The radiation-induced polymerization of formaldehyde has been studied in the solid state. The time of addition of one new link to a polymer chain increases exponentially in accordance with the Arrhenius law at 140 to 80 K, but approaches a constant value (approximately 10(-2) second) at temperatures below 10 K. Thus, a low-temperature limit to a chemical reaction rate has been observed. It is interpreted as a quantum effect caused by tunneling from the zero vibration level of the initial state, and a semiquantitative theory is given. The phenomenon should be taken into account for understanding tunneling of electrons in biological systems when such tunneling is accompanied by conformational changes. It could also be significant in slow, exothermic chemical reactions at low and ultralow temperatures, which may have had a role in chemical and biological evolution (cold prehistory of life?).

The temperature dependence of the mean square displacement of the iron atom in reduced and oxidized cytochrome c has been studied by Mössbauer spectroscopy. The flexibility of the protein, labeled by the modes coupling to the iron, is diminished upon reduction. The differences in flexibility are sufficient to explain the differences in physicochemical properties between the oxidized and the reduced forms.

No abstract

No abstract

No abstract