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Edward Mills Purcell, Henry Cutler Torrey and Robert Vivian Pound observed nuclear magnetic resonance through absorption in a bulk solid. A static magnetic field separates nuclear magnetic energy levels, and an applied radiofrequency field drives resonant transitions. Measuring the absorbed signal connects a microscopic nuclear moment with a laboratory electromagnetic circuit. The experiment helped make nuclear-spin behavior accessible in ordinary condensed samples.^[ref]

A physicist.^[ref]

An experimental physicist who coauthored observation of nuclear magnetic resonance in a solid with Edward Mills Purcell and Robert Vivian Pound. A radiofrequency field drives transitions of nuclear magnetic moments in an applied magnetic field; resonance appears as enhanced absorption. The method provided access to nuclear properties without requiring a freely traveling atomic beam.^[ref]

Awarded jointly to Felix Bloch and Edward Mills Purcell for new methods of precise nuclear magnetic measurement and related discoveries. The nuclear magnetic resonance article explains their distinct experiments.^[ref]

For an exponentially correlated local field, a single-frequency illustrative relaxation rate is $T_1^{-1}=C{\tau }_c/(1+{\omega }_0^2{\tau }_c^2)$. Its derivative with respect to ${\tau }_c$ changes sign at ${\omega }_0{\tau }_c=1$. Slow motion gives $T_1\propto {\tau }_c$, and fast motion gives $T_1\propto 1/{\tau }_c$; an Arrhenius plot consequently has a minimum of $T_1$ between opposite-slope limits.

For identical spin-one-half nuclei with homonuclear dipolar relaxation, include both transition frequencies:Writing $x={\omega }_0{\tau }_c$, the maximum of the rate satisfiesLet $\ell$ be jump length, ${\tau }_j$ the total waiting time, ${\tau }_c=c{\tau }_j$, and $f_D$ the diffusion jump correlation factor. In three dimensions $D=f_D{\ell }^2/(6{\tau }_j)=f_{D}c{\ell }^2/(6{\tau }_c)$. Combining this with $D=D_0\exp [-E_D/(k_{B}T)]$ givesThe numerical constant is one for the single-frequency illustration and 0.616 for the homonuclear dipolar model. Assumptions are a single activated process, exponential field correlations, a temperature-independent prefactor and coupling amplitude, and an established relation between local correlation and translational motion. Defect creation can enter the measured activation energy; it cannot automatically be identified with a bare migration barrier. The fluctuation-spectrum approach originates in the relaxation theory of Nicolaas Bloembergen, Edward Mills Purcell and Robert Pound.^[ref]

Edward Mills Purcell, Henry Cutler Torrey, and Robert Vivian Pound placed paraffin wax in a capacitively loaded coaxial cavity near 30 MHz between magnet poles. Coupling loops supplied and extracted power; oscillating and steady fields were perpendicular. Output balanced against a generator reference fed amplification, detection and a microammeter. A slow field sweep revealed absorption above fluctuations at room temperature. Weak drive avoided population equalization. Calibration was rough; field inhomogeneity could contribute to linewidth.^[ref]

These are driven experiments with continuous radiofrequency excitation and changing static field, not demonstrations of modern pulsed Fourier transform nuclear magnetic resonance. Bloch's theoretical paper explicitly distinguishes proposed free precession after a pulse from the forced precession actually studied.^[ref]

An experimental failure need not mean absent nuclear magnetic moments. In the model below, excessive drive reduces the population imbalance through nuclear magnetic resonance saturation; waiting too briefly can leave insufficient polarization. Separately, ordinary electrical losses can cause heating without identifying a nuclear resonance. The absorption experiment measured a balanced electrical signal, rather than using heating as its readout. Useful diagnostic checks include moving off resonance, changing the frequency, checking field uniformity and reducing drive. These are general checks; the historical operations actually documented are specified above.

In 1938, Isidor Isaac Rabi, Jerrold Zacharias, Sidney Millman and Polykarp Kusch introduced molecular-beam magnetic resonance. Their 1939 account describes a heated oven, vacuum slits, inhomogeneous A/B magnetic fields with opposite gradients, and a uniform static C magnetic field. Conductors supplied transverse oscillatory radiofrequency (RF) fields. Transitions spoiled refocusing, reducing the tungsten-filament detector signal. Alignment compared A-only and B-only attenuation; C-field sweeps at fixed RF frequency limited oscillator pickup. Matching frequency/field ratios across compounds checked nuclear assignments. Magnetic field calibration limited absolute magnetic moments; weak intervening fields caused unwanted transitions.^[ref]

The readout has a useful logical structure: A and the apertures admit trajectories correlated with a magnetic moment projection; B tests whether that projection has survived C. The two deflectors compensate for unchanged states, whereas a changed projection experiences a different force in B. A dip followed by recovery as the static magnetic field passes through resonance is therefore a population-sensitive signal. A comparison with RF absent or far from resonance is the natural baseline in this functional model; RF pickup, drift or background loss must not be mistaken for a state transition. A dip alone does not establish a pure initial quantum state or resolve an entire time-domain Rabi cycle.

This beam method measures transmitted particles after state-dependent deflection. The later bulk nuclear magnetic resonance methods of Felix Bloch and Edward Mills Purcell instead use a macroscopic sample and detect nuclear induction or RF absorption; NMR spectroscopy builds on that bulk setting. The common resonant coupling does not make their preparations or readouts interchangeable.^[ref][ref]