Ümit Demirbaş , Zehra Özçifçi , Hakkı Türker Akçay
{"title":"带有氟甲基喹啉取代基的新型酞菁:合成、表征、光物理和光化学特性","authors":"Ümit Demirbaş , Zehra Özçifçi , Hakkı Türker Akçay","doi":"10.1016/j.jorganchem.2024.123421","DOIUrl":null,"url":null,"abstract":"<div><div>The novel 4-((6-fluoro-2-methylquinolin-4-yl)oxy)phthalonitrile (<strong>3a</strong>), 3-((6-fluoro-2-methylquinolin-4-yl)oxy)phthalonitrile <strong>(3b),</strong> tetra 6-fluoro-2-methylquinolin-4-yl)oxy substituted zinc(II) phthalocyanines <strong>(4a</strong> and <strong>4b)</strong> and their water soluble derivatives <strong>(5a</strong> and <strong>5b)</strong> were prepared. The proposed structures of novel compounds were comfirmed via FT-IR, <sup>1</sup>HNMR , UV–Vis and MALDI-TOF mass data. The aggregation tendency, fluorescence quantum yield, singlet oxygen quantum yield and photodegradation measurements were performed to examine the photodynamic therapy potential of both peripherally tetra substituted zinc(II) phthalocyanines <strong>(4a</strong> and <strong>4b)</strong> and the water soluble quaternized tetra substituted zinc(II) phthalocyanines <strong>(5a</strong> and <strong>5b)</strong>. The result showed that both the novel tetra 6-fluoro-2-methylquinolin-4-yl)oxy substituted zinc(II) phthalocyanines <strong>(4a</strong> and <strong>4b)</strong> and their water soluble derivatives <strong>(5a</strong> and <strong>5b)</strong> could be used as photosensitizer agents in PDT thanks to their lack of aggregation tendency, having sufficient fluorescence emission for monitoring and produce high amount of singlet oxygen to destroy cancerous tissues and having moderate photostability.</div></div>","PeriodicalId":374,"journal":{"name":"Journal of Organometallic Chemistry","volume":"1022 ","pages":"Article 123421"},"PeriodicalIF":2.1000,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Novel phthalocyanines bearing fluoro-methylquinolin substituents: Synthesis, characterization, photophysical and photochemical properties\",\"authors\":\"Ümit Demirbaş , Zehra Özçifçi , Hakkı Türker Akçay\",\"doi\":\"10.1016/j.jorganchem.2024.123421\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The novel 4-((6-fluoro-2-methylquinolin-4-yl)oxy)phthalonitrile (<strong>3a</strong>), 3-((6-fluoro-2-methylquinolin-4-yl)oxy)phthalonitrile <strong>(3b),</strong> tetra 6-fluoro-2-methylquinolin-4-yl)oxy substituted zinc(II) phthalocyanines <strong>(4a</strong> and <strong>4b)</strong> and their water soluble derivatives <strong>(5a</strong> and <strong>5b)</strong> were prepared. The proposed structures of novel compounds were comfirmed via FT-IR, <sup>1</sup>HNMR , UV–Vis and MALDI-TOF mass data. The aggregation tendency, fluorescence quantum yield, singlet oxygen quantum yield and photodegradation measurements were performed to examine the photodynamic therapy potential of both peripherally tetra substituted zinc(II) phthalocyanines <strong>(4a</strong> and <strong>4b)</strong> and the water soluble quaternized tetra substituted zinc(II) phthalocyanines <strong>(5a</strong> and <strong>5b)</strong>. The result showed that both the novel tetra 6-fluoro-2-methylquinolin-4-yl)oxy substituted zinc(II) phthalocyanines <strong>(4a</strong> and <strong>4b)</strong> and their water soluble derivatives <strong>(5a</strong> and <strong>5b)</strong> could be used as photosensitizer agents in PDT thanks to their lack of aggregation tendency, having sufficient fluorescence emission for monitoring and produce high amount of singlet oxygen to destroy cancerous tissues and having moderate photostability.</div></div>\",\"PeriodicalId\":374,\"journal\":{\"name\":\"Journal of Organometallic Chemistry\",\"volume\":\"1022 \",\"pages\":\"Article 123421\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-10-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Organometallic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022328X24004169\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organometallic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022328X24004169","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
The novel 4-((6-fluoro-2-methylquinolin-4-yl)oxy)phthalonitrile (3a), 3-((6-fluoro-2-methylquinolin-4-yl)oxy)phthalonitrile (3b), tetra 6-fluoro-2-methylquinolin-4-yl)oxy substituted zinc(II) phthalocyanines (4a and 4b) and their water soluble derivatives (5a and 5b) were prepared. The proposed structures of novel compounds were comfirmed via FT-IR, 1HNMR , UV–Vis and MALDI-TOF mass data. The aggregation tendency, fluorescence quantum yield, singlet oxygen quantum yield and photodegradation measurements were performed to examine the photodynamic therapy potential of both peripherally tetra substituted zinc(II) phthalocyanines (4a and 4b) and the water soluble quaternized tetra substituted zinc(II) phthalocyanines (5a and 5b). The result showed that both the novel tetra 6-fluoro-2-methylquinolin-4-yl)oxy substituted zinc(II) phthalocyanines (4a and 4b) and their water soluble derivatives (5a and 5b) could be used as photosensitizer agents in PDT thanks to their lack of aggregation tendency, having sufficient fluorescence emission for monitoring and produce high amount of singlet oxygen to destroy cancerous tissues and having moderate photostability.
期刊介绍:
The Journal of Organometallic Chemistry targets original papers dealing with theoretical aspects, structural chemistry, synthesis, physical and chemical properties (including reaction mechanisms), and practical applications of organometallic compounds.
Organometallic compounds are defined as compounds that contain metal - carbon bonds. The term metal includes all alkali and alkaline earth metals, all transition metals and the lanthanides and actinides in the Periodic Table. Metalloids including the elements in Group 13 and the heavier members of the Groups 14 - 16 are also included. The term chemistry includes syntheses, characterizations and reaction chemistry of all such compounds. Research reports based on use of organometallic complexes in bioorganometallic chemistry, medicine, material sciences, homogeneous catalysis and energy conversion are also welcome.
The scope of the journal has been enlarged to encompass important research on organometallic complexes in bioorganometallic chemistry and material sciences, and of heavier main group elements in organometallic chemistry. The journal also publishes review articles, short communications and notes.