X-ray powder structure determination of Li6P6O18·3H2O

1998 ◽  
Vol 35 (10-11) ◽  
pp. 689-697 ◽  
Author(s):  
M. Toumi ◽  
F. Hlel ◽  
T. Ben Chaabane ◽  
L. Smiri ◽  
Y. Laligant ◽  
...  
1981 ◽  
Vol 46 (12) ◽  
pp. 3063-3073 ◽  
Author(s):  
Jana Podlahová ◽  
Bohumil Kratochvíl ◽  
Vratislav Langer ◽  
Josef Šilha ◽  
Jaroslav Podlaha

The equilibria and mechanism of addition of protons to the ethylenediphosphinetetraacetate anion (L4-) were studied in solution by the UV, IR, 1H and 31P NMR spectroscopic methods. A total of six protons can be bonded to the anion. They are added stepwise, first with partial formation of zwitterions containing P-H bonds, which then dissociate with formation of the free acid, H4L, where all four protons are bonded in carboxyl groups. The formation of zwitterions is strongly dependent on the concentration. In the final stage, the acid bonds two additional protons to form the bis-phosphonium cation, H6L2+. A number of isostructural salts containing this cation, H4L.2 HX (X = Cl, Br, I), have been prepared. The X-ray crystal structure determination of the bromide confirmed the expected arrangement. The bromide crystals are monoclinic, a = 578.2, b = 1 425.0, c = 1 046.7 pm, β = 103.07° with a space group of P21/c, Z = 2. The final R factor was 0.059 based on 1 109 observed reflections. The structure consists of H6L2+ cations containing protons bonded to phosphorus atoms (P-H distance 134 pm) and of bromide anions, located in gaps which are also sufficiently large for I- anions in the isostructural iodide. The interbonding of phosphonium cations proceeds through hydrogen bonds, C-OH...O=C, in which the O...O distance is 275.3 pm.


1999 ◽  
Vol 23 (3) ◽  
pp. 196-197
Author(s):  
Timothy J. Houghton ◽  
Stephen C. Wallwork

X-Ray structure determination of the complex salts [MeNC5H4Me]+[TCNQ2]- [1,4-dimethylpyridinium 2(7,7,8,8-tetracyanoquinodimethane) (1-); I] and [Me(NC5H4)(Me)CH-CH(Me)(C5H4N)Me]2+[TCNQ4]2- [ meso-2,3-bis( N-methyl-4-pyridyl)butane(2+) 4(7,7,8,8-tetracyanoquinodimethane) (2-); II], where TCNQ=(CN)2C(C6H4)C(CN)2, shows that, although in both salts the TCNQ moieties are stacked in columns, lateral shifts break these columns into diads for I and tetrads for II causing their electrical conductivities to be only moderate (Σ = 2–4 × 10−3 ohm−1 cm−1).


Polyhedron ◽  
2008 ◽  
Vol 27 (17) ◽  
pp. 3477-3483 ◽  
Author(s):  
Milan Nádvorník ◽  
Vratislav Langer ◽  
Robert Jirásko ◽  
Michal Holčapek ◽  
Tomáš Weidlich ◽  
...  

1998 ◽  
Vol 63 (9) ◽  
pp. 3125-3127 ◽  
Author(s):  
Richard Vaughan Williams ◽  
W. Daniel Edwards ◽  
Ashwani Vij ◽  
Robert W. Tolbert ◽  
Reginald H. Mitchell

2013 ◽  
Vol 88 ◽  
pp. 107-109 ◽  
Author(s):  
J.J. Nair ◽  
O.Q. Munro ◽  
M. Pošta ◽  
H.B. Papenfus ◽  
P. Beier ◽  
...  

1994 ◽  
Vol 89 (7) ◽  
pp. 583-586 ◽  
Author(s):  
Toshihiro Shimada ◽  
Yukito Furukawa ◽  
Etsuo Arakawa ◽  
Kunikazu Takeshita ◽  
Tadashi Matsushita ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document