A Kinetic Study of the Reaction between the 2-Ċ3H7 Radical and i-C4H8: Enthalpy of Formation of the (CH3)2CHCH2Ċ(CH3)2 Radical

Verfasser / Beitragende:
[László Seres, Martin Dinse, Miklós Görgényi]
Ort, Verlag, Jahr:
2004
Enthalten in:
Zeitschrift für Physikalische Chemie/International journal of research in physical chemistry and chemical physics, 218/4/2004(2004-04-01), 469-478
Format:
Artikel (online)
ID: 378913638
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024 7 0 |a 10.1524/zpch.218.4.469.29200  |2 doi 
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245 0 2 |a A Kinetic Study of the Reaction between the 2-Ċ3H7 Radical and i-C4H8: Enthalpy of Formation of the (CH3)2CHCH2Ċ(CH3)2 Radical  |h [Elektronische Daten]  |c [László Seres, Martin Dinse, Miklós Görgényi] 
520 3 |a The reversible addition reaction 2-Ċ3H7 + i-C4H8 ⇔ (CH3)2CHCH2Ċ(CH3)2 was studied in the temperature range 491-543K by product analysis in experiments in which 2-Ċ3H7 radicals were generated by the thermal decomposition of azoisopropane. The enthalpy of formation of the radical (CH3)2CHCH2Ċ(CH3)2 was determined, the value obtained being ΔfH° = -21.8 ± 5.2kJ mol-1. From this result, the following group value was deduced: ΔfH°[Ċ-(C)3] = 177.1kJ mol-1. From the latter, ΔfH°(t-Ċ4H9) = 51.6kJ mol-1 was estimated. The rate constant of self-combination of the radical (CH3)2CHCH2Ċ(CH3)2 was determined for the first time: log(k12/(dm3mol-1s-1)) = 7.3. 
540 |a © 2004 Oldenbourg Wissenschaftsverlag GmbH 
690 7 |a Thermodynamics & statistical physics  |2 nationallicence 
690 7 |a Laboratory techniques, experiments  |2 nationallicence 
690 7 |a Physical chemistry  |2 nationallicence 
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700 1 |a Dinse  |D Martin  |4 aut 
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