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Experimental standard molar enthalpies of formation of crystalline 3,5-dimethylpyrazole, 3,5-dimethyl-4-nitrosopyrazole, 1,3,5-trimethyl-4-nitrosopyrazole, and 3,5-dimethyl-1-phenyl-4-nitrosopyrazole

✍ Scribed by Maria D.M.C. Ribeiro da Silva; Susana C.C. Ferreira; Ivone A.P. Rodrigues; Luı́s C.M. da Silva; William E. Acree Jr; Siddharth Pandey; Lindsay E. Roy


Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
99 KB
Volume
33
Category
Article
ISSN
0021-9614

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✦ Synopsis


The standard ( p o = 0.1 MPa) molar enthalpies of combustion in oxygen, at T = 298.15 K, for crystalline 3,5-dimethylpyrazole (Me 2 Pyr), 3,5-dimethyl-4-nitrosopyrazole (Me 2 PyrNO), 1,3,5-trimethyl-4-nitrosopyrazole (Me 3 PyrNO), and 3,5-dimethyl-1phenyl-4-nitrosopyrazole (Me 2 PhPyrNO) were measured by static-bomb calorimetry. These values were used to derive the standard molar enthalpies of formation of the crystalline compounds. The standard molar enthalpies of sublimation for these four compounds were measured by microcalorimetry.

c H o m (cr)/(kJ • mol -1 ) g cr H o m /(kJ • mol -1 ) Me 2 Pyr 3129.8 ± 1.6 83.4 ± 2.4 Me 2 PyrNO 3079.2 ± 2.8 102.9 ± 3.0 Me 3 PyrNO 3759.2 ± 1.9 88.0 ± 2.0 Me 2 PhPyrNO 6110.4 ± 1.5 100.4 ± 2.2

The experimental results obtained allow us to derive the values of the standard molar enthalpies of formation, in the gaseous state, for the monomeric compounds involved in this work. These last values are discussed comparatively with results previously obtained for some aromatic nitroso derivatives.


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Formation and structure of 1-Amino-4-met
✍ Donato Donati; Stefania Fusi; Fabio Ponticelli 📂 Article 📅 1998 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 281 KB 👁 1 views

The title compound 3 was obtained during the rearrangement of isoxazol-5-yl hydrazine 1 to 1 -aminopyrazolone 2 at \(115^{\circ}\). X-ray analysis of the corresponding benzylidene derivative allowed us to achieve the structure assignment.