A mononuclear Fe(III) complex showing thermally induced spin crossover and slow magnetic relaxation with reciprocating thermal behaviour.

AC susceptibility measurements of [FeIII(L5)(NCSe)] reveal a field supported slow magnetic relaxation. On cooling, the relaxation time of the high-frequency fraction decreases which is a sign of reciprocating thermal behaviour. The relaxation time for the low-frequency mode at T = 2.0 K is as high as τ(LF) = 2.0 s.

Pressing of Functionalized Polymer Composite Materials to Improve Mössbauer Measurement Signals.

Coordination compounds, like iron(II) triazole complexes, exhibit spin crossover (SCO) behavior at around room temperature. Therefore, they are interesting for a variety of possible applications, and it is convenient to integrate them into polymers. Due to a reduction of the iron content and thus also 57Fe content in the sample through integration in polymers, Mössbauer measurements are only possible with greater difficulty or very long measurement times without expensive enrichment of the samples with 57Fe. So, other ways of improving the Mössbauer signal for these composite materials are necessary. Therefore, we pressed these composite materials to improve the Mössbauer spectra. In this study, we synthesized an iron(II) triazole spin crossover complex and an electrospun polymer complex composite nanofiber material including the same complex. For both products, Mössbauer measurements were performed at room temperature before and after using a press to show that the complex composite is not harmed through pressing. We investigate the influence of the pressing impact on the Mössbauer measurements in the context of measurement statistics and the measured signals. We show that pressing is not connected to any changes in the sample regarding the spin and oxidation state. We present that pressing improves the statistics of the Mössbauer measurements significantly. Furthermore, we use SEM measurements and PXRD to investigate whether or not the obtained fiber mats are destroyed in the pressing process.

Investigation of the molecular switching process between spin crossover states of triazole complexes as basis for optical sensing applications.

With the advent of the first laser sources and suitable detectors, optical sensor applications immediately also came into focus. During the last decades, a huge variety of optical sensor concepts were developed, yet the forecast for the future application potential appears even larger. In this context, the development of new sensor probes at different scales down to the atomic or molecular level open new avenues for research and development. We investigated an iron based triazole molecular spin-crossover complex changing its absorption characteristics significantly by varying environmental parameters such as humidity, temperature, magnetic or electric field, respectively, with respect to its suitability for a new class of versatile molecular sensor probes. Hereby, besides the investigation of synthesized pure bulk material using different analyzing methods, we also studied amorphous micro particles which were applied in or onto optical waveguide structures. We found that significant changes of the reflection spectra can also be obtained after combining the particles with different types of optical waveguides.The obtained results demonstrate the suitability of the material complex for a broad field of future sensor applications.

Development of a Novel Passive Monitoring Technique to Showcase the 3D Distribution of Tritiated Water (HTO) Vapor in Indoor Air of a Nuclear Facility.

Tritiated water (HTO), a ubiquitous byproduct of the nuclear industry, is a radioactive contaminant of major concern for environmental authorities. Although understanding spatiotemporal heterogeneity of airborne HTO vapor holds great importance for radiological safety as well as diagnosing a reactor's status, comprehensive HTO distribution dynamics inside nuclear facilities has not been studied routinely yet due to a lack of appropriate monitoring techniques. For current systems, it is difficult to simultaneously achieve high representativeness, sensitivity, and spatial resolution. Here, we developed a passive monitoring scheme, including a newly designed passive sampler and a tailored analytical protocol for the first comprehensive 3D distribution characterization of HTO inside a nuclear reactor facility. The technique enables linear sampling in any environment at a one-day resolution and simultaneous preparation of hundreds of samples within 1 day. Validation experiments confirmed the method's good metrological properties and sensitivity to the HTO's spatial dynamics. The air in TU Wien's reactor hall exhibits a range of 3H concentrations from 75-946 mBq m-3 in the entire 3D matrix. The HTO release rate estimated by the mass-balance model (3199 ± 306 Bq h-1) matches the theoretical calculation (2947 ± 254 Bq h-1), suggesting evaporation as the dominant HTO source in the hall. The proposed method provides reliable and quality-controlled 3D monitoring at low cost, which can be adopted not only for HTO and may also inspire monitoring schemes of other indoor pollutants.

Incorporation and Deposition of Spin Crossover Materials into and onto Electrospun Nanofibers.

We synthesized iron(II)-triazole spin crossover compounds of the type [Fe(atrz)3]X2 and incorporated and deposited them on electrospun polymer nanofibers. For this, we used two separate electrospinning methods with the goal of obtaining polymer complex composites with intact switching properties. In view of possible applications, we chose iron(II)-triazole-complexes that are known to exhibit spin crossover close to ambient temperature. Therefore, we used the complexes [Fe(atrz)3]Cl2 and [Fe(atrz)3](2ns)2 (2ns = 2-Naphthalenesulfonate) and deposited those on fibers of polymethylmethacrylate (PMMA) and incorporated them into core-shell-like PMMA fiber structures. These core-shell structures showed to be inert to outer environmental influences, such as droplets of water, which we purposely cast on the fiber structure, and it did not rinse away the used complex. We analyzed both the complexes and the composites with IR-, UV/Vis, Mössbauer spectroscopy, SQUID magnetometry, as well as SEM and EDX imaging. The analysis via UV/Vis spectroscopy, Mössbauer spectroscopy, and temperature-dependent magnetic measurements with the SQUID magnetometer showed that the spin crossover properties were maintained and were not changed after the electrospinning processes.

Untangling the intertwined: metallic to semiconducting phase transition of colloidal MoS2 nanoplatelets and nanosheets.

2D semiconducting transition metal dichalcogenides (TMDCs) are highly promising materials for future spin- and valleytronic applications and exhibit an ultrafast response to external (optical) stimuli which is essential for optoelectronics. Colloidal nanochemistry on the other hand is an emerging alternative for the synthesis of 2D TMDC nanosheet (NS) ensembles, allowing for the control of the reaction via tunable precursor and ligand chemistry. Up to now, wet-chemical colloidal syntheses yielded intertwined/agglomerated NSs with a large lateral size. Here, we show a synthesis method for 2D mono- and bilayer MoS2 nanoplatelets with a particularly small lateral size (NPLs, 7.4 nm ± 2.2 nm) and MoS2 NSs (22 nm ± 9 nm) as a reference by adjusting the molybdenum precursor concentration in the reaction. We find that in colloidal 2D MoS2 syntheses initially a mixture of the stable semiconducting and the metastable metallic crystal phase is formed. 2D MoS2 NPLs and NSs then both undergo a full transformation to the semiconducting crystal phase by the end of the reaction, which we quantify by X-ray photoelectron spectroscopy. Phase pure semiconducting MoS2 NPLs with a lateral size approaching the MoS2 exciton Bohr radius exhibit strong additional lateral confinement, leading to a drastically shortened decay of the A and B exciton which is characterized by ultrafast transient absorption spectroscopy. Our findings represent an important step for utilizing colloidal TMDCs, for example small MoS2 NPLs represent an excellent starting point for the growth of heterostructures for future colloidal photonics.

Development and calibration of a modifiable passive sampler for monitoring atmospheric tritiated water vapor in different environments.

Anthropogenic release of tritium from nuclear facilities is expected to increase significantly in the coming decades, which may cause radiation exposure to humans through the contamination of water and food chains. It is necessary and urgent to acquire detailed information about tritium in various environments for studying its behavior and assessing the potential radiation risk. In the atmosphere, although the passive sampling technique provides a low-cost and convenient way to characterize the dynamics of tritiated water vapor (HTO), a single, simple sampler configuration makes it difficult to collect sufficient and representative samples within the expected period from different environments. In this study, we systematically studied the impacts of sampler configurations on sampling performance and proposed a modifiable sampler design by scaling sampler geometry and adjusting absorbent to achieve different monitoring demands. The samplers were subsequently deployed at five sites in China and Germany for the field calibration and the measured results exhibited a good agreement between the adsorption process obtained in sites corrected with diffusion coefficient and the one calibrated in Shanghai. This suggests the feasibility of predicting sampling performance in the field based on known data. Finally, we developed a strategy for sampler modification and selection in different environments and demonstrated that using easily obtainable environmental data, our sampler can be optimized for any area without any time-consuming preliminary experiments. This work provides a scientific basis for establishing high-resolution atmospheric HTO database and expands the conventional empirical sampler design paradigm by demonstrating the feasibility of using quantitative indices for sampler performance customization.

Second harmonic generation on chiral cyanido-bridged FeII-NbIV spin-crossover complexes.

Incorporating chiral organic ligands into cyanido-bridged FeII-NbIV assemblies synthesized chiral spin-crossover complexes, FeII2[NbIV(CN)8](L)8·6H2O (L = R-, S-, or rac-1-(3-pyridyl)ethanol: R-FeNb, S-FeNb, or rac-FeNb). Rietveld analyses based on a racemic complex of rac-FeNb indicate that the chiral complexes have a cubic crystal structure in the I213 space group with a three-dimensional cyanido-bridged FeII-NbIV coordination network. All the complexes exhibit spin crossover between the high-spin (HS) and the low-spin (LS) FeII states without thermal hysteresis. Chiral complexes of R-FeNb and S-FeNb show second harmonic generation (SHG) due to their non-centrosymmetric structure. The I213 space group provides second-order susceptibility tensor elements of χxyz, χyzx, and χzxy, which contribute to SHG. The temperature-dependent second harmonic light intensity change is due to spin crossover between FeIIHS and FeIILS.

Polymer Optical Waveguide Sensor Based on Fe-Amino-Triazole Complex Molecular Switches.

We report on a polymer-waveguide-based temperature sensing system relying on switchable molecular complexes. The polymer waveguide cladding is fabricated using a maskless lithographic optical system and replicated onto polymer material (i.e., PMMA) using a hot embossing device. An iron-amino-triazole molecular complex material (i.e., [Fe(Htrz)2.85(NH2-trz)0.15](ClO4)2) is used to sense changes in ambient temperature. For this purpose, the core of the waveguide is filled with a mixture of core material (NOA68), and the molecular complex using doctor blading and UV curing is applied for solidification. The absorption spectrum of the molecular complex in the UV/VIS light range features two prominent absorption bands in the low-spin state. As temperature approaches room temperature, a spin-crossover transition occurs, and the molecular complex changes its color (i.e. spectral properties) from violet-pink to white. The measurement of the optical power transmitted through the waveguide as a function of temperature exhibits a memory effect with a hysteresis width of approx. 12 °C and sensitivity of 0.08 mW/°C. This enables optical rather than electronic temperature detection in environments where electromagnetic interference might influence the measurements.

Spin-crossover in an iron(III) complex showing a broad thermal hysteresis.

A pentadentate Schiff-base ligand 3,5Cl-L2- and NCSe- form an iron(iii) mononuclear complex, namely [Fe(3,5Cl-L)(NCSe)], which shows a thermally induced spin crossover with a broad hysteresis width of 24 K between 123 K (warming) and 99 K (cooling). Analogous complexes of the [Fe(3,5X-L)(Y)] type, where X = Cl or Br and Y = Cl-, N3-, NCS-, and NCSe-, are high-spin over the whole temperature interval.

Octacyanidorhenate(V) Ion as an Efficient Linker for Hysteretic Two-Step Iron(II) Spin Crossover Switchable by Temperature, Light, and Pressure.

A two-step hysteretic FeII spin crossover (SCO) effect was achieved in programmed layered Cs{[Fe(3-CNpy)2 ][Re(CN)8 ]}⋅H2 O (1) (3-CNpy=3-cyanopyridine) assembly consisting of cyanido-bridged FeII -ReV square grid sheets bonded by Cs+ ions. The presence of two non-equivalent FeII sites and the conjunction of 2D bimetallic coordination network with non-covalent interlayer interactions involving Cs+ , [ReV (CN)8 ]3- ions, and 3-CNpy ligands, leads to the occurrence of two steps of thermal SCO with strong cooperativity giving a double thermal hysteresis loop. The resulting spin-transition phenomenon could be tuned by an external pressure giving the room-temperature range of SCO, as well as by visible-light irradiation, inducing an efficient recovery of the high-spin FeII state at low temperatures. We prove that octacyanidorhenate(V) ion is an outstanding metalloligand for induction of a cooperative multistep, multiswitchable FeII SCO effect.

Slow magnetic relaxation in a high-spin pentacoordinate Fe(iii) complex.

A mononuclear pentacoordinate iron(iii) complex shows slow magnetic relaxation with three relaxation channels. The high-frequency relaxation time of the order of microseconds is prolonged on cooling in accordance with the direct and Raman processes. The low frequency relaxation time is little dependent on temperature and varies in the range τ(LF) = 0.52-0.79 s.

Solid-State Hydrogen-Bond Alterations in a [Co2 Fe2 ] Complex with Bifunctional Hydrogen-Bonding Donors.

A hydrogen-bonding donor-acceptor system, [Co2 Fe2 (bpy*)4 (CN)6 (tp*)2 ](PF6 )2 ⋅2ABA⋅4BN⋅2PE (1 solv ), was prepared by co-crystallization of an external stimuli-responsive cyanide-bridged tetranuclear [Co2 Fe2 ] complex and bifunctional hydrogen-bonding donors, p-aminobenzoic acid. Compound 1 solv exhibited a gradual electron-transfer-coupled spin transition (ETCST), and the removal of solvent molecules led to an abrupt thermal ETCST behavior with increased transition temperature. X-ray structural analysis revealed that the modification of ETCST was caused by a significant alteration of a hydrogen-bonding mode between the tetranuclear [Co2 Fe2 ]2+ cations and ABA molecules. Variable temperature IR measurements indicated that the desolvated form, 1 desolv , showed dynamic alteration of hydrogen-bonding interactions coupled with thermal ETCST behavior. These results suggested that the tetranuclear [Co2 Fe2 ] complex shows solid-state modulations of hydrogen-bond strengths by external stimuli.

A Brønsted-Ligand-Based Iron Complex as a Molecular Switch with Five Accessible States.

A mononuclear FeII complex, prepared with a Brønsted diacid ligand, H2 L (H2 L=2-[5-phenyl-1H-pyrazole-3-yl] 6-benzimidazole pyridine), shows switchable physical properties and was isolated in five different electronic states. The spin crossover (SCO) complex, [FeII (H2 L)2 ](BF4 )2 (1A ), exhibits abrupt spin transition at T1/2 =258 K, and treatment with base yields a deprotonated analogue [FeII (HL)2 ] (1B ), which shows gradual SCO above 350 K. A range of FeIII analogues were also characterized. [FeIII (HL)(H2 L)](BF4 )Cl (1C ) has an S=5/2 spin state, while the deprotonated complexes [FeIII (L)(HL)], (1D ), and (TEA)[FeIII (L)2 ], (1E ) exist in the low-spin S=1/2 state. The electronic properties of the five complexes were fully characterized and we demonstrate in situ switching between multiple states in both solution and the solid-state. The versatility of this simple mononuclear system illustrates how proton donor/acceptor ligands can vastly increase the range of accessible states in switchable molecular devices.

Effect of the degree of inversion on optical properties of spinel ZnFe2O4.

Spinel ferrites (T[M1-xFex]O[MxFe2-x]O4 with 0 ≤ x ≤ 1, where M is a bivalent metal ion and the superscripts denote tetrahedral and octahedral sites) are materials commonly used in electronics due to their outstanding magnetic properties. Thus, the effect of the degree of inversion, x, on these properties is well known. However, its effect on other properties of these materials has rarely been investigated in detail. Since ferrites gained much attention during the last decade as visible light active photocatalysts and photoelectrocatalysts, understanding the effect of the degree of inversion on the optical properties became necessary. Among photocatalytically and photoelectrocatalytically active spinel ferrites, zinc ferrite (ZnFe2O4, ZFO) is one of the most widely studied materials. In this work, five ZFO samples with degrees of inversion varying from 0.07 to 0.20 were prepared by a solid-state reaction employing different annealing temperatures and subsequent quenching. Raman and UV-Vis-NIR spectra were measured and analyzed together with theoretical results obtained from ab initio calculations. Changes in the UV-Vis-NIR spectra associated with electronic transitions of tetrahedrally and octahedrally coordinated Fe3+ ions are distinguished. However, the optical band gap of the material remains unchanged as the degree of inversion varies. Based on the experimental and theoretical results, a new assignment for the Raman active internal modes and the electronic transitions of ZFO is proposed.

Mixture of PLA-PEG and biotinylated albumin enables immobilization of avidins on electrospun fibers.

The application of nanotechnology in biomedical field has enormous potential in basic and applied research. Micro or nanofibers produced by electrospinning technique offer excellent properties because of large specific surface area, high porosity, and ability to incorporate functional additives. Here we embedded biotinylated bovine serum albumin into polylactic acid (PLA)-polyethylene glycol (PEG) fibers, which enabled specific immobilization of fluorescently labelled avidin. An alkaline phosphatase enzyme was immobilized via biotin-streptavidin interaction on the hybrid nanofibers, demonstrating the suitability of the material for biosensing applications. These functional nanofibers provide a promising platform for development of biosensors and other biofunctional materials utilizing avidin-biotin as a generic and robust immobilization method. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 356-362, 2017.

Spin state switching of metal complexes by visible light or hard X-rays.

Electromagnetic stimuli of spin crossover compounds restricted to UV-vis light irradiation for many years could be recently extended to X-ray excitation. This review covers a large variety of light-induced effects, as well as recent analogues stimulated by X-ray irradiation which have not yet been reviewed. The focus is also on multistable multinuclear spin crossover compounds which are the subject of lively discussions within the spin crossover community. Their spin transition often occurs incompletely and with different switching mechanisms. In this review, we recall a predicted sequential switching induced thermally as well as a concerted stimulation mechanism by light irradiation for these interesting multifunctional materials.

Simultaneous cancer control and diagnosis with magnetic nanohybrid materials.

Coated magnetite nanoparticles were linked to (68)Ga complexes used in the positron emission tomography (PET) for a new technical approach to detect cancer tissue with radiopharmaceuticals. By substitution of the Ga isotope with an alpha emitter the same compound could be used for cancer treatment. Furthermore the nanoparticles were connected to pH-sensitive complexes, enabling a pH-controlled assembly/disassembly and therefore the spreading of the particles in the tissue. With this novel method of combining detection and treatment simultaneously, the amount of medical exposure could be minimized for the patient. The results demonstrate that magnetite nanoparticles can effectively be functionalized with PET isotopes and pH sensitive complexes in order to use them as a new type of radiopharmaceuticals.

[Fe19 ] "Super-Lindqvist" Aggregate and Large 3D Interpenetrating Coordination Polymer from Solvothermal Reactions of [Fe2 (OtBu)6 ] with Ethanol.

The syntheses, crystal structures, and physical properties of [HFe19 O14 (OEt)30 ] and {Fe11 (OEt)24 }∞ are reported. [HFe19 O14 (OEt)30 ] has an octahedral shape. Its core with a central Fe metal ion surrounded by six µ6 -oxo ligands is arranged in the rock salt structure. {Fe11 (OEt)24 }∞ is a mixed-valence coordination polymer in which Fe(III) metal ions form three 3D interpenetrating (10,3)-b nets. The arrangement of the Fe(III) ions can also be compared to that of Si ions in α-ThSi2 . Thus, the described structures are at the interface between molecular and solid-state chemistry.

Mixed-valence heptanuclear iron complexes with ferromagnetic interaction.

Three new Prussian blue analogues, heptanuclear mixed-valence iron complexes of the type [Fe(II)(CN)(6){Fe(III)(1(-2H))}(6)]Cl(2)·nH(2)O, were synthesized and structurally and spectrally characterized, and their magnetic properties were investigated (1(-2H) corresponds to doubly deprotoned Schiff-base pentadentate ligands 1a, N,N'-bis(2-hydroxybenzylidene)-1,5-diamino-3-azapentane, 1b, N,N'-bis(3-ethoxy-2-hydroxybenzylidene)-1,7-diamino-4-azaheptane, or 1c, N,N'-bis(3-methoxy-2-hydroxybenzylidene)-1,6-diamino-3-azahexane). These compounds were formed by assembling the [Fe(CN)(6)](4-) building block with mononuclear complexes of the [Fe(1(-2H))Cl] type. X-ray structure analysis revealed that the complexes adopt a star-like architecture: the Fe(II) ion lies at the very center, and on its octahedral nodes the Fe(III) sites are coordinated in the Fe(II)-C≡N-Fe(III) manner. The Schiff-base pentadentate ligand moiety 1(-2H) coordinates a single Fe(III) center in two complexes 3b and 3c. Ligands 1a(-2H) in the complex cation of 3a adopt an unusual coordination mode: three donor atoms of the same ligand (one O and two N) coordinate one Fe(III), whereas the remaining N' and O' donor atoms coordinate the neighboring Fe(III) center creating the {Fe(ON(2))(N'O')N″} chromophore involving two 1a(-2H) ligand moieties. Moreover, three Fe(III) centers are interconnected with three 1a(-2H) ligands in such a manner that two {Fe(III)(3)(1a(-2H))(3)} units form two intramolecular rings. Magnetic investigation of the heptanuclear complexes revealed the high-spin state of all six Fe(III) coordination sites (s = 5/2), while the very central Fe(II) site is in the low-spin state (s = 0). At low temperature, the ferromagnetic exchange interactions stay evident for all three complexes. Mössbauer spectra of compounds 3a and 3b revealed a presence of two different doublets for both compounds: the major doublet is related to six Fe(III) high-spin coordination sites and the minor doublet refers to the low-spin very central Fe(II).