Search results for "Nuclear Magnetic Resonance"

Characterization and Tuning of Ultra High Gradient Permanent Magnet Quadrupoles

2009

The application of quadrupole devices with high field gradients and small apertures requires precise control over higher order multipole field components. We present a new scheme for performance control and tuning, which allows the illumination of most of the quadrupole device aperture because of the reduction of higher order field components. Consequently, the size of the aperture can be minimized to match the beam size achieving field gradients of up to $500\text{ }\text{ }\mathrm{T}\text{ }{\mathrm{m}}^{\ensuremath{-}1}$ at good imaging quality. The characterization method based on a Hall probe measurement and a Fourier analysis was confirmed using the high quality electron beam at the M…

Zur protonenkatalysierten Aralkylierung von 1,2,3-Trimethylindol und 1,2,3,4-Tetrahydrocarbazol mit Arylaldehyden

1987

1,2,3-Trimethylindol (2) liefert mit Benzaldehyden die Kondensationsprodukte 5 und 6, wahrend aus den NH-Indolen 1 und 3 die Verbindungen 7 und 8 entstehen. Proton-catalyzed Aralkylation of 1,2,3-Trimethylindole and 1,2,3,4-Tetrahydrocarbazole with Arylaldehydes Reaction of 1,2,3-trimethylindole (2) with benzaldehydes leads to the condensation compounds 5 and 6, the NH-indoles 1 and 3, however, give 7 and 8.

Off-stoichiometry in Co2FeSi thin films sputtered from stoichiometric targets revealed by nuclear magnetic resonance

2009

Co2FeSi is predicted to be a half-metallic ferromagnet with an extraordinary high magnetic moment and Curie temperature. However, a low tunnel magneto-resistance ratio, a lower spin polarization and a lower magnetic moment were experimentally observed in thin film samples. Consequently, thin Co2FeSi films of different groups were studied using spin-echo nuclear magnetic resonance (NMR). NMR probes the local hyperfine fields of the active atoms, which strongly depend on the local environment. NMR is thus able to reveal the next neighbouring shells of the Co-59 nuclei in the Co2FeSi thin films. As expected, our NMR study shows the main resonance line corresponding to Co-59 nuclei in the L2(1)…

Characterization of sulfobetaine monomers by nuclear magnetic resonance spectroscopy: a note

1995

A set of zwitterionic monomers bearing the 3-ammoniopropanesulfonate moiety is analysed in CDCl3, CD3OD and D2O by one- and two-dimensional H-1 n.m.r. and C-13 n.m.r. spectroscopy. Absolute and relative positions of the n.m.r, signals are determined depending on the solvent used; the refined assignments of the signals in the vicinity of the ammonium group deviate from previously proposed assignments based on standard n.m.r, shift tables. Still, there is no convincing evidence for a special ring current effect due to a six-membered ring conformation of the betaine moiety.

ChemInform Abstract: High-Resolution Solid-State NMR Spectroscopy of Steroids and Their Derivatives

2013

Abstract: Steroids are an important class of organic compounds containing a vast array of biologically and physiologically essential molecules. Due to their availability, relatively straightforward derivatizability, and endogeneity, they are widely used in pharmacological applications. The investigation of molecular and physicochemical properties of active pharmaceutical ingredients (APIs) in the solid state is important, because these properties are directly related to their pharmacological activity. Several methods are available for this purpose. Solid-state NMR spectroscopy offers a nondestructive and flexible technique, providing both structural and dynamic information. It can be applie…

High-Resolution Solid-State NMR Spectroscopy of Steroids and Their Derivatives

2013

Abstract: Steroids are an important class of organic compounds containing a vast array of biologically and physiologically essential molecules. Due to their availability, relatively straightforward derivatizability, and endogeneity, they are widely used in pharmacological applications. The investigation of molecular and physicochemical properties of active pharmaceutical ingredients (APIs) in the solid state is important, because these properties are directly related to their pharmacological activity. Several methods are available for this purpose. Solid-state NMR spectroscopy offers a nondestructive and flexible technique, providing both structural and dynamic information. It can be applie…

Analgetische Wirkstoffe, 11. Mitt. Diacylderivate des Butyroguanamins

1986

Reaktionen von elektronenreichen Heterocyclen mit Orthocarbonsäure-Derivaten, 9. Acylierungsreaktionen von Indol und Methylindolen mit Dialkoxycarben…

1986

Indol und einige Methylderivate 1 lassen sich unter milden Bedingungen mit den Dialkoxycarbenium-tetrafluoroboraten 2 in meist guten Ausbeuten regioselektive acylieren. Mit dem Formylkation-Aquivalent 2a′ werden mit uberschussigem 1 auch die Bisindolycarbenium-tetrafluoroborate 13a – d erhalten. Reactions of Electron-rich Heterocycles with Orthocarboxylic Acid Derivatives, 9. – Acylation of Indole and Methylindoles with Dialkoxycarbenium Tetrafluoroborates Indole and some methylindoles 1 were acylated regioselectively with dialkoxycarbenium tetrafluoroborates 2 under mild conditions. The formyl cation equivalent 2a′ reacts with excess of indoles 1 to give the bisindolylcarbenium tetrafluoro…

Antikonvulsiva, 1. Mitt. Thiocarbamoylbutyroguanamine

1986

Durch Anlagerung von Butyroguanamin (1) an die Isothiocyanate 2a-c sind die Thiocarbamoylbutyroguanamine 3a-c zuganglich. Auf dem Wege der Acylierung von 3 sind unsymmetrisch substituierte Butyroguanamine 4 erhaltlich. Unter den neu entwickelten Verbindungen zeichnet sich insbesondere 3c durch antikonvulsive, fungizide und die Magensauresekretion hemmende Wirkungen aus. Anticonvulsivic Agents, I: Thiocarbamoylbutyroguanamines The thiocarbamoylbutyroguanamines 3a-c are accessible by addition of butyroguanamine (1) to the isothiocyanates 2a-c. Unsymmetrically substituted butyroguanamines 4 are obtainable by acylation of 3. Among the newly prepared compounds, 3c in particular exhibits anticonv…

The identification of vicinally substituted cyclohexane isomers in their mixtures by 1H and 13C NMR spectroscopy.

2000

The radical addition reactions of organobromine compounds, XBr (X = CH2COOMe, PhCH2, CHBr2 and CCl3) with cyclohexene afforded mixtures of cis/trans isomer pairs of 1-X-2-Br-cyclohexanes. In addition to benzyl benzoyloxy derivatives are formed also, when benzoyl peroxide is used as an initiator. Owing to the great difficulties in separating these cis/trans isomer pairs, they are identified directly in their mixtures by NMR spectroscopy. In addition to one-dimensional (ID) 1H, proton decoupled 13C and DEPT-135, also two-dimensional (2D) 13C-13C INADEQUATE as well as 1H-13C HMQC experiments have been used in assigning the signals of each compound in their mixtures. The identification of each …