{"title":"Synthesis, characterization, and spectroscopic properties of the new type of aminoquinoline-modified cyclotriphosphazenes","authors":"Duygu Palabıyık , Ceylan Mutlu Balcı","doi":"10.1080/10426507.2022.2046570","DOIUrl":null,"url":null,"abstract":"<div><p>The aminolysis reactions of hexachlorocyclotriphosphazene, [N<sub>3</sub>P<sub>3</sub>Cl<sub>6</sub>] (<strong>1a</strong>) and dispiro-2,2′-biphenoxydichlorocyclotriphosphazene [N<sub>3</sub>P<sub>3</sub>Cl<sub>2</sub>[(2,2′-biphenoxy)<sub>2</sub>] (<strong>1b</strong>) with 6-aminoquinoline (<strong>2</strong>) were carried out to examine the spectroscopic properties of cyclotriphosphazene derivatives combined with 6-aminoquinoline. For the first time, two new aminoquinoline-substituted cyclotriphosphazene derivatives (<strong>3a</strong>, <strong>b</strong>) were obtained in this study. Both compounds (<strong>3a</strong>, <strong>b</strong>) have been characterized by elemental analysis, FT-IR analysis, MALDI-TOF mass spectrometry, <sup>13</sup>C, <sup>1</sup>H, and <sup>31</sup>P NMR spectroscopies. The molecular structure of <strong>3b</strong> has been confirmed by single crystal X-Ray crystallography. The crystal structure of <strong>3b</strong> was investigated in detail to determine the remarkable intermolecular interactions. Furthermore, the photophysical properties of compounds <strong>3a</strong> and <strong>3b</strong> were determined by using UV/vis and fluorescence spectroscopies.</p></div>","PeriodicalId":1,"journal":{"name":"Accounts of Chemical Research","volume":null,"pages":null},"PeriodicalIF":16.4000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Accounts of Chemical Research","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S104265072201231X","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 1
Abstract
The aminolysis reactions of hexachlorocyclotriphosphazene, [N3P3Cl6] (1a) and dispiro-2,2′-biphenoxydichlorocyclotriphosphazene [N3P3Cl2[(2,2′-biphenoxy)2] (1b) with 6-aminoquinoline (2) were carried out to examine the spectroscopic properties of cyclotriphosphazene derivatives combined with 6-aminoquinoline. For the first time, two new aminoquinoline-substituted cyclotriphosphazene derivatives (3a, b) were obtained in this study. Both compounds (3a, b) have been characterized by elemental analysis, FT-IR analysis, MALDI-TOF mass spectrometry, 13C, 1H, and 31P NMR spectroscopies. The molecular structure of 3b has been confirmed by single crystal X-Ray crystallography. The crystal structure of 3b was investigated in detail to determine the remarkable intermolecular interactions. Furthermore, the photophysical properties of compounds 3a and 3b were determined by using UV/vis and fluorescence spectroscopies.
期刊介绍:
Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance.
Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.