Photophysical behaviour of asymmetrically substituted metal free, Mg and Zn phthalocyanines in the presence of folic acid
- Nombona, Nolwazi, Chidawanyika, Wadzanai J U, Nyokong, Tebello
- Authors: Nombona, Nolwazi , Chidawanyika, Wadzanai J U , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247705 , vital:51608 , xlink:href="https://doi.org/10.1016/j.poly.2010.11.033"
- Description: This work reports on the synthesis, characterisation and photophysical properties of new asymmetric metal free, magnesium and zinc phthalocyanines containing a mono carboxylic acid group for possible linking to biological molecules via an amide bond. Successful synthesis of the phthalocyanines was achieved through the statistical condensation method. The phthalocyanines were mixed with folic acid and their photophysical properties were examined. The triplet quantum yield values for all the complexes in DMSO were between 0.49 and 0.74 and in the presence of folic acid they were between 0.37 and 0.63. The lifetimes were generally good ranging from 70 to 290 μs in the absence or presence of folic acid.
- Full Text:
- Date Issued: 2011
- Authors: Nombona, Nolwazi , Chidawanyika, Wadzanai J U , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247705 , vital:51608 , xlink:href="https://doi.org/10.1016/j.poly.2010.11.033"
- Description: This work reports on the synthesis, characterisation and photophysical properties of new asymmetric metal free, magnesium and zinc phthalocyanines containing a mono carboxylic acid group for possible linking to biological molecules via an amide bond. Successful synthesis of the phthalocyanines was achieved through the statistical condensation method. The phthalocyanines were mixed with folic acid and their photophysical properties were examined. The triplet quantum yield values for all the complexes in DMSO were between 0.49 and 0.74 and in the presence of folic acid they were between 0.37 and 0.63. The lifetimes were generally good ranging from 70 to 290 μs in the absence or presence of folic acid.
- Full Text:
- Date Issued: 2011
Photophysical characterization of dysprosium, erbium and lutetium phthalocyanines tetrasubstituted with phenoxy groups at non-peripheral positions
- Zugle, Ruphino, Litwinski, Christian, Nyokong, Tebello
- Authors: Zugle, Ruphino , Litwinski, Christian , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247561 , vital:51595 , xlink:href="https://doi.org/10.1016/j.poly.2011.03.030"
- Description: Dysprosium bis-phthalocyanine and monomeric phthalocyanines of erbium and lutetium with non-peripheral phenoxy substituents have been synthesized using two different preparative routes. Photophysical studies on these phthalocyanines revealed that the triplet states of dysprosium and erbium are not populated while the monomeric phthalocyanine complex of lutetium is populated with a quantum yield of 0.83 and a lifetime of 25 μs in DMSO. It was further found that the phthalocyanine complex of lutetium was capable of photochemical generation of singlet state molecular oxygen with yield of 0.71 in THF, thus a promising photosensitizer. However, the three phthalocyanine molecules have very low fluorescence quantum yields of less than 0.01.
- Full Text:
- Date Issued: 2011
- Authors: Zugle, Ruphino , Litwinski, Christian , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247561 , vital:51595 , xlink:href="https://doi.org/10.1016/j.poly.2011.03.030"
- Description: Dysprosium bis-phthalocyanine and monomeric phthalocyanines of erbium and lutetium with non-peripheral phenoxy substituents have been synthesized using two different preparative routes. Photophysical studies on these phthalocyanines revealed that the triplet states of dysprosium and erbium are not populated while the monomeric phthalocyanine complex of lutetium is populated with a quantum yield of 0.83 and a lifetime of 25 μs in DMSO. It was further found that the phthalocyanine complex of lutetium was capable of photochemical generation of singlet state molecular oxygen with yield of 0.71 in THF, thus a promising photosensitizer. However, the three phthalocyanine molecules have very low fluorescence quantum yields of less than 0.01.
- Full Text:
- Date Issued: 2011
Phototransformation of 4-nitrophenol using Pd phthalocyanines supported on single walled carbon nanotubes
- Ogunbayo, Taofeek B, Nyokong, Tebello
- Authors: Ogunbayo, Taofeek B , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247800 , vital:51619 , xlink:href="https://doi.org/10.1016/j.molcata.2011.01.016"
- Description: Adsorption of palladium phthalocyanines complexes on single walled carbon nanotubes was carried out. The resulting composites were employed as catalysts for heterogeneous photocatalytic oxidation of 4-nitrophenol (4-NP) in aqueous media. Singlet oxygen was found to be involved in the phototransformation of 4-NP. Gas chromatographic separation gave hydroquinone and benzoquinone as the phototransformation products. Langmuir–Hinshelwood (L–H) model was employed to evaluate the adsorption and desorption equilibria of the reactants and the products. 2,3,9,10,16,17,23,24-octakis(dodecylthiophthalocyaninato) palladium(II) and 1,4,8,11,15,18,22,25-octakis(dodecylthio phthalocyaninato) palladium, containing the longest alkyl chain gave the best performances.
- Full Text:
- Date Issued: 2011
- Authors: Ogunbayo, Taofeek B , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247800 , vital:51619 , xlink:href="https://doi.org/10.1016/j.molcata.2011.01.016"
- Description: Adsorption of palladium phthalocyanines complexes on single walled carbon nanotubes was carried out. The resulting composites were employed as catalysts for heterogeneous photocatalytic oxidation of 4-nitrophenol (4-NP) in aqueous media. Singlet oxygen was found to be involved in the phototransformation of 4-NP. Gas chromatographic separation gave hydroquinone and benzoquinone as the phototransformation products. Langmuir–Hinshelwood (L–H) model was employed to evaluate the adsorption and desorption equilibria of the reactants and the products. 2,3,9,10,16,17,23,24-octakis(dodecylthiophthalocyaninato) palladium(II) and 1,4,8,11,15,18,22,25-octakis(dodecylthio phthalocyaninato) palladium, containing the longest alkyl chain gave the best performances.
- Full Text:
- Date Issued: 2011
Porphyrin nanorods modified glassy carbon electrode for the electrocatalysis of dioxygen, methanol and hydrazine
- George, Reama C, Mugadza, Tawanda, Khene, Samson, Egharevba, Gabriel O, Nyokong, Tebello
- Authors: George, Reama C , Mugadza, Tawanda , Khene, Samson , Egharevba, Gabriel O , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247388 , vital:51576 , xlink:href="https://doi.org/10.1002/elan.201100081"
- Description: Porphyrin nanorods (PNR) were prepared by ionic self-assembly of two oppositely charged porphyrin molecules consisting of free base meso-tetraphenylsulfonate porphyrin (H4TPPS42−) and meso-tetra(N-methyl-4-pyridyl) porphyrin (MTMePyP4+M=Sn, Mn, In, Co). These consist of H4TPPS42−SnTMePyP4+, H4TPPS42−CoTMePyP4+, H4TPPS42−InTMePyP4+ and H4TPPS42−MnTMePyP4+ porphyrin nanorods. The absorption spectra and transmission electron microscopic (TEM) images of these structures were obtained. These porphyrin nanostructures were used to modify a glassy carbon electrode for the electrocatalytic reduction of oxygen, and the oxidation of hydrazine and methanol at low pH. The cyclic voltammogram of PNR-modified GCE in pH 2 buffer solution has five irreversible processes, two distinct reduction processes and three oxidation processes. The porphyrin nanorods modified GCE produce good responses especially towards oxygen reduction at −0.50 V vs. Ag|AgCl (3 M KCl). The process of electrocatalytic oxidation of methanol using PNR-modified GCE begins at 0.71 V vs. Ag|AgCl (3 M KCl). The electrochemical oxidation of hydrazine began at around 0.36 V on H4TPPS42−SnTMePyP4+ modified GCE. The GCE modified with H4TPPS42−CoTMePyP4+ H4TPPS42−InTMePyP4+ and H4TPPS42−MnTMePyP4+ porphyrin nanorods began oxidizing hydrazine at 0.54 V, 0.59 V and 0.56 V, respectively.
- Full Text:
- Date Issued: 2011
- Authors: George, Reama C , Mugadza, Tawanda , Khene, Samson , Egharevba, Gabriel O , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247388 , vital:51576 , xlink:href="https://doi.org/10.1002/elan.201100081"
- Description: Porphyrin nanorods (PNR) were prepared by ionic self-assembly of two oppositely charged porphyrin molecules consisting of free base meso-tetraphenylsulfonate porphyrin (H4TPPS42−) and meso-tetra(N-methyl-4-pyridyl) porphyrin (MTMePyP4+M=Sn, Mn, In, Co). These consist of H4TPPS42−SnTMePyP4+, H4TPPS42−CoTMePyP4+, H4TPPS42−InTMePyP4+ and H4TPPS42−MnTMePyP4+ porphyrin nanorods. The absorption spectra and transmission electron microscopic (TEM) images of these structures were obtained. These porphyrin nanostructures were used to modify a glassy carbon electrode for the electrocatalytic reduction of oxygen, and the oxidation of hydrazine and methanol at low pH. The cyclic voltammogram of PNR-modified GCE in pH 2 buffer solution has five irreversible processes, two distinct reduction processes and three oxidation processes. The porphyrin nanorods modified GCE produce good responses especially towards oxygen reduction at −0.50 V vs. Ag|AgCl (3 M KCl). The process of electrocatalytic oxidation of methanol using PNR-modified GCE begins at 0.71 V vs. Ag|AgCl (3 M KCl). The electrochemical oxidation of hydrazine began at around 0.36 V on H4TPPS42−SnTMePyP4+ modified GCE. The GCE modified with H4TPPS42−CoTMePyP4+ H4TPPS42−InTMePyP4+ and H4TPPS42−MnTMePyP4+ porphyrin nanorods began oxidizing hydrazine at 0.54 V, 0.59 V and 0.56 V, respectively.
- Full Text:
- Date Issued: 2011
Prospects for the biological control of submerged macrophytes in South Africa
- Coetzee, Julie A, Bownes, Angela, Martin, Grant D
- Authors: Coetzee, Julie A , Bownes, Angela , Martin, Grant D
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/452295 , vital:75118 , https://hdl.handle.net/10520/EJC32899
- Description: Historically, biological control efforts against aquatic plants in South Africa have focused on floating species, and as a result, there has been a dearth of research into the invasion and control of submerged macrophytes. With numerous submerged invasive species already established in South Africa, thriving horticultural and aquarium industries, nutrient-rich water systems, and a limited knowledge of the drivers of invasions of submerged macrophytes, South Africa is highly vulnerable to a second phase of aquatic plant problems. Experience gained in the U.S.A. on biological control against submerged weeds, such as hydrilla, Hydrilla verticillata (L.f.) Royle (Hydrocharitaceae) and spiked / Eurasian watermilfoil, Myriophyllum spicatum L. (Haloragaceae), have provided South African researchers with the necessary foundation to initiate programmes against these weeds. Research in South Africa is currently focused on pre-release studies on the biological control of H. verticillata, using an undescribed fly, Hydrellia sp. (Diptera: Ephydridae) and a weevil, Bagous hydrillae O'Brien (Coleoptera: Curculionidae); and on M. spicatum using a North American weevil, Euhrychiopsis lecontei Dietz (Coleoptera: Curculionidae). Feasibility studies into biological control of some incipient submerged weeds are also being conducted, including Brazilian water weed, Egeria densa Planch. (Hydrocharitaceae), Canadian water weed, Elodea canadensis Mitch. (Hydrocharitaceae) and cabomba, Cabomba caroliniana A. Gray (Cabombaceae). Progress with, and potential constraints that may limit these programmes, are discussed.
- Full Text:
- Date Issued: 2011
- Authors: Coetzee, Julie A , Bownes, Angela , Martin, Grant D
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/452295 , vital:75118 , https://hdl.handle.net/10520/EJC32899
- Description: Historically, biological control efforts against aquatic plants in South Africa have focused on floating species, and as a result, there has been a dearth of research into the invasion and control of submerged macrophytes. With numerous submerged invasive species already established in South Africa, thriving horticultural and aquarium industries, nutrient-rich water systems, and a limited knowledge of the drivers of invasions of submerged macrophytes, South Africa is highly vulnerable to a second phase of aquatic plant problems. Experience gained in the U.S.A. on biological control against submerged weeds, such as hydrilla, Hydrilla verticillata (L.f.) Royle (Hydrocharitaceae) and spiked / Eurasian watermilfoil, Myriophyllum spicatum L. (Haloragaceae), have provided South African researchers with the necessary foundation to initiate programmes against these weeds. Research in South Africa is currently focused on pre-release studies on the biological control of H. verticillata, using an undescribed fly, Hydrellia sp. (Diptera: Ephydridae) and a weevil, Bagous hydrillae O'Brien (Coleoptera: Curculionidae); and on M. spicatum using a North American weevil, Euhrychiopsis lecontei Dietz (Coleoptera: Curculionidae). Feasibility studies into biological control of some incipient submerged weeds are also being conducted, including Brazilian water weed, Egeria densa Planch. (Hydrocharitaceae), Canadian water weed, Elodea canadensis Mitch. (Hydrocharitaceae) and cabomba, Cabomba caroliniana A. Gray (Cabombaceae). Progress with, and potential constraints that may limit these programmes, are discussed.
- Full Text:
- Date Issued: 2011
Range extension of the Lufira Masked Weaver Ploceus ruweti, endemic to Katanga province, Democratic Republic of Congo
- Craig, Adrian J F K, Hasson, Michel, Jordaens, Kurt, Breman, Floris C, Louette, Michel
- Authors: Craig, Adrian J F K , Hasson, Michel , Jordaens, Kurt , Breman, Floris C , Louette, Michel
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/449489 , vital:74825 , https://www.tandfonline.com/doi/pdf/10.2989/00306525.2010.523018
- Description: For many years the status of Ploceus ruweti Louette and Benson 1982, described from the unique male type specimen obtained in 1960 at Lake Lufira (an artificial impoundment on the Lufira River), remained obscure. However, in 2009 MH revisited the type locality, photographed the birds breeding there (including females and young birds), and rec-orded their song; nests and eggs were described for the first time, and a second male specimen was obtained from local fishermen (Louette and Hasson 2009; collection number RMCA A9-18-A-1). This species had been treated in the authoritative series The Birds of Africa as the Lake Lufira Weaver (Oschadleus 2004), and appears under this name in current checklists and fieldguides (eg Sinclair and Ryan 2003). Since the lake is now known as Lake Tshangalele and, based on our data from a recent field trip to the region, the bird is not restricted to the lake, an appropriate common name for P. ruweti is ‘Lufira Masked Weaver’as recommended by Gill and Wright (2006), and as used in a forthcoming volume of the other authoritative series Handbook of the Birds of the World (Craig 2010).
- Full Text:
- Date Issued: 2011
- Authors: Craig, Adrian J F K , Hasson, Michel , Jordaens, Kurt , Breman, Floris C , Louette, Michel
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/449489 , vital:74825 , https://www.tandfonline.com/doi/pdf/10.2989/00306525.2010.523018
- Description: For many years the status of Ploceus ruweti Louette and Benson 1982, described from the unique male type specimen obtained in 1960 at Lake Lufira (an artificial impoundment on the Lufira River), remained obscure. However, in 2009 MH revisited the type locality, photographed the birds breeding there (including females and young birds), and rec-orded their song; nests and eggs were described for the first time, and a second male specimen was obtained from local fishermen (Louette and Hasson 2009; collection number RMCA A9-18-A-1). This species had been treated in the authoritative series The Birds of Africa as the Lake Lufira Weaver (Oschadleus 2004), and appears under this name in current checklists and fieldguides (eg Sinclair and Ryan 2003). Since the lake is now known as Lake Tshangalele and, based on our data from a recent field trip to the region, the bird is not restricted to the lake, an appropriate common name for P. ruweti is ‘Lufira Masked Weaver’as recommended by Gill and Wright (2006), and as used in a forthcoming volume of the other authoritative series Handbook of the Birds of the World (Craig 2010).
- Full Text:
- Date Issued: 2011
Redox activity of CdTe quantum dots linked to nickel tetraaminophthalocyanine
- Khene, Samson, Nyokong, Tebello
- Authors: Khene, Samson , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/246457 , vital:51478 , xlink:href="https://doi.org/10.1016/j.microc.2011.06.024"
- Description: Cadmium tellurite quantum dots (CdTe-QDs) are linked to nickel tetraamino phthalocyanine (CdTe-QDs-NiTAPc) through an amide bond. Differential pulse voltammetry shows that that NiTAPc stabilizes the QDs against oxidative disintegration into metallic products on oxidation. Electrocatalytic oxidation of 2, 4-dichlorophenol (DCP) and pentachlorophenol (PCP) on CdTe-QDs and CdTe-QDs-NiTAPc adsorbed or electrodeposited onto a gold electrode were studied. Adsorbed CdTe-QDs-NiTAPc shows the lowest potential for DCP and PCP oxidation and it is also more stable to fouling by PCP and its oxidation products compared to adsorbed CdTe-QDs without NiTAPc. Electrodeposited CdTe-QDs or CdTe-QDs-NiTAPc show the best activity in terms of enhanced currents towards the oxidation of the chlorophenols.
- Full Text:
- Date Issued: 2011
- Authors: Khene, Samson , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/246457 , vital:51478 , xlink:href="https://doi.org/10.1016/j.microc.2011.06.024"
- Description: Cadmium tellurite quantum dots (CdTe-QDs) are linked to nickel tetraamino phthalocyanine (CdTe-QDs-NiTAPc) through an amide bond. Differential pulse voltammetry shows that that NiTAPc stabilizes the QDs against oxidative disintegration into metallic products on oxidation. Electrocatalytic oxidation of 2, 4-dichlorophenol (DCP) and pentachlorophenol (PCP) on CdTe-QDs and CdTe-QDs-NiTAPc adsorbed or electrodeposited onto a gold electrode were studied. Adsorbed CdTe-QDs-NiTAPc shows the lowest potential for DCP and PCP oxidation and it is also more stable to fouling by PCP and its oxidation products compared to adsorbed CdTe-QDs without NiTAPc. Electrodeposited CdTe-QDs or CdTe-QDs-NiTAPc show the best activity in terms of enhanced currents towards the oxidation of the chlorophenols.
- Full Text:
- Date Issued: 2011
Regulation and risk assessment for importations and releases of biological control agents against invasive alien plants in South Africa
- Klein, Hildegard, Hill, Martin P, Zachariades, Costas, Zimmermann, Helmuth G
- Authors: Klein, Hildegard , Hill, Martin P , Zachariades, Costas , Zimmermann, Helmuth G
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/451481 , vital:75052 , https://hdl.handle.net/10520/EJC32898
- Description: The importation and release of biological control agents against invasive alien plants in South Africa are subject to regulation by the Department of Agriculture, Forestry and Fisheries (DAFF), under its Agricultural Pests Act, and by the Department of Environmental Affairs (DEA), initially under its Environment Conservation Act, subsequently under the National Environmental Management Act and eventually, as soon as the relevant regulations have been developed, under the National Environmental Management: Biodiversity Act. Peer review, both within South Africa, and with colleagues in other countries, has helped to ensure the integrity of the science and practice of weed biological control in South Africa. This paper traces the development of the regulatory system from the first weed biological control project in 1913, through a dispensation when importations and releases were authorized by DAFF only to a dual regulatory system involving two government departments. Inappropriate legislation, lack of knowledge about biological control amongst the relevant authorities and the costs of employing compulsory private consultants are some of the reasons for significant delays that have become a feature in the authorization of biological control agent releases. These delays have set back several control programmes. Holding agents in quarantine while awaiting decisions ties up expensive space and staff time and increases the risk of losing colonies through accidents or decreased genetic vigour. It seems likely that changes in legislation within DEA will streamline the regulatory process in the near future.
- Full Text:
- Date Issued: 2011
- Authors: Klein, Hildegard , Hill, Martin P , Zachariades, Costas , Zimmermann, Helmuth G
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/451481 , vital:75052 , https://hdl.handle.net/10520/EJC32898
- Description: The importation and release of biological control agents against invasive alien plants in South Africa are subject to regulation by the Department of Agriculture, Forestry and Fisheries (DAFF), under its Agricultural Pests Act, and by the Department of Environmental Affairs (DEA), initially under its Environment Conservation Act, subsequently under the National Environmental Management Act and eventually, as soon as the relevant regulations have been developed, under the National Environmental Management: Biodiversity Act. Peer review, both within South Africa, and with colleagues in other countries, has helped to ensure the integrity of the science and practice of weed biological control in South Africa. This paper traces the development of the regulatory system from the first weed biological control project in 1913, through a dispensation when importations and releases were authorized by DAFF only to a dual regulatory system involving two government departments. Inappropriate legislation, lack of knowledge about biological control amongst the relevant authorities and the costs of employing compulsory private consultants are some of the reasons for significant delays that have become a feature in the authorization of biological control agent releases. These delays have set back several control programmes. Holding agents in quarantine while awaiting decisions ties up expensive space and staff time and increases the risk of losing colonies through accidents or decreased genetic vigour. It seems likely that changes in legislation within DEA will streamline the regulatory process in the near future.
- Full Text:
- Date Issued: 2011
Selection and characterization of suitable lipid excipients for use in the manufacture of didanosine-loaded solid lipid nanoparticles and nanostructured lipid carriers
- Kasongo, Kasongo W, Pardeike, Jana, Muller, Rainer H, Walker, Roderick B
- Authors: Kasongo, Kasongo W , Pardeike, Jana , Muller, Rainer H , Walker, Roderick B
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/184016 , vital:44156 , xlink:href="https://doi.org/10.1002/jps.22711"
- Description: This research aimed to evaluate the suitability of lipids for the manufacture of solid lipid nanoparticles (SLNs) and nanostructured lipid carriers (NLCs) loaded with the hydrophilic drug, didanosine (DDI). The crystalline state and polymorphism of lipids with the best‐solubulizing potential for DDI was investigated using differential scanning calorimetry (DSC) and wide‐angle X‐ray scattering (WAXS). DSC and WAXS were also used to determine potential interactions between the bulk lipids and DDI. Precirol® ATO 5 and Transcutol® HP showed the best‐solubilizing potential for DDI. Precirol® ATO 5 exists in the β‐modification before heating; however, a mixture of both α‐ and β‐modifications were detected following heating. Addition of Transcutol® HP to Precirol® ATO 5 changes the polymorphism of the latter from the β‐modification to a form that exhibits coexistence of the α‐ and β‐modifications. DDI exists in a crystalline state when dispersed at 5% (w/w) in Precirol® ATO 5 or in a Precirol® ATO 5/Transcutol® HP mixture. DSC and WAXS profiles of DDI/bulk lipids mixture obtained before and after exposure to heat revealed no interactions between DDI and the lipids. Precirol® ATO 5 and a mixture of Precirol® ATO 5 and Transcutol® HP may be used to manufacture DDI‐loaded SLN and NLC, respectively.
- Full Text:
- Date Issued: 2011
- Authors: Kasongo, Kasongo W , Pardeike, Jana , Muller, Rainer H , Walker, Roderick B
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/184016 , vital:44156 , xlink:href="https://doi.org/10.1002/jps.22711"
- Description: This research aimed to evaluate the suitability of lipids for the manufacture of solid lipid nanoparticles (SLNs) and nanostructured lipid carriers (NLCs) loaded with the hydrophilic drug, didanosine (DDI). The crystalline state and polymorphism of lipids with the best‐solubulizing potential for DDI was investigated using differential scanning calorimetry (DSC) and wide‐angle X‐ray scattering (WAXS). DSC and WAXS were also used to determine potential interactions between the bulk lipids and DDI. Precirol® ATO 5 and Transcutol® HP showed the best‐solubilizing potential for DDI. Precirol® ATO 5 exists in the β‐modification before heating; however, a mixture of both α‐ and β‐modifications were detected following heating. Addition of Transcutol® HP to Precirol® ATO 5 changes the polymorphism of the latter from the β‐modification to a form that exhibits coexistence of the α‐ and β‐modifications. DDI exists in a crystalline state when dispersed at 5% (w/w) in Precirol® ATO 5 or in a Precirol® ATO 5/Transcutol® HP mixture. DSC and WAXS profiles of DDI/bulk lipids mixture obtained before and after exposure to heat revealed no interactions between DDI and the lipids. Precirol® ATO 5 and a mixture of Precirol® ATO 5 and Transcutol® HP may be used to manufacture DDI‐loaded SLN and NLC, respectively.
- Full Text:
- Date Issued: 2011
Selective adsorption of PVP on the surface of silver nanoparticles
- Mdluli, Phumlani S, Sosibo, Ndabenhle M, Mashazi, Philani N, Nyokong, Tebello, Tshikhudo, Robert T, Skepu, Amanda, van der Lingen, Elma
- Authors: Mdluli, Phumlani S , Sosibo, Ndabenhle M , Mashazi, Philani N , Nyokong, Tebello , Tshikhudo, Robert T , Skepu, Amanda , van der Lingen, Elma
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247143 , vital:51550 , xlink:href="https://doi.org/10.1016/j.molstruc.2011.07.049"
- Description: The use of surfactants to affect the shape evolution of silver nanoparticles is explored. This allows one to fine-tune the morphological evolution and the optical properties of the metal nanoparticles. Polyvinyl pyrrolidone (PVP) has been used as a surfactant to control the growth of silver nanoparticles at room temperature. In this paper, molecular dynamics simulations were performed to understand regio-selective adsorption of PVP that leads to the preferential growth of silver nanoparticles in dimethylformamide (DMF). The interaction energies between PVP and Ag(1 1 0), Ag(1 0 0) and Ag(1 1 1) crystal planes were calculated and in addition the length density profile of the surfactant on silver surfaces was also examined. Importantly, it has been demonstrated that the length distribution profiles analysis obtained from the molecular dynamics study fully explained the adsorption of PVP on the surface of silver nanoparticles through the carbonyl group of the PVP ring. The application of molecular dynamics simulation technique is important in understanding the evolution of silver nanoparticles and is vital in choosing the right surfactants.
- Full Text:
- Date Issued: 2011
- Authors: Mdluli, Phumlani S , Sosibo, Ndabenhle M , Mashazi, Philani N , Nyokong, Tebello , Tshikhudo, Robert T , Skepu, Amanda , van der Lingen, Elma
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247143 , vital:51550 , xlink:href="https://doi.org/10.1016/j.molstruc.2011.07.049"
- Description: The use of surfactants to affect the shape evolution of silver nanoparticles is explored. This allows one to fine-tune the morphological evolution and the optical properties of the metal nanoparticles. Polyvinyl pyrrolidone (PVP) has been used as a surfactant to control the growth of silver nanoparticles at room temperature. In this paper, molecular dynamics simulations were performed to understand regio-selective adsorption of PVP that leads to the preferential growth of silver nanoparticles in dimethylformamide (DMF). The interaction energies between PVP and Ag(1 1 0), Ag(1 0 0) and Ag(1 1 1) crystal planes were calculated and in addition the length density profile of the surfactant on silver surfaces was also examined. Importantly, it has been demonstrated that the length distribution profiles analysis obtained from the molecular dynamics study fully explained the adsorption of PVP on the surface of silver nanoparticles through the carbonyl group of the PVP ring. The application of molecular dynamics simulation technique is important in understanding the evolution of silver nanoparticles and is vital in choosing the right surfactants.
- Full Text:
- Date Issued: 2011
Simulating Collective agency: Joint purpose, presence and power as Constraints to learning in a social Context
- Authors: Kulundu, Injairu
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/386530 , vital:68149 , xlink:href="https://www.ajol.info/index.php/sajee/article/view/122249"
- Description: This paper reflects on the practice of social learning by using my experiences as a social development practitioner in two projects. The first, the Arkwork Collective, is an art-junk process that engages marginalised youth in Grahamstown, South Africa in a process that uses creative sculpture and drama to explore personal and social issues that exist in their immediate context. The second, Jonga Phambili Sinethemba looks into the impact of climate change and HIV/AIDS (amongst other issues) in the rural and peri-urban communities of Willowvale and Lesseyton in the Eastern Cape, South Africa. It seeks to provide a platform where members of each community can define the vulnerabilities, capabilities, social networks in their areas with the aim of bolstering the adaptive capacity of these communities. Snippets of my experiences in these projects are shared with the intention of demonstrating constraints to learning in a social context. Key ideas that the paper explores include honouring the lived experiences of participants as part of the process, prioritising the participation of each individual present as part of the ongoing conversation, the challenge of surfacing the vital independent links of a collective, drawing on the reflective capacity of a diverse group, assessing the quality of participation, building capabilities for ‘response-ability’ and rethinking facilitation. Each section sets out challenges and questions for practitioners in this field to reflect on. The paper suggests that in order to achieve the laudable aims of social learning, we need to peel back the common rhetoric of its participatory aims and acknowledge the complexity, flexibility and dedication that it requires.
- Full Text:
- Date Issued: 2011
- Authors: Kulundu, Injairu
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/386530 , vital:68149 , xlink:href="https://www.ajol.info/index.php/sajee/article/view/122249"
- Description: This paper reflects on the practice of social learning by using my experiences as a social development practitioner in two projects. The first, the Arkwork Collective, is an art-junk process that engages marginalised youth in Grahamstown, South Africa in a process that uses creative sculpture and drama to explore personal and social issues that exist in their immediate context. The second, Jonga Phambili Sinethemba looks into the impact of climate change and HIV/AIDS (amongst other issues) in the rural and peri-urban communities of Willowvale and Lesseyton in the Eastern Cape, South Africa. It seeks to provide a platform where members of each community can define the vulnerabilities, capabilities, social networks in their areas with the aim of bolstering the adaptive capacity of these communities. Snippets of my experiences in these projects are shared with the intention of demonstrating constraints to learning in a social context. Key ideas that the paper explores include honouring the lived experiences of participants as part of the process, prioritising the participation of each individual present as part of the ongoing conversation, the challenge of surfacing the vital independent links of a collective, drawing on the reflective capacity of a diverse group, assessing the quality of participation, building capabilities for ‘response-ability’ and rethinking facilitation. Each section sets out challenges and questions for practitioners in this field to reflect on. The paper suggests that in order to achieve the laudable aims of social learning, we need to peel back the common rhetoric of its participatory aims and acknowledge the complexity, flexibility and dedication that it requires.
- Full Text:
- Date Issued: 2011
SOA driven architectures for service creation through enablers in an IMS testbed
- Tsietsi, Mosiuoa, Terzoli, Alfredo, Wells,George C
- Authors: Tsietsi, Mosiuoa , Terzoli, Alfredo , Wells,George C
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/430726 , vital:72711 , https://ieeexplore.ieee.org/abstract/document/6144230
- Description: Standards development organisations have long been in agreement that the most appropriate and cost effective way of developing services for the IP Multimedia Subsystem (IMS) is through the use - and re-use - of service capabilities, which are the building blocks for developing complex services. IMS specifications provide a theoretical framework for how service capabilities can be aggregated into large service appli-cations. However, there is little evidence that mainstream IMS service development is capability-based, and many services are still designed in a monolithic way, with no re-use of existing functionality. Telecom-munication networks are well positioned to stimulate the Internet ser-vices market by exposing these service enablers to third parties. In this paper, we marry the two issues by defining an extended IMS service layer (EISL) that provides a service broker that is the central agent in both service interaction management and the execution of external re-quests from third parties. A prototypical implementation of the service broker is described that was developed using a converged SIP servlet container, and a discussion is also provided that details how third party developers could use HTTP APIs to interact with a service broker in or-der to gain access to network capabilities.
- Full Text:
- Date Issued: 2011
- Authors: Tsietsi, Mosiuoa , Terzoli, Alfredo , Wells,George C
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/430726 , vital:72711 , https://ieeexplore.ieee.org/abstract/document/6144230
- Description: Standards development organisations have long been in agreement that the most appropriate and cost effective way of developing services for the IP Multimedia Subsystem (IMS) is through the use - and re-use - of service capabilities, which are the building blocks for developing complex services. IMS specifications provide a theoretical framework for how service capabilities can be aggregated into large service appli-cations. However, there is little evidence that mainstream IMS service development is capability-based, and many services are still designed in a monolithic way, with no re-use of existing functionality. Telecom-munication networks are well positioned to stimulate the Internet ser-vices market by exposing these service enablers to third parties. In this paper, we marry the two issues by defining an extended IMS service layer (EISL) that provides a service broker that is the central agent in both service interaction management and the execution of external re-quests from third parties. A prototypical implementation of the service broker is described that was developed using a converged SIP servlet container, and a discussion is also provided that details how third party developers could use HTTP APIs to interact with a service broker in or-der to gain access to network capabilities.
- Full Text:
- Date Issued: 2011
Some considerations when comparing SABAP 1 with SABAP 2 data
- Authors: Bonnevie, Bo T
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/448327 , vital:74722 , https://doi.org/10.2989/00306525.2011.603486
- Description: Generally, one should be cautious when comparing data that have not been collected in the same manner. The data collection methods of the South African Bird Atlas Projects, SABAP 1 (Harrison et al. 1997) and SABAP 2 (in progress at the time of writing), differ both spatially and temporally. On the spatial scale SABAP 1 used predominantly quarter degree cells (15′ by 15′), whereas SABAP 2 uses pentads (5′ by 5′; one quarter-degree cell containing nine pentads). On a temporal scale SABAP 1 used one calendar month, whereas SABAP 2 is using one pentade (five days). Where possible, however, SABAP 1 used pentades post hoc for seasonality modelling (Harrison et al. 1997, pp lviii–lix). Because of, but possibly not limited to, this, caution will need to be exercised when comparing data between the two projects. It is naturally desirable to compare the data between these projects, particularly to seek long-term trends in population densities and in the potential changes in the distribution of species.
- Full Text:
- Date Issued: 2011
- Authors: Bonnevie, Bo T
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/448327 , vital:74722 , https://doi.org/10.2989/00306525.2011.603486
- Description: Generally, one should be cautious when comparing data that have not been collected in the same manner. The data collection methods of the South African Bird Atlas Projects, SABAP 1 (Harrison et al. 1997) and SABAP 2 (in progress at the time of writing), differ both spatially and temporally. On the spatial scale SABAP 1 used predominantly quarter degree cells (15′ by 15′), whereas SABAP 2 uses pentads (5′ by 5′; one quarter-degree cell containing nine pentads). On a temporal scale SABAP 1 used one calendar month, whereas SABAP 2 is using one pentade (five days). Where possible, however, SABAP 1 used pentades post hoc for seasonality modelling (Harrison et al. 1997, pp lviii–lix). Because of, but possibly not limited to, this, caution will need to be exercised when comparing data between the two projects. It is naturally desirable to compare the data between these projects, particularly to seek long-term trends in population densities and in the potential changes in the distribution of species.
- Full Text:
- Date Issued: 2011
Stable isotope methods: the effect of gut contents on isotopic ratios of zooplankton
- Hill, Jaclyn M, McQuaid, Christopher D
- Authors: Hill, Jaclyn M , McQuaid, Christopher D
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/444623 , vital:74255 , https://doi.org/10.1016/j.ecss.2011.02.002
- Description: In the past decade there has been an increased awareness of the potential for methodological bias resulting from multiple pre-analytical procedures in foodweb interpretations based on stable isotope techniques. In the case of small organisms, this includes the effect of gut contents on whole body signatures. Although gut contents may not reflect actual assimilation, their carbon and nitrogen values will be isotopically lighter than after the same material has been assimilated. The potential skewing of isotopic ratios in whole organism samples is especially important for aquatic environments as many studies involve trophic relationships among small zooplankton. This is particularly important in pelagic waters, where herbivorous zooplankton comprise small taxa. Hence this study investigated the effect of gut contents on the δ13C and δ15N ratios of three size classes of zooplankton (1.0–2.0, 2.0–4.0 and >4.0mm) collected using bongo net tows in the tropical waters of the south-west Indian Ocean. Animals were collected at night, when they were likely to be feeding, sieved into size classes and separated into genera. We focused on Euphausia spp which dominated zooplankton biomass. Three treatment types were processed: bulk animals, bulk animals without guts and tail muscle from each size class at 10 bongo stations.
- Full Text:
- Date Issued: 2011
- Authors: Hill, Jaclyn M , McQuaid, Christopher D
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/444623 , vital:74255 , https://doi.org/10.1016/j.ecss.2011.02.002
- Description: In the past decade there has been an increased awareness of the potential for methodological bias resulting from multiple pre-analytical procedures in foodweb interpretations based on stable isotope techniques. In the case of small organisms, this includes the effect of gut contents on whole body signatures. Although gut contents may not reflect actual assimilation, their carbon and nitrogen values will be isotopically lighter than after the same material has been assimilated. The potential skewing of isotopic ratios in whole organism samples is especially important for aquatic environments as many studies involve trophic relationships among small zooplankton. This is particularly important in pelagic waters, where herbivorous zooplankton comprise small taxa. Hence this study investigated the effect of gut contents on the δ13C and δ15N ratios of three size classes of zooplankton (1.0–2.0, 2.0–4.0 and >4.0mm) collected using bongo net tows in the tropical waters of the south-west Indian Ocean. Animals were collected at night, when they were likely to be feeding, sieved into size classes and separated into genera. We focused on Euphausia spp which dominated zooplankton biomass. Three treatment types were processed: bulk animals, bulk animals without guts and tail muscle from each size class at 10 bongo stations.
- Full Text:
- Date Issued: 2011
Syntheses and electrochemical characterization of new water soluble octaarylthiosubstituted manganese phthalocyanines
- Booysen, Irvin N, Matemadombo, Fungisai, Durmus, Mahmut, Nyokong, Tebello
- Authors: Booysen, Irvin N , Matemadombo, Fungisai , Durmus, Mahmut , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247614 , vital:51600 , xlink:href="https://doi.org/10.1016/j.dyepig.2010.09.012"
- Description: This paper reports on the synthesis and characterization of new manganese phthalocyanine (MnPc) complexes: 2,3-octakis-[(2-mercaptopyridine) phthalocyaninato] acetato manganese (III) (1) and its quaternized (hence water soluble) derivative: 2,3-octakis-{[(N-methyl-2-mercaptopyridine) phthalocyaninato] acetato manganese (III)} sulphate (2). The complexes were used to form self assembled monolayers (SAMs). Voltammetry proved that both of the SAMs are well packed, strongly passivating and act as selective and efficient barriers to ion permeability. Furthermore, surface coverage studies confirmed that the MPc macrocycles adsorb onto the gold electrode as monolayers. Both MPc SAMs were successfully used as electrochemical sensors of nitrite.
- Full Text:
- Date Issued: 2011
- Authors: Booysen, Irvin N , Matemadombo, Fungisai , Durmus, Mahmut , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247614 , vital:51600 , xlink:href="https://doi.org/10.1016/j.dyepig.2010.09.012"
- Description: This paper reports on the synthesis and characterization of new manganese phthalocyanine (MnPc) complexes: 2,3-octakis-[(2-mercaptopyridine) phthalocyaninato] acetato manganese (III) (1) and its quaternized (hence water soluble) derivative: 2,3-octakis-{[(N-methyl-2-mercaptopyridine) phthalocyaninato] acetato manganese (III)} sulphate (2). The complexes were used to form self assembled monolayers (SAMs). Voltammetry proved that both of the SAMs are well packed, strongly passivating and act as selective and efficient barriers to ion permeability. Furthermore, surface coverage studies confirmed that the MPc macrocycles adsorb onto the gold electrode as monolayers. Both MPc SAMs were successfully used as electrochemical sensors of nitrite.
- Full Text:
- Date Issued: 2011
Syntheses, electrochemical and spectroelectrochemical properties of novel ball-type and mononuclear Co (II) phthalocyanines substituted at the peripheral and non-peripheral positions with binaphthol groups
- Canlıca, Mevlüde, Booysen, Irvin Noel, Nyokong, Tebello
- Authors: Canlıca, Mevlüde , Booysen, Irvin Noel , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247837 , vital:51622 , xlink:href="https://doi.org/10.1016/j.poly.2010.11.017"
- Description: Mononuclear cobalt phthalocyanine (CoPc) substituted at the non-peripheral 8 and peripheral positions 9 with 1,1′-binaphthyl-8,8′-diol and ball-type dinuclear Co2Pc2 substituted at the non-peripheral 10 and peripheral 11 positions with the same substituent are reported. The complexes with 1,1′-binaphthol-bridges were prepared from the corresponding phthalonitriles 4–7. The effects of the position of substituent on spectral, electrochemical and spectroelectrochemical properties of these complexes were also explored. The mononuclear complexes 8 and 9 exhibited one metal reduction, one ring reduction and one ring oxidation. The redox properties of the ball-type complexes 10 and 11 exhibited two reduction processes assigned to [(CoIPc−2)2]2−/[(CoIPc−3)2]4− (I), (CoIIPc−2)2/[(CoIPc−2)2]2− (II) and one oxidation process assigned to [(CoIIIPc−2)2]2+/CoIIPc−2)2 (III). The ball-type complexes are much easier to oxidize and more difficult to reduce than the corresponding monomers 8 and 9.
- Full Text:
- Date Issued: 2011
- Authors: Canlıca, Mevlüde , Booysen, Irvin Noel , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247837 , vital:51622 , xlink:href="https://doi.org/10.1016/j.poly.2010.11.017"
- Description: Mononuclear cobalt phthalocyanine (CoPc) substituted at the non-peripheral 8 and peripheral positions 9 with 1,1′-binaphthyl-8,8′-diol and ball-type dinuclear Co2Pc2 substituted at the non-peripheral 10 and peripheral 11 positions with the same substituent are reported. The complexes with 1,1′-binaphthol-bridges were prepared from the corresponding phthalonitriles 4–7. The effects of the position of substituent on spectral, electrochemical and spectroelectrochemical properties of these complexes were also explored. The mononuclear complexes 8 and 9 exhibited one metal reduction, one ring reduction and one ring oxidation. The redox properties of the ball-type complexes 10 and 11 exhibited two reduction processes assigned to [(CoIPc−2)2]2−/[(CoIPc−3)2]4− (I), (CoIIPc−2)2/[(CoIPc−2)2]2− (II) and one oxidation process assigned to [(CoIIIPc−2)2]2+/CoIIPc−2)2 (III). The ball-type complexes are much easier to oxidize and more difficult to reduce than the corresponding monomers 8 and 9.
- Full Text:
- Date Issued: 2011
Synthesis and electrocatalytic behavior of cobalt (II)-tris (benzyl-mercapto)-monoaminophthalocyanine–single walled carbon nanotube nanorods
- Mugadza, Tawanda, Nyokong, Tebello
- Authors: Mugadza, Tawanda , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247882 , vital:51626 , xlink:href="https://doi.org/10.1016/j.electacta.2010.11.016"
- Description: In this paper we report on synthesis and electrocatalytic behavior of cobalt (II)-tris(benzyl-mercapto)-monoaminophthalocyanine–single walled carbon nanotube nanorods towards the oxidation of amitrole. SWCNTs that were terminally functionalized with carboxylic acid groups were chemically linked to cobalt (II)-tris(benzyl-mercapto) monoaminophthalocyanine (CoMAPc) via an amide bond to form nanorods. UV–vis, FTIR, TEM, Raman and XRD spectroscopies were used in characterization of the nanorods (CoMAPc–SWCNT-linked), while cyclic voltammetry and chronoamperometry were used during the characterization of amitrole on the modified glassy carbon electrode. The linear dynamic range for the amitrole was from 1.0 × 10−6 M to 1.2 × 10−4 M, with a sensitivity of 6.76 A mol−1 L cm−2. The estimated limit of detection for amitrole was 0.10 μM, using the 3δ criterion. The catalytic rate constant was found to be 1.09 × 105 M−1 s−1.
- Full Text:
- Date Issued: 2011
- Authors: Mugadza, Tawanda , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247882 , vital:51626 , xlink:href="https://doi.org/10.1016/j.electacta.2010.11.016"
- Description: In this paper we report on synthesis and electrocatalytic behavior of cobalt (II)-tris(benzyl-mercapto)-monoaminophthalocyanine–single walled carbon nanotube nanorods towards the oxidation of amitrole. SWCNTs that were terminally functionalized with carboxylic acid groups were chemically linked to cobalt (II)-tris(benzyl-mercapto) monoaminophthalocyanine (CoMAPc) via an amide bond to form nanorods. UV–vis, FTIR, TEM, Raman and XRD spectroscopies were used in characterization of the nanorods (CoMAPc–SWCNT-linked), while cyclic voltammetry and chronoamperometry were used during the characterization of amitrole on the modified glassy carbon electrode. The linear dynamic range for the amitrole was from 1.0 × 10−6 M to 1.2 × 10−4 M, with a sensitivity of 6.76 A mol−1 L cm−2. The estimated limit of detection for amitrole was 0.10 μM, using the 3δ criterion. The catalytic rate constant was found to be 1.09 × 105 M−1 s−1.
- Full Text:
- Date Issued: 2011
Synthesis and electrochemical behavior of novel peripherally and non-peripherally substituted ball-type cobalt phthalocyanine complexes
- Canlıca, Mevlüde, Booysen, Irvin Noel, Nyokong, Tebello
- Authors: Canlıca, Mevlüde , Booysen, Irvin Noel , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247848 , vital:51623 , xlink:href="https://doi.org/10.1016/j.poly.2010.11.028"
- Description: The syntheses of new ball-type Co(II) phthalocyanines containing 4,4′-(9H-fluorene-9,9-diyl)diphenol substituents at non-peripheral (complex 6) and peripheral (complex 7) positions are presented. These complexes were characterized by UV–Vis, FT-IR, mass spectroscopy and electrochemical methods. Both complexes exhibit metal and ring based redox processes, typical of cobalt phthalocyanine complexes. For 6, the metal based reduction was observed at −0.46 V followed by a ring based reduction at −1.40 V. The metal oxidation for 6 was observed at +0.16 V and the ring based oxidation at +1.05 V. For 7, reductions are easier but the oxidations are more difficult. The metal based reduction for 7 was observed at −0.38 V followed by a ring based reduction at −1.03 V. The metal oxidation for 7 was observed at +0.20 V and the ring based oxidation at +1.35 V.
- Full Text:
- Date Issued: 2011
- Authors: Canlıca, Mevlüde , Booysen, Irvin Noel , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247848 , vital:51623 , xlink:href="https://doi.org/10.1016/j.poly.2010.11.028"
- Description: The syntheses of new ball-type Co(II) phthalocyanines containing 4,4′-(9H-fluorene-9,9-diyl)diphenol substituents at non-peripheral (complex 6) and peripheral (complex 7) positions are presented. These complexes were characterized by UV–Vis, FT-IR, mass spectroscopy and electrochemical methods. Both complexes exhibit metal and ring based redox processes, typical of cobalt phthalocyanine complexes. For 6, the metal based reduction was observed at −0.46 V followed by a ring based reduction at −1.40 V. The metal oxidation for 6 was observed at +0.16 V and the ring based oxidation at +1.05 V. For 7, reductions are easier but the oxidations are more difficult. The metal based reduction for 7 was observed at −0.38 V followed by a ring based reduction at −1.03 V. The metal oxidation for 7 was observed at +0.20 V and the ring based oxidation at +1.35 V.
- Full Text:
- Date Issued: 2011
Synthesis and electrochemical properties of new tetra substituted cobalt phthalocyanine complexes, and their application in electrode modification for the electrocatalysis of l-cysteine
- Erdoğmuş, Ali, Booysen, Irvin Noel, Nyokong, Tebello
- Authors: Erdoğmuş, Ali , Booysen, Irvin Noel , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247893 , vital:51627 , xlink:href="https://doi.org/10.1016/j.synthmet.2010.11.028"
- Description: This study investigates the synthesis and characterization new peripherally (β) tetra-substituted 4-(2-mercaptoquinoline phthalocyaninato) Co(II) (CoPcSHQn, 3), and 4-(2-phenoxy-4-trifluoromethylpyridine phthalocyaninato) Co(II) (CoPcOHPy, 4). These complexes were characterized by elemental analysis, IR, mass and electronic spectroscopies and electrochemical methods. Both complexes show well resolved redox peaks attributed to both ring and metal based processes. Spectroelectrochemistry was used to confirm the assignments of the redox processes. For CoPcSHQn (3): CoIPc−2/CoIPc−3 (E1/2 = −1.25 V, I), CoIIPc−2/CoIPc−2 (E1/2 = −0.57 V, II), CoIIIPc−2/CoIIPc−2 (E1/2 = +0.45 V, IV) and an irreversible process at Ep = +1.05 V vs Ag|AgCl for CoIIIPc−1/CoIIIPc−2 (V). Redox couple III at E1/2 = −0.15 V was ascribed to aggregation. In the case of CoPcOHPy (4): CoIPc−2/CoIPc−3 (E1/2 = −1.13 V, I), CoIIPc−2/CoIPc−2 (E1/2 = −0.45 V, II), CoIIIPc−2/CoIIPc−2 at E1/2 = +0.21 V (IV), and CoIIIPc−1/CoIIIPc−2 (E1/2 = +1.01 V vs Ag|AgCl, V). Again III is associated with the aggregated species. Both complexes were electrodeposited on a glassy carbon electrode (GCE). For complex 3 self-assembled monolayers was also formed. The modified (CoPc-GCE) electrodes electrocatalytically detected L-cysteine at Ep = 0.62 V (3-GCE) and 0.59 V (4-GCE) vs Ag|AgCl.
- Full Text:
- Date Issued: 2011
- Authors: Erdoğmuş, Ali , Booysen, Irvin Noel , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247893 , vital:51627 , xlink:href="https://doi.org/10.1016/j.synthmet.2010.11.028"
- Description: This study investigates the synthesis and characterization new peripherally (β) tetra-substituted 4-(2-mercaptoquinoline phthalocyaninato) Co(II) (CoPcSHQn, 3), and 4-(2-phenoxy-4-trifluoromethylpyridine phthalocyaninato) Co(II) (CoPcOHPy, 4). These complexes were characterized by elemental analysis, IR, mass and electronic spectroscopies and electrochemical methods. Both complexes show well resolved redox peaks attributed to both ring and metal based processes. Spectroelectrochemistry was used to confirm the assignments of the redox processes. For CoPcSHQn (3): CoIPc−2/CoIPc−3 (E1/2 = −1.25 V, I), CoIIPc−2/CoIPc−2 (E1/2 = −0.57 V, II), CoIIIPc−2/CoIIPc−2 (E1/2 = +0.45 V, IV) and an irreversible process at Ep = +1.05 V vs Ag|AgCl for CoIIIPc−1/CoIIIPc−2 (V). Redox couple III at E1/2 = −0.15 V was ascribed to aggregation. In the case of CoPcOHPy (4): CoIPc−2/CoIPc−3 (E1/2 = −1.13 V, I), CoIIPc−2/CoIPc−2 (E1/2 = −0.45 V, II), CoIIIPc−2/CoIIPc−2 at E1/2 = +0.21 V (IV), and CoIIIPc−1/CoIIIPc−2 (E1/2 = +1.01 V vs Ag|AgCl, V). Again III is associated with the aggregated species. Both complexes were electrodeposited on a glassy carbon electrode (GCE). For complex 3 self-assembled monolayers was also formed. The modified (CoPc-GCE) electrodes electrocatalytically detected L-cysteine at Ep = 0.62 V (3-GCE) and 0.59 V (4-GCE) vs Ag|AgCl.
- Full Text:
- Date Issued: 2011
Synthesis and evaluation of phosphonated N-heteroarylcarboxamides as DOXP-reductoisomerase (DXR) inhibitors
- Bodill, Taryn, Conibear, Anne C, Blatch, Gregory L, Lobb, Kevin A, Kaye, Perry T
- Authors: Bodill, Taryn , Conibear, Anne C , Blatch, Gregory L , Lobb, Kevin A , Kaye, Perry T
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/448939 , vital:74772 , xlink:href="https://doi.org/10.1016/j.bmc.2010.11.062"
- Description: The diethyl esters and disodium salts of a range of heteroarylcarbamoylphosphonic acids have been prepared and evaluated as analogues of the highly active DOXP-reductoisomerase (DXR) inhibitor, fosmidomycin. Computer-simulated docking studies, Saturation Transfer Difference (STD) NMR analysis and enzyme inhibition assays have been used to explore enzyme-binding and -inhibition potential, while in silico analysis of the DXR active site has highlighted the importance of including a well-parameterised metal co-factor in docking studies and has revealed the availability of an additional binding pocket to guide future drug design.
- Full Text:
- Date Issued: 2011
- Authors: Bodill, Taryn , Conibear, Anne C , Blatch, Gregory L , Lobb, Kevin A , Kaye, Perry T
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/448939 , vital:74772 , xlink:href="https://doi.org/10.1016/j.bmc.2010.11.062"
- Description: The diethyl esters and disodium salts of a range of heteroarylcarbamoylphosphonic acids have been prepared and evaluated as analogues of the highly active DOXP-reductoisomerase (DXR) inhibitor, fosmidomycin. Computer-simulated docking studies, Saturation Transfer Difference (STD) NMR analysis and enzyme inhibition assays have been used to explore enzyme-binding and -inhibition potential, while in silico analysis of the DXR active site has highlighted the importance of including a well-parameterised metal co-factor in docking studies and has revealed the availability of an additional binding pocket to guide future drug design.
- Full Text:
- Date Issued: 2011