Acetophenone substituted phthalocyanines and their graphene quantum dots conjugates as photosensitizers for photodynamic antimicrobial chemotherapy against Staphylococcus aureus
- Openda, Yolande I, Sen, Pinar, Managa, Muthumuni, Nyokong, Tebello
- Authors: Openda, Yolande I , Sen, Pinar , Managa, Muthumuni , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/186507 , vital:44506 , xlink:href="https://doi.org/10.1016/j.pdpdt.2019.101607"
- Description: This work reports on the synthesis and characterization of novel acetophenone substituted phthalocyanines along with the self-assembled nanoconjugates formed via π-π stacking interaction between the synthesized unmetalated (2), zinc (3) and indium (4) phthalocyanines and graphene quantum dots (GQDs) to form 2@GQDs, 3@GQDs and 4@GQDs. The complexes and conjugates exhibited high singlet oxygen ranging from 0.20 to 0.79 in DMSO for Pcs and nanoconjugates where in all cases, the indium complexes showed the highest singlet oxygen quantum yields. The photodynamic antimicrobial chemotherapy activity of both phthalocyanines and nanoconjugates were tested against Staphylococcus aureus. 4@GQDs was found to be highly effective causing a 9.68 log reduction of the bacteria at 10 μM (based on Pc) when compared to 3.77 log reduction of 3@GQDs.
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- Authors: Openda, Yolande I , Sen, Pinar , Managa, Muthumuni , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/186507 , vital:44506 , xlink:href="https://doi.org/10.1016/j.pdpdt.2019.101607"
- Description: This work reports on the synthesis and characterization of novel acetophenone substituted phthalocyanines along with the self-assembled nanoconjugates formed via π-π stacking interaction between the synthesized unmetalated (2), zinc (3) and indium (4) phthalocyanines and graphene quantum dots (GQDs) to form 2@GQDs, 3@GQDs and 4@GQDs. The complexes and conjugates exhibited high singlet oxygen ranging from 0.20 to 0.79 in DMSO for Pcs and nanoconjugates where in all cases, the indium complexes showed the highest singlet oxygen quantum yields. The photodynamic antimicrobial chemotherapy activity of both phthalocyanines and nanoconjugates were tested against Staphylococcus aureus. 4@GQDs was found to be highly effective causing a 9.68 log reduction of the bacteria at 10 μM (based on Pc) when compared to 3.77 log reduction of 3@GQDs.
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Development of manganese phthalocyanine decorated with silver nanoparticles nanocomposite for improved electrocatalytic oxidation of hydrazine:
- Mpeta, Lekhetho S, Sen, Pinar, Nyokong, Tebello
- Authors: Mpeta, Lekhetho S , Sen, Pinar , Nyokong, Tebello
- Date: 2020
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/148472 , vital:38742 , https://doi.org/10.1016/j.jelechem.2020.114173
- Description: In this study we report on the synthesis of tetrakis [4-(4-(5-chloro-1H-benzo [d]imidazol-2-yl) phenoxy phthalocyaninato] manganese (III) chloride (MnPc). The MnPc was first used to modify a glassy carbon electrode, followed by the growth of silver nanoparticles (AgNPs) onto the MnPc modified electrode to form MnPc-AgNPs modified electrode. The modified electrode was characterized using cydic voltammetry, chronoamperometry, scanning electrochemical microscopy and electrochemical impedance spectroscopy. The modified MnPc-AgNPs electrode was employed for the detection of hydrazine. The MnPc-AgNPs gave better current responses for electrooxidation of hydrazine relative to MnPc and AgNPs, individually. The catalytic rate constant was 1.90 x 10(5 )M(-1) S-1, with the detection limit (LoD) of 2.42 pM (using 3 sigma notation), and sensitivity of 61.56 mu A mM(-1), for MnPc-AgNPs. (C) 2020 Elsevier B.V. All rights reserved.
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- Authors: Mpeta, Lekhetho S , Sen, Pinar , Nyokong, Tebello
- Date: 2020
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/148472 , vital:38742 , https://doi.org/10.1016/j.jelechem.2020.114173
- Description: In this study we report on the synthesis of tetrakis [4-(4-(5-chloro-1H-benzo [d]imidazol-2-yl) phenoxy phthalocyaninato] manganese (III) chloride (MnPc). The MnPc was first used to modify a glassy carbon electrode, followed by the growth of silver nanoparticles (AgNPs) onto the MnPc modified electrode to form MnPc-AgNPs modified electrode. The modified electrode was characterized using cydic voltammetry, chronoamperometry, scanning electrochemical microscopy and electrochemical impedance spectroscopy. The modified MnPc-AgNPs electrode was employed for the detection of hydrazine. The MnPc-AgNPs gave better current responses for electrooxidation of hydrazine relative to MnPc and AgNPs, individually. The catalytic rate constant was 1.90 x 10(5 )M(-1) S-1, with the detection limit (LoD) of 2.42 pM (using 3 sigma notation), and sensitivity of 61.56 mu A mM(-1), for MnPc-AgNPs. (C) 2020 Elsevier B.V. All rights reserved.
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Direct nonlinear optical absorption measurements of asymmetrical zinc (II) phthalocyanine when covalently linked to semiconductor quantum dots
- Mgidlana, Sithi, Sen, Pinar, Nyokong, Tebello
- Authors: Mgidlana, Sithi , Sen, Pinar , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/186056 , vital:44459 , xlink:href="https://doi.org/10.1016/j.molstruc.2020.128729"
- Description: We report on nonlinear optical properties of tris[(4-tert-butyl)-2-thio (phenyl)acetic acid (1) and tris(dimethyl-5-(3,4-phenoxy) isophthalate (2) phthalocyaninato zinc (II) complexes. The synthesized complexes were covalently conjugated to glutathione-capped CdTe/ZnSe/ZnO quantum dots. We observed an increase in triplet quantum yield with corresponding decrease in fluorescence quantum yield of conjugates compared to Pc complexes alone. Z-scan technique was employed to experimentally test the nonlinear optical response of complexes and nanoconjugates in solution at laser excitation wavelength of 532 nm with 7 ns pulse. Nonlinear absorption coefficient, third-order optical susceptibility and optical limiting threshold of the materials were obtained from the Z-scan data. The nonlinear absorption parameters improved in the presence of CdTe/ZnSe/ZnO, with 1 and 1-CdTe/ZnSe/ZnO, giving the best results due to the presence of electron donating substituents.
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- Authors: Mgidlana, Sithi , Sen, Pinar , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/186056 , vital:44459 , xlink:href="https://doi.org/10.1016/j.molstruc.2020.128729"
- Description: We report on nonlinear optical properties of tris[(4-tert-butyl)-2-thio (phenyl)acetic acid (1) and tris(dimethyl-5-(3,4-phenoxy) isophthalate (2) phthalocyaninato zinc (II) complexes. The synthesized complexes were covalently conjugated to glutathione-capped CdTe/ZnSe/ZnO quantum dots. We observed an increase in triplet quantum yield with corresponding decrease in fluorescence quantum yield of conjugates compared to Pc complexes alone. Z-scan technique was employed to experimentally test the nonlinear optical response of complexes and nanoconjugates in solution at laser excitation wavelength of 532 nm with 7 ns pulse. Nonlinear absorption coefficient, third-order optical susceptibility and optical limiting threshold of the materials were obtained from the Z-scan data. The nonlinear absorption parameters improved in the presence of CdTe/ZnSe/ZnO, with 1 and 1-CdTe/ZnSe/ZnO, giving the best results due to the presence of electron donating substituents.
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Enhanced Light-Driven Antimicrobial Activity of Cationic Poly (oxanorbornene) s by Phthalocyanine Incorporation into Polymer as Pendants
- Ahmetali, Erem, Sen, Pinar, Süer, N Ceren, Aksu, Burak, Nyokong, Tebello, Eren, Tarik, Sener, Kasim M
- Authors: Ahmetali, Erem , Sen, Pinar , Süer, N Ceren , Aksu, Burak , Nyokong, Tebello , Eren, Tarik , Sener, Kasim M
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/185976 , vital:44453 , xlink:href=" https://doi.org/10.1002/macp.202000386"
- Description: Amphiphilic poly(oxanorbornene)s are promising synthetic polymers that mimic the structural properties and antimicrobial functions of naturally occurring antimicrobial peptides. Here, poly(oxanorbornene)s bearing pendant zinc(II) phthalocyanine and triphenyl(ethyl) phosphonium functionalities are synthesized by ring-opening metathesis polymerization (ROMP). Fluorescence, singlet oxygen and triplet quantum yields of polymers are measured in dimethyl sulfoxide and aqueous medium. The singlet oxygen quantum yields of copolymers with the highest triphenyl and triethyl phosphonium content are found to be 0.29 and 0.41, respectively. Then, antimicrobial activities of polymers against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) are investigated under both dark and light conditions. Synergistic effect of zinc(II) phthalocyanine and phosphonium-containing poly(oxanorbornene) is observed that the conjugate possessing the most triphenyl phosphonium side chains has the highest activity under light against both gram-positive and gram-negative bacterial strains after 80 min irradiation, reducing the survival of E. coli or S. aureus by 99.9999%. Hemolytic concentrations of the copolymers are found between 8 and 512 µg mL−1. Scanning electron microscopy (SEM) proves that the bacteria membrane deforms after contacting with the biocidal polymer.
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- Authors: Ahmetali, Erem , Sen, Pinar , Süer, N Ceren , Aksu, Burak , Nyokong, Tebello , Eren, Tarik , Sener, Kasim M
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/185976 , vital:44453 , xlink:href=" https://doi.org/10.1002/macp.202000386"
- Description: Amphiphilic poly(oxanorbornene)s are promising synthetic polymers that mimic the structural properties and antimicrobial functions of naturally occurring antimicrobial peptides. Here, poly(oxanorbornene)s bearing pendant zinc(II) phthalocyanine and triphenyl(ethyl) phosphonium functionalities are synthesized by ring-opening metathesis polymerization (ROMP). Fluorescence, singlet oxygen and triplet quantum yields of polymers are measured in dimethyl sulfoxide and aqueous medium. The singlet oxygen quantum yields of copolymers with the highest triphenyl and triethyl phosphonium content are found to be 0.29 and 0.41, respectively. Then, antimicrobial activities of polymers against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) are investigated under both dark and light conditions. Synergistic effect of zinc(II) phthalocyanine and phosphonium-containing poly(oxanorbornene) is observed that the conjugate possessing the most triphenyl phosphonium side chains has the highest activity under light against both gram-positive and gram-negative bacterial strains after 80 min irradiation, reducing the survival of E. coli or S. aureus by 99.9999%. Hemolytic concentrations of the copolymers are found between 8 and 512 µg mL−1. Scanning electron microscopy (SEM) proves that the bacteria membrane deforms after contacting with the biocidal polymer.
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Investigation of electrocatalytic behaviour of low symmetry cobalt phthalocyanines when clicked to azide grafted carbon electrodes
- Mpeta, Lakethe S, Sen, Pinar, Nyokong, Tebello
- Authors: Mpeta, Lakethe S , Sen, Pinar , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/186304 , vital:44483 , xlink:href="https://doi.org/10.1016/j.jelechem.2020.113896"
- Description: This work describes the electrochemical properties of low symmetry cobalt phthalocyanines namely, tris-[(4-tert-butylphenoxy)-4-(pent-4-yn-1-yloxy) phthalocyaniato] cobalt (II) (3) and tris-[(4-tert-butylphenoxy)-4-(4-ethybylbenzyl-oxy) phthalocyaniato] cobalt (II) (5). The complexes were characterized by a number of techniques including UV–Vis, mass, and infrared spectra, as well as elemental analysis. The glassy carbon electrodes were first azide functionalized then clicked to low symmetry phthalocyanines. The click reaction was confirmed using X-ray photoelectron spectra. The constructed electrodes showed excellent electrocatalytic activity towards hydrazine oxidation. Oxidation peaks with low potentials of 0.21 V and 0.26 V, for complexes 3 and 5, respectively were obtained. Complex-5 gave a better detection limit of 0.94 μM and electrocatalytic rate constant of 5.6 × 106 M−1 s−1.
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- Authors: Mpeta, Lakethe S , Sen, Pinar , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/186304 , vital:44483 , xlink:href="https://doi.org/10.1016/j.jelechem.2020.113896"
- Description: This work describes the electrochemical properties of low symmetry cobalt phthalocyanines namely, tris-[(4-tert-butylphenoxy)-4-(pent-4-yn-1-yloxy) phthalocyaniato] cobalt (II) (3) and tris-[(4-tert-butylphenoxy)-4-(4-ethybylbenzyl-oxy) phthalocyaniato] cobalt (II) (5). The complexes were characterized by a number of techniques including UV–Vis, mass, and infrared spectra, as well as elemental analysis. The glassy carbon electrodes were first azide functionalized then clicked to low symmetry phthalocyanines. The click reaction was confirmed using X-ray photoelectron spectra. The constructed electrodes showed excellent electrocatalytic activity towards hydrazine oxidation. Oxidation peaks with low potentials of 0.21 V and 0.26 V, for complexes 3 and 5, respectively were obtained. Complex-5 gave a better detection limit of 0.94 μM and electrocatalytic rate constant of 5.6 × 106 M−1 s−1.
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New difluoroboron complexes based on N, O-chelated Schiff base ligands: Synthesis, characterization, DFT calculations and photophysical and electrochemical properties
- Sen, Pinar, Mpeta, Lekhetho S, Mack, John, Nyokong, Tebello
- Authors: Sen, Pinar , Mpeta, Lekhetho S , Mack, John , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/186207 , vital:44473 , xlink:href="https://doi.org/10.1016/j.jlumin.2020.117262"
- Description: The synthesis of new Schiff bases and their dinuclear boron complexes is described, along with their characterization by 1H and 13C NMR, FT-IR, and UV–visible absorption spectroscopy, mass spectrometry, and EDX for elemental analysis. The optical and photophysical properties were examined in terms of their absorption and emission behavior, fluorescence quantum yields and fluorescence lifetimes. The flexible dinuclear boron complexes that are linked by a flexible carbon chain exhibited large Stokes shifts in the range from 92 nm to 115 nm in contrast to BODIPY dyes. Those properties make these complexes precious for applications in fluorescence materials. And also theoretical calculations were obtained by using Density Functional Theory (DFT) methods.
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- Authors: Sen, Pinar , Mpeta, Lekhetho S , Mack, John , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/186207 , vital:44473 , xlink:href="https://doi.org/10.1016/j.jlumin.2020.117262"
- Description: The synthesis of new Schiff bases and their dinuclear boron complexes is described, along with their characterization by 1H and 13C NMR, FT-IR, and UV–visible absorption spectroscopy, mass spectrometry, and EDX for elemental analysis. The optical and photophysical properties were examined in terms of their absorption and emission behavior, fluorescence quantum yields and fluorescence lifetimes. The flexible dinuclear boron complexes that are linked by a flexible carbon chain exhibited large Stokes shifts in the range from 92 nm to 115 nm in contrast to BODIPY dyes. Those properties make these complexes precious for applications in fluorescence materials. And also theoretical calculations were obtained by using Density Functional Theory (DFT) methods.
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Synthesis of novel Schiff base cobalt (II) and iron (iii) complexes as cathode catalysts for microbial fuel cell applications
- Sen, Pinar, Akagunduz, Dilan, Aghdam, Araz S, Cebeci, Fevzi C, Nyokong, Tebello, Catal, Tunc
- Authors: Sen, Pinar , Akagunduz, Dilan , Aghdam, Araz S , Cebeci, Fevzi C , Nyokong, Tebello , Catal, Tunc
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/190861 , vital:45035 , xlink:href="https://doi.org/10.1007/s10904-019-01286-x"
- Description: In this study, the synthesis and characterization of a new Schiff base and its cobalt(II) and iron(III) complexes were performed fully characterized by common spectroscopic techniques such as 1H-NMR, 13C-NMR, FT-IR, UV–Vis and MS and elemental analysis. The cathodes prepared with only activated carbon, Co-Schiff base complex, and Fe-Schiff base complex mixed with activated carbon as the carrier were examined in single chamber air cathode microbial fuel cells (MFCs). The spectroscopic results confirm the structure of novel Schiff base and its complexes with cobalt (II) and Fe(III). MFC results showed that Fe-Schiff base complex generated higher voltage generation using glucose as the carbon source. Cyclic voltammetry results showed the conductivity and catalytic features of the cathodes developed in this study. Scanning electron microscopic results showed the distribution the complexes on the cathode surface. In conclusion, a novel Schiff base and its complexes with cobalt (II) and iron (III) can be employed into MFC technology to be used in green electricity production, and might help decreasing the operating costs of wastewater treatment plants.
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- Authors: Sen, Pinar , Akagunduz, Dilan , Aghdam, Araz S , Cebeci, Fevzi C , Nyokong, Tebello , Catal, Tunc
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/190861 , vital:45035 , xlink:href="https://doi.org/10.1007/s10904-019-01286-x"
- Description: In this study, the synthesis and characterization of a new Schiff base and its cobalt(II) and iron(III) complexes were performed fully characterized by common spectroscopic techniques such as 1H-NMR, 13C-NMR, FT-IR, UV–Vis and MS and elemental analysis. The cathodes prepared with only activated carbon, Co-Schiff base complex, and Fe-Schiff base complex mixed with activated carbon as the carrier were examined in single chamber air cathode microbial fuel cells (MFCs). The spectroscopic results confirm the structure of novel Schiff base and its complexes with cobalt (II) and Fe(III). MFC results showed that Fe-Schiff base complex generated higher voltage generation using glucose as the carbon source. Cyclic voltammetry results showed the conductivity and catalytic features of the cathodes developed in this study. Scanning electron microscopic results showed the distribution the complexes on the cathode surface. In conclusion, a novel Schiff base and its complexes with cobalt (II) and iron (III) can be employed into MFC technology to be used in green electricity production, and might help decreasing the operating costs of wastewater treatment plants.
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Synthesis of novel Schiff base cobalt (II) and iron (iii) complexes as cathode catalysts for microbial fuel cell applications
- Sen, Pinar, Akagunduz, Dilan, Aghdam, Araz Sheibani, Cebeci, Fevzi C, Nyokong, Tebello
- Authors: Sen, Pinar , Akagunduz, Dilan , Aghdam, Araz Sheibani , Cebeci, Fevzi C , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/187015 , vital:44556 , xlink:href="https://doi.org/10.1007/s10904-019-01286-x"
- Description: In this study, the synthesis and characterization of a new Schiff base and its cobalt(II) and iron(III) complexes were performed fully characterized by common spectroscopic techniques such as 1H-NMR, 13C-NMR, FT-IR, UV–Vis and MS and elemental analysis. The cathodes prepared with only activated carbon, Co-Schiff base complex, and Fe-Schiff base complex mixed with activated carbon as the carrier were examined in single chamber air cathode microbial fuel cells (MFCs). The spectroscopic results confirm the structure of novel Schiff base and its complexes with cobalt (II) and Fe(III). MFC results showed that Fe-Schiff base complex generated higher voltage generation using glucose as the carbon source. Cyclic voltammetry results showed the conductivity and catalytic features of the cathodes developed in this study. Scanning electron microscopic results showed the distribution the complexes on the cathode surface. In conclusion, a novel Schiff base and its complexes with cobalt (II) and iron (III) can be employed into MFC technology to be used in green electricity production, and might help decreasing the operating costs of wastewater treatment plants.
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- Authors: Sen, Pinar , Akagunduz, Dilan , Aghdam, Araz Sheibani , Cebeci, Fevzi C , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/187015 , vital:44556 , xlink:href="https://doi.org/10.1007/s10904-019-01286-x"
- Description: In this study, the synthesis and characterization of a new Schiff base and its cobalt(II) and iron(III) complexes were performed fully characterized by common spectroscopic techniques such as 1H-NMR, 13C-NMR, FT-IR, UV–Vis and MS and elemental analysis. The cathodes prepared with only activated carbon, Co-Schiff base complex, and Fe-Schiff base complex mixed with activated carbon as the carrier were examined in single chamber air cathode microbial fuel cells (MFCs). The spectroscopic results confirm the structure of novel Schiff base and its complexes with cobalt (II) and Fe(III). MFC results showed that Fe-Schiff base complex generated higher voltage generation using glucose as the carbon source. Cyclic voltammetry results showed the conductivity and catalytic features of the cathodes developed in this study. Scanning electron microscopic results showed the distribution the complexes on the cathode surface. In conclusion, a novel Schiff base and its complexes with cobalt (II) and iron (III) can be employed into MFC technology to be used in green electricity production, and might help decreasing the operating costs of wastewater treatment plants.
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The effects of asymmetry in combination with reduced graphene oxide nanosheets on hydrazine electrocatalytic detection on cobalt phthalocyanines
- Mpeta, Lekhetho S, Sen, Pinar, Nyokong, Tebello
- Authors: Mpeta, Lekhetho S , Sen, Pinar , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/186023 , vital:44456 , xlink:href="https://doi.org/10.1002/elan.202060094"
- Description: New symmetric {tetrakis [4-(4-(5-chloro-1Hbenzo[d]imidazol-2-yl) phenoxy phthalocyaninato] Co (II) (CoTPc)} and low symmetry {tris tert butyl phenoxy mono [4-(4-(5-chloro-1H-benzo[d]imidazol-2-yl) phenoxy phthalocyaninato]} Co (II) (CoMPc) were successfully synthesised and combined with reduced graphene oxide nanosheets (rGONS) for electrocatalytic detection of hydrazine. Prior to electrocatalysis, the probes were characterised using cyclic voltammetry and electrochemical impedance spectroscopy. Chronoamperometry was used to determine catalytic rate constant and the limit of detection (LOD). CoMPc-rGONS gave catalytic rate constant and LOD of 1.37×106 M 1 s 1 and 0.82 μM respectively, rendering it a more suitable probe for hydrazine, due to low symmetry.
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- Authors: Mpeta, Lekhetho S , Sen, Pinar , Nyokong, Tebello
- Date: 2020
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/186023 , vital:44456 , xlink:href="https://doi.org/10.1002/elan.202060094"
- Description: New symmetric {tetrakis [4-(4-(5-chloro-1Hbenzo[d]imidazol-2-yl) phenoxy phthalocyaninato] Co (II) (CoTPc)} and low symmetry {tris tert butyl phenoxy mono [4-(4-(5-chloro-1H-benzo[d]imidazol-2-yl) phenoxy phthalocyaninato]} Co (II) (CoMPc) were successfully synthesised and combined with reduced graphene oxide nanosheets (rGONS) for electrocatalytic detection of hydrazine. Prior to electrocatalysis, the probes were characterised using cyclic voltammetry and electrochemical impedance spectroscopy. Chronoamperometry was used to determine catalytic rate constant and the limit of detection (LOD). CoMPc-rGONS gave catalytic rate constant and LOD of 1.37×106 M 1 s 1 and 0.82 μM respectively, rendering it a more suitable probe for hydrazine, due to low symmetry.
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