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Full-Text Articles in Engineering
Ionic Liquids As Crystallization Media: Weakly-Coordinating Anions Do Coordinate In 1∞[Eu(Otf)3(Ch3cn)3], Sifu Tang, Anja V. Mudring
Ionic Liquids As Crystallization Media: Weakly-Coordinating Anions Do Coordinate In 1∞[Eu(Otf)3(Ch3cn)3], Sifu Tang, Anja V. Mudring
Anja V. Mudring
Tris(acetonitrile)tris(trifluoromethanesulfonato)-europium(III), 1∞[Eu(OTf)3(CH3CN)3], is the first structurally characterized Ln(OTf)3-solvate where triflate is still in the coordination sphere of the Ln(III) cation and not substituted by solvate molecules. This fact is attributed to the unique crystallization conditions that an ionic liquid provides: 1∞[Eu(OTf)3(CH3CN)3] was obtained from a solution of europium(III) triflate, Eu(OTf)3, with acetonitrile in the ionic liquid [C4py][OTf] (1-butylpyridinium triflate). The crystal structure (triclinic, P1̅ (no. 2), a = 5.734(1) Å, b = 10.500(2) Å, c = 19.088(4) Å, α = 98.09(3)°, β = 93.79(3)°, γ = 91.46(3)°, V = 1134.5(4) Å3, Z = 2, R1 for 4388 reflections with Io …
Efficient Quantum Cutting In Hexagonal Nagdf4:Eu3+ Nanorods, Pushpal Ghosh, Sifu Tang, Anja V. Mudring
Efficient Quantum Cutting In Hexagonal Nagdf4:Eu3+ Nanorods, Pushpal Ghosh, Sifu Tang, Anja V. Mudring
Anja V. Mudring
An ionic liquid (IL) assisted solvothermal method is employed to prepare single phase, oxygen free, hexagonal NaGdF4:Eu3+ (2 mol%) nanorods with a visible quantum efficiency of 187%. In contrast, for mixed materials containing cubic and hexagonal NaGdF4:Eu3+, the quantum efficiency is much less (127%). Thus, synthesis parameters have to be carefully chosen in order to get the high performance hexagonal material. Not only the influence of the IL but also of the Gd : F ratio during synthesis as well as the temperature were studied. It is found that the IL stabilizes the formation of hexagonal NaGdF4:Eu3+, likewise a fluoride …
Stability And Growth Behavior Of Transition Metal Nanoparticles In Ionic Liquids Prepared By Thermal Evaporation: How Stable Are They Really?, Kai Richter, Alexander Birkner, Anja V. Mudring
Stability And Growth Behavior Of Transition Metal Nanoparticles In Ionic Liquids Prepared By Thermal Evaporation: How Stable Are They Really?, Kai Richter, Alexander Birkner, Anja V. Mudring
Anja V. Mudring
Recently we developed an access to metal- and metal-oxide colloids based on thermal evaporation of metals into ionic liquids (ILs). Here we present systematic studies on the long-time stability of gold and copper nanoparticles (NPs) in different ILs. The influence of metal concentration and temperature on the ripening of the as-prepared gold NPs in different ILs was investigated by transmission electron microscopy (TEM) and UV-vis absorption measurements. Short alkyl chain-length-methyl-imidazolium salts with weakly coordinating perfluorinated counter anions (PF6, BF4 or Tf2N, bis(trifluoromethanesulfonyl)amide) were found to be better stabilizers compared to ILs with cations bearing long alkyl chains (trihexyltetradecylphosphonium, 1-octyl-3-methylimidazolium) and …
Structures, Electronic Properties And Solid State Luminescence Of Cu(I) Iodide Complexes With 2,9-Dimethyl-1,10-Phenanthroline And Aliphatic Aminomethylphosphines Or Triphenylphosphine, Radoslaw Starosta, Malgorzata Puchalska, Joanna Cybinska, Maciej Barys, Anja V. Mudring
Structures, Electronic Properties And Solid State Luminescence Of Cu(I) Iodide Complexes With 2,9-Dimethyl-1,10-Phenanthroline And Aliphatic Aminomethylphosphines Or Triphenylphosphine, Radoslaw Starosta, Malgorzata Puchalska, Joanna Cybinska, Maciej Barys, Anja V. Mudring
Anja V. Mudring
The luminescent complexes of triphenylphosphine and two interesting aminomethylphosphines: P(CH2N(CH2CH2)2NCH3)3 and P(CH2N(CH2CH2)2O)3 with copper(I) iodide and 2,9-dimethyl-1,10-phenanthroline (dmp): [CuI(dmp)PPh3], [CuI(dmp)P(CH2N(CH2CH2)2NCH3)3] and [CuI(phen)P(CH2N(CH2CH2)2O)3] are presented in this work. These complexes were characterized in solution by means of NMR spectroscopy and their structures were crystallographically determined in the solid state. All complexes crystallize as the discrete dimers bound by π-stacking interactions between dmp rings. The coordination geometry about the Cu(I) centre is pseudo-tetrahedral showing small flattening and large rocking distortions. The investigated compounds exhibit intense orange photoluminescence in the solid state (emission peaks at r.t.: λmax = 588–592 nm; τ = 1.7–2.2 …
In-Situ Crystal Growth And Properties Of The Magnetic Ionic Liquid [C2mim][Fecl4], Tobias Backer, Oliver Breunig, Klaus Merz, Vera Vasylyeva, Anja V. Mudring
In-Situ Crystal Growth And Properties Of The Magnetic Ionic Liquid [C2mim][Fecl4], Tobias Backer, Oliver Breunig, Klaus Merz, Vera Vasylyeva, Anja V. Mudring
Anja V. Mudring
[C2mim][FeCl4] behaves like a paramagnetic liquid at room temperature. Specific heat measurements indicate that there is a magnetic ordering below 3.8 K. The released entropy is far from the expected value for a J = 5/2 system, implying that the magnetic state is partly disordered. Full magnetic polarization was reached in fields above 4 T, and the anomaly in the magnetic susceptibility can be fully suppressed in higher B fields. Hence, the suggested magnetic ground state is superparamagnetic. In order to better understand the magnetic nature of this compound, structural investigations were carried out. Raman and IR-spectroscopy as well as …
A New Open-Framework Iron Borophosphate From Ionic Liquids: Kfe[Bp2o8(Oh)], Guangmei Wang, Anja V. Mudring
A New Open-Framework Iron Borophosphate From Ionic Liquids: Kfe[Bp2o8(Oh)], Guangmei Wang, Anja V. Mudring
Anja V. Mudring
A new open-framework iron borophosphate, KFe[BP2O8(OH)], has been obtained by ionothermal synthesis from KH2PO4, FeCl3∙4H2O, H3BO3 and [C4mpyr]Br (1-butyl-1-methylpyrrolidinium bromide). Single-crystal X-ray diffraction analysis shows that KFe[BP2O8(OH)] (monoclinic, P21/c, a = 9.372(2) Å , b = 8.146(2)Å , c = 9.587(2) Å, β = 101.18(3)°, V = 718.0(2)Å3 and Z = 4) has a three-dimensional (3-D) framework structure composed by {Fe(III)O5(OH)} octahedra as well as {BO3(OH)} and {PO4} tetrahedra. As anionic structural sub-unit, KFe[BP2O8(OH)], contains an infinite open-branched {[BP2O8(OH)]4-} chain which is formed by alternating {BO3(OH)} and {PO4} tetrahedra. {Fe(III)O5(OH)} octahedra share common O corners with five phosphate tetrahedra and …
The First Lanthanide Telluride-Bromide: La3te4br, A Valence Compound, Markus Larres, Anja V. Mudring, Gerd Meyer
The First Lanthanide Telluride-Bromide: La3te4br, A Valence Compound, Markus Larres, Anja V. Mudring, Gerd Meyer
Anja V. Mudring
The first ternary lanthanide telluride-bromide La3Te4Br was obtained from a mixture of LaTe and LaBr3 (in the presence of iridium) in a sealed tantalum container at elevated temperatures. The crystal structure (orthorhombic, Pnma, a = 1634.3(2), b = 435.0(1), c = 1426.6(2) pm, Z = 4, R1 (I0 > 2s(I0)) = 0.0349) is built from dicapped trigonal prisms of tellurium and bromine atoms surrounding lanthanum in two different ways. The dicapped trigonal prisms are connected via common edges to a threedimensional structure, in the same fashion as is known for the binary U3Te5. La3Te4Br is a valence compound according to (La3+)3(Te2-)4(Br-) …
Linear Trimeric Hafnium Clusters In Hf0.86(1)I3, Jan Beekhuizen, Anja V. Mudring, Gerd Meyer
Linear Trimeric Hafnium Clusters In Hf0.86(1)I3, Jan Beekhuizen, Anja V. Mudring, Gerd Meyer
Anja V. Mudring
The reduction of hafnium tetraiodide, HfI4, with aluminum at 600 °C or 850 °C in the presence of a NaI flux resulted in black single crystals of Hf0.86(1)I3. This composition corresponds well to the upper end of the non-stoichiometry range 0.89 ≤ x ≤ 1.00 previously reported for HfxI3. The crystal structure (a = 1250.3(2), c = 1999.6(3) pm, R-3m, Z = 18) is made up of hexagonal closest packed layers of iodide ions. One third of the octahedral holes would be filled as in TiI3 or ZrI3 if it were Hf1.00I3. In Hf0.86(1)I3, one out of six octahedral holes …
(B15c5)Bii3(I2): Molecular Benzo-15-Crown-5―Bii3 Complexes Bridged By Iodine Molecules To Chains, Christoph Fiolka, Mark Richter, Ingo Pantenburg, Anja V. Mudring, Gerd Meyer
(B15c5)Bii3(I2): Molecular Benzo-15-Crown-5―Bii3 Complexes Bridged By Iodine Molecules To Chains, Christoph Fiolka, Mark Richter, Ingo Pantenburg, Anja V. Mudring, Gerd Meyer
Anja V. Mudring
The reaction of bismuth triiodide with iodine and benzo-15-crown-5 in ethanol/dichloromethane yielded red single crystals of (b15c5)BiI3(I2) (monoclinic, P21/c (no. 14), a = 1376.9(1), b = 1172.7(1), c = 1700.2(2) pm, b = 115.197(6), V = 2484.1(4)·106 pm3, Z = 4). Neutral pseudo-octahedral complexes (b15c5)BiI3 are connected by secondary bonding interactions via iodine molecules to chains. Electronic structure calculations of the neutral complex (b15c5)BiI3 reveal that the compound can indeed be described as b15c5 interacting with a molecular BiI3 unit. However, bonding has to be mainly electrostatic as the interactions of the bismuth 6s lone pair with the 2p orbitals …
Europium(Iii) Fluoride Nanoparticles From Ionic Liquids: Structural, Morphological, And Luminescent Properties, Chantal Lorbeer, Joanna Cybinska, Anja V. Mudring
Europium(Iii) Fluoride Nanoparticles From Ionic Liquids: Structural, Morphological, And Luminescent Properties, Chantal Lorbeer, Joanna Cybinska, Anja V. Mudring
Anja V. Mudring
Inorganic luminescent materials (phosphors) find widespread scientific and industrial applications. For potential applications, nanoscale phosphors are favored because of the reduced scattering and the possibility to miniaturize devices. In such materials, the optical behavior is strongly dependent on impurities or defects in the crystal lattice, so that a well-defined reaction protocol with fixed parameters is compulsory to ensure the quality of the obtained material. The fast and facile conversion of europium acetate via microwave radiation with and in different tetrafluoroborate ionic liquids to oxygen-free, hexagonal EuF3 nanoparticles is investigated in detail. The study of the influence of the different reaction …