Single crystal study of the one dimensional Ca Co O compound: five stable configurations for the Ising triangular lattice

2000 ◽  
Vol 15 (4) ◽  
pp. 657-663 ◽  
Author(s):  
A. Maignan ◽  
C. Michel ◽  
A.C. Masset ◽  
C. Martin ◽  
B. Raveau
2015 ◽  
Vol 115 (16) ◽  
Author(s):  
Yuesheng Li ◽  
Gang Chen ◽  
Wei Tong ◽  
Li Pi ◽  
Juanjuan Liu ◽  
...  

2018 ◽  
Vol 74 (2) ◽  
pp. 131-138 ◽  
Author(s):  
Pamela Allan ◽  
Jean-Baptiste Arlin ◽  
Alan R. Kennedy ◽  
Aiden Walls

Ten isostructural single-crystal diffraction studies of mixed cation Ca/Sr salt forms of the salicylate anion are presented, namely catena-poly[[diaquacalcium(II)/strontium(II)]-bis(μ2-2-hydroxybenzoato)], [Ca1–x Sr x (C7H5O3)2(H2O)2] n , where x = 0, 0.041, 0.083, 0.165, 0.306, 0.529, 0.632, 0.789, 0.835 and 1. The structure of an isostructural Sr/Ba species, namely catena-poly[[diaquastrontium(II)/barium(II)]-bis(μ2-2-hydroxybenzoato)], [Sr0.729Ba0.271(C7H5O3)2(H2O)2], is also described. The Ca/Sr structures form a series where, with increasing Sr content, the unit cell expands in both the crystallographic a and c directions (by 1.80 and 3.18%, respectively), but contracts slightly in the b direction (−0.31%). The largest percentage structural expansion lies parallel to the direction of propagation of the one-dimensional coordination polymer that is the primary structural feature. This structural expansion is thus associated with increased M—O distances. Aqueous solubility measurements show that solubility generally increases with increasing Sr content. Thus, tuning the composition of these mixed counter-ion salt forms leads to systematic structural changes and allows solubility to be tuned to values between those for the pure Ca and Sr species.


1997 ◽  
Vol 50 (6) ◽  
pp. 671 ◽  
Author(s):  
Effendy ◽  
John D. Kildea ◽  
Allan H. White

The synthesis and room-temperature single-crystal X-ray structure determination of the 1 : 1 adduct of silver(I) nitrate with triphenylstibine, AgNO3/SbPh3 (1 : 1), is recorded, being monoclinic, Cc,a 12·824(2), b 15·794(4),c 9·796(2) Å, β 117·50(1)°, Z= 4; conventional R on F was 0·030 for 2881 independent ‘observed’ (I > 3σ(I)) reflections. The complex is a one-dimensional polymer with bridging nitrate groups, resembling in this respect its phosphine and arsine analogues. The completion of this study, along with related species recorded in accompanying papers, means that full structural data are now available for the complete array AgNO3/EPh3 (1 : n), E = P, As, Sb, n = 1–4, with the one exception of E = Sb, n = 2.


2006 ◽  
Vol 21 (11) ◽  
pp. 2904-2910 ◽  
Author(s):  
P. Gouma ◽  
K. Kalyanasundaram ◽  
A. Bishop

Single-crystal MoO3 nanowires were produced using the electrospinning technique. High-resolution transmission electron microscopy revealed that the one-dimensional nanostructures are 10–50 nm in diameter, on the order of 1–2 μm in length, and have the orthorhombic MoO3 structure. The structure, crystallinity, and sensoric character of these electrostatically processed nanowires are discussed. It has been demonstrated that the nonwoven network of MoO3 nanowires exhibits an order of magnitude higher sensitivity compared with that of a sol-gel based sensor. This is promising for use of the nanowire sensors in nanomedicine.


1977 ◽  
Vol 24 (4) ◽  
pp. 313-316 ◽  
Author(s):  
K. Le Dang ◽  
P. Veillet ◽  
J.-P. Renard

2008 ◽  
Vol 460 (1-3) ◽  
pp. 93-99 ◽  
Author(s):  
R.J. Papoular ◽  
B.H. Toby ◽  
V.A. Davydov ◽  
A.V. Rakhmanina ◽  
A. Dzyabchenko ◽  
...  

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