dipyrromethene and tetrahydrofuran

dipyrromethene has been researched along with tetrahydrofuran* in 2 studies

Other Studies

2 other study(ies) available for dipyrromethene and tetrahydrofuran

ArticleYear
Rational Design of Near-Infrared-Absorbing Pt(II)-Chelated Azadipyrromethene Dyes as a New Generation of Photosensitizers for Synergistic Phototherapy.
    Inorganic chemistry, 2020, Dec-21, Volume: 59, Issue:24

    Pt(II) photosensitizers are emerging as novel Pt anticancer agents for cancer photodynamic therapy (PDT) to avoid uncontrollable toxicity of cisplatin. However, the application of Pt(II) photosensitizers is limited by tumor hypoxia and the poor penetration depth of excitation light. To overcome these drawbacks, exploiting the next generation of Pt anticancer agents is of urgent need. According to theoretical calculations, novel near-infrared (NIR)-absorbing Pt(II)-chelated azadipyrromethene dyes (

    Topics: Furans; HeLa Cells; Humans; Infrared Rays; Molecular Structure; Photosensitizing Agents; Phototherapy; Platinum Compounds; Porphobilinogen; Spectrophotometry, Infrared

2020
Multiantenna artificial photosynthetic reaction center complex.
    The journal of physical chemistry. B, 2009, May-21, Volume: 113, Issue:20

    In order to ensure efficient utilization of the solar spectrum, photosynthetic organisms use a variety of antenna chromophores to absorb light and transfer excitation to a reaction center, where photoinduced charge separation occurs. Reported here is a synthetic molecular heptad that features two bis(phenylethynyl)anthracene and two borondipyrromethene antennas linked to a hexaphenylbenzene core that also bears two zinc porphyrins. A fullerene electron acceptor self-assembles to both porhyrins via dative bonds. Excitation energy is transferred very efficiently from all four antennas to the porphyrins. Singlet-singlet energy transfer occurs both directly and by a stepwise funnel-like pathway wherein excitation moves down a thermodynamic gradient. The porphyrin excited states donate an electron to the fullerene with a time constant of 3 ps to generate a charge-separated state with a lifetime of 230 ps. The overall quantum yield is close to unity. In the absence of the fullerene, the porphyrin excited singlet state donates an electron to a borondipyrromethene on a slower time scale. This molecule demonstrates that by incorporating antennas, it is possible for a molecular system to harvest efficiently light throughout the visible from ultraviolet wavelengths out to approximately 650 nm.

    Topics: Absorption; Anthracenes; Benzene; Biomimetics; Electrons; Energy Transfer; Fullerenes; Furans; Light; Metalloporphyrins; Models, Molecular; Molecular Conformation; Photosynthetic Reaction Center Complex Proteins; Porphobilinogen; Spectrum Analysis; Time Factors

2009