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1.
An unusual infrared chemiluminescence emission (8130Å) of methylene blue, and other thiazine dyes, sensitized by singlet molecular oxygen is reported. This chemiluminescence does not correspond to the ordinary fluorescence of the dye and cannot be explained by previously proposed mechanisms for singlet oxygen sensitized emissions of dyes. From energetic considerations singlet molecular oxygen in its 1Σg+ state is postulated as the sensitizing agent for the thiazine dye chemiluminescences. Schemes in which 1Σg+ oxygen transfers electronic excitation energy (a) to the lowest triplet state of the dye, (b) to a combined multiplicity state of the lowest triplet state of the dye, and triplet molecular oxygen, or (c) to a charge-transfer state between the dye and oxygen, are compared. The chemiluminescence of methylene blue in aqueous solution may be used as a luminescent probe for 1Σg+ oxygen.  相似文献   

2.
Abstract— The aerobic xanthine oxidase reaction causes the co-oxidation of 2,5-dimethylfuran to cis-diacetylethylene and the bleaching of rubrene tetracarboxylate. These actions were suppressed by superoxide dismutase, catalase, desferoxamine and by benzoate and other hydroxyl radical scavengers. The bleaching of rubrene tetracarboxylate was not enhanced in D20. These results suggest that OHv, generated from O2- plus H2O2 by an iron-catalyzed Haber Weiss reaction, was the responsible agent and that singlet oxygen was not detectably involved. Control experiments, in which singlet oxygen was generated photochemically, demonstrated that replacement of H2O by D2O caused the expected enhancement of the chemical reactivity of singlet oxygen under the conditions of these experiments and that O2-, at concentrations achieved by the xanthine oxidase reaction, did not detectably quench singlet oxygen. We conclude that singlet oxygen, if produced at all during the aerobic xanthine oxidase reaction, cannot exceed 0.1% of the production of O2-.  相似文献   

3.
Here, we report an experimental study of the effect of toxic metal ions on photosensitized singlet oxygen generation for photodegradation of PAH derivatives, Anthracene‐9,10‐dipropionic acid disodium salt (ADPA) and 1,5‐dihydroxynapthalene (DHN) and photoinactivation of Escherichia coli bacteria by using cationic meso‐tetra(N‐methyl‐4‐pyridyl)porphine tetrachloride (TMPyP) as a singlet oxygen photosensitizer. Three s‐block metals ions, such as Na+, K+ and Ca2+ and five toxic metals such as Cd2+, Cu2+, Hg2+, Zn2+ and Pb2+ were studied. The s‐block metal ions showed no change in the rate of photodegradation of ADPA or DHN by TMPyP, whereas a dramatic change in the photodegradation of ADPA and DHN was observed in the presence of toxic metals. The maximum photodegradation rate constants of ADPA and DHN were observed for Cd2+ ions [(3.91 ± 0.20) × 10?3 s?1 and (7.18 ± 0.35) × 10?4 s?1, respectively]. Strikingly, the photodegradation of ADPA and DHN was almost completely inhibited in the presence of Hg2+ ions and Cu2+ ions. A complete inhibition of growth of E. coli was observed upon visible light irradiation of E. coli solutions with TMPyP and toxic metal ions particularly, Cd2+, Hg2+, Zn2+ and Pb2+ ions, except for Cu2+ ions where a significantly slow inhibition of E. coli's growth was observed.  相似文献   

4.
We developed the detection apparatus that equipped with the two-photomultiplier tubes for chemiluminescence from singlet oxygen. Singlet oxygen was generated with reaction between sodium hypochlorite and hydrogen peroxide. The chemiluminescence from singlet oxygen, the dimol light emission (ca. 634 nm) and the monomol light emission (ca. 1270 nm), was observed simultaneously for the same reaction cell. The effects of sodium azide as an antioxidant, human serum albumin, and α-amino acids on the chemiluminescence based on the both emissions were examined; the observed chemiluminescence could provide direct information with regard to the reaction between singlet oxygen and antioxidant/biomolecules. The apparent rate constants for quenching singlet oxygen in the presence of human serum albumin were calculated to be ca. 3.3 × 109 and ca. 8.8 × 108 M−1 s−1 for the dimol and monomol light emissions, respectively, under the present conditions. The chemiluminescence intensities of the dimol emission decreased in the presence of His, Asp, Phe, Ser, and Tyr, and that of the monomol decreased in the presence of Cys and Trp. The chemiluminescence observed in the presence of biomolcules was discussed together with the reactivities of sodium hypochlorite and hydrogen peroxide to biomolecules.  相似文献   

5.
The yield of singlet oxygen (1О2) in the decomposition of a number of hydrotrioxides of alcohols (cyclobutanol, cyclopentanol, cyclohexanol, cycloheptanol, cyclooctanol, L-menthol, 1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol, 1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol, heptan-4-ol, propanol-2, and 1-cyclopropylethanol) has been determined using the IR chemiluminescence technique. It has been shown that cyclopentanol, 1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol and 1-cyclopropylethanol hydrotrioxides are efficient sources of singlet oxygen; the yield of 1О2 reaches up to 58%.  相似文献   

6.
A diblock copolymer (P98N100) composed of a biocompatible water‐soluble block (PMPC) and a lower critical solution temperature (LCST) type thermo‐responsive block (PNIPAM) was prepared via controlled radical polymerization. To dissolve fullerene (C60) in water, the C60/P98N100 complex was prepared by mixing C60 and P98N100 powders. The maximum solubilized C60 concentration in water was 1.39 g/L, as estimated from UV–vis adsorption, when the polymer concentration was 5.0 g/L. The percent transmittance of the aqueous solution of the C60/P98N100 complex decreased above 36 °C due to inter‐complex association above the LCST for the PNIPAM block. While the hydrodynamic radius of C60/P98N100 complex was 135 nm at 20 °C, it increased to 161 nm at 50 °C. Despite the observation of 1H NMR signals from PMPC and PNIPAM blocks for the C60/P98N100 complex in D2O at room temperature, the signals from PNIPAM disappeared above 35 °C due to restricted motion of PNIPAM. Generation of singlet oxygen (1O2) from the C60/P98N100 complex by photo‐irradiation was confirmed using 9,10‐anthracene dipropionic acid (ADPA). The absorbance of ADPA decreased with increasing irradiation time due to oxidation of ADPA by 1O2. It is expected that the C60/P98N100 complex can be applied as a thermo‐responsive carrier for photodynamic therapy. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 2432–2439  相似文献   

7.
Horseradish peroxidase catalyzes the aerobic oxidation of 2-phenylpropanal and diphenylacetaldehyde at physiological pH to yield acetophenone and benzophenone partly in the triplet state, respectively. These excited products plus formic acid are expected from the thermolysis of dioxetane intermediates. The presence of acetophenone was demonstrated spectrophotometr-ically and the chemiluminescence spectrum (δmax - 430 nm) was consistent with its triplet state. Energy transfer to 9,10-dibromoanthracene-2-sulfonate ion, a triplet carbonyl counter, but not to anthracene-2-sulfonate ion, a singlet carbonyl acceptor, occurred, confirming the triplet nature of the main emitter. In the case of the diphenylacetaldehydelperoxidase system, benzophenone could also be detected spectrophotometrically but the corresponding chemiluminescence spectrum showed only red emission (δmax - 630 nm), which was tentatively attributed to singlet oxygen formed by triplet-triplet energy transfer to ground state oxygen. Horseradish peroxidase can be replaced by other he-meproteins such as myoglobin, hemoglobin and micro-peroxidase as catalyst of the chemiluminescent reaction. The distinct emission spectra achieved with different hemeproteins suggest a role of the microenvi-ronment in totally or partly protecting the excited species from oxygen collisions, resulting in emission maxima around 430 nm, 630 nm or both.  相似文献   

8.
Abstract— Photo-irradiation of aqueous basic solutions of soil humic acids and synthetic melanins with UV and visible light (Λ > 320 nm) under oxygen or nitrogen atmospheres generates electronic exicted states and radicals. These processes give rise to a long-lived chemiluminescence with emission maxima at 480–500, 570 and 615–650 nm, as well as a paramagnetic resonance (EPR) signal with g-value at 2.006 and ΔH~ 3Gs. Chemiluminescence intensity and EPR signals follow multistep kinetics. An increase of the ratio of OD at 260/400 nm and 400/600 nm and a decrease of amplitude of an EPR signal after prolonged photo-irradiation were observed. Long irradiation also causes a decrease of fluorescence intensity bands with maxima at 535 nm and 495 nm (Λex 480 and 400 nm, respectively), and an increase of the short wavelength band with a maximum at 450 nm (Λex 260 nm). The data indicate that a complex chain of reactions initiated by reactive species leads to the degradation of the aromatic core of the polymers. Oxygen efficiently enhances the chemiluminescence intensity and the rate of photodegradation. The mechanism of photodegradative oxidation and chemiluminescence probably involves an energy transfer process and singlet oxygen formation. The possibility of its occurrence in nature and its significance are discussed.  相似文献   

9.
A new tetrathiafulvalene-anthracene dyad 1 with two “tetraethylene glycol” units was synthesized and characterized. Strong chemiluminescence was observed upon reaction of dyad 1 with singlet oxygen (1O2), and this reaction shows fairly good selectivity toward 1O2 over other reactive oxygen species. Due to the introduction of two hydrophilic “tetraethylene glycol” units, the detection of 1O2 with dyad 1 can be performed in alcohol/water solution, which is relatively a mild medium when compared with water/tetrahydrofuran solution required by other tetrathiafulvalene-anthracene dyads. Dyad 1 may have a wider use for detection of 1O2 in biological systems.  相似文献   

10.
The reactions of singlet molecular oxygen (O21Δg) with a series of organic compounds have been studied in the gas phase at 298°K. The concentration of singlet molecular oxygen was determined by titration with 2,5-dimethylfuran. The titration technique was checked using a photoionization technique. Absolute rate constants were measured on the basis of the loss of organic reactant and, in some cases, of singlet molecular oxygen. It was found that the usual method of producing singlet molecular oxygen in the gas phase can also, under some conditions, allow reactive species other than singlet molecular oxygen to enter the reactor, leading to serious errors in the determination of rate constants. This problem was eliminated by carrying out the rate measurements in the presence of a small amount of nitrogen dioxide a radical scavenger.  相似文献   

11.
夏文生  张达  翁维正  万惠霖 《催化学报》2013,34(11):2130-2137
采用密度泛函理论方法考察了La-O团簇上超氧物种与过氧物种间转化的连接途径. 单重态下, 团簇上单个超氧物种可通过一系列臭氧物种转化为过氧物种, 且转化能垒较高;三重态下, 单个超氧物种则并无与过氧物种间连接的途径. 然而, La-O团簇上两超氧物种间的相互作用及其转化也具单重态和三重态两条途径. 三重态下, 超氧物种可很容易地转化为过氧物种(O2- + O2-↔O22- + O2), 超氧物种与过氧物种处于快速的交换状态之中;单重态下, 超氧物种转化为过氧物种则需较高的活化能垒, 表明在单重态下这些氧物种具有较高的稳定性.  相似文献   

12.
Traditional photodynamic therapy (PDT) is dependent on externally applied light and oxygen, and the depth of penetration of these factors can be insufficient for the treatment of deep infections. The short half-life and short diffusion distance of reactive oxygen species (ROS) also limit the antibacterial efficiency of PDT. Herein, we designed a targeting singlet oxygen delivery system, CARG-Py, for irradiation-free and oxygen-free PDT. This system was converted to the “singlet oxygen battery” CARG-1O2 and released singlet oxygen without external irradiation or oxygen. CARG-1O2 is composed of pyridones coupled to a targeting peptide that improves the utilization of singlet oxygen in deep multidrug-resistant bacterial infections. CARG-1O2 was shown to damage DNA, protein, and membranes by increasing the level of reactive oxygen inside bacteria; the attacking of multiple biomolecular sites caused the death of methicillin-resistant Staphylococcus aureus (MRSA). An in vivo study in a MRSA-infected mouse model of pneumonia demonstrated the potential of CARG-1O2 for the efficient treatment of deep infections. This work provides a new strategy to improve traditional PDT for irradiation- and oxygen-free treatment of deep infections while improving convenience of PDT.  相似文献   

13.
It was found that irradiation of the solution of 4,4"-diazidodiphenyl in ethyl alcohol with UV-light at a wavelength longer than 280 nm in the presence of dissolved oxygen resulted in appearance of post-luminescence. The luminescence intensity increases with increasing the oxygen concentration; the luminescence virtually disappears after purging the solution with argon. The observed emission of light was attributed to chemiluminescence of the products of photooxidation of 4,4"-diazidodiphenyl. The rate dependence of the afterglow shows two maxima. The first is observed immediately after cessation of the UV irradiation of the solution and its transfer to a photometric cell. The intensity of the corresponding chemiluminescence decreases by an exponential law with e= 5 s. The second maximum appears after a certain time interval after the first one. Addition of a triplet sensitizer (Michler's ketone) to the reaction mixture results in quenching of the chemiluminescence from the photooxidation products, whereas the addition of substances that stabilize electrophilic species in the singlet state leads to an increase in the chemiluminescence intensity. It was suggested that the chemiluminescence resulted from reactions involving the singlet nitrene adduct with oxygen.  相似文献   

14.
The quantum yields of singlet oxygen formation (ØΔ) by the quenching of triplet states of organic sensitizers are measured at various concentrations of the sensitizers by using the time-resolved thermal lens method. Above a certain concentration, ØΔ is independent of the sensitizer concentration. Below the threshold, ØΔ gradually decreases as the concentration of the sensitizer decreases. The extrapolation of ØΔ to zero concentration indicates that singlet oxygen formation is not necessarily dominant in the quenching process even for the 3ππ* state in benzene.  相似文献   

15.
The purple bridged bimetallic complex [CH3N(PF2)2]3Co2(CO)2 undergoes successive chemically and electrochemically reversible one-electron reductions to the corresponding green radical anion and pale-yellow dianion. The radical anion is relatively unreactive towards oxygen and methyl iodide. The dianion is not only reactive towards oxygen and methyl iodide but also captures small positively charged species (e.g. Li+ and H+) with significant alteration of its chemical properties.  相似文献   

16.
The spectroscopy and photophysics of the photosensitizer hypericin when in homogeneous solutions and when bound to liposomes were studied. Hypericin was found to partition efficiently into DMPC liposomes, with a binding constant of 58 (mg lipid/mL)?1. In these liposomes the singlet oxygen production quantum yield was 0.43 ± 0.09. To determine the deactivation constant of singlet oxygen in lipid bilayers for the first time, we calculated extrapolated values from its quenching by DMPC and lecithin in homogeneous solutions and obtained decay times of 36.4 and 12.2 μs, respectively. We also measured the quenching of singlet oxygen, sensitized by hypericin in DMPC liposomes, by NaN3, diphenyl isobenzofuran and H2,O: D2O mixtures and explained the results on the basis of singlet oxygen diffusing rapidly out of the lipid bilayer into the aqueous medium. The observed temperature effect on the lifetime of singlet oxygen of about 50% over a 15°C range in liposome suspension contrasts with a 3% change in a homogeneous solution in 1-nonanol and is explained by the temperature effect on the diffusion out of the liposome. A strong pH effect was observed, indicating that the deprotonated species formed above about pH 10 is a much weaker photosensitizer of singlet oxygen than the native, protonated species.  相似文献   

17.
The rates of accumulation of oxygen-containing species in photooxidation have been determined for a series of polymers such as polystyrene, polyisoprene, and polybutadiene in a wide range of singlet oxygen stationary concentrations in the polymers. An increase in singlet oxygen (1O2) concentration was achieved by introducing a dye which is a 1O2 donor into a polymer and by irradiating a sample with an additional source of light absorbed by the dye only. To decrease 1O2 concentration, 1,2,5-trimethyl-4-hydroxyphenylpiperidine, which is a quencher of 1O2, was introduced into a sample. The 1O2 stationary concentration in an oxidized polymer was measured via singlet oxygen oxidation of 2,2,6,6-tetramethyl-4-oxypiperidine which leads to the formation of the corresponding nitroxyl radical. The photooxidation rate has been found to vary only slightly with 1O2 concentration, even when the concentration changes 10–25-fold. Thus, 1O2 does not participate appreciably in the process of polymer photooxidation. It may be due to the lowering of 1O2 reactivity toward unsaturated groups in the polymer matrix as compared with that in solution.  相似文献   

18.
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.  相似文献   

19.
Dendrimers with a C60 core have been obtained by cyclization of dendritic bis-malonate derivatives at the carbon sphere. The resulting bis-methanofullerene derivatives have been characterised by electrospray (ES) and/or MALDI-TOF mass spectrometries. UV-VIS absorption spectra, fluorescence spectra, and fullerene singlet excited state lifetimes have been determined in solvents of different polarity (toluene, dichloromethane, acetonitrile). These data suggest a tighter core/periphery contact upon increase of solvent polarity and dendrimer size. In all the investigated solvents, the fullerene triplet lifetimes are steadily increased with the dendrimer volume, reflecting lower diffusion rates of O2 inside the dendrimers along the series. Measurements of quantum yields of singlet oxygen sensitization indicate that longer lived triplet states generate lower amounts of singlet oxygen (1O2) in dichloromethane but not in apolar toluene suggesting a tighter contact between the dendritic branches and the fullerene core in CH2Cl2. In acetonitrile, the trend in singlet oxygen production is peculiar. Effectively, enhanced singlet oxygen production is monitored for the largest dendrimer. This reflects specific interactions of excited 1O2 molecules with the dendritic wedges, as probed by singlet oxygen lifetime measurements, possibly as a consequence of trapping effects.  相似文献   

20.
The triplet state of ergosterol (provitamin D2) has been produced in benzene by pulse radiolysis and characterised in terms of absorption spectrum, lifetime, self-quenching properties and relaxed triplet energy. The amount of singlet oxygen, O2(1Δg), produced as a consequence of the oxygen quenching of this species has been determined by kinetic infrared emission spectroscopy. Ergosterol is significantly more efficient as a singlet oxygen sensitiser in benzene than is naphthalene, the absolute standard employed in this work.  相似文献   

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