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Biomedical subjects

Petre Ionita

Publications and source records attributed to Petre Ionita.

6 recordsLinked to original sources
PubMed2006

Hydrazyl-nitrones, novel hybrid molecules in free radical research.

This work describes the synthesis and characterisation of some novel hybrid molecules which contains in the same molecule a free radical moiety of hydrazyl type and a spin-trap moiety of nitrone type. The new compounds synthesized have multiple and easy to follow spectroscopic properties, making them useful as sensors or probes in radical chemistry. The new class of hydrazyl-nitrone molecules can act, in a single step process, as both generator and spin-trap of short-lived radicals. The hybrid molecules can be also involved in acid-base or redox processes, and the chemical processes can be easily monitored by visible or electron paramagnetic resonance spectroscopy. The excellent generator and trap properties recommend them as valuable sensors and probes in radical chemistry.

Electron Spin Resonance Spectroscopy↗
PubMed2005

Dipole-dipole interactions in spin-labeled au nanoparticles as a measure of interspin distances.

A series of Au nanoparticles modified with a nitroxide-functionalized ligand was prepared with a range of spin-label coverage. The X-band EPR spectra of frozen solutions of these nanoparticles showed coverage-dependent line-broadening due to dipole-dipole interactions between spin labels. We developed a methodology to analyze such spectra in terms of geometrical features of the nanoparticles (e.g., Au core size and the length of the spin-labeled ligand). Our method is based on the assumption that the spectral line shape is determined by the average distance between nearest-neighboring spin labels adsorbed on the Au particle. Geometrical and statistical analysis then relates this distance to the line shape parameter d1/d, which was calibrated using a model system. Application of this methodology to the experimental spectra provided information about the conformation of ligands on the Au surface. We found that, if the spin-labeled ligand is substantially longer than the surrounding protecting layer, it does not adopt a fully stretched conformation but wraps around the particle immediately above the layer of surrounding ligand. Our results also show that the ligands do not adsorb cooperatively on the Au surface.

Journal Article↗
PubMed2004

Mechanistic study of a place-exchange reaction of Au nanoparticles with spin-labeled disulfides.

The mechanism of a place-exchange reaction of ligand-protected Au nanoparticles was investigated using diradical disulfide spin labels. Analysis of reaction mixtures using a combination of GPC and EPR allowed us to determine concentration profile and propose a kinetic model for the reaction. In this model, only one branch of the disulfide ligand is adsorbed on the Au surface during exchange; the other branch forms mixed disulfide with the outgoing ligand. The two branches of the disulfide ligand therefore do not adsorb in adjacent positions on the surface of Au nanoparticles; this was ultimately proven by the powder EPR spectra of frozen exchange reaction mixtures. Our data also suggest the presence of different binding sites with different reactivity in the exchange reaction. The most-active sites are likely to be nanoparticle surface defects.

Journal Article↗
PubMed2004

Spin-labelled Au nanoparticles.

A series of Au nanoparticles functionalised with nitroxide spin labels has been prepared and studied by EPR spectroscopy. Samples with low coverage of the spin label were used to investigate the dynamics of the surface-attached labels at different distances from the Au surface. The rotational correlation times of spin labels vary from 10(-10) s to more than 3 x 10(-9) s, depending on the chain length of the label and the surrounding ligand. The samples with higher coverage of the spin label show an increasing contribution of the exchange interaction between nitroxides adsorbed in a close proximity to each other on the same nanoparticle. Quantitative analysis of the EPR spectra of these samples suggests the presence of non-equivalent binding sites on the surface of Au nanoparticles. Additionally, EPR signals of isolated radical pairs were observed at intermediate coverage.

Journal Article↗
PubMed2002

EPR study of a place-exchange reaction on Au nanoparticles: two branches of a disulfide molecule do not adsorb adjacent to each other.

An EPR study of a place-exchange reaction of a diradical disulfide with butanethiol-protected Au nanoparticles showed that the two branches of the disulfide molecule do not adsorb adjacent to each other on the Au surface. The most likely mechanism includes adsorption of only one branch of the disulfide molecule in the exchange process. The exchange reaction was found to be zeroth-order with respect to the diradical, indicative of a dissociative "SN1"-type mechanism.

Journal Article↗