Kawon Oum

Bromine activation in the troposphere by the dark reaction of O3 with seawater ice

There is increasing evidence that bromine atoms play a role in tropospheric chemistry in the marine boundary layer. In addition, they are believed to lead to rapid depletion of surface level ozone in the Arctic at polar sunrise. While mechanisms have been proposed for recycling bromine atoms from sea salt particles, the initial reaction(s) leading to the formation of bromine atom precursors is not known. We report here the formation of gaseous Br2 from the reaction of seawater ice with O3 in the dark. These observations suggest that this reaction is a potential source of tropospheric photolyzable bromine in high latitude coastal regions in winter. In addition, it may be the source of the photolyzable bromine gas measured recently in the Arctic by Impey et al. (1997), which is believed to be responsible for the ozone destruction at polar sunrise.

Heterogeneous chemistry in the troposphere: Experimental approaches and applications to the chemistry of sea salt particles

Halogen atoms, particularly chlorine atoms, are well known to be highly reactive and to play a central role in the chemistry of the upper atmosphere. A large potential source of these halogens in the lower atmosphere (troposphere) exists in the form of sea salt particles. A variety of laboratory, field and modelling studies strongly suggests that there are heterogeneous reactions of sea salt particles which generate photochemically active halogen species such as Cl in marine areas. In addition, there is increasing evidence for a contribution of bromine atoms to tropospheric chemistry in marine regions at high latitudes. We review here briefly the potential importance of such halogen reactions and evidence for their role in the chemistry of the troposphere. Studies carried out in this laboratory to elucidate, at a molecular level, the mechanisms of reaction of synthetic sea salt and its components with gases of tropospheric interest are reviewed. Initial results obtained using a new aerosol apparatus recen...

Synthesis and Photochemical Investigations of Tetrasubstituted Alkenes as Molecular Switches—The Effect of Substituents

Molecular switches based on helical tetrasubstituted alkenes, substituted with either electron-withdrawing (CF(3), F, CN; 2a-c, 3a,c) or -donating substituents (Me, OMe; 2d,e), have been synthesized from acyclic precursors 4 and 5 in a domino carbopalladation/Stille reaction. This palladium-catalyzed process allowed the rapid assembly of two C-C bonds, two six-membered rings, and the tetrasubstituted double bond in a completely diastereoselective fashion. The electronic effects of the substituents on the overall switching process were investigated by alternating irradiation of two different wavelength regions. Although the substituents had only a small influence on the absorption maxima, drastic differences in the switching behavior were observed.

Synthesis of chiroptical molecular switches by pd-catalyzed domino reactions.

New photochromic switches based on helical alkenes can quickly and efficiently be accessed by Pd-catalyzed domino reactions using a modular approach; this allows a wide variability in product formation with the advantages of a convergent synthetic route. The alkenes have been synthesized in excellent enantioselectivity and their switching properties assessed by stimulation with nanosecond laser pulses at two different wavelengths in over 1000 switching cycles.

On the nature of interactions between ionic liquids and small amino-acid-based biomolecules.

During the last decade, ionic liquids (ILs) have revealed promising properties and applications in many research fields, including biotechnology and biological sciences. The focus of this contribution is to give a critical review of the phenomena observed and current knowledge of the interactions occurring on a molecular basis. As opposed to the huge advances made in understanding the properties of proteins in ILs, complementary investigations dealing with interactions between ILs and peptides or oligopeptides are underrepresented and are mostly only of phenomenological nature. However, the field has received more attention in the last few years. This Review features a meta-analysis of the available data and findings and should, therefore, provide a basis for a scientifically profound understanding of the nature and mechanisms of interactions between ILs and structured or nonstructured peptides. Fundamental aspects of the interactions between different peptides/oligopeptides and ILs are complemented by sections on the experimental (spectroscopy, structural biology) and theoretical (computational chemistry) possibilities to explain the phenomena reported so far in the literature. In effect, this should lead to the development of novel applications and support the understanding of IL-solute interactions in general.

Femtosecond pump-supercontinuum probe and transient lens spectroscopy of adonixanthin.

The ultrafast internal conversion (IC) dynamics of adonixanthin in organic solvents were studied by pump-supercontinuum probe (PSCP) and transient lens (TL) spectroscopy after photoexcitation to the S(2) state. Transient PSCP spectra in the range 344-768 nm provided the spectral evolution of the S(0)-->S(2) ground state bleach and S(1)-->S(n) excited state absorption. Time constants were tau(2) =115 and 111 fs for the S(2)-->S(1) IC and tau(1)=6.4 and 5.8 ps for the S(1)-->S(0) IC in acetone and methanol, respectively. There was only an insignificant polarity dependence of tau(1), underlining the negligible importance of intramolecular charge transfer (ICT) in the lowest-lying excited state of C(40) carotenoids with carbonyl substitution on the beta-ionone ring. A blueshift and a spectral narrowing of the S(1)-->S(n) ESA band, likely due to solvation dynamics, and formation of the adonixanthin radial cation at high pump energies via resonant two-photon ionization were found.

Electron and hole transfer dynamics of a triarylamine-based dye with peripheral hole acceptors on TiO2 in the absence and presence of solvent.

We investigated photoinduced primary charge transfer processes of the sensitizer E6 on TiO2 without solvent and in contact with the organic solvent acetonitrile and the ionic liquid 1-ethyl-3-methylimidazolium tetracyanoborate [C2mim](+)[B(CN)4](-) using transient absorption spectroscopy, spectroelectrochemistry, and DFT/TDDFT calculations. E6, which belongs to a family of triarylamine dyes for solar cell applications, features two peripheral triarylamine units which are connected via diether spacer groups to the core chromophore and are designed to act as hole traps. This function was confirmed by spectroelectrochemistry, where the E6˙(+) radical cation shows a considerably blue-shifted absorption compared to dyes without these two substituents. This indicates that one of the terminal triarylamine units must carry the positive charge. After photoexcitation of E6 at 520 nm (S0 → S1 band), electrons are injected into TiO2 predominantly within the cross-correlation time (<80 fs), with some subsequent delayed electron injection (τ ca. 250 fs). Importantly, a transient Stark shift (electrochromism) is observed (time constants ca. 0.8 and 12 ps) which is related to a changing electric field generated by the E6˙(+) radical cations and injected electrons. This field induces absorption shifts of the dye species on the surface. Interestingly, these dynamics are largely unaffected by solvent molecules. However, pronounced differences are observed on longer timescales. In contact with solvent, one observes an increase in the E6˙(+) absorption band above 600 nm with a time constant of 75 ps. This is assigned to hole transfer from the core chromophore to one of the peripheral triarylamine substituents. Electron-cation recombination occurs on much longer timescales and is multiexponential, with time constants of ca. 100 μs, 1 ms and 15 ms. Because of hole trapping, it is slower than for similar dyes lacking the peripheral triarylamines. Additional experiments were performed for E6 attached to the wide band gap semiconductor ZrO2. Here, electron injection occurs into surface trap states with subsequent recombination. Another fraction of non-injecting E6 molecules in S1 quickly decays to S0 (time constants 1 and 35 ps).

Four‐ and Sixfold Tandem‐Domino Reactions Leading to Dimeric Tetrasubstituted Alkenes Suitable as Molecular Switches

A highly efficient palladium-catalyzed fourfold tandem-domino reaction consisting of two carbopalladation and two C-H-activation steps was developed for the synthesis of two types of tetrasubstituted alkenes 3 and 6 with intrinsic helical chirality starting from substrates 1 and 4, respectively. A sixfold tandem-domino reaction was also developed by including a Sonogashira reaction. 20 compounds with different substitution patterns were prepared with yields of up to 97 %. Structure elucidation by X-ray crystallography confirmed helical chirality of the two alkene moieties. Photophysical investigations of some of the compounds showed pronounced switching properties through light-controlled changes of their stereochemical configuration.

The role of the radical-complex mechanism in the ozone recombination/dissociation reaction

The data bases for low-pressure rate coefficients of the dissociation of O3 and the reverse recombination of O with O2 in the bath gases M=He, Ar, N2, CO2 and SF6 are carefully analyzed. At very high temperatures, the rate constants have to correspond solely to the energy transfer (ET) mechanism. On condition that this holds for Ar and N2 near 800 K, average energies transferred per collision of -DeltaE/hc=18 and 25 cm-1 are derived, respectively. Assuming an only weak temperature dependence of DeltaE as known in similar systems, rate coefficients for the ET-mechanism are extrapolated to lower temperatures and compared with the experiments. The difference between measured and extrapolated rate coefficients is attributed to the radical complex (RC) mechanism. The derived rate coefficients for the RC-mechanism are rationalized in terms of equilibrium constants for equilibria of van der Waals complexes of O (or O2) with the bath gases and with rate coefficients for oxygen abstraction from these complexes. The latter are of similar magnitude as rate coefficients for oxygen isotope exchange which provides support for the present interpretation of the reaction in terms of a superposition of RC- and ET-mechanisms. We obtained rate coefficients for the ET-mechanism of k/[Ar]=2.3x10(-34) (T/300)(-1.5) and k/[N2]=3.5x10(-34) (T/300)(-1.5) cm6 molecule-2 s-1 and rate coefficients for the RC-mechanism of k/[Ar]=1.7x10(-34) (T/300)(-3.2) and k/[N2]=2.5x10(-34) (T/300)(-3.3) cm6 molecule-2 s-1. The data bases for M=He, CO2 and SF6 are less complete and only approximate separations of RC- and ET-mechanism were possible. The consequences of the present analysis for an analysis of isotope effects in ozone recombination are emphasized.

On-line in-situ characterization of CO2 RESS processes for benzoic acid, cholesterol and aspirin

Rapid expansions of supercritical solutions (RESS) of benzoic acid, cholesterol and aspirin in supercritical CO2 have been used to investigate the influence of a systematic variation of the pre-expansion temperature and pressure, the distance from the RESS nozzle and the amount of added co-solvent on properties like the average particle diameter Dav and the width of the particle size distribution σ. The properties of the CO2 expansion have been characterized by a 1-dimensional flow-field model using the Span–Wagner equation of state. Particle detection was performed on-line and in-situ using laser-based three wavelength extinction measurements (3-WEM). For benzoic acid we found a decrease in Dav with increasing pre-expansion pressure, and an increase in Dav with increasing pre-expansion temperature. This is probably due to a lower mass flow rate, which is associated with a lower pre-expansion pressure or higher pre-expansion temperature. This in turn results in a longer residence time in the expansion region and thus a longer particle growth time. Furthermore, a decrease in pre-expansion pressure or an increase in pre-expansion temperature is associated with a decrease in saturation, corresponding to an increase in the critical particle radius and a decrease in the nucleation rate. The size of the benzoic acid particles ranged from about 100 to 500 nm. In addition, we found no obvious correlation between Dav and the distance from the RESS nozzle for benzoic acid and aspirin particles. The particle size was roughly 350 nm and 160 nm for these two solutes, respectively. Obviously, the particle growth processes have already ceased not too far away from the Mach disc. In addition, for cholesterol expansions in CO2 there was no correlation between the amount and type of co-solvent added. Particle sizes of ∼100 nm were obtained for methanol, ethanol and isopropanol co-solvents. This is most likely due the low solubility of cholesterol in supercritical CO2, compared with molecules such as benzoic acid, which results in a change of Dav which is too small to be detected using 3-WEM.