TMSCH(2)Li and TMSCH(2)Li-LiDMAE have been used efficiently for bromine-lithium exchange in 2-bromo-, 3-bromo-, and 2,5-dibromopyridines under noncryogenic conditions, while low temperatures (-78 to -100 degrees C) are always needed with n-BuLi. The aminoalkoxide LiDMAE induced a remarkable C-2 selectivity with 2,5-dibromopyridines in toluene at 0 degrees C, which was unprecedented at such a temperature. The lithiopyridines were successfully reacted with electrophiles also under noncryogenic conditions giving the expected adducts in good yields.
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http://dx.doi.org/10.1021/jo070620j | DOI Listing |
Nanotechnology
November 2024
Department of Electronics Engineering, Chungnam National Univ, Daehak-ro, Yuseong-gu, Daejeon 305-764, Republic of Korea.
This study investigates the effect of silicon carbon nitride (SiCN) as an interlayer for ZnO-based resistive random access memory (RRAM). SiCN was deposited using plasma-enhanced chemical vapor deposition with controlled carbon content, achieved by varying the partial pressure of tetramethylsilane (4MS). Our results indicate that increasing the carbon concentration enhances the endurance of RRAM devices but reduces the on/off ratio.
View Article and Find Full Text PDFJ Magn Reson
October 2024
Department of Chemistry, University of Wisconsin-Madison, Madison, WI, United States; National Magnetic Resonance Facility at Madison (NMRFAM), University of Wisconsin-Madison, Madison, WI, United States; Department of Biochemistry, University of Wisconsin-Madison, Madison, WI, United States. Electronic address:
The development of magic angle spinning (MAS) at rates ranging from 30 kHz to greater than 100 kHz has substantially advanced solid-state nuclear magnetic resonance (SSNMR) spectroscopy H-detection methods. The small rotors required for such MAS rates have a limited sample volume and low C-detection sensitivity, rendering the traditional set of standard compounds for SSNMR insufficient or highly inconvenient for shimming and magic-angle calibration. Additionally, the reproducibility of magic angle setting, chemical shift referencing, and probe position can be especially critical for SSNMR experiments at high fields.
View Article and Find Full Text PDFMagn Reson Chem
July 2024
University of Lodz, Faculty of Chemistry, Department of Physical Chemistry, Theoretical and Structural Chemistry Group, Łódź, Poland.
This study aimed to obtain the title spectra and verify the temperature dependence of δ of the HOD signal from DO of the NMR sample. However, the analysis of the collected δ data, extended by the results of other closely related measurements reported in the literature, provided important guidelines for performing routine H/C NMR spectra in aqueous solvents externally referenced to neat liquid TMS contained in a coaxial capillary. Therefore, it is recommended that the previously proposed correction of δ data thus determined, which is mainly due to the difference in volume magnetic susceptibility χ between the sample and the external standard used, usually called the bulk magnetic susceptibility (BMS) correction, has been increased by +0.
View Article and Find Full Text PDFNMR Biomed
November 2023
Magnetic Resonance Imaging and Spectroscopy Lab, Department of Biomedical Engineering, The University of Memphis, Memphis, Tennessee, USA.
Nuclear magnetic resonance (NMR) spectroscopy is a powerful tool for quantitative metabolomics; however, quantification of metabolites from NMR data is often a slow and tedious process requiring user input and expertise. In this study, we propose a neural network approach for rapid, automated lipid identification and quantification from NMR data. Multilayered perceptron (MLP) networks were developed with NMR spectra as the input and lipid concentrations as output.
View Article and Find Full Text PDFChem Sci
July 2023
Department of Chemistry and Biochemistry, Texas State University 601 University Dr San Marcos TX 78666 USA
We report unprecedented photochemistry for the diamidocarbene 1. Described within are the double cyclopropanation of 1-bromonaphthalene, the double addition to pyridine, and remarkably, the insertion into the unactivated sp C-H bonds of cyclohexane, tetramethylsilane, and -pentane to give compounds 2-6, respectively. All compounds have been fully characterized, and the solid state structure of 4 was obtained using single crystal electron diffraction.
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