1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How...

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1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition, or forbidden) judged by the range of = 10 4 -10 5 L mol -1 cm -1 , strong absorption < 10 3 L mol -1 cm -1 , low intensity * M h M excitation

Transcript of 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How...

Page 1: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

1.1 Range of molar absorptivity

Electronic excitation of outer valence (i.e. bonding) electron

How probable for this electronic excitation? (allowed transition, or forbidden)

judged by the range of = 104 -105 L mol-1 cm-1, strong absorption

< 103 L mol-1 cm-1, low intensity

*MhM excitation

Page 2: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

1.2 Which electron get excited?

1.2.1 Organic molecules

, (bonding) and n (non-bonding) orbitals

*, * (anti-bonding) orbitals

* E large ( < 150 nm, out of range)

= 10 -10,000 Lmol-1cm-1

n * E smaller ( = 150 - 250 nm)

= 200-2000 Lmol-1cm-1

*

n * E smallest ( = 200 - 700 nm)

= 10-10,000 Lmol-1cm-1

Ideal for UV-Vis spectrometry of organic chromophore

Page 3: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,
Page 4: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

1.2.2 Inorganic moleculesMost transition metal ions are colored (absorption in Vis) due to d d electronic transition

Fig. 14-4 (p.371)Fig. 14-3 (p.370)

Page 5: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

1.2.3 Charge-transfer absorption

A: electron donor, metal ions

D: electron acceptor, ligand

> 10,000

DAhAD excitation

Fig. 14-5 (p.371)

Page 6: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

2.1Approximation of T and A

A = -log T = log (P0/P) = ··b·c

: molar absorptivity at one particular wavelength (L·mol-1cm-1)

b: path length of absorption (cm)

c: molar concentration (mol·L-1)Fig. 6-25 (p.158)

Fig. 13-1 (p.337)

Light loss due to reflection (17.3%), scattering, …

Page 7: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

P

P

P

PA

P

P

P

PT

solution

solvent

solvent

solution

0

0

loglog

Page 8: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

2.2 Application of Beer’s law to mixtures

Absorbance is additive

Atotal = A1 + A2 + … = 1bc1 + 2bc2

For a 2-component mixture, we measure the absorption at two different wavelength, respectively

A1 = 1,1·b·c1 + 2,1·b·c2

A2 = 1,2·b·c1 + 2,2·b·c2

Page 9: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

2.3 Limitations of Beer’s law

2.3.1 Real deviations

At low concentration

A = -log T = log (P0/P) = ··b·c

At c > 0.01 M solute-solute interaction, hydrogen-bond, …can alter the electronic absorption at a given wavelength

dilute the solution

Page 10: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

2.3.2 Chemical effects analyte associates, dissociates or reacts with a solvent to

give molecule with different

Example: acid-base equilibrium of an indicator

430 570 HIn 6.30 x102 7.12x103 (measured in HCl solution)In- 2.06 x 1049.61 x102 (measured in NaOH solution)

What’s the absorbance of unbuffered solution at c = 2 x 10-5M?

073.0][][

236.0][][

1088.0][

1012.1][

570,570,570

430,430,430

5

5

HInbInbA

HInbInbA

MHIn

MIn

HInIn

HInIn

5 a 102.1K InHHIn

][][

][][

1042.1][

]][[ 5

IncHIn

InH

HIn

InHKa

Page 11: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

Fig. 13-3 (p.340)=[HIn] + [In-]

InHHIn

Page 12: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

2.3.3 Instrumental deviations due to polychromatic radiation

Beer’s law applies for monochromatic absorption only.

If a band of radiation consisting of two wavelength ’, and ”

Assuming Beer’s law applies to each wavelength

bc"bcm

bc"

bc

PP

PP

PP

PPA

PP"

PP

bcP

PA

"0

''0

"0

'0

"0

'0

"0

''0

'0

1010log

"'log

absorbance Measured

10

"h wavelengtsecond For the

10'

''

log'

length first waveFor

Fig. 7-11 (p.176)

Page 13: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

2.3.3 Instrumental deviations due to polychromatic radiation

bc"bcm PP

PP

PP

PPA

"0

'0

"0

'0

"0

'0

1010log

"'log

absorbance Measured

Fig. 13-4 (p.341)

′″

′″

′″ Non-linear calibration curve

Page 14: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

How to avoid :

Select a wavelength band near its maximum absorption where the absorptivity changes little with wavelength

Fig. 13-5 (p.341)

Page 15: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

2.3.4 Other physical effects

stray light – the scattering, reflection radiation from the instrument, outside the nominal wavelength band chosen for measurement

mismatched cell for the sample and the blank

Page 16: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

3.1 Standard deviation of c

TT

s

c

ss

s

T

cbTT

c

Tb

c

Tc

TT

cc

Tc

log

434.0

)(

434.0

log1

2

2

222

Page 17: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

3.2 Sources of instrumental noise Case I Limited readout resolution (31/2-digit displays 0.1% uncertainty from 0%T -100% T) Thermal noise in thermal detector, etc (particularly for IR and neat IR spectrophotometer)

Case IIShot noise in photon detector (random emission of photon from the light source orrandom emission of electrons from the cathode in a detector)

Case III Flicker noise,

Fail to position sample and blank cells reproducibly in replicate measurements (as a result, different sections of cell window are exposed to radiation, and reflection and scattering losses change)

1ksT

TTksT 22

TksT 3

Page 18: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

3.2 Sources of instrumental noise

Fig. 13-3 (p.344)

Page 19: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

4.1 Designsa. Single beam

b. Double-beam-in-space

c. Double-beam-in-time

Advantage of double beam configuration

• Compensate for fluctuation in the radiant output, drift in transducer, etc.

• Continuous recording of spectra

Fig. 13-13 (p.352)

Page 20: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

Shimadzu UV-2450 Spectrophotometer

Page 21: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

Wavelength Range

190 to 900nm (performance guaranteed range). Extendable to 1,100nm through the use of the optional photomultiplier. (The measurable range maybe restricted in the shorter wavelength side depending on the type of photomultipler used.)

Monochromator System

UV-2450: Single monochromator with a high-performance blazed holographic grating in the aberration corrected Czerny-Turner mounting.

Resolution 0.1nm

Spectral Bandwidth

0.1, 0.2, 0.5, 1, 2 and 5nm

Wavelength Accuracy

±0.3nm

Wavelength Repeatability

±0.01nm

Wavelength Scanning Speed

FAST, MEDIUM, SLOW, and SUPER SLOW

Light Source 50W halogen lamp (2,000 hours of life) and D2lamp (500 hours of life)

Light Source lamp switching

Selectable between 282nm and 393nm

Stray Light UV-2450: Less than 0.015% at 220nm and 340nm

Detector Photomultiplier R-928

Photometric System

Double beam, direct ratio system with dynode feedback

Photometric Mode Absorbance (Abs.), transmittance (%), reflectance (%) and energy (E).

Photometric Range

Abosrbance: -4~5 Abs. (0.001 Abs. increments)Transmittance: 0~999.9% (0.01 increments)Reflectance: 0~999.9% (0.01% increments)

Photometric Accuracy

±0.002Abs(0~0.5Abs), ±0.004Abs(0.5~1Abs),±0.3T (0~100%T) (all determined with NIST 930D standard filter)

Photometric Repeatability

0.001Abs (0~0.5Abs), ±0.1%T

Baseline Correction

Selectable with storage in firmware

Baseline FlatnessWithin ±0.001Abs. (excluding noise, 2nm slit width and SLOW wavelength scanning speed)

Drift Less than 0.0004 Abs. per hour (after 2 hours warm-up)

Dimensions 570 (W) x 660 (D) x 275 (H) (mm)

Weight 36kg

Power Supply AC 100V/120V/220V/240V, 50/60Hz 250VA (swithc-selectable)

Page 22: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

Shimadzu UV-2450 Spectrophotometer

Page 23: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

d. Effects of monchromator exit slit width on spectra

Narrow exit slit width improves the spectrum resolution

but it also significantly reduce the radiant power

Trade-off between resolution and S/N ratio

Page 24: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

e. Multichannel spectrometer

No monochromator,

but disperses transmitted light and measures “all wavelength at once”

No Scanning-simple and fast

More expensive

Limited resolution

Fig. 13-15 (p.353)

Page 25: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

5.1Quanlitative spectra

Solvent effects on the UV-Vis spectra

Polar solvents “blur” vibrational features

Polar solvents shift absorption maxima

n * blue shift

* red shift -

UV-Vis not reliable for qualitative but excellent for quantitative analysis

Page 26: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

5.2 Quantitative analysis- Determining the relationship between A and c

External Standards

Standard-Addition

Page 27: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

Fig. 14-14 (p.382)

5.3 Spectrophotometric kinetics

Page 28: 1.1 Range of molar absorptivity Electronic excitation of outer valence (i.e. bonding) electron How probable for this electronic excitation? (allowed transition,

Fig. 14-16 (p.384)