X -ray scattering and covalent bonding in germanium

The effects of covalent bonding on Bragg X -ray scattering in germanium are predicted in terms of the results which have emerged from detailed studies of such effects evident in accurate X -ray data for silicon and diamond. Alternative possibilities consistent with trends found in these lighter systems are considered, and it is shown that one of the possibilities is in accord with a recent observation that | f (222)| = 0⋅14 ± 0⋅01. The predictions of nonspherical scattering in the orthodox data for this system are compared with the X -ray measurements of DeMarco & Weiss to illustrate how the requirements of high accuracy in experimental results rise steeply with increase in atomic number. It is shown that, on the present evidence from the 222 reflexion, the effects of covalent bonding in germanium will produce a peak of approximately 0⋅18 e/Å 3 at the midpoint of each bond. The need for more precise measurements in the future is pointed out.

2012 ◽  
Vol 108 (6) ◽  
Author(s):  
J. T. Okada ◽  
P. H.-L. Sit ◽  
Y. Watanabe ◽  
Y. J. Wang ◽  
B. Barbiellini ◽  
...  

2014 ◽  
Vol 9 (4) ◽  
pp. 304-313 ◽  
Author(s):  
Fernanda Peyronel ◽  
Bonnie Quinn ◽  
Alejandro G. Marangoni ◽  
David A. Pink

Author(s):  
Eva-Maria Mandelkow ◽  
Eckhard Mandelkow ◽  
Joan Bordas

When a solution of microtubule protein is changed from non-polymerising to polymerising conditions (e.g. by temperature jump or mixing with GTP) there is a series of structural transitions preceding microtubule growth. These have been detected by time-resolved X-ray scattering using synchrotron radiation, and they may be classified into pre-nucleation and nucleation events. X-ray patterns are good indicators for the average behavior of the particles in solution, but they are difficult to interpret unless additional information on their structure is available. We therefore studied the assembly process by electron microscopy under conditions approaching those of the X-ray experiment. There are two difficulties in the EM approach: One is that the particles important for assembly are usually small and not very regular and therefore tend to be overlooked. Secondly EM specimens require low concentrations which favor disassembly of the particles one wants to observe since there is a dynamic equilibrium between polymers and subunits.


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