Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download IR spectroscopy
Document related concepts
Transcript
Infrared Spectroscopy L.O. To understand the principles of IR spectroscopy. To be able to interpret simple IR spectra. Infrared Spectroscopy Different covalent bonds have different strengths as a result of the masses of the different atoms at either end of the bond. As a result, the bonds vibrate at different frequencies The frequency of vibration can be found by detecting when the molecules absorb electro-magnetic radiation. The different types of vibrations include... STRETCHING and BENDING SYMMETRIC STRETCHING BENDING ASYMMETRIC STRETCH The spectrophotometer Process: 1. A beam of infra red radiation is passed through the sample and a similar beam is passed through the reference cell 2. The frequency of radiation is varied and bonds vibrating with a similar frequency absorb the radiation 3. The amount of radiation absorbed by the sample is compared with the reference and the results are collected, stored and plotted The Infrared Spectrophotometer A bond will absorb radiation of a frequency similar to its vibration(s) normal vibration vibration having absorbed energy USES Particular bonds can be identified if they have characteristic peaks in specific, identifiable parts of the spectrum. For example, O-H and C=O. Compounds can be identified by comparing spectra. The only way to do this using IR alone is to compare its spectrum with a known reference sample. The “fingerprint region” of the IR spectrum is unique to each compound. Infra-red spectra are complex as each molecule can have many different vibrations occurring. Total characterisation based only on a substances’ IR spectrum is almost impossible unless you have computerised data handling facilities for comparison of the obtained spectrum with known ones in the computer memory. The technique is useful when used with other methods -nuclear magnetic resonance spectroscopy and mass spectroscopy. Interpretation The position of peaks depends on bond strength and the masses of the atoms joined by the bond. For example: strong bonds absorb at lower wavenumbers Light atoms absorb at lower wavenumbers weak bonds absorb at high wavenumbers heavy atoms absorb at high wavenumbers Interpretation Vertical axis Absorbance the stronger the absorbance the larger the peak Horizontal axis Frequency Wavelength wavenumber (waves per centimetre) / cm-1 microns (m); 1 micron = 1000 nanometres Fingerprint region • • • • organic molecules have a lot of C-C and C-H bonds within their structure spectra obtained will have peaks in the 1400 cm-1 to 800 cm-1 range this is referred to as the “fingerprint” region the pattern obtained is characteristic of a particular compound the frequency of any absorption is also affected by adjoining atoms or groups. IR spectrum of a carbonyl compound N.B: Carbonyl compounds show a sharp, strong absorption between 1700 and 1760 cm-1, which is due to the presence of the C=O bond IR spectrum of an alcohol N.B: Alcohols show a broad absorption between 3200 and 3600 cm-1, which is due to the presence of the O-H bond IR spectrum of a carboxylic acid N.B: Carboxylic acids show a broad absorption between 3200 and 3600 cm-1, which is due to the presence of the O-H bond. They also show a strong absorption around 1700 cm-1, which is due to the presence of the C=O bond IR spectrum of an ester N.B: Esters show a strong absorption between 1750 cm-1 and 1730 cm-1, which is due to the presence of the C=O bond What is it? One can tell the difference between alcohols, aldehydes and carboxylic acids by comparison of their spectra. O-H STRETCH ALCOHOL C=O STRETCH ALDEHYDE O-H STRETCH AND C=O STRETCH CARBOXYLIC ACID Characteristic frequencies N-H CN O-H C-Cl C=O C-H C-O Aromatic C-C C=C C-C alkanes Characteristic absorption frequencies Bond Class of compound Range / cm-1 Intensity C-H C-C C=C Alkane Alkane Alkene 2965 - 2850 1200 - 700 1680 - 1620 strong weak variable C=O Ketone Aldehyde Carboxylic acid Ester Amide Alcohol, ester, acid, ether 1725 - 1705 1740 - 1720 1725 - 1700 1750 - 1730 1700 - 1630 1300 - 1000 strong strong strong strong strong strong O-H Alcohol (monomer) Alcohol (H-bonded) Carboxylic acid (H-bonded) 3650 - 3590 3420 - 3200 3300 - 3250 variable, sharp strong, broad variable, broad N-H CN Amine, Amide Nitrile 3500 (approx) 2260 - 2240 medium medium C-X Chloride Bromide Iodide 800 - 600 600 - 500 500 (approx) strong strong strong C-O
