2021
DOI: 10.1039/d1cc03620c
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An Ir3L2 complex with anion binding pockets: photocatalytic EZ isomerization via molecular recognition

Abstract: A molecular host with photosensitizing centers provides photo-responsive host–guest properties based on its molecular recognition ability. Here, we construct a self-assembled photoactive Ir(III) cage-shaped complex that contains anion binding pockets...

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Cited by 17 publications
(4 citation statements)
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“…Enantiopure C46 cage (a) self-assembly, (b) substrate selectivity of the photocatalytic E – Z isomerization between 111 and 113 by Λ-C46 . (c) Crystal structure of Λ-C46 atoms: C = gray, F = lime green, N = dark blue, P = orange, Ir = navy blue …”
Section: Photoredox Catalysis For the Synthesis Of Complex Moleculesmentioning
confidence: 99%
“…Enantiopure C46 cage (a) self-assembly, (b) substrate selectivity of the photocatalytic E – Z isomerization between 111 and 113 by Λ-C46 . (c) Crystal structure of Λ-C46 atoms: C = gray, F = lime green, N = dark blue, P = orange, Ir = navy blue …”
Section: Photoredox Catalysis For the Synthesis Of Complex Moleculesmentioning
confidence: 99%
“…The Fujita group has developed a cage-based photocatalyst ( Δ/Λ-3 ) using Ir( iii ) as a metal node. 61 The iridium( iii ) complex usually serves as a versatile precursor for this photoresponsive system, yet it is seldom employed as the metal component of the coordinating host. Upon heating a 2 : 3 mixture of 2,4,6-tri(3-pyridyl)benzene and the iridium complex at 60 °C in CD 3 NO 2 , a clear yellow solution was obtained.…”
Section: Application Of Porous Coordination Cages In Photocatalysismentioning
confidence: 99%
“…In nature, the coordination of metal ions with organic substrates has been exploited to create various functional compounds, such as chlorophyll, vitamin B 12 , hemoglobin, etc. Compared to other weak noncovalent interactions, coordination bonds are advantageous in terms of their directionality and predictability. Inspired by nature, chemists have utilized coordination-driven self-assembly strategies to construct discrete architectures from two-dimensional (2D) rings to three-dimensional (3D) cages with precise sizes and shapes, which have applications in areas such as catalysis, cancer treatment, and optical materials; , among these architectures, 2,2′:6′,2″-terpyridine (tpy) as a building block has gained widespread attention owing to its remarkable binding ability to different transition-metal ions. , Compared to 2D rings, 3D nanocages demonstrate promising applications for anion recognition, C 60 encapsulation, and controlled release because of their regular configuration with fixed-size cavities that can selectively encapsulate guest molecules …”
Section: Introductionmentioning
confidence: 99%