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Uni Rgbg

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In this way we follow the concentration time profiles of the reaction intermediates in the time range from 50 ns to 10 ms.

We use a special and unique experimental setup built around a streak camera see below. This enables us to measure simultaneously the concentration time profiles kinetics and the spectra of the intermediates.

Method: Transient absorption spectroscopy with a streak camera. The transient spectral data form a matrix A whose columns represent wavelengths and the rows represent time.

Simple pump-probe experiments measure a single data point of the matrix A for each excitation cycle. The efficiency can be improved by measuring a complete time profile for each excitation cycle at one fixed wavelength, which corresponds to the measurement of a column of the matrix A.

In order to obtain the full matrix A this measurement must be repeated at different wavelengths, keeping all other parameters of the apparatus constant.

Alternatively, the whole transient absorption spectrum can be measured for fixed delay times with a short white light pulse, a monochromator, and an optical multichannel detector.

This corresponds to the measurement of a row of the matrix A. The time needed for the determination of the complete matrix A will be similar to that for the column-wise measurements.

We measure the complete data matrix A for each excitation cycle by a double multiplex method, using the combination of a continuous white probe light, a monochromator, and a streak camera.

This results in a multiplex factor of more than , i. The pulse duration is typically 8 ns, and the energy typi-cally 10 mJ.

The probe light is generated by a pulsed xenon flash lamp which produces a white light pulse with very flat intensity profile of ca.

The lenses used in the original setup for the probe light path were replaced by toroidal mirrors. This makes the light path achromatic.

An additional aperture and shutter in the probe light path re-duces the white light falling on the sample outside of the time window of the measure-ment.

After passing through the sample the probe light is dispersed by a spectrograph and then temporally analyzed by the streak camera.

The latter consists of two parts: the streak tube which produces an image on a phosphor screen, and a CCD camera which digitizes this image.

In this domain, the photoactive cysteine C57 of the wild type is replaced by glycine. This introduces a "short-cut" into the photocycle which now proceeds from the triplet state of the flavin back to the ground state with a time constant of ca.

The left side of the figure shows a false color representation of the two-dimensional spectral data. The fluorescence of flavin is clearly visible as the narrow blue horizontal stripe.

The bleaching of the flavin ground state appears as a green vertical stripe centered at nm. Red colored stripes on both sides indicate transient absorption by the triplet state.

A global fit to these data sets reveals two lifetime components. One is short with fitted decay times between 40 - 60 ns.

Andreas Schmaunz Dipl. Andreas Wenge Dr. Angela Kessler Dr. Thorsten Obernhuber Dr. Reinhold Seiler Dr. Robert Aures.

Photodissociation dynamics of nitroso compounds Since NO is a stable radical, the X-N bond in nitroso compounds X-NO is usually weak and can be broken by thermal or photochemical excitation.

After excitation to the second absorption band of NNPy dissociation into two different electronic states of the NPy radical has been observed.

In all three compounds the dissociation occurs on a purely repulsive potential energy surface and on a time scale of a few femtoseconds.

The same apparatus as for VMI is used. However, the ionization laser is tuned over all REMPI resonances of NO, and for each ion that hits the detector the position and the wavelength are recorded.

The figure below shows a histogram of the ion counts as a function of wavelength horizontal axis and distance from the center vertical axis of the detector.

Blue and green colors indicates low ion count, yellow and red colors corresponds to large counts. The picture consist of many stripes that are narrow along the wavelength axis and extend along the R-axis.

A simultaneous fit to these data yields, for each quantum state, the velocity distribution, but also the population in this particular fragment channel.

VMI: Velocity Map Imaging Photodissociation with a linearly polarized laser produces a velocity distribution of the fragments which is rotationally symmetric around the polarization direction.

These ions are accelerated towards a two-dimensional detector MCP, see figure below. The vector from the center of the MCP to the position of ion impact is proportional to the in-plane component of the fragment velocity.

The "ion image" is thus the projection of the velocity distribution onto a plane. The original three-dimensional velocity distribution can be reconstructed from the ion image by Abel inversion, or a fit of a model function.

References: Kessler, A.

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Uni Rgbg - Mukoviszidose-Test zum Trinken

Das bedeutet konkret, dass die Aussetzung der Abgabefrist mit dieser Bekanntgabe aufgrund eines Beschlusses der Prüfungsausschüsse Physik und Nanoscience zum Dank ihrer späten Gründung kann sich die Universität des jüngsten und modernsten Klinikums Europas rühmen, das sich dennoch in kürzester Zeit einen hervorragenden Ruf in Forschung und Lehre erobern konnte. Um ausreichend Platz für die Vorträge und Präsentationen der 5. Ein Abmeldelink ist am Ende jedes Newsletters enthalten. Bei den Regensburger Schlossfestspielen besuchen bis zu

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Imagefilm der Universität Regensburg Uni Rgbg

In the DFG Graduiertenkolleg Research Training Group GRK several research teams from organic, inorganic, and physical chemistry cooperate in the design and understanding of new photochemical systems.

Our part in this is the study of the reaction mechanisms. We do this by transient absorption measurements following a short laser flash.

In this way we follow the concentration time profiles of the reaction intermediates in the time range from 50 ns to 10 ms.

We use a special and unique experimental setup built around a streak camera see below. This enables us to measure simultaneously the concentration time profiles kinetics and the spectra of the intermediates.

Method: Transient absorption spectroscopy with a streak camera. The transient spectral data form a matrix A whose columns represent wavelengths and the rows represent time.

Simple pump-probe experiments measure a single data point of the matrix A for each excitation cycle. The efficiency can be improved by measuring a complete time profile for each excitation cycle at one fixed wavelength, which corresponds to the measurement of a column of the matrix A.

In order to obtain the full matrix A this measurement must be repeated at different wavelengths, keeping all other parameters of the apparatus constant.

Alternatively, the whole transient absorption spectrum can be measured for fixed delay times with a short white light pulse, a monochromator, and an optical multichannel detector.

This corresponds to the measurement of a row of the matrix A. The time needed for the determination of the complete matrix A will be similar to that for the column-wise measurements.

We measure the complete data matrix A for each excitation cycle by a double multiplex method, using the combination of a continuous white probe light, a monochromator, and a streak camera.

This results in a multiplex factor of more than , i. The pulse duration is typically 8 ns, and the energy typi-cally 10 mJ.

The probe light is generated by a pulsed xenon flash lamp which produces a white light pulse with very flat intensity profile of ca.

The lenses used in the original setup for the probe light path were replaced by toroidal mirrors. This makes the light path achromatic.

An additional aperture and shutter in the probe light path re-duces the white light falling on the sample outside of the time window of the measure-ment.

After passing through the sample the probe light is dispersed by a spectrograph and then temporally analyzed by the streak camera.

The latter consists of two parts: the streak tube which produces an image on a phosphor screen, and a CCD camera which digitizes this image. In this domain, the photoactive cysteine C57 of the wild type is replaced by glycine.

This introduces a "short-cut" into the photocycle which now proceeds from the triplet state of the flavin back to the ground state with a time constant of ca.

The left side of the figure shows a false color representation of the two-dimensional spectral data. The fluorescence of flavin is clearly visible as the narrow blue horizontal stripe.

The bleaching of the flavin ground state appears as a green vertical stripe centered at nm. Nicole Berner. Bernhard Dick.

Former Group Members:. Roger-Jan Kutta Dr. Andreas Schmaunz Dipl. Andreas Wenge Dr. Angela Kessler Dr.

Thorsten Obernhuber Dr. Reinhold Seiler Dr. Robert Aures. Photodissociation dynamics of nitroso compounds Since NO is a stable radical, the X-N bond in nitroso compounds X-NO is usually weak and can be broken by thermal or photochemical excitation.

After excitation to the second absorption band of NNPy dissociation into two different electronic states of the NPy radical has been observed.

In all three compounds the dissociation occurs on a purely repulsive potential energy surface and on a time scale of a few femtoseconds.

The same apparatus as for VMI is used. However, the ionization laser is tuned over all REMPI resonances of NO, and for each ion that hits the detector the position and the wavelength are recorded.

The figure below shows a histogram of the ion counts as a function of wavelength horizontal axis and distance from the center vertical axis of the detector.

Blue and green colors indicates low ion count, yellow and red colors corresponds to large counts.

The picture consist of many stripes that are narrow along the wavelength axis and extend along the R-axis.

A simultaneous fit to these data yields, for each quantum state, the velocity distribution, but also the population in this particular fragment channel.

VMI: Velocity Map Imaging Photodissociation with a linearly polarized laser produces a velocity distribution of the fragments which is rotationally symmetric around the polarization direction.

These ions are accelerated towards a two-dimensional detector MCP, see figure below.

Uni Rgbg k Followers, Following, Posts - See Instagram photos and videos from Universität Regensburg (@belgiumrescuedogs.beburg). Eingang Universitätsklinikum Regensburg. Aktuell Die deutschen Universitätsklinika Universität Regensburg Siegel Aktion Saubere Hände. Focus Top. 62 Bewertungen zum Studium Betriebswirtschaftslehre an der Uni Regensburg. ✓82% der Studenten empfehlen das Studium weiter. So funktioniert das Jurastudium an der Uni Regensburg: Ablauf, NC, Studentenmeinungen, Schwerpunktbereiche, Notenschnitt und vieles mehr. Diese Artikel finden Sie nur bei Bücher Pustet auf dem Campus der Uni Regensburg oder hier direkt im Online-Shop. Bestellung zur Abholung oder Direktversand. Mega Millions Jackpot, A. The same apparatus as for VMI is used. Andreas Schmaunz Dipl. Bernhard Dick. A, Uwe Kensy Dipl. Alignment and velocity distribution of the NO fragments from the UV Mr And Lady dissociation of jet-cooled nitrosobenzene studied by LIF and Doppler profile measurements.

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