Benzophenoxazine-based colorimetric and fluorescent probe for highly sensitive detection of amines and food freshness

Hongjin Wang1, Wenzhu Yin2, Hui Ma3

  • 1College of Chemistry and Environmental Science, Yili Normal University, Yining 835000, PR China; State Key Laboratory of Coordination Chemistry, State Key Laboratory of Analytical Chemistry for Life Science, Jiangsu Key Laboratory Advanced Organic Materials, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, PR China.

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NMR Spectroscopy Of Amines01:19

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In proton NMR spectroscopy, primary amines and secondary amines showcase their N–H protons as a broad signal in the chemical shift range between δ 0.5 and 5 ppm. The exact position in this range depends on several factors, including sample concentration, hydrogen bonding, and the type of solvent used. Since amine protons undergo fast proton exchange in solution, the protons are labile and therefore do not participate in any splitting with adjacent protons. Thus, the observed peak is...
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Physical Properties of Amines01:26

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Amines with low molecular weight are usually gaseous at room temperature, while those with high molecular weight are liquid or solids in nature. Usually, low molecular weight amines have a rotten fish-like smell. Diamines typically have a pungent smell. For instance, cadaverine and putrescine, depicted in Figure 1, are two molecules responsible for decaying tissue.
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Amines to Sulfonamides: The Hinsberg Test

The Hinsberg test is a method to identify primary, secondary and tertiary amines, named after its pioneer, Oscar Hinsberg. Here, amines are treated with benzenesulfonyl chloride, also known as the Hinsberg reagent, in the presence of an excess of aqueous base, followed by acidification. Based on the nature of the amines, different changes are observed.
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