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The standard (p 0=0.1 MPa) molar enthalpies of formation, Δf H m 0, for crystalline phthalimides: phthalimide, N-ethylphthalimide and N-propylphthalimide were derived from the standard molar enthalpies of combustion, in oxygen, at the temperature 298.15 K, measured by static bomb-combustion calorimetry, as, respectively, – (318.01.7), – (350.12.7) and – (377.32.2) kJ mol–1. The standard molar enthalpies of sublimation, Δcr g H m 0, at T=298.15 K were derived by the Clausius-Clapeyron equation, from the temperature dependence of the vapour pressures for phthalimide, as (106.91.2) kJ mol–1 and from high temperature Calvet microcalorimetry for phthalimide, N-ethylphthalimide and N-propylphthalimide as, respectively, (106.31.3), (91.01.2) and (98.21.4) kJ mol–1. The derived standard molar enthalpies of formation, in the gaseous state, are analysed in terms of enthalpic increments and interpreted in terms of molecular structure.

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from phthalimide and fully characterized by spectroscopic and thermal methods. Experimental General In general, reactions were carried out in a dry (all glassware was dried in an oven overnight at 120 °C

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DTA and TG has been used to study the thermal stability of cross-linked epoxidized polydienes. Cross-linking has been achieved using some derivatives of hydroxycarbostyrils, triazines and phthalimide. The new properties of the polymers after curing are interpreted on the basis of the results of DTA and TG.

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Journal of Thermal Analysis and Calorimetry
Authors: Ju-Lan Zeng, Sai-Bo Yu, Bo Tong, Li-Xian Sun, Zhi-Cheng Tan, Zhong Cao, Dao-Wu Yang, and Jing-Nan Zhang

. Ribeiro da Silva , MAV , Santos , CPF , Monte , MJS , Sousa , CAD . Thermochemical studies of phthalimide and two N -alkylsubstituted phthalimides (alkyl = ethyl and n -propyl) . J Therm Anal Calorim 2006 83 : 533 – 539 10.1007/s10973

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. “ Photodecarboxylative addition of carboxylates to phthalimides: A concise access to biologically active 3-(alkyl and aryl)methylene- H -isoindolin-1-ones ” F. Hatoum , J. Engler , C. Zelmer , J. Wißen , C. A. Motti , J. Lex , M. Oelgemöller Tetrahedron Letters

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¢-dimethoxybenzophenone mediated photodecarboxylation reactions involving phthalimides” O. Shvydkiv , K. Nolan , M. Oelgemöller Beilstein Journal of Organic Chemsitry 2011 , 7 , 1055 – 1063 . “ Homocoupling of aryl halides in flow: Space

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Reaction Kinetics, Mechanisms and Catalysis
Authors: K. V. Novikova, M. O. Kompanets, O. V. Kushch, S. P. Kobzev, M. M. Khliestov, and I. O. Opeida

methods of oxidation with dioxygen are carried out under harsh conditions, utilize a corrosive reagent mixture with limited conversion and selectivity. Ishii and co-workers [ 1 ] discovered that N -hydroxyphthalimide (NHPI), the precursor of phthalimide

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distilled before use. Ethyliene dichloride, potassium hydroxide, phthalimide, and hydrazine hydrate were used as received. Epoxy resin was a liquid diglycidyl ether of bisphenol A (DGEBA), W ep = 196, and the curing agent 4,4′-diaminobiphenyl (DABP) was of

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, which is an increase or decrease of the detector response. Results and Discussion Captan ( N -(trichloromethylthio)cyclohex-4-ene-1,2-dicarboximide, IUPAC) and folpet ( N -(trichloromethylthio)phthalimide, IUPAC

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