This document summarizes UV-Vis spectroscopy. It describes how UV-Vis spectroscopy can provide information about unsaturated functional groups and concentration. It also discusses absorption and emission, the Frank-Condon principle, selection rules for electronic transitions, and calculation of electronic spectra using time-dependent density functional theory.
Uv-Vis spectroscopy: electronic spectroscopy, absorption and emission, Terms describing UV absorptions, absorbing species containing s,n and pi, absorbing species,sigma and pi orbitals, electronic transitions, Absorption: physical Basis and lineshape,UV-Spectra.
Applications of Infrared spectroscopy
Identification of organic compounds,
Structure determination
Qualitative analysis of functional group
Quantitative analysis
Distinction between two types of hydrogen bonding
Study of chemical reaction
Study of Keto-Enol tautomerism
Conformational analysis
Geometrical isomerism
Study of complex molecules
Detection of impurity in a compound
Identification of the organic compounds by IR
Hydrocarbons, Aromatic compounds, Alcohol, Phenols, Ethers, Aldehydes, Ketones, Esters, Acid chlorides, Anhydrides, Amides, Amines, Nitriles, Isocynates, Isothiocynates, Imines and Nitro compounds.
UV/Vis spectroscopy is routinely used in analytical chemistry for the quantitative determination of different analytes, such as transition metal ions, highly conjugated organic compounds, and biological macromolecules. Molecules containing bonding and non-bonding electrons undergo electronic transitions and absorb energy in the form of ultraviolet or visible light to excite these electrons to higher anti-bonding molecular orbitals.
UV spectroscopy is an analytical method used to detct the numbers of double and triple bonds present in dienes ,trienes and polyenes compounds.The energy corresponds to EM radiation in the ultraviolet (UV) region, 100-350 nm, and visible (VIS) regions 350-700 nm of the spectrum is known as UV spectrum.
Introduction to Spectroscopy,
Introduction to UV, electronic transitions, terminology, chromophore, Auxochrome, Examples and Applications.
Introduction to IR, Fundamental vibrations, Types of Vibrations, Factors affecting the vibrational freaquencies, Group frequencies, examples and applications.
Uv-Vis spectroscopy: electronic spectroscopy, absorption and emission, Terms describing UV absorptions, absorbing species containing s,n and pi, absorbing species,sigma and pi orbitals, electronic transitions, Absorption: physical Basis and lineshape,UV-Spectra.
Applications of Infrared spectroscopy
Identification of organic compounds,
Structure determination
Qualitative analysis of functional group
Quantitative analysis
Distinction between two types of hydrogen bonding
Study of chemical reaction
Study of Keto-Enol tautomerism
Conformational analysis
Geometrical isomerism
Study of complex molecules
Detection of impurity in a compound
Identification of the organic compounds by IR
Hydrocarbons, Aromatic compounds, Alcohol, Phenols, Ethers, Aldehydes, Ketones, Esters, Acid chlorides, Anhydrides, Amides, Amines, Nitriles, Isocynates, Isothiocynates, Imines and Nitro compounds.
UV/Vis spectroscopy is routinely used in analytical chemistry for the quantitative determination of different analytes, such as transition metal ions, highly conjugated organic compounds, and biological macromolecules. Molecules containing bonding and non-bonding electrons undergo electronic transitions and absorb energy in the form of ultraviolet or visible light to excite these electrons to higher anti-bonding molecular orbitals.
UV spectroscopy is an analytical method used to detct the numbers of double and triple bonds present in dienes ,trienes and polyenes compounds.The energy corresponds to EM radiation in the ultraviolet (UV) region, 100-350 nm, and visible (VIS) regions 350-700 nm of the spectrum is known as UV spectrum.
Introduction to Spectroscopy,
Introduction to UV, electronic transitions, terminology, chromophore, Auxochrome, Examples and Applications.
Introduction to IR, Fundamental vibrations, Types of Vibrations, Factors affecting the vibrational freaquencies, Group frequencies, examples and applications.
UV-visible spectroscopy is a technique that measures the amount of light absorbed by a chemical substance. The ultraviolet (UV) region scanned is normally from 200 to 400 nm, and the visible portion is from 400 to 800 nm.
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3. Absortpion ssppeeccttrroossccooppyy
• Provide information about presence and absence of
unsaturated functional groups
• Useful adjunct to IR
• Determination of concentration, especially in
chromatography
• For structure proof, usually not critical data, but
essential for further studies
• NMR, MS not good for purity
4. Absorption and Emission
Emission
Absorption: A transition from a lower level to a higher
level with transfer of energy from the radiation field to
an absorber, atom, molecule, or solid.
Emission: A transition from a higher level to a lower
level with transfer of energy from the emitter to the
radiation field. If no radiation is emitted, the transition
from higher to lower energy levels is called nonradiative
decay.
Absorption
http://www.chemistry.vt.edu/chem-ed/spec/spectros.html
5. Frank-Condon Principle
• The nuclear motion (10-13 s) is negligible during the time required for an
electronic excitation (10-16 s).
• Since the nuclei do not move during the excitation, the internuclear distances
remain constant and “the most probable component of an electronic transition
involves only the vertical transitions”.
6. Absorption and emission
pathways
McGarvey and Gaillard, Basic Photochemistry at
http://classes.kumc.edu/grants/dpc/instruct/index2.htm
7. Origin of electronic spectra
Absorptions of UV-vis photons by molecule results in
electronic excitation of molecule with chromophore.
chromophore Any group of atoms that absorbs light whether or not a color is
thereby produced.
The electronic transition involves promotion of electron
from a electronic ground state to higher energy state,
usually from a molecular orbital called HOMO to LUMO.
8. Biological chromophores
1. The peptide bonds and amino acids in proteins
• The p electrons of the peptide group are delocalized over the
carbon, nitrogen, and oxygen atoms. The n-p* transition is
typically observed at 210-220 nm, while the main p-p* transition
occurs at ~190 nm.
• Aromatic side chains contribute to absorption at l> 230 nm
2. Purine and pyrimidine bases in nucleic acids and
their derivatives
3. Highly conjugated double bond systems
9.
10.
11. Selection Rules
11.. SSppiinn sseelleeccttiioonn rruullee:: DS = 0
allowed transitions: singlet ® singlet or triplet ® triplet
forbidden transitions: singlet ® triplet or triplet ® singlet
CChhaannggeess iinn ssppiinn mmuullttiipplliicciittyy aarree ffoorrbbiiddddeenn
http://www.shu.ac.uk/schools/sci/chem/tutorials/molspec/lumin1.htm
12. Selection rules
22.. LLaappoorrttee sseelleeccttiioonn rruullee:: there must be a change in the parity
(symmetry) of the complex
Electric dipole transition can occur only between states of opposite parity.
Laporte-allowed transitions: g ® u or u ® g
Laporte-forbidden transitions: g ® g or u ® u
g stands for gerade – compound with a center of symmetry
u stands for ungerade – compound without a center of symmetry
Selection rules can be relaxed due to:
•vibronic coupling
•spin-orbit coupling
•geometry relaxation during transition
13. • Spin-forbidden transitions
– Transitions involving a change in the spin
state of the molecule are forbidden
– Strongly obeyed
– Relaxed by effects that make spin a poor
quantum number (heavy atoms)
• Symmetry-forbidden transitions
– Transitions between states of the same
parity are forbidden
– Particularly important for centro-symmetric
molecules (ethene)
– Relaxed by coupling of electronic
transitions to vibrational transitions
(vibronic coupling)
14. Excited state symmetry
Formaldehyde
The symmetry of the first excited state
of formaldehyde (as a result of HOMO-LUMO
transition)
15. Calculation of electronic spectra
• TD-DFT (time-dependent DFT)
– #P TD(nstates=5) B3LYP/6-31+G(d,p)
• Run this job on an optimized geometry of formaldehyde
16. Plot the HOMO-2, HOMO-1, HOMO, LUMO, LUMO+1, LUMO+2,
LUMO+3 orbitals, using the Gaussview program.
Use a chk file in your Gaussian calculation