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Surprising differences in the reactivity of cyanoaromatic radical anions generated by photoinduced electron transfer
In this paper, the authors report some studies that indicate that the reactivity of photogenerated cyanoaromatic anion radicals is strongly affected by the medium in which they are generated; interestingly they report conditions under which potentially reactive anion radicals of strongly affected by...
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Published in: | Journal of the American Chemical Society 1991-01, Vol.113:1 |
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container_title | Journal of the American Chemical Society |
container_volume | 113:1 |
creator | Kellett, M.A. Whitten, D.G. Gould, I.R. Bergmark, W.R. |
description | In this paper, the authors report some studies that indicate that the reactivity of photogenerated cyanoaromatic anion radicals is strongly affected by the medium in which they are generated; interestingly they report conditions under which potentially reactive anion radicals of strongly affected by the medium in which they are generated; interestingly they report conditions under which potentially reactive anion radicals of DCA and 2,6,9,10-tetracyanoanthracene (TCA) can be the stable end products of photoinduced redox reactions. |
doi_str_mv | 10.1021/ja00001a052 |
format | article |
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Whitten, D.G. ; Gould, I.R. ; Bergmark, W.R.</creator><creatorcontrib>Kellett, M.A. ; Whitten, D.G. ; Gould, I.R. ; Bergmark, W.R.</creatorcontrib><description>In this paper, the authors report some studies that indicate that the reactivity of photogenerated cyanoaromatic anion radicals is strongly affected by the medium in which they are generated; interestingly they report conditions under which potentially reactive anion radicals of strongly affected by the medium in which they are generated; interestingly they report conditions under which potentially reactive anion radicals of DCA and 2,6,9,10-tetracyanoanthracene (TCA) can be the stable end products of photoinduced redox reactions.</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/ja00001a052</identifier><language>eng</language><publisher>United States</publisher><subject>400500 - Photochemistry ; ANTHRACENE ; AROMATICS ; CHEMICAL REACTIONS ; CONDENSED AROMATICS ; 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interestingly they report conditions under which potentially reactive anion radicals of strongly affected by the medium in which they are generated; interestingly they report conditions under which potentially reactive anion radicals of DCA and 2,6,9,10-tetracyanoanthracene (TCA) can be the stable end products of photoinduced redox reactions.</description><subject>400500 - Photochemistry</subject><subject>ANTHRACENE</subject><subject>AROMATICS</subject><subject>CHEMICAL REACTIONS</subject><subject>CONDENSED AROMATICS</subject><subject>DATA</subject><subject>ELECTRON TRANSFER</subject><subject>EXPERIMENTAL DATA</subject><subject>HYDROCARBONS</subject><subject>INFORMATION</subject><subject>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</subject><subject>MEASURING METHODS</subject><subject>NUMERICAL DATA</subject><subject>ORGANIC COMPOUNDS</subject><subject>PHOTOCHEMICAL REACTIONS</subject><subject>REDOX REACTIONS</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNotT0tPAyEYJEYTa_XkHyDeV4EFFo6m8ZU08aCem2_h2y5NhQaoSf-9JDqXycxhHoTccnbPmeAPO2ANHJgSZ2TBlWCd4kKfk0WzRTcY3V-Sq1J2TUph-ILUj2M-5FBC3FIfpgkzRoeFhkjrjDQjuBp-Qj3RNFF3gpggp2-owdEMPjjYU4ghxUK3GDFDRU_HEz3MqaYQ_dE1jXt0NaeWmCGWVnFNLibYF7z55yX5en76XL126_eXt9Xjukuci9pNg-dacTP1zCk-eIl-MEpLj9YqKYRsT40dLYMRYLRWjM5oy1Ay7b2TQ78kd3-5qdSwKS5UdLNLMbY9G8W1sXbofwGVrF7j</recordid><startdate>19910102</startdate><enddate>19910102</enddate><creator>Kellett, M.A.</creator><creator>Whitten, D.G.</creator><creator>Gould, I.R.</creator><creator>Bergmark, W.R.</creator><scope>OTOTI</scope></search><sort><creationdate>19910102</creationdate><title>Surprising differences in the reactivity of cyanoaromatic radical anions generated by photoinduced electron transfer</title><author>Kellett, M.A. ; 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interestingly they report conditions under which potentially reactive anion radicals of strongly affected by the medium in which they are generated; interestingly they report conditions under which potentially reactive anion radicals of DCA and 2,6,9,10-tetracyanoanthracene (TCA) can be the stable end products of photoinduced redox reactions.</abstract><cop>United States</cop><doi>10.1021/ja00001a052</doi></addata></record> |
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source | ACS CRKN Legacy Archives |
subjects | 400500 - Photochemistry ANTHRACENE AROMATICS CHEMICAL REACTIONS CONDENSED AROMATICS DATA ELECTRON TRANSFER EXPERIMENTAL DATA HYDROCARBONS INFORMATION INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY MEASURING METHODS NUMERICAL DATA ORGANIC COMPOUNDS PHOTOCHEMICAL REACTIONS REDOX REACTIONS |
title | Surprising differences in the reactivity of cyanoaromatic radical anions generated by photoinduced electron transfer |
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