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פותח על ידי קלירמאש פתרונות בע"מ -
CHEMICAL REACTIONS OF SUPEROXIDE ANION RADICAL IN APROTIC SOLVENTS
Year:
1978
Source of publication :
Photochemistry and Photobiology
Authors :
רוזנטל, יונל
;
.
Volume :
28
Co-Authors:
Frimer, A.A., Department of Chemistry, Bar Ilan University, Ramat Gan, Israel, Department of Organic Chemistry, The Weizmann Institute of Science, Rehovot, Israel
Rosenthal, I., Department of Chemistry, Bar Ilan University, Ramat Gan, Israel, Department of Organic Chemistry, The Weizmann Institute of Science, Rehovot, Israel
Facilitators :
From page:
711
To page:
717
(
Total pages:
7
)
Abstract:
Abstract— While superoxide anion radical does not normally react with olefins, it does react with activated double bonds. Thus O‐ 2 oxidatively cleaves certain α,β‐unsaturated ketones such as chalcones and tetracyclone and electron poor olefins such as 1,1‐dicyano and 1,1‐dinitro olefins. Similarly O‐ 2 can react with substituted nitrobenzenes to yield the corresponding nitrophenols. EPR and oxygen labeling (KO36 2) experiments confirm an electron transfer mechanism. Copyright © 1978, Wiley Blackwell. All rights reserved
Note:
Related Files :
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תוכן קשור
More details
DOI :
10.1111/j.1751-1097.1978.tb07005.x
Article number:
Affiliations:
Database:
סקופוס
Publication Type:
מאמר
;
.
Language:
אנגלית
Editors' remarks:
ID:
19707
Last updated date:
02/03/2022 17:27
Creation date:
16/04/2018 23:31
Scientific Publication
CHEMICAL REACTIONS OF SUPEROXIDE ANION RADICAL IN APROTIC SOLVENTS
28
Frimer, A.A., Department of Chemistry, Bar Ilan University, Ramat Gan, Israel, Department of Organic Chemistry, The Weizmann Institute of Science, Rehovot, Israel
Rosenthal, I., Department of Chemistry, Bar Ilan University, Ramat Gan, Israel, Department of Organic Chemistry, The Weizmann Institute of Science, Rehovot, Israel
CHEMICAL REACTIONS OF SUPEROXIDE ANION RADICAL IN APROTIC SOLVENTS
Abstract— While superoxide anion radical does not normally react with olefins, it does react with activated double bonds. Thus O‐ 2 oxidatively cleaves certain α,β‐unsaturated ketones such as chalcones and tetracyclone and electron poor olefins such as 1,1‐dicyano and 1,1‐dinitro olefins. Similarly O‐ 2 can react with substituted nitrobenzenes to yield the corresponding nitrophenols. EPR and oxygen labeling (KO36 2) experiments confirm an electron transfer mechanism. Copyright © 1978, Wiley Blackwell. All rights reserved
Scientific Publication
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