超分子中锌细菌叶绿素-d类似物从BODIPY到自聚集的激发能转移

IF 4.7 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-07-01 Epub Date: 2025-02-15 DOI:10.1016/j.jphotochem.2025.116344
Yuna Mori, Hitoshi Tamiaki
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引用次数: 0

摘要

在无氧光合绿细菌的主要光收集天线(叶绿体)中,吸收绿光的光激发类胡萝卜素将单线态激发能提供给细菌叶绿素(BChls)自聚集体-c/d/e,其位点能量位于远红光区。为了模拟能量转移体系,在1%(v/v)的四氢呋喃和己烷中研究了锌bcl -d类似物与二吡咯甲烷硼(BODIPY)衍生物共价连接。在极性较低的有机溶剂中,共轭物中的Zn-BChl-d部分与叶绿体中类似自聚集,并接受来自BODIPY部分的激发能,在绿光区吸收约500 nm。利用可见吸收光谱和荧光发射光谱分析了共轭物超分子自组装过程中BODIPY*向(Zn-BChl-d)n的激发能转移。
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Excitation energy transfer from BODIPY to self-aggregate of zinc bacteriochlorophyll-d analog in supramolecule
In the main light-harvesting antennas (chlorosomes) of anoxygenic photosynthetic green bacteria, photoexcited carotenoids absorbing green light donate singlet excitation energy to self-aggregates of bacteriochlorophylls(BChls)-c/d/e with their site energies in a far-red light region. To mimic the energy transfer systems, a zinc BChl-d analog covalently linked with a boron dipyrromethene (BODIPY) derivative was investigated in 1%(v/v) tetrahydrofuran and hexane. In the less polar organic solvent, the Zn-BChl-d part in the conjugate self-aggregated similarly as in chlorosomes and accepted excitation energy from the BODIPY part with absorption around 500 nm in a green light region. The excitation energy transfer from BODIPY* to (Zn-BChl-d)n in the supramolecular self-assembly of the conjugate was analyzed by visible absorption and fluorescence emission spectroscopy.
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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