03 Fakultät Chemie
Permanent URI for this collectionhttps://elib.uni-stuttgart.de/handle/11682/4
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Item Open Access High‐performance carbon fibers prepared by continuous stabilization and carbonization of electron beam‐irradiated textile grade polyacrylonitrile fibers(2021) König, Simon; Bauch, Volker; Herbert, Christian; Wego, Andreas; Steinmann, Mark; Frank, Erik; Buchmeiser, Michael R.The manufacturing of high‐performance carbon fibers (CFs) from low‐cost textile grade poly(acrylonitrile) (PAN) homo‐ and copolymers using continuous electron beam (EB) irradiation, stabilization, and carbonization on a kilogram scale is reported. The resulting CFs have tensile strengths of up to 3.1 ± 0.6 GPa and Young's moduli of up to 212 ± 9 GPa, exceeding standard grade CFs such as Toray T300. Additionally, the Weibull strength and modulus, the microstructure, and the morphology of these CFs are determined.Item Open Access Melt-spinning of an intrinsically flame-retardant polyacrylonitrile copolymer(2020) König, Simon; Kreis, Philipp; Herbert, Christian; Wego, Andreas; Steinmann, Mark; Wang, Dongren; Frank, Erik; Buchmeiser, Michael R.Poly(acrylonitrile) (PAN) fibers have two essential drawbacks: they are usually processed by solution-spinning, which is inferior to melt spinning in terms of productivity and costs, and they are flammable in air. Here, we report on the synthesis and melt-spinning of an intrinsically flame-retardant PAN-copolymer with phosphorus-containing dimethylphosphonomethyl acrylate (DPA) as primary comonomer. Furthermore, the copolymerization parameters of the aqueous suspension polymerization of acrylonitrile (AN) and DPA were determined applying both the Fineman and Ross and Kelen and Tüdõs methods. For flame retardancy and melt-spinning tests, multiple PAN copolymers with different amounts of DPA and, in some cases, methyl acrylate (MA) have been synthesized. One of the synthesized PAN-copolymers has been melt-spun with propylene carbonate (PC) as plasticizer; the resulting PAN-fibers had a tenacity of 195 ± 40 MPa and a Young’s modulus of 5.2 ± 0.7 GPa. The flame-retardant properties have been determined by Limiting Oxygen Index (LOI) flame tests. The LOI value of the melt-spinnable PAN was 25.1; it therefore meets the flame retardancy criteria for many applications. In short, the reported method shows that the disadvantage of high comonomer content necessary for flame retardation can be turned into an advantage by enabling melt spinning.Item Open Access Macrocyclization of dienes under confinement with cationic tungsten imido/oxo alkylidene N‐heterocyclic carbene complexes(2023) Ziegler, Felix; Bruckner, Johanna R.; Nowakowski, Michal; Bauer, Matthias; Probst, Patrick; Atwi, Boshra; Buchmeiser, Michael R.Macrocyclization reactions are still challenging due to competing oligomerization, which requires the use of small substrate concentrations. Here, the cationic tungsten imido and tungsten oxo alkylidene N-heterocyclic carbene complexes [[W(N-2,6-Cl2-C6H3)(CHCMe2Ph(OC6F5)(pivalonitrile)(IMes)+ B(ArF)4-] (W1) and [W(O (CHCMe2Ph(OCMe(CF3)2)(IMes)(CH3CN)+ B(ArF)4-] (W2) (IMes=1,3-dimesitylimidazol-2-ylidene; B(ArF)4-=tetrakis(3,5-bis(trifluoromethyl)phenyl borate) have been immobilized inside the pores of ordered mesoporous silica (OMS) with pore diameters of 3.3 and 6.8 nm, respectively, using a pore-selective immobilization protocol. X-ray absorption spectroscopy of W1@OMS showed that even though the catalyst structure is contracted due to confinement by the mesopores, both the oxidation state and structure of the catalyst stayed intact upon immobilization. Catalytic testing with four differently sized α,ω-dienes revealed a dramatically increased macrocyclization (MC) and Z-selectivity of the supported catalysts compared to the homogenous progenitors, allowing high substrate concentrations of 25 mM. With the supported complexes, a maximum increase in MC-selectivity from 27 to 81 % and in Z-selectivity from 17 to 34 % was achieved. In general, smaller mesopores exhibited a stronger confinement effect. A comparison of the two supported tungsten-based catalysts showed that W1@OMS possesses a higher MC-selectivity, while W2@OMS exhibits a higher Z-selectivity which can be rationalized by the structures of the catalysts.Item Open Access Asymmetric Rh diene catalysis under confinement : isoxazole ring‐contraction in mesoporous solids(2024) Marshall, Max; Dilruba, Zarfishan; Beurer, Ann‐Katrin; Bieck, Kira; Emmerling, Sebastian; Markus, Felix; Vogler, Charlotte; Ziegler, Felix; Fuhrer, Marina; Liu, Sherri S. Y.; Kousik, Shravan R.; Frey, Wolfgang; Traa, Yvonne; Bruckner, Johanna R.; Plietker, Bernd; Buchmeiser, Michael R.; Ludwigs, Sabine; Naumann, Stefan; Atanasova, Petia; Lotsch, Bettina V.; Zens, Anna; Laschat, SabineCovalent immobilization of chiral dienes in mesoporous solids for asymmetric heterogeneous catalysis is highly attractive. In order to study confinement effects in bimolecular vs monomolecular reactions, a series of pseudo‐C2‐symmetrical tetrahydropentalenes was synthesized and immobilized via click reaction on different mesoporous solids (silica, carbon, covalent organic frameworks) and compared with homogeneous conditions. Two types of Rh‐catalyzed reactions were studied: (a) bimolecular nucleophilic 1,2‐additions of phenylboroxine to N‐tosylimine and (b) monomolecular isomerization of isoxazole to 2H‐azirne. Polar support materials performed better than non‐polar ones. Under confinement, bimolecular reactions showed decreased yields, whereas yields in monomolecular reactions were only little affected. Regarding enantioselectivity the opposite trend was observed, i. e. effective enantiocontrol for bimolecular reactions but only little control for monomolecular reactions was found.Item Open Access Sulfur‐composites derived from poly(acrylonitrile) and poly(vinylacetylene) : a comparative study on the role of pyridinic and thioamidic nitrogen(2023) Kappler, Julian; Klostermann, Sina V.; Lange, Pia L.; Dyballa, Michael; Veith, Lothar; Schleid, Thomas; Weil, Tanja; Kästner, Johannes; Buchmeiser, Michael R.Sulfurized poly(acrylonitrile) (SPAN) is a prominent example of a highly cycle stable and rate capable sulfur/polymer composite, which is solely based on covalently bound sulfur. However, so far no in‐depth study on the influence of nitrogen in the carbonaceous backbone, to which sulfur in the form of thioketones and poly(sulfides) is attached, exists. Herein, we investigated the role of nitrogen by comparing sulfur/polymer composites derived from nitrogen‐containing poly(acrylonitrile) (PAN) and nitrogen‐free poly(vinylacetylene) (PVac). Results strongly indicate the importance of a nitrogen‐rich, aromatic carbon backbone to ensure full addressability of the polymer‐bound sulfur and its reversible binding to the aromatic backbone, even at high current rates. This study also presents key structures, which are crucial for highly cycle and rate stable S‐composites.Item Open Access Predicting catalytic activity from 13CCH alkylidene chemical shift in cationic tungsten oxo alkylidene N‐heterocyclic carbene complexes(2021) Musso, Janis V.; Schowner, Roman; Falivene, Laura; Frey, Wolfgang; Cavallo, Luigi; Buchmeiser, Michael R.A series of cationic tungsten oxo alkylidene N‐heterocyclic carbene (NHC) complexes was synthesized and structurally characterized by single crystal X‐ray diffraction. The 13C NMR chemical shifts of the alkylidene C atoms of these complexes were correlated with the diamagnetic, paramagnetic and spin‐orbit chemical shifts calculated by DFT. A good correlation (R2=0.90) between the DFT isotropic chemical shifts and the experimental chemical shift as well as a strong correlation between the DFT isotropic chemical shifts and the TOF1min for the RCM of 1,7‐octadiene was found. Further, a comparison of the catalyst geometries allowed for assigning tetracoordinate pseudotetrahedral catalysts to the most deshielded alkylidenes and to the highest TOF1min, pentacoordinate square‐planar catalysts to the intermediate deshielded alkylidenes and intermediate TOF1min, and hexacoordinate and octahedral catalyst to the most shielded alkylidene and lowest TOF1min. Analysis of the magnetic shielding tensors allowed for ascribing variations in the chemical shifts to electronic transitions between occupied molecular orbitals corresponding to the alkylidene‐C and alkylidene‐H σ‐bonds and the empty molecular orbital corresponding to the W‐alkylidene σ*‐bond.Item Open Access Olefin metathesis under spatial confinement and continuous flow : investigation of isomeric side reactions with a Grubbs-Hoveyda type catalyst(2023) Böth, André; Roider, Thomas; Ziegler, Felix; Xie, Xiulan; Buchmeiser, Michael R.; Tallarek, UlrichA 2nd‐generation Grubbs-Hoveyda type catalyst was immobilized inside mesoporous silica and used in the ring‐closing metathesis (RCM) of an α,ω‐diene to a large macro(mono)cycle. The goal was to investigate the relationship between substrate concentration, reaction time, and overall experiment time on the rate of isomerization under spatial (mesopore space) confinement with continuous‐flow microreactors. RCM reactions are commonly monitored by 1H NMR analysis, however, elucidation of reaction mixtures yielding large rings with a difference of only a single carbon atom remains difficult, because NMR signals are sometimes indistinguishable. In this work, an analytical platform with on‐line separation and detection of UV‐active substrate as well as (side) products by high‐performance liquid chromatography and a UV/Vis‐diode array detector (DAD) plus mass spectrometry served as enabling technology to quantify yield and selectivity under the respective reaction conditions. Using this setup, competitive reaction equilibria and isomerization reactions, in particular, could be resolved. Identification and quantification of relevant compounds of the reaction scheme under spatial confinement became possible despite chemical similarity. Kinetic data revealed that isomerization increases with higher substrate concentrations (up to 250 mM) and longer reaction times (from 1.2 to 18.6 min), but shows a distinct decline for prolonged overall experiment times (up to ∼250 min).Item Open Access Olefin ring‐closing metathesis under spatial confinement and continuous flow(2021) Ziegler, Felix; Roider, Thomas; Pyschik, Markus; Haas, Christian P.; Wang, Dongren; Tallarek, Ulrich; Buchmeiser, Michael R.We report on the use of a 2nd‐generation Hoveyda-Grubbs‐type catalyst immobilized inside mesoporous silica for the application in selective macro(mono)cyclization (MMC) of an α,ω‐diene under spatially confined and continuous‐flow conditions. Reactions carried out with different flow rates allow for variations in residence time; conversion and MMC selectivity can be determined for well‐defined reaction times. Analysis of the reaction mixtures obtained for different reaction times and temperatures in a single flow experiment by NMR and MALDI‐TOF‐MS allows to address confinement effects and to determine olefin metathesis pathways. These investigations revealed that ring‐chain equilibria are quickly established but substantially affected by residence time and flow, allowing for the determination of conditions under which MMC selectivity reaches a maximum. In contrast to reactions carried out in solution, in which oligomers up to the hexamer were observed, MMC under confinement predominantly proceeds via ring‐closing metathesis of the monomer and backbiting from the dimer and trimer, but not from higher oligomers as their formation is suppressed. This leads to the observed high MMC selectivity, reaching 60 % at a 25 mM substrate concentration.Item Open Access Olefin ring‐closing metathesis under spatial confinement : morphology-transport relationships(2020) Tallarek, Ulrich; Hochstrasser, Janika; Ziegler, Felix; Huang, Xiaohui; Kübel, Christian; Buchmeiser, Michael R.Spatial confinement effects on hindered transport in mesoporous silica particles are quantified using reconstructions of their morphology obtained by electron tomography as geometrical models in direct diffusion simulations for passive, finite‐size tracers. We monitor accessible porosity and effective diffusion coefficients resulting from steric and hydrodynamic interactions between tracers and pore space confinement as a function of λ=dtracer/dmeso, the ratio of tracer to mean mesopore size. For λ=0, pointlike tracers reproduce the true diffusive tortuosities. For λ>0, derived hindrance factors quantify the extent to which diffusion through the materials is hindered compared with free diffusion in the bulk liquid. Morphology‐transport relationships are then discussed with respect to the immobilization, formation, and transport of key molecular species in the ring‐closing metathesis of an α,ω‐diene to macro(mono)cyclization product and oligomer, with a 2nd‐generation Hoveyda‐Grubbs type catalyst immobilized inside the mesopores of the particles.Item Open Access Differences in electrochemistry between fibrous SPAN and fibrous S/C cathodes relevant to cycle stability and capacity(2017) Warneke, Sven; Eusterholz, Michael; Zenn, Roland K.; Hintennach, Andreas; Dinnebier, Robert E.; Buchmeiser, Michael R.Two different Li/S cathodes are compared in terms of capacity (mA.h.gsulfur-1) and intermediates during discharge and charge. One cathode material is based on fibrous SPAN, a sulfur-containing material obtained via the thermal conversion of poly(acrylonitrile), PAN, in the presence of sulfur. In this material, sulfur is covalently bound to the polymeric backbone. The second cathode material is based on porous activated carbon fibers (ACFs) with elemental sulfur embedded inside the ACFs’ micropores. Cyclic voltammetry clearly indicates different discharge and charge chemistry of the two materials. While S-containing ACFs show the expected redox-chemistry of sulfur, SPAN does not form long-chain polysulfides during discharge; instead, sulfide is chopped off the polymer-bound sulfur chains to directly form Li2S. The high reversibility of this process accounts for both the high cycle stability and capacity of SPAN-based cathode materials.