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Low-temperature Fluorination of Perfluoro-2,4-dimethyl-3-ethylpent-2-ene

Sadulla Reimovich Allayarov 1
Sadulla Reimovich Allayarov
Igor Mstislavovich Barkalov 1
Igor Mstislavovich Barkalov
Ida Pavlovna Kim 1
Ida Pavlovna Kim
Published 1992-12-31
CommunicationVolume 2, Issue 4, 139-141
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Allayarov S. R., Barkalov I. M., Kim I. P. Low-temperature Fluorination of Perfluoro-2,4-dimethyl-3-ethylpent-2-ene // Mendeleev Communications. 1992. Vol. 2. No. 4. pp. 139-141.
GOST all authors (up to 50) Copy
Allayarov S. R., Barkalov I. M., Kim I. P. Low-temperature Fluorination of Perfluoro-2,4-dimethyl-3-ethylpent-2-ene // Mendeleev Communications. 1992. Vol. 2. No. 4. pp. 139-141.
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TY - JOUR
DO - 10.1070/MC1992v002n04ABEH000173
UR - https://mendcomm.colab.ws/publications/10.1070/MC1992v002n04ABEH000173
TI - Low-temperature Fluorination of Perfluoro-2,4-dimethyl-3-ethylpent-2-ene
T2 - Mendeleev Communications
AU - Allayarov, Sadulla Reimovich
AU - Barkalov, Igor Mstislavovich
AU - Kim, Ida Pavlovna
PY - 1992
DA - 1992/12/31
PB - Mendeleev Communications
SP - 139-141
IS - 4
VL - 2
ER -
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@article{1992_Allayarov,
author = {Sadulla Reimovich Allayarov and Igor Mstislavovich Barkalov and Ida Pavlovna Kim},
title = {Low-temperature Fluorination of Perfluoro-2,4-dimethyl-3-ethylpent-2-ene},
journal = {Mendeleev Communications},
year = {1992},
volume = {2},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1992v002n04ABEH000173},
number = {4},
pages = {139--141},
doi = {10.1070/MC1992v002n04ABEH000173}
}
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Allayarov, Sadulla Reimovich, et al. “Low-temperature Fluorination of Perfluoro-2,4-dimethyl-3-ethylpent-2-ene.” Mendeleev Communications, vol. 2, no. 4, Dec. 1992, pp. 139-141. https://mendcomm.colab.ws/publications/10.1070/MC1992v002n04ABEH000173.

Abstract

Calorimetric and EPR investigations of the low temperature (77–300 K) fluorination of unsaturated perfluorocarbons have shown that, in glassy systems, the formation of molecular complexes of fluorine with a C=C bond is possible during the transition to the supercooled liquid state; chain addition of fluorine to the title compound stops at the first stage, after formation of stable, long-lived radicals.

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