摘要:
A signal function S(t 1 , t 2 ) is obtained from a plurality of coherence transfer pathways in a single acquisition by preparing a molecular system in a coherent non-equilibrium state, and alternately and sequentially detecting signals at individual sampling points, in t 2 , from the plurality of coherence transfer pathways by using gradient refocusing of a new pathway after signal detection at a sampling point in another pathway. The gradient encoding and refocusing of coherence pathways can use inhomogeneous rf-pulses (B 1 gradients) or B 0 field gradients. The coherence transfer pathways can be sequentially selected in an arbitrary order.
摘要:
A signal function S(t₁, t₂) is obtained from a plurality of coherence transfer pathways in a single acquisition by preparing a molecular system in a coherent non-equilibrium state, and alternately and sequentially detecting signals at individual sampling points, in t₂, from the plurality of coherence transfer pathways by using gradient refocusing of a new pathway after signal detection at a sampling point in another pathway. A frequency domain spectrum S(ω₁,ω₂) is another pathway. A frequency domain spectrum S(ω₁,ω₂) is constructed by first Fourier transforming the time domain signals S(t₁, t₂) in the t₂ dimension and producing real and imaginary components which modulate as sine and cosine signals in t₁. The real (ω₂) cosine (t₁) components are combined with the imaginary (ω₂)sine (t₁) components to form a complex data set S(t₁, ω₂) that is amplitude modulated in t₁. The complex data set is then Fourier transformed in the t₁ dimension to construct in frequency domain spectrum S(ω₁, ω₂) which contains construct in frequency domain spectrum S(ω₁, ω₂) which contains pure absorption lineshapes.