X-ray diffraction and chemical bonding
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X-ray diffraction and chemical bonding

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Published by Twente University of Technology in Enschede .
Written in English


  • Chemical bonds.,
  • X-rays -- Diffraction.

Book details:

Edition Notes

Statementby Jan Willem Bats.
The Physical Object
Pagination110 p. :
Number of Pages110
ID Numbers
Open LibraryOL22003506M

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  This book deals with the electron density distribution in molecules and solids as obtained experimentally by X-ray diffraction. It is a comprehensive treatment of the methods involved, and the interpretation of the experimental results in terms of Author: Philip Coppens. The book's middle chapters describe the instrumentation and procedures used in X-ray diffraction, including X-ray sources, X-ray detection, and production of monochromatic radiation. The chapter devoted to instrument design and calibration is followed by an examination of specimen preparation methods, data collection, and reduction. Conventionally, the core electron density (ED) of atoms in molecules is considered to be virtually unperturbed by chemical bonding effects. Here we report a combined experimental and theoretical investigation of the ED of cubic boron nitride including a detailed modeling of the core ED. By modeling structure factors obtained from very-high-resolution synchrotron powder X-ray diffraction data. PART I INTRODUCTION. CHAPTER 1 Origin, Scope, and Plan of this Book. In July the fiftieth anniversary of Max von Laue’s discovery of the Diffraction of X-rays by crystals is going to be celebrated in Munich by a large international group of crystallographers, physicists, chemists, spectroscopists, biologists, industrialists, and many others who are employing the methods based on Laue.

C–H⋯O (ether) hydrogen bonding along the () direction in polyglycolic acid studied by infrared spectroscopy, wide-angle X-ray diffraction, quantum chemical calculations and natural bond . An X-ray powder diffraction pattern is a plot of the intensity of X-rays scattered at different angles by a sample • The detector moves in a circle around the sample –The detector position is recorded as the angle 2theta (2θ) –The detector records the number of X-rays observed at each angle 2θ –The X-ray intensity is usually.   Part of the Structure and Bonding book series (STRUCTURE, volume ) Abstract. We review the basic theoretical formulation for pulsed X-ray scattering on nonstationary molecular states. Møller K.B., Henriksen N.E. () Time-Resolved X-Ray Diffraction: The Dynamics of the Chemical Bond. In: Mingos D., Day P., Dahl J. (eds) Molecular. X-Ray Diffraction: A Practical Approach C. Suryanarayana, M. Grant Norton (auth.) In this, the only book available to combine both theoretical and practical aspects of x-ray diffraction, the authors emphasize a "hands on" approach through experiments and examples based on actual laboratory data.

This paper supplies tabulated data on the diffraction patterns of chemical substances and gives a scheme of classification which makes possible a routine and valuable use in the chemical laboratory of the Hull method of X-ray analysis. In Hull9 described a new method of chemical analysis by means of X-ray diffraction. He gave the ex-. X-Ray diffraction methods remain the definitive structural proof, and the number of X-ray studies on 1,2,3-thiadiazoles published has been steadily increasing. The bond lengths and bond angles are listed in Table 2 for 4- and for 5-monosubstituted and 4,5-disubstituted 1,2,3-thiadiazoles 1, Cite this chapter as: Corey R.B. () X-Ray Diffraction Studies of Crystalline Amino Acids and Peptides. In: Fortschritte der Chemie Organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products / Progrès Dans la Chimie des Substances Organiques Naturelles. ISBN: OCLC Number: Description: xiii, pages: illustrations ; 24 cm. Contents: Ch. 1. Scattering of x-rays and neutrons --Ch. Effect of thermal vibrations on the intensities of the diffracted beams --Ch. al bonding and the x-ray scattering formalism --Ch. -squares methods and their use in charge density analysis --Ch. 5.