GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more...
Transcript of GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more...
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GPAT Online Class for B.Pharm Students
Pharmaceutical Analysis – Part 2 (2nd July 2020)
By
Dr P Ramlingam, M.Pharm., PhD
Director – ResearchRaghavendra Institute of Pharmaceutical Education and Research – Autonomous
Affil: JNT University Anantapur, Anantapur, Andhra Pradesh, India
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GPAT Online Class for B.Pharm Students
Pharmaceutical Analysis – Part 2UV-Visible Spectroscopy : Woodward rules
& IR Spectroscopy
By
Dr P Ramlingam, M.Pharm., PhD
Director – ResearchRaghavendra Institute of Pharmaceutical Education and Research – Autonomous
Affil: JNT University Anantapur, Anantapur, Andhra Pradesh, India
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Disclaimer
“ The contents in this presentation are compiled from different sources, this presentation is delivered at the interest of students and not involved any commercial
benefits. Thus the presenter shall not claim any copyright for this presentation, and not responsible for
any copyright issues if arise”
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Woodward- Feiser Rules
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These are several sets of empirically derived rules which
attempt to predict the wavelength of the absorption
maximum (λ max ) in an ultraviolet–visible spectrum of a
given compound.
Its applied to,
•Conjugated dienes
•Alpha-beta unsaturated carbonyl compounds,
•Substituted benzoyl compounds
•Polyenes
Woodward rules
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▪ Rules developed by Woodward in
1941 then expanded by Feiser in
1948.
▪ Woodward rules work well for
conjugated dienes and polyenes
with up to 4-double bonds or less.
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▪In 1959 Fieser modified these rules with more
experimental data, and the modified rule is
known as Woodward- Feiser Rules.
▪The Fieser rule must be applied for certain
plants pigments such as carotenoids with even
more than 4 conjugated double bonds.
▪This may be differs from observed values by 5-
6.5 nm
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According to Woodward’s rules the λ max of the
molecule can be calculated using a formula:
Here the base value depends upon whether the
diene is a heteroannular or homoannular diene or
cyclic or acyclic.
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Class of Compounds that suitable for wood ward rules
Conditions: Structure should posses conjugation
1. 1,3 butadiene
2. α, β- unsaturated carbonyl compounds
3. Benzoyl compounds
4. Polyenes
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Simplified formula for remembrance
Absorption maxima = B + A + E + R + S
B - Basic value
A - Additional conjugation
E - Exocyclic double bond
R - Ring residue
S - Substitution on double bonded carbon only
ʎ max for 1,3-butadiene
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Basic Value215 nm
253 nm
217 nm
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DescriptorsValue to be considered in
calculation (in nm) Homoannular (cisoid) diene 253 nmHeteroannular (transoid) diene 217 nm
Acyclic diene 215 nm
Double bond extending conjugation 30 nm
Alkyl substituent or ring residue 5 nm
Exocyclic double bond 5 nm-OC(O)CH3 0 nm-OR 6 nm-Cl, -Br 5 nm-NR2 60 nm-SR 30 nmPhenyl ring 75 nm
Values to be used in calculations
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Additional ConjugationBonds in alternative position are considered to beextending conjugation. In the below structure thebond between C6 and C7 is isolated from diene, so itcannot be considered as extending conjugation oraddition conjugation. Thus it has 0 (zero) value incalculation.
In the below structure, there is aONE extended or additionalconjugation to diene. So (1 × 30nm) 30 nm has to be added in thecalculation.
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Exocyclic Double Bond
The above structure has both Heteroannular diene andHomoannular diene. But basic value has to be based onHomoannular diene.
The exocyclic double bond has to be calculated based on the position, thus above structure has THREE exocyclic double bond ( 3 × 5 = 15 nm)
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Ring Residue
It is the number of bond cleavage to be doneon the ring structure to isolate the entireconjugated chain, thus above structure has fivering residue (5 × 5 = 25 nm) and 25 nm has toadded in the calculation
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Example 1
Formula Value Final value
B 253 253nm
A 0 0nm
E 2x5nm 10nm
R 4x5nm 20nm
S 0 0nm
Total 283nm
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Example 2
Formula Value Final value
B 253 253nm
A 1x30nm 30nm
E 1x5nm 5nm
R 4x5nm 20nm
S 0 0nm
Total 303nm
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Problems
Calculate the λ max by using Woodward- Fieser rule for above structures
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Unsaturated Carbonyl System
Basic value for Cyclic Unsaturated Carbonyl System
Base value:
(a) Acyclic α, β unsaturated ketones = 214 nm
(b) 6 membered cyclic α, β unsaturated ketones= 215 nm
(c) 5 membered cyclic α, β unsaturated ketones= 202 nm
(d) α, β unsaturated aldehydes = 210 nm
(e) α, β unsaturated carboxylic acids & esters = 195 nm
(f) Homoannular diene = 39 nm
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Auxochrome Alpha Beta Gamma delta
OH 35 30 -- 50
OR (-OCH3) 35 30 17 31
Br 25 30 -- --
Cl 15 12 -- --
CH3 or Any alkyl group 10 12 18 18
Ring residue 10 12 18 18
-OCOR 6 6 6 6
NR2 -- 95 -- --
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Formula Value Final value
B 214 214nm
A 0 0nm
E 0 0nm
R 0 0nm
S α= 10nm
β= 2x12= 24nm
34nm
Total 248nm
Example 1
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Example 2
Formula Value Final value
B 215 215nm
A 1x30nm 30nm
E 1x39nm 39nm
R 1x18nm 18nm
S 0 0nm
Total 302nm
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Problems
Calculate the λ max by using Woodward- Fieser rule for above structures
![Page 27: GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more experimental data, and the modified rule is known as Woodward-FeiserRules. The Fieser rule](https://reader036.fdocuments.in/reader036/viewer/2022062403/5fdb9d26bc4c56610d54cbad/html5/thumbnails/27.jpg)
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ʎ max Calculation for Aromatic (benzoyl system) compounds
ʎ max = B+S
λ max = Basic value + Substitution effect (ortho or meta or para)Basic values:
• (a) Ar -COR ( ketone) = 246 nm
• (b) Ar -CHO (Aldehyde) = 250 nm
• (c) Ar -CO2H ( Acid) = 230 nm
• (d) Ar -CO2R ( Ester) = 230 nm
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Auxochrome ortho meta para
-NR2 ( amine) 20 20 85
-NH2 13 13 58
-NHCH3 - - 73
-NHCOCH3 20 20 45
-OH , -OR 7 7 25
Aliphatic ( - R) 3 3 10
-Br 2 2 15
-Cl 0 0 10
-O+ ( oxonium) 11 20 78
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Example 1
Formula Value Final value
B 230 230nm
S m- 2x7= 14nm
p- 1x25nm
39nm
Total 269nm
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Problems
Calculate the λ max by using Woodward- Fieser rule for above structures ?
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•Infrared spectroscopy (IR spectroscopy) is a type of absorptionspectroscopy based on absorption of Middle infrared region(MID-IR radiation) of the electromagnetic spectrum.
•MID-IR is absorbed by the vibrating bonds in the molecule(dipole moment should not be Zero).
•It is used to identify the chemical compound based on functionalgroups, bonds, isomerism (except optical isomerism) andchemicals derivatives.
Infra-Red Spectroscopy
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•A basic IR spectrum is based on infrared light absorbance (or %transmittance) on the vertical Y-axis Vs frequency (Hz) orwavelength (micron) or wave number (Cm-1) on the horizontalX-axis.•More commonly, wave number (reciprocal centimeters ofwavelength) is used in interpretation of spectra.
•A common laboratory instrument in present day is a Fouriertransform infrared (FTIR) spectrometer.
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IR Spectrum
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Region Frequency Effect on molecule
Near IR 14000–4000 cm−1
(0.8–2.5 μm)
The higher-energy near-IR,approximately can excite overtone orharmonic vibrations
Middle IR 4000–400 cm−1
(2.5–25 μm)
The mid-infrared approximately may beused to study the fundamentalvibrations and associated rotational-vibrational structure. (organic andpharmaceuticals)
Far IR 400–10 cm−1
(25–1000 μm),
The far-infrared, approximately lyingadjacent to the microwave region, haslow energy and may be used forrotational spectroscopy
Different units and regions of IR radiation andtheir effect on organic molecules
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Molecular Vibration and IR Absorption: Hooke’s Law
Every bond in the molecule is under vibration, due to variety of reasons. If, m1 and m2 are mass of the atom and K is the force constant, the vibration of bond can be calculated using Hooke’s law
Fundamental frequency of the bond (natural) =
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NOTE: For a molecule to be "IR active (absorbsIR radiation), it must be associated withchanges in the dipole, remember thatpermanent dipole is not necessary, but requiresonly a change in dipole moment.
•Simple diatomic molecules have only one bondand only one Vibrational band.
•If the molecule is symmetrical, e.g. N2, H2, Cl2,
etc, the band is not observed in the IR spectrumbut observed only in the Raman spectrum.
•Asymmetrical diatomic molecules, e.g. CO,absorb in the IR spectrum.
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Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Number of vibrations in a molecule
A molecule can vibrate in several ways (called vibrational mode). If, N’ is the number of atoms in a molecule,
•Linear molecules will have 3N – 5 degrees of Vibrational modes.
•Nonlinear molecules will have 3N – 6 degrees of Vibrational modes
As an example H2O, a non-linear molecule, will have 3 × 3 – 6 = 3 degrees of Vibrational freedom, or modes.
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RIPERAUTONOMOUS
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Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
In carbon dioxide, bond under symmetricalstretching bond (dipole moment = 0) does notabsorb IR frequency, but it scatter the IRfrequency with Raman shift.
Thus Raman Spectroscopy is the complimentarytechnique to IR spectroscopy
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Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Types of vibrations in an organic molecules.
![Page 40: GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more experimental data, and the modified rule is known as Woodward-FeiserRules. The Fieser rule](https://reader036.fdocuments.in/reader036/viewer/2022062403/5fdb9d26bc4c56610d54cbad/html5/thumbnails/40.jpg)
RIPERAUTONOMOUS
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Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
IR absorption by a vibrating bondThe irradiated IR radiation is absorbed by the bond when fundamental frequency is equal to the applied IR frequency, as a result the change vibration energy takes place (V0 to V1).
In Overtone is due to
Vo to V2 or V3.
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Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Group frequency region (4000-1100 cm-1) and finger print region (1100-400 cm-1). Finger print region is very sensitive for small change in the structure, so it can be used for identification and authentication.
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Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Group Cm-1 (str)
Cm-1bend
Group Cm-1Str
Group Cm-1
O-H 3600 1100 C=O 1700 C-O 1200
N-H 3300 1200 C=N 1600 C-N 1100
C-H (Ar) 3000 1400 C=C 1500 C-S 1000
C-H (Ali) 2900 1400 C=S 1500 C-X 800-1000
C-H(Ald) 2800 1400 N=O 1400 Phenyl 800-600
S=O 1300
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RIPERAUTONOMOUS
NAAC &
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
![Page 44: GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more experimental data, and the modified rule is known as Woodward-FeiserRules. The Fieser rule](https://reader036.fdocuments.in/reader036/viewer/2022062403/5fdb9d26bc4c56610d54cbad/html5/thumbnails/44.jpg)
RIPERAUTONOMOUS
NAAC &
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
![Page 45: GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more experimental data, and the modified rule is known as Woodward-FeiserRules. The Fieser rule](https://reader036.fdocuments.in/reader036/viewer/2022062403/5fdb9d26bc4c56610d54cbad/html5/thumbnails/45.jpg)
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Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Identify the functional group in the given IR-Spectrum
![Page 46: GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more experimental data, and the modified rule is known as Woodward-FeiserRules. The Fieser rule](https://reader036.fdocuments.in/reader036/viewer/2022062403/5fdb9d26bc4c56610d54cbad/html5/thumbnails/46.jpg)
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Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
Identify the functional group in the given IR-Spectrum
![Page 47: GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more experimental data, and the modified rule is known as Woodward-FeiserRules. The Fieser rule](https://reader036.fdocuments.in/reader036/viewer/2022062403/5fdb9d26bc4c56610d54cbad/html5/thumbnails/47.jpg)
Factors affecting the Vibrational frequency of the bond
• Coupled vibration (AX2 system)
• Electronic effect
• Overtone
• Fermi-Resonance
• Resonance – Electronic factors
• Hydrogen bonding
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RIPERAUTONOMOUS
NAAC &
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
![Page 49: GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more experimental data, and the modified rule is known as Woodward-FeiserRules. The Fieser rule](https://reader036.fdocuments.in/reader036/viewer/2022062403/5fdb9d26bc4c56610d54cbad/html5/thumbnails/49.jpg)
RIPERAUTONOMOUS
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
![Page 50: GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more experimental data, and the modified rule is known as Woodward-FeiserRules. The Fieser rule](https://reader036.fdocuments.in/reader036/viewer/2022062403/5fdb9d26bc4c56610d54cbad/html5/thumbnails/50.jpg)
RIPERAUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
![Page 51: GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more experimental data, and the modified rule is known as Woodward-FeiserRules. The Fieser rule](https://reader036.fdocuments.in/reader036/viewer/2022062403/5fdb9d26bc4c56610d54cbad/html5/thumbnails/51.jpg)
RIPERAUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
![Page 52: GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more experimental data, and the modified rule is known as Woodward-FeiserRules. The Fieser rule](https://reader036.fdocuments.in/reader036/viewer/2022062403/5fdb9d26bc4c56610d54cbad/html5/thumbnails/52.jpg)
RIPERAUTONOMOUS
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SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
![Page 53: GPAT Online Class for B.Pharm Students · In 1959 Fieser modified these rules with more experimental data, and the modified rule is known as Woodward-FeiserRules. The Fieser rule](https://reader036.fdocuments.in/reader036/viewer/2022062403/5fdb9d26bc4c56610d54cbad/html5/thumbnails/53.jpg)
RIPERAUTONOMOUS
NAAC &
NBA (UG)
SIRO- DSIR
Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
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RIPERAUTONOMOUS
NAAC &
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Raghavendra Institute of Pharmaceutical Education and Research - AutonomousK.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721
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H-Bonding in IR spectra(Broadening effect)
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FT-IR Spectrophotometer
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