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Kinetics and Thermodynamics of the Formation of the Donor Acceptor Complex of Tetracyanoethylene with Hexamethyl benzene in Solution, by a Microwave Temperature-jump method

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dc.contributor.author Caldin, E. F.
dc.contributor.author Crooks, J. E.
dc.contributor.author O’Donnell, D.
dc.contributor.author Smith, D.
dc.contributor.author Toner, S.
dc.date.accessioned 2025-02-07T02:17:18Z
dc.date.available 2025-02-07T02:17:18Z
dc.date.issued 1972
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17310
dc.description.abstract The rate of formation of the donor-acceptor complex between tetracyanoethylene and hexamethylbenzene, in 1-chlorobutane as solvent, has been measured at –83°C by a temperature-jump method using microwave heating. Equilibrium constants have also been determined over a range of temperature. The rate constant is (1.45 ± 0.3)× 108 l. mol–1 s–1(the uncertainty referring to the estimated limits of error). This is smaller by an order of magnitude than the calculated value for a diffusion-controlled reaction. The reason for this is discussed and it is concluded that there is possibly an energy barrier due to solvation changes. The rate constant in a solvent consisting of chlorobenzene + n-heptane (40–60 v-v) has also been determined, allowance being made for the parallel complex-formation between chlorobenzene and tetracyanoethylene; at –60°C, it was found to be (8 ± 3)× 108 l. mol–1 s–1. en_US
dc.language.iso en en_US
dc.publisher Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1972, 68 (5) en_US
dc.subject Chemistry en_US
dc.subject Donor-Acceptor Complex en_US
dc.subject Tetracyanoethylene en_US
dc.subject Hexamethylbenzene en_US
dc.subject Microwave Temperature-Jump en_US
dc.subject Journal of the Chemical Society : Faraday Transaction - I en_US
dc.title Kinetics and Thermodynamics of the Formation of the Donor Acceptor Complex of Tetracyanoethylene with Hexamethyl benzene in Solution, by a Microwave Temperature-jump method en_US
dc.type Article en_US


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