Temperature jump measurements employing optical rotation to follow transients show an upper limit of 10μsec. on the half time of the helix‐random coil relaxation in poly‐α, L ‐glutamic acid. No relaxations are observed under conditions where the polymer exists in completely helical or completely random coil form. Assuming that the helix‐coil transition can be described kinetically as a pure growth process, expressions for the relaxation time are derived for three special cases. A comparison is made between the rate of the helix‐coil transition and the rate of imide proton exchange.
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Lumry et al. (1964) studied this question.
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