• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

聚电解质多层膜中5,10,15,20-四(4-磺酸钠苯基)卟啉的J聚集体与H聚集体之间的pH诱导相互转化

pH-induced interconversion between J-aggregates and H-aggregates of 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin in polyelectrolyte multilayer films.

作者信息

Egawa Yuya, Hayashida Ryosuke, Anzai Jun-ichi

机构信息

Graduate School of Pharmaceutical Sciences, Tohoku University, Aramaki, Aoba, Sendai 980-8578, Japan.

出版信息

Langmuir. 2007 Dec 18;23(26):13146-50. doi: 10.1021/la701957b. Epub 2007 Nov 10.

DOI:10.1021/la701957b
PMID:17994773
Abstract

We fabricated a layer-by-layer (LbL) film composed of 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin (TPPS) and poly(allylamine) (PAA) and investigated its pH response by UV-visible spectrometry. When the (PAA/TPPS)5PAA film was immersed in a pH 1.5 solution, J-aggregate bands were observed at 484 and 691 nm. Above pH 3.0, the J-aggregates were completely dissociated and an H-aggregate band was observed at 405 nm. The interconversion between the J-aggregates and H-aggregates in the LbL film was repeatable and controllable by changing the pH of the solutions.

摘要

我们制备了一种由5,10,15,20-四(4-磺酸钠苯基)卟啉(TPPS)和聚烯丙胺(PAA)组成的逐层(LbL)薄膜,并通过紫外可见光谱研究了其pH响应。当将(PAA/TPPS)5PAA薄膜浸入pH为1.5的溶液中时,在484和691nm处观察到J-聚集体带。在pH 3.0以上,J-聚集体完全解离,在405nm处观察到H-聚集体带。通过改变溶液的pH值,LbL薄膜中J-聚集体和H-聚集体之间的相互转化是可重复且可控的。

相似文献

1
pH-induced interconversion between J-aggregates and H-aggregates of 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin in polyelectrolyte multilayer films.聚电解质多层膜中5,10,15,20-四(4-磺酸钠苯基)卟啉的J聚集体与H聚集体之间的pH诱导相互转化
Langmuir. 2007 Dec 18;23(26):13146-50. doi: 10.1021/la701957b. Epub 2007 Nov 10.
2
Multilayer nanostructured porphyrin arrays constructed by layer-by-layer self-assembly.通过层层自组装构建的多层纳米结构卟啉阵列。
Langmuir. 2009 Sep 1;25(17):9873-8. doi: 10.1021/la900953a.
3
Studies on the effects of metal ions and counter anions on the aggregate behaviors of meso-tetrakis(p-sulfonatophenyl)porphyrin by absorption and fluorescence spectroscopy.通过吸收光谱和荧光光谱研究金属离子和抗衡阴离子对中位四(对磺酸基苯基)卟啉聚集行为的影响。
Spectrochim Acta A Mol Biomol Spectrosc. 2008 Nov 1;71(1):153-60. doi: 10.1016/j.saa.2007.11.020. Epub 2007 Nov 29.
4
Chiral induction, memory, and amplification in porphyrin homoaggregates based on electrostatic interactions.基于静电相互作用的卟啉同聚集体中的手性诱导、记忆和放大。
Chemphyschem. 2009 Apr 14;10(6):954-62. doi: 10.1002/cphc.200800810.
5
J- and H-aggregates of 5,10,15,20-tetrakis-(4-sulfonatophenyl)-porphyrin and interconversion in PEG-b-P4VP micelles.5,10,15,20-四(4-磺酸苯基)卟啉的J-聚集体和H-聚集体以及在聚乙二醇-b-聚4-乙烯基吡啶胶束中的相互转化
Biomacromolecules. 2008 Oct;9(10):2601-8. doi: 10.1021/bm8004808. Epub 2008 Aug 14.
6
Porphyrin J-aggregates stabilized by ferric myoglobin in neutral aqueous solution.在中性水溶液中由高铁肌红蛋白稳定的卟啉J聚集体。
J Phys Chem B. 2008 Nov 20;112(46):14402-8. doi: 10.1021/jp802567b. Epub 2008 Jul 18.
7
Molecular organization in self-assembled binary porphyrin nanotubes revealed by resonance Raman spectroscopy.共振拉曼光谱揭示自组装二元卟啉纳米管中的分子组织。
Phys Chem Chem Phys. 2010 Apr 28;12(16):4072-7. doi: 10.1039/b926068d. Epub 2010 Mar 9.
8
Novel porphyrin-incorporated hydrogels for photoactive intraocular lens biomaterials.用于光活性人工晶状体生物材料的新型卟啉复合水凝胶。
J Phys Chem B. 2007 Jan 25;111(3):527-34. doi: 10.1021/jp066217i.
9
Interaction of meso-tetrakis(4-sulphonatophenyl)porphine with chitosan in aqueous solutions.中-四(4-磺酸基苯基)卟啉与壳聚糖在水溶液中的相互作用
Spectrochim Acta A Mol Biomol Spectrosc. 2007 Feb;66(2):225-35. doi: 10.1016/j.saa.2006.02.046. Epub 2006 Jul 10.
10
Investigation on solvation and protonation of meso-tetrakis(p-sulfonatophenyl)porphyrin in imidazolium-based ionic liquids by spectroscopic methods.通过光谱方法研究中-四(对-磺酸钠苯基)卟啉在咪唑基离子液体中的溶剂化和质子化作用。
Spectrochim Acta A Mol Biomol Spectrosc. 2009 Oct 1;74(2):502-8. doi: 10.1016/j.saa.2009.06.057. Epub 2009 Jul 8.

引用本文的文献

1
Porphyrin Aggregation under Homogeneous Conditions Inhibits Electrocatalysis: A Case Study on CO Reduction.均相条件下卟啉聚集对电催化的抑制作用:以CO还原为例的研究
ACS Cent Sci. 2024 Jun 3;10(6):1251-1261. doi: 10.1021/acscentsci.4c00121. eCollection 2024 Jun 26.
2
Supramolecular Self-Assembly of Porphyrin and Metallosurfactant as a Drug Nanocontainer Design.卟啉与金属表面活性剂的超分子自组装作为药物纳米容器设计
Nanomaterials (Basel). 2022 Jun 9;12(12):1986. doi: 10.3390/nano12121986.
3
Photodynamic Inactivation of Bacteria with Porphyrin Derivatives: Effect of Charge, Lipophilicity, ROS Generation, and Cellular Uptake on Their Biological Activity In Vitro.
卟啉衍生物的光动力细菌灭活:体外电荷、亲脂性、ROS 生成和细胞摄取对其生物学活性的影响。
Int J Mol Sci. 2020 Nov 18;21(22):8716. doi: 10.3390/ijms21228716.
4
pH-Responsive Polyketone/5,10,15,20-Tetrakis-(Sulfonatophenyl)Porphyrin Supramolecular Submicron Colloidal Structures.pH响应性聚酮/5,10,15,20-四(磺化苯基)卟啉超分子亚微米胶体结构
Polymers (Basel). 2020 Sep 3;12(9):2017. doi: 10.3390/polym12092017.
5
Utilizing Polymer Micelle to Control Dye J-aggregation and Enhance Its Theranostic Capability.利用聚合物胶束控制染料J-聚集并增强其诊疗能力。
iScience. 2019 Dec 20;22:229-239. doi: 10.1016/j.isci.2019.11.022. Epub 2019 Nov 16.
6
A de novo strategy for predictive crystal engineering to tune excitonic coupling.一种用于调节激子耦合的预测性晶体工程的从头算策略。
Nat Commun. 2019 May 3;10(1):2048. doi: 10.1038/s41467-019-10011-8.
7
Enforcing Extended Porphyrin J-Aggregate Stacking in Covalent Organic Frameworks.在共价有机框架中实现扩展卟啉J-聚集体堆积
J Am Chem Soc. 2018 Dec 5;140(48):16544-16552. doi: 10.1021/jacs.8b08088. Epub 2018 Nov 19.
8
Potentiation by potassium iodide reveals that the anionic porphyrin TPPS4 is a surprisingly effective photosensitizer for antimicrobial photodynamic inactivation.碘化钾的增效作用表明,阴离子卟啉TPPS4是一种用于抗菌光动力灭活的极其有效的光敏剂。
J Photochem Photobiol B. 2018 Jan;178:277-286. doi: 10.1016/j.jphotobiol.2017.10.036. Epub 2017 Oct 31.
9
Self-organized porphyrinic materials.自组装卟啉材料。
Chem Rev. 2009 May;109(5):1630-58. doi: 10.1021/cr8002483.