Search Results
.4 (C-5′), δ C 10.6 (C-6′), δ C 23.3 (C-7′), and δ C 13.7 (C-8′), on the basis of its spectral data compound 4 was identified as di-(2-ethylhexyl) phthalate [ 29 , 30 ]. Compound 5 was obtained as fine powder ( R f upon PC in 15% AcOH
-12), 113.8 (C-13), and 133.3 (C-14) ppm. The anomeric proton assigned at δ 5.01 ppm (d, J = 5.4 Hz) through its one-bond correlation in Heteronuclear Single Quantum Coherence (HSQC) with its own anomeric carbon signal at δ 100.5 ppm was an
products of this process are: allyl-glycidyl ether, and 3-allyloxy-1,2-propanediol. These compounds are formed with selectivities of 5 mol% (20 °C)—13 mol% (60 °C). Bis(allyl) ether is formed with the selectivity 3–5 mol%, and acroleine with 1
fraction) was resuspended in the saponin buffer with 1% TritonX-100, heated for 2–3 s at 95 °C, and centrifuged (5 min; 4 °C; 13,000 rpm). The solubilized membrane fraction present in the supernatant was retained, as well as the insoluble proteins in the
,c 17 (5.7%) 3 (1.7%) 20 3.39 (1.01–11.4) Campylobacter spp. b,c 13 (4.4%) 2 (1.1%) 15 3.89 (0.89–17.05) Yersinia spp. 0 0 0 a One individual was co-infected with Salmonella spp. and Shigella spp./EIEC. b One individual was co-infected with
Magnesium sulphate complexes with hexamethylenetetramine and 1,10-phenanthroline
Thermal, structural and spectroscopic properties
dimensions (Å, °): a = 12.0010(10), b = 10.0779(7), c = 13.8536(10), α = 90.00, β = 113.459(8), γ = 90.00; volume (Å 3 ): 1537.0(2); reflections collected/unique: 15987/2735 (R (int) = 0.0512); data/restraints/parameters: 2735/0/214; GooF: 1.157; final
Alters who gamble 3.72 (5.26) a 7.30 (7.17) b 9.38 (6.73) c 9.85 (6.91) c 13.01 (7.30) d Welch (4, 386.02) = 48.26, p < .001
= 0.34 e (7–42) (7.5–35) BSCS 32.5 ± 5.3 35.6 ± 6.1 P = 0.17 c (25–43) (25–43) BIS 20.9 ± 3.1 19.8 ± 3.8 P = 0.54 c (13–25) (14–28) BAS-drive 11.2 ± 1.3 11.8 ± 2.0 P = 0.37 c (9–14) (8–15) BAS-fun seeking 11.8 ± 2.2 12.2 ± 1.6 P = 0.61 c (8–15) (9
= 0.34 e (7–42) (7.5–35) BSCS 32.5 ± 5.3 35.6 ± 6.1 P = 0.17 c (25–43) (25–43) BIS 20.9 ± 3.1 19.8 ± 3.8 P = 0.54 c (13–25) (14–28) BAS-drive 11.2 ± 1.3 11.8 ± 2.0 P = 0.37 c (9–14) (8–15) BAS-fun seeking 11.8 ± 2.2 12.2 ± 1.6 P = 0.61 c (8–15) (9
