Rotational and vibrational spectroscopy

Chemist20
Messages
80
Reaction score
0
Hello there!

Im studying microwave spectroscopy, and I'm stuck because I don't see why the spacing between rotational energy levels increases as J does. Can anyone explain please?

Also, about IR, I see everywhere that the selction rule is Δv=±1. Correct me if I'm wrong but I'm guessing that's only when you use IR light. If you where to use UV, where an electronic transition can take place, we could also go from l=1 v=0 to l=2 v=0 and hence Δv=±0,1. (excluding overtones of this) . Is this correct?

Thanks!
 
Physics news on Phys.org
In electronic transitions you usually observe a whole series of transitions of possible v values (so called Franck Condon progression) as the equilibrium positions of the electronic ground and excited state do not coincide.
 
Insights auto threads is broken atm, so I'm manually creating these for new Insight articles. Towards the end of the first lecture for the Qiskit Global Summer School 2025, Foundations of Quantum Mechanics, Olivia Lanes (Global Lead, Content and Education IBM) stated... Source: https://www.physicsforums.com/insights/quantum-entanglement-is-a-kinematic-fact-not-a-dynamical-effect/ by @RUTA
If we release an electron around a positively charged sphere, the initial state of electron is a linear combination of Hydrogen-like states. According to quantum mechanics, evolution of time would not change this initial state because the potential is time independent. However, classically we expect the electron to collide with the sphere. So, it seems that the quantum and classics predict different behaviours!
Back
Top