Supramolecular and covalent metal-BODIPY hybrids for photocatalytic hydrogen production
用于光催化制氢的超分子和共价金属-BODIPY杂化物
基本信息
- 批准号:323851644
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:德国
- 项目类别:Research Grants
- 财政年份:2016
- 资助国家:德国
- 起止时间:2015-12-31 至 2020-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Based on preliminary results on photocatalytic hydrogen production using a multicomponent system based on BODIPY dyes and Pd compounds as the proton reducing species, this joint project is aiming at a better understanding of this this reaction. For this purpose, comparative and mechanistic studies will be performed that will result in a functional optimisation of stability and hydrogen production activity of the systems. The following points will be adressed:1. correlation of structure, optical properties and catalytic activitya. system (catalysis and kinetic studies)b. photophysical behaviour2. covalent linking of BODIPY and Pd, maintaining activity and stability for a directed intramolecular electron transfer3. enhancement of supramolecular aggregation of dye and nanoparticle by using functionalised (oligo)BODIPYs with coordination sites for weak interactions.
基于以BODIPY染料和Pd化合物为质子还原物质的多组分体系光催化制氢的初步结果,本联合项目旨在更好地理解这一反应。为此目的,将进行比较和机理研究,这将导致系统稳定性和制氢活性的功能优化。将讨论以下几点:结构、光学性质与催化活性的关系。系统(催化和动力学研究)光物理behaviour2。BODIPY和Pd的共价连接,维持定向分子内电子转移的活性和稳定性。利用具有弱相互作用配位的功能化(寡聚)BODIPYs增强染料和纳米颗粒的超分子聚集。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Professor Dr. Torsten Beweries其他文献
Professor Dr. Torsten Beweries的其他文献
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{{ truncateString('Professor Dr. Torsten Beweries', 18)}}的其他基金
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Quantification of the interactions of group 8 and group 10 metal fluorides with hydrogen and halogen donors in solution - contributions to a better understanding of the nature of the metal fluoride bond
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Catalytic ways to new inorganic polymers: development of transition metal catalysts for highly selective dehydropolymerisation of amine boranes
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Metallacyclobuta-2,3-dienes as organometallic analogs of the smallest cyclic allene – classical metallacyles or unusual transition metal biradcals?
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