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Why do some absorbing compounds fluoresce but others do not?

Short Answer

Expert verified

Molecules which have smaller relaxation time will show flourescence.

Step by step solution

01

Step 1. Given information

Fluorescence is one of the ways that an excited molecule might return to its original state. The molecule is stimulated by radiation absorption and returns to its ground state in a variety of methods, both radiative and non-radiative.

02

Step 2. Reason for some absorbing compounds fluoresce but others do not 

Fluorescence is one of the raciative ways in which the molecule returns to its ground state. Nonradiative decay techniques such as internal conversion and vibrational relaxation occur at a faster pace than fluorescence for the other molecules that do not demonstrate this. Non-fluorescent molecules have a longer relaxation time, which means they stay in the excited state for longer and return to the ground state slowly, whereas fluorescent molecules have a shorter relaxation time.

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Most popular questions from this chapter

Iron(II) ions catalyze the oxidation of luminol by H2O2. The intensity of the resulting chemiluminescence has been shown to increase linearly with iron(II) concentration from 10-10 to 10-8 M.

Exactly 1.00 mL of water was added to a 2.00-mL aliquot of an unknown Fe(II) solution, followed by 2.00 mL of a dilute H2O2 solution and 1.00 mL of an alkaline solution of luminol. The chemiluminescence from the mixture was integrated over a 10.0-s period and found to be 12.7. To a second 2.00-mL aliquot of the sample was added 1.00 mL of a 3.27 x 10-5 M Fe(II) solution followed by the same volume of H2O2 and luminol. The integrated intensity was 27.9. Find the concentration of Fe(II)

in the sample.

Why is spectrofluorometry potentially more sensitive than spectrophotometry?

Explain the difference between a fluorescence emission spectrum and a fluorescence excitation spectrum. Which more closely resembles an absorption spectrum?

The following lifetimes were measured for the chloride quenching of quinine sulfate given in Example 15-1. The fluorescence intensities are given in the example.

(a) Plot fluorescence intensity versus [Cl-].

(b) Plot the ratio of intensity to lifetime, F-t versus [Cl-].

(c) Develop a normalization factor to correct the measured fluorescence intensity to that of the solution without quencher.

(d) Plot on the same graph F versus [Cl-] and Fcorr versus [Cl-] .

Quinine in a 1.553-gantimalarial tablet was dissolved in sufficient 0.10MHClto give 250mLof solution. A 10.00-mLaliquot was then diluted to 50.00mLwith the acid. The fluorescence intensity for the diluted sample at 347.5nmprovided a reading of 196on an arbitrary scale. A standard 100-ppmquinine solution registered125when measured under conditions identical to those for the diluted sample. Calculate the mass in milligrams of quinine in the tablet.

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