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. 2019 Jun 21;75(Pt 7):1041–1045. doi: 10.1107/S2056989019008685

Table 2. Experimental details.

  Rb2KDy(VO4)2 Cs1.52K1.48Gd(VO4)2
Crystal data
M r 602.42 646.74
Crystal system, space group Trigonal, P Inline graphic m1 Trigonal, P Inline graphic m1
Temperature (K) 296 296
a, c (Å) 5.9728 (1), 7.7780 (1) 6.0321 (1), 7.9821 (2)
V3) 240.30 (1) 251.53 (1)
Z 1 1
Radiation type Mo Kα Mo Kα
μ (mm−1) 20.10 14.37
Crystal size (mm) 0.35 × 0.28 × 0.25 0.34 × 0.26 × 0.22
 
Data collection
Diffractometer Bruker X8 APEX Bruker X8 APEX
Absorption correction Multi-scan (SADABS; Krause et al., 2015) Multi-scan (SADABS; Krause et al., 2015)
T min, T max 0.357, 0.749 0.639, 0.747
No. of measured, independent and observed [I > 2σ(I)] reflections 10549, 647, 631 14472, 678, 666
R int 0.049 0.038
(sin θ/λ)max−1) 0.926 0.925
 
Refinement
R[F 2 > 2σ(F 2)], wR(F 2), S 0.016, 0.042, 1.11 0.010, 0.028, 1.09
No. of reflections 647 678
No. of parameters 24 25
Δρmax, Δρmin (e Å−3) 1.35, −1.35 0.63, −0.94

Computer programs: APEX2 and SAINT-Plus (Bruker, 2009), SHELXT2014 (Sheldrick, 2015a ), SHELXL2018 (Sheldrick, 2015b ), ORTEP-3 for Windows (Farrugia, 2012), DIAMOND (Brandenburg, 2006), Mercury (Macrae et al., 2008) and publCIF (Westrip, 2010).