The ammonium salts of the complex anions trans-diiodobis(ethanedial-dioximato)-cobaltate(III), [Col2(GH)2]-, and trans-diiodobis(ethanedial-dioximato)rhodate(III), [RhI2(GH)2]- (GH- = ethanedial dioximate or glyoximate), have been synthesized and their structures determined from single crystal X-ray diffraction data at room temperature. The crystals of the two salts are monoclinic, space group C2/c. NH4[CoI2(GH)2] (I) crystallizes as dark-brown prisms with a greenish reflectance; its crystal data are: C4H10Col2N5O4, Mr = 504.90; a = 8.910(6), b = 11.700(9), c = 11.691(6) Å; β = 93.55(5)°; V = 1216.4 Å3; Z = 4; Dc = 2.78 Mg m-3. NH4[RhI2(GH)2] (II) crystallizes as yellow-brown blocks with crystal data: C4H10I2N5O4Rh, Mr = 548.88; a = 9.038(4), b = 11.949(5), c = 11.770(3) Å; β = 95.54(3)°; V = 1265.16 A3; Z = 4; Dc = 2.87 Mg m-3. The two structures were refined to a final RW = 0.045 for 1209 observed independent reflections and 95 parameters for I, and to a final RW = 0.040 for 1922 observed independent reflections and 87 parameters for II. The coordination geometry around Co or Rh in the anionic complexes is a distorted (4 + 2) octahedron of four equatorial chelating N atoms and two apical iodides. The H atoms of the hydroxyl groups are involved, as usual, in intramolecular O—H—O bridges with uniform Ο···Ο separations of 2.582 Å for I, and 2.713 Å for II. The rectilinear I—Co—I or I—Rh—I triads form “infinite” zigzag chains extending parallel to the ab plane, with a weak I—I contact of 3.988 Å for I, and 4.010 Å for II.
Saccharified Uranyl Ions: Self‐Assembly of UO
2
2+
into Trinuclear Anionic Complexes by the Coordination of Glucosamine‐Derived Schiff Bases
