NMR Samples - PowerPoint PPT Presentation

About This Presentation
Title:

NMR Samples

Description:

Title: PowerPoint Presentation Last modified by: Notebook User Created Date: 1/1/1601 12:00:00 AM Document presentation format: On-screen Show Other titles – PowerPoint PPT presentation

Number of Views:71
Avg rating:3.0/5.0
Slides: 22
Provided by: chemirisC
Category:
Tags: nmr | effect | samples | solvent

less

Transcript and Presenter's Notes

Title: NMR Samples


1
NMR Samples
  • Types of NMR tubes
  • Sample preparation

2
Types of NMR Tubes
Solution NMR Sample Tube Spinners
Solid State Sample Rotors
NMR Sample Tubes with Caps
3
NMR Sample Preparation
  • Use clean dry NMR tubes and caps (tubes can
    be re-used, caps should not!)
  • 0.5 ml deuterated solvent (i.e. CDCl ,C D
    , acetone-d ,etc.)
  • substrate requirements for routine spectra
    10 mg for proton NMR 100 mg for carbon-13 NMR
  • min. filling height of tube 2 inches (5 cm)
  • Cleaning of tubes 1. rinse with solvent you
    were using 2. rinse with acetone 3. dry in
    (vacuum-)oven at low temperature

5 mm
3
6
6
6
4
NMR Sample Preparation
Clean clear solution
Suspension or opaque solution
Precipitate
Not enough solvent
Two phases
Concentration gradient

GOOD!
B a d S a m p l e s !
5
Good and bad NMR Spectra
  • are the result of
  • Sample preparation
  • Choice of solvent
  • Homogeneity of magnetic field
  • Data acquisition parameters
  • Processing procedures

6
Good spectrum
ppm
ppm
7
Good spectrum
ppm
Peak picking
Integrals
ppm
ppm scale
8
Good spectrum
ppm
ppm
9
Bad spectrum ?
10
Bad spectrum !
No units specified for axis and peak picking
Signal/Noise ratio bad
11
Bad spectrum ?
12
Bad spectrum !
Tall signals are cut off
13
Bad spectrum ?
14
Bad spectrum !
Signals too small (only allowed to
compare signal intensities between different
spectra)
15
Bad spectrum ?
16
Bad spectrum !
Broad signals(bad sample, poor shimming, wrong
processing parameters)
17
Bad spectrum ?
18
Bad spectrum !
Signals are distorted (automatic phase
correction is often insufficient)
Excessive peak picking (low p.p.
threshold,also due to improper phasing)
19
Bad spectrum ?
20
Bad spectrum ?
Areas without signals should be excluded. (If you
want to print all your spectra with a default
range, i.e. 0-10 ppm, dont forget to print
detailed expansions.)
21
Lab Assignments
Duration Spectrometer Experiment
sample requirement
(per 0.5 ml solution) 1. 2X2 hrs 100
360 MHz Comprehensive 1H NMR Indirect 13C
Observation 100 mg 2. 3 hrs 100 or
360 MHz Pulse Width Calibration and B1 100 mg
3. 2X2 hrs 100 360 MHz Rare spin
NMR concentrated (80-90) 4. 3 hrs 360
MHz Decoupling 1H from 13C and B2 100 mg 5. 2
hrs 100 300 MHz Spin Echo and
Spin/Spin Relaxation, T2 100 mg 6. 2 hrs
100 300 MHz Spin/Lattice Relaxation,
T1 100 mg 7. 3 hrs 360 MHz Nuclear
Overhauser Effect 25 mg 8. 2 hrs 360
MHz Polarization Transfer and DEPT 100 mg
9. 3 hrs 300 MHz 13C CP/MAS in Solids (sample
provided) 10. 2 hrs 360 MHz HETCOR (1H/13C
COSY) 100 mg 11. 2 hrs 360 MHz 1H COSY /
NOESY (optional) 25 mg Use your own samples,
if possible. Familiarize yourselves with the
procedures for each experiment, before you come
to the lab. Print the manuals.
Write a Comment
User Comments (0)
About PowerShow.com