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Journal of Thermal Analysis and Calorimetry
Authors: I. Blanco, L. Abate, F. A. Bottino and P. Bottino

), 6.76 (dd, 1H), 1.85 (m, 7H), 0.97 (m, 42 H), 0.62 (m, 14H). Anal. Calcd for C 34 H 66 F 2 Si 8 O 12 : C 43.96, H 7.16. Found: C 43.72, H 7.18. IR spectroscopy The Fourier Transform Infrared (FTIR

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compounds were identified by elemental analysis as the formula C 9 H 8 O 5 Na 2 (Calculated: C, 44.64%; H, 3.33%; O, 33.04%. Found: C, 44.26%; H, 3.61%; O, 33.28%) and C 8 H 5 O 4.5 Na 2 (Calculated: C, 43.85%; H, 2.30%; O, 32.86%. Found: C, 43.29%; H, 2

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Thermal and structural properties of surfactant–picrate compounds

Effect of the alkyl chain number on the same ammonium head group

Journal of Thermal Analysis and Calorimetry
Authors: Tea Mihelj, Zoran Štefanić and Vlasta Tomašić

) found: C, 62.90; H, 9.56; N, 9.16%; requires C, 62.92; H, 9.57; N, 9.17%; for C 43 H 80 N 4 O 7 ( 3 ) found: C, 67.48; H, 10.56; N, 7.33%; requires C, 67.50; H, 10.54; N, 7.32%. Scheme 1 The scheme of the

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) 2 (phen)]Cl 2 : Decomposition temperature: 245 °C; yield: 91%; IR(KBr) cm −1 : 1,615, 1,502, 988 (C = C and C = N); 1,216, 1,090, 810 (C–H deformations); Anal. (C 24 H 32 N 6 S 4 Cl 2 Mn) Found: C 43.54; H 4.70; N 12.41; S 19.25; Mn 8.36; Cl 10

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Journal of Thermal Analysis and Calorimetry
Authors: Francesca Caterina Izzo, Elisabetta Zendri, Guido Biscontin and Eleonora Balliana

/>400 °C 43.5 151 °C; 397 °C; 501 °C 391 °C; 449 °C  2 years /1/100–250 °C;/2/250–400 °C;/3/>400 °C

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−47 °C −15 °C 100 Hz 6 °C43 °C −12 °C DMA/max. tan δ

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.5 (128–244) HDL-C 43.21 ± 0.92 47.57 ± 2.26 <0.05 43 (18–60) 47.5 (30

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loss in a mouse model of autism. Pharmacol Biochem Behav 126C, 43–49 (2014) Matsuda T Chronic treatment with valproic acid or sodium butyrate attenuates novel object recognition

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Reaction Kinetics, Mechanisms and Catalysis
Authors: Andrés Pena, Santiago Veiga, Mariángeles Sapelli, Natalia Martínez, Victoria Márquez, Eduardo Dellacassa and Juan Bussi

presence of pure oxygen. In contrast, the reaction of limonene takes place when a NiAl-HT catalyst is present, with increasing reaction rates up to 90 °C as shown in Fig. 3 . Conversions at 6 h of reaction time were 16.7 % at 70 °C, 43.9 % at 80 °C and 51

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]copper(I) bromide . Acta Crystallogr 1987 C43 : 1685 – 1688 . 9. Bombicz , P , Mutikainen , I , Krunks , M , Leskela , T , Madarasz , J , Niinisto , LA . Synthesis, vibrational spectra and

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