Occluded molecular surface: Analysis of protein packing

1995 ◽  
Vol 8 (6) ◽  
pp. 334-344 ◽  
Author(s):  
N. Pattabiraman ◽  
K. B. Ward ◽  
P. J. Fleming
Author(s):  
Robert W. Odom

Time-of-flight secondary ion mass spectrometry (TOF-SIMS) performs surface sensitive analysis of the elemental and molecular composition of solids. TOFSIMS is a relatively new embodiment of static secondary ion mass spectrometry (SSIMS) in which the dose of primary ions incident on the surface is typically less than 1012 ions/cm2. Since typical solid surfaces have an atomic density of 1015 atoms/cm2, this primary ion dose nominally removes less than 0.1% of a monolayer. Hence, SIMS analyses performed under these static conditions represent near surface analysis in which secondary ions are produced from the top few monolayers of the surface. The actual sampling depth is determined by the primary ion momentum, angle of incidence and chemistry of the surface. Since low dose primary ions cause minimal perturbation of the chemistry of the solid surface, SSIMS analyses often produce molecular or pseudo-molecular ions characteristic of the chemical composition of the surface. Thus, molecular ions or structurally significant fragment ions are often observed in SSIMS analyses of surfaces containing inorganic and organic residues, polymers surfaces, coatings, and biological materials such as tissues and membranes.


2006 ◽  
Vol 14 (5) ◽  
pp. 1630-1643 ◽  
Author(s):  
Tomasz Magdziarz ◽  
Bozena Łozowicka ◽  
Rafał Gieleciak ◽  
Andrzej Bąk ◽  
Jarosław Polański ◽  
...  

2003 ◽  
Vol 69 (1-2) ◽  
pp. 51-59 ◽  
Author(s):  
Kiyoshi Hasegawa ◽  
Kenji Morikami ◽  
Yasuhiko Shiratori ◽  
Tatsuo Ohtsuka ◽  
Yuko Aoki ◽  
...  

Author(s):  
Sergei Rigin ◽  
Beatrice Armijo ◽  
Arcadius V. Krivoshein ◽  
Marina Fonari ◽  
Tatiana Timofeeva

A new polymorph of the title compound, C10H13NO, was obtained by recrystallization of the commercial product from a water/ethanol mixture (1:1 v/v). Crystals of the previously reported racemic and homochiral forms of 2-phenylbutyramide were grown from water–acetonitrile solution in 1:1 volume ratio [Khrustalev et al. (2014). Cryst. Growth Des. 14, 3360–3369]. While the previously reported racemic and enantiopure forms of the title compound adopt very similar supramolecular structures (hydrogen-bonded ribbons), the new racemic polymorph is stabilized by a single N—H...O hydrogen bond that links molecules into chains along the c-axis direction with an antiparallel (centrosymmetric) packing in the crystal. Hirshfeld molecular surface analysis was employed to compare the intermolecular interactions in the polymorphs of the title compound.


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