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. 2014 Jun 23;70(Pt 7):27–30. doi: 10.1107/S1600536814011015

Table 3. Experimental details.

Crystal data
Chemical formula (NH4)(VO2)(VO2)(TeO3)
M r 359.52
Crystal system, space group Orthorhombic, P n a21
Temperature (K) 293
a, b, c (Å) 18.945 (2), 7.0277 (8), 5.4402 (6)
V3) 724.29 (14)
Z 4
Radiation type Mo Kα
μ (mm−1) 6.52
Crystal size (mm) 0.17 × 0.02 × 0.02
 
Data collection
Diffractometer Bruker SMART1000 CCD
Absorption correction Multi-scan (SADABS; Bruker, 2000)
T min, T max 0.404, 0.881
No. of measured, independent and observed [I > 2σ(I)] reflections 7528, 2368, 1595
R int 0.047
(sin θ/λ)max−1) 0.756
 
Refinement
R[F 2 > 2σ(F 2)], wR(F 2), S 0.040, 0.082, 0.98
No. of reflections 2368
No. of parameters 101
No. of restraints 1
Δρmax, Δρmin (e Å−3) 0.99, −1.13
Absolute structure Flack (1983), 1201 Friedel pairs
Absolute structure parameter 0.5 (1)

Computer programs: SMART and SAINT (Bruker, 2000), SHELXS97 and SHELXL97 (Sheldrick, 2008), ORTEP-3 for Windows (Farrugia, 2012) and ATOMS (Dowty, 1999).