TY - JOUR
T1 - Two-dimensional RF pulses
T2 - A new approach to selectively exciting J-coupled spins in nuclear magnetic resonance
AU - Lupulescu, Adonis
AU - Aharon, Hannah
AU - Frydman, Lucio
N1 - ERC [246754]; ISF [795/13]; EU'S BioNMR [261863]; Helen and Kimmel Award for Innovative Investigation; Perlman Family FoundationFinancial support from the ERC Advanced Grant No. 246754, ISF Grant No. 795/13, EU'S BioNMR Grant No. 261863, a Helen and Kimmel Award for Innovative Investigation, and the generosity of the Perlman Family Foundation, are gratefully acknowledged.
PY - 2013/10/14
Y1 - 2013/10/14
N2 - A new scheme for the excitation of spins according to the joint values of their heteronuclear or homonuclear J couplings and of their chemical shifts, is proposed and demonstrated. The principles of the new pulses involved derive from those employed in NMR imaging for exciting arbitrary 2D spatial shapes, using so-called "multidimensional" RF pulses. It is shown that if recast in a suitable spectroscopic framework, the distinction that π-pulses enable to establish between linear and bilinear interactions, support the selective excitation of coherences possessing arbitrary combinations of chemical shift and J-coupling values - a flexibility akin to that provided by a 2D J-resolved NMR spectrum. Details on the execution of the resulting 2D "J-shift" RF pulses are given, and examples where excitation only addresses spins with particular chemical shift offsets fulfilling specific J-coupling displacements, are demonstrated. Additional instances where such pulses could be applied, as well as main limitations of this new approach, are briefly discussed.
AB - A new scheme for the excitation of spins according to the joint values of their heteronuclear or homonuclear J couplings and of their chemical shifts, is proposed and demonstrated. The principles of the new pulses involved derive from those employed in NMR imaging for exciting arbitrary 2D spatial shapes, using so-called "multidimensional" RF pulses. It is shown that if recast in a suitable spectroscopic framework, the distinction that π-pulses enable to establish between linear and bilinear interactions, support the selective excitation of coherences possessing arbitrary combinations of chemical shift and J-coupling values - a flexibility akin to that provided by a 2D J-resolved NMR spectrum. Details on the execution of the resulting 2D "J-shift" RF pulses are given, and examples where excitation only addresses spins with particular chemical shift offsets fulfilling specific J-coupling displacements, are demonstrated. Additional instances where such pulses could be applied, as well as main limitations of this new approach, are briefly discussed.
UR - http://www.scopus.com/inward/record.url?scp=84886927804&partnerID=8YFLogxK
U2 - https://doi.org/10.1063/1.4823772
DO - https://doi.org/10.1063/1.4823772
M3 - مقالة
SN - 0021-9606
VL - 139
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 14
M1 - 144204
ER -