THE PHOTOLYSIS OF TRYPTOPHAN WITH 337.1 nm LASER RADIATION

Abstract— Aqueous solutions of L-tryptophan were photolyzed by exposure to 337.1 nm radiation from a pulsed nitrogen laser. These data were compared with results for the 290 nm conventional-source photolysis of tryptophan. The progress of photolysis was monitored by fluorescence analysis of tryptophan. UV absorption spectroscopy, HPLC, TLC, and proton NMR spectroscopy. The loss of Trp was observed to be first order for 290 nm photolysis but of mixed order for 337.1 nm photolysis. Five photolysis products were detected by TLC analysis, including: N-formylkynurenine. kynurenine, tryptamine (detected after 290 nm photolysis but not 337.1 nm photolysis) and two unknown products. The tryptophan-containing peptides N-acetyl-tryptophanamide (NATA) and tryptophylglycine (Trp-Gly) were also observed to photolyze upon 337.1 nm laser radiation demonstrating that this phenomenon is not restricted to free tryptophan monomer.
Since Trp is not ordinarily thought to absorb U V radiation at wavelengths as long as 337.1 nm. a number of experiments were performed in an effort to determine the mechanism of photolysis at this wavelength. Evidence is presented which indicates that the 337.1 nm laser photolysis of Trp does not result from two photon absorption, dielectric breakdown, or other laser-specific processes. Instead. it is concluded that this photolysis results either from a very weak absorption tail extending to 337.1 nm in tryptophan itself or from a reaction involving an impurity sensitizer which absorbs the 337.1 nm radiation. The sensitizing impurity. if present, could not. however, be removed by preparative HPLC and could not be detected by TLC or fluorescence analysis.     

Significance of water quality and radiation wavelength for UV photolysis of PhCs in simulated mixed solutions

Ultraviolet (UV) photolysis of sixteen pharmaceutical compounds (PhCs) in mixed solutions with four types of water and two sets of UV radiation was investigated. UVC (254 nm) photolysis was ineffective at eliminating a large number of PhCs while a big number of them were refractory. However, vacuum UV (VUV: 185 nm + 254 nm) photolysis in the same experimental conditions eliminated the PhCs almost completely. The eliminations in ultrapure water (UPW), tap water (TW) and Neya River water (NRW) and their organic/inorganic contents were inversely correlated, which was more evident in VUV photolysis. Natural organic matter (NOM) in NRW did not have an impact in indirect photolysis, but effluent organic matter (EfOM) in secondary-treated effluent (NWTPE) enhanced indirect photolysis, which was more evident in VUV photolysis underlining the point that radiation wavelength/intensity can be a limiting factor in organic-rich waters. Moreover, VUV photolysis was far superior (90% mineralization) to UVC photolysis (10% mineralization) for PhCs mineralization. The greatly enhanced elimination and mineralization efficiencies observed for VUV photolysis were attributed to accelerated direct photolysis with 185 nm wavelength and indirect photolysis involving ^·OH. The results demonstrated efficacy of VUV photolysis in wastewater treatment and its potential use as a tertiary treatment.      

The laser two-photon photolysis of liquid carbon tetrachloride

The two-photon photolysis of liquid CCl4 with 25 ps pulses of 266 nm light has been studied and compared with similar studies with high energy radiation. Both neutral and ionic species are produced from excited states and ionization. The emphasis of the study is on the ionic processes, while some data related to excited states and free radicals are presented. In both radiolysis and photolysis, a solvent separated charged pair, CCl3+ // Cl-, exhibiting a lambda(max) at 475 nm, is observed that exhibits a total growth over 38 to 100 ps. Solutes with ionization potentials less than that of CCl4 (11.47 eV) reduce the yield of the 475 nm species producing radical cations of the solute. The efficiency of this process is about 10-fold larger in radiolysis compared with photolysis. Analysis of the data suggest that the lower energy of two-photon photolysis produces a charge pair CCl4+ // CCl4-, which decays in about 3 ps to CCl4+ // Cl-. This species then decays to CCl3+ // Cl-. The lifetime of the growth of the 475 nm is measured as 46 ps. These studies clearly show areas where radiolysis and photolysis can be quite similar and also areas where the vast difference in excitation energy introduces stark differences in the observed radiation and photoinduced chemistry.     

Megawatt infrared laser photochemistry of ketene

Multiphoton laser-induced decomposition is reported here for photolysis ketene with 9.260 μm radiation from a pulsed CO₂ TEA laser. Chemical end products of this photolysis were primarily H₂ and CO. Visible chemiluminescence, attributed to C₂ Swan band emission, was observed during the first ≈ 1 μs following photolysis. A collision-assisted dissociation, followed by rephotolysis of the transient products, is proposed to account for the results.     

The photolysis of trans-3,4-dimethylcyclopentanone. II. Short Wavelengths

The photolysis of trans-3,4-dimethylcyclopentanone has been investigated in the gas phase at 100°C using light of 206 and 193 nm. The photolytic products are propene, 1,2-dimethylcyclobutane, and the butene isomers. Small quantities of 3,4-dimethylpent-4-enal were also detected. Relative yields of these products were determined as a function of the ketone pressure and also of that of added nitrogen. A mechanism for the photochemical decomposition based on that suggested for the photolysis of cyclopentanone using short wavelength radiation, is consistent with the experimental results and is simpler than that required to account for the long wavelength photolysis reported earlier.     

Photochemical oxidation of persistent cyanide-related compounds

Russian Journal of Physical Chemistry A - Kinetic regularities of the photolysis of thiocyanate solutions using of mono- and polychromatic UV radiation sources with different spectral ranges are...     

Role of ionic defects in photolysis of lithium hydride

Kinetic parameters of photoconductivity and dark conductivity of lithium hydride under uv irradiation have been investigated. A kinetic scheme of lithium hydride photolysis is suggested. Kinetic features of hydrogen evolution under uv irradiation of lithium hydride are explained. The contributions of radiation induced defects and equilibrium cation vacancies to processes leading to gas evolution under photolysis are determined.     

Ultraviolet Photolysis and Ortho-Phthalaldehyde-Mercaptoethanol Derivatization of Pharmaceuticals for Enhanced Fluorescence Detection in HPLC

Abstract

Several classes of nitrogenous pharmaceutical were examined for fluorescence after ultraviolet (UV) radiation induced photolysis followed by reaction with o-phthalaldehyde-2-mercaptoethanol (OPA-MERC), and after UV photolysis alone. Photolyses were examined in water, mixtures of methanol/water (1:1), and acetonitrile/water (1:1). Acetone was assessed as a photosensitizer to enhance photolysis and fluorescence response. Flow injection analysis and high-performance liquid chromatographic techniques were used for several pharmaceuticals. The analytes were subjected to UV photolysis and reaction with OPA-MERC reagent for generation of fluorophores that responded to fluorescence detection. During photolysis, solvent type as well as the presence of photosensitizers seem to play a significant role in the formation of primary amines and fluorophores. Photochemical transformation products of some of the pharmaceutical chemicals are proposed. Analytical figures of merit were determined for some analytes. This fluorescence detection approach is applicable for a number of pharmaceuticals at nanogram level.     

THE EFFECT OF pH ON THE AEROBIC and ANAEROBIC PHOTOLYSIS OF TRYPTOPHAN AND SOME TRYPTOPHAN-CONTAINING DIPEPTIDES

Abstract— Rates of photolysis, quantum yields of fluorescence, and fluorescence emission maxima for the dipeptides glycyltryptophan (Gly-Trp) and tryptophylglycine (Trp-Gly) and for free tryptophan (Trp) were determined under both degassed and aerated conditions in the pH range 4.5-10.0. The photolyses were performed at 25°C using 290 nm radiation from a 1000 W xenon lamp. Photolysis rates were determined by monitoring tryptophan fluorescence loss with time. It was found that Trp-Gly and free Trp showed similar behavior in that their fluorescence quantum yields and photolysis rates increased significantly above neutral pH. In contrast, the Gly-Trp fluorescence yield was smaller than that of Trp or Trp-Gly, showing no significant increase at high pH and the photolysis rate for Gly-Trp decreased with increasing pH. In comparing aerated to degassed samples, it was found that degassing had a far greater effect on the photolysis rates of Trp and Trp-Gly than on the photolysis rate of Gly-Trp especially at higher pH. But, degassing did not change the relative fluorescence quantum yields or fluorescence emission maxima of any of the three compounds. Possible mechanisms for photolysis under various experimental conditions were examined in light of the data.     

Synthesis of charged phenyl radicals and biradicals by laser photolysis in a Fourier-transform ion cyclotron resonance mass spectrometer

The feasibility of generating substituted phenyl radicals and biradicals (with a charged substituent) in the gas phase by laser photolysis was examined by using a Fourier-transform ion cyclotron resonance mass spectrometer. The precursors were generated by ipso-substitution of a halogen atom in the radical cation of a di- or trihalobenzene by various nucleophiles. Photolytic cleavage of the remaining carbon-halogen bond(s) with 266-nm radiation was found to produce many substituted phenyl radicals in greater yields than the earlier employed method, sustained off-resonance irradiated collision-activated dissociation (SORI-CAD). Furthermore, ion generation by photolysis leads to isomerization less often than collisional activation. Finally, not only phenyl-bromine and phenyl-iodine but also certain phenyl-chlorine bonds can be cleaved by photolysis, whereas the synthetic utility of SORI-CAD appears to be largely limited to the cleavage of phenyl-iodine bonds. Hence, laser photolysis greatly expands the variety of substituted phenyl radicals and biradicals that can be synthesized inside a mass spectrometer.     

THE VACUUM ULTRAVIOLET PHOTOCHEMISTRY OF NUCLEOTIDES

Abstract— Photodestruction of nucleotides by vacuum UV (λ < 200 nm) and near UV radiation in thin films has been studied; the products were analyzed by thin-layer chromatography. Vacuum UV photolysis leads to the rupture of the N-glycosidic bond with liberation of bases, the quantum yield of the process being about 2 × 10^-4 for guanosine-5'-monophosphate. No bases have been found among the products of near UV photolysis.
Vacuum UV irradiation of aqueous solutions of adenosine-5'-monophosphate and guanosine-5'-monophosphate produces, along with bases, some other fluorescent substances. The identity of photoproducts of vacuum UV photolysis with those of γ-radiolysis is established. The mechanism of photochemical conversion is discussed.     

PHOTOLYSIS AND RADIOLYSIS OF NITROMETHANE AND NITROETHANE

Abstract— Prolonged photolysis of nitromethane and nitroethane in liquid and vapour phases, with simultaneous photolysis of the nitrogen dioxide formed, was studied in the absence and presence of cupric oxide. A high-pressure quartz immersion lamp providing the full range of visible and u.v. spectrum, with a high output of radiation at 366 and 313 mμ, was employed as source of light. The products of photolysis were detected by microanalytical methods, infrared-absorption spectrum analysis and gas chromatography. Photolysis of liquid nitro-alkanes resulted in formation of many compounds; saturated hydrocarbons, and in the case of nitroethane, ethylene, were submitted to detailed examination. Photolysis in the vapour phase was carried out in a specially designed glass apparatus. The main products were nitrogen dioxide, aldehydes and polyaldehydes; hydrocarbons were not estimated.
Liquid nitromethane and nitroethane were also irradiated with γ-rays from a ⁶⁰Co source. The radiolysis products were similiar to those obtained on photolysis. The mechanism of photolytic decomposition of nitroalkanes is proposed and discussed.     

Solid-state photochromism and photoreactivity of o- and p-anisaldehydes. Remarkable stabilization of o-xylylenols

[reaction: see text] All of the crystalline o-anisaldehyde derivatives 1 and 3 change to brick-red color upon brief exposure to UV-vis radiation. The red color, attributed to (E)-xylylenol, is remarkably persistent for hours (ca. 10 h) in the case of 1c; such a long lifetime for the reactive o-xylylenols is unprecedented. In contrast, the p-anisaldehydes 2 undergo cyclization. Solid-state photolysis of 2b affords the benzocyclobutenol 7b regioselectively, which is not accessible from solution-phase photolysis.     

Photolytic processing of secondary organic aerosols dissolved in cloud droplets

The effect of UV irradiation on the molecular composition of aqueous extracts of secondary organic aerosol (SOA) was investigated. SOA was prepared by the dark reaction of ozone and d-limonene at 0.05-1 ppm precursor concentrations and collected with a particle-into-liquid sampler (PILS). The PILS extracts were photolyzed by 300-400 nm radiation for up to 24 h. Water-soluble SOA constituents were analyzed using high-resolution electrospray ionization mass spectrometry (HR-ESI-MS) at different stages of photolysis for all SOA precursor concentrations. Exposure to UV radiation increased the average O/C ratio and decreased the average double bond equivalent (DBE) of the dissolved SOA compounds. Oligomeric compounds were significantly decreased by photolysis relative to the monomeric compounds. Direct pH measurements showed that acidic compounds increased in abundance upon photolysis. Methanol reactivity analysis revealed significant photodissociation of molecules containing carbonyl groups and the formation of carboxylic acids. Aldehydes, such as limononaldehyde, were almost completely removed. The removal of carbonyls was further confirmed by the UV/Vis absorption spectroscopy of the SOA extracts where the absorbance in the carbonyl n→π* band decreased significantly upon photolysis. The effective quantum yield (the number of carbonyls destroyed per photon absorbed) was estimated as ～0.03. The total concentration of peroxides did not change significantly during photolysis as quantified with an iodometric test. Although organic peroxides were photolyzed, the likely end products of photolysis were smaller peroxides, including hydrogen peroxide, resulting in a no net change in the peroxide content. Photolysis of dry limonene SOA deposited on substrates was investigated in a separate set of experiments. The observed effects on the average O/C and DBE were similar to the aqueous photolysis, but the extent of chemical change was smaller in dry SOA. Our results suggest that biogenic SOA dissolved in cloud and fog droplets will undergo significant photolytic processing on a time scale of hours to days. This type of photolytic processing may account for the discrepancy between the higher values of O/C measured in the field experiments relative to the laboratory measurements on SOA in smog chambers. In addition, the direct photolysis of oligomeric compounds may be responsible for the scarcity of their observation in the field.     

Direct photolysis of chlorophenols in aqueous solutions by UV radiation from excilamps

Direct photolysis of 2- and 4-chlorophenol and 2,4-dichlorophenol in aqueous solutions by UV radiation from XeBr (282 nm) and KrCl (222 nm) excilamps at various pH values was subjected to a comparative study.     

THE PHOTOLYSIS RATES OF SOME DI- AND TRIPEPTIDES OF TRYPTOPHAN

We have measured the relative rates of photolysis of free tryptophan (trp), the dipeptides Gly-Trp, Trp-Gly, Leu-Trp, and Trp-Leu, and the tripeptides Gly-Trp-Gly and Leu-Trp-Leu. The photolyses were performed in neutral 0.1 mM aqueous solutions at 25°C using monochromatic 290 nm Xe arc radiation. Tryptophan loss was monitored by absorption, fluorescence and phosphorescence spectroscopy. The rate of tryptophan fluorescence loss was found to be different in the di-and tripeptides than in tryptophan monomer. These rate differences depended on both the identity of the neighboring amino acid (gly or leu) and on the nature of the linkage, e.g., the rate of Gly-Trp photolysis was more than 10 times greater than the rate of Trp-Gly photolysis. Degassing was found to markedly reduce (factor of 8) the photolysis rates of Trp, Trp-Gly, and Trp-Leu, but degassing only slightly reduced (less than a factor of 2) the photolysis rates of the other di-and tri-peptides. Photochemical product structures were not determined, but absorption and fluorescence spectra were obtained and products could be inferred in some cases by comparison with data of previous workers. The products appeared to differ greatly among the various peptides studied; Trp, Trp-Gly, and Trp-Leu gave oxidation products, while Gly-Trp and Leu-Trp apparently gave ring closure products, not requiring oxygen.     

Kinetics and mechanism of CH3Br,CHF2Br,and C2HF4Br photolysis in the presence of dioxygen under the action of λ = 253.7 nm light

The photolysis of CH₃Br, CHF₂Br, and C₂HF₄Br mixed with oxygen under radiation emitted by a bactericidal mercury lamp (radiation intensity maximum at λ = 253.7 nm) has been investigated. Oxygen was added in order to simulate natural conditions. A photolysis mechanism has been suggested, the corresponding model calculations have been carried out, and the calculated data have been compared with experimental data. The calculated absorption cross sections are in agreement with the literature, thus proving the validity of the mechanism suggested. The ratios between the rate constants of the reactions of the photolytically generated CH₃, CHF₂, and C₂HF₄ radicals with molecular bromine and oxygen have been determined.     

Changes in the composition and properties of graphene oxide films under monochromatic vacuum UV radiation

The photolysis of a graphene oxide film by monochromatic vacuum UV radiation with a wavelength of 123.6 nm has been studied. It has been shown that photoreduction as a result of the detachment of the C?O polar groups is also accompanied by an increase in the conductivity, wettability, and surface energy of the graphene oxide film.     

Increase in isotopic selectivity with pressure in the multiphoton infrared decomposition of CF3Br

The C-13 isotopic selectivity in the multiphoton decomposition of CF₃Br has been shown to increase with increasing pressure of substrate for photolysis far to the red of the resonant, low intensity absorption band using relatively low fluence radiation. However, the quantum efficiency would appear to decrease as pressure is increased.     

酞花菁及金属酞菁化物紫外光解的ESR研究

在较强的紫外辐射作用下,即使较为稳定的酞菁化合物也可能发生光解。水文用自旋捕捉与ESR技术相结合的方法检出了在光解中生成的氮中心自由基。