{"title":"二卤二羰基rhodate(I)阴离子与2-氨基吡啶反应动力学研究","authors":"F.H. Jumean, Y.A. Asha","doi":"10.1016/0022-1902(81)80501-5","DOIUrl":null,"url":null,"abstract":"<div><p>The kinetic behavior of the reaction between dihalodicarbonylrhodate(I) anions, [RhX<sub>2</sub>(CO)<sub>2</sub>]<sup>−1</sup>, where X = Cl, Br, and the chelating agent 2-aminopyridine was investigated spectrophotometrically. The reaction for both halo analogues was found to obey third order kinetics, first order in the complex anion and second order in the 2-aminopyridine concentrations. The third order rate constants for the chloro and bromo complex anions had the values, at 25°C, of 779 and 156 l<sup>2</sup> mol<sup>−2</sup> min<sup>−1</sup>, respectively, and the corresponding activation energies were 3.00 and 5.50 Kcal mol<sup>−1</sup>. A mechanism is proposed to account for these observations.</p></div>","PeriodicalId":16275,"journal":{"name":"Journal of Inorganic and Nuclear Chemistry","volume":"43 3","pages":"Pages 557-559"},"PeriodicalIF":0.0000,"publicationDate":"1981-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0022-1902(81)80501-5","citationCount":"2","resultStr":"{\"title\":\"Kinetic studies of the reaction between dihalodicarbonylrhodate(I) anions and 2-aminopyridine\",\"authors\":\"F.H. Jumean, Y.A. Asha\",\"doi\":\"10.1016/0022-1902(81)80501-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The kinetic behavior of the reaction between dihalodicarbonylrhodate(I) anions, [RhX<sub>2</sub>(CO)<sub>2</sub>]<sup>−1</sup>, where X = Cl, Br, and the chelating agent 2-aminopyridine was investigated spectrophotometrically. The reaction for both halo analogues was found to obey third order kinetics, first order in the complex anion and second order in the 2-aminopyridine concentrations. The third order rate constants for the chloro and bromo complex anions had the values, at 25°C, of 779 and 156 l<sup>2</sup> mol<sup>−2</sup> min<sup>−1</sup>, respectively, and the corresponding activation energies were 3.00 and 5.50 Kcal mol<sup>−1</sup>. A mechanism is proposed to account for these observations.</p></div>\",\"PeriodicalId\":16275,\"journal\":{\"name\":\"Journal of Inorganic and Nuclear Chemistry\",\"volume\":\"43 3\",\"pages\":\"Pages 557-559\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1981-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0022-1902(81)80501-5\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Inorganic and Nuclear Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0022190281805015\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Inorganic and Nuclear Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0022190281805015","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Kinetic studies of the reaction between dihalodicarbonylrhodate(I) anions and 2-aminopyridine
The kinetic behavior of the reaction between dihalodicarbonylrhodate(I) anions, [RhX2(CO)2]−1, where X = Cl, Br, and the chelating agent 2-aminopyridine was investigated spectrophotometrically. The reaction for both halo analogues was found to obey third order kinetics, first order in the complex anion and second order in the 2-aminopyridine concentrations. The third order rate constants for the chloro and bromo complex anions had the values, at 25°C, of 779 and 156 l2 mol−2 min−1, respectively, and the corresponding activation energies were 3.00 and 5.50 Kcal mol−1. A mechanism is proposed to account for these observations.