Molecular structure of hydrated complex of 1,4-dimethylpiperazine di-betaine with l-tartaric acid

2008 ◽  
Vol 892 (1-3) ◽  
pp. 353-359 ◽  
Author(s):  
Z. Dega-Szafran ◽  
A. Katrusiak ◽  
M. Szafran
2011 ◽  
Vol 991 (1-3) ◽  
pp. 178-185 ◽  
Author(s):  
Z. Dega-Szafran ◽  
G. Dutkiewicz ◽  
Z. Kosturkiewicz ◽  
M. Szafran ◽  
P. Barczyński

2016 ◽  
Vol 61 (2) ◽  
pp. 209-215 ◽  
Author(s):  
V. S. Sergienko ◽  
E. A. Chebanenko ◽  
I. I. Seifullina ◽  
A. V. Churakov ◽  
E. E. Martsinko

1996 ◽  
Vol 31 (9) ◽  
pp. 1127-1131 ◽  
Author(s):  
Yu Wentao ◽  
Lu Mengkai ◽  
Meng Fanqing

2002 ◽  
Vol 14 (1) ◽  
pp. 67-74 ◽  
Author(s):  
Alessia Bacchi ◽  
Giancarlo Pelizzi ◽  
George M. Sheldrick ◽  
Gabriele Amari ◽  
Maurizio Delcanale ◽  
...  

2013 ◽  
Vol 781-784 ◽  
pp. 135-138
Author(s):  
Xiao Xia Sun ◽  
Ying Chun Li ◽  
Xiao Xiao Zhuang ◽  
Yu Hu

An effective resolving agent, (D)-dibenzoyl tartaric acid (2b), was screened to yield direct resolution of (S)- ethyl nipecotate (1) with high optical purity and yield. Molecular recognition was studied by 1H NMR, IR, DSC and single crystal diffraction of the pair of diastereomeric salts. The less-soluble salt formed a supra molecular structure by enantio differentiating self-assembly.


Author(s):  
Wah Chiu ◽  
David Grano

The periodic structure external to the outer membrane of Spirillum serpens VHA has been isolated by similar procedures to those used by Buckmire and Murray (1). From SDS gel electrophoresis, we have found that the isolated fragments contain several protein components, and that the crystalline structure is composed of a glycoprotein component with a molecular weight of ∽ 140,000 daltons (2). Under an electron microscopic examination, we have visualized the hexagonally-packed glycoprotein subunits, as well as the bilayer profile of the outer membrane. In this paper, we will discuss some structural aspects of the crystalline glycoproteins, based on computer-reconstructed images of the external cell wall fragments.The specimens were prepared for electron microscopy in two ways: negatively stained with 1% PTA, and maintained in a frozen-hydrated state (3). The micrographs were taken with a JEM-100B electron microscope with a field emission gun. The minimum exposure technique was essential for imaging the frozen- hydrated specimens.


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