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. 2016 Nov 10;72(Pt 12):1783–1785. doi: 10.1107/S2056989016017734

Table 2. Experimental details.

Crystal data
Chemical formula C26H28N5O2 +·Cl·CH4O
M r 510.03
Crystal system, space group Triclinic, P Inline graphic
Temperature (K) 296
a, b, c (Å) 10.5572 (5), 11.0764 (4), 11.4408 (5)
α, β, γ (°) 104.622 (1), 97.327 (2), 90.695 (1)
V3) 1282.57 (10)
Z 2
Radiation type Mo Kα
μ (mm−1) 0.19
Crystal size (mm) 0.50 × 0.46 × 0.38
 
Data collection
Diffractometer Rigaku R-AXIS RAPID/ZJUG
Absorption correction Multi-scan (ABSCOR; Higashi, 1995)
T min, T max 0.91, 0.93
No. of measured, independent and observed [I > 2σ(I)] reflections 11090, 5000, 3865
R int 0.044
(sin θ/λ)max−1) 0.617
 
Refinement
R[F 2 > 2σ(F 2)], wR(F 2), S 0.053, 0.154, 1.00
No. of reflections 5000
No. of parameters 328
H-atom treatment H-atom parameters constrained
Δρmax, Δρmin (e Å−3) 0.31, −0.43

Computer programs: PROCESS-AUTO (Rigaku, 2006), CrystalStructure (Rigaku, 2007), SHELXS97 and SHELXL97 (Sheldrick, 2008), ORTEP-3 for Windows and WinGX (Farrugia, 2012).