Product operator (NMR)

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In the various fields of nuclear magnetic resonance, the product operator mathematical formalism is often used to simplify both the design and the interpretation of often very complex sequences of radio frequency electromagnetic pulses applied to samples under study. Basically, it is a short hand mathematical construct, a set of equations, that is used in place of more complex, although equivalent, matrix multiplication. The formalism uses a rotating frame of reference, in which the central irradiation frequency, say 800 MHz, is fixed on the X- or Y-axis, and the magnetic field, by convention, points towards the postive Z-axis. By convention, I and S indicate magnetic vectors associated with protons or heteroatom, respectively. Subscripts are used to indicate the axial orientation of the magnetic vector. At equilibrium, the net proton magnetic vector is thus Iz. Although even 2 pulse experiments on only 2 protons can lead to equations with 32 parts in the final equation due to chemical shifts, pulses and various forms of coupling, the use and knowledge of phase-cycling techniques or gradients to wipe out most of the terms leads to simplified final equations once accounted for.

Single Pulses (rotations)

Arbitrary pulses (rotations)

Ix -->(x) --> Ix

Ix -->(y) --> Ixcos() + Izsin()

Ix -->(z) --> Ixcos() - Iysin()


Iy -->(x) --> Iycos() - Izsin()

Iy -->(y) --> Iy

Iy -->(z) --> Iycos() + Ixsin()


Iz -->(x) --> Izcos() + Iysin()

Iz -->(y) --> Izcos() - Ixsin()

Iz -->(z) --> Iz


90 degree pulses

So called 90 degree (/2) pulses, in which magnetization is rotated from one axis to another, are the most widely used single pulses in NMR spectroscopy and the above equations simplify to the following for such pulses.


Ix -->(90x) --> Ix

Ix -->(90y) --> Iz

Ix -->(90z) --> -Iy


Iy -->(90y) --> Iy

Iy -->(90z) --> Ix

Iy -->(90x) --> -Iz


Iz -->(90z) --> Iz

Iz -->(90x) --> -Iy

Iz -->(90y) --> -Ix


Chemical Shift Operators

Nuclei rotate around the XY plane at different frequencies. For example, assuming an 800 MHz central proton frequency, some protons will rotate 800 Hertz, or 1 part-per-million (ppm), faster, while others will rotate about the field more slowly. This difference from the central frequency, expressed in ppm, is called a chemical shift, which is sybolized as . The actual frequency, is sybolized as in radians/second or if expressed in Hertz. = 2. Remembering that the central frequency is fixed on the X-axis, the chemical shifts of each proton will cause them to rotate away from the X-axis towards the Y-axis for faster frequencies and towards the minus Y-axis for slower frequencies. The total angle of the rotation is time dependent, so that during time delay , the angle extended is

=

Note that chemical shifts only evolved in the XY plane.


Ix -->{} --> Ix cos() + Iy sin()

Iy -->{} --> Iy cos() - Iy sin()

Iz -->{} --> Iz

The one pulse experiment

Ignoring relaxation, coupling and other effects then, for a simple single proton starting at equilibrium, excited with a -90y pulse, the time-dependent signal observed is:

Iz --> Ix --> Ix cos() + Iy sin()

Relaxation Operators

Although the previous equations imply that the NMR signal would ring out indefinitely, a number of relaxation processes cause the excited NMR states to relax back to equilibrium. Although these effects can be separated into rates R1 and R2, longitudinal (Z-axis) and transverse (XY-plane) effects, respectively, for simplicity one can consider the effect relaxation rate, R, and its characteristic relaxation time T = 1/R. Relaxation effects cause an exponential decay of the observable signal. The effects of relaxation then are expressed as:

Ix -->{} --> Ix cos() + Iy sin() --> {R()} --> Ix cos()e{-/T} + Iy sin()e{-/T}

J-coupling Operators