https://commons.ru.ac.za/vital/access/manager/Index ${session.getAttribute("locale")} 5 Nonlinear optical responses of phthalocyanines in the presence of nanomaterials or when embedded in polymeric materials https://commons.ru.ac.za/vital/access/manager/Repository/vital:25548 Wed 12 May 2021 20:07:23 SAST ]]> Nonlinear optical responses of targeted phthalocyanines when conjugated with nanomaterials or fabricated into polymer thin films https://commons.ru.ac.za/vital/access/manager/Repository/vital:29926 Wed 12 May 2021 19:50:04 SAST ]]> Phthalocyanine-nanoparticle conjugates for photodynamic therapy of cancer and phototransformation of organic pollutants https://commons.ru.ac.za/vital/access/manager/Repository/vital:4538 Wed 12 May 2021 19:02:23 SAST ]]> Photophysical studies of Zinc phthalocyanine-silica nanoparticles conjugates https://commons.ru.ac.za/vital/access/manager/Repository/vital:4537 Wed 12 May 2021 17:56:16 SAST ]]> Nonlinear optical studies of phthalocyanines and their conjugates with nanomaterials https://commons.ru.ac.za/vital/access/manager/Repository/vital:4545 Wed 12 May 2021 17:12:36 SAST ]]> Photophysical properties and photodynamic therapy activities of symmetrical and asymmetrical porphyrins embedded into Pluronic polymer micelles and nonlinear optical properties of an asymmetrical phthalocyanine https://commons.ru.ac.za/vital/access/manager/Repository/vital:29122 90% cell survival. The photodynamic activity of water insoluble porphyrins improved when encapsulated into the micelles. Novel asymmetrical phthalocyanines were also synthesised for nonlinear optics (NLO) studies in solution and thin films.]]> Wed 12 May 2021 16:05:57 SAST ]]> Determination of nonlinear optical properties of phthalocyanine regioisomers using computational models https://commons.ru.ac.za/vital/access/manager/Repository/vital:41337 Wed 12 May 2021 15:02:23 SAST ]]> The electrocatalytic response of metallophthalocyanines when clicked to electrodes and to nanomaterials https://commons.ru.ac.za/vital/access/manager/Repository/vital:42174 Wed 12 May 2021 15:00:21 SAST ]]> Evaluation of metallophthalocyanine functionalized photocatalytic asymmetric polymer membranes for pollution control and antimicrobial activity https://commons.ru.ac.za/vital/access/manager/Repository/vital:42052 Wed 12 May 2021 14:30:41 SAST ]]> Effects of Axial Ligands on the Photosensitising Properties of Silicon Octaphenoxyphthalocyanines https://commons.ru.ac.za/vital/access/manager/Repository/vital:4553 600 nm) in dimethylsulphoxide solution. All the ligands were transformed into the dihydroxy silicon octaphenoxyphthalocyanine with varying degrees of phototransformation quantum yields ranging in order from 10⁻³ to 10⁻⁵ depending on the axial ligand involved. During and after axial ligand transformations a photodegredation of the dihydroxy silicon octaphenoxy phthalocyanine was observed upon continued irradiation. The oligomers were found to undergo the same axial ligand transformation process with a phototransformation quantum yield of 10⁻⁵ The singlet oxygen quantum yields of the unaggregated monomeric silicon octaphenoxy phthalocyanines were all found to be approximately 0.2 with the exception of a compound with two (trihexyl)siloxy axial substituents that had a singlet oxygen quantum yield of approximately 0.4 in dimethylsulphoxide solutions. The oligomers showed a surprising trend of an increase in singlet oxygen quantum yield with an increase in phthalocyanine ring number up to the pentamer and then a dramatic decrease to the nonamer. The triplet quantum yield and triplet lifetime were determined by laser flash photolysis for selected compounds and no correlation was observed with any of these properties and the singlet oxygen quantum yields. These selected compounds all fluoresce and a very good correlation was found between the fluorescence lifetimes determined experimentally by laser photolysis and the Strickler-Berg equation for the non-aggregated compounds. Electrochemical measurements also indicate the importance of the axial ligands upon the behaviour of the phthalocyanines as cyclic voltammetric behaviour was determined by the nature of the axial ligand.]]> Thu 13 May 2021 14:52:35 SAST ]]> Metallophthalocyanine-gold nanoparticle conjugates for photodynamic antimicrobial chemotherapy https://commons.ru.ac.za/vital/access/manager/Repository/vital:4543 Thu 13 May 2021 11:46:40 SAST ]]> Physicochemical properties and photodynamic therapy activities of indium and zinc phthalocyanine-nanoparticle conjugates https://commons.ru.ac.za/vital/access/manager/Repository/vital:30589 50Îll viability at concentrations≤ 160μg/mL, however the conjugates showed<50% cell viabilityatconcentrations≤ 160μg/mLprobably due to the enhanced singlet oxygen quantum yield. The findings from this work show the importance of linking photosensitises such as phthalocyanines to metal nanoparticles for the enhancement ofsinglet oxygen quantum yield and ultimately the photodynamic effect.]]> Thu 13 May 2021 08:10:17 SAST ]]> Low symmetry metallophthalocyanines and their nanoparticle conjugates for photodynamic antimicrobial chemotherapy https://commons.ru.ac.za/vital/access/manager/Repository/vital:4278 Thu 13 May 2021 07:14:17 SAST ]]> Electrode surface modification using metallophthalocyanines and metal nanoparticles : electrocatalytic activity https://commons.ru.ac.za/vital/access/manager/Repository/vital:4541 Thu 13 May 2021 07:06:37 SAST ]]> Effects of substituents on the photosensitizing and electrocatalytic properties of phthalocyanines https://commons.ru.ac.za/vital/access/manager/Repository/vital:4554 SnPc>ZnPc. Triplet lifetimes of the GePc (168-340μs) are very similar to that of the ZnPc (197 - 366μs), but the triplet lifetimes of the SnPc are ten fold shorter (10 - 32μs ). Triplet quantum yields are higher for the GePc (0.20 - 0.50) and SnPc (0.08 - 0.45) than for the ZnPc (0.02 - 0.25). Fluorescence lifetimes of GePc ( 4.0 - 5.1 ns) are significantly longer than that of ZnPc (1.9 - 3.0 ns) and SnPc (0.2 - 0.4 ns). Fluorescence quantum yields decrease in the following order: GePc(0.21-0.31)>ZnPc(0.02-0.21)>SnPc(0.02- 0.06). Ring-substituted cobalt phthalocyanine complexes of the form CoPc(R)4 (R= NH2, N02, C(CH3)3, S03H and COOH) are compared for their catalytic activities towards the oxidation of cysteine. The potential for the electrocatalytic oxidation of cysteine is closely related to the Com/Co11 couple of the CoPc(R)4 complexes in acidic media and to the Con/Co1 couple in basic media. The catalytic current and the oxidation potential for cysteine are dependent on the pH of the solution, the potential becoming less positive and the currents increasing with increase in pH.]]> Thu 13 May 2021 06:41:11 SAST ]]> Electrochemical sensing and immunosensing using metallophthalocyanines and biomolecular modified surfaces https://commons.ru.ac.za/vital/access/manager/Repository/vital:5580 Thu 13 May 2021 06:37:27 SAST ]]> Photophysicochemical properties and in vitro photodynamic therapy activities of zinc phthalocyanine conjugates with biomolecules and single-walled carbon nanotubes https://commons.ru.ac.za/vital/access/manager/Repository/vital:4544 Thu 13 May 2021 03:36:01 SAST ]]> Graphene quantum dots and their metallophthalocyanines nanoconjugates as novel photoluminescent nanosensors https://commons.ru.ac.za/vital/access/manager/Repository/vital:27821 Thu 13 May 2021 01:17:53 SAST ]]>