Complexes with coordination number nine

The lanthanum complex (Scheme 9) has the coordination number nine with two NO3 ions bidentately bound in the solid state, while in solution only one nitrate group is coordinated. H2dapsox is symmetrically pentadentately coordinated in the a-oxyazine form (Scheme 9). 

Note that the cis isomer lacks an improper axis of rotation and is therefore chiral, but that the trans isomer has a plane of symmetry and will be achiral in the absence of an asymmetric carbon in the phosphine ligand-28 As in the case of the previously encountered cyclopentadienyl complex (page 476), it can be argued whether the coordination number is 5 or 9. In either semantic interpretation these compounds are of considerable interest since isomerism in nine-coordinate complexes Is even less well documented than in those with coordination number 5. 

There are few structures known with coordination numbers larger than 8. The existence of coordination number 12 in some crystal lattices was mentioned above. Discrete nine-coordinate structures are known for complexes such as (LnlH.O) )1 and for the hydnde complexes [MHJ2- (where M = Tc or Re). These structures are formed by adding a ligand to each of the rectangular feces of a trigonal prism (Fig. 12.40). 

A number of chloride complexes include Pr(terpy)Cl3.8H2O X-ray diffraction established the presence of a [Pr(terpy)C1(H20)5] + ion. Lanthanide nitrates react with 1 mole of terpy in MeCN to give [La(terpy)(N03)3(H20) ] (Ln = La, = 2 Ln = Ce-Ho, n = 1 Ln = Er-Lu, n = 0) with coordination numbers decreasing from 11 (La) to 9 (Er-Lu) if these are crystallized from water [Ln(terpy)(N03)2(H20)4] NO3 (Ln = La-Gd) and [Ln(terpy)(N03)2(H20)3]N03.2H20 (Ln = Tb-Lu) are formed these have both biden-tate and ionic nitrate and nine- and eight-coordinate lanthanides, respectively. Thiocyanate complexes Ln(terpy)2(NCS)3(Ln = Pr, Nd) are also nine coordinate. 

Preston (1985) described the solvent extraction behavior of a large number of metal cations including rare earth nitrates in solutions of Versatic 10 (2-ethyl-2-methylheptanoic acid), naphthenic, 2-bromodecanoic and 3,5-diisopropylsalicylic acids in xylene. The last two acids extract metal cations under more acidic conditions, pH 1-2. For Versatic 10 the order of extraction of yttrium and lanthanides is La < Ce < Nd < Gd < Y < Ho < Yb and for naphthenic acids it is La < Ce < Y < Nd < Gd k Ho Yb. The lanthanides tend to form complexes of predominantly ionic nature. In the case of Versatic 10, the stability of the complexes increases uniformly with atomic number due to the increase in electrostatic energy as a result of the decrease in ionic radius. The primary branched naphthenic acid allows the formation of complexes with high coordination number, nine for La to Nd, eight and eventually six as the metal ionic radius decreases. In general, the extraction of a metal ion by a carboxylic acid H2A2 can be represented by the reaction... 

With diethylenetriamine two types of complexes are formed with nitrate as the anion (Forsberg and Walthen, 1971) R(dien)3(N03)3 (R=La-Gd) and R(dien)2(N03)3 (R = La-Yb, Y). The tris complexes contain only ionic nitrate whereas the bis complexes contain both ionic and coordinated nitrate groups. Coordination number nine was thus assigned to the tris complexes but the coordination number in the bis complexes remains undetermined due to the impossibility of determining the relative numbers of ionic and coordinated nitrate groups solely by means of the infrared spectra. 

Probably, the first series of lanthanide complexes with neutral oxygen donor ligands is that of AP with the lanthanide nitrates. In 1913, Kolb (79) reported tris-AP complexes with lighter lanthanide nitrates and tetrakis-AP complexes with heavier lanthanide nitrates. Subsequently, complexes of lanthanide nitrates with AP which have a L M of 6 1 and 3 1 have also been prepared (80-82). Bhandary et al. (83) have recently shown through an X-ray crystal and molecular structure study of Nd(AP)3(N03)3 that all the nitrates are bidentate and hence the coordination number for Nd(III) is nine in this complex. Complexes of AP with lanthanide perchlorates (81, 84), iodides (81, 85), and isothiocyanates (66, 86, 87) are known. While the perchlorates and iodides in the respective complexes remain ionic, two of the isothiocyanates are coordinated in the corresponding complexes of AP with lanthanide isothiocyanates. 

---