Preparation and characterization of regioisomerically pure 1,7-disubstituted perylene bisimide dyes

A detailed study on bromination and subsequent imidization of perylene bisanhydride with cyclohexylamine is reported. The present results reveal that previously reported 1,7-difunctionalized perylene bisimides are presumably contaminated with the respective 1,6 regioisomers. N,N'-Dicyclohexyl-1,7-dibromoperylene bisimide 1,7-3 is obtained for the first time in isomerically pure form, and its structure is unequivocally confirmed by X-ray analysis. By using regioisomerically pure 1,7-dibromoperylene bisimide 1,7-3, 1,7-dipyrrolidinylperylene bisimides 4a-c and 1,7-dipyrrolidinylperylene bisanhydride 5 as well as the unsymmetrically difunctionalized 1-bromo-7-pyrrolidinyl- and 1-cyano-7-pyrrolidinylperylene bisimides 7 and 8 are synthesized in good yield.     

MRI observation of heavy metal transport in aquifer matrices down to sub-mg quantities

In this contribution, we report results from MRI studies of the propagation of heavy metal ions through columns packed with sandy aquifer materials. Both sorption of low concentrations of heavy metal ions from water flowing through the column and the formation of sorption traces produced from initially localized higher concentrations of heavy metal ions, and the remobilisation of adsorbed ions with time and changing hydrochemical conditions were studied. Multislice spin-echo and FLASH techniques were used for the imaging experiments. Advantages and problems of the different imaging protocols for the study of aquifer materials are discussed.     

On the feasibility of performing non-linear autocorrelation with attosecond pulse trains

We present experimental results in which a second-order effect, namely two-photon ionization of atomic He induced by a superposition of harmonics, is observed. The harmonics are generated in a Xe gas-jet using a 790-nm 10-Hz femtosecond Ti:sapphire laser and are subsequently focused into a He gas-jet with a Kirkpatrick–Baez arrangement. The superposition is formed by using a thin In filter and it comprises the 7th to 13th harmonics. Solving the time-dependent Schrödinger equation for He in a polychromatic laser field, the He ⁺ ion yield is calculated as a function of the total XUV intensity. Using the calculated yield and taking into account the focusing and transmission properties of the arrangement, the number of He ⁺ ions produced per laser pulse is estimated and is found to be in reasonable agreement with its measured value. The total number of ions produced non-resonantly follows a nearly quadratic dependence on the harmonic intensity, thus establishing the feasibility of a second-order auto-correlation measurement of the superposition of harmonics, i.e., of a direct temporal characterization of attosecond pulse trains.     

High-intensity laser induced ion acceleration from heavy-water droplets

Fusion neutrons from a heavy water droplet target irradiated with laser pulses of 3 x 10(19) W/cm(2) and from a deuterated secondary target are observed by a time-of-flight (TOF) neutron spectrometer. The observed TOF spectrum can be explained by fusion of deuterium ions simultaneously originating from two different sources: ion acceleration in the laser focus by ponderomotively induced charge separation and target-normal sheath acceleration off the target rear surface. The experimental findings agree well with 3D particle-in-cell simulations.     

Numerical simulations for performance optimization of a few-cycle terawatt NOPCPA system

We present a systematic numerical design and performance study of an ultra-broadband noncollinear optical parametric chirped pulse amplification (NOPCPA) system. Using a split-step Fourier approach, we model a three-stage amplifier system which is designed for the generation of 7 fs pulses with multi-terawatt peak intensity. The numerical results are compared with recent experimental data. Several important aspects and design parameters specific to NOPCPA are identified, and the values of these parameters required to achieve optimal working conditions are investigated. We identify and analyze wavelength-dependent gain saturation effects, which are specific to NOPCPA and have a strong influence on the parametric amplification process. PACS 42.65.Yj; 42.65.Re     

Controlled formation of ag nanoparticles by means of long-chain sodium polyacrylates in dilute solution

A new tool is presented to control formation of Ag nanoparticles. Small amounts of silver ions were added to dilute solutions of long-chain sodium polyacrylates (NaPA). Four NaPA samples covering a molar mass regime of 97 kD < or = Mw < or = 650 kD have been used. With amounts of added Ag(+) as low as 1-2% of the COO(-) groups of the polyanionic chains, significant changes could already be induced in the NaPA coils with 650 kD. If the NaPA concentration was kept below 0.1 g/L, the coils with 650 kD exhibited a significant coil shrinking in stable solutions. At larger NaPA concentrations, addition of Ag+ initiates an aggregation of the polyacrylate coils toward compact structures. Coil shrinking and aggregation was revealed by means of time-resolved static light scattering. If exposed to UV-radiation, small Ag particles formed within the shrunken anionic polyacrylate coils. The Ag nanoparticles were identified by means of an enhanced light scattering and a characteristic plasmon absorption band around 410 nm. No such Ag particle formation could be observed even at 5 times larger concentrations of Ag(+) and NaPA if the two smallest polyacrylate samples have been used under otherwise equal conditions. This molar mass sensitive response of NaPA to Ag(+)-addition suggests an interesting phenomenon: if the coil size of the NaPa chains, which act as Ag(+) collectors, is large enough, local Ag(+) concentration in these coil-shaped Ag(+) containers exceeds a critical value, and irradiation with UV generates Ag nanoparticles.     

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Ohne Zusammenfassung     

Camphor and nopinone derivatives as new photosensitive chiral dopants

E-Z photoisomerizable chiral dopants are a class of materials that can be used to prepare birefringent optical components with patterned optical properties. Two new photoisomerizable chiral dopants have been synthesized and analysed. The materials were derived from nopinone and camphor. The properties of these compounds were compared with the properties of the methone derivative described in earlier publications. The E-isomers of the nopinone and camphor derivatives had helical twisting powers of 2.7 and 1.7 μm^-1, respectively. This is a factor of about 10 lower than the value obtained for the menthone derivative (-19 μm^-1). Due to the high absorption of the Z-isomers relative to the E-isomers of the nopinone and camphor derivatives, isomerization during 365 nm UV exposure proceeded to a much lesser extent than the isomerization of the menthone derivative. At shorter wavelengths, the absorption of the Z-isomer is much lower than that of the E-isomer and much higher degrees of conversion could be achieved.     

Modern Variants of the Mannich Reaction

Important building blocks for the synthesis of drugs or natural products are found in Mannich bases and their derivatives. Modern variants of the Mannich reaction that expand the potential of the classical intermolecular reaction significantly and enable efficient control of the regioselectivity and stereoselectivity are therefore the topic of intensive research. Intramolecular reactions, in particular as part of domino reaction sequences, often afford astoundingly simple and elegant approaches to complex target compounds.