# Rotation of the plane of polarization of light by glucose

• greg_rack
In summary, Glucose molecules in a solution have a property called circular birefringence, which means that they rotate the plane of polarisation of light passing through them. This rotation angle depends on the frequency of the light, which is related to the shape of the molecules. This phenomenon is called "optical activity" and can be observed by passing white light through a glucose solution and a polarizing filter.
greg_rack
Gold Member
Hi guys,

Online I found this really cool experiment that uses a glucose solution(e.g. in a beaker) to rotate the plane of polarization of a polarized light beam passing through it, of an angle ##\theta## which depends on the frequency of the EM wave.
Then, for example, watching white light emitted from a monitor(polarized white light) through the beaker containing glucose, with a polarizing filter, allows you to watch the white beam split into a certain frequency of the visible spectrum depending on how you tilt the filter.

Hence, I wanted to ask you why do glucose molecules cause this rotation of EM waves, depending on frequency? I know this has something to do with the shape of the molecules, but online I couldn't find much and I would really appreciate a detailed explanation of the phenomenon :)

Greg

greg_rack and Motore
Nice question! There's a property of an optically active medium called birefringence, which just means that the refractive index of the medium depends on how the light is polarised.

A glucose solution exhibits circular birefringence, where left-handed and right-handed circularly polarised light propagate with different speeds. This sort of birefringence occurs when the sample contains net non-zero amount of molecules of a certain chirality [(D) or (L)]; chirality is just a fancy way of saying that if you reflect the molecule in a mirror then you can't superimpose it on the original molecule. For example glucose is chiral because it contains a number of carbon atoms each of which are connected to four distinct groups.

For a plane EM wave traveling along the ##z## axis you can generally write the electric field as ##\mathbf{E}(z,t) = \mathcal{Re} \left[(a \hat{\boldsymbol{x}} + b \hat{\boldsymbol{y}})e^{i(kz - \omega t)} \right]## where ##a## and ##b## are the complex amplitudes (##a = a_0 e^{i \phi_x}##, ##b = b_0 e^{i \phi_y}##) in the ##x## and ##y## directions.

First you have a linearly polarised wave from the polariser (that is, ##\phi_x = \phi_y##), for which without loss of generality you can just take ##\mathbf{E}(z,t) = \mathcal{Re} [(A \hat{\boldsymbol{x}}) e^{i(kz - \omega t)}]## for some real number ##A##. You can write this equivalently as the sum of two oppositely circularly polarised (##\phi_y = \phi_x \pm \frac{\pi}{2}##) waves,$$\mathbf{E}(z,t) = \frac{1}{2} \mathcal{Re} \left[ A(\hat{\boldsymbol{x}} + i \hat{\boldsymbol{y}} ) e^{i(k_1 z - \omega t)} \right] + \frac{1}{2} \mathcal{Re} \left[ A(\hat{\boldsymbol{x}} - i \hat{\boldsymbol{y}} ) e^{i(k_2 z - \omega t)} \right]$$Outside of the circularly birefringent material you'll have ##k_1 = k_2 = k = n \omega / c##, but once the light passes into the material ##n_1 \omega / c = k_1 \neq k_2 = n_2 \omega / c##, if the two refractive indices are ##n_1## and ##n_2##. In other words, the two waves begin to accumulate phase with increasing ##z## at a relative rate of ##\frac{\omega}{c} (n_2 - n_1) := \frac{\omega \Delta n}{c}##. If you let ##\xi## be the distance the light has traveled in the medium (i.e. let ##z = z_0 + \xi##, where ##z_0## is the coordinate of the start of the material), then the change in relative phase over this distance will be ##\delta(\xi) := \frac{\omega \xi \Delta n}{c}##. So the equation of the electric field on the other side of the material is the sum of two contributions with a relative phase ##\delta(L)## (abbreviated ##\delta##),
\begin{align*} \mathbf{E}(z,t) &= \frac{1}{2} \mathcal{Re} \left[ A(\hat{\boldsymbol{x}} + i \hat{\boldsymbol{y}} ) e^{i(kz - \omega t)} \right] + \frac{1}{2} \mathcal{Re} \left[ A(\hat{\boldsymbol{x}} - i \hat{\boldsymbol{y}} ) e^{i(kz - \omega t)} e^{i\delta} \right] \\ \\ &= \frac{1}{2} \mathcal{Re} \left[Ae^{i (kz - \omega t + \frac{\delta}{2})} \left( (\hat{\boldsymbol{x}} + i \hat{\boldsymbol{y}} )e^{-\frac{i \delta}{2}} + (\hat{\boldsymbol{x}} - i \hat{\boldsymbol{y}} )e^{\frac{i \delta}{2}} \right) \right] \\ \\ &= \mathcal{Re} \left[Ae^{i (kz - \omega t + \frac{\delta}{2})} \left(\frac{e^{\frac{i \delta}{2}} + e^{-\frac{i \delta}{2}}}{2} \hat{\boldsymbol{x}} - \frac{e^{\frac{i \delta}{2}} - e^{-\frac{i \delta}{2}}}{2} i \hat{\boldsymbol{y}} \right)\right] \\ \\ &= \mathcal{Re} \left[Ae^{i (kz - \omega t + \frac{\delta}{2})} \left( \cos{\frac{\delta}{2} } \hat{\boldsymbol{x}} + \sin{\frac{\delta}{2} } \hat{\boldsymbol{y}} \right)\right] = \mathcal{Re}[(A \hat{\boldsymbol{n}})e^{i(kz - \omega t+ \frac{\delta}{2})}] \end{align*}where ##\hat{\boldsymbol{n}} = \cos{\frac{\delta}{2}} \hat{\boldsymbol{x}} + \sin{\frac{\delta}{2}} \hat{\boldsymbol{y}}## is the unit vector obtained by rotating ##\hat{\boldsymbol{x}}## anti-clockwise by ##\delta / 2##. In other words, the plane of polarisation has tilted by an angle ##\delta / 2##!

Because ##\delta \propto \omega##, the angle by which the plane of polarisation tilts depends on the frequency of the light passing through the glucose. If you observe with white light incident on crossed polars, then those particular frequencies which have their polarisation angle tilted by a multiple of ##\pi## will pass through the glucose un-rotated, so are not transmitted through the analyser (which is at ##\frac{\pi}{2}## to the polariser). The colour seen is then the so-called "complementary colour", which you can determine by looking at the Michel-Levy chart.

Last edited by a moderator:
greg_rack and vanhees71
greg_rack said:
Hi guys,

Online I found this really cool experiment that uses a glucose solution(e.g. in a beaker) to rotate the plane of polarization of a polarized light beam passing through it, of an angle ##\theta## which depends on the frequency of the EM wave.
Then, for example, watching white light emitted from a monitor(polarized white light) through the beaker containing glucose, with a polarizing filter, allows you to watch the white beam split into a certain frequency of the visible spectrum depending on how you tilt the filter.

Hence, I wanted to ask you why do glucose molecules cause this rotation of EM waves, depending on frequency? I know this has something to do with the shape of the molecules, but online I couldn't find much and I would really appreciate a detailed explanation of the phenomenon :)

Greg

Condon's paper is a classic:

https://journals.aps.org/rmp/pdf/10.1103/RevModPhys.9.432

In essence, the optically active molecule needs to be asymmetric.

greg_rack, vanhees71 and etotheipi
etotheipi said:
Nice question! There's a property of an optically active medium called birefringence, which just means that the refractive index of the medium depends on how the light is polarised.

A glucose solution exhibits circular birefringence, where left-handed and right-handed circularly polarised light propagate with different speeds. This sort of birefringence occurs when the sample contains net non-zero amount of molecules of a certain chirality [(D) or (L)]; chirality is just a fancy way of saying that if you reflect the molecule in a mirror then you can't superimpose it on the original molecule. For example glucose is chiral because it contains a number of carbon atoms each of which are connected to four distinct groups.

For a plane EM wave traveling along the ##z## axis you can generally write the electric field as ##\mathbf{E}(z,t) = \mathcal{Re} \left[(a \hat{\boldsymbol{x}} + b \hat{\boldsymbol{y}})e^{i(kz - \omega t)} \right]## where ##a## and ##b## are the complex amplitudes (##a = a_0 e^{i \phi_x}##, ##b = b_0 e^{i \phi_y}##) in the ##x## and ##y## directions.

First you have a linearly polarised wave from the polariser (that is, ##\phi_x = \phi_y##), for which without loss of generality you can just take ##\mathbf{E}(z,t) = \mathcal{Re} [(A \hat{\boldsymbol{x}}) e^{i(kz - \omega t)}]## for some real number ##A##. You can write this equivalently as the sum of two oppositely circularly polarised (##\phi_y = \phi_x \pm \frac{\pi}{2}##) waves,$$\mathbf{E}(z,t) = \frac{1}{2} \mathcal{Re} \left[ A(\hat{\boldsymbol{x}} + i \hat{\boldsymbol{y}} ) e^{i(k_1 z - \omega t)} \right] + \frac{1}{2} \mathcal{Re} \left[ A(\hat{\boldsymbol{x}} - i \hat{\boldsymbol{y}} ) e^{i(k_2 z - \omega t)} \right]$$Outside of the circularly birefringent material you'll have ##k_1 = k_2 = k = n \omega / c##, but once the light passes into the material ##n_1 \omega / c = k_1 \neq k_2 = n_2 \omega / c##, if the two refractive indices are ##n_1## and ##n_2##. In other words, the two waves begin to accumulate phase with increasing ##z## at a relative rate of ##\frac{\omega}{c} (n_2 - n_1) := \frac{\omega \Delta n}{c}##. If you let ##\xi## be the distance the light has traveled in the medium (i.e. let ##z = z_0 + \xi##, where ##z_0## is the coordinate of the start of the material), then the change in relative phase over this distance will be ##\delta(\xi) := \frac{\omega \xi \Delta n}{c}##. So the equation of the electric field on the other side of the material is the sum of two contributions with a relative phase ##\delta(L)## (abbreviated ##\delta##),
\begin{align*} \mathbf{E}(z,t) &= \frac{1}{2} \mathcal{Re} \left[ A(\hat{\boldsymbol{x}} + i \hat{\boldsymbol{y}} ) e^{i(kz - \omega t)} \right] + \frac{1}{2} \mathcal{Re} \left[ A(\hat{\boldsymbol{x}} - i \hat{\boldsymbol{y}} ) e^{i(kz - \omega t)} e^{i\delta} \right] \\ \\ &= \frac{1}{2} \mathcal{Re} \left[Ae^{i (kz - \omega t + \frac{\delta}{2})} \left( (\hat{\boldsymbol{x}} + i \hat{\boldsymbol{y}} )e^{-\frac{i \delta}{2}} + (\hat{\boldsymbol{x}} - i \hat{\boldsymbol{y}} )e^{\frac{i \delta}{2}} \right) \right] \\ \\ &= \mathcal{Re} \left[Ae^{i (kz - \omega t + \frac{\delta}{2})} \left(\frac{e^{\frac{i \delta}{2}} + e^{-\frac{i \delta}{2}}}{2} \hat{\boldsymbol{x}} - \frac{e^{\frac{i \delta}{2}} - e^{-\frac{i \delta}{2}}}{2} i \hat{\boldsymbol{y}} \right)\right] \\ \\ &= \mathcal{Re} \left[Ae^{i (kz - \omega t + \frac{\delta}{2})} \left( \cos{\frac{\delta}{2} } \hat{\boldsymbol{x}} + \sin{\frac{\delta}{2} } \hat{\boldsymbol{y}} \right)\right] = \mathcal{Re}[(A \hat{\boldsymbol{n}})e^{i(kz - \omega t+ \frac{\delta}{2})}] \end{align*}where ##\hat{\boldsymbol{n}} = \cos{\frac{\delta}{2}} \hat{\boldsymbol{x}} + \sin{\frac{\delta}{2}} \hat{\boldsymbol{y}}## is the unit vector obtained by rotating ##\hat{\boldsymbol{x}}## anti-clockwise by ##\delta / 2##. In other words, the plane of polarisation has tilted by an angle ##\delta / 2##!

Because ##\delta \propto \omega##, the angle by which the plane of polarisation tilts depends on the frequency of the light passing through the glucose. If you observe with white light incident on crossed polars, then those particular frequencies which have their polarisation angle tilted by a multiple of ##\pi## will pass through the glucose un-rotated, so are not transmitted through the analyser (which is at ##\frac{\pi}{2}## to the polariser). The colour seen is then the so-called "complementary colour", which you can determine by looking at the Michel-Levy chart.
Brilliant! Thanks man, appreciate it :)

etotheipi

## 1. What is the "rotation of the plane of polarization of light by glucose"?

The rotation of the plane of polarization of light by glucose refers to the phenomenon where the plane of polarization of linearly polarized light is rotated when passing through a solution of glucose. This is due to the chiral nature of glucose molecules, which causes a difference in the refractive index for left- and right-circularly polarized light.

## 2. What causes the rotation of the plane of polarization of light by glucose?

The rotation of the plane of polarization of light by glucose is caused by the chiral nature of glucose molecules. This means that the molecules are not superimposable on their mirror images, resulting in a difference in the refractive index for left- and right-circularly polarized light.

## 3. How is the rotation of the plane of polarization of light by glucose measured?

The rotation of the plane of polarization of light by glucose is measured using a polarimeter. This instrument measures the angle of rotation of the plane of polarization of light passing through a sample of glucose solution. The amount of rotation is directly proportional to the concentration of glucose in the solution.

## 4. What is the significance of the rotation of the plane of polarization of light by glucose?

The rotation of the plane of polarization of light by glucose is an important phenomenon in the field of analytical chemistry. It is used in the quantitative analysis of glucose in various solutions, such as in blood samples for diabetes diagnosis. It is also used in the study of chiral molecules and their interactions with polarized light.

## 5. Are there any other substances that can cause the rotation of the plane of polarization of light?

Yes, there are many other substances that can cause the rotation of the plane of polarization of light, including other chiral molecules such as amino acids and proteins. In addition, certain materials like quartz and sugar solutions can also exhibit this phenomenon due to their crystal structure or molecular arrangement.

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