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Dr. Antony Williams received a Ph.D. in analytical chemistry (NMR) from the University of London, UK in 1988.
NMR spectra were performed using an Avance III HD 600 MHz NMR from Bruker by NanoQAM (Université du Québec à Montréal).
Figure 9 shows an integrated analysis of the presence of micropores based on the well log, thin section, MICP, and NMR from Well-9.
(a) At 0°C, (b) at 80°C, and (c) the resultant1H NMR from (a) upon heating at 170°C for 4 h.
However, these reactions render these so-called thermally rearranged (TR) polymers insoluble in common solvents, which prevent the use of certain experimental characterization techniques such as solution-state nuclear magnetic resonance (NMR) from identifying their chemical structure.
Oligonucleotides for NMR (from Oligosetc or IDT) were dissolved in D2O to make an ∼10 mM stock solution.
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The proline at P5 induced a helical turn in the lipopeptide, as deduced from NMR studies, from P6 to P2 in membrane mimetic solvents.
Bottom: residuals from the subtraction of the 29Si NMR signals from hydrous glasses minus those from anhydrous glasses.
The 29Si NMR signal from the anhydrous glasses suffers from a very long T 1 relaxation time.
The carbon chemical shift assignments were obtained from comparison with the C NMR spectra from wood samples [ 25, 26] and acid-alkaline pretreated sugarcane bagasse [ 17].
Although this approach is perfectly valid for simple H NMR spectra from pure compounds, H NMR spectra from brain extracts contain many partially overlapping resonances.
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