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By Janne Marie Soetbeer

Janne Marie Soetbeer determines the optimum dynamical decoupling (DD) scheme for effective aid of electron spin coherence loss in version platforms for spin labelled biomolecules looking on their specific rest habit. Extending the nth order DD scheme to double electron-electron resonance (DEER) experiments require the addition of a number of pump pulses for 1. Incomplete excitation of pump spin packets introduce sign artefacts that are minimized via pump pulse optimization together with linear-chirp and uneven hyperbolic secant pulses. Prolonging the dipolar evolution time with diminished sign artefact permits to volume the measurable interspin distances in biomolecules which have been differently now not obtainable because of spin echo leisure.

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From Fig. 92 µs, if the echo time of the 4-DEER experiment is treated as the beginning of the relaxation process. Fig. 10: Illustration of how the acquisition time in a T2 relaxation experiment influences the relaxation parameter Tm and ξ. 6 µs), stretched exponential fitting yields different values for ξ and Tm . e. later starting points of the fitting routine, indicated by the stars, decreasing ξ and Tm values are obtained. Hence, a slower apparent relaxation behaviour is observed with increasingly later acquisition time.

Applying the same assumptions as used for simplying equation (36) to (37), leads to V 9’-Uhrig (t) / hp4 cos [d (2⌧1 3 +p (1 p) cos [d (2⌧2 2⌧2 + T + ⌧ + 3t)] + p3 (1 ⌧1 T ⌧ 3 2t)] + p (1 p) cos [d (2⌧2 p) cos [d (⌧1 ⌧1 ⌧2 ⌧ 3t)] T + t)]]i (39) Note, how the fourth signal contribution in equation (38) (p3 q50 p7 p90 ) vanishes for t1 = t3 . Considering the main signal modulation with weight p4 , the minimum dipolar evolution 9’-Uhrig time is reached at t1,min = t2,min = t3,min = T and corresponds to tdip, min = 2⌧1 4 T + ⌧ .

6. To measure the relaxation of the pure refocused echo the stimulated and refocused echo needed to be separated in time by shifting the second π pulse by the delay δτ as illustrated in Fig. 6b. Delay δτ was chosen such that it only corresponds to a fraction of the total sequence time. This allows to neglect any relaxation occuring during the additional δτ time. Setting δτ = 0 in a relaxation measurements leads to an underestimation of the real relaxation time as the stimulated echo signal contribution decays with approximately T1 .

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