We investigated the effect of different organic coatings on the H-NMR relaxation properties of ultra-small iron-oxide-based magnetic nanoparticles. The first set of nanoparticles, with a magnetic core diameter ds1 = 4.4 ± 0.7 nm, was coated with polyacrylic acid (PAA) and dimercaptosuccinic acid (DMSA), while the second set, ds2 = 8.9 ± 0.9 nm, was coated with aminopropylphosphonic acid (APPA) and DMSA. At fixed core diameters but different coatings, magnetization measurements revealed a similar behavior as a function of temperature and field. On the other hand, the H-NMR longitudinal r1 nuclear relaxivity in the frequency range ν = 10 kHz ÷ 300 MHz displayed, for the smallest particles (diameter ds1), an intensity and a frequency behavior dependent on the kind of coating, thus indicating different electronic spin dynamics. Conversely, no differences were found in the r1 relaxivity of the biggest particles (ds2) when the coating was changed. It is concluded that, when the surface to volume ratio, i.e., the surface to bulk spins ratio, increases (smallest nanoparticles), the spin dynamics change significantly, possibly due to the contribution of surface spin dynamics/topology.
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http://dx.doi.org/10.3390/nano13050804 | DOI Listing |
Sensors (Basel)
November 2024
School of Engineering and Architecture, Universidad La Salle Oaxaca, Camino a San Agustín No. 407, Santa Cruz Xoxocotlán, Oaxaca 71230, Mexico.
Nuclear magnetic resonance relaxation of the proton spins of liquid molecules and their evolution during processes such as drying, fluid flow, and phase change of a sample can be monitored in a nondestructive way. A unilateral H NMR sensor made with a permanent magnet array, inspired by the NMR MOUSE, with an RF coil tuned to 11.71 MHz was developed.
View Article and Find Full Text PDFActa Biomater
December 2024
Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus UAB, E-08193 Bellaterra, Spain; CIBER de Bioingeniería, Biomateriales y Nanomedicina, Instituto de Salud Carlos III, Campus UAB, 08913 Bellaterra, Spain. Electronic address:
This study introduces a series of water-soluble radical dendrimers (G0 to G5) as promising magnetic resonance imaging (MRI) contrast agents that could potentially address clinical safety concerns associated with current gadolinium-based contrast agents. By using a simplified synthetic approach based on a cyclotriphosphazene core and lysine-derived branching units, we successfully developed a G5 dendrimer containing up to 192 units of 2,2,6,6-Tetramethylpiperidinyloxy (TEMPO) radical. This synthesis offers advantages including ease of preparation, purification, and tunable water solubility through the incorporation of glutamic acid anion residues.
View Article and Find Full Text PDFPhys Chem Chem Phys
December 2024
Graduate School of Nanobioscience, Yokohama City University, Kanazawa-ku, Yokohama, 236-0027, Japan.
Eight salts of [NEtMe(i-Pr)][BEtMe] ( = 1-3, = 0, 1) were prepared to reduce Coulombic interactions in the crystals. These novel ionic plastic crystals exhibited low activation energies for isotropic rotational motion () and ion diffusion (). The lattice constant in the cubic structure indexed to a CsCl-type was larger than that of the corresponding plastic crystals of [NEtMe][BEtMe] (nonbranched sample).
View Article and Find Full Text PDFJ Phys Chem B
November 2024
Leibniz Institut für Analytische Wissenschaften-ISAS-e.V., Dortmund 44139, Germany.
The formation and transport of ionic charges in formic acid-water (HCOOH-HO) mixtures with initial water mole fractions ranging from X = 0 to 1 were investigated using C and H NMR, FTIR spectroscopy, viscosity, conductivity, and pH measurements. The maximum molar concentration of ions (HO and HCOO), along with the relative differences between theoretical and experimental densities, spin-lattice relaxation times (), activation energies (), viscosity (η), and conductivity (σ), were identified within the range of X ≈ 0.5-0.
View Article and Find Full Text PDFDalton Trans
November 2024
Dipartimento di Scienze Chimiche e Geologiche e UdR INSTM, Università degli Studi di Modena e Reggio Emilia, via G. Campi 103, 41125 Modena, Italy.
First prepared in the late 70s, the pro-ligand 1,3-bis(3,5-dioxo-1-hexyl)benzene (Hbdhb) contains two acetoacetyl terminations linked to a central 1,3-phenylene unit through dimethylene bridges. Since each termination can be either in diketonic or keto-enolic form, in organic solution it exists as a mixture of three spectroscopically resolvable tautomers. In the presence of pyridine, Co and the bdhb anion form a crystalline dimeric compound with formula [Co(bdhb)(py)] (2) and a Co⋯Co separation of more than 11 Å.
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