Direct Catalytic Benzene Hydroxylation under Mild Reaction Condition by Using a Monocationic μ-Nitrido-Bridged Iron Phthalocyanine Dimer with 16 Peripheral Methyl Groups

Direct catalytic hydroxylation of benzene under mild reaction conditions proceeded efficiently in the presence of a monocationic μ-nitrido-bridged iron phthalocyanine dimer with 16 peripheral methyl groups in an acetonitrile solution...

Role of Iron Phthalocyanine Coordination in Catecholamines Detection

Catecholamines are an important class of neurotransmitters responsible for regularizing, controlling, and treating neural diseases. Based on control and diseases treatment, the development of methodology and dives to sensing is a promissory technology area. This work evaluated the role of iron phthalocyanine coordination (FePc) with the specific groups from catecholamine molecules (L-dopa, dopamine, epinephrine, and the amino acid tyrosine) and the effect of this coordination on electrochemical behavior. The in situ coordination analysis was performed through isotherms π-A of FePc Langmuir films in the absence and presence of catecholamines. The π-A isotherm indicates a strong interaction between FePc monolayer and L-Dopa and DA, which present a catechol group and a side chain with a protonated amino group (-NH3+). These strong interactions with catechol and amine groups were confirmed by characterization at the molecular level using the surface-enhanced Raman spectroscopy (SERS) from a Langmuir–Schaefer monolayer deposited onto Ag surfaces. The electrochemical measurements present a similar tendency, with lower oxidation potential observed to DA>L-Dopa>Ep. The results corroborate that the coordination of the analyte on the electron mediator surface plays an essential role in an electrochemical sensing application. The FePc LS film was applied as a sensor in tablet drug samples, showing a uniformity of content of 96% for detecting active compounds present in the L-Dopa drug samples.

Substituent effect on iron phthalocyanines as cyclohexene oxidation catalysts

Two iron phthalocyanines peripherally octasubstituted either with electron-withdrawing isobutylsulfonyl moities or electron-donating isobutoxy moieties were designed to investigate the effect of the substitution pattern on their oxidation catalytic activity, and were then tested in oxidation of cyclohexene as a reaction model. For both catalysts, the main product of oxidation was 2-cyclohexen-1-ol which is an allylic oxidation product. The electron-withdrawing isobutylsulfonyl substituted iron phthalocyanine 1exhibited better catalytic activities than the electron-donating isobutoxy substituted iron phthalocyanine 2.

Synthesis of Multi-Walled Carbon Nanotubes by Chemical Vapour Deposition and Post-Synthesis Treatment by Dielectrophoresis

<p>Carbon nanotubes (CNTs) are a group of pure carbon solid materials that possess one-dimensional structures with diameters down to less than one nanometre. They have interesting physical properties such as very high tensile strength, metallic and semiconducting conductivity, and great potential for applications. This work investigates the synthesis, alignment and purification of multi-walled carbon nanotubes, which were characterized by Electron Microscopy, measurement of electrical properties and Raman scattering. Synthesis of multi-walled carbon nanotubes (MWNTs) was carried out by Chemical Vapour Deposition, using three different precursors: Fe(NO3)3, ferrocene and iron phthalocyanine. Vertically aligned "forests" of large numbers of MWNTs were achieved using ferrocene and iron phthalocyanine as precursors. Products from iron phthalocyanine yield more graphitic CNT nanostructures, as determined by Scanning Electron Microscopy, Transmission Electron Microscopy, Thermogravity Analysis, Raman microscopy and Energy Dispersive X-ray spectroscopy. Patterned growth of vertical MWNTs arrays with a resolution of 2 microns was also obtained, using a predeposited substrate. A High Resolution Transmission Electron Microscope was employed to investigate the inner structures of individual MWNTs, giving well-resolved images of concentric nanostructures with inter-lattice spacings of 0.34 nm. Techniques for purification and manipulation of CNTs are required before CNTs' excellent properties can be exploited. In this thesis, dielectrophoresis (DEP) under high-frequency AC voltages using an array of micron-scale electrodes was adopted as the technique to align MWNTs between these, electrodes. This technique is effective for MWNTs since their long cylindrical structure and the high mobility of their charge carriers allow them to be electrically polarised. As a result, MWNTs experience large DEP forces in an AC electric field. In our experiments, inter-digitated electrodes were used to apply the electric field to CNT suspensions in various solvents. Alignment of CNTs along their axis was achieved within the gaps between adjacent electrodes at a frequency larger than 1.1 MHz, The AC admittance changes between the electrodes were monitored and were observed to be a clear reflection of the accumulation process of MWNTs. Also it was identified that distilled water was a better solvent than ethanol and isopropanol for DEP purpose on MWNTs. In addition, a prototype device was built to selectively purify MWNTs from as-grown samples by combining DEP and re-circulating fluid flow. It was found that this device is able to decrease the impurity content of MWNTs, which is collected on the electrode array, from the suspension of as-grown samples.</p>