scholarly journals How to determine the number of inner-sphere water molecules in Lanthanide(III) complexes by17O NMR spectroscopy. A technical note

2007 ◽  
Vol 2 (2) ◽  
pp. 67-71 ◽  
Author(s):  
Kristina Djanashvili ◽  
Joop. A. Peters
1988 ◽  
Vol 8 (2) ◽  
pp. 191-199 ◽  
Author(s):  
Carlos F. G. C. Geraldes ◽  
A. Dean Sherry ◽  
William P. Cacheris ◽  
Kah-Tiong Kuan ◽  
Rodney D. Brown ◽  
...  
Keyword(s):  

1992 ◽  
Vol 114 (10) ◽  
pp. 3690-3697 ◽  
Author(s):  
Daniella Goldfarb ◽  
Hong Xin Li ◽  
Mark E. Davis

1998 ◽  
Vol 282 (4) ◽  
pp. 847-858 ◽  
Author(s):  
Maria Sunnerhagen ◽  
Vladimir P Denisov ◽  
Kandadai Venu ◽  
Alexandre M.J.J Bonvin ◽  
Jannette Carey ◽  
...  

2010 ◽  
Vol 37 (3-4) ◽  
pp. 91-100 ◽  
Author(s):  
Z.T. Lalowicz ◽  
G. Stoch ◽  
A. Birczyński ◽  
M. Punkkinen ◽  
M. Krzystyniak ◽  
...  

2020 ◽  
Vol 56 (69) ◽  
pp. 9998-10001 ◽  
Author(s):  
Thirupathi Ravula ◽  
Bikash R. Sahoo ◽  
Xiaofeng Dai ◽  
Ayyalusamy Ramamoorthy

Measurement of ordering of water molecules in magnetically aligned polymer-nanodiscs using an integrated 17O NMR and MD simulation.


Author(s):  
M. Carmen Alpoim ◽  
Ana M. Urbano ◽  
Carlos F. G. C. Geraldes ◽  
Joop A. Peters
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2021 ◽  
Author(s):  
Fernán Berride ◽  
Victor M. Sánchez-Pedregal ◽  
Bruno Dacuña ◽  
Eurico Cabrita ◽  
Armando Navarro-Vázquez ◽  
...  

The X-ray crystal structure of the gelator 1,3:2,4-dibenzylidene-D-sorbitol (DBS) is reported here. DBS is an important gelating molecule known for nearly 130 years, that has eluded crystallization until now. The crystal obtained presents an axial stacking of DBS molecules stabilized by both Van der Waals interactions and intermolecular hydrogen bonds of the side chain hydroxyl groups with either neighboring DBS or water molecules. The crystal structure shows definitive evidence for the frequently assumed “butterfly” type aggregation mode and experimentally proves the equatorial placement of the phenyl rings. The conformation of DBS has been analyzed in the crystal structure and compared with that determined in solution through NMR spectroscopy.


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