Abstract
Spontaneous hydrobromination of allyl chloride (AC) proceeds in the liquid phase (180–220 K, thermal effect ΔH= 17 kcal mor−1) to give 1-chloro-2-bromopropane; active centres produced by radiolysis at 77 K at the glass transition (87–95 K) initiate a chain addition reaction of HBr to AC to form 1-chloro-3-bromopropane (thermal effect Δ13.2 kcal mor−1). This is the first example of hydrobromination at matrix devitrification; a local brittle fracture of the irradiated sample of AC + HBr gives an autowave of chemical conversion spread over the sample.
References
1.
10.1070/MC1993v003n02ABEH000226_bib1
Sergeev
Zh. Vses. Khim. Ova im. D. I. Mendeleeva,
1973
2.
10.1070/MC1993v003n02ABEH000226_bib2
Sergeev
Kriokhimiya (Cryochemistry) M. Khimiya,
1978
3.
10.1070/MC1993v003n02ABEH000226_bib3
Kiryukhin
Dokl. Akad. Nauk SSSR,
1978
4.
10.1070/MC1993v003n02ABEH000226_bib4
Zanin
Dokl. Akad. Nauk SSSR,
1980
5.
Kiryukhin D.P., Barkalov I.M., Goldanskii V.L.
Journal de Chimie Physique,
2017
6.
10.1070/MC1993v003n02ABEH000226_bib6
Goldanskii
Tunnelnye Ayvleniay v Khimicheskoi Fizike (Tunnel Appearances in Chemical Physics),
1986
7.
Barelko V.V., Barkalov I.M., Goldanskii V.I., Kiryukhin D.P., Zanin A.M.
Advances in Chemical Physics,
1988
8.
Barelko V.V., Barkalov I.M., Gol'danskii V.I., Zanin A.M., Kiryukhin D.P.
Russian Chemical Reviews,
1990
9.
10.1070/MC1993v003n02ABEH000226_bib9
Barkalov
Vysokomol. Soedin, Ser. A,
1980
10.
10.1070/MC1993v003n02ABEH000226_bib10
Barkalov
Khim. Vys. Energ.,
1990
11.
10.1070/MC1993v003n02ABEH000226_bib11
Zanin
Dokl. Akad. Nauk SSSR,
1981
12.
10.1070/MC1993v003n02ABEH000226_bib12
Kovaliev
Dokl. Akad. Nauk SSSR,
1965
13.
10.1070/MC1993v003n02ABEH000226_bib13
Kovaliev
Vestn. MGU, Ser. Khim.,
1976
14.
10.1070/MC1993v003n02ABEH000226_bib14
Cox
Thermochemistry of Organic and Organometallic Compounds,
1970
15.
10.1070/MC1993v003n02ABEH000226_bib15
Kiryukhin
Khimicheskaya Fizika,
1992