Feasibility study for production of 99mTc by neutron irradiation of MoO3 in a 250 kW TRIGA Mark II reactor

The subject of this paper is to explore the possibility to obtain ^99mTc from activation of ⁹⁸Mo, using the TRIGA Mark II low flux research reactor (Vienna, Austria). Irradiation of both natural and enriched in ⁹⁸Mo molybdenum oxides was compared. Aims of this work included the determination of neutron fluxes and ⁹⁸Mo(n, γ)⁹⁹Mo reaction effective cross section in the TRIGA Mark II reactor irradiation channels, calculation of ⁹⁹Mo specific activities, determination of optimal irradiation conditions for the subsequent ^99mTc separation from MoO₃ targets using concentrating technologies.     

Synthesis of tris(β,β,γ-oximinoalkyl)amines from aliphatic nitro compounds and methyl vinyl ketone

A general strategy for the assembly of previously unknown tris(β,β,γ-oximinoalkyl)amines from aliphatic nitro compounds and methyl vinyl ketone is described. The strategy involves N,N-bis(siloxy)enamines as key intermediates. The latter are accessible by double silylation of alkylnitro compounds. Nickel(II) and copper(II) complexes of tris(β,β,γ-oximinoalkyl)amines are prepared and structurally characterized.     

The effect of ply properties in paperboard converting operations: a way to increase formability

Cellulose - This study addresses the question of how the difference in mechanical properties of the individual layers in a multi-ply commercial paperboard affects the outcome of the tray-forming...     

Third Generation Buchwald Precatalysts with XPhos and RuPhos: Multigram Scale Synthesis,Solvent-Dependent Isomerization of XPhos Pd G3 and Quality Control by 1H- and 31P-NMR Spectroscopy

The third generation Buchwald precatalysts Pd(ABP)(Phos)(OMs) (also known as Phos Pd G3)) with XPhos and RuPhos were prepared in multigram scale by a modified procedure (ABP = fragment of C-deprotonated 2-aminobiphenyl, XPhos = 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl, RuPhos = 2-dicyclohexylphosphino-2′,6′-diisopropoxybiphenyl, OMs⁻ = CH₃SO₃⁻). The ¹H- and ³¹P-NMR spectra of the title complexes and some impurities, measured by various 1D and 2D techniques, were analyzed in detail. The solvent-dependent isomerization of Pd(ABP)(XPhos)(OMs) was studied by NMR, and the X-ray structures of two isomers were determined. The impurities in precatalysts, such as Pd(ABP)(HABP)(OMs) (HABP—neutral 2-aminobiphenyl coordinated to Pd²⁺ in N-monodentate mode) and PdCl₂(XPhos)₂, were identified and characterized by single crystal X-ray diffraction. A simple method for the quick quality control (QC) of the precatalysts, suitable for routine use, was proposed. The method was based on the assessment of the impurity content on the basis of the ¹H-NMR spectra analysis.     

Ferromagnetically Coupled S=1 Chains in Crystals of Verdazyl-Nitronyl Nitroxide Diradicals

Thermally stable organic diradicals with a triplet ground state along with large singlet-triplet energy gap have significant potential for advanced technological applications. A series of phenylene-bridged diradicals with oxoverdazyl and nitronyl nitroxide units were synthesized via a palladium-catalyzed cross-coupling reaction of iodoverdazyls with a nitronyl nitroxide-2-ide gold(I) complex with high yields. The diradicals exhibit high stability and do not decompose in an inert atmosphere up to 180 °C. For the diradicals, both substantial AF (ΔE_ST≈−64 cm⁻¹) and FM (ΔE_ST≥25 and 100 cm⁻¹) intramolecular exchange interactions were observed. The sign of the exchange interaction is determined both by the bridging moiety (para- or meta-phenylene) and by the type of oxoverdazyl block (C-linked or N-linked). Upon crystallization, diradicals with the triplet ground state form unique one-dimensional exchange-coupled chains with strong intra- and weak inter-diradical ferromagnetic coupling.     

Preparation and Crystal Structure of a New Uranyl Sulfate Templated by a Bis-isothiouronium Cation

Crystals of a new uranyl sulfate (C₂N₄H₈S₂)[UO₂(SO₄)₂] · 0.3H₂O ( 1 ) templated by a relatively rare bis-isothiouronium cation, were formed upon evaporation of aqueous solutions containing uranyl acetate, thiourea, and excess sulfuric acid. The new compound is orthorhombic, P2₁2₁2₁, a = 6.928(2) Å, b = 13.398(3) Å, c = 15.225(3) Å, Z = 2. Its crystal structure is comprised of [UO₂(SO₄)₂] moieties linked by hydrogen bonds formed between the template cations and terminal oxygen atoms of the sulfate tetrahedra. The C₂N₄H₈S₂²⁺ template is most likely formed in situ during a redox reaction between uranyl cation and thiourea in a strongly acidic medium, with UO₂²⁺ partially reduced to U⁴⁺.     

Monocrystalline Quartz ICP Etching: Road to High-Temperature Dry Etching

Plasma Chemistry and Plasma Processing - In this study, the dry plasma-chemical etching process of monocrystalline SiO2 (quartz) in a fluoride-based (sulfur hexafluoride, SF6) inductively coupled...     

Noninvasive Temperature Measurement in Dental Materials Using Nd3+, Yb3+ Doped Nanoparticles Emitting in the Near Infrared Region

In this work, the application of near infrared (NIR)-emitting NaYbF₄:1%Tm³⁺@NaLuF₄:30%Nd³⁺ core–shell nanoparticles is reported for noninvasive probing and monitoring the temperature during photopolymerization of dental materials. When excited at 808 nm, the synthesized nanoparticles emit NIR photoluminescence (PL) with two distinctive peaks at 865 and 980 nm which correspond to radiative transitions from the doped Nd³⁺ and Yb³⁺ ions, respectively. Luminescence intensity ratio between these two bands is found to vary with temperature due to temperature-dependent electronic excitation energy transfer between Nd³⁺ and Yb³⁺ ions at the core/shell interface. This finding allows luminescence ratiometric evaluation of the in situ temperature during photopolymerization of resin cement (doped with nanoparticles) in a veneer placement procedure. In addition, the NIR emission also enables PL imaging of the distribution of the adhesive under the veneer. The results highlight that rare-earth ions–doped nanoparticles with both excitation and emission in the NIR spectral range are advantageous for both PL-based nanothermometry and imaging due to the reduced attenuation of NIR light by dental ceramics.