ABSTRACT
Cluster compounds of the general formula A(2)[W(6)Cl(18)] containing singly charged A cations (A = K, Rb, Ag, Tl, NH(4), N(C(2)H(5))(4), N(n-C(3)N(7))(4), N(n-C(4)H(9))(4)) and [W(6)Cl(18)](2-) anions have been synthesized. Compounds were obtained by W(6)Cl(18) reduction using methanol and the corresponding metal or (alkyl-)ammonium salts. The use of CoCp(2) as reducing agent in inert solvents such as tetrahydrofurane also leads to the ionic compound (Co(C(5)H(5))(2))(2)[W(6)Cl(18)]. All compounds described here evidence the existence of octahedral clusters of the M(6)X(12) type with 20 cluster electrons occupying metal centered states, thus exceeding the conventional number of 16 electrons for this cluster type. Electrospray ionization (ESI) mass spectra were recorded for the neutral compound W(6)Cl(18) and for the ionic salts K(2)[W(6)Cl(18)], Cs(2)[W(6)Cl(18)], and (Co(C(5)H(5))(2))(2)[W(6)Cl(18)], showing that the cluster W(6)Cl(18) unit in these compounds is preserved in solution. The base peak in the ESI spectra for all compounds corresponds to the [W(6)Cl(18)](2-) anion, so that neutral W(6)Cl(18) is prone to undergo a two electron reduction process. This result is confirmed by cyclic voltammetry experiments, which makes of W(6)Cl(18) a very clean mild oxidizing agent. The preparation of the complete series of ionic A(2)[W(6)Cl(18)] (A = K, Cs, CoCp(2)) clusters allows to systematically investigate their structural trends as function of the distinctive cations, which is the main focus of the present work.
ABSTRACT
Crystalline samples of rare earth carbodiimides were synthesized by solid-state metathesis reactions of rare earth trichlorides with lithium cyanamide in sealed silica ampules. Two distinct structures were determined by single-crystal X-ray diffraction. The structure determined for Sm2(CN2)3 [C2/m, Z = 2, a = 14.534(2) A, b = 3.8880(8) A, c = 5.2691(9) A, beta = 95.96(2) degrees , R1 = 0.0267, and wR2 = 0.0667] was assigned for RE2(CN2)3 compounds with RE = Y, Pr, Nd, Sm, Gd, Tb, Dy, Ho, and Er, and the structure determined for Lu2(CN2)3 [R32, Z = 3, a = 6.2732(8) A, c = 14.681(2) A, R1 = 0.0208, and wR2 = 0.0526] was assigned for the smallest rare earth ions with RE = Tm, Yb, and Lu by powder X-ray diffraction. Both types of crystal structures are characterized by layers of [NCN](2-) ions whose arrangements can be derived from the motif of a closest packed layer of sticks. These layers alternate with layers of rare earth ions in a one-by-one sequence. Different tilting arrangements of the N-C-N-axes relative to the stacking directions (c) and different arrangements of RE3+ ions within metal atom layers account for the two distinct structures in which Sm3+ and Lu3+ ions adopt the coordination numbers 7 and 6, respectively.
