Ready for Take-Off –
Crystallography in Undergraduate Education
August 29, 2012 1
Ready for Take-Off – Crystallography in Undergraduate Education
August 29, 2012 2
Dr. Michael Ruf Product Manager – Crystallography Bruker AXS Inc. Madison, WI, USA Dr. Roger Sommer Assistant Professor Department of Chemistry DePaul University Chicago, IL, USA Dr. Nigam Rath Director of the X-ray Diffraction Lab Department of Chemistry & Biochemistry University of Missouri St. Louis, MO, USA
• Introduction - Michael Ruf
• Experiences at DePaul University, Chicago - Roger Sommer
- CHE480: Special Topics in Chemistry: X-ray Crystallography
- From growing and handling crystals to preparing reports of experimental data for publication
• Experiences at University of Missouri, St. Louis - Nigam Rath
- Organic and inorganic chemistry experiments: syntheses, crystallization and structure determination of organic and inorganic compounds
Ready for Take-Off – Crystallography in Undergraduate Education
August 29, 2012 3
Is there a steep learning curve in crystallography?
August 29, 2012 4
• Crystallization
• X-rays
• Reciprocal space
• Fast Fourier Indexing
• Data collection strategies
• Kappa geometry
• Patterson methods
• SIRAS, SAD, MAD …
August 29, 2012 5
• Should we require that students understand structure factors and comprehend the concept of reciprocal space to be able to determine a structure?
• How can we interest students in crystallographic methods for structure determination?
• Can we interest students in crystallography by providing easy access to structure determination?
• Can we make it easier?
• Is automation a viable option?
• Can automation provide reliable and accurate structural information?
How can we interest students in crystallography?
August 29, 2012 6
• It is possible to take good quality pictures without any knowledge of
- Exposure times
- F-stops
- CMOS or CCD technology
- Image processing
- Or even one look at the users manual
Point and shoot in photography
VS.
August 29, 2012 7
• Is it possible to successfully apply this concept to structure determination?
• Would this concept lower the barrier to getting students interested in crystallography?
Point and shoot in crystallography?
VS.
August 29, 2012 8
SMART X2S benchtop diffractometer
The SMART X2S is
• a true benchtop system which can be placed anywhere in your laboratory
• extremely compact, lightweight and completely air-cooled – no cooling water is needed
• Requires single phase power only and draws ten times less power than a conventional diffractometer
August 29, 2012 9
SMART X2S benchtop diffractometer
• Completely automated operation
- Sample mounting and alignment
- Data collection
- Structure solution
- Report generation
- High success rate
• 100% data compatibility with APEX2 – the crystallography software suite
SMART X2S in a teaching environment
Roger Sommer
DePaul University
Department of Chemistry
August 29, 2012 11
In your opinion, what is the major hurdle to teaching crystallography to undergraduates?
a) Growing crystals
b) Availability of instrumentation
c) Safety
d) Need for local expertise
e) Availability of time in curriculum
Audience Poll
CHE480: Special Topics in Chemistry X-ray Crystallography
• 2 credit hour (1/2 regular course) – 1.5 hours lecture once a week for 10 weeks – 6 Masters, 3 senior undergrads
• Specific objectives of the course is to teach students how to: – Grow and handle crystals. – Run an experiment using the Bruker SMART X2S – Refine model to best fit the data. Evaluate the quality of the
structure based on common metrics. – Make useful high quality graphics of solid state structures. – Prepare report of experimental data for possible
publication.
My Objectives
• Students become independent users of SMART X2S
– Able to complete a routine experiment without direct intervention of crystallographer (instructor)
• Teach chemistry through crystallography
– CHE321 substitute (Int. Inorg. Chem.)
– Chemical intuition guides model refinement
Course Schedule Date Topics Events
9/13/2010
A look at the instrument, setup of experiment, how
data gets collected, a basic look at Bragg’s law, start a
dataset, look at unit cell, Miller indices, diffraction
planes. Get started using software.
9/20/2010
Crystal systems, Bravais lattices, space groups,
symmetry operations in unit cell, systematic absences,
look at international tables, evaluating crystal quality
under microscope.
Project 1 selection
9/27/2010
Completing and refining structure model, look at
extended structure (intermolecular interactions),
microscope/lab time
10/4/2010 Growing crystals, project selection/start crystallizations Project 1 due,
Project 2 selection
10/11/2010
Structure refinement - atom identification
project time, discussion of examples/specific issues
with student projects
10/18/2010 Techniques for dealing with solvated structures,
disorder and other problems, project 2 selection. Project 3 selection
10/25/2010 Project time/discussions Project 2 due
11/1/2010 Project time/discussions
11/8/2010 Project time/discussions
11/15/2010 Project time/discussions
11/22/2010 Project 3 due
Project 1: Do a structure of a pre-made crystal
• In the lab – Assess sample quality and select viable
specimen (microscope/X2S) – Mount crystal and start data collection – Observe unit cell determination and check
CSD for matches
• Homework – Refine structure
• X2S, OLEX2, or APEX2/XShell with instructor help
– Practice generating useful graphics – Write useful captions
• Report – One paragraph description of structure – Quality graphic of asymm. unit or molecule – Packing diagram from Hg including
characteristic symm. element
nickel sulfate taurine hexamethylenetetramine sucrose copper(II)acetate dihydrate vanadyl sulfate
Project 1: Instructor input
• 30-45 minutes outside lecture per student
– Microscope training and crystal selection/mounting
• 30 minutes Lecture time introducing software
• 3 hours of office hours troubleshooting structure refinement
Student illustrations of symmetry and Miller planes from Mercury
Si on 2 fold axis in P21212 222 plane
Mercury CSD 2.0 - New Features for the Visualization and Investigation of Crystal Structures C. F. Macrae, I. J. Bruno, J. A. Chisholm, P. R. Edgington, P. McCabe, E. Pidcock, L. Rodriguez-Monge, R. Taylor, J. van de Streek and P. A. Wood, J. Appl. Cryst., 41, 466-470, 2008 http://www.ccdc.cam.ac.uk/
Project 1 pictures: Illustrate symmetry elements
Figure: The unit cell of NiSO4H2O. The cell has
the dimensions 6.78597Å x 6.78597Å x
18.2992Å and the green lines indicate the
location of the 2-fold rotation axes through the
sulfur and nickel atoms of the compound. Figure 1: 2-Fold symmetry with (0.5-x,
0.5+y, 0.5-z) transformation was used to
generate above figure.
J. Appl. Cryst., 41, 466-470, 2008
Project 2: Grow your own crystals, improve graphics/descriptions
• In the lab – Students grow, select, and mount
their own crystals
• Homework – Refine structure using OLEX2, ShelXL
– Add appropriate labeling scheme and improve graphic/caption quality
• Report – Similar to 1 but better quality
graphics, improved language/descriptions
1) Dolomanov, O.V.; Bourhis, L.J.; Gildea, R.J.; Howard, J.A.K.; Puschmann, H., OLEX2: A complete structure solution, refinement and analysis program J. Appl. Cryst. 2009, 42, 339-341
2) SHELXL, G.M. Sheldrick, Acta Cryst. 2008 A64, 112-122
Project 2: Instructor input
• Lectures and discussion on refining structure and improving reports
• ~30-45 min/student on crystallizations
- Students spent more time • Office hour questions on
software and refinement
• 5-10 minutes per student for access to X-ray lab
Project 3: Finishing the structure • In the lab (optional)
– Some students used pre-collected data – Some got extensions to grow crystals of new compounds over winter break
• Homework
– Refine structure to convergence (OLEX2) – Merge and write .cif file (OLEX2) – Edit and complete .cif file (enCIFer) – Use CheckCIF and address as many issues as possible
• Report
– Quality graphics and description, "completed" .cif file
– A copy of the "initial" and "final" CheckCIF report – Standard tables for a paper
CIF applications. XV. enCIFer: a program for viewing, editing and visualising CIFs. F. H. Allen, O. Johnson, G. P. Shields, B. R. Smith, M. Towler, J. Applied Cryst., 2004 , 37, 335-338.
Student response
• Enthusiastic and engaged
• “Hands-on”
• “My own Data”
• “Practical application”
• Students used compounds from their own Master’s project
• Several students ready to publish
The numbers from CHE480
• Samples studied: ~50
– Includes many samples from student research that did not diffract
• Datasets collected: ~25
• Structures: 20
• New structures: 10
Students wanted more of…
• Discussion of Cambridge Structural Database
• A CSD-based project
– Analyze intermolecular interactions etc.
Student frustrations
• Growing crystals
• “A lot of software to learn…”
Student engagement
Kristy On Tue, Nov 30, 2010 at 6:14 PM, Kristina Streu < wrote: Dr. Sommer, I'm in the lab playing around with some of the crystals of the 2-acetamidobiphenyl that we grew. I got one loaded onto a mount and I started the experiment. However the instrument has stopped while loading the sample. It has been showing the "please insert the sample" screen for about 5 minutes, and has reported a loading error. I was hoping you would have some insight as to what I might need to do to retrieve the sample and fix this loading issue. In the loading process the instrument seems to have stalled at teh point where the sample has been taken down, however the door has not closed. My number is if you wanted to call me, I will be in the lab for a while working on Project 3 and some research. Or you can e-mail me back, whatever is convenient for you. Thanks, Kristy
Student engagement
Pca21
From: Kristina Streu [mailto: ] Sent: Tuesday, November 30, 2010 6:42 PM To: [email protected] Subject: Re: Crystals Dr. Sommer, Tom came in and advised me to try turning the instrument on and letting it re-initialize. This fixed the problem. The 2-acetamidobiphenyl crystal is running just fine now. Hopefully we get something from it. Kristy
Summer research with the X2S
• Two students in Sommer Lab
– Rising sophomores
• Ready to “go solo” within a week
• Three more structures for colleagues
Summer research results presented as a poster Spring ACS meeting 2011
August 29, 2012 30
Poll Results
In your opinion, what is the major hurdle to teaching crystallography to undergraduates?
a) Growing crystals
b) Availability of instrumentation
c) Safety
d) Need for local expertise
e) Availability of time in curriculum
Crystallography Experiments for
Undergraduate Laboratory
Nigam P. Rath,
Department of Chemistry and Biochemistry and Center for Nanoscience
University of Missouri - St. Louis
Outline
Introduction
Organic chemistry experiments: Multi-step syntheses, crystallization and structure
determination of organic compounds
Inorganic chemistry experiments: Synthesis, crystallization and structure determination of
transition metal p-toluenesulfonates
Student response
Conclusion
Introduction
Advanced techniques in undergraduate laboratories
Local and regional workforce requires students with expertise in advanced instrumentation and techniques
What can we teach and what can students learn with limited exposure to X-ray diffraction?
The “black box” approach?
The experiments The experiments can be carried out in modules
In the absence of access to X-ray instrumentation, available data sets can be used to provide a good flavor for crystallography using public domain software
The transition metal p-toluenesulfonates are good starting materials, reasonably inexpensive and demonstrate synthetic techniques under inert atmosphere
Criteria for selection of the experiments
The compound synthesis should be doable in a typical senior level laboratory course
The experiments should be easily reproducible
In the absence of a diffractometer, it should be possible to use available data sets for crystallography
A Typical Lab One-hour lecture – “everything you always wanted to know
about crystallography in 50 minutes”
A 4-hour lab period for data collection in batches
A 5-hour lab period with everyone in front of a computer to solve and refine the structure and generate figures and tables
Individual “help time” as needed
August 29, 2012 37
Do you plan on adding X-ray crystallography to your undergraduate teaching curriculum?
a) Yes, within the next year
b) Yes, within the next 1-2 years
c) Yes, within the next 3-5 years
d) Not sure
e) No plans at this time
Audience Poll
Reaction of Vanillin with Acetic Anhydride
O
O
O
O
4-acetoxy-3-methoxybenzaldehyde
O
O
HO
+
OO
O
acetic anhydride
NaOH
H2SO4
Vanillin
Vanyllyl Acetate
Unexpected Reaction ProductIdentfy with X-ray dif f raction
Crystallization
The product can be recrystallized from various solvents including methanol, ethanol and acetone.
The crystals shown are from slow evaporation of an acetone solution.
Crystal Data and Structure Refinement Parameters
Empirical formula C14 H16 O7
Formula weight 296.27
Temperature 100(2) K
Wavelength 0.71073 Å
Crystal system Orthorhombic
Space group Pbca
Unit cell dimensions a = 8.9131(8) Å
b = 7.8741(7) Å
c= 41.266(4) Å
Volume 2896.2(4) Å3
Z 8
Density (calculated) 1.359 Mg/m3
Absorption coefficient 0.110 mm-1
F(000) 1248
Crystal size 0.34 x 0.32 x 0.31 mm3
Theta range for data collection 1.97 to 40.43°.
Index ranges -16≤h≤16, -14≤k≤14, -75≤l≤ 74
Reflections collected 120135
Independent reflections 9191 [R(int) = 0.0329]
Absorption correction Semi-empirical from equivalents
Max. and min. transmission 0.9667 and 0.9637
Refinement method Full-matrix least-squares on F2
Data / restraints / parameters 9191 / 0 / 194
Goodness-of-fit on F2 1.042
Final R indices [I>2sigma(I)] R1 = 0.0437, wR2 = 0.1133
R indices (all data) R1 = 0.0593, wR2 = 0.1218
Largest diff. peak and hole 0.633 and -0.343 e.Å-3
Structure of the tri-acetate
Acid Catalyzed Esterification
O
O
HO
+
OO
O
acetic anhydride
Vanillin
H+/H2SO4
O
O
O
O
O
O
O
Condensation of Citral and Malonic Acid
Crystallization
The compound can be easily crystallized by slow evaporation of methanol, ethanol or acetone solutions.
Crystals shown are from methanol.
Crystal Data and Structure Refinement for the Lactone
Empirical formula C13 H18 O4
Formula weight 238.27
Temperature 100(2) K
Wavelength 0.71073 Å
Crystal system Monoclinic
Space group P21/c
Unit cell dimensions a = 8.6592(5) Å
b = 19.6679(11) Å = 107.049(2)°
c = 7.0735(4) Å
Volume 1151.74(11) Å3
Z 4
Density (calculated) 1.374 Mg/m3
Absorption coefficient 0.101 mm-1
F(000) 512
Crystal size 0.41 x 0.35 x 0.30 mm3
Theta range for data collection 2.07 to 36.59°.
Index ranges -14≤h≤14, -32≤k≤32, -11≤l≤11
Reflections collected 30631
Independent reflections 5644 [R(int) = 0.0242]
Completeness to theta = 36.59° 99.2 %
Absorption correction Semi-empirical from equivalents
Max. and min. transmission 0.9704 and 0.9597
Refinement method Full-matrix least-squares on F2
Data / restraints / parameters 5644 / 0 / 226
Goodness-of-fit on F2 1.045
Final R indices [I>2sigma(I)] R1 = 0.0324, wR2 = 0.0906
R indices (all data) R1 = 0.0394, wR2 = 0.0960
Largest diff. peak and hole 0.482 and -0.197 e.Å-3
Molecular Structure of the Lactone
An “ideal” compound for a crystallography experiment
During the reaction, a fused ring system is produced which is difficult to characterize and predict, at least at the level this experiment is carried out
This compound is hard to characterize by NMR as the 1H-spectrum is featureless
Forms well-formed crystals easily
Student Reports
Students submit a report on synthesis and characterization of the compounds.
They are introduced to mercury and CSD for further analysis of the structure (H-bonding, short contacts, comparison of geometrical parameters with similar structures, etc.).
Vanillin Acetate or Tricyclic Lactone? Both are good experiments for multi-step synthesis
and form good crystals.
The lactone experiment has been used lately for crystallography because the structure is relatively difficult to derive without X-ray.
The lactone experiment needs more time for synthetic steps - well planning needed.
Experiments for Inorganic Laboratory: synthesis and X-ray crystallography The following experiments have been carried out in the
senior inorganic chemistry laboratory course Chem4433 for last three years
Transition metal p-toluenesulfonates Binary salts of Mn(II), Fe(II), Co(II) and Ni(II) can be
synthesized by the reaction of the metal with p-toluenesulfonic acid monohydrate (HOTs.H2O) M + 2HOTs.H2O + 3H2O [M(OH2) 4][OTs] 2.H2O + H2
Monomeric tosylates [M(OTs) 2(DMF) 4] and polymeric tosylates [M(OTs) 2(DMF) 2]n can be crystallized by slowly diffusing (layering) Et2O into a solution of M(OTs) 2 in DMF.
X-ray structure determination Students screen, select and mount their own crystals
Data sets are collected under the supervision of a faculty member
The structure solution and refinement is carried out in a 4-5 hour laboratory period
The instructor and all students have used SHELX-TL software for X-ray structure determination
Students prepare the laboratory reports using the J. Am. Chem. Soc. Communication template. The report includes synthesis and characterization of the compound using X-ray diffraction, as well as other spectroscopic methods.
Structure of mononuclear and polymeric [Tm p-Toluenesulfonates]
Typically one of the two forms are produced: - a mono-nuclear trans-[M(OTs)2(DMF)4] or some of the DMF’s
replaced by water molecules
- A polymeric [M(OTs)2(DMF)2]n
Structure of trans-Fe(OTs)2(DMF)4]
Crystal Data and Structure Refinement for [Fe(OTs2)DMF4] Empirical formula C26 H42 Fe N4 O10 S2
Formula weight 690.61
Temperature 100(2) K
Wavelength 0.71073 Å
Crystal system Monoclinic
Space group P21/n
Unit cell dimensions a = 7.8561(7) Å
b = 24.663(2) Å = 111.155(3)°
c = 8.8289(7) Å
Volume, Z 1595.4(2) Å3 ,2
Density (calculated) 1.438 Mg/m3
Absorption coefficient 0.662 mm-1
F(000) 728
Crystal size 0.33 x 0.15 x 0.11 mm3
Theta range for data collection 2.61 to 34.98°.
Index ranges -12≤h≤12, -36≤k≤39, -14≤l≤8
Reflections collected 43608
Independent reflections 6993 [R(int) = 0.0474]
Absorption correction Semi-empirical from equivalents
Max. and min. transmission 0.9295 and 0.8131
Refinement method Full-matrix least-squares on F2
Data / restraints / parameters 6993 / 0 / 201
Goodness-of-fit on F2 1.021
Final R indices [I>2sigma(I)] R1 = 0.0299, wR2 = 0.0754
R indices (all data) R1 = 0.0407, wR2 = 0.0816
Largest diff. peak and hole 0.513 and -0.337 e.Å-3
Structure of trans-Mn(OTs)2(DMF)2(H2O)2]
Crystal Data and Structure Refinement for [Mn(OTs2)(DMF)2(H2O)2] Empirical formula C20 H32 Mn N2 O10 S2
Formula weight 579.54
Temperature 100(2) K
Wavelength 0.71073 Å
Crystal system Triclinic
Space group P-1
Unit cell dimensions a = 6.3281(5) Å = 90.105(5)°.
b = 12.2134(12) Å = 98.940(4)°.
c = 17.1863(17) Å = 95.606(4)°.
Volume, Z 1305.7(2) Å3 ,2
Density (calculated) 1.474 Mg/m3
Absorption coefficient 0.720 mm-1
F(000) 606
Crystal size 0.51 x 0.13 x 0.08 mm3
Theta range for data collection 1.20 to 33.14°.
Index ranges -9≤h≤9, -18≤k≤18, -23≤l≤26
Reflections collected 41188
Independent reflections 9751 [R(int) = 0.0445]
Absorption correction Semi-empirical from equivalents
Max. and min. transmission 0.9467 and 0.7117
Refinement method Full-matrix least-squares on F2
Data / restraints / parameters 9751 / 6 / 338
Goodness-of-fit on F2 1.034
Final R indices [I>2sigma(I)] R1 = 0.0381, wR2 = 0.0897
R indices (all data) R1 = 0.0639, wR2 = 0.1034
Largest diff. peak and hole 0.601 and -0.394 e.Å-3
Structure of [Mn(OTs)2(DMF) 2]n
Crystal Data and Structure Refinement for [Mn(OTs)2(DMF)2]n Empirical formula C20 H28 Mn N2 O8 S2
Formula weight 543.50
Temperature 100(2) K
Wavelength 0.71073 Å
Crystal system Monoclinic
Space group P21/n
Unit cell dimensions a = 14.8262(8) Å = 90°.
b = 5.2111(3) Å = 107.948(3)°.
c = 16.2554(9) Å = 90°.
Volume, Z 1194.79(12) Å3 ,2
Density (calculated) 1.511 Mg/m3
Absorption coefficient 0.775 mm-1
F(000) 566
Crystal size 0.30 x 0.08 x 0.05 mm3
Theta range for data collection 2.23 to 30.86°.
Index ranges -21≤h≤21, -7≤k≤6, -23≤l≤23
Reflections collected 16816
Independent reflections 3769 [R(int) = 0.0445]
Absorption correction Semi-empirical from equivalents
Max. and min. transmission 0.9645 and 0.8002
Refinement method Full-matrix least-squares on F2
Data / restraints / parameters 3769 / 0 / 154
Goodness-of-fit on F2 1.017
Final R indices [I>2sigma(I)] R1 = 0.0360, wR2 = 0.0862
R indices (all data) R1 = 0.0551, wR2 = 0.0972
Largest diff. peak and hole 0.592 and -0.485 e.Å-3
August 29, 2012 60
Do you plan on adding X-ray crystallography to your undergraduate teaching curriculum?
a) Yes, within the next year
b) Yes, within the next 1-2 years
c) Yes, within the next 3-5 years
d) Not sure
e) No plans at this time
Poll Results
Conclusions The organic laboratory experiments have been
successfully incorporated into our curriculum for the past several years.
Student response has been very enthusiastic (anecdotal and anonymous course evaluations).
These experiments add significant learning to the respective labs.
Acknowledgements Professor Christopher Spilling and students in his
organic laboratory course Chem3643
Professor Stephen Holmes and students in the inorganic laboratory course Chem4433
Undergraduate and high school students who have checked the recrystallization of the samples
NSF-MRI funding for the purchase of X-ray diffractometers
Bruker AXS for a benchtop diffractometer for evaluation
X-ray Diffraction Facility at UMSL
Housed in the custom-designed laboratory space in the Center for Nanoscience.
Current instrumentation includes two single crystal and one powder diffractometers.
August 29, 2012 64
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