This document discusses UV-Vis spectroscopy. It begins by defining the ultraviolet and visible wavelength ranges from 190-780 nm. It then explains that UV-Vis spectroscopy involves electronic transitions of molecules when exposed to these wavelengths, promoting electrons from ground states to excited states. The document discusses terms like chromophores, auxochromes, and bathochromic/hypsochromic shifts related to UV absorptions. It also describes different types of electronic transitions that can be detected by UV-Vis spectroscopy, including σ→σ*, n→σ*, n→p*, and p→p* transitions involving different orbital types.
4. Electronic Spectroscopy
• This is the earliest method of molecular
spectroscopy.
• A phenomenon of interaction of molecules with
ultraviolet and visible lights.
• Absorption of photon results in electronic
transition of a molecule, and electrons are
promoted from ground state to higher electronic
states.
5. Absorption and Emission
Emission
Absorption: A transition from a lower level to a higher level
with transfer of energy to an absorber, atom, molecule, or
solid.
Emission: A transition from a higher level to a lower level
Absorption
6. Terms describing UV absorptions
1. Chromophores: functional groups that give
electronic transitions.
2. Auxochromes: substituents with unshared pair e's like
OH, NH, SH ..., when attached to π chromophore they
generally move the absorption max. to longer λ.
3. Bathochromic shift: shift to longer λ, also called red
shift.
4. Hypsochromic shift: shift to shorter λ, also called blue
shift.
7. Absorbing species containing p , s, and
n electrons
• Absorption of ultraviolet and visible radiation
in organic molecules is restricted to certain
functional groups (chromophores) that contain
valence electrons of low excitation energy.
• UV-VIS spectroscopy is used to detect the
presence of chromophores like dienes,
aromatics, polyenes, and conjugated ketones,
etc
8. Absorbing species
• Electronic transitions
– p, s, and n electrons
– d and f orbital electrons
– Charge transfer reactions
• p, s, and n (non-bonding) electrons
12. s s Transitions
• An electron in a bonding s orbital is excited to
the corresponding antibonding orbital. The
energy required is large. For example, methane
(which has only C-H bonds, and can only
undergo s s transitions) shows an
absorbance maximum at 125 nm.
• Absorption maxima due to s s transitions
are not seen in typical UV-VIS spectra (200 -
700 nm)
13. n s Transitions
• Saturated compounds containing atoms with
lone pairs (non-bonding electrons) are capable
of n s transitions. These transitions
usually need less energy than s s
transitions. They can be initiated by light
whose wavelength is in the range 150 - 250 nm
• . The number of organic functional groups
with n s peaks in the UV region is small.
14. n p and p p Transitions
• Most absorption spectroscopy of organic
compounds is based on transitions of n or p
electrons to the p excited state.
• These transitions fall in an experimentally
convenient region of the spectrum (200 - 700
nm). These transitions need an unsaturated
group in the molecule to provide the p
electrons.
16. Absorption: Physical Basis
Absorption occurs when the energy contained in a photon is
absorbed by an electron resulting in a transition to an
excited state
Since photon and electron energy levels are quantized, we
can only get specific allowed transitions
~ 115 nm
~ 200 – 400 nm
~ 150-250
nm
~ 400 - 700
nm
E=h (h = 6.626*10-34 Js)
18. Internal Energy of Molecules
Etotal=Eelec+Evib+Erot+Etrans
Eelec: electronic transitions (UV, X-ray)
Evib: vibrational transitions (Infrared)
Erot: rotational transitions (Microwave)
19. Absorption: Lineshape
This is because molecules are always rotating and vibrating.
Each rotational or vibrational state slightly changes the
energy of the transition.
Distrubtion of these states is…a random walk.
So the lineshape of our
absorption spectra is…
normally distributed