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Jahn-Teller effect observation

A minor success is also seen in complexes of d and d" ions, in which the distorted octahedral geometries observed may be rationalized (and indeed predicted) in terms of the Jahn-Teller effect, and ultimately in terms of the steric activity of the open d shell. This is a common feature in copper(n) chemistry, and you will... [Pg.171]

The Jahn-Teller effect is always to be expected when degenerate orbitals are unevenly occupied with electrons. In fact, it is observed for the following electronic configurations ... [Pg.75]

RhAr6]+ ions are octahedral. As shown in Fig. 5, these observations are a manifestation of the Jahn-Teller effect in the gas phase. It must be stressed that other donor molecules easily displace these weak ligands this will be discussed in Section III.C.l. [Pg.371]

As far as the trication [Ni(bipy)3]3+ is concerned, both EPR spectroscopy166 and the magnetic moment (2.10 8) 67 confirm its Ni(III) nature (d7-t6ge>). Contrary to what has been observed for the corresponding Ni(II) complex, for which all the Ni-N distances are identical, in this case the equatorial Ni-N distances (2.02 A) are about 0.1 A longer than the axial Ni-N distances.166 This has been attributed to the Jahn-Teller effect. [Pg.299]

As there are no other sodium compounds Na2MeF4 hitherto known it may well be presumed, that the existence of this type is closely connected with the Jahn-Teller effect, that may stabilize the structure. There is a conspicuous increase of the molecular volumes of about 2% as compared to the sum of the volumes, the component fluorides have in their binary compounds NaF, CrF2 and CuF2 resp. Generally a decrease of volumes is observed during formation of compounds. [Pg.35]

Cotton, F. A., and M. D. Meyers Magnetic and spectral properties of the spin-free 3d -systems FeFj" and CoF Probable observation of dynamic Jahn. Teller effects. J. Am. Chem. Soc. 82, 5023 (1960). [Pg.76]

The Cupric, Cu2+ or Cu(II) State, 3d9 The most important and stable oxidation state for copper is divalent. There is a well-defined aqueous chemistry of the Cu2+ ion, which generates the familiar blue solution when complexed with water. A large number of copper coordination compounds exist and these have been studied extensively. A strong Jahn-Teller distortion is associated with the 3d9 electronic configuration of this ion. This implies that a regular tetrahedron or octahedron about the Cu2+ ion is never observed, except in the rare occurrence of a dynamic Jahn-Teller effect. The tetragonal distortion about an octahedron can lead to a square-planar coordination which is often observed in Cu(II) oxides. [Pg.54]

The preceding three reduced molybdenum clusters indicate that rhomboidal cluster units are common among this kind of oxide, and the Mo-Mo distances in the cluster units are dependent on CVE assignable to the Mo4 units. MO calculations on Mo4 molecular cluster compounds containing 10 CVE and 8 CVE have shown that the 8-electron clusters distort from a second-order Jahn-Teller effect (116). Such a distortion has been observed in the 8-electron W4(OEt)16 (117). [Pg.81]

TL OEt) ]224 with distortions due to M—M bonding. Crystal structure analysis of [W4(OEt)i6] (Figure 22) reveals the presence of two short W—W bonds (2.645 and 2.76 A) and two long bonds of 2.93 A. In this structure, there is a total of five possible W—W interactions, and thus, to form five bonds of order one, ten electrons are required. Only eight metal electrons are available for metal-metal bonding, which leads to the observed distortions. It has been suggested that this distortion results from a novel second order Jahn-Teller effect.225... [Pg.993]

Two additional factors that can contribute to line breadth and shape are spin-orbil coupling, which is particularly prevalent in complexes of the heavier transition metals, and departures from cubic symmetry, such as through the Jahn-Teller effect. This latter effect, which will be discussed later in this chapter, is believed to be responsible for the low-frequency shoulder observed on the absorption line for [TKH30)6)2 (Fig. 11.8). [Pg.233]


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