Use the fluorescent spectra provided in Figure 3-2 and3-3, discuss and explain the difference between the emitted colors of Ălq3and Eu(tta)3(phen). What are the most likely electronic transitions that are responsible for the emissions? Why is the intensity of the emission for both complexes weak when excited by 254 nm UV light, yet strong when excited by 365 nm UV light. Page < 6 > of 7 O 20OM + 1.2 1.2 Ex. 340 nm Em. 612 Ex. 394 nm Em. 516 1 0.8 0.8 0.6 0.6 0.4 0.4 0.2 0.2 300 350 400 450 500 550 600 650 700 200 300 400 500 600 700 Wavelength (nm) Wavelength (nm) Intensity Intensity
Carbohydrates
Carbohydrates are the organic compounds that are obtained in foods and living matters in the shape of sugars, cellulose, and starch. The general formula of carbohydrates is Cn(H2O)2. The ratio of H and O present in carbohydrates is identical to water.
Starch
Starch is a polysaccharide carbohydrate that belongs to the category of polysaccharide carbohydrates.
Mutarotation
The rotation of a particular structure of the chiral compound because of the epimerization is called mutarotation. It is the repercussion of the ring chain tautomerism. In terms of glucose, this can be defined as the modification in the equilibrium of the α- and β- glucose anomers upon its dissolution in the solvent water. This process is usually seen in the chemistry of carbohydrates.
L Sugar
A chemical compound that is represented with a molecular formula C6H12O6 is called L-(-) sugar. At the carbon’s 5th position, the hydroxyl group is placed to the compound’s left and therefore the sugar is represented as L(-)-sugar. It is capable of rotating the polarized light’s plane in the direction anticlockwise. L isomers are one of the 2 isomers formed by the configurational stereochemistry of the carbohydrates.
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