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. 2019 Aug 23;75(Pt 9):1339–1343. doi: 10.1107/S2056989019011265

Table 3. Experimental details.

  I II
Crystal data
Chemical formula C33H30Si C27H26OSi
M r 454.66 394.57
Crystal system, space group Triclinic, P Inline graphic Monoclinic, P21/c
Temperature (K) 173 173
a, b, c (Å) 10.3879 (7), 10.5037 (7), 13.6350 (9) 11.8576 (5), 13.2995 (6), 14.3948 (6)
α, β, γ (°) 68.8212 (7), 70.6364 (7), 84.7947 (8) 90, 110.363 (3), 90
V3) 1308.06 (15) 2128.20 (16)
Z 2 4
Radiation type Mo Kα Cu Kα
μ (mm−1) 0.11 1.08
Crystal size (mm) 0.21 × 0.21 × 0.17 0.10 × 0.09 × 0.08
 
Data collection
Diffractometer Bruker APEXII CCD Bruker APEXII CCD
Absorption correction Multi-scan (SADABS; Bruker, 2013) Multi-scan (SADABS; Bruker, 2013
T min, T max 0.695, 0.745 0.624, 0.754
No. of measured, independent and observed [I > 2σ(I)] reflections 16773, 4803, 3734 11901, 4113, 2414
R int 0.036 0.096
(sin θ/λ)max−1) 0.603 0.617
 
Refinement
R[F 2 > 2σ(F 2)], wR(F 2), S 0.045, 0.120, 1.08 0.062, 0.171, 0.97
No. of reflections 4803 4113
No. of parameters 308 267
H-atom treatment H-atom parameters constrained H atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å−3) 0.34, −0.22 0.29, −0.36

Computer programs: APEX2 and SAINT (Bruker, 2013), SHELXS (Sheldrick, 2008), SHELXL (Sheldrick, 2015), OLEX2 (Dolomanov et al., 2009; Bourhis et al., 2015) and CrystalMaker (Palmer, 2007).