نتایج جستجو برای: nuclear independent chemical shift

تعداد نتایج: 1149737  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1976
S J Opella J P Yesinowski J S Waugh

Proton-enhanced 13C nuclear magnetic resonance is used to obtain signals from labeled cholesterols in lecithin dispersions. The [26-(13)C]cholesterol resonance indicates that the aliphatic tail of the molecule undergoes reorientation fast enough to average completely the chemical shift anisotropy. In contrast, [4-(13)C]cholesterol signals are characteristic of limited anisotropic reorientation....

Journal: :Physical review letters 2009
Balázs Dóra Ferenc Simon

A theory of nuclear magnetic resonance (NMR) in graphene is presented. The canonical form of the electron-nucleus hyperfine interaction is strongly modified by the linear electronic dispersion. The NMR shift and spin-lattice relaxation time are calculated as a function of temperature, chemical potential, and magnetic field, and three distinct regimes are identified: Fermi-, Dirac-gas, and extre...

2013
Leonhard Geist Anna Zawadzka-Kazimierczuk Saurabh Saxena Szymon Żerko Wiktor Koźmiński Robert Konrat

Brain acid-soluble protein 1 (BASP1, CAP-23, NAP-22) appears to be implicated in diverse cellular processes. An N-terminally myristoylated form of BASP1 has been discovered to participate in the regulation of actin cytoskeleton dynamics in neurons, whereas non-myristoylated nuclear BASP1 acts as co-suppressor of the potent transcription regulator WT1 (Wilms' Tumor suppressor protein 1). Here we...

Journal: :Science 2005
Juan Perlo Vasiliki Demas Federico Casanova Carlos A Meriles Jeffrey Reimer Alexander Pines Bernhard Blümich

We report construction of a portable nuclear magnetic resonance sensor with a single-sided open probe design. The resulting magnetic field inhomogeneity is compensated by a pulse sequence that takes advantage of parallel inhomogeneity in the applied radio frequency field. We can thereby acquire fluorine-19 spectra of liquid fluorocarbons with 8 parts per million resolution, surmounting the long...

2013
Luca Menichetti Francesca Frijia Alessandra Flori Vincenzo Lionetti Matteo Liserani Giulio Giovannetti Giacomo Bianchi Simone L Romano Vincenzo Positano Jan Henrik Ardenkjaer-Larsen Rolf F Schulte Fabio A Recchia Luigi Landini Maria Filomena Santarelli Massimo Lombardi

Background 13C Dynamic Nuclear Polarization (DNP) with rapid dissolution together with Magnetic Resonance Chemical Shift Imaging (CSI) have been used for non-invasive real-time metabolic assessment in cardiac experimental models on a clinical 3T scanner. Here, we report an in vivo comparison of hyperpolarized [1-13C] pyruvate and [1-13C] acetate perfusion and metabolism: a method based on a 3D ...

2017
Hanna Andersson Emma Danelius Patrik Jarvoll Stephan Niebling Ashley J. Hughes Sebastian Westenhoff Ulrika Brath Máté Erdélyi

We have evaluated the ability of nuclear magnetic resonance (NMR) and circular dichroism (CD) spectroscopies to describe the difference in the folding propensities of two structurally highly similar cyclic β-hairpins, comparing the outcome to that of molecular dynamics simulations. NAMFIS-type NMR ensemble analysis and CD spectroscopy were observed to accurately describe the consequence of alte...

Journal: :Physical review letters 2004
L-B Wang P Mueller K Bailey G W F Drake J P Greene D Henderson R J Holt R V F Janssens C L Jiang Z-T Lu T P O'Connor R C Pardo K E Rehm J P Schiffer X D Tang

We have performed precision laser spectroscopy on individual 6He (t(1/2)=0.8 s) atoms confined and cooled in a magneto-optical trap, and measured the isotope shift between 6He and 4He to be 43 194.772+/-0.056 MHz for the 2(3)S1-3(3)P2 transition. Based on this measurement and atomic theory, the nuclear charge radius of 6He is determined for the first time in a method independent of nuclear mode...

Ebrahim Balali Hadi Lari Masoome Sheikhi,

The N-(2-benzoyl-phenyl) oxalyl derivatives are important models for studying of three-centered intramolecular hydrogen bonding in organic molecules. The quantum theoretical calculations for two crystal structures of N-(2-benzoyl-phenyl) oxalyl (compounds I and II) were performed by Density Functional Theory (B3LYP method and 6-311+G* basis set). From the optimized structures, geometric paramet...

Journal: :Journal of Synthetic Organic Chemistry, Japan 1997

Journal: :Journal of Biomolecular NMR 2013

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