TY - JOUR A1 - Pawlik, Alf A1 - König, R. A1 - Scholz, G. A1 - Kemnitz, E. A1 - Brunklaus, G. A1 - Bertmer, M. A1 - Jäger, Christian T1 - Access to local structures of HS-AIF3 and its precursor determined by high-resolution solid-state NMR KW - Aluminium fluoride KW - 27Al NMR KW - MQMAS KW - Amorphous materials KW - Catalysts PY - 2009 DO - https://doi.org/10.1021/jp904626k SN - 1932-7447 SN - 1089-5639 VL - 113 IS - 38 SP - 16674 EP - 16680 PB - Soc. CY - Washington, DC AN - OPUS4-20463 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mehner, Hartmut A1 - Feist, M. A1 - Stößer, R. A1 - Scholz, G. A1 - Kemnitz, E. A1 - Dwelk, H. T1 - Halogeno metallates of transition elements with cations of nitrogen-containing heterocyclic bases, IX. Moessbauer and ESR spectroscopic investigation of aquachloro- and bromoferrates(III). On the compatibility of structural information obtained by spectroscopic and diffraction methods N2 - The 57Fe-Moessbauer spectrum of (dmpipzH2)2[FeIII(H2O)2Cl4][FeIII Cl4]Cl2 (1) consists of two doublets caused by a strongly distorted octahedral and a non-distorted tetrahedral component. Both (dmpipzH2)[FeIIIBr4]2 (2) and (trienH2)[FeIIIBr4]Br (3) show only one doublet indicating a more strongly distorted iron(III) species for 2 and a less-distorted one in the case of 3. For all compounds investigated, the ESR spectra reveal the existence of ground states with predominant antiferromagnetic coupling. The Néel temperatures amount to <4.2 K for 1, 4 K for 3 and 48 K for 2. In the case of 2, both the Moessbauer and the ESR spectra reveal the formation of exchange-coupled {FeBr4} units which has been attributed to a significant cation influence. The fine structure of residual paramagnetic [FeBr4]- subunits remaining in the crystalline matrix could be directly determined. Temperature dependent AC and DC susceptibility measurements of 2 and 3 confirmed the results. KW - Iron coordination KW - Antiferromagnetic coupling KW - Exchange-coupled units KW - ESR fine structure KW - Magnetic susceptibility PY - 2002 DO - https://doi.org/10.1016/S1293-2558(01)01193-1 SN - 1293-2558 SN - 1873-3085 VL - 4 IS - 1 SP - 109 EP - 115 PB - Elsevier CY - Amsterdam AN - OPUS4-1311 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hemmann, F. A1 - Scholz, G. A1 - Scheurell, K. A1 - Kemnitz, E. A1 - Jäger, Christian T1 - Time-optimized 15N qNMR determination of Lewis and Brønsted site concentrations and chemical bonding of pyridine at Brønsted sites in amorphous aluminium hydroxide fluoride N2 - Time-optimized 15N quantitative NMR (qNMR) is described for the precise determination of Lewis and Brønsted site concentrations per gram catalyst, enabling a measurement time reduction of more than a factor of 10. The proof-of-principle is demonstrated for amorphous aluminum hydroxide fluorides with their tunable Lewis to Brønsted functionalities and relevance to highly active and selective heterogeneous catalysis using pyridine as a widely accepted probe molecule for Lewis and Brønsted sites. Two different Lewis centers were found, and reliable site concentrations down to the micromole per gram region can be determined. Furthermore, 1H{15N} REDOR NMR for the acid proton at the Brønsted site yields a distance of the 15N atom of bonded pyridine to this acid proton of (0.112 ± 0.002) nm, such that fast motion/diffusion of the Brønsted site-bonded pyridine at the surface can be excluded. KW - Catalysis KW - Lewis/Brønsted acid sites KW - Acid site concentration KW - Pyridine KW - Quantitative NMR KW - 15N KW - REDOR PY - 2012 DO - https://doi.org/10.1021/jp212045w SN - 1932-7447 SN - 1089-5639 VL - 116 IS - 19 SP - 10580 EP - 10585 PB - Soc. CY - Washington, DC AN - OPUS4-27724 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - König, R. A1 - Scholz, G. A1 - Veiczi, M. A1 - Jäger, Christian A1 - Troyanov, S.I. A1 - Kemnitz, E. T1 - New crystalline aluminium alkoxide oxide fluorides: evidence of the mechanism of the fluorolytic sol-gel reaction N2 - This study reports three new crystalline aluminum isopropoxide oxide fluorides with molar ratios of Al:F equal to 1:1 and 1:1.25. These are the first three representatives isolated without the incorporation of external donor molecules. Compound 1 Al4F4(µ4-O)(µ-O'Pr)5[H(O'Pr)2] contains a tetranuclear unit consisting of two different five fold coordinated AlFO4-units, with F exclusively in the terminal position. Compound 2, Al4F4(µ4-O)(µ-O'Pr)5[H(O'Pr)2]·Al5F5(µ5-O)(µ-O'Pr)8, contains both a tetranuclear unit (as in 1) and a pentanuclear Al-unit. Al-atoms in the latter are five- and six fold coordinated. Compound 3, Al16F20(µ4-O)4(µ-O'Pr)20·2('PrOH), exhibits a slightly higher fluorination degree and contains an oligomeric chain of four F-linked tetranuclear Al-units. In addition to X-ray structure analysis, compound 1 was characterized by different solid state MAS NMR techniques, including 27Al triple quantum MAS NMR and 1H, 1H→13C CP, 19F and 27Al MAS NMR. On the basis of the collected data, a reliable decomposition of 27Al single pulse MAS NMR spectra and an unambiguous assignment of the resonances to the respective structural AlFO4-units are given. The new crystalline aluminum isopropoxide oxide fluorides are direct evidence of the fluorolytic sol–gel mechanism previously discussed. KW - Aluminium fluorine KW - MAS NMR KW - Qudrupolar nuclei KW - Crystalline aluminium isopropoxide fluoride PY - 2011 DO - https://doi.org/10.1039/c1dt10514k SN - 1477-9226 SN - 1477-9234 SN - 1364-5447 VL - 40 IS - 34 SP - 8701 EP - 8710 PB - RSC CY - Cambridge AN - OPUS4-26245 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - König, R. A1 - Scholz, G. A1 - Kemnitz, E. A1 - Jäger, Christian A1 - Pawlik, Alf A1 - van Rossumm, B. A1 - Oschkinat, H. T1 - Crystalline aluminium hydroxy fluorides: Structural insights obtained by high field solid state NMR and 27Al chemical shift trend analysis T2 - Gesellschaft Deutscher Chemiker CY - Regensburg, Germany DA - 2008-09-22 PY - 2008 AN - OPUS4-17956 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - König, R. A1 - Scholz, G. A1 - Kemnitz, E. A1 - Jäger, Christian A1 - Pawlik, Alf A1 - van Rossumm, B. A1 - Oschkinat, H. T1 - Crystalline aluminium hydroxyl fluorides: Structural insights obtained by high-field solid state NMR and 27Al chemical shift trend analysis T2 - Gesellschaft Deutscher Chemiker CY - Regensburg, Germany DA - 2008-09-22 PY - 2008 AN - OPUS4-17957 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - König, R. A1 - Scholz, G. A1 - Pawlik, Alf A1 - Jäger, Christian A1 - van Rossumm, B. A1 - Oschkinat, H. A1 - Kemnitz, E. T1 - Crystalline Aluminium Hydroxy Fluorides: Structural Insights Obtained by High Field Solid State NMR and Trend Analyses N2 - A series of crystalline aluminum hydroxy fluorides in cubic pyrochlore structure AlFx(OH)3-x·H2O with variable F-content x were investigated by solid-state NMR by applying different magnetic fields up to 21.1 T. Distinguishable octahedral species AlFx(OH)6-x (x = 1-6) were identified in the crystalline aluminum hydroxy fluorides. The subsequent analysis of the highfield 27Al MAS NMR data allows the derivation of the trend analysis graphs giving correlations between the 27Al chemical shifts and the quadrupolar frequencies and the F-content x in AlFx(OH)6-x. Clear trends were obtained for both, which are, along with the 19F MAS chemical-shift trend analysis presented earlier, valuable tools for the interpretation of MAS NMR spectra of amorphous AlFx(OX)3-x compounds (X = H, alkyl). Following the dehydration of the pyrochlores by solid-state NMR eventually reveals a remarkable influence of the incorporated solvent molecules (H2O) on the 19F chemical shift. On that basis, a new chemical-shift trend analysis for 19F chemical shifts in correlation with x in AlFx(OH)6-x units for proton-poor substances (in the Al, F, O, H system) was determined. By using this correlation, high-surface AlF3 has a mean bulk Al:F ratio similar to that found for ACF, namely, AlF2.8(O/OH)0.2. KW - Aluminium-27 KW - Crystalline aluminium hydroxy fluorides KW - Chemical shift trend analysis KW - High field solid state NMR KW - Quadrupolar nuclei PY - 2008 DO - https://doi.org/10.1021/jp804662f SN - 1932-7447 SN - 1089-5639 VL - 112 IS - 40 SP - 15708 EP - 15720 PB - Soc. CY - Washington, DC AN - OPUS4-18365 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Scholz, G. A1 - Emmerling, Franziska A1 - Dreger, M. A1 - Kemnitz, E. T1 - Mechanochemical synthesis and characterization of hydrated and dehydrated crystalline strontium terephtalates N2 - A successful mechanochemical synthesis of strontium terephthalate trihydrate is described for the first time. The dehydration of Sr(C8H4O4)·3H2O occurs at about 100 °C and results in a well-defined strontium terephtalate, Sr(C8H4O4), thermally stable up to 550 °C. Both compounds are not described so far in the literature. Their structures were solved by ab initio structure determination and subsequent Rietveld refinement of the powder diffraction data. Further methods like DTA-TG, MAS NMR and FT-IR spectroscopy, and BET measurements were used to characterize these compounds. KW - Mechanochemical synthesis KW - Ab initio structure determination KW - MAS NMR spectroscopy KW - Strontium PY - 2013 DO - https://doi.org/10.1002/zaac.201200550 SN - 0044-2313 SN - 1521-3749 SN - 0372-7874 SN - 0863-1786 SN - 0863-1778 VL - 639 IS - 5 SP - 689 EP - 693 PB - Wiley-VCH CY - Weinheim AN - OPUS4-29117 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - König, R. A1 - Scholz, G. A1 - Pawlik, Alf A1 - Jäger, Christian A1 - Rossum, B. van A1 - Kemnitz, E. T1 - Identification of AIFx(OR)y species in strongly disordered aluminium isopropoxide fluoride solids: a field-dependent MAS NMR study KW - Ultra high-field MAS NMR (21.1T) KW - 27 Al MAS solid state NMR KW - Fluoride xerogels KW - Sol-gel process KW - Fluorolysis KW - Quadrupolar nuclei PY - 2009 DO - https://doi.org/10.1021/jp9066795 SN - 1932-7447 SN - 1089-5639 VL - 113 IS - 35 SP - 15576 EP - 15585 PB - Soc. CY - Washington, DC AN - OPUS4-20461 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - König, R. A1 - Scholz, G. A1 - Scheurell, K. A1 - Heidemann, D. A1 - Buchem, I. A1 - Unger, Wolfgang A1 - Kemnitz, E. T1 - Spectroscopic characterization of crystalline AIF3 phases N2 - A comprehensive spectroscopic characterization of all known crystalline AlF3 phases (α-, β-, η-, κ-, θ-AlF3) is presented for the first time in this study. Beside their X-ray diffraction powder patterns, which were already published in the literature, 27Al and 19F MAS NMR, FT IR and XPS spectroscopic techniques were applied for all phases in a consistent manner. For all phases prepared the utilization of 27Al satellite transition (SATRAS) NMR allowed to determine the quadrupolar parameters of the aluminium sites including their distributions. In addition, η-AlF3 was isolated with high phase purity and characterized following a new preparation path different from those known so far in the literature. KW - Crystalline aluminium fluorides KW - Solid state NMR KW - FT IR KW - XPS PY - 2010 DO - https://doi.org/10.1016/j.jfluchem.2009.10.015 SN - 0022-1139 SN - 1873-3328 VL - 131 IS - 1 SP - 91 EP - 97 PB - Elsevier CY - Amsterdam AN - OPUS4-20991 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -