Cationic dipyridylamine substituted zinc tetrapyrazinoporphyrazine derivatives for photodynamic therapy
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Park, Jong Min | - |
dc.contributor.author | Yao, Wang | - |
dc.contributor.author | Jung, Chang Young | - |
dc.contributor.author | Cho, Joong Hyun | - |
dc.contributor.author | Kim, Dae Hyun | - |
dc.contributor.author | Jaung, Jae Yun | - |
dc.date.accessioned | 2021-07-30T05:07:33Z | - |
dc.date.available | 2021-07-30T05:07:33Z | - |
dc.date.issued | 2017-09 | - |
dc.identifier.issn | 1010-6030 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/3196 | - |
dc.description.abstract | Two kinds of cationic zinc tetrapyrazinoporphyrazine derivatives substituted with ortho- or para-methylpyridinium groups on the peripheral position were synthesized and characterized. The solubility and aggregation behavior of each material were estimated in various solvents, which show different aspect depending on the position of nitrogen on methylpyridinium groups. The fluorescence quantum yield (Phi(F)) values of both cationic tetrapyrazinoporphyrazines were measured and the singlet oxygen quantum (Phi(Delta) ) yield value were measured by indirect method with DPBF (1,3-diphenylisobenzofuran) in DMSO. Both Phi(F) and Phi(Delta) of cationic zinc tetrapyrazinoporphyrazine derivatives exhibited reasonable values for photodynamic therapy application. The cationic zinc tetrapyrazinoporphyrazine derivatives substituted methylpyridinium groups increased solubility in aqueous solvent but also showed the suitable properties as the photosensitizers for photodynamic therapy. | - |
dc.format.extent | 7 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | ELSEVIER SCIENCE SA | - |
dc.title | Cationic dipyridylamine substituted zinc tetrapyrazinoporphyrazine derivatives for photodynamic therapy | - |
dc.type | Article | - |
dc.publisher.location | 스위스 | - |
dc.identifier.doi | 10.1016/j.jphotochem.2017.05.050 | - |
dc.identifier.scopusid | 2-s2.0-85020279349 | - |
dc.identifier.wosid | 000407526200013 | - |
dc.identifier.bibliographicCitation | JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, v.346, pp 126 - 132 | - |
dc.citation.title | JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY | - |
dc.citation.volume | 346 | - |
dc.citation.startPage | 126 | - |
dc.citation.endPage | 132 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | sci | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
dc.subject.keywordPlus | QUANTUM YIELDS | - |
dc.subject.keywordPlus | PHTHALOCYANINE | - |
dc.subject.keywordPlus | PHOTOSENSITIZERS | - |
dc.subject.keywordPlus | CANCER | - |
dc.subject.keywordPlus | PORPHYRINS | - |
dc.subject.keywordPlus | SPECTRA | - |
dc.subject.keywordPlus | SOLVENT | - |
dc.subject.keywordAuthor | Cationic tetrapyrazinoporphyrazine | - |
dc.subject.keywordAuthor | Photodynamic therapy | - |
dc.subject.keywordAuthor | Photosensitizer | - |
dc.subject.keywordAuthor | Aggregation behavior | - |
dc.identifier.url | https://reader.elsevier.com/reader/sd/pii/S1010603016312436?token=D61039E530FA055E61905148E72C325EB81949D6888A6F09E0606CA110630F566454F2B84C92248AA692BBD2DB153D9D&originRegion=us-east-1&originCreation=20230509012454 | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
222, Wangsimni-ro, Seongdong-gu, Seoul, 04763, Korea+82-2-2220-1365
COPYRIGHT © 2021 HANYANG UNIVERSITY.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.