281 likes | 1.04k Views
Infrared Spectroscopy. Electromagnetic radiation. Ultraviolet 190 nm to 400 nm Electronic transitions s to s * p to p * Visible 400 nm to 700 nm Electronic transitions involving molecular orbitals. Electromagnetic Radiation. Infrared 800 nm to 2500 nm Near infrared
E N D
Electromagnetic radiation • Ultraviolet • 190 nm to 400 nm • Electronic transitions s to s* p to p* • Visible • 400 nm to 700 nm • Electronic transitions involving molecular orbitals
Electromagnetic Radiation • Infrared • 800 nm to 2500 nm • Near infrared • 2500 nm (4000 cm-1) to 15000 nm (667 cm-1) • Ordinary infrared • 15000 nm to 200000 nm • Far infrared
Energy and vibrations • Energy is measured in cm-1 • 4000 cm-1 is the high energy end and 667 cm-1 is the low energy end. • Vibrations • Stretching (require higher energy) • Bending (normally involve several bonds) • C=C at higher energy than C-C
NonaneC-H stretch and C-H bends CH2 bend CH3 bend C-H stretch, sp3
1-OcteneC-H stretch, C=C stretch, CH bend sp2 CH str C=C str sp3 CH str CH bends
1-OctyneCH stretch, C≡C stretch C≡C str sp CH str CO2
m-XyleneAromatic peaks 2000-1667 CH > 3000 1600,1500 650-800
PhenanthreneAromatic peaks CH > 3000 and 650-800 cm-1
1-PentanolOH stretch, CH stretch, CH bend, CO stretch C-O str, 1000-1200
4-MethylacetophenoneCH stretch, C=O stretch C=O < 1700, conjugated
PentanalCH and CHO stretches, C=O stretch Water C=O stretch
BenzaldehydeCH and CHO stretches, C=O stretch, aromatic peaks CHO stretches C=O str < 1700
Hexanoic acidOH stretch and C=O stretch OH stretch C=O str
Ethyl benzoateCH stretch, C=O and C-O stretches C=O str, 1725 cm-1 C-O stretch
BenzonitrileCN stretch C≡N stretch Aromatic
NitrobenzeneNO stretches (asymmetric and symmetric) NO stretch