G. A. Ksendzova, N. I. Ostrovskaya, R. L. Sverdlov, V. L. Sorokin
{"title":"4,6-二叔丁基-2,3-二羟基苯甲醛亚甲胺衍生物对涉及烷基和-羟基烷基自由基的辐射诱导反应的影响","authors":"G. A. Ksendzova, N. I. Ostrovskaya, R. L. Sverdlov, V. L. Sorokin","doi":"10.1134/s0018143923060085","DOIUrl":null,"url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Abstract</h3><p>The effects of azomethine derivatives of 4,6-di-<i>tert</i>-butyl-2,3-dihydroxybenzaldehyde on the formation of radiolysis products of deaerated <i>n</i>-hexane and ethanol have been studied. It was shown that the catechol moiety in the tested compounds did not significantly affect their reactions with carbon-centered radicals. The aldimine group exhibited high activity as an α-hydroxyalkyl radical scavenger and low activity as a scavenger of alkyl radicals. The introduction of additional radical-inhibiting groups –OH, –SH, –NO<sub>2</sub>, and =N–NH– into the side fragment of a molecule led to a significant increase in the antiradical activity with respect to various types of carbon-centered radicals.</p>","PeriodicalId":12893,"journal":{"name":"High Energy Chemistry","volume":"29 1","pages":""},"PeriodicalIF":0.9000,"publicationDate":"2023-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of Azomethine Derivatives of 4,6-Di-tert-Butyl-2,3-Dihydroxybezaldehyde on Radiation-Induced Reactions Involving Alkyl and Alpha-Hydroxyalkyl Radicals\",\"authors\":\"G. A. Ksendzova, N. I. Ostrovskaya, R. L. Sverdlov, V. L. Sorokin\",\"doi\":\"10.1134/s0018143923060085\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<h3 data-test=\\\"abstract-sub-heading\\\">Abstract</h3><p>The effects of azomethine derivatives of 4,6-di-<i>tert</i>-butyl-2,3-dihydroxybenzaldehyde on the formation of radiolysis products of deaerated <i>n</i>-hexane and ethanol have been studied. It was shown that the catechol moiety in the tested compounds did not significantly affect their reactions with carbon-centered radicals. The aldimine group exhibited high activity as an α-hydroxyalkyl radical scavenger and low activity as a scavenger of alkyl radicals. The introduction of additional radical-inhibiting groups –OH, –SH, –NO<sub>2</sub>, and =N–NH– into the side fragment of a molecule led to a significant increase in the antiradical activity with respect to various types of carbon-centered radicals.</p>\",\"PeriodicalId\":12893,\"journal\":{\"name\":\"High Energy Chemistry\",\"volume\":\"29 1\",\"pages\":\"\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2023-11-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"High Energy Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1134/s0018143923060085\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"High Energy Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1134/s0018143923060085","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Effects of Azomethine Derivatives of 4,6-Di-tert-Butyl-2,3-Dihydroxybezaldehyde on Radiation-Induced Reactions Involving Alkyl and Alpha-Hydroxyalkyl Radicals
Abstract
The effects of azomethine derivatives of 4,6-di-tert-butyl-2,3-dihydroxybenzaldehyde on the formation of radiolysis products of deaerated n-hexane and ethanol have been studied. It was shown that the catechol moiety in the tested compounds did not significantly affect their reactions with carbon-centered radicals. The aldimine group exhibited high activity as an α-hydroxyalkyl radical scavenger and low activity as a scavenger of alkyl radicals. The introduction of additional radical-inhibiting groups –OH, –SH, –NO2, and =N–NH– into the side fragment of a molecule led to a significant increase in the antiradical activity with respect to various types of carbon-centered radicals.
期刊介绍:
High Energy Chemistry publishes original articles, reviews, and short communications on molecular and supramolecular photochemistry, photobiology, radiation chemistry, plasma chemistry, chemistry of nanosized systems, chemistry of new atoms, processes and materials for optical information systems and other areas of high energy chemistry. It publishes theoretical and experimental studies in all areas of high energy chemistry, such as the interaction of high-energy particles with matter, the nature and reactivity of short-lived species induced by the action of particle and electromagnetic radiation or hot atoms on substances in their gaseous and condensed states, and chemical processes initiated in organic and inorganic systems by high-energy radiation.