Dypas2Ein Computerprogramm zur Simulation dynamischer PHIP-NMR-Spektroskopie auf Basis des Superoperatorformalismus
Dypas2
Ein Computerprogramm zur Simulation dynamischer PHIP-NMR-Spektroskopie auf Basis des Superoperatorformalismus
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DissertationPrüfungsdatum
24.06.2003Datum der Veröffentlichung
2003Erstgutachter
Bargon, JoachimZweitgutachter
Woelk, KlausMetadaten
Zur Langanzeige
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Inhalt
For in situ studies of reaction mechanisms using parahydrogen it is desirable to compare experimentally recorded NMR spectra with those theoretically expected. Likewise it is advantageous to know, how the individual intensities of the intermediates and reaction products depend on time.
For this purpose we have developed a computer simulation program DYPAS2 which is based on the density matrix formalism using superoperators, implemented under the C++ class library GAMMA.
DYPAS2 offers a large variety of simulation modes and allows to calculate the polarization patterns of the expected NMR spectra derived either from parahydrogen or orthodeuterium. Furthermore, the individual boundary conditions can be taken into account, under which the hydrogenations take place. Accordingly, the magnetic field dependence of the resulting polarization patterns can be predicted, for example in spectra based on the PASADENA or ALTADENA effect, respectively.
The kinetics of the hydrogenation transfer is covered by the use of an exchange superoperator assuming a pseudo first order reaction. Thereby competing hydrogenations of the substrate to more than one product can also be accommodated. In addition, the consequences of relaxation effects or NOE's can be included into the simulations if desired. Furthermore, it is possible to simulate the consequences of different types of pulse sequences, such as PH-INEPT or INEPT+, which have previously been developed for the transfer of polarization from the parahydrogen-derived protons to hetero nuclei like 13C or 15N. The individual delays required in these pulse sequences are critical parameters for the associated magnitude of the transferred polarization, but it is not trivial to estimate their optimal values. Therefore, - and in particular for large spin systems, - it is desirable to obtain access to intensity plots, which display the calculated intensities of the polarization-enhanced NMR spectra of the hetero nuclei as a function of the individual delay times. DYPAS2 contains this option and provides an even greater variety of other possibilities.
For this purpose we have developed a computer simulation program DYPAS2 which is based on the density matrix formalism using superoperators, implemented under the C++ class library GAMMA.
DYPAS2 offers a large variety of simulation modes and allows to calculate the polarization patterns of the expected NMR spectra derived either from parahydrogen or orthodeuterium. Furthermore, the individual boundary conditions can be taken into account, under which the hydrogenations take place. Accordingly, the magnetic field dependence of the resulting polarization patterns can be predicted, for example in spectra based on the PASADENA or ALTADENA effect, respectively.
The kinetics of the hydrogenation transfer is covered by the use of an exchange superoperator assuming a pseudo first order reaction. Thereby competing hydrogenations of the substrate to more than one product can also be accommodated. In addition, the consequences of relaxation effects or NOE's can be included into the simulations if desired. Furthermore, it is possible to simulate the consequences of different types of pulse sequences, such as PH-INEPT or INEPT+, which have previously been developed for the transfer of polarization from the parahydrogen-derived protons to hetero nuclei like 13C or 15N. The individual delays required in these pulse sequences are critical parameters for the associated magnitude of the transferred polarization, but it is not trivial to estimate their optimal values. Therefore, - and in particular for large spin systems, - it is desirable to obtain access to intensity plots, which display the calculated intensities of the polarization-enhanced NMR spectra of the hetero nuclei as a function of the individual delay times. DYPAS2 contains this option and provides an even greater variety of other possibilities.
Schlagwörter
NMR, PHIP, Spektroskopie, Simulation
Klassifikation (DDC)
540 ChemieSchmidt, Thorsten: Dypas2 : Ein Computerprogramm zur Simulation dynamischer PHIP-NMR-Spektroskopie auf Basis des Superoperatorformalismus. - Bonn, 2003. - Dissertation, Rheinische Friedrich-Wilhelms-Universität Bonn.
Online-Ausgabe in bonndoc: https://nbn-resolving.org/urn:nbn:de:hbz:5n-02293
Online-Ausgabe in bonndoc: https://nbn-resolving.org/urn:nbn:de:hbz:5n-02293
@phdthesis{handle:20.500.11811/1917,
urn: https://nbn-resolving.org/urn:nbn:de:hbz:5n-02293,
author = {{Thorsten Schmidt}},
title = {Dypas2 : Ein Computerprogramm zur Simulation dynamischer PHIP-NMR-Spektroskopie auf Basis des Superoperatorformalismus},
school = {Rheinische Friedrich-Wilhelms-Universität Bonn},
year = 2003,
note = {For in situ studies of reaction mechanisms using parahydrogen it is desirable to compare experimentally recorded NMR spectra with those theoretically expected. Likewise it is advantageous to know, how the individual intensities of the intermediates and reaction products depend on time.
For this purpose we have developed a computer simulation program DYPAS2 which is based on the density matrix formalism using superoperators, implemented under the C++ class library GAMMA.
DYPAS2 offers a large variety of simulation modes and allows to calculate the polarization patterns of the expected NMR spectra derived either from parahydrogen or orthodeuterium. Furthermore, the individual boundary conditions can be taken into account, under which the hydrogenations take place. Accordingly, the magnetic field dependence of the resulting polarization patterns can be predicted, for example in spectra based on the PASADENA or ALTADENA effect, respectively.
The kinetics of the hydrogenation transfer is covered by the use of an exchange superoperator assuming a pseudo first order reaction. Thereby competing hydrogenations of the substrate to more than one product can also be accommodated. In addition, the consequences of relaxation effects or NOE's can be included into the simulations if desired. Furthermore, it is possible to simulate the consequences of different types of pulse sequences, such as PH-INEPT or INEPT+, which have previously been developed for the transfer of polarization from the parahydrogen-derived protons to hetero nuclei like 13C or 15N. The individual delays required in these pulse sequences are critical parameters for the associated magnitude of the transferred polarization, but it is not trivial to estimate their optimal values. Therefore, - and in particular for large spin systems, - it is desirable to obtain access to intensity plots, which display the calculated intensities of the polarization-enhanced NMR spectra of the hetero nuclei as a function of the individual delay times. DYPAS2 contains this option and provides an even greater variety of other possibilities.},
url = {https://hdl.handle.net/20.500.11811/1917}
}
urn: https://nbn-resolving.org/urn:nbn:de:hbz:5n-02293,
author = {{Thorsten Schmidt}},
title = {Dypas2 : Ein Computerprogramm zur Simulation dynamischer PHIP-NMR-Spektroskopie auf Basis des Superoperatorformalismus},
school = {Rheinische Friedrich-Wilhelms-Universität Bonn},
year = 2003,
note = {For in situ studies of reaction mechanisms using parahydrogen it is desirable to compare experimentally recorded NMR spectra with those theoretically expected. Likewise it is advantageous to know, how the individual intensities of the intermediates and reaction products depend on time.
For this purpose we have developed a computer simulation program DYPAS2 which is based on the density matrix formalism using superoperators, implemented under the C++ class library GAMMA.
DYPAS2 offers a large variety of simulation modes and allows to calculate the polarization patterns of the expected NMR spectra derived either from parahydrogen or orthodeuterium. Furthermore, the individual boundary conditions can be taken into account, under which the hydrogenations take place. Accordingly, the magnetic field dependence of the resulting polarization patterns can be predicted, for example in spectra based on the PASADENA or ALTADENA effect, respectively.
The kinetics of the hydrogenation transfer is covered by the use of an exchange superoperator assuming a pseudo first order reaction. Thereby competing hydrogenations of the substrate to more than one product can also be accommodated. In addition, the consequences of relaxation effects or NOE's can be included into the simulations if desired. Furthermore, it is possible to simulate the consequences of different types of pulse sequences, such as PH-INEPT or INEPT+, which have previously been developed for the transfer of polarization from the parahydrogen-derived protons to hetero nuclei like 13C or 15N. The individual delays required in these pulse sequences are critical parameters for the associated magnitude of the transferred polarization, but it is not trivial to estimate their optimal values. Therefore, - and in particular for large spin systems, - it is desirable to obtain access to intensity plots, which display the calculated intensities of the polarization-enhanced NMR spectra of the hetero nuclei as a function of the individual delay times. DYPAS2 contains this option and provides an even greater variety of other possibilities.},
url = {https://hdl.handle.net/20.500.11811/1917}
}
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