Signposts on the road toward transformative governance: how a stronger focus on diverse values can enhance environmental policies
- Keleman, Eszter, Subramanian, Suneetha M, de Vos, Alta, Amaruzaman, Sacha, Porter-Bolland, Luciana, Islar, Mine, Kosmus, Marina, Nakangu, Barbara, Nuesiri, Emmanuel, Robles, Gabriela A, Yiu, Evonne, Emerton, Lucy, Zólyomi, Ágnes
- Authors: Keleman, Eszter , Subramanian, Suneetha M , de Vos, Alta , Amaruzaman, Sacha , Porter-Bolland, Luciana , Islar, Mine , Kosmus, Marina , Nakangu, Barbara , Nuesiri, Emmanuel , Robles, Gabriela A , Yiu, Evonne , Emerton, Lucy , Zólyomi, Ágnes
- Date: 2023
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/415927 , vital:71301 , xlink:href="https://doi.org/10.1016/j.cosust.2023.101351"
- Description: Transformative change toward sustainability is increasingly recognized as inevitable to avoid the collapse of socioecological systems. However, for a deep and system-wide transformation, governance approaches and policymaking need to be changed too. This paper discusses how a diverse value approach in environmental policymaking could be undertaken to foster transformative governance that can further lead to system-wide transitions. Based on the analysis of different policy options’ transformative potential, we argue that the more diverse values addressed by a policy instrument, the bigger its transformative potential. Weaving values into policy decision-making is possible at several junctures of the policy process, but context-specificities should always be considered, and capacities must be enhanced at all levels, both for public and private actors.
- Full Text:
- Date Issued: 2023
- Authors: Keleman, Eszter , Subramanian, Suneetha M , de Vos, Alta , Amaruzaman, Sacha , Porter-Bolland, Luciana , Islar, Mine , Kosmus, Marina , Nakangu, Barbara , Nuesiri, Emmanuel , Robles, Gabriela A , Yiu, Evonne , Emerton, Lucy , Zólyomi, Ágnes
- Date: 2023
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/415927 , vital:71301 , xlink:href="https://doi.org/10.1016/j.cosust.2023.101351"
- Description: Transformative change toward sustainability is increasingly recognized as inevitable to avoid the collapse of socioecological systems. However, for a deep and system-wide transformation, governance approaches and policymaking need to be changed too. This paper discusses how a diverse value approach in environmental policymaking could be undertaken to foster transformative governance that can further lead to system-wide transitions. Based on the analysis of different policy options’ transformative potential, we argue that the more diverse values addressed by a policy instrument, the bigger its transformative potential. Weaving values into policy decision-making is possible at several junctures of the policy process, but context-specificities should always be considered, and capacities must be enhanced at all levels, both for public and private actors.
- Full Text:
- Date Issued: 2023
A contemporary phenomenology of menstruation: Understanding the body in situation and as situation in public health interventions to address menstruation-related challenges
- Kelland, Lindsay, Paphitis, Sharli A, Macleod, Catriona I
- Authors: Kelland, Lindsay , Paphitis, Sharli A , Macleod, Catriona I
- Date: 2017
- Subjects: To be catalogued
- Language: English
- Type: text , book chapter
- Identifier: http://hdl.handle.net/10962/434293 , vital:73045 , ISBN 1879-243X , https://doi.org/10.1016/j.wsif.2017.09.004
- Description: Social science and public health research has pointed to, firstly, the challenges women face in terms of the management of menstruation and, secondly, to the negative symbolic associations made with the menstruating body. This research, however, seldom engages with philosophical issues relating to embodied subjectivity in order to explain and understand the trends noted. In this paper, we attempt to bridge the divide between feminist theory and current research on the menstruation-related challenges facing women today. We provide a feminist phenomenological account of menstruation in which women's shared bodily lived experiences of menstruation—the body as situation—are set within contexts that enable and/or restrain freedom—the body in situation. This account allows us to understand the universal and differentiated aspects of menstruation and menstrual management, thereby providing a nuanced picture of the interplay between the physical occurrence of menstruation, the symbolic associations made with menstruation, and the socio-material, historical and political conditions within which women live. Such an account, we suggest, should inform advocacy around public policy and institutional civic society that promotes the freedom of women to engage in important life projects, and ground public health interventions around menstruation related challenges.
- Full Text:
- Date Issued: 2017
- Authors: Kelland, Lindsay , Paphitis, Sharli A , Macleod, Catriona I
- Date: 2017
- Subjects: To be catalogued
- Language: English
- Type: text , book chapter
- Identifier: http://hdl.handle.net/10962/434293 , vital:73045 , ISBN 1879-243X , https://doi.org/10.1016/j.wsif.2017.09.004
- Description: Social science and public health research has pointed to, firstly, the challenges women face in terms of the management of menstruation and, secondly, to the negative symbolic associations made with the menstruating body. This research, however, seldom engages with philosophical issues relating to embodied subjectivity in order to explain and understand the trends noted. In this paper, we attempt to bridge the divide between feminist theory and current research on the menstruation-related challenges facing women today. We provide a feminist phenomenological account of menstruation in which women's shared bodily lived experiences of menstruation—the body as situation—are set within contexts that enable and/or restrain freedom—the body in situation. This account allows us to understand the universal and differentiated aspects of menstruation and menstrual management, thereby providing a nuanced picture of the interplay between the physical occurrence of menstruation, the symbolic associations made with menstruation, and the socio-material, historical and political conditions within which women live. Such an account, we suggest, should inform advocacy around public policy and institutional civic society that promotes the freedom of women to engage in important life projects, and ground public health interventions around menstruation related challenges.
- Full Text:
- Date Issued: 2017
In vitro cytotoxic effects of chemical constituents of Euphorbia grandicornis Blanc against breast cancer cells
- Kemboi, Douglas, Peter, Xolani, Langat, Moses K, Mhlanga, Richwell, Vukea, Nyeleti, de la Mare, Jo-Anne, Siwe-Noundou, Xavier, Krause, Rui W M, Tembu, Vuyelwa J
- Authors: Kemboi, Douglas , Peter, Xolani , Langat, Moses K , Mhlanga, Richwell , Vukea, Nyeleti , de la Mare, Jo-Anne , Siwe-Noundou, Xavier , Krause, Rui W M , Tembu, Vuyelwa J
- Date: 2021
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/191747 , vital:45160 , xlink:href="https://doi.org/10.1016/j.sciaf.2021.e01002"
- Description: Euphorbia grandicornis Blanc is widely utilized in traditional medicine for a variety of ailments including body pains associated with skin irritations, inflammation, and snake or scorpion bites. Compounds from E. grandicornis were characterized using spectroscopic techniques, NMR, IR, MS, and melting points and alongside the extracts were evaluated for in vitro anticancer activity against several cancer cell lines. The root extract afforded known, β-glutinol (1), β-amyrin (2), 24-methylenetirucalla-8-en-3β-ol (3), tirucalla-8,25-diene-3β,24R-diol (4), stigmasterol (5), sitosterol (6), and hexyl (E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenoate (7) based on their NMR spectroscopic data for the first report in E. grandicornis. The extracts and isolated compounds were evaluated for anticancer activities against hormone receptor-positive breast cancer (MCF-7), triple-negative breast cancer (HCC70), and non-tumorigenic mammary epithelial (MCF-12A) cell lines. The CH2Cl2 extract exhibited potent, cytotoxicity against MCF-7, HCC70, and MCF-12A cells. The aerial extract exhibited IC50 values of 1.03, 0.301, and 1.68 µg/mL, and root extract displayed IC50 values of 0.83, 0.83 and 3.98 µg/mL against MCF-7, HCC70, and MCF-12A cells respectively. The root extract thus showed selectivity for the cancer cell lines over the non-cancerous control cell line (SI = 4.80). Hexyl (E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenoate (7) showed significant activity with IC50 values of 23.41, 29.45 and 27.01 µM against MCF-7, HCC70 and MCF-12A cells respectively, suggesting non-specific cytotoxicity.
- Full Text:
- Date Issued: 2021
- Authors: Kemboi, Douglas , Peter, Xolani , Langat, Moses K , Mhlanga, Richwell , Vukea, Nyeleti , de la Mare, Jo-Anne , Siwe-Noundou, Xavier , Krause, Rui W M , Tembu, Vuyelwa J
- Date: 2021
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/191747 , vital:45160 , xlink:href="https://doi.org/10.1016/j.sciaf.2021.e01002"
- Description: Euphorbia grandicornis Blanc is widely utilized in traditional medicine for a variety of ailments including body pains associated with skin irritations, inflammation, and snake or scorpion bites. Compounds from E. grandicornis were characterized using spectroscopic techniques, NMR, IR, MS, and melting points and alongside the extracts were evaluated for in vitro anticancer activity against several cancer cell lines. The root extract afforded known, β-glutinol (1), β-amyrin (2), 24-methylenetirucalla-8-en-3β-ol (3), tirucalla-8,25-diene-3β,24R-diol (4), stigmasterol (5), sitosterol (6), and hexyl (E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenoate (7) based on their NMR spectroscopic data for the first report in E. grandicornis. The extracts and isolated compounds were evaluated for anticancer activities against hormone receptor-positive breast cancer (MCF-7), triple-negative breast cancer (HCC70), and non-tumorigenic mammary epithelial (MCF-12A) cell lines. The CH2Cl2 extract exhibited potent, cytotoxicity against MCF-7, HCC70, and MCF-12A cells. The aerial extract exhibited IC50 values of 1.03, 0.301, and 1.68 µg/mL, and root extract displayed IC50 values of 0.83, 0.83 and 3.98 µg/mL against MCF-7, HCC70, and MCF-12A cells respectively. The root extract thus showed selectivity for the cancer cell lines over the non-cancerous control cell line (SI = 4.80). Hexyl (E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenoate (7) showed significant activity with IC50 values of 23.41, 29.45 and 27.01 µM against MCF-7, HCC70 and MCF-12A cells respectively, suggesting non-specific cytotoxicity.
- Full Text:
- Date Issued: 2021
The use of experimental design in the development of an HPLC–ECD method for the analysis of captopril
- Khamanga, Sandile M, Walker, Roderick B
- Authors: Khamanga, Sandile M , Walker, Roderick B
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/184056 , vital:44163 , xlink:href="https://doi.org/10.1016/j.talanta.2010.11.025"
- Description: An accurate, sensitive and specific high performance liquid chromatography–electrochemical detection (HPLC–ECD) method that was developed and validated for captopril (CPT) is presented. Separation was achieved using a Phenomenex® Luna 5 μm (C18) column and a mobile phase comprised of phosphate buffer (adjusted to pH 3.0): acetonitrile in a ratio of 70:30 (v/v). Detection was accomplished using a full scan multi channel ESA Coulometric detector in the “oxidative-screen” mode with the upstream electrode (E1) set at +600 mV and the downstream (analytical) electrode (E2) set at +950 mV, while the potential of the guard cell was maintained at +1050 mV. The detector gain was set at 300. Experimental design using central composite design (CCD) was used to facilitate method development. Mobile phase pH, molarity and concentration of acetonitrile (ACN) were considered the critical factors to be studied to establish the retention time of CPT and cyclizine (CYC) that was used as the internal standard. Twenty experiments including centre points were undertaken and a quadratic model was derived for the retention time for CPT using the experimental data. The method was validated for linearity, accuracy, precision, limits of quantitation and detection, as per the ICH guidelines. The system was found to produce sharp and well-resolved peaks for CPT and CYC with retention times of 3.08 and 7.56 min, respectively. Linear regression analysis for the calibration curve showed a good linear relationship with a regression coefficient of 0.978 in the concentration range of 2–70 μg/mL. The linear regression equation was y = 0.0131x + 0.0275. The limits of detection (LOQ) and quantitation (LOD) were found to be 2.27 and 0.6 μg/mL, respectively. The method was used to analyze CPT in tablets. The wide range for linearity, accuracy, sensitivity, short retention time and composition of the mobile phase indicated that this method is better for the quantification of CPT than the pharmacopoeial methods.
- Full Text:
- Date Issued: 2011
- Authors: Khamanga, Sandile M , Walker, Roderick B
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/184056 , vital:44163 , xlink:href="https://doi.org/10.1016/j.talanta.2010.11.025"
- Description: An accurate, sensitive and specific high performance liquid chromatography–electrochemical detection (HPLC–ECD) method that was developed and validated for captopril (CPT) is presented. Separation was achieved using a Phenomenex® Luna 5 μm (C18) column and a mobile phase comprised of phosphate buffer (adjusted to pH 3.0): acetonitrile in a ratio of 70:30 (v/v). Detection was accomplished using a full scan multi channel ESA Coulometric detector in the “oxidative-screen” mode with the upstream electrode (E1) set at +600 mV and the downstream (analytical) electrode (E2) set at +950 mV, while the potential of the guard cell was maintained at +1050 mV. The detector gain was set at 300. Experimental design using central composite design (CCD) was used to facilitate method development. Mobile phase pH, molarity and concentration of acetonitrile (ACN) were considered the critical factors to be studied to establish the retention time of CPT and cyclizine (CYC) that was used as the internal standard. Twenty experiments including centre points were undertaken and a quadratic model was derived for the retention time for CPT using the experimental data. The method was validated for linearity, accuracy, precision, limits of quantitation and detection, as per the ICH guidelines. The system was found to produce sharp and well-resolved peaks for CPT and CYC with retention times of 3.08 and 7.56 min, respectively. Linear regression analysis for the calibration curve showed a good linear relationship with a regression coefficient of 0.978 in the concentration range of 2–70 μg/mL. The linear regression equation was y = 0.0131x + 0.0275. The limits of detection (LOQ) and quantitation (LOD) were found to be 2.27 and 0.6 μg/mL, respectively. The method was used to analyze CPT in tablets. The wide range for linearity, accuracy, sensitivity, short retention time and composition of the mobile phase indicated that this method is better for the quantification of CPT than the pharmacopoeial methods.
- Full Text:
- Date Issued: 2011
Exploring molecular insights into the interaction mechanism of cholesterol derivatives with the Mce4A: A combined spectroscopic and molecular dynamic simulation studies
- Khan, Shagufta, Khan, Faez I, Khan, Parvez, Hasan, Gulam M, Lobb, Kevin A, Islam, Asimul, Ahmad, Faizan, Hassan, M Imtaiyaz
- Authors: Khan, Shagufta , Khan, Faez I , Khan, Parvez , Hasan, Gulam M , Lobb, Kevin A , Islam, Asimul , Ahmad, Faizan , Hassan, M Imtaiyaz
- Date: 2018
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/447041 , vital:74579 , xlink:href="https://doi.org/10.1016/j.ijbiomac.2017.12.160"
- Description: Mammalian cell entry protein (Mce4A) is a member of MCE-family, and is being considered as a potential drug target of Mycobacterium tuberculosis infection because it is required for invasion and latent survival of pathogen by utilizing host's cholesterol. In the present study, we performed molecular docking followed by 100 ns MD simulation studies to understand the mechanism of interaction of Mce4A to the cholesterol derivatives and probucol. The selected ligands, cholesterol, 25-hydroxycholesterol, 5-cholesten-3β-ol-7-one and probucol bind to the predicted active site cavity of Mce4A, and complexes remain stable during entire simulation of 100 ns. In silico studies were further validated by fluorescence-binding studies to calculate actual binding affinity and number of binding site(s). The non-toxicity of all ligands was confirmed on human monocytic cell (THP1) by MTT assay. This work provides a deeper insight into the mechanism of interaction of Mce4A to cholesterol derivatives, which may be further exploited to design potential and specific inhibitors to ameliorate the Mycobacterium pathogenesis.
- Full Text:
- Date Issued: 2018
- Authors: Khan, Shagufta , Khan, Faez I , Khan, Parvez , Hasan, Gulam M , Lobb, Kevin A , Islam, Asimul , Ahmad, Faizan , Hassan, M Imtaiyaz
- Date: 2018
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/447041 , vital:74579 , xlink:href="https://doi.org/10.1016/j.ijbiomac.2017.12.160"
- Description: Mammalian cell entry protein (Mce4A) is a member of MCE-family, and is being considered as a potential drug target of Mycobacterium tuberculosis infection because it is required for invasion and latent survival of pathogen by utilizing host's cholesterol. In the present study, we performed molecular docking followed by 100 ns MD simulation studies to understand the mechanism of interaction of Mce4A to the cholesterol derivatives and probucol. The selected ligands, cholesterol, 25-hydroxycholesterol, 5-cholesten-3β-ol-7-one and probucol bind to the predicted active site cavity of Mce4A, and complexes remain stable during entire simulation of 100 ns. In silico studies were further validated by fluorescence-binding studies to calculate actual binding affinity and number of binding site(s). The non-toxicity of all ligands was confirmed on human monocytic cell (THP1) by MTT assay. This work provides a deeper insight into the mechanism of interaction of Mce4A to cholesterol derivatives, which may be further exploited to design potential and specific inhibitors to ameliorate the Mycobacterium pathogenesis.
- Full Text:
- Date Issued: 2018
Microwave synthesis and photophysics of new tetrasulfonated tin (II) macrocycles
- Khene, Samson, Ogunsipe, Abimbola, Antunes, Edith M, Nyokong, Tebello
- Authors: Khene, Samson , Ogunsipe, Abimbola , Antunes, Edith M , Nyokong, Tebello
- Date: 2007
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/281269 , vital:55708 , xlink:href="https://doi.org/10.1142/S108842460700014X"
- Description: This work reports on the microwave synthesis of tetrasulfonated tin phthalocyanine and tetrasulfonated tin α,β,γ-tetrabenzcorrole. The latter was only formed at low ratios (more than 1:8) of 4-sulfophthalic acid to urea. Both complexes are aggregated in aqueous media, but can be partly or fully disaggregated by the addition of Triton X-100. The α,β,γ-tetrabenzcorrole complex has lower triplet life times and yields, while the binding constant and quenching (of bovine serum albumin) constant are lower for α,β,γ-tetrabenzcorrole compared to tetrasulfonated tin phthalocyanine.
- Full Text:
- Date Issued: 2007
- Authors: Khene, Samson , Ogunsipe, Abimbola , Antunes, Edith M , Nyokong, Tebello
- Date: 2007
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/281269 , vital:55708 , xlink:href="https://doi.org/10.1142/S108842460700014X"
- Description: This work reports on the microwave synthesis of tetrasulfonated tin phthalocyanine and tetrasulfonated tin α,β,γ-tetrabenzcorrole. The latter was only formed at low ratios (more than 1:8) of 4-sulfophthalic acid to urea. Both complexes are aggregated in aqueous media, but can be partly or fully disaggregated by the addition of Triton X-100. The α,β,γ-tetrabenzcorrole complex has lower triplet life times and yields, while the binding constant and quenching (of bovine serum albumin) constant are lower for α,β,γ-tetrabenzcorrole compared to tetrasulfonated tin phthalocyanine.
- Full Text:
- Date Issued: 2007
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
Voltammetry and electrochemical impedance spectroscopy of gold electrodes modified with CdTe quantum dots and their conjugates with nickel tetraamino phthalocyanine
- Khene, Samson, Moeno, Sharon, Nyokong, Tebello
- Authors: Khene, Samson , Moeno, Sharon , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247187 , vital:51554 , xlink:href="https://doi.org/10.1016/j.poly.2011.06.002"
- Description: This work reports on the synthesis of conjugates of cadmium telluride quantum dots (CdTe-QDs) caped with thioglycolic acid and peripherally substituted nickel tetraamino phthalocyanine (NiTAPc) complex. The conjugates are characterized using cyclic (CV) and differential pulse (DPV) voltammetries, electrochemical impedance spectroscopy, X-ray powder diffraction, infrared spectroscopy, Raman spectroscopy, atomic force microscopy and time correlated single photon counting. CV and DPV show that NiTAPc stabilizes the CdTe QDs against oxidation to metallic products.
- Full Text:
- Date Issued: 2011
- Authors: Khene, Samson , Moeno, Sharon , Nyokong, Tebello
- Date: 2011
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/247187 , vital:51554 , xlink:href="https://doi.org/10.1016/j.poly.2011.06.002"
- Description: This work reports on the synthesis of conjugates of cadmium telluride quantum dots (CdTe-QDs) caped with thioglycolic acid and peripherally substituted nickel tetraamino phthalocyanine (NiTAPc) complex. The conjugates are characterized using cyclic (CV) and differential pulse (DPV) voltammetries, electrochemical impedance spectroscopy, X-ray powder diffraction, infrared spectroscopy, Raman spectroscopy, atomic force microscopy and time correlated single photon counting. CV and DPV show that NiTAPc stabilizes the CdTe QDs against oxidation to metallic products.
- Full Text:
- Date Issued: 2011
Interaction between nickel hydroxy phthalocyanine derivatives with p-chlorophenol
- Khene, Samson, Lobb, Kevin A, Nyokong, Tebello
- Authors: Khene, Samson , Lobb, Kevin A , Nyokong, Tebello
- Date: 2010
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/248461 , vital:51688 , xlink:href="https://doi.org/10.1016/j.electacta.2010.10.007"
- Description: In this work the interaction between peripherally (β) substituted nickel tetrahydroxyphthalocyanines (β-NiPc(OH)4 and β-Ni(O)Pc(OH)4) with p-chlorophenol is theoretically rationalised by performing calculations at B3LYP/6-31G(d) level. Density functional theory (DFT) and molecular orbital theory are used to calculate the condensed Fukui function for phthalocyanine derivatives and p-chlorophenol, in order to determine the reactive sites involved when p-chlorophenol is oxidized, and to compare theoretically predicted reactivity to experimentally determined electrocatalytic activity. Electrocatalytic activities of adsorbed NiPc derivatives: ads-α-NiPc(OH)8-OPGE (OPGE = ordinary poly graphite electrode), ads-α-NiPc(OH)4-OPGE and ads-β-NiPc(OH)4-OPGE are compared with those of the polymerized counterparts: poly-α-Ni(O)Pc(OH)8-OPGE, poly-α-NiPc(OH)4-OPGE and poly-β-NiPc(OH)4-OPGE, respectively.
- Full Text:
- Date Issued: 2010
- Authors: Khene, Samson , Lobb, Kevin A , Nyokong, Tebello
- Date: 2010
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/248461 , vital:51688 , xlink:href="https://doi.org/10.1016/j.electacta.2010.10.007"
- Description: In this work the interaction between peripherally (β) substituted nickel tetrahydroxyphthalocyanines (β-NiPc(OH)4 and β-Ni(O)Pc(OH)4) with p-chlorophenol is theoretically rationalised by performing calculations at B3LYP/6-31G(d) level. Density functional theory (DFT) and molecular orbital theory are used to calculate the condensed Fukui function for phthalocyanine derivatives and p-chlorophenol, in order to determine the reactive sites involved when p-chlorophenol is oxidized, and to compare theoretically predicted reactivity to experimentally determined electrocatalytic activity. Electrocatalytic activities of adsorbed NiPc derivatives: ads-α-NiPc(OH)8-OPGE (OPGE = ordinary poly graphite electrode), ads-α-NiPc(OH)4-OPGE and ads-β-NiPc(OH)4-OPGE are compared with those of the polymerized counterparts: poly-α-Ni(O)Pc(OH)8-OPGE, poly-α-NiPc(OH)4-OPGE and poly-β-NiPc(OH)4-OPGE, respectively.
- Full Text:
- Date Issued: 2010
Characterization of nickel tetrahydroxy phthalocyanine complexes and the electrocatalytic oxidation of 4-chlorophenol
- Khene, Samson M, Lobb, Kevin A, Nyokong, Tebello
- Authors: Khene, Samson M , Lobb, Kevin A , Nyokong, Tebello
- Date: 2009
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/263308 , vital:53616 , xlink:href="https://doi.org/10.1016/j.ica.2009.08.019"
- Description: This work reports on the use of nickel(II) tetrahydroxy (NiPc(OH)4) and (poly-Ni(OH)Pc(OH)4) phthalocyanine complexes as films on ordinary poly graphite electrode (OPGE) for the electrochemical oxidation of 4-chlorophenol (4-CP). The NiPc(OH)4 film was electrotransformed to Ni(OH)Pc(OH)4 film in aqueous 0.1 M NaOH solution to the ‘O–Ni–O oxo’ bridge form. The result showed that the Ni(OH)Pc(OH)4 film on OPGE was more electroactive in terms of increase in current and less catalytic in terms of potential compared to the adsorbed NiPc(OH)4 on OPGE. The reactivity of the two molecules was explained by theoretical calculations. The energies of the frontier orbitals of NiPc(OH)4, Ni(OH)Pc(OH)4 and 4-chlorophenol were calculated using density functional theory (DFT) method. The inter molecular hardness (η) and donor–acceptor hardness (ηDA) of Ni(OH)Pc(OH)4, NiPc(OH)4, Ni(OH)Pc(OH)4/4-chlorophenol and NiPc(OH)4/4-chlorophenol were estimated. The Ni(OH)Pc(OH)4, showed stronger interaction with 4-chlorophenol than NiPc(OH)4. DFT method was also used to model IR and Raman spectrum of H2Pc(OH)4 and NiPc(OH)4.
- Full Text:
- Date Issued: 2009
- Authors: Khene, Samson M , Lobb, Kevin A , Nyokong, Tebello
- Date: 2009
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/263308 , vital:53616 , xlink:href="https://doi.org/10.1016/j.ica.2009.08.019"
- Description: This work reports on the use of nickel(II) tetrahydroxy (NiPc(OH)4) and (poly-Ni(OH)Pc(OH)4) phthalocyanine complexes as films on ordinary poly graphite electrode (OPGE) for the electrochemical oxidation of 4-chlorophenol (4-CP). The NiPc(OH)4 film was electrotransformed to Ni(OH)Pc(OH)4 film in aqueous 0.1 M NaOH solution to the ‘O–Ni–O oxo’ bridge form. The result showed that the Ni(OH)Pc(OH)4 film on OPGE was more electroactive in terms of increase in current and less catalytic in terms of potential compared to the adsorbed NiPc(OH)4 on OPGE. The reactivity of the two molecules was explained by theoretical calculations. The energies of the frontier orbitals of NiPc(OH)4, Ni(OH)Pc(OH)4 and 4-chlorophenol were calculated using density functional theory (DFT) method. The inter molecular hardness (η) and donor–acceptor hardness (ηDA) of Ni(OH)Pc(OH)4, NiPc(OH)4, Ni(OH)Pc(OH)4/4-chlorophenol and NiPc(OH)4/4-chlorophenol were estimated. The Ni(OH)Pc(OH)4, showed stronger interaction with 4-chlorophenol than NiPc(OH)4. DFT method was also used to model IR and Raman spectrum of H2Pc(OH)4 and NiPc(OH)4.
- Full Text:
- Date Issued: 2009
Electrochemical and photophysical characterization of non-peripherally-octaalkyl substituted dichlorotin (IV) phthalocyanine and tetrabenzotriazaporphyrin compounds
- Khene, Samson M, Cammidge, Andrew N, Cook, Michael J, Nyokong, Tebello
- Authors: Khene, Samson M , Cammidge, Andrew N , Cook, Michael J , Nyokong, Tebello
- Date: 2007
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/271216 , vital:54522 , xlink:href="https://doi.org/10.1142/S1088424607000886"
- Description: Three non-peripherally substituted tin(IV) macrocylic compounds, octahexylphthalocyaninato dichlorotin(IV) (3a), octahexyltetrabenzo-5,10,15- triazaporphyrinato dichlorotin(IV) (3b) and octadecylphthalocyaninato dichlorotin(IV) (3c) were synthesized and their photophysical and electrochemical behavior studied. Complex 3b, containing a CH group in place of one of the aza nitrogen atoms of the phthalocyanine core, shows a split Q-band due to its lower symmetry. The triplet state quantum yields were found to be lower than would be expected on the basis of the heavy atom effect of tin as the central metal for phthalocyanine derivatives (3a and 3c). In contrast, 3b shows a triplet quantum yield ΦT = 0.78. The triplet state lifetimes were solvent dependent, and were higher in tetrahydrofuran than in toluene. Cyclic voltammetry and spectroelectrochemistry of the complexes revealed only ring-based redox processes.
- Full Text:
- Date Issued: 2007
- Authors: Khene, Samson M , Cammidge, Andrew N , Cook, Michael J , Nyokong, Tebello
- Date: 2007
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/271216 , vital:54522 , xlink:href="https://doi.org/10.1142/S1088424607000886"
- Description: Three non-peripherally substituted tin(IV) macrocylic compounds, octahexylphthalocyaninato dichlorotin(IV) (3a), octahexyltetrabenzo-5,10,15- triazaporphyrinato dichlorotin(IV) (3b) and octadecylphthalocyaninato dichlorotin(IV) (3c) were synthesized and their photophysical and electrochemical behavior studied. Complex 3b, containing a CH group in place of one of the aza nitrogen atoms of the phthalocyanine core, shows a split Q-band due to its lower symmetry. The triplet state quantum yields were found to be lower than would be expected on the basis of the heavy atom effect of tin as the central metal for phthalocyanine derivatives (3a and 3c). In contrast, 3b shows a triplet quantum yield ΦT = 0.78. The triplet state lifetimes were solvent dependent, and were higher in tetrahydrofuran than in toluene. Cyclic voltammetry and spectroelectrochemistry of the complexes revealed only ring-based redox processes.
- Full Text:
- Date Issued: 2007
Synthesis, electrochemical characterization of tetra-and octa-substituted dodecyl-mercapto tin phthalocyanines in solution and as self-assembled monolayers
- Khene, Samson M, Geraldo, Daniela A, Togo, Chamunorwa A, Limson, Janice L, Nyokong, Tebello
- Authors: Khene, Samson M , Geraldo, Daniela A , Togo, Chamunorwa A , Limson, Janice L , Nyokong, Tebello
- Date: 2008
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/264541 , vital:53743 , xlink:href="https://doi.org/10.1016/j.electacta.2008.08.018"
- Description: Non-peripherally (α) tetra- (9) and octa-(7) substituted dodecyl-mercapto tin(IV) phthalocyanines were synthesized and their electrochemical behavior studied. Cyclic voltammetry and spectroelectrochemistry show ring-based reductions for 7 and 9, the former shows two ring oxidations, while the latter shows only one ring-based oxidation. The adsorption kinetics of (7) and (9) on gold electrode were investigated by electrochemical impedance spectroscopy (EIS). The equilibrium constant (K) for the adsorption and the Gibbs free energy (ΔGads) of the SAMs were evaluated based on the Frumkin isotherm.
- Full Text:
- Date Issued: 2008
- Authors: Khene, Samson M , Geraldo, Daniela A , Togo, Chamunorwa A , Limson, Janice L , Nyokong, Tebello
- Date: 2008
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/264541 , vital:53743 , xlink:href="https://doi.org/10.1016/j.electacta.2008.08.018"
- Description: Non-peripherally (α) tetra- (9) and octa-(7) substituted dodecyl-mercapto tin(IV) phthalocyanines were synthesized and their electrochemical behavior studied. Cyclic voltammetry and spectroelectrochemistry show ring-based reductions for 7 and 9, the former shows two ring oxidations, while the latter shows only one ring-based oxidation. The adsorption kinetics of (7) and (9) on gold electrode were investigated by electrochemical impedance spectroscopy (EIS). The equilibrium constant (K) for the adsorption and the Gibbs free energy (ΔGads) of the SAMs were evaluated based on the Frumkin isotherm.
- Full Text:
- Date Issued: 2008
Photocatalytic behaviour of zinc tetraamino phthalocyanine-silver nanoparticles immobilized on chitosan beads
- Khoza, Phindile, Nyokong, Tebello
- Authors: Khoza, Phindile , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7250 , http://hdl.handle.net/10962/d1020256
- Description: Photocatalytic degradation of Rhodamine 6G using unconjugated zinc tetraamino phthalocyanine (ZnTAPc) or when conjugated to Ag nanoparticles (ZnTAPc–AgNPs) is reported. Upon conjugating ZnTAPc to silver nanoparticles, the singlet oxygen production of the phthalocyanine was slightly increased. ZnTAPc and ZnTAPc–AgNPs were immobilized onto chitosan beads for ease of recovery after photocatalysis. Chitosan beads were characterized by FTIR, XRD and TGA. The photodegradation of Rhodamine 6G was used to evaluate the efficiency of the immobilized photocatalysts. In the presence of AgNPs, the photodegradation of Rhodamine 6G was enhanced. The apparent rates (k) were found to be 8.51 × 10−8 and 1.61 × 10−7 mol L−1 min−1 for chitosan supported ZnTAPc or ZnTAPc–AgNPs, respectively. The observation of good photocatalytic activity of the ZnTAPc when immobilized on chitosan proves the uncompromised efficiency of the photocatalysts even when confined in beads, showing great potential for the functionalized beads as heterogeneous catalysts. , Original publication is available at http://dx.doi.org/10.1016/j.molcata.2015.01.017
- Full Text: false
- Authors: Khoza, Phindile , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7250 , http://hdl.handle.net/10962/d1020256
- Description: Photocatalytic degradation of Rhodamine 6G using unconjugated zinc tetraamino phthalocyanine (ZnTAPc) or when conjugated to Ag nanoparticles (ZnTAPc–AgNPs) is reported. Upon conjugating ZnTAPc to silver nanoparticles, the singlet oxygen production of the phthalocyanine was slightly increased. ZnTAPc and ZnTAPc–AgNPs were immobilized onto chitosan beads for ease of recovery after photocatalysis. Chitosan beads were characterized by FTIR, XRD and TGA. The photodegradation of Rhodamine 6G was used to evaluate the efficiency of the immobilized photocatalysts. In the presence of AgNPs, the photodegradation of Rhodamine 6G was enhanced. The apparent rates (k) were found to be 8.51 × 10−8 and 1.61 × 10−7 mol L−1 min−1 for chitosan supported ZnTAPc or ZnTAPc–AgNPs, respectively. The observation of good photocatalytic activity of the ZnTAPc when immobilized on chitosan proves the uncompromised efficiency of the photocatalysts even when confined in beads, showing great potential for the functionalized beads as heterogeneous catalysts. , Original publication is available at http://dx.doi.org/10.1016/j.molcata.2015.01.017
- Full Text: false
Photocatalytic behaviour of zinc tetraamino phthalocyanine-silver nanoparticles immobilized on chitosan beads
- Khoza, Phindile, Nyokong, Tebello
- Authors: Khoza, Phindile , Nyokong, Tebello
- Date: 2015
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/189468 , vital:44849 , xlink:href="https://doi.org/10.1016/j.molcata.2015.01.017"
- Description: Photocatalytic degradation of Rhodamine 6G using unconjugated zinc tetraamino phthalocyanine (ZnTAPc) or when conjugated to Ag nanoparticles (ZnTAPc–AgNPs) is reported. Upon conjugating ZnTAPc to silver nanoparticles, the singlet oxygen production of the phthalocyanine was slightly increased. ZnTAPc and ZnTAPc–AgNPs were immobilized onto chitosan beads for ease of recovery after photocatalysis. Chitosan beads were characterized by FTIR, XRD and TGA. The photodegradation of Rhodamine 6G was used to evaluate the efficiency of the immobilized photocatalysts. In the presence of AgNPs, the photodegradation of Rhodamine 6G was enhanced. The apparent rates (k) were found to be 8.51 × 10−8 and 1.61 × 10−7 mol L−1 min−1 for chitosan supported ZnTAPc or ZnTAPc–AgNPs, respectively. The observation of good photocatalytic activity of the ZnTAPc when immobilized on chitosan proves the uncompromised efficiency of the photocatalysts even when confined in beads, showing great potential for the functionalized beads as heterogeneous catalysts.
- Full Text:
- Date Issued: 2015
- Authors: Khoza, Phindile , Nyokong, Tebello
- Date: 2015
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/189468 , vital:44849 , xlink:href="https://doi.org/10.1016/j.molcata.2015.01.017"
- Description: Photocatalytic degradation of Rhodamine 6G using unconjugated zinc tetraamino phthalocyanine (ZnTAPc) or when conjugated to Ag nanoparticles (ZnTAPc–AgNPs) is reported. Upon conjugating ZnTAPc to silver nanoparticles, the singlet oxygen production of the phthalocyanine was slightly increased. ZnTAPc and ZnTAPc–AgNPs were immobilized onto chitosan beads for ease of recovery after photocatalysis. Chitosan beads were characterized by FTIR, XRD and TGA. The photodegradation of Rhodamine 6G was used to evaluate the efficiency of the immobilized photocatalysts. In the presence of AgNPs, the photodegradation of Rhodamine 6G was enhanced. The apparent rates (k) were found to be 8.51 × 10−8 and 1.61 × 10−7 mol L−1 min−1 for chitosan supported ZnTAPc or ZnTAPc–AgNPs, respectively. The observation of good photocatalytic activity of the ZnTAPc when immobilized on chitosan proves the uncompromised efficiency of the photocatalysts even when confined in beads, showing great potential for the functionalized beads as heterogeneous catalysts.
- Full Text:
- Date Issued: 2015
Photocatalytic behavior of phthalocyanine-silver nanoparticle conjugates supported on polystyrene fibers
- Khoza, Phindile, Nyokong, Tebello
- Authors: Khoza, Phindile , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7317 , http://hdl.handle.net/10962/d1020561
- Description: Herein, carbazole derivatized non-peripheral (1,(4)-tetra(carbazol-2-yloxy)phthalocyaninatozinc(II), 3-TCbZnPc) and peripheral (2,(3)-tetra(carbazol-2-yloxy)phthalocyaninato zinc(II), 4-TCbZnPc) are conjugated to silver nanoparticles and their photochemical and photophysical behavior are reported. The presence of silver nanoparticles resulted in reduced fluorescence, and increased triplet and singlet oxygen quantum yields. The conjugates were further electrospun into polystyrene fibers, and employed for the photodegradation of methyl orange. The photodegradation of methyl orange using all functionalized fibers followed first order kinetics, and was faster when the conjugates with silver nanoparticles were used. The non-peripherally substituted 3-TCbZnPc gave better photocatalytic activity compared to its peripherally substituted counterpart (4-TCbZnPc). The hybrid electrospun fibers provide great potential as active photocatalysts for degrading organic pollutants. , Online publication is available at http://dx.doi.org/10.1016/j.molcata.2014.07.031
- Full Text: false
- Authors: Khoza, Phindile , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7317 , http://hdl.handle.net/10962/d1020561
- Description: Herein, carbazole derivatized non-peripheral (1,(4)-tetra(carbazol-2-yloxy)phthalocyaninatozinc(II), 3-TCbZnPc) and peripheral (2,(3)-tetra(carbazol-2-yloxy)phthalocyaninato zinc(II), 4-TCbZnPc) are conjugated to silver nanoparticles and their photochemical and photophysical behavior are reported. The presence of silver nanoparticles resulted in reduced fluorescence, and increased triplet and singlet oxygen quantum yields. The conjugates were further electrospun into polystyrene fibers, and employed for the photodegradation of methyl orange. The photodegradation of methyl orange using all functionalized fibers followed first order kinetics, and was faster when the conjugates with silver nanoparticles were used. The non-peripherally substituted 3-TCbZnPc gave better photocatalytic activity compared to its peripherally substituted counterpart (4-TCbZnPc). The hybrid electrospun fibers provide great potential as active photocatalysts for degrading organic pollutants. , Online publication is available at http://dx.doi.org/10.1016/j.molcata.2014.07.031
- Full Text: false
Photophysichochemical behavior of carbazole derivatized zinc phthalocyanine in the presence of ZnO microparticles and when embedded in electrospun fibers
- Khoza, Phindile, Antunes, Edith M, Nyokong, Tebello
- Authors: Khoza, Phindile , Antunes, Edith M , Nyokong, Tebello
- Date: 2014
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/193860 , vital:45400 , xlink:href="https://doi.org/10.1016/j.dyepig.2013.12.019"
- Description: The synthesis of a zinc phthalocyanine complex tetrasubstituted with carbazole functionality at the peripheral position (complex 4) is reported. The singlet oxygen quantum yield of the complex was found to be 0.83 in dimethylformamide (DMF). The complex was subsequently conjugated to zinc oxide microparticles (ZnOMPs), the conjugation (formation of the amide bond) was confirmed by IR spectroscopy. The presence of ZnOMPs was found to reduce the singlet oxygen produced (ΦΔ = 0.63) in DMF. Polystyrene electrospun fibers of complex 4 alone and its conjugate to ZnOMPs were found to be thermally stable. The singlet oxygen quantum yield of the modified electrospun fibers was determined in aqueous media with ADMA as a singlet oxygen quencher and were 0.25 and 0.20 for complex 4 and 4-ZnOMPs embedded in fibers, respectively.
- Full Text:
- Date Issued: 2014
- Authors: Khoza, Phindile , Antunes, Edith M , Nyokong, Tebello
- Date: 2014
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/193860 , vital:45400 , xlink:href="https://doi.org/10.1016/j.dyepig.2013.12.019"
- Description: The synthesis of a zinc phthalocyanine complex tetrasubstituted with carbazole functionality at the peripheral position (complex 4) is reported. The singlet oxygen quantum yield of the complex was found to be 0.83 in dimethylformamide (DMF). The complex was subsequently conjugated to zinc oxide microparticles (ZnOMPs), the conjugation (formation of the amide bond) was confirmed by IR spectroscopy. The presence of ZnOMPs was found to reduce the singlet oxygen produced (ΦΔ = 0.63) in DMF. Polystyrene electrospun fibers of complex 4 alone and its conjugate to ZnOMPs were found to be thermally stable. The singlet oxygen quantum yield of the modified electrospun fibers was determined in aqueous media with ADMA as a singlet oxygen quencher and were 0.25 and 0.20 for complex 4 and 4-ZnOMPs embedded in fibers, respectively.
- Full Text:
- Date Issued: 2014
Synthesis and photophysicochemical studies of a water soluble conjugate between folic acid and zinc tetraaminophthalocyanine
- Khoza, Phindile, Antunes, Edith M, Chen, Ji-Yao, Nyokong, Tebello
- Authors: Khoza, Phindile , Antunes, Edith M , Chen, Ji-Yao , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/242142 , vital:51005 , xlink:href="https://doi.org/10.1016/j.jlumin.2012.06.048"
- Description: This work reports on the synthesis of zinc tetraaminophthalocyanine (ZnTAPc) functionalized with folic acid (FA), forming ZnTAPcFA. The conjugate between FA and ZnTAPc was soluble in water whereas ZnTAPc alone is not. The structure of ZnTAPcFA conjugate was elucidated by 1H NMR, MALDI-TOF mass and FTIR spectra. Photophysical and photochemical studies of ZnTAPcFA were conducted in DMSO. The increase in fluorescence quantum yield of the conjugate was accompanied by a decrease in the triplet and singlet oxygen quantum yields. The changes in triplet quantum and singlet oxygen quantum yields were marginal when ZnTAPc was simply mixed with FA without a chemical bond.
- Full Text:
- Date Issued: 2013
- Authors: Khoza, Phindile , Antunes, Edith M , Chen, Ji-Yao , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/242142 , vital:51005 , xlink:href="https://doi.org/10.1016/j.jlumin.2012.06.048"
- Description: This work reports on the synthesis of zinc tetraaminophthalocyanine (ZnTAPc) functionalized with folic acid (FA), forming ZnTAPcFA. The conjugate between FA and ZnTAPc was soluble in water whereas ZnTAPc alone is not. The structure of ZnTAPcFA conjugate was elucidated by 1H NMR, MALDI-TOF mass and FTIR spectra. Photophysical and photochemical studies of ZnTAPcFA were conducted in DMSO. The increase in fluorescence quantum yield of the conjugate was accompanied by a decrease in the triplet and singlet oxygen quantum yields. The changes in triplet quantum and singlet oxygen quantum yields were marginal when ZnTAPc was simply mixed with FA without a chemical bond.
- Full Text:
- Date Issued: 2013
Synthesis and photophysicochemical properties of zinc phthalocyanine derivatized with benzothiazole or carbazole photosensitizers
- Khoza, Phindile, Antunes, Edith M, Nyokong, Tebello
- Authors: Khoza, Phindile , Antunes, Edith M , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241728 , vital:50964 , xlink:href="https://doi.org/10.1016/j.poly.2013.05.046"
- Description: The synthesis of new zinc phthalocyanine complexes containing 3-(2-benzothiazol-2-yloxy) (complex 3) and 3-(carbazol-2-yloxy) (complex 4) substituents at the non-peripheral positions are reported. The new compounds were characterized by elemental analysis, FT-IR, 1H NMR, mass spectrometry and UV–Vis spectroscopy. The effects of carbazole and benzothiazole substitutents on the photophysical and photochemical parameters of ZnPc are reported. These new phthalocyanines are non-aggregated in common solvents and show improved photophysicochemical properties. The 3-(2-benzothiazol-2-yloxy) substituted complex showed the longest triplet lifetime ever reported for a zinc phthalocyanine (1.7 ms).
- Full Text:
- Date Issued: 2013
- Authors: Khoza, Phindile , Antunes, Edith M , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241728 , vital:50964 , xlink:href="https://doi.org/10.1016/j.poly.2013.05.046"
- Description: The synthesis of new zinc phthalocyanine complexes containing 3-(2-benzothiazol-2-yloxy) (complex 3) and 3-(carbazol-2-yloxy) (complex 4) substituents at the non-peripheral positions are reported. The new compounds were characterized by elemental analysis, FT-IR, 1H NMR, mass spectrometry and UV–Vis spectroscopy. The effects of carbazole and benzothiazole substitutents on the photophysical and photochemical parameters of ZnPc are reported. These new phthalocyanines are non-aggregated in common solvents and show improved photophysicochemical properties. The 3-(2-benzothiazol-2-yloxy) substituted complex showed the longest triplet lifetime ever reported for a zinc phthalocyanine (1.7 ms).
- Full Text:
- Date Issued: 2013
Photophysichochemical behavior of carbazole derivatized zinc phthalocyanine in the presence of ZnO microparticles and when embedded in electrospun fibers
- Khoza, Phindile, Antunes, Edith M, Nyokong, Tebello
- Authors: Khoza, Phindile , Antunes, Edith M , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7303 , http://hdl.handle.net/10962/d1020380
- Description: The synthesis of a zinc phthalocyanine complex tetrasubstituted with carbazole functionality at the peripheral position (complex 4) is reported. The singlet oxygen quantum yield of the complex was found to be 0.83 in dimethylformamide (DMF). The complex was subsequently conjugated to zinc oxide microparticles (ZnOMPs), the conjugation (formation of the amide bond) was confirmed by IR spectroscopy. The presence of ZnOMPs was found to reduce the singlet oxygen produced (ΦΔ = 0.63) in DMF. Polystyrene electrospun fibers of complex 4 alone and its conjugate to ZnOMPs were found to be thermally stable. The singlet oxygen quantum yield of the modified electrospun fibers was determined in aqueous media with ADMA as a singlet oxygen quencher and were 0.25 and 0.20 for complex 4 and 4-ZnOMPs embedded in fibers, respectively. , Original publication is available at http://dx.doi.org/10.1016/j.dyepig.2013.12.019
- Full Text: false
- Authors: Khoza, Phindile , Antunes, Edith M , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7303 , http://hdl.handle.net/10962/d1020380
- Description: The synthesis of a zinc phthalocyanine complex tetrasubstituted with carbazole functionality at the peripheral position (complex 4) is reported. The singlet oxygen quantum yield of the complex was found to be 0.83 in dimethylformamide (DMF). The complex was subsequently conjugated to zinc oxide microparticles (ZnOMPs), the conjugation (formation of the amide bond) was confirmed by IR spectroscopy. The presence of ZnOMPs was found to reduce the singlet oxygen produced (ΦΔ = 0.63) in DMF. Polystyrene electrospun fibers of complex 4 alone and its conjugate to ZnOMPs were found to be thermally stable. The singlet oxygen quantum yield of the modified electrospun fibers was determined in aqueous media with ADMA as a singlet oxygen quencher and were 0.25 and 0.20 for complex 4 and 4-ZnOMPs embedded in fibers, respectively. , Original publication is available at http://dx.doi.org/10.1016/j.dyepig.2013.12.019
- Full Text: false
Photocatalytic behavior of phthalocyanine-silver nanoparticle conjugates supported on polystyrene fibers
- Khozile, Phindile, Nyokong, Tebello
- Authors: Khozile, Phindile , Nyokong, Tebello
- Date: 2014
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/189909 , vital:44946 , xlink:href="https://doi.org/10.1016/j.molcata.2014.07.031"
- Description: Herein, carbazole derivatized non-peripheral (1,(4)-tetra(carbazol-2-yloxy)phthalocyaninatozinc(II), 3-TCbZnPc) and peripheral (2,(3)-tetra(carbazol-2-yloxy)phthalocyaninato zinc(II), 4-TCbZnPc) are conjugated to silver nanoparticles and their photochemical and photophysical behavior are reported. The presence of silver nanoparticles resulted in reduced fluorescence, and increased triplet and singlet oxygen quantum yields. The conjugates were further electrospun into polystyrene fibers, and employed for the photodegradation of methyl orange. The photodegradation of methyl orange using all functionalized fibers followed first order kinetics, and was faster when the conjugates with silver nanoparticles were used. The non-peripherally substituted 3-TCbZnPc gave better photocatalytic activity compared to its peripherally substituted counterpart (4-TCbZnPc). The hybrid electrospun fibers provide great potential as active photocatalysts for degrading organic pollutants.
- Full Text:
- Date Issued: 2014
- Authors: Khozile, Phindile , Nyokong, Tebello
- Date: 2014
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/189909 , vital:44946 , xlink:href="https://doi.org/10.1016/j.molcata.2014.07.031"
- Description: Herein, carbazole derivatized non-peripheral (1,(4)-tetra(carbazol-2-yloxy)phthalocyaninatozinc(II), 3-TCbZnPc) and peripheral (2,(3)-tetra(carbazol-2-yloxy)phthalocyaninato zinc(II), 4-TCbZnPc) are conjugated to silver nanoparticles and their photochemical and photophysical behavior are reported. The presence of silver nanoparticles resulted in reduced fluorescence, and increased triplet and singlet oxygen quantum yields. The conjugates were further electrospun into polystyrene fibers, and employed for the photodegradation of methyl orange. The photodegradation of methyl orange using all functionalized fibers followed first order kinetics, and was faster when the conjugates with silver nanoparticles were used. The non-peripherally substituted 3-TCbZnPc gave better photocatalytic activity compared to its peripherally substituted counterpart (4-TCbZnPc). The hybrid electrospun fibers provide great potential as active photocatalysts for degrading organic pollutants.
- Full Text:
- Date Issued: 2014