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chemia: Boron porphyrins

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The central four nitrogen atoms in a porphyrin macrocycle form a unique molecular pocket which is known to accommodate transition metals of various sizes and oxidation states.
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Boron porphyrins are a variety of porphyrin, a common macrocycle used for photosensitization and metal trapping applications, that incorporate boron. The central four nitrogen atoms in a porphyrin macrocycle form a unique molecular pocket which is known to accommodate transition metals of various sizes and oxidation states. Due to the diversity of binding modes available to porphyrin, there is a growing interest in introducing other elements (i.e. main group elements) into this pocket. Boron in particular has been shown to prefer binding to porphyrin in a 2:1 stoichiometry, primarily due to its small atomic radius, but the Group XIII element will bind in a 1:1 ratio with corrole, a macromolecule with a structure similar to porphyrin but with a smaller N4 pocket. Boron porphyrins are of interest because of the unique geometric environment to which both boron and porphyrin are subjected upon B-N(pyrrole) bond formation. These new geometric motifs lead to novel reactivity, one of the most surprising examples being sterically-induced reductive coupling. Possible applications for boron porphyrins include BNCT delivery agents and OLED devices. Also of interest are molecules containing both boron and porphyrin moieties, but without B-N(pyrrole) bonds. Examples include diketonate-porphyrin compounds and dyads (two-component molecules) containing the classic BODIPY dye.
Kategoria: chemia
Rodzina: chemia
Jakość źródła: 65/100
Próby weryfikacji: 3
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Wikipedia ENpomocniczeniezależne

Evidence: 100 • authority: 72

Boron porphyrins are a variety of porphyrin, a common macrocycle used for photosensitization and metal trapping applications, that incorporate boron. The central four nitrogen atoms in a porphyrin macrocycle form a unique molecular pocket which is known to accommodate transition metals of various sizes and oxidation states. Due to the diversity of binding modes available to porphyrin, there is a growing interest in introducing other elements (i.e. main group elements) into this pocket. Boron in particular has been shown to prefer binding to porphyrin in a 2:1 stoichiometry, primarily due to its small atomic radius, but the Group XIII element will bind in a 1:1 ratio with corrole, a macromol…

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American Chemical Society (ACS)pomocniczeniezależne

Evidence: 36 • authority: 80

Cobalt Porphyrin with a Fine-Tuned Molecular Pocket Bottleneck for Improved Oxygen Reduction Reaction

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American Chemical Society (ACS)pomocniczeniezależne

Evidence: 36 • authority: 80

Cobalt Porphyrin with a Fine-Tuned Molecular Pocket Bottleneck for Improved Oxygen Reduction Reaction

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American Chemical Society (ACS)pomocniczeniezależne

Evidence: 36 • authority: 80

Cobalt Porphyrin with a Fine-Tuned Molecular Pocket Bottleneck for Improved Oxygen Reduction Reaction

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American Chemical Society (ACS)pomocniczeniezależne

Evidence: 36 • authority: 80

Cobalt Porphyrin with a Fine-Tuned Molecular Pocket Bottleneck for Improved Oxygen Reduction Reaction

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American Chemical Society (ACS)pomocniczeniezależne

Evidence: 36 • authority: 80

Near-Infrared Chemiluminescence Supramolecular Porphyrin Hydrogel Containing Fe/Mn Double Transition Metals for Wound Healing

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Europe PMC / Journal of coordination chemistrypomocniczeniezależne

Evidence: 36 • authority: 92

Beyond BODIPY: dipyrrin complexes of P-block elements.. Dipyrrin has proven to be a versatile ligand platform for metals across the periodic table. Since much of the coordination chemistry has focused on transition metals, main-group dipyrrin chemistry has been underexplored, particularly in the case of heavy p-block elements. Boron dipyrrin complexes (also known as BODIPY) were initially reported in 1968, yet the first well-characterized example of a heavy p-block dipyrrin complex was in 2006. This nascent area of research has undergone a significant surge, where nearly half of the reports in this field have been published since 2019. Given this renewed interest and rapid development, we p…

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Europe PMC / ACS omegapomocniczeniezależne

Evidence: 36 • authority: 92

Advances in Ligand Development for Wacker-Type Oxidation.. Wacker-type oxidation is a cornerstone catalytic transformation for alkene-to-carbonyl conversion in organic synthesis, with immense industrial and academic impact over six decades. However, the classic Wacker-Tsuji system suffers from inherent limitations, including corrosive chloride reliance, poor regiocontrol, noble metal dependence, catalyst deactivation, and sustainability issues, which severely restrict its synthetic utility. Ligand engineering has emerged as the central strategy to revolutionize this field, yet no comprehensive review dedicated to ligand-controlled Wacker-type oxidation has been reported to date. Herein, we…

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