Recent advances of triplet–triplet annihilation upconversion in photochemical transformations DOI

Jihao Jin,

Tianjun Yu,

Jinping Chen

и другие.

Current Opinion in Green and Sustainable Chemistry, Год журнала: 2023, Номер 43, С. 100841 - 100841

Опубликована: Июнь 19, 2023

Язык: Английский

Low-energy photoredox catalysis DOI
David C. Cabanero, Tomislav Rovis

Nature Reviews Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 11, 2024

Язык: Английский

Процитировано

10

Detour to success: photoswitching via indirect excitation DOI Creative Commons
Kim Kuntze, Jussi Isokuortti, Jacob Jan van der Wal

и другие.

Chemical Science, Год журнала: 2024, Номер 15(30), С. 11684 - 11698

Опубликована: Янв. 1, 2024

Photoswitching via indirect excitation allows harnessing low-energy photons to control molecular configuration. Herein, the state of art predominant photoswitching methods is presented.

Язык: Английский

Процитировано

8

Metal–Organic Bichromophore Lowers the Upconversion Excitation Power Threshold and Promotes UV Photoreactions DOI Creative Commons
Han Li, Cui Wang, Felix Glaser

и другие.

Journal of the American Chemical Society, Год журнала: 2023, Номер 145(20), С. 11402 - 11414

Опубликована: Май 15, 2023

Sensitized triplet–triplet annihilation upconversion is a promising strategy to use visible light for chemical reactions requiring the energy input of UV photons. This avoids unsafe ultraviolet sources and can mitigate photo-damage provide access reactions, which filter effects hamper direct excitation. Here, we report new approach make blue-to-UV more amenable photochemical applications. The tethering naphthalene unit cyclometalated iridium(III) complex yields bichromophore with high triplet (2.68 eV) naphthalene-based reservoir featuring lifetime 72.1 μs, roughly factor 20 longer than photoactive excited state parent complex. In combination three different annihilators, consistently lower thresholds crossover from quadratic into linear excitation power dependence regime were observed compared system composed 2,5-diphenyloxazole annihilator sufficiently robust under long-term blue irradiation continuously high-energy singlet-excited that drive normally light. Both photoredox transfer catalyses feasible using this concept, including reductive N–O bond cleavage Weinreb amides, C–C coupling reaction based on aryl debromination, two Paternò–Büchi [2 + 2] cycloaddition reactions. Our work seems relevant in context developing strategies driving energetically demanding photochemistry low-energy

Язык: Английский

Процитировано

20

First‐Row d6 Metal Complex Enables Photon Upconversion and Initiates Blue Light‐Dependent Polymerization with Red Light DOI Creative Commons
Cui Wang, Christina Wegeberg, Oliver S. Wenger

и другие.

Angewandte Chemie International Edition, Год журнала: 2023, Номер 62(43)

Опубликована: Сен. 8, 2023

Photosensitizers for sensitized triplet-triplet annihilation upconversion (sTTA-UC) often rely on precious heavy metals, whereas coordination complexes based abundant first-row transition metals are less common. This is mainly because long-lived triplet excited states more difficult to obtain 3d particularly when the d-subshell only partially filled. Here, we report first example of sTTA-UC a 3d6 metal photosensitizer yielding an performance competitive with metal-based analogues. Using newly developed Cr0 featuring equally good photophysical properties as OsII benchmark complex in combination acetylene-decorated anthracene annihilator, red-to-blue achievable. The efficiency under optimized conditions 1.8 %, and excitation power density threshold reach strong limit 5.9 W/cm2 . These factors, along high photostability, permit initiation acrylamide polymerization by red light, radiative energy transfer between delayed annihilator fluorescence blue light absorbing photo-initiator. Our study provides proof-of-concept photon elusive analogues widely employed d6 photosensitizers, their application photochemical reactions triggered wavelengths close near-infrared.

Язык: Английский

Процитировано

19

Red-Shifting Blue Light Photoredox Catalysis for Organic Synthesis: A Graphical Review DOI Creative Commons
Tomislav Rovis, Logan R. Beck,

Katherine A. Xie

и другие.

SynOpen, Год журнала: 2023, Номер 07(01), С. 76 - 87

Опубликована: Фев. 1, 2023

Abstract Photoredox catalysis has revolutionized synthetic chemistry in recent decades. However, the field traditionally used high-energy blue/ultraviolet light to activate chromophores. High-energy irradiation is associated with several drawbacks (e.g., activation of sensitive functional groups, undesired metal-ligand homolysis, background molecules, and poor penetration), which led researchers develop alternative systems lower energy deep red (DR) or near-infrared (NIR) light. This graphical review provides a concise overview photophysical principles relevant photoredox catalysis. Several applications that benefit from low-energy irradiation, such as large-scale batch reactions, photodynamic therapy, biological labeling, multi-photon excitation are reviewed.

Язык: Английский

Процитировано

16

Recent advancements in the molecular design of deep-red to near-infrared light-absorbing photocatalysts DOI
Minling Zhong, Yujie Sun

Chem Catalysis, Год журнала: 2024, Номер 4(8), С. 100973 - 100973

Опубликована: Апрель 17, 2024

Язык: Английский

Процитировано

7

Photocyclization by a triplet–triplet annihilation upconversion pair in water – avoiding UV-light and oxygen removal DOI Creative Commons

Rubaishan Jeyaseelan,

Martin Utikal,

Constantin G. Daniliuc

и другие.

Chemical Science, Год журнала: 2023, Номер 14(40), С. 11040 - 11044

Опубликована: Янв. 1, 2023

We present a formal [2 + 2]-cycloaddition of unsaturated ketones enabled by green-to-ultraviolet triplet-triplet annihilation upconversion (TTA-UC) pair, using commercially available Ru(bpy)32+ and pyrene as sensitizer annihilator, respectively. In the developed protocol, visible light irradiation at λmax = 520 nm allows for reaction to proceed without need UV-light aqueous medium eliminates oxygen removing protocols. Through this study, application readily pair is broadened include cyclization reactions. showcase utility system generating bicyclo[2.1.1]hexanes that are valuable bioisosteres ortho-substituted benzenes, promising motif pharmaceuticals.

Язык: Английский

Процитировано

14

Red-Light-Promoted Radical Cascade Reaction to Access Tetralins and Dialins Enabled by Zinc(II)porphyrin, A Light-Flexible Catalyst DOI

Yusuke Okanishi,

Otoki Takemoto,

Sanpou Kawahara

и другие.

Organic Letters, Год журнала: 2024, Номер 26(18), С. 3929 - 3934

Опубликована: Апрель 26, 2024

[5,15-Bis(pentafluorophenyl)-10,20-diphenylporphinato]zinc(II) (1), a metalloporphyrin derivative that was recently reported as an efficient photocatalyst driven by blue LEDs our group, found to catalyze red-light-promoted (630 nm LEDs) radical cascade reaction of N-3-arylpropionyloxyphthalimides with radicophiles including electron-deficient alkenes and alkynes, providing access range functionalized tetralin dialin derivatives. The catalyzed 1 took place via oxidative quenching cycle in DMSO, where no sacrificial electron donor required, uncovering unique solvent effect capable promoting the porphyrin catalysis.

Язык: Английский

Процитировано

5

Steric and Electronic Influence of Excited-State Decay in Cu(I) MLCT Chromophores DOI
Felix N. Castellano, Michael C. Rosko

Accounts of Chemical Research, Год журнала: 2024, Номер 57(19), С. 2872 - 2886

Опубликована: Сен. 11, 2024

ConspectusFor the past 11 years, a dedicated effort in our research group focused on fundamentally advancing photophysical properties of cuprous

Язык: Английский

Процитировано

5

Π‐Radical Photosensitizer for Highly Efficient and Stable Near‐Infrared Photon Upconversion DOI
Yaxiong Wei,

Kebin An,

Xinsheng Xu

и другие.

Advanced Optical Materials, Год журнала: 2023, Номер 12(6)

Опубликована: Сен. 10, 2023

Abstract Near‐infrared (NIR)‐to‐blue triplet–triplet annihilation upconversion (TTA‐UC) exhibits substantial potential for diverse applications, encompassing photovoltaics, photocatalysis, bioimaging, and photodynamic therapy. A major challenge in this field, however, is attaining high quantum yields ( Φ UC ) without using transition metals as NIR photosensitizers. This research presents an innovative organic π‐radical photosensitizer (TTM‐TPA) featuring extended absorption the region (≈760 nm) that capable of generating pronounced anti‐Stokes emissions when coupled with suitable triplet acceptors. By eliminating energy loss associated intersystem crossing promoting rapid doublet–triplet transfer processes, binary TTM‐TPA/perylene system achieves values up to 6.8% shift 0.93 eV. Notably, TTA‐UC demonstrates exceptional stability subjected intense 733 nm laser irradiation (4 W cm −2 ), maintaining nearly constant intensity after 4 h. These findings underscore considerable doublet‐sensitized a broad array practical applications.

Язык: Английский

Процитировано

12