A quantitative study of susceptibility and additional frequency shift of three common materials in MRI.

Purpose: This work quantifies magnetic susceptibilities and additional frequency shifts derived from different samples.

Methods: Twenty samples inside long straws were imaged with a multiecho susceptibility weighted imaging and analyzed with two approaches for comparisons. One approach applied our complex image summation around a spherical or cylindrical object method to phase distributions outside straws.

Magnetic moment quantifications of small spherical objects in MRI.

Purpose: The purpose of this work is to develop a method for accurately quantifying effective magnetic moments of spherical-like small objects from magnetic resonance imaging (MRI). A standard 3D gradient echo sequence with only one echo time is intended for our approach to measure the effective magnetic moment of a given object of interest.

Methods: Our method sums over complex MR signals around the object and equates those sums to equations derived from the magnetostatic theory.

Phase-coexistence and thermal hysteresis in samples comprising adventitiously doped MnAs nanocrystals: programming of aggregate properties in magnetostructural nanomaterials.

Small changes in the synthesis of MnAs nanoparticles lead to materials with distinct behavior. Samples prepared by slow heating to 523 K (type-A) exhibit the characteristic magnetostructural transition from the ferromagnetic hexagonal (α) to the paramagnetic orthorhombic (β) phase of bulk MnAs at Tp = 312 K, whereas those prepared by rapid nucleation at 603 K (type-B) adopt the β structure at room temperature and exhibit anomalous magnetic properties. The behavior of type-B nanoparticles is due to P-incorporation (up to 3%), attributed to reaction of the solvent (trioctylphosphine oxide).

Diverse structural and magnetic properties of differently prepared MnAs nanoparticles.

Discrete nanoparticles of MnAs with distinct magnetostructural properties have been prepared by small modifications of solution-phase arrested precipitation reactions. Rietveld and X-ray atomic pair distribution function based approaches were used to explore the evolution of the structure of the samples with temperature, and these data were compared to the magnetic response measured with ac susceptibility. Relative to a bulk standard, one type of MnAs nanoparticles was found to demonstrate similar but smaller structural transitions and corresponding magnetic changes.

Control of phase in phosphide nanoparticles produced by metal nanoparticle transformation: Fe2P and FeP.

The transformation of Fe nanoparticles by trioctylphosphine (TOP) to phase-pure samples of either Fe(2)P or FeP is reported. Fe nanoparticles were synthesized by the decomposition of Fe(CO)(5) in a mixture of octadecene and oleylamine at 200 degrees C and were subsequently reacted with TOP at temperatures in the region of 350-385 degrees C to yield iron phosphide nanoparticles. Shorter reaction times favored an iron-rich product (Fe(2)P), and longer reaction times favored a phosphorus-rich product (FeP).

Discrete, dispersible MnAs nanocrystals from solution methods: phase control on the nanoscale and magnetic consequences.

Nanocrystals of thermodynamically stable alpha-MnAs (hexagonal NiAs-type) and metastable beta-MnAs (orthorhombic MnP-type) have been synthesized by the reaction of triphenylarsine oxide (Ph(3)AsO) and dimanganesedecacarbonyl (Mn(2)CO(10)) at temperatures ranging from 250 to 330 degrees C in the presence of the coordinating solvent trioctylphosphine oxide (TOPO). Morphologically, both alpha- and beta-MnAs nanoparticles adopt a core-shell type structure with a crystalline core and low-contrast noncrystalline shell. In contrast to prior studies on MnAs particles, disks, and films, the present bottom-up synthesis yields discrete, dispersible MnAs nanoparticles without a structural support.

Magnetic-field-induced optical anisotropy in ferrofluids: a time-dependent light-scattering investigation.

We report an experimental investigation of time dependent anisotropic light scattering by an aqueous suspension of tetramethyl ammonium hydroxide coated Fe3O4 nanoparticles (approximately 6 nm) under the ON-OFF transient of an external dc magnetic field. The study employs the synchronized recording and measurement of the two magnetic-field-induced light-scattering patterns produced by two identical orthogonal He-Ne laser beams passing through the ferrofluid sample and propagating parallel and perpendicular to the applied field, respectively. From these patterns, we extract the time dependence of the induced optical anisotropy, which provides a measure of the characteristic time scale and kinematic response for field-induced structure formation in the sample.

Quantifying magnetic nanoparticles in non-steady flow by MRI.

Objective: This work compares the measured R*2 of magnetic nanoparticles to their corresponding theoretical values in both gel phantoms and dynamic water flows on the basis of the static dephasing theory.

Materials And Methods: The magnetic moment of a nanoparticle solution was measured by a magnetometer. The R*2 of the nanoparticle solution doped in a gel phantom was measured at both 1.

Assembly of triangular trimetallic complexes by triamidophosphine ligands: spin-frustrated Mn2+ plaquettes and diamagnetic Mg2+ analogues with a combined through-space, through-bond pathway for 31P-31P spin-spin coupling.

The reactions of 2 equiv of the ligand precursor P(CH2NHPh)3 or P[CH2NH-3,5-(CF3)2C6H3]3 with 3 equiv of Mn[N(SiMe3)2]2 provide high-yielding routes to the triangular trinuclear Mn(II) complexes [P(CH2NPh)3]2Mn3(THF)3.1.5THF and [P(CH2N-3,5-(CF3)2C6H3)3]2Mn3(THF)3.