Example: Identification

Similar documents
Refine & Validate. In the *.res file, be sure to add the following four commands after the UNIT instruction and before any atoms: ACTA CONF WPDB -2

3. The solved structure is not the expected compound, but this unexpected twist is beside the point:

Space Objects. Section. When you finish this section, you should understand the following:

3D - Structure Graphics Capabilities with PDF-4 Database Products

Login -the operator screen should be in view when you first sit down at the spectrometer console:

Refinement of Disorder with SHELXL

You w i ll f ol l ow these st eps : Before opening files, the S c e n e panel is active.

4. Constraints and Hydrogen Atoms

Physical Chemistry Analyzing a Crystal Structure and the Diffraction Pattern Virginia B. Pett The College of Wooster

SeeSAR 7.1 Beginners Guide. June 2017

Preparing a PDB File

BUILDING BASICS WITH HYPERCHEM LITE

Application Note. U. Heat of Formation of Ethyl Alcohol and Dimethyl Ether. Introduction

NMR Predictor. Introduction

PDF-4+ Tools and Searches

PDF-4+ Tools and Searches

X-Seed 4.0. A program for supramolecular crystallography

APPENDIX E. Crystallographic Data for TBA Eu(DO2A)(DPA) Temperature Dependence

Space Group & Structure Solution

Tutorial 23 Back Analysis of Material Properties

BOND LENGTH WITH HYPERCHEM LITE

Irrational Thoughts. Aim. Equipment. Irrational Investigation: Teacher Notes

Performing a Pharmacophore Search using CSD-CrossMiner

Creating a Pharmacophore Query from a Reference Molecule & Scaffold Hopping in CSD-CrossMiner

Synthetic, Structural, and Mechanistic Aspects of an Amine Activation Process Mediated at a Zwitterionic Pd(II) Center

3D Molecule Viewer of MOGADOC (JavaScript)

ISIS/Draw "Quick Start"

Seth B. Harkins and Jonas C. Peters

Let s continue our discussion on the interaction between Fe(III) and 6,7-dihydroxynaphthalene-2- sulfonate.

Chem 253. Tutorial for Materials Studio

Introduction to Hartree-Fock calculations in Spartan

Pymol Practial Guide

ion, as obtained from a search of the Cambridge Structural database (CSD), December 2013.

BD1. Reciprocal space and Fourier transforms. IB Mineral Sciences Module B: Reciprocal Space, Symmetry and Crystallography

CALIFORNIA INSTITUTE OF TECHNOLOGY BECKMAN INSTITUTE X-RAY CRYSTALLOGRAPHY LABORATORY

HSC Chemistry 7.0 User's Guide

Ethylene Trimerization Catalysts Based on Chromium Complexes with a. Nitrogen-Bridged Diphosphine Ligand Having ortho-methoxyaryl or

Cages on a plane: a structural matrix for molecular 'sheets'

Assignment 1: Molecular Mechanics (PART 1 25 points)

Experiment 2a Models of the Solid State*

An area chart emphasizes the trend of each value over time. An area chart also shows the relationship of parts to a whole.

PDF-2 Tools and Searches

VCell Tutorial. Building a Rule-Based Model

Lab #10 Atomic Radius Rubric o Missing 1 out of 4 o Missing 2 out of 4 o Missing 3 out of 4

Tutorial. Getting started. Sample to Insight. March 31, 2016

Calculating Bond Enthalpies of the Hydrides

PQSMol. User s Manual

Finite Element Modules for Enhancing Undergraduate Transport Courses: Application to Fuel Cell Fundamentals

Rigid body Rigid body approach

1 Introduction & Objective. 2 Warm-up. Lab P-16: PeZ - The z, n, and O! Domains

Supplementary Material (ESI) for CrystEngComm This journal is The Royal Society of Chemistry 2010

Dock Ligands from a 2D Molecule Sketch

Electric Fields and Equipotentials

CHEMDRAW ULTRA ITEC107 - Introduction to Computing for Pharmacy. ITEC107 - Introduction to Computing for Pharmacy 1

HOW TO ANALYZE SYNCHROTRON DATA

Introduction to Computer Tools and Uncertainties

ICM-Chemist How-To Guide. Version 3.6-1g Last Updated 12/01/2009

Homework 1 (not graded) X-ray Diffractometry CHE Multiple Choice. 1. One of the methods of reducing exposure to radiation is to minimize.

Table of Contents. Table of Contents LAMMPS trajectories into QuantumATK

Endothermic and Exothermic Reactions

Harvard Life Science Outreach December 7, 2017 Measuring ecosystem carbon fluxes using eddy covariance data ACTIVITIES I. NAME THAT ECOSYSTEM!

The Rain in Spain - Tableau Public Workbook

Comparing whole genomes

OECD QSAR Toolbox v.4.1. Step-by-step example for predicting skin sensitization accounting for abiotic activation of chemicals

ScienceWord and PagePlayer Chemical formulae. Dr Emile C. B. COMLAN Novoasoft Representative in Africa

DSP First. Laboratory Exercise #10. The z, n, and ˆω Domains

IncuCyte ZOOM NeuroTrack Fluorescent Processing

MAGNETITE OXIDATION EXAMPLE

Skin Damage Visualizer TiVi60 User Manual

Chemistry 14CL. Worksheet for the Molecular Modeling Workshop. (Revised FULL Version 2012 J.W. Pang) (Modified A. A. Russell)

Reaction Landscape of a Pentadentate N5-Ligated Mn II Complex with O 2

Eur. J. Inorg. Chem WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, 2013 ISSN SUPPORTING INFORMATION

Signal Processing First Lab 11: PeZ - The z, n, and ˆω Domains

Lab 1 Uniform Motion - Graphing and Analyzing Motion

Exercises for Windows

Solving Differential Equations on 2-D Geometries with Matlab

CLASSIFIY ROCKS THAT ARE SHARED BETWEEN TWO OR MORE GLACIERS AS "NODATA"

PHYSICS 220 LAB #5: WORK AND ENERGY

Spin crossover in polymeric and heterometallic Fe II species containing polytopic dipyridylamino-substituted-triazine ligands.

TECDIS and TELchart ECS Weather Overlay Guide

Entropy rules! Disorder Squeeze

Working with protein structures. Benjamin Jack

Electric Fields and Potential

Exploring the World of Ordinary Kriging. Dennis J. J. Walvoort. Wageningen University & Research Center Wageningen, The Netherlands

Introduction to Structure Preparation and Visualization

Examples of Protein Modeling. Protein Modeling. Primary Structure. Protein Structure Description. Protein Sequence Sources. Importing Sequences to MOE

1 An Experimental and Computational Investigation of the Dehydration of 2-Butanol

The Hückel Approximation Consider a conjugated molecule i.e. a molecule with alternating double and single bonds, as shown in Figure 1.

Advanced Crystallography: Refinement of Disordered Structures. November 13, 2012 Disorder Webinar

RT3D Rate-Limited Sorption Reaction

Section III - Designing Models for 3D Printing

Ligand Scout Tutorials

Geography 281 Map Making with GIS Project Four: Comparing Classification Methods

Chem 1 Kinetics. Objectives. Concepts

Supporting Information

Computational Study of Chemical Kinetics (GIDES)

Mnova Software for Analyzing Reaction Monitoring NMR Spectra

1 Introduction to Computational Chemistry (Spartan)

Harmonic Motion. Mass on a Spring. Physics 231: General Physics I Lab 6 Mar. 11, Goals:

ON SITE SYSTEMS Chemical Safety Assistant

Transcription:

Example: Identification In this structure we will explore Atom identification Working with maps Working with projections Eliminating diffusely diffracting solvent Disorder modeling Restrain application The proposed structure of a Pd(II) complex is shown below. It was crystallized from acetone and hexanes. 1. We start with files identification.res and identification.hkl. The structure has been solved and all atoms we are sure about are shown. 2. Run a refinement (CTRL-R). Label the highest peak of 7.3 e/å 3 as follows: Under Work Toolbox Work click on the button. The cursor goes into the labeling mode, and the name of the next atom to be labeled is displayed. In this case it is O4. 1

Click on the highest Q peak to rename it and run an anisotropic refinement by clicking on the button. 3. The new O4 atom looks a little large. O4 To examine the Fourier difference map go to Tools Maps Electron Denisty and click on the button. Pull the Level slider all the way to the left and start pulling it to the right. The dark-colored meshwork around O4 indicates a hole; clearly too much electron density was assigned at this location: Click on the Map button again to hide the map. Moreover, if you type grow to examine the structure, the coordination from O4 to the Pd atom is inconsistent with the typical bridging coordination geometry of the acetate. We conclude that O4 is in fact a carbon, and the ligand is acetonate. Type fuse to reduce the molecule to the asymmetric unit, relabel O4 to be C5 and re-refine the structure. Then position the H atoms on C5 and refine the structure again this is done by clicking on under Work Toolbox Work: The meaning to the checkbox to the left of the Add H button is to ensure that a refinement is launched immediately after H atoms are assigned. If you wish to check the correctness of H atoms placement prior to the refinement uncheck the box. 2

4. There are some peaks of electron density that belong to the solvent molecules. They reside in the solvent accessible voids. To visualize their positions: a) make sure the Q peaks are displayed (press CTRL-Q if necessary). b) to make sure that each Pd atom forms no more than four bonds select Pd1 and type conn 4 c) type pack to generate a packing diagram. d) type cell to display the unit cell boundaries. e) to orient the unit cell along the a axis type matr 1 or matr a. In this case the best view is along the c axis (matr 3 or matr c): View along the c axis 5. Modeling the solvent in this case is left as an exercise for the reader. We ll mask the solvent out in a procedure alternative to SQUEEZE. More info on how OLEX2 masking compares to SQUEEZE and some literature references is available in Ilia Guzei s Notes on OLEX2 at xray.chem.wisc.edu/lab.html. Reduce the view to the asymmetric unit by typing run fuse>>cell>>compaq The run command allows command concatenation (useful if you plan to repeat a succession of commands in the future by pressing the key). Under Tools Maps Masks click on the Mask button. 3

Type cell to display the cell. Under the Maps menu check the Extended checkbox channels in the lattice: to see the solvent accessible voids as The numerical output is also generated in the console part of the GUI. It can also be examined in the output.txt file that is opened by clicking on the atop the GUI panel. The masking procedure computed a total of 138.4 electrons for the diffusely diffracted species in the voids of 755 Å 3 : Void Vol/Ang^3 #Electrons 1 377.5 69.2 2 377.5 69.2 For comparison, SQUEEZE computed a volume of 735.8 Å 3 and 156 electrons. Click on the MASK button to hide the mask, and hide the cell either by typing cell or by View Symmetry Generation Symmetry Tools Show Cell. To refine the structure with the solvent masked out go to Work Refine and check the Run a refinement with CTRL-R. use solvent mask box. 6. The extended nature of the structure can be examined in a number of ways with View Symmetry Generation Symmetry Tools. We are not going to do that due to the self-explanatory nature of these tools. Instead, type mode grow 4

to enable manual generation of symmetry-related atoms. The dashed lines show where symmetry related atoms are located (diagram on the left). Extend the structure by clicking on the dashes: Press ESC to exit the grow mode. The text in the GUI can be toggled with CTRL-T. The H atoms can be toggled with CTRL- H. To determine the direction of the propagation of this polymeric structure select two Pd atoms in the direction of the propagation by clicking on them and type line n The line command draws lines, but when used with the n switch no line is generated and the structure is oriented so that this line is perpendicular to the screen: The drawing is oriented along the Pd Pd lines on the right. Type direction to numerically express the lattice direction perpendicular to the screen (in our case it is the direction defined by the two Pd atoms, thanks to the line n command). In this case the following output is generated: Direction: (-0.033*A, -0.000*B, 0.999*C) View along 000-001 (normalised deviation: 0.022A) View along 100-101 (normalised deviation: 0.022A) 5

View along 010-011 (normalised deviation: 0.022A) View along 110-111 (normalised deviation: 0.022A) Thus, the direction of propagation is along the c axis. OLEX2 also prints major directions if they are close to the direction of the current projection. 7. Reduce the structure to the asymmetric unit (fuse) and let us model the disorder of the CF 3 group. This is seriously cool. The idea is to split atoms F1, F2, F3 into two sets by rotating the CF 3 group about the C1-C2 axis. Select atoms C2 F1 F2 F3 by clicking on them in this order. In general, a selection can be made by drawing a box around the atoms of interest (by holding down the SHIFT key and dragging the mouse with the left button depressed), but in this case the order in which the atoms are selected is important. In the GUI type mode fit -s=1 to indicate that we will be fitting the whole group to a new location, but one atom (the first atom of the selection) will not be split. The colors change somewhat, but importantly, the C1 C2 bond is highlighted: Right click on the C1 C2 bond once. Press the left mouse button and drag on the C1 C2 bond to rotate the F atoms about the C1 C2 axis. When you find good positions for the new F atoms, press ESC. The anisotropic F atoms have been split into two sets of isotropic atoms: FVAR 0.20168 0.75 PART 1 F1 5 0.27260 0.87054 0.57380 21.00000 0.07766 F2 5 0.31045 0.91385 0.76109 21.00000 0.10564 F3 5 0.22327 0.78921 0.69629 21.00000 0.11074 PART 2 F2a 5 0.32353 0.93217 0.71783-21.00000 0.05000 F3a 5 0.24159 0.81252 0.75254-21.00000 0.05000 F1a 5 0.24608 0.83512 0.57664-21.00000 0.05000 6

Note that the F atoms are assigned to two parts with occupancies 21 and -21 and that the second free variable with a value of 0.75 has been added to the FVAR line. Run a refinement. The C F distances seem to vary between 1.26 and 1.43 Å, and the use of restraints is warranted. OLEX2 has a neat utility of restraining 1-2 distances and 1 3 distances with a couple of clicks. Select atom C2. Then select Tools SHELX compatible restraints SADI (from the drop-down menu). When you click on the GO button in this option, all C2-F and C2-C1 distances will be restrained to be similar and all F F separations will get a similarity restraint as follows: SADI 0.04 F1 F2 F1 F3 F2 F3 F2A F3A F2A F1A F3A F1A SADI C2 C1 C2 F1 C2 F2 C2 F3 C2 F2A C2 F3A C2 F1A These commands are automatically inserted in the INS file. Of course the C2 C1 bond on the second line does not belong and one may elect to assign different esd s on the SADI cards. To edit this command open the INS file by typing edit. In my case these two commands are modified to eliminate the C2 C1 bond and to assign tighter esd s: SADI 0.02 F1 F2 F1 F3 F2 F3 F2A F3A F2A F1A F3A F1A SADI 0.01 C2 F1 C2 F2 C2 F3 C2 F2A C2 F3A C2 F1A Another refinement does even out the C F distances and CF 3 group geometries. It also suggests that the CF 3 group may be split over three positions (see the ball-n-stick diagram on the left), a preprogrammed feature for splitting a group into three or more is being considered. 7