Peter Bigler
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Peter Bigler has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
Thomas Sprang
Department of Chemistry and Biochemistry, University of Berne, Freiestrasse 3, CH-3012 Berne, Switzerland
2 shared publicationsChristian Schorn
Department of Chemistry and Biochemistry, University of Berne, Freiestrasse 3, CH‐3012 Berne, Switzerland
1 shared publicationRainer Kümmerle
Bruker BioSpin AG, Industriestrasse 26, CH-8117 Fällanden, Switzerland
1 shared publicationRémy Burger
Department of Chemistry and Biochemistry, University of Berne, Freiestrasse 3, CH‐3012 Berne, Switzerland
1 shared publicationWolfgang Bermel
BRUKER BioSpin GmbH, Am Silberstreifen 4, D-76287 Rheinstetten, Germany
1 shared publication
Latest Publications
- 20 June 2008
- Published by Taylor & Francis in Spectroscopy Letters
- Vol. 41 (4) , 162-165
Fast 13 C-NMR Spectral Editing for Determining CH n Multiplicities
With an improved version of the 13C DEPTQ NMR experiment all carbon multiplicities (Cq, CH, CH2 und CH3) can be identified unequivocally and most conveniently in two experiments and at best with only one scan each. This simplifies the analysis of 13C-NMR data on a routine level in general. With higher sample amounts and/or exploiting the high sensitivity of cryogenically cooled 13C probeheads the efficiency of such investigations may be improved. This makes this method attractive for fast 13C analysis of small-to-medium sized molecules in high-throughput laboratories.
- 20 June 2008
- Published by Taylor & Francis in Spectroscopy Letters
- Vol. 41 (4) , 162-165
Fast 13 C-NMR Spectral Editing for Determining CH n Multiplicities
With an improved version of the 13C DEPTQ NMR experiment all carbon multiplicities (Cq, CH, CH2 und CH3) can be identified unequivocally and most conveniently in two experiments and at best with only one scan each. This simplifies the analysis of 13C-NMR data on a routine level in general. With higher sample amounts and/or exploiting the high sensitivity of cryogenically cooled 13C probeheads the efficiency of such investigations may be improved. This makes this method attractive for fast 13C analysis of small-to-medium sized molecules in high-throughput laboratories.
- 17 April 2007
- Published by Wiley in Magnetic Resonance in Chemistry
- Vol. 45 (6) , 469-472
Multiplicity editing including quaternary carbons: improved performance for the 13C‐DEPTQ pulse sequence
An improved version of the DEPTQ experiment yielding the signal and multiplicity information for all carbon types including the signals of quaternary carbons is proposed. It encompasses all the known advantages of the basic DEPT experiment. In comparison to the original version, signals of the sensitivity‐limiting quaternary carbons are markedly increased: the initial 13C pulse may be adjusted to the Ernst angle, the NOE build‐up period is prolonged by the split relaxation delay and a partial recovery of signal losses due to instrumental imperfections is achieved by the incorporation of composite adiabatic 13C refocussing pulses. Furthermore, pure absorption lineshapes for all carbon types are obtained with only one single scan. These attributes make this experiment attractive for 13C analysis of small molecules (including spectral editing), particularly in high‐throughput analysis laboratories. Copyright © 2007 John Wiley & Sons, Ltd.
- 17 April 2007
- Published by Wiley in Magnetic Resonance in Chemistry
- Vol. 45 (6) , 469-472
Multiplicity editing including quaternary carbons: improved performance for the 13C‐DEPTQ pulse sequence
An improved version of the DEPTQ experiment yielding the signal and multiplicity information for all carbon types including the signals of quaternary carbons is proposed. It encompasses all the known advantages of the basic DEPT experiment. In comparison to the original version, signals of the sensitivity‐limiting quaternary carbons are markedly increased: the initial 13C pulse may be adjusted to the Ernst angle, the NOE build‐up period is prolonged by the split relaxation delay and a partial recovery of signal losses due to instrumental imperfections is achieved by the incorporation of composite adiabatic 13C refocussing pulses. Furthermore, pure absorption lineshapes for all carbon types are obtained with only one single scan. These attributes make this experiment attractive for 13C analysis of small molecules (including spectral editing), particularly in high‐throughput analysis laboratories. Copyright © 2007 John Wiley & Sons, Ltd.
- 9 December 2003
- Published by Wiley in Magnetic Resonance in Chemistry
- Vol. 42 (1) , 55-60
HMBC–RELAY: a combined technique for the differentiation of simultaneously detected 2J(C,H) and nJ(C,H) connectivities
We present a new pulse sequence that detects simultaneously nJ(C,H) and 2J(C,H) connectivities. The corresponding coherences are created along independent pathways and therefore can be separated into two different subspectra. One spectrum is to show all nJ(C,H) connectivities and the other is to show exclusively 2J(C,H) connectivities. In contrast to the previously published 2J/nJ experiment, this sequence detects the 2J(C,H) connectivities via a C,H,H‐RELAY pathway leading to an intensification of the 2J(C,H) signals. Strictly, the 2J(C,H) spectrum does not show 2J(C,H) but 3J(H,H) coupling interactions within 13CHk–12CHl fragments. Therefore, 2J(C,H) signals can appear even if the corresponding 2J(C,H) coupling constant is zero. Copyright © 2003 John Wiley & Sons, Ltd.
- 9 December 2003
- Published by Wiley in Magnetic Resonance in Chemistry
- Vol. 42 (1) , 55-60
HMBC–RELAY: a combined technique for the differentiation of simultaneously detected 2J(C,H) and nJ(C,H) connectivities
We present a new pulse sequence that detects simultaneously nJ(C,H) and 2J(C,H) connectivities. The corresponding coherences are created along independent pathways and therefore can be separated into two different subspectra. One spectrum is to show all nJ(C,H) connectivities and the other is to show exclusively 2J(C,H) connectivities. In contrast to the previously published 2J/nJ experiment, this sequence detects the 2J(C,H) connectivities via a C,H,H‐RELAY pathway leading to an intensification of the 2J(C,H) signals. Strictly, the 2J(C,H) spectrum does not show 2J(C,H) but 3J(H,H) coupling interactions within 13CHk–12CHl fragments. Therefore, 2J(C,H) signals can appear even if the corresponding 2J(C,H) coupling constant is zero. Copyright © 2003 John Wiley & Sons, Ltd.
- 1 March 2003
- Published by Wiley in Magnetic Resonance in Chemistry
- Vol. 41 (3) , 177-182
A new technique for differentiating between2J(C,H) and3/4J(C,H) connectivities
- 1 March 2003
- Published by Wiley in Magnetic Resonance in Chemistry
- Vol. 41 (3) , 177-182
A new technique for differentiating between2J(C,H) and3/4J(C,H) connectivities
- 13 October 2000
- Published by Wiley in Magnetic Resonance in Chemistry
- Vol. 38 (11) , 963-969
BIRD–HMBC: improved detection of heteronuclear long‐range couplings
- 13 October 2000
- Published by Wiley in Magnetic Resonance in Chemistry
- Vol. 38 (11) , 963-969
BIRD–HMBC: improved detection of heteronuclear long‐range couplings