Tris(2,2'-bipyridine)ruthenium(2+)-mediated photoreduction of olefins with 1-benzyl-1,4-dihydronicotinamide: a mechanistic probe for electron-transfer reactions of NAD(P)H-model compounds
“…All these examples provided important early evidence that various dyes can function as remarkable accelerators of some lightinduced reductions. Another type of transformations photosensitized by [Ru(bpy) 3 ] 2+ have been independently discovered by the group of Pac (Scheme 4) 19,20 . In their work, Pac et al studied reactions of various olefins with 1-benzyl-1,4-dihydronicotinamide (BNAH) as an NADH model.…”
Section: Early Examples From the 1970s To 1990smentioning
confidence: 99%
“…The reaction course was found to be governed by the structural parameters 19,20 ) of the used carbonyl compound. Thus, di-2-pyridylketone (17) led to the alcohol 18 together with a dimeric dihydronicotinamide structure 10, whereas benzaldehyde was converted to a secondary alcohol 19 in high 21,22 ) yield.…”
Section: Early Examples From the 1970s To 1990smentioning
Reactions triggered by light constitute a treasure trove of unique synthetic methods that are available to chemists. Photoinduced redox processes using visible light in conjunction with sensitizing dyes offer a great variety of catalytic transformations useful in the realm of organic synthesis. The recent literature amply shows that this preparative toolbox is expanding substantially. This review discusses historical and contemporary work in the area of photoredox catalysis with [Ru(bpy)3]2+. Elegant examples from the most recent literature document the importance of this fast developing area of research. The photoredox chemistry has also emerged as a promising bond-making and bond-breaking tool for chemical biology and materials chemistry. A review with 96 references.
“…All these examples provided important early evidence that various dyes can function as remarkable accelerators of some lightinduced reductions. Another type of transformations photosensitized by [Ru(bpy) 3 ] 2+ have been independently discovered by the group of Pac (Scheme 4) 19,20 . In their work, Pac et al studied reactions of various olefins with 1-benzyl-1,4-dihydronicotinamide (BNAH) as an NADH model.…”
Section: Early Examples From the 1970s To 1990smentioning
confidence: 99%
“…The reaction course was found to be governed by the structural parameters 19,20 ) of the used carbonyl compound. Thus, di-2-pyridylketone (17) led to the alcohol 18 together with a dimeric dihydronicotinamide structure 10, whereas benzaldehyde was converted to a secondary alcohol 19 in high 21,22 ) yield.…”
Section: Early Examples From the 1970s To 1990smentioning
Reactions triggered by light constitute a treasure trove of unique synthetic methods that are available to chemists. Photoinduced redox processes using visible light in conjunction with sensitizing dyes offer a great variety of catalytic transformations useful in the realm of organic synthesis. The recent literature amply shows that this preparative toolbox is expanding substantially. This review discusses historical and contemporary work in the area of photoredox catalysis with [Ru(bpy)3]2+. Elegant examples from the most recent literature document the importance of this fast developing area of research. The photoredox chemistry has also emerged as a promising bond-making and bond-breaking tool for chemical biology and materials chemistry. A review with 96 references.
“…Both MOFs were tested for photocatalytic CO2 reduction under visible light irradiation. The reaction was conducted in 5 mL of a mixed solution of 4:1 (v/v) acetonitrile (MeCN)-triethanolamine (TEOA, as a sacrificial base), and 0.1 M 1-benzyl-1,4-dihydronicotinamide (BNAH, as a sacrificial reductant) [27][28][29]. The suspension, which contained 5 mg of MOF, was purged with 1 bar of CO2 gas for 30 min followed by light irradiation by a 300 W Xe lamp.…”
Postsynthetic exchange (PSE) of Ti(IV) into a Zr(IV)-based MOF enabled photocatalytic CO2 reduction to HCOOH under visible light irradiation with the aid of BNAH and TEOA. Use of a mixed-ligand strategy enhanced the photocatalytic activity of the MOF by introducing new energy levels in the band structure of the MOF.
“…The other common sensitization mechanism involves electron transfer between photoexcited M and ground-state substrate. In the exam ple outlined in Scheme 15 (46,47), visible-light irradiation of the photosensitizer Ru(bipy) 3…”
Section: (Prophos Is 13-bis(diphenylphosphino)propane) (45)mentioning
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