{"title":"ds-双(苯腈)二氯铂(II)在氯仿中的光取代动力学","authors":"E. M. Jaryszak, Son L. Phan, P. Hoggard","doi":"10.1515/irm-1999-0206","DOIUrl":null,"url":null,"abstract":"Abstract Under 254 nm irradiation cis-[Pt(C6H5CN)2Cl2] is converted to H2PtCl6. Absorption of light by both the metal complex and the solvent contribute to the first step of this process, suggested to form HPt(C6H5CN) Cl3. A linear dependence of the reaction rate on light intensity appears to rule out chlorination by trichloromethyl radicals. However, at higher light intensities a higher order dependence on intensity develops, and under 313 nm irradiation is dominant, and a reaction between trichloromethyl radical and the excited state complex is proposed to account for this.","PeriodicalId":8996,"journal":{"name":"BioInorganic Reaction Mechanisms","volume":"113 1","pages":"129 - 136"},"PeriodicalIF":0.0000,"publicationDate":"1999-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":"{\"title\":\"Kinetics of the Photosubstitution of ds-Bis(benzonitrile)dichloroplatinum(II) in Chloroform\",\"authors\":\"E. M. Jaryszak, Son L. Phan, P. Hoggard\",\"doi\":\"10.1515/irm-1999-0206\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract Under 254 nm irradiation cis-[Pt(C6H5CN)2Cl2] is converted to H2PtCl6. Absorption of light by both the metal complex and the solvent contribute to the first step of this process, suggested to form HPt(C6H5CN) Cl3. A linear dependence of the reaction rate on light intensity appears to rule out chlorination by trichloromethyl radicals. However, at higher light intensities a higher order dependence on intensity develops, and under 313 nm irradiation is dominant, and a reaction between trichloromethyl radical and the excited state complex is proposed to account for this.\",\"PeriodicalId\":8996,\"journal\":{\"name\":\"BioInorganic Reaction Mechanisms\",\"volume\":\"113 1\",\"pages\":\"129 - 136\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1999-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BioInorganic Reaction Mechanisms\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1515/irm-1999-0206\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BioInorganic Reaction Mechanisms","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/irm-1999-0206","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Kinetics of the Photosubstitution of ds-Bis(benzonitrile)dichloroplatinum(II) in Chloroform
Abstract Under 254 nm irradiation cis-[Pt(C6H5CN)2Cl2] is converted to H2PtCl6. Absorption of light by both the metal complex and the solvent contribute to the first step of this process, suggested to form HPt(C6H5CN) Cl3. A linear dependence of the reaction rate on light intensity appears to rule out chlorination by trichloromethyl radicals. However, at higher light intensities a higher order dependence on intensity develops, and under 313 nm irradiation is dominant, and a reaction between trichloromethyl radical and the excited state complex is proposed to account for this.
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