Preparation and structural characterization of [Ph3Sn(IV)]+ complexes with pyridine-carboxylic acids or hydroxypyridine, -pyrimidine and -quinoline

2006 ◽  
Vol 691 (8) ◽  
pp. 1622-1630 ◽  
Author(s):  
Attila Szorcsik ◽  
László Nagy ◽  
Michelangelo Scopelliti ◽  
Andrea Deák ◽  
Lorenzo Pellerito ◽  
...  
Il Farmaco ◽  
2005 ◽  
Vol 60 (6-7) ◽  
pp. 519-527 ◽  
Author(s):  
Jerzy Kossakowski ◽  
Kinga Ostrowska ◽  
Elżbieta Hejchman ◽  
Irena Wolska

Author(s):  
Alessandro Mariani ◽  
Alessandro Innocenti ◽  
Alberto Varzi ◽  
Stefano Passerini

Herein we report the first in-dept structural characterization of simple linear carboxylic acids with alkyl tail length ranging from one to six carbon atoms. By means of SWAXS technique, a...


Polyhedron ◽  
2013 ◽  
Vol 64 ◽  
pp. 268-279
Author(s):  
Wesley Sattler ◽  
Joshua H. Palmer ◽  
Christy C. Bridges ◽  
Lucy Joshee ◽  
Rudolfs K. Zalups ◽  
...  

Polyhedron ◽  
2018 ◽  
Vol 141 ◽  
pp. 208-214 ◽  
Author(s):  
Alice De Palo ◽  
Lorenzo Biancalana ◽  
Marco Bortoluzzi ◽  
Maria Alessandra Martini ◽  
Fabio Marchetti ◽  
...  

Author(s):  
S. F. Hayes ◽  
M. D. Corwin ◽  
T. G. Schwan ◽  
D. W. Dorward ◽  
W. Burgdorfer

Characterization of Borrelia burgdorferi strains by means of negative staining EM has become an integral part of many studies related to the biology of the Lyme disease organism. However, relying solely upon negative staining to compare new isolates with prototype B31 or other borreliae is often unsatisfactory. To obtain more satisfactory results, we have relied upon a correlative approach encompassing a variety EM techniques, i.e., scanning for topographical features and cryotomy, negative staining and thin sectioning to provide a more complete structural characterization of B. burgdorferi.For characterization, isolates of B. burgdorferi were cultured in BSK II media from which they were removed by low speed centrifugation. The sedimented borrelia were carefully resuspended in stabilizing buffer so as to preserve their features for scanning and negative staining. Alternatively, others were prepared for conventional thin sectioning and for cryotomy using modified procedures. For thin sectioning, the fixative described by Ito, et al.


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