Steering Photoinduced Electron Transfer in Intramolecular Photocatalysts by Peripheral Ligand Control

Benedikt Bagemihl, Prof. Carolin Müller, Dr. Georgina E. Shillito, Marco Hartkorn, Dr. Alexander K. Mengele, Dr. Stephan Kupfer, Prof. Benjamin Dietzek-Ivanšić, Prof. Sven Rau
{"title":"Steering Photoinduced Electron Transfer in Intramolecular Photocatalysts by Peripheral Ligand Control","authors":"Benedikt Bagemihl,&nbsp;Prof. Carolin Müller,&nbsp;Dr. Georgina E. Shillito,&nbsp;Marco Hartkorn,&nbsp;Dr. Alexander K. Mengele,&nbsp;Dr. Stephan Kupfer,&nbsp;Prof. Benjamin Dietzek-Ivanšić,&nbsp;Prof. Sven Rau","doi":"10.1002/ceur.202300084","DOIUrl":null,"url":null,"abstract":"<p>Bridged photosensitizer-catalyst systems are promising models to study photocatalytic hydrogen evolution. However, the systems in the literature structurally diverse and therefore hard to compare. Many systems show highly complex photophysics including several accepting orbitals for the excited state, as a result catalytic activity is hard to predict. Here we present a bimetallic Ru−Pt photocatalyst bearing peripheral spectator ligands at the ruthenium(II) photocenter as a member of the Ru-tpphz-Pt family. Consequently, it features a single acceptor tpphz ligand and so-called unidirectional electron transfer, <i>i. e</i>., electron transfer without co-occurring transfer to peripheral ligands, from the excited state. Thus – and in contrast to recently used peripheral ligands – the new spectator ligands do not disrupt electron transfer towards the catalytic center. By comparison to known systems, this facilitates unprecedented insight into the importance of electron transfer from the bridge to the catalytic center moving towards more rational design of oligonuclear photocatalysts.</p>","PeriodicalId":100234,"journal":{"name":"ChemistryEurope","volume":"2 6","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ceur.202300084","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemistryEurope","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ceur.202300084","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Bridged photosensitizer-catalyst systems are promising models to study photocatalytic hydrogen evolution. However, the systems in the literature structurally diverse and therefore hard to compare. Many systems show highly complex photophysics including several accepting orbitals for the excited state, as a result catalytic activity is hard to predict. Here we present a bimetallic Ru−Pt photocatalyst bearing peripheral spectator ligands at the ruthenium(II) photocenter as a member of the Ru-tpphz-Pt family. Consequently, it features a single acceptor tpphz ligand and so-called unidirectional electron transfer, i. e., electron transfer without co-occurring transfer to peripheral ligands, from the excited state. Thus – and in contrast to recently used peripheral ligands – the new spectator ligands do not disrupt electron transfer towards the catalytic center. By comparison to known systems, this facilitates unprecedented insight into the importance of electron transfer from the bridge to the catalytic center moving towards more rational design of oligonuclear photocatalysts.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
通过外围配体控制引导分子内光催化剂中的光诱导电子转移
桥式光敏剂催化剂系统是研究光催化氢气进化的有前途的模型。然而,文献中的系统结构多种多样,因此很难进行比较。许多系统显示出高度复杂的光物理,包括激发态的多个接受轨道,因此催化活性难以预测。在这里,我们介绍了一种双金属 Ru-Pt 光催化剂,它作为 Ru-tpphz-Pt 家族的一员,在钌(II)光中心带有外围旁观配体。因此,这种催化剂具有单一受体 tpphz 配体和所谓的单向电子转移(即电子从激发态转移而不同时转移到外围配体)的特点。因此,与最近使用的外围配体不同,新的旁观配体不会干扰电子向催化中心的转移。与已知系统相比,这有助于深入了解电子从桥转移到催化中心的重要性,从而更合理地设计低核光催化剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Front Cover: Luminescence and Single-Molecule Magnet Properties in Ideal Symmetry Compounds: Example of a Near-Planar Tricoordinate Ytterbium(III) Amide (ChemistryEurope 6/2024) Cover Feature: Water Chemistry at the Nanoscale: Clues for Resolving the “Water Paradox” Underlying the Emergence of Life (ChemistryEurope 6/2024) Luminescence and Single-Molecule Magnet Properties in Ideal Symmetry Compounds: Example of a Near-Planar Tricoordinate Ytterbium(III) Amide Steering Photoinduced Electron Transfer in Intramolecular Photocatalysts by Peripheral Ligand Control Water Chemistry at the Nanoscale: Clues for Resolving the “Water Paradox” Underlying the Emergence of Life
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1