactive and active state (laser induced) on melanoma skin cancer cells, healthy normal skin fibroblast and keratinocyte cells. Experimentally, 3 x 10(4) cells/ml were seeded in 24-well plates before treatment with different concentrations of aluminum tetrasulfophthalocyanines. After 2 h, cells were irradiated with a light dose of 4.5 J/cm(2). Post-irradiated cells were incubated for 24 h before cell viability was measured using the CellTiter-Blue Viability Assay. Results showed that aluminum tetrasulfophthalocyanines at high concentrations were cytotoxic to melanoma cells in the absence of laser activation. In the presence of laser activation of aluminum tetrasulfophthalocyanines at a concentration of 40 mu g/ml decreased cell viability of melanoma cells to 45%, fibroblasts to 78% and keratinocytes to 73%. At this photosensitizing concentration of aluminum tetrasulfophthalocyanines the efficacy of the treatment light dose 4.5 J/cm(2) and the cell death mechanism induced by photoactivated aluminum tetrasulfophthalocyanines was evaluated. A light dose of 4.5 J/cm(2) was more efficient in killing a higher number of melanoma cells and a lower number of fibroblast and keratinocyte cells than the other light doses of 2.5 J/cm(2), 7.5 J/cm(2) and 10.5 J/cm(2). Apoptosis features such as blebbing, nucleus condensation, nucleus fragmentation and the formation of apoptotic bodies were seen in the photodynamic therapy treated melanoma skin cancer cells. This in vitro photodynamic therapy study concludes that using aluminum tetrasulfophthalocyanines at a photosensitizing concentration of 40 mu g/ml in combination with a laser dose of 4.5 J/cm(2) was potentially lethal for melanoma skin cancer cells and less harmful for the normal healthy skin cells. (c) 2011 Elsevier B.V. All rights reserved.
- Full Text:
- Date Issued: 2012
- Authors: Maduray, Kaminee , Odhay, Bharti , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/245762 , vital:51403 , xlink:href="https://doi.org/10.1016/j.pdpdt.2011.07.001"
- Description: Photodynamic therapy is a medical treatment that uses an inactive dye/drug and lasers as a light source to activate the dye/drug to produce a toxic form of oxygen that destroys the cancer cells. This study aimed at investigating the cytotoxic effects of different concentrations of aluminum tetrasulfophthalocyanines in its inactive and active state (laser induced) on melanoma skin cancer cells, healthy normal skin fibroblast and keratinocyte cells. Experimentally, 3 x 10(4) cells/ml were seeded in 24-well plates before treatment with different concentrations of aluminum tetrasulfophthalocyanines. After 2 h, cells were irradiated with a light dose of 4.5 J/cm(2). Post-irradiated cells were incubated for 24 h before cell viability was measured using the CellTiter-Blue Viability Assay. Results showed that aluminum tetrasulfophthalocyanines at high concentrations were cytotoxic to melanoma cells in the absence of laser activation. In the presence of laser activation of aluminum tetrasulfophthalocyanines at a concentration of 40 mu g/ml decreased cell viability of melanoma cells to 45%, fibroblasts to 78% and keratinocytes to 73%. At this photosensitizing concentration of aluminum tetrasulfophthalocyanines the efficacy of the treatment light dose 4.5 J/cm(2) and the cell death mechanism induced by photoactivated aluminum tetrasulfophthalocyanines was evaluated. A light dose of 4.5 J/cm(2) was more efficient in killing a higher number of melanoma cells and a lower number of fibroblast and keratinocyte cells than the other light doses of 2.5 J/cm(2), 7.5 J/cm(2) and 10.5 J/cm(2). Apoptosis features such as blebbing, nucleus condensation, nucleus fragmentation and the formation of apoptotic bodies were seen in the photodynamic therapy treated melanoma skin cancer cells. This in vitro photodynamic therapy study concludes that using aluminum tetrasulfophthalocyanines at a photosensitizing concentration of 40 mu g/ml in combination with a laser dose of 4.5 J/cm(2) was potentially lethal for melanoma skin cancer cells and less harmful for the normal healthy skin cells. (c) 2011 Elsevier B.V. All rights reserved.
- Full Text:
- Date Issued: 2012
Synthesis and physicochemical behaviour of aluminium trikis and tetrakis (diaquaplatinum) octacarboxyphthalocynine
- Malinga, Nduduzo, Dolotova, Olga, Bulgakov, Roman, Antunes, Edith M, Nyokong, Tebello
- Authors: Malinga, Nduduzo , Dolotova, Olga , Bulgakov, Roman , Antunes, Edith M , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/242687 , vital:51068 , xlink:href="https://doi.org/10.1016/j.dyepig.2012.05.011"
- Description: The combination of chemotherapy and photodynamic therapy was investigated by the synthesis and characterisation of phthalocyanine conjugates with Pt complexes. The complexes synthesized are: hydroxoaluminum trikis(diaquaplatinum) octacarboxyphthalocyanine (OHAlOCPc(Pt)3) and hydroxoaluminum tetrakis(diaquaplatinum) octacarboxyphthalocyanine (OHAlOCPc(Pt)4). The platinated phthalocyanine complexes gave long triplet lifetimes of 577 and 526 μs for OHAlOCPc(Pt)3 and OHAlOCPc(Pt)4, respectively. The triplet quantum yields were found to be 0.45 for OHAlOCPc(Pt)3 and 0.57 OHAlOCPc(Pt)4 while the singlet oxygen quantum yields were found to be 0.38 and 0.48, respectively.
- Full Text:
- Date Issued: 2012
- Authors: Malinga, Nduduzo , Dolotova, Olga , Bulgakov, Roman , Antunes, Edith M , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/242687 , vital:51068 , xlink:href="https://doi.org/10.1016/j.dyepig.2012.05.011"
- Description: The combination of chemotherapy and photodynamic therapy was investigated by the synthesis and characterisation of phthalocyanine conjugates with Pt complexes. The complexes synthesized are: hydroxoaluminum trikis(diaquaplatinum) octacarboxyphthalocyanine (OHAlOCPc(Pt)3) and hydroxoaluminum tetrakis(diaquaplatinum) octacarboxyphthalocyanine (OHAlOCPc(Pt)4). The platinated phthalocyanine complexes gave long triplet lifetimes of 577 and 526 μs for OHAlOCPc(Pt)3 and OHAlOCPc(Pt)4, respectively. The triplet quantum yields were found to be 0.45 for OHAlOCPc(Pt)3 and 0.57 OHAlOCPc(Pt)4 while the singlet oxygen quantum yields were found to be 0.38 and 0.48, respectively.
- Full Text:
- Date Issued: 2012
The photophysical and energy transfer behaviour of low symmetry phthalocyanine complexes conjugated to coreshell quantum dots
- Masilela, Nkosiphile, Nyokong, Tebello
- Authors: Masilela, Nkosiphile , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243051 , vital:51111 , xlink:href="https://doi.org/10.1016/j.jphotochem.2012.07.016"
- Description: This work reports on the synthesis of new coreshell quantum dots (QDs)-low symmetry phthalocyanines conjugates. The energy transfer from QDs (donor) to phthalocyanines (acceptor) was investigated when the two are mixed together or chemically linked to each other. Ti monocarboxy phthalocyanine QDs-linked and Sn monocarboxy phthalocyanine QDs-linked gave the smallest centre-to-centre separation distance (r) corresponding to their higher Förster resonance energy transfer efficiencies which are estimated at 0.76 and 0.85 respectively. Higher energy transfer behaviour was achieved for all the covalently linked conjugates compared to their corresponding mixed counterparts. An improvement in triplet quantum yields and lifetimes was achieved for all the complexes in the presence of quantum dots, with the linked counterparts displaying excellent triplet state behaviour.
- Full Text:
- Date Issued: 2012
- Authors: Masilela, Nkosiphile , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243051 , vital:51111 , xlink:href="https://doi.org/10.1016/j.jphotochem.2012.07.016"
- Description: This work reports on the synthesis of new coreshell quantum dots (QDs)-low symmetry phthalocyanines conjugates. The energy transfer from QDs (donor) to phthalocyanines (acceptor) was investigated when the two are mixed together or chemically linked to each other. Ti monocarboxy phthalocyanine QDs-linked and Sn monocarboxy phthalocyanine QDs-linked gave the smallest centre-to-centre separation distance (r) corresponding to their higher Förster resonance energy transfer efficiencies which are estimated at 0.76 and 0.85 respectively. Higher energy transfer behaviour was achieved for all the covalently linked conjugates compared to their corresponding mixed counterparts. An improvement in triplet quantum yields and lifetimes was achieved for all the complexes in the presence of quantum dots, with the linked counterparts displaying excellent triplet state behaviour.
- Full Text:
- Date Issued: 2012
Synthesis and physicochemical behavior of new low symmetry Ge, Ti and Sn phthalocyanines
- Masilela, Nkosiphile, Nyokong, Tebello
- Authors: Masilela, Nkosiphile , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/242421 , vital:51040 , xlink:href="https://doi.org/10.1016/j.synthmet.2012.07.028"
- Description: The synthesis and photophysicochemical properties of new low symmetrically Ge, Sn and Ti phthalocyanines substituted with one carboxy containing group are reported. Broading and splitting in the absorption spectra were observed for some of the complexes in particular for both the titanium Pcs due to loss of symmetry. Higher fluorescence quantum yields and lifetimes were obtained for the Pcs substituted with three benzyloxy (5–7) compared to their corresponding counterparts substituted with six 2-diethylaminoethylthiol groups (9–11). The germanium Pc complexes gave the highest triplet and singlet oxygen quantum yields compared to all the other complexes studied in DMF. All the complexes showed reasonable ability to generate singlet oxygen with quantum yields ranging from 0.54 to 0.69.
- Full Text:
- Date Issued: 2012
- Authors: Masilela, Nkosiphile , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/242421 , vital:51040 , xlink:href="https://doi.org/10.1016/j.synthmet.2012.07.028"
- Description: The synthesis and photophysicochemical properties of new low symmetrically Ge, Sn and Ti phthalocyanines substituted with one carboxy containing group are reported. Broading and splitting in the absorption spectra were observed for some of the complexes in particular for both the titanium Pcs due to loss of symmetry. Higher fluorescence quantum yields and lifetimes were obtained for the Pcs substituted with three benzyloxy (5–7) compared to their corresponding counterparts substituted with six 2-diethylaminoethylthiol groups (9–11). The germanium Pc complexes gave the highest triplet and singlet oxygen quantum yields compared to all the other complexes studied in DMF. All the complexes showed reasonable ability to generate singlet oxygen with quantum yields ranging from 0.54 to 0.69.
- Full Text:
- Date Issued: 2012
Comparison of carbon screen-printed and disk electrodes in the detection of antioxidants using CoPc derivatives
- Matemadombo, Fungisai, Apetrei, Constantin, Nyokong, Tebello, Rodríguez-Méndez, María Luz, de Saja, José Antonio
- Authors: Matemadombo, Fungisai , Apetrei, Constantin , Nyokong, Tebello , Rodríguez-Méndez, María Luz , de Saja, José Antonio
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/244371 , vital:51251 , xlink:href="https://doi.org/10.1016/j.snb.2012.02.088"
- Description: Cobalt phthalocyanine (CoPc) and cobalt phthalocyanine carboxylic derivatives (CoTCPc and CoOCPc) have been used as electrocatalysts for the detection of the antioxidants vanillic acid, caffeic acid, pyrogallol, and ascorbic acid on screen-printed carbon and disk electrode surfaces. The cobalt phthalocyanines were used to detect vanillic acid (with limit of detection ranging from 1.15 μM to 2.42 μM at potentials of 0.55–0.88 V vs. Ag|AgCl), caffeic acid (with limit of detection ranging from 1.17 μM to 2.20 μM at potentials of 0.30–0.81 V vs. Ag|AgCl), pyrogallol (with limit of detection ranging from 1.16 μM to 3.63 μM at potentials of 0.52–0.63 V vs. Ag|AgCl), and ascorbic acid (with limit of detection ranging from 1.16 μM to 1.58 μM at potentials of 0.34–0.46 V vs. Ag|AgCl). The kinetic studies also demonstrate diffusion-controlled processes at the electrode surface. The SPCE electrodes have better detection properties towards vanillic acid, caffeic acid, pyrogallol while the disk electrodes had better ascorbic acid detection properties as proven by kinetic studies. Both types CoPc-influenced electrodes show 100% discrimination of the antioxidants.
- Full Text:
- Date Issued: 2012
- Authors: Matemadombo, Fungisai , Apetrei, Constantin , Nyokong, Tebello , Rodríguez-Méndez, María Luz , de Saja, José Antonio
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/244371 , vital:51251 , xlink:href="https://doi.org/10.1016/j.snb.2012.02.088"
- Description: Cobalt phthalocyanine (CoPc) and cobalt phthalocyanine carboxylic derivatives (CoTCPc and CoOCPc) have been used as electrocatalysts for the detection of the antioxidants vanillic acid, caffeic acid, pyrogallol, and ascorbic acid on screen-printed carbon and disk electrode surfaces. The cobalt phthalocyanines were used to detect vanillic acid (with limit of detection ranging from 1.15 μM to 2.42 μM at potentials of 0.55–0.88 V vs. Ag|AgCl), caffeic acid (with limit of detection ranging from 1.17 μM to 2.20 μM at potentials of 0.30–0.81 V vs. Ag|AgCl), pyrogallol (with limit of detection ranging from 1.16 μM to 3.63 μM at potentials of 0.52–0.63 V vs. Ag|AgCl), and ascorbic acid (with limit of detection ranging from 1.16 μM to 1.58 μM at potentials of 0.34–0.46 V vs. Ag|AgCl). The kinetic studies also demonstrate diffusion-controlled processes at the electrode surface. The SPCE electrodes have better detection properties towards vanillic acid, caffeic acid, pyrogallol while the disk electrodes had better ascorbic acid detection properties as proven by kinetic studies. Both types CoPc-influenced electrodes show 100% discrimination of the antioxidants.
- Full Text:
- Date Issued: 2012
Characterization of 2,(3)-tetra-(4-oxo-benzamide) phthalocyaninato cobalt (II)—single walled carbon nanotube conjugate platforms and their use in electrocatalysis of amitrole
- Mugadza, Tawanda, Arslanoğlu, Yasin, Nyokong, Tebello
- Authors: Mugadza, Tawanda , Arslanoğlu, Yasin , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/244382 , vital:51252 , xlink:href="https://doi.org/10.1016/j.electacta.2012.02.041"
- Description: In this paper we report on the use of carboxylic acid functionalized single walled carbon nanotubes (SWCNT) in the synthesis of 2,(3)-tetra-(4-oxo-benzamide)phthalocyaninato cobalt (II)–single walled carbon nanotube conjugates (CoTOBPc–SWCNT), their characterization and application in the electrocatalytic oxidation of amitrole. Cyclic voltammetry, chronoamperometry and electrochemical impedance spectroscopy were used for the detection of amitrole on the modified glassy carbon electrode. The catalytic rate constant was 1.6 × 103 M−1 s−1 and the apparent electron rate transfer constant was 1.5 × 10−5 cm s−1. The linear dynamic range was 1.0 × 10−6–3.0 × 10−5 M, with a sensitivity of ∼1.13 A mol−1 L cm−2.
- Full Text:
- Date Issued: 2012
- Authors: Mugadza, Tawanda , Arslanoğlu, Yasin , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/244382 , vital:51252 , xlink:href="https://doi.org/10.1016/j.electacta.2012.02.041"
- Description: In this paper we report on the use of carboxylic acid functionalized single walled carbon nanotubes (SWCNT) in the synthesis of 2,(3)-tetra-(4-oxo-benzamide)phthalocyaninato cobalt (II)–single walled carbon nanotube conjugates (CoTOBPc–SWCNT), their characterization and application in the electrocatalytic oxidation of amitrole. Cyclic voltammetry, chronoamperometry and electrochemical impedance spectroscopy were used for the detection of amitrole on the modified glassy carbon electrode. The catalytic rate constant was 1.6 × 103 M−1 s−1 and the apparent electron rate transfer constant was 1.5 × 10−5 cm s−1. The linear dynamic range was 1.0 × 10−6–3.0 × 10−5 M, with a sensitivity of ∼1.13 A mol−1 L cm−2.
- Full Text:
- Date Issued: 2012
Photophysical and photochemical studies of sulfur containing phthalocyanine derivatives in the presence of folic acid
- Nombona, Nolwazi, Nyokong, Tebello
- Authors: Nombona, Nolwazi , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243180 , vital:51124 , xlink:href="https://doi.org/10.1016/j.ica.2012.03.051"
- Description: The syntheses of zinc and magnesium 9,16,23-tris-(5-trifluoromethyl-2-mercaptopyridine)-2-(carboxy)phthalocyaninato complexes are described for the first time. The photophysical and photochemical parameters of these molecules in the absence or presence of folic acid are compared to the corresponding oxygen bridged complexes and to 2,9,17,23-tetrakis-[(1,6-hexanedithiol)phthalocyaninato]zinc(II), [8,15,22-tris-(naptho)-2-(amidoethanethiol)phthalocyaninato]zinc(II) and zinc phthalocyanine tetrasulfonate. In the absence of folic acid, the complexes show relatively good triplet quantum yields (ranging from 0.52 to 0.88) in DMSO with reasonable triplet lifetime between 140 and 470 μs. The complexes showed high singlet oxygen quantum yield values ranging from 0.27 to 0.66 in the absence of folic acid. In the presence of folic acid, the triplet quantum yield values were between 0.37 and 0.75 and the lifetimes were significantly reduced (70–320 μs).
- Full Text:
- Date Issued: 2012
- Authors: Nombona, Nolwazi , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/243180 , vital:51124 , xlink:href="https://doi.org/10.1016/j.ica.2012.03.051"
- Description: The syntheses of zinc and magnesium 9,16,23-tris-(5-trifluoromethyl-2-mercaptopyridine)-2-(carboxy)phthalocyaninato complexes are described for the first time. The photophysical and photochemical parameters of these molecules in the absence or presence of folic acid are compared to the corresponding oxygen bridged complexes and to 2,9,17,23-tetrakis-[(1,6-hexanedithiol)phthalocyaninato]zinc(II), [8,15,22-tris-(naptho)-2-(amidoethanethiol)phthalocyaninato]zinc(II) and zinc phthalocyanine tetrasulfonate. In the absence of folic acid, the complexes show relatively good triplet quantum yields (ranging from 0.52 to 0.88) in DMSO with reasonable triplet lifetime between 140 and 470 μs. The complexes showed high singlet oxygen quantum yield values ranging from 0.27 to 0.66 in the absence of folic acid. In the presence of folic acid, the triplet quantum yield values were between 0.37 and 0.75 and the lifetimes were significantly reduced (70–320 μs).
- Full Text:
- Date Issued: 2012
Synthesis of phthalocyanine conjugates with gold nanoparticles and liposomes for photodynamic therapy
- Nombona, Nolwazi, Maduray, Kaminee, Antunes, Edith M, Karsten, Aletta, Nyokong, Tebello
- Authors: Nombona, Nolwazi , Maduray, Kaminee , Antunes, Edith M , Karsten, Aletta , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/245798 , vital:51406 , xlink:href="https://doi.org/10.1016/j.jphotobiol.2011.11.007"
- Description: The efficiency of [2,9,17,23-tetrakis-(1,6-hexanedithiol)phthalocyaninato]zinc(II) as a photodynamic therapy (PDT) agent was investigated. This compound belongs to the second generation of photosensitizers currently tested for the cellular photo-damage of cancer cells. The production of reactive oxygen species (ROS) and phototoxicity of the photosensitizer were assessed. Healthy fibroblast cells and breast cancer (MCF-7) cells were treated with either free phthalocyanine or phthalocyanine bound to either gold nanoparticles or encapsulated in liposomes. Cell viability studies showed the optimum phototoxic effect on non-malignant cells to be 4.5 J cm−2. The PDT effect of the liposome bound phthalocyanine showed extensive damage of the breast cancer cells. Gold nanoparticles only showed a modest improvement in PDT activity.
- Full Text:
- Date Issued: 2012
- Authors: Nombona, Nolwazi , Maduray, Kaminee , Antunes, Edith M , Karsten, Aletta , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/245798 , vital:51406 , xlink:href="https://doi.org/10.1016/j.jphotobiol.2011.11.007"
- Description: The efficiency of [2,9,17,23-tetrakis-(1,6-hexanedithiol)phthalocyaninato]zinc(II) as a photodynamic therapy (PDT) agent was investigated. This compound belongs to the second generation of photosensitizers currently tested for the cellular photo-damage of cancer cells. The production of reactive oxygen species (ROS) and phototoxicity of the photosensitizer were assessed. Healthy fibroblast cells and breast cancer (MCF-7) cells were treated with either free phthalocyanine or phthalocyanine bound to either gold nanoparticles or encapsulated in liposomes. Cell viability studies showed the optimum phototoxic effect on non-malignant cells to be 4.5 J cm−2. The PDT effect of the liposome bound phthalocyanine showed extensive damage of the breast cancer cells. Gold nanoparticles only showed a modest improvement in PDT activity.
- Full Text:
- Date Issued: 2012
Spectroscopic and physicochemical behavior of magnesium phthalocyanine derivatives mono-substituted with a carboxylic acid group
- Nombona, Nolwazi, Chidawanyika, Wadzanai J U, Nyokong, Tebello
- Authors: Nombona, Nolwazi , Chidawanyika, Wadzanai J U , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/244450 , vital:51258 , xlink:href="https://doi.org/10.1016/j.molstruc.2011.12.051"
- Description: This work reports on the synthesis of novel unsymmetrically substituted magnesium phthalocyanine complexes containing one carboxyl group. The physicochemical behavior of these complexes were compared with those of their unmetallated and zinc counterparts. The MgPcs showed interesting absorption spectra with [8,15,22-Tris-(naphtho)-4,5-(3-carboxy-1,2-dioxyphenyl)phthalocyaninato]magnesium (II) showing a large split in the Q band whereas [8,15,22-Tris-(naphtho)-2-(carboxy) phthalocyaninato]magnesium(II) presented only a small splitting. The magnesium phthalocyanine derivatives displayed higher fluorescence quantum yields compared to unmetallated and zinc phthalocyanine counterparts. The latter gave admirable triplet and singlet oxygen quantum yields. These molecules can distinctly be employed in the field of photodynamic therapy in combination with fluorescence imaging.
- Full Text:
- Date Issued: 2012
- Authors: Nombona, Nolwazi , Chidawanyika, Wadzanai J U , Nyokong, Tebello
- Date: 2012
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/244450 , vital:51258 , xlink:href="https://doi.org/10.1016/j.molstruc.2011.12.051"
- Description: This work reports on the synthesis of novel unsymmetrically substituted magnesium phthalocyanine complexes containing one carboxyl group. The physicochemical behavior of these complexes were compared with those of their unmetallated and zinc counterparts. The MgPcs showed interesting absorption spectra with [8,15,22-Tris-(naphtho)-4,5-(3-carboxy-1,2-dioxyphenyl)phthalocyaninato]magnesium (II) showing a large split in the Q band whereas [8,15,22-Tris-(naphtho)-2-(carboxy) phthalocyaninato]magnesium(II) presented only a small splitting. The magnesium phthalocyanine derivatives displayed higher fluorescence quantum yields compared to unmetallated and zinc phthalocyanine counterparts. The latter gave admirable triplet and singlet oxygen quantum yields. These molecules can distinctly be employed in the field of photodynamic therapy in combination with fluorescence imaging.
- Full Text:
- Date Issued: 2012