Welcome to Nanalysis’ benchtop NMR Blog

We love benchtop NMR! In this blog section, you will find all things benchtop NMR. Please contact us if you would like to discuss about your project.

Educational Godfrey Wills Educational Godfrey Wills

Using NMR to observe the restricted rotation in amide bonds

NMR is a great tool for the analysis of molecular properties such as the amide bond, which has a restricted rotation around the C–N bond. In Biochemistry, the amide bond is referred to as the peptide bond. This bond is formed by the union of a carboxyl group of one amino acid with the amino group of another amino acid. Read more.

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Educational Alexander Maier Educational Alexander Maier

β-Diketone (Beta-diketone) tautomerization ratio determined via 60 MHz benchtop NMR

Tautomers are constitutional isomers that interconvert into each other by an exchange reaction, most commonly a proton transfer. Such two isomers can for example be a ketone and an enol. Keto-enol tautomerism (KET) becomes possible when there are hydrogen atoms adjacent to a carbonyl group (these hydrogen atoms are called α hydrogens). This tautomerism is depicted in Scheme 1 and is also discussed…

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Educational Alexander Maier Educational Alexander Maier

β-Diketone (Beta-diketone) tautomerization ratio determined via 60 MHz benchtop NMR

Tautomers are constitutional isomers that interconvert into each other by an exchange reaction, most commonly a proton transfer. Such two isomers can for example be a ketone and an enol. Keto-enol tautomerism (KET) becomes possible when there are hydrogen atoms adjacent to a carbonyl group (these hydrogen atoms are called α hydrogens). This tautomerism is depicted in Scheme 1 and is also discussed…

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Educational Susie Riegel Educational Susie Riegel

Teeter-Tautomers

2,4-pentanedione (aka acetylacetone, acetylacetonato or acacH) is not only a ubiquitous ligand (AND ligand precursor!) for beautifully coloured organometallic complexes[1-3].. Read more.

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