New ways to measure and suppress 1H-1H ...
Type de document :
Communication dans un congrès avec actes
URL permanente :
Titre :
New ways to measure and suppress 1H-1H couplings in 1H-13C experiments
Auteur(s) :
Sinnaeve, Davy [Orateur]
Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 [RID-AGE]
Biologie Structurale Intégrative [ERL 9002 - INSERM U1167 - BSI]

Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 [RID-AGE]
Biologie Structurale Intégrative [ERL 9002 - INSERM U1167 - BSI]
Titre de la manifestation scientifique :
43rd FGMR Annual Discussion Meeting
Organisateur(s) de la manifestation scientifique :
Division of Magnetic Resonance of the German Chemical society
Ville :
Karlsruhe
Pays :
Allemagne
Date de début de la manifestation scientifique :
2022-09-12
Mot(s)-clé(s) en anglais :
NMR spectroscopy
Discipline(s) HAL :
Chimie/Chimie analytique
Résumé en anglais : [en]
In organic molecules, 1H-1H couplings are abundant and their measurement contributes greatly to constitutional, configurational and conformational structure elucidation studies. The downside of their abundance is that it ...
Lire la suite >In organic molecules, 1H-1H couplings are abundant and their measurement contributes greatly to constitutional, configurational and conformational structure elucidation studies. The downside of their abundance is that it results in complex and broad multiplets that may overlap, obstructing extraction of individual couplings or other spectral information. Pure shift experiments alleviate the overlap problem by delivering fully homodecoupled 1H spectra, boosting spectral resolution by an order of magnitude [1]. They can elegantly be combined with selective 2D J-resolved experiments, such as SERF, G-SERF or PSYCHEDELIC [2], allowing individual coupling measurement at pure shift resolution. Unfortunately, in situations where coupled protons have very small chemical shift differences (strong coupling), pure shift and 2DJ methods often break down. A way to circumvent this issue is by focusing on the 13C isotopomer signals instead, since at natural abundance the large 1JCH coupling breaks the chemical shift degeneracy between protons relative to the all-12C isotopomer [3].I will first introduce a new selective 2DJ method that allows selective observation of the 13C isotopomer signals by making good use of the BIRD pure shift element [3]. This provides access to 1H-1H couplings unattainable with SERF or PSYCHEDELIC.Unfortunately, a major drawback of BIRD pure shift methods is that geminal 1H-1H couplings are not suppressed, which is especially problematic for compounds rich in methylene groups. This is a general limitation for pure shift 1H-13C HSQC experiments. Proposed solutions have been the use of constant-time acquisition, the perfect echo, or J-resolved echo processing [4-6], but all these methods have particular shortcomings that complicate their application under molecular alignment conditions, for medium to large size molecules, or for selective 2DJ experimental design.I will present a generally applicable pure shift method compatible with 1H-13C HSQC experiments that circumvents all aforementioned shortcomings at a reasonable price in sensitivity relative to the parent pure shift HSQC experiment. The new method, coined CYBORG, allows maximum pure shift resolution for 1H-13C HSQC experiments, holds promise for the study of larger compounds such as peptides or protein side-chains, and is easily combined with selective 2DJ methods.Literature:[1] K. Zangger, Prog. Nucl. Magn. Reson. Spectrosc. 2015, 86-87, 1. [2] D. Sinnaeve, eMagRes 2021, 9, 267. [3] J. Aguilar et al., Angew. Chem. Int. Ed. 2011, 50, 9716. [4] T. Reinsperger et al., J. Magn. Reson. 2014, 239, 110. [5] L. Kaltschnee et al., Chem. Commun. 2014, 50, 15702. [6] P. Sakhaii et al., Sci. Rep. 2021, 11, 21566.Lire moins >
Lire la suite >In organic molecules, 1H-1H couplings are abundant and their measurement contributes greatly to constitutional, configurational and conformational structure elucidation studies. The downside of their abundance is that it results in complex and broad multiplets that may overlap, obstructing extraction of individual couplings or other spectral information. Pure shift experiments alleviate the overlap problem by delivering fully homodecoupled 1H spectra, boosting spectral resolution by an order of magnitude [1]. They can elegantly be combined with selective 2D J-resolved experiments, such as SERF, G-SERF or PSYCHEDELIC [2], allowing individual coupling measurement at pure shift resolution. Unfortunately, in situations where coupled protons have very small chemical shift differences (strong coupling), pure shift and 2DJ methods often break down. A way to circumvent this issue is by focusing on the 13C isotopomer signals instead, since at natural abundance the large 1JCH coupling breaks the chemical shift degeneracy between protons relative to the all-12C isotopomer [3].I will first introduce a new selective 2DJ method that allows selective observation of the 13C isotopomer signals by making good use of the BIRD pure shift element [3]. This provides access to 1H-1H couplings unattainable with SERF or PSYCHEDELIC.Unfortunately, a major drawback of BIRD pure shift methods is that geminal 1H-1H couplings are not suppressed, which is especially problematic for compounds rich in methylene groups. This is a general limitation for pure shift 1H-13C HSQC experiments. Proposed solutions have been the use of constant-time acquisition, the perfect echo, or J-resolved echo processing [4-6], but all these methods have particular shortcomings that complicate their application under molecular alignment conditions, for medium to large size molecules, or for selective 2DJ experimental design.I will present a generally applicable pure shift method compatible with 1H-13C HSQC experiments that circumvents all aforementioned shortcomings at a reasonable price in sensitivity relative to the parent pure shift HSQC experiment. The new method, coined CYBORG, allows maximum pure shift resolution for 1H-13C HSQC experiments, holds promise for the study of larger compounds such as peptides or protein side-chains, and is easily combined with selective 2DJ methods.Literature:[1] K. Zangger, Prog. Nucl. Magn. Reson. Spectrosc. 2015, 86-87, 1. [2] D. Sinnaeve, eMagRes 2021, 9, 267. [3] J. Aguilar et al., Angew. Chem. Int. Ed. 2011, 50, 9716. [4] T. Reinsperger et al., J. Magn. Reson. 2014, 239, 110. [5] L. Kaltschnee et al., Chem. Commun. 2014, 50, 15702. [6] P. Sakhaii et al., Sci. Rep. 2021, 11, 21566.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Collections :
Source :
Date de dépôt :
2025-04-03T03:52:09Z