Photoinduced Electron‐Transfer Oxidation of Olefins with Molecular Oxygen Sensitized by Tetrasubstituted Dimethoxybenzenes: A Non‐Singlet‐Oxygen Mechanism

α‐Methylstyrene ( 1 ) was photo‐oxidized in the presence of a series of alkylated dimethoxybenzenes as sensitizers in an oxygen‐saturated MeCN solution to afford the cleaved ketone 2 , epoxide 3 , as well as a small amount of the ene product 4 in ca. 1 : 1 : 0.04 ratio. The relative rate of conversion was well‐correlated with the fluorescence quantum yield of sensitizers. Thus, a non‐singlet‐oxygen mechanism is proposed, in which an excited sensitizer is quenched by (ground‐state) molecular oxygen to produce a sensitizer radical cation and a superoxide ion (O), the former of which oxidizes the substrate, while the latter reacts with the resulting olefin radical cation ( 1 ^{+ .}) to give the major oxidation products. Photodurability of such electron‐donating sensitizers is dramatically improved by substituting four aromatic H‐atoms in 1,4‐dimethoxybenzene with Me or fused alkyl groups, which provides us with an environmentally friendly, clean method of photochemical functionalization with molecular oxygen, alternative to the ene reaction via singlet oxygenation.     

以二氰蒽为敏化剂的聚异戊二烯敏化光降解

<正> 近年来,以二氰蒽(DGA)为敏化剂对烯类化合物进行光敏氧化研究颇受重视。Foote等曾对此作过系统工作,他们从热力学、闪光光解以及对氧化产物进行分析等方法确认其间存在着电子转移。最近Steichen等指出:二氰蒽也可做为单线态氧敏化剂在光氧化反应中发挥作用。可以认为二氰蒽作为敏化剂兼有电子转移和能量转移的能     

Low energy light-triggered oxidative cleavage of olefins

A series of substituted olefins were tested for their reactivity with singlet oxygen as a singlet oxygen-mediated cleavable linker. Low intensity light of 200 mW/cm² was irradiated to the solution of an olefin and 5,10,15-triphenyl-20-(4-hydroxyphenyl)-21H,23H-porphyrin under atmospheric condition. Among the tested olefins, 1,2-cis-diphenoxyethylene reacted fast with singlet oxygen, >80% within 15 min yielding a stoichiometric conversion to aldehyde product without any side reactions.     

Photochemistry of A1E, a retinoid with a conjugated pyridinium moiety: competition between pericyclic photooxygenation and pericyclization

The photochemistry of the retinoid analogue A1E shows an oxygen and solvent dependence. Irradiation of A1E with visible light (lambda(irr) = 425 nm) in methanol solutions resulted in pericyclization to form pyridinium terpenoids. Although the quantum yield for this cyclization is low (approximately 10(-4)), nevertheless the photochemical transformation occurs with quantitative chemical yield with remarkable chemoselectivity and diastereoselectivity. Conversely, irradiation of A1E under the same irradiation conditions in air-saturated carbon tetrachloride or deuterated chloroform produced a cyclic 5,8-peroxide as the major product. Deuterium solvent effects, experiments utilizing endoperoxide, phosphorescence, and chemiluminescence quenching studies strongly support the involvement of singlet oxygen in the endoperoxide formation. It is proposed that, upon irradiation, in the presence of oxygen, A1E acts as a sensitizer for generation of singlet oxygen from triplet oxygen present in the solution; the singlet oxygen produced reacts with A1E to produce cyclic peroxide. Thus, the photochemistry of A1E is characterized by two competing reactions, cyclization and peroxide formation. The dominant reaction is determined by the concentration of oxygen, the concentration of A1E, and the lifetime of singlet oxygen in the solvent employed. If the lifetime of singlet oxygen in a given solvent is long enough, then oxidation (peroxide formation) is the major reaction. If the singlet oxygen produced is quenched by the protonated solvent molecules faster than singlet oxygen reacts with A1E, then cyclization dominates.     

9, 10-DICYANOANTHRACENE-SENSITIZED PHOTOOXYGENATION OF α,α'-DIMETHYLSTILBENES. MECHANISM AND KINETICS OF THE COMPETING SINGLET OXYGEN AND ELECTRON TRANSFER PHOTOOXYGENATION REACTIONS

Abstract— The 9, lodicyanoanthracene-sensitized photooxygenation of 2-methyl-2-butene and (+)-limonene proceeds via the singlet oxygen pathway in carbon tetrachloride as well as in acetonitrile, although the fluorescence of the sensitizer in acetonitrile is quenched by these olefins in an electron transfer quenching mechanism. The 9, 10-dicyanoanthracene-sensitized photooxygenation of cis- and trans-ä, ä′-dimethylstilbenes occurs exclusively via the singlet oxygen pathway in carbon tetrachloride; in acetonitrile, however, singlet oxygen and electron transfer photooxygenation reactions compete with one another. Addition of tetra-n-butyl ammonium bromide and increasing oxygen concentrations favor the formation of the singlet oxygen product, whereas addition of anisole, increasing substrate concentrations and decreasing oxygen concentrations favor the electron transfer photooxygenation products. In carbon tetrachloride, exciplexes of the sensitizer and the dimethylstilbenes are formed which give rise to cidrrans-isomerization of the substrates. In acetonitrile, neither exciplex formation nor cisltrans-isomerization are observed. A mechanism is proposed which allows us to calculate product distributions of the competing singlet oxygen/electron transfer photooxygenation reactions and thus to determine the efficiencies with which encounters between the singlet excited sensitizer and the substrates finally result in electron transfer photooxygenation products. Using (I) these efficiencies, (2) the β-value obtained from singlet oxygen photooxygenation sensitized by rose bengal, and (3) the appropriate k-values determined from fluorescence quenching of 9, 10-dicyanoanthracene in MeCN by oxygen and the stilbene, allows the calculation of the quantum yield of oxygen consumption by this stilbene. The quantum yield thus calculated is strictly proportional to the rate of oxygen consumption experimentally obtained; this result is considered as convincing evidence for the mechanism proposed.     

A Tandem Mass Spectrometric Method for Singlet Oxygen Measurement

Singlet oxygen, a harmful reactive oxygen species, can be quantified with the substance 2,2,6,6‐tetramethylpiperidine (TEMP) that reacts with singlet oxygen, forming a stable nitroxyl radical (TEMPO). TEMPO has earlier been quantified with electron paramagnetic resonance (EPR) spectroscopy. In this study, we designed an ultra–high‐performance liquid chromatographic—tandem mass spectrometric (UHPLC‐ESI‐MS/MS) quantification method for TEMPO and showed that the method based on multiple reaction monitoring (MRM) can be used for the measurements of singlet oxygen from both nonbiological and biological samples. Results obtained with both UHPLC‐ESI‐MS/MS and EPR methods suggest that plant thylakoid membranes produce 3.7 × 10^?7 molecules of singlet oxygen per chlorophyll molecule in a second when illuminated with the photosynthetic photon flux density of 2000 μmol m^?2 s^?1.     

Reaction of triarylphosphine radical cations generated from photoinduced electron transfer in the presence of oxygen

[reaction: see text] The 9,10-dicyanoanthracene (DCA)-sensitized photoreaction of triarylphosphines (1) was carried out in acetonitrile under aerobic conditions. Phosphine 1 was oxidized to the corresponding phosphine oxide with no appreciable side reactions. Product analysis and laser flash photolysis experiments suggest that the radical cation of 1 formed by the electron transfer from 1 to DCA in the singlet excited state ((1)DCA) reacts with O(2) to eventually afford the phosphine oxide.     

“Olefin metathesis” reactions of (η5-C5H5)NiRu3(μ-H)(CO)9-(μ4-η2)-(CCHBut) and related complexes

The complex (η⁵-C₅H₅)NiRu₃(μ-H)(CO)₉(μ₄-η²-CCHBu^t) (1a) reacts with olefins to give several organic products, including species derived from the coupling of the vinylidene ligand with an olefin-derived =CRR′ fragment, representing the first example of a (non catalytic) olefin metathesis reaction involving a metal cluster; other complexes structurally or chemically related to the compound 1a have also been treated with olefins and alkynes.     

Kinetics Study on Reaction of Atenolol with Singlet Oxygen by Directly Monitoring the 1O2 Phosphorescence

The pharmaceutically active compound atenolol, a kind of $\beta$-blockers, may result in adverse effects both for human health and ecosystems if it is excreted to the surface water resources. To effectively remove atenolol in the environment, both direct and indirect photodegradation, driven by sunlight play an important role. Among indirect photodegradation, singlet oxygen (¹O₂), as a pivotal reactive species, is likely to determine the fates of atenolol. Nevertheless, the kinetic information on the reaction of atenolol with singlet oxygen has not been well investigated and the reaction rate constant is still ambiguous. Herein, the reaction rate constant of atenolol with singlet oxygen is investigated directly through observing the decay of the ¹O₂ phosphorescence at 1270 nm. It is determined that the reaction rate constant between atenolol and ¹O₂ is 7.0×10⁵ (mol/L)$^{-1}\cdot$s^-1 in D₂O, 8.0×10⁶ (mol/L)$^{-1}\cdot$s^-1 in acetonitrile, and 8.4×10⁵ (mol/L)$^{-1}\cdot$s^-1 in EtOH, respectively. Furthermore, the solvent effects on the title reaction were also investigated. It is revealed that the solvents with strong polarity and weak hydrogen donating ability are suitable to achieve high rate constant values. These kinetics information on the reaction of atenolol with singlet oxygen may provide fundamental knowledge to the indirect photodegradation of $\beta$-blockers.     

Allylic amidation. An investigation of nitrosocarbonylmethane for direct allylic functionalization of olefins

Nitrosocarbonylmethane reacts with a variety of olefins $\text{via}$ an ene pathway, yielding N-substituted hydroxamic acid products in a preparatively useful reaction. With unsymmetrical olefins, observed regiochemical preferences can be rationalized by a mechanism involving electrophilic addition of nitrogen to the olefin.     

Photooxidation of Troglitazone,a New Antidiabetic Drug *

Troglitazone (CS-045) is a new oral antidiabetic drug reported to be effective in insulin-resistant diabetes and to show antihypertensive effects. Photooxidation of troglitazone gave the quinone and quinone epoxide as the major final stable products. An intermediate observed by NMR spectroscopy was shown to be the hydroperoxydi-enone, which is moderately stable at room temperature. The rate constant of singlet oxygen quenching by troglitazone is 2.14 × 10⁸M^?1s^?1 and the reaction rate constant in acetone-d, is 8.64 × 10, M^?1 s^?1. Only the chroman ring of troglitazone reacts with and quenches singlet oxygen significantly, and its reactivity and products are analogous to those of a-tocopherol. The reactivity of CS-045 toward singlet oxygen is much larger than that of the related compounds lacking the chroman ring.     

Photo-oxygenations de composes aromatiques sensibilisees par des accepteurs d'electron

Photo-oxygenation of aromatic compounds sensitized by electron acceptors, like 9-10 dicyanoanthracene (DCA) is shown to proceed by two distinct mechanisms each one beginning by an electron-transfer step: in the first way superoxide ion [O₂^?] is involved and in the second one singlet oxygen [¹O₂^*] is produced according to an unusual process.     

The mechanism of the singlet oxygen ene reaction

A complex between singlet oxygen and olefins is proposed in which frontier orbital interactions between the oxygen and both the olefin π orbitals and C-H bonds are important. Formation of this complex is proposed to dominate the chemistry of this reaction and is shown to be consistent with the available data.     

Photooxygenations par transfert d'electron sensibilisees par le dicyano-9,10 anthracene. Role du solvant et formation d'oxygene singulet.

Photooxygenation of naphtalenic compounds sensitized by electron acceptors like 9,10 dicyanoanthracene (DCA) is shown to proceed by two distinct ways depending on the solvent polarity. In a polar solvent superoxide ion (O₂^-.) as well as singlet oxygen (¹O₂★) are involved while in a non polar solvent only singlet oxygen is produced.     

Studies on reactivity of benzoyl and benzoylperoxy radicals produced by laser flash photolysis of dibenzoyldiazene in aerated solutions

Photolysis of dibenzoyldiazene gives benzoyl radicals. In aerated solutions, the benzoyl radicals react with oxygen to yield benzoylperoxy radicals. Spin trapping studies indicate that 5,5′dimethyl-1-pyrroline N-oxide reacts with the benzoylperoxy radicals to produce the adduct which exhibits ESR parameters, A_N = 13.8 G and A_Hβ = 10.1 G. Laser photolysis studies reveal that the rate constants for the reaction between the benzoyl radical and oxygen are ca. 4 × 10⁹ M^-1 s^-1 in toluene, acetone, and ethyl acetate. The benzoylperoxy radicals undergo one-electron oxidation of tetramethyl-p-phenylenediamine, TMPD, to give an ion pair. The ion pair has an absorption spectrum similar to that of the TMPD cation radical. The formation of the ion pair is detected by monitoring the absorbance change at 600 nm after laser pulsing. From the kinetic studies for the formation of the ion pair in the presence of olefins, the bimolecular rate constants for reactions between several olefins and the benzoylperoxy radical are determined. The electrophilic addition of the benzoylperoxy radicals to olefins is discussed in comparison with the addition reactions of thiyl radicals to olefins. The detection and determination of the dipole moments of both the benzoylperoxy radicals and the ion pair are carried out with the use of the time-resolved microwave dielectric absorption technique. The distance between the positive and negative ions in the ion pair is estimated as 0.20 nm.     

Charge-transfer interactions,exciplex formations and ionic dissociations in singlet oxygen reactions

Intermolecular perturbation and configuration interaction calculations have been carried out to elucidate the attacking modes of singlet molecular oxygen (¹O₂) to allyl olefins and electron-rich olefins, which are classified into four groups from their molecular structures. It is found: (1) that the attacking modes are dependent on the molecular structure of substrates ; (2) that the charge-transfer (CT) interactions between ¹O₂ and substrates are particularly important for the formation of exciplexes through which the ene and (2+2) reactions of ¹O₂ proceed ; and (3) that the CT energy levels are important in governing the fraction of ionic dissociation to produce Superoxide anion and the relative ratio between the (4+2) and (2+2) reactions of ¹O₂ with dienes, heterocycles and related species.     

FTIR, 13C NMR,and GPC analysis of high‐propylene content co‐ and terpolymers with ethylene and higher α‐olefins synthesized with EtInd2ZrCl2/MAO

This article reports the results of propylene/α‐olefin copolymerization and propylene/ethylene/α‐olefin terpolymerization using low concentrations (less than 5 mol %) of long α‐olefins such as 1‐octene, 1‐decene, and 1‐dodecene. Kinetics data are presented and discussed. The highest activity was found with the longest α‐olefin studied (1‐dodecene). A possible explanation is proposed for this and other characteristics of the polymers obtained. The effect of low‐ethylene contents (4 mol % in the gas phase) on the copolymerization of propylene/α‐olefins was also examined. The polymers synthesized were characterized by ¹³C NMR, gel permeation chromatography, DSC, Fourier transform infrared spectroscopy, and wide‐angle X‐ray scattering. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 2005–2018, 2001     

Ozone as an oxygen source for alkene ene-reactions

Summary A strategy was developed which uses the adduct of ozone and triphenyl phosphite as a substitute for photochemically generated singlet oxygen in ene reactions of olefins. The resulting allylic hydroperoxide can be conveniently reduced by a second mole of phosphite to yield the corresponding allylic alcohol. The aryl phosphate produced as the by-product can either be recycled by reduction or used itself as a commodity. As an example, the two key steps of the rose oxide synthesis involving singlet oxygen can thus be reduced to a one pot procedure. With respect to the reaction mechanism, additional arguments for the direct reaction of the olefin with the phosphite ozonide were gathered. A simple decomposition of the ozonide to produce singlet oxygen was made rather unlikely.

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Ozon als Sauerstoffquelle für En-Reaktionen von Olefinen

Zusammenfassung Es wurde eine Strategie zum Ersatz von photochemisch erzeugtem Singlett-Sauerstoff durch das Addukt aus Ozon und Triphenylphosphit zum Einsatz in En-Reaktionen von Olefinen entwickelt. Das entstehende allylische Hydroperoxid kann durch ein zweites Molekül Phosphit einfach zum entsprechenden allylischen Alkolhol reduziert werden. Das als Nebenprodukt entstehende Arylphosphat kann entweder durch Reduktion recycliert oder direkt als Handelsware weiterverwendet werden. Auf diese Weise können zum Beispiel die beiden Stufen der Rosenoxidsynthese, an denen Singlett-Sauerstoff beteiligt ist, zu einer Eintopfreaktion vereinfacht werden. Bezüglich des Reaktionsmechanismus wurden zusätzliche Hinweise auf die direkte Reaktion des Phosphitozonids mit dem Olefin gefunden. Eine Zersetzung des Ozonids unter Bildung von Singlettsauerstoff ist nicht wahrscheinlich.

     

A Remarkable cis‐ and trans‐Spanning Dibenzylidene Acetone Diphosphine Chelating Ligand (dbaphos)

A multidentate and flexible diolefin–diphosphine ligand, based on the dibenzylidene acetone core, namely dbaphos ( 1 ), is reported herein. The ligand adopts an array of different geometries at Pt, Pd and Rh. At Pt^II the dbaphos ligand forms cis‐ and trans‐diphosphine complexes and can be defined as a wide‐angle spanning ligand. ¹H NMR spectroscopic analysis shows that the β‐hydrogen of one olefin moiety interacts with the Pt^II centre (an anagostic interaction), which is supported by DFT calculations. At Pd⁰ and Rh^I, the dbaphos ligand exhibits both olefin and phosphine interactions with the metal centres. The Pd⁰ complex of dbaphos is dinuclear, with bridging diphosphines. The complex exhibits the coordination of one olefin moiety, which is in dynamic exchange (intramolecular) with the other “free” olefin. The Pd⁰ complex of dbaphos reacts with iodobenzene to afford trans‐[Pd^II(dbaphos)I(Ph)]. In the case of Rh^I, dbaphos coordinates to form a structure in which the phosphine and olefin moieties occupy both axial and equatorial sites, which stands in contrast to a related bidentate olefin, phosphine ligand (“Lei” ligand), in which the olefins occupy the equatorial sites and phosphines the axial sites, exclusively.