Crystal structures and solution dynamics of mono- and di-nuclear rhodium complexes of heterodinucleating macrocyclic ligands containing the 2,6-di(thiomethyl)pyridine sub-unit

Author(s):  
Ian M. Helps ◽  
Karen E. Matthes ◽  
David Parker ◽  
George Ferguson
2001 ◽  
Vol 30 (2) ◽  
pp. 168-169 ◽  
Author(s):  
Xiao-Yan Yu ◽  
Masahiko Maekawa ◽  
Mitsuru Kondo ◽  
Susumu Kitagawa ◽  
Guo-Xin Jin

Author(s):  
Laurent Barloy ◽  
Shailesh Ramdeehul ◽  
John A. Osborn ◽  
Claire Carlotti ◽  
Francis Taulelle ◽  
...  

1984 ◽  
Vol 62 (2) ◽  
pp. 332-335 ◽  
Author(s):  
Christopher Robin Paige ◽  
Mary Frances Richardson

HgCl2 and CdCl2 form 1:1 complexes with 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6). The complexes are isostructural. The metal coordination is hexagonal bipyramidal, with chlorine atoms strongly coordinated in the axial positions and the 18-crown-6 in the equatorial place. The symmetry of the complex is crystallographically required to be [Formula: see text], but is very nearly [Formula: see text]. The Hg—Cl, Hg—O, Cd—Cl, and Cd—O distances are 2.314(1), 2.825(4), 2.3645(5), and 2.752(1) Å, respectively. Crystals of HgCl2•18-crown-6 are rhombohedral, space group [Formula: see text], a = 7.746(2) Å, α = 95.26(3)°, Z = 1 unit of HgCl2C12H24O6, R = 0.026 for 543 independent reflections with θ < 25°, I > 3σ(I). Crystals of CdCl2•18-crown-6 are also rhombohedral, space group [Formula: see text], a = 7.712(3) Å, α = 95.57(2)°, Z = 1 unit of CdCl2C12H24O6, R = 0.022 for 534 independent reflections with θ < 25°, I > 3σ(I).


Sign in / Sign up

Export Citation Format

Share Document