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Venceslav Kaucic

Publications and source records attributed to Venceslav Kaucic.

4 recordsLinked to original sources

31P NMR as a tool for studying incorporation of Ni, Co, Fe, and Mn into aluminophosphate zeotypes.

The incorporation of moderate amounts of Ni(II), Co(II), Fe(II/III), and Mn(II/III) into aluminophosphate zeotype AlPO4-34 and Fe(II/III) into aluminophosphate zeotype AlPO4-36 was studied by broadline 31P NMR. The technique provided direct evidence on isomorphous substitution of framework aluminum by transition metals and allowed us to determine the extent of the substitution. 31P NMR proved to be complementary to other spectroscopic techniques such as X-ray absorption spectroscopy (XAS), Mössbauer, electron paramagnetic resonance (EPR), and electron nuclear double resonance (ENDOR) spectroscopies. The position of the NMR signal belonging to phosphorus in the P(OAl)3(OMe) environment depended mostly on the magnitude of the hyperfine interaction between a phosphorus nucleus and an unpaired electron, which was delocalized from the transition metal atom Me by covalent bonding. The width of the NMR signal was dominated by dipolar coupling among phosphorus nuclei and nearest paramagnetic centers. In addition, broadline NMR of ethylenediamine-templated manganese phosphate (C2H10N2)[Mn2(HPO4)3(H2O)], which was used as a model compound, showed that on the basis of line positions and line widths different 31P signals could easily be assigned to different phosphorus crystallographic sites. The technique could thus be applied to extract valuable structural information about metal phosphates as well.

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Enhancing sensitivity or resolution of homonuclear correlation experiment for half-integer quadrupolar nuclei.

We have recently introduced double-quantum homonuclear correlation NMR experiment for half-integer quadrupolar nuclei in solids, which was based on rotary resonance recoupling [J. Chem. Phys. 120 (2004) 2835]. In this contribution we show on two 23Na (I=3/2) containing samples, Na2SO4 and Na2HPO4, that the efficiency of the experiment can be substantially enhanced by adding rotor assisted population transfer (RAPT) and Carr-Purcell-Meiboom-Gill (CPMG) sequences to it. We also present an upgraded two-dimensional experiment, in which double- and six-quantum coherences are correlated during t1 evolution period, yielding a high-resolution isotropic spectrum along an indirectly detected dimension. The sensitivity of the upgraded experiment is, however, greatly reduced compared to the sensitivity of the original experiment, so that its application is feasible only when RAPT and CPMG can be used as well.

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Atomic force microscopy study of the molecular sieve MnAPO-50.

Atomic force microscopy (AFM) imaging of MnAPO-50 reveals multiply-nucleated, elliptical terraces, oriented in registry with the facet edges with step heights ranging from one to six template repeat distances on the [100] facets and terraces with step heights ranging from one to thirty three times the c unit cell parameter on the [001] facets.

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Synthesis, structural and spectroscopic properties of two new ethylenediamine-templated gallophosphate-oxalate layered materials.

Two new layered gallophosphate-oxalate materials have been prepared hydrothermally using ethylenediamine and oxalic acid as structure-directing agents. The compounds (C2N2H10)2[Ga2(C2O4)2(HPO4)3].H2O 1 and (C2N2H10)3- [Ga4(C2O4)4(HPO4)4(H2PO4)2] 2 are closely related, consisting of anionic double chains built of alternating paris of GaO6 and HPO4 polyhedra. These double chains are linked via bridging HPO4 or H2PO4 tetrahedra to form corrugated layers containing eight-membered rings. The oxalate group acts as a bidentate ligand to each of the GaO6 octahedron. The corrugated layers are held together by strong to weak hydrogen-bonding interactions between oxalate groups, water and diprotonated ethylenediamine molecules, and the framework components. The compounds were characterized by single-crystal X-ray diffraction, thermogravimetric analysis, and infrared and Raman spectroscopy. Crystal data for 1: monoclinic, space group P21/C (No. 14), a = 6.355(1) A, b = 39.362(8) A, c = 9.249(2) A, beta = 106.7(1) degrees, Z = 2. Crystal data for 2: triclinic, space group P1 (No. 2), a = 8.730(1) A, b = 11.575(1) A, c = 11.696(1) A, alpha = 115.12(1) degree, beta = 90.07(1) degree, gamma = 111.23(1) degree, Z = 2.

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