Derive the relation between the P & R branches

In summary, the conversation is discussing the assignment to derive two expressions involving rotational constants and transition/energy differences between energy levels. The conversation also mentions selection rules for transitions and how R(J) and P(J) refer to the energy of specific transitions. The poster is struggling to understand how to put all of this information together and is requesting additional help.
  • #1
Bananen
8
0
Moved from a technical forum, so homework template missing
Hi,

I have an assignment to derive the two following expressions:

R(J)-P(J)=2B'(2J+1)
R(J-1)-P(J+1)=2B''(2J+1)
where Bis the rotational constant and prime ' stands for upper level and bis '' for lower level.
Bv=Be-α(v+1/2)

using the selection rules (I guess in this case ΔJ=±1) and ΔT=G(v')-G(v'')+F(J')-F(J'') where ΔT is the transition/energy difference
between two energy levels expressed in wavenumbers and F(J)=BJ(J+1)
G(v)=ωe(v+1/2)-ωexe(v+1/2)2.

I don't understand how I'm going to put all of this together and I don't understand what they mean with R(J) and P(J) etc.
Thankful for any help!
 
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  • #2
You'll have to give more background. Can you provide with the exact problem statement?
 
  • #3
It's difficult to determine if there is a precise question in OP's post.

R(J) refers to the energy of an R-branch transition originating from the J'th rotational state. Ditto for P(J) (for a P-branch transition). You might spend some time poring over this diagram:
https://en.wikipedia.org/wiki/Rotat...scopy#/media/File:Vibrationrotationenergy.svg

Also, presumably this is comparing P and R branches of the same vibrational transition, so you don't have to worry about most of the expressions you've listed involving vibrational quantum numbers. Maybe, as @DrClaude suggested, you could give us a more focused question?
 

Related to Derive the relation between the P & R branches

1. What is the P & R branch in spectroscopy?

The P & R branches in spectroscopy refer to the spectral lines formed by the transitions between rotational energy levels in a molecule. The P branch is the group of lines with lower energy transitions, while the R branch is the group of lines with higher energy transitions.

2. How do we derive the relation between the P & R branches?

The relation between the P & R branches can be derived using the rigid rotor approximation, which assumes that the molecule is a rigid rotor with a fixed bond length. The energy levels in this approximation are given by the expression E(J) = BJ(J+1), where B is the rotational constant and J is the quantum number representing the rotational state.

3. What is the significance of the P & R branches in spectroscopy?

The P & R branches provide important information about the rotational energy levels and the rotational constant of a molecule. They also help in identifying the type of molecule and its structure, as each molecule has a unique set of P & R branch transitions.

4. How does the P & R branch relate to the molecular geometry?

The P & R branch transitions are affected by the molecular geometry, as the rotational constant B is dependent on the bond length and the moments of inertia of the molecule. Therefore, analyzing the P & R branches can provide insights into the molecular geometry and its changes upon molecular motion.

5. Can the P & R branch transitions be used for quantitative analysis?

Yes, the P & R branch transitions can be used for quantitative analysis in spectroscopic techniques such as Raman and infrared spectroscopy. By measuring the intensity and position of these transitions, the concentration and quantity of a particular molecule can be determined.

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