The practically diamagnetic phase of the title biradical underwent a solid-state phase transition at 350 K with a drastic χmol
T jump by an almost ideal value of 1 cm3 K mol-1 to give a stable S = 1 paramagnetic state.
The structure of ferricytochrome c' extracted from Rhodospirillum rubrum has been determined by the X-ray crystallographic method. Crystals in hexagonal space group P6(1), with unit-cell dimensions a = b = 51.72 A and c = 155.49 A, contain one dimer molecule composed of chemically identical polypeptide chains (monomer I and monomer II) per asymmetric unit. An electron density map has been calculated at a resolution of 2.8 A by the multiple isomorphous replacement method using four-circle diffractometer data from native crystals and two heavy-atom derivatives. The quality of the map was improved by averaging the electron density about the non-crystallographic 2-fold axis relating the two monomers. The initial three-dimensional model of monomer I was built on a computer graphics system and that of monomer II was derived from monomer I using the non-crystallographic symmetry matrices. The dimer structure has been refined using a combination of simulated annealing and conventional restrained least-squares crystallographic refinement. The current model includes 244 amino acid residues (122 x 2) and 2 hemes, with a root-mean-square deviation in bond lengths from ideal values of 0.022 A. The current crystallographic R-factor is 23.3% for 4,481 independent reflections [magnitude of Fo greater than or equal to sigma (F)] between 5.0 and 2.8 A resolution. The monomer molecule is structurally organized as an array of four nearly parallel alpha-helices which construct a left-twisted bundle. One end of the bundle, in which a covalently bound protoheme IX prosthetic group is incorporated, is more divergent than the other.(ABSTRACT TRUNCATED AT 250 WORDS)
[reaction--see text] Optically active diphenyl dichalcogenides were isolated in bulk for the first time by chiral crystallization. The absolute configuration of the P-helical enantiomer of diphenyl disulfide was determined by X-ray crystallography. On the basis of this determination and considering the similarities of the Cotton effects of diphenyl diselenide and ditelluride, the absolute configuration of optically active diphenyl dichalcogenides could be assigned. Furthermore, stereochemistry of chiral crystallization could be controlled by using an optically active crystal as a seed crystal.
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