Abstract:Intermetallic compounds with the equiatomic composition CeTX that crystallize with the orthorhombic TiNiSi-type structure can be synthesized with electronrich transition metals (T) and X = Zn, Al, Ga, Si, Ge, Sn, As, Sb, and Bi. The present review focusses on the crystal chemistry and chemical bonding of these CeTX phases and on their physical properties, 119 Sn and 121 Sb Mössbauer spectra, high-pressure effects, hydrogenation reactions and the formation of solid solutions in order to elucidate structure-prop… Show more
“…[22,23] In contrast to the equiatomic compounds we observe two different colorings for Bärnighausen formalism [24][25][26] is presented in Figure 2. The symmetry reduction proceeds by the hexagonal branch of the Bärnighausen tree from the aristotype by the Ni 2 In [27] / ZrBeSi type [28] to the pair UPt 2 [29] / YAlGe.…”
Abstract. The quaternary germanides RE 3 TRh 4 Ge 4 (RE = Ce, Pr, Nd; T = Nb, Ta) were synthesized from the elements by arc-melting and subsequent annealing in a muffle furnace. The structure of Ce 3 TaRh 4 Ge 4 was refined from single-crystal X-ray diffractometer data: new type, Pbam, a = 719.9(2), b = 1495.0(3), c = 431.61(8), wR 2 = 0.0678, 1004 F 2 values, and 40 variables. Isotypy of the remaining phases was evident from X-ray powder patterns. Ce 3 TaRh 4 Ge 4 is a new superstructure variant of the aristotype AlB 2 with an ordering of cerium and tantalum on the aluminum site, whereas the honey-comb network is built up by a 1:1 ordering of rhodium and germanium. This crystal-chemical relationship is discussed based on a group-subgroup scheme. The distinctly different size of tantalum and cerium leads to a pronounced puckering of the [Rh 4 Ge 4 ] network, which shows the shortest interatomic distances (253-271 pm Rh-Ge) within the
“…[22,23] In contrast to the equiatomic compounds we observe two different colorings for Bärnighausen formalism [24][25][26] is presented in Figure 2. The symmetry reduction proceeds by the hexagonal branch of the Bärnighausen tree from the aristotype by the Ni 2 In [27] / ZrBeSi type [28] to the pair UPt 2 [29] / YAlGe.…”
Abstract. The quaternary germanides RE 3 TRh 4 Ge 4 (RE = Ce, Pr, Nd; T = Nb, Ta) were synthesized from the elements by arc-melting and subsequent annealing in a muffle furnace. The structure of Ce 3 TaRh 4 Ge 4 was refined from single-crystal X-ray diffractometer data: new type, Pbam, a = 719.9(2), b = 1495.0(3), c = 431.61(8), wR 2 = 0.0678, 1004 F 2 values, and 40 variables. Isotypy of the remaining phases was evident from X-ray powder patterns. Ce 3 TaRh 4 Ge 4 is a new superstructure variant of the aristotype AlB 2 with an ordering of cerium and tantalum on the aluminum site, whereas the honey-comb network is built up by a 1:1 ordering of rhodium and germanium. This crystal-chemical relationship is discussed based on a group-subgroup scheme. The distinctly different size of tantalum and cerium leads to a pronounced puckering of the [Rh 4 Ge 4 ] network, which shows the shortest interatomic distances (253-271 pm Rh-Ge) within the
“…In continuation of our systematic studies on equiatomic cerium intermetallics [1][2][3], we have recently investigated the chemical bonding peculiarities in the ZrNiAl type series CeMgGa vs. CeMgPd [17]. Electronic structure calculations revealed a substantially higher cohesive energy and a more directional bonding for the palladium as compared to the gallium compound.…”
Section: A N U S C R I P Tmentioning
confidence: 99%
“…2) which again shows a change in structure type. The bonding peculiarities of the structurally related stannides and plumbides CeNiSn, CePtSn and CePdPb have already been studied and are summarized in review articles [1][2][3].…”
Section: A N U S C R I P Tmentioning
confidence: 99%
“…Roughly one can subdivide these phases into three groups: (i) CeTX intermetallics with ZrNiAl type structure, (ii) CeTX phases with TiNiSi structure, and (iii) CeTX compounds with more complex structures. These three groups of materials have recently been reviewed [1][2][3]. The magnetic ground state of these CeTX intermetallics strongly depends on the Ce(4f )-T(nd) hybridization, leading to intermediate valence, non-magnetic Kondo lattices, antiferromagnetic or ferromagnetic ordering.…”
“…For ternary intermetallic compounds, the tetragonal body-centered ThCr 2 Si 2 -type (I4/mmm, >3250 entries) [8], the orthorhombic TiNiSi-type (Pnma, >1550 entries), and the hexagonal ZrNiAl-type (P62m, >1450 entries) [9] representatives show a broad variety of compounds with numerous, different elemental combinations. The structures and physical properties of the equiatomic RETX (RE = rare-earth element, T = transition metal, X = element of group [12][13][14][15] representatives have been recently summarized in a series of review articles [10][11][12][13].…”
Abstract:The REPt 2 Al 3 compounds of the late rare-earth metals (RE = Y, Dy-Tm) were found to crystallize isostructural. Single-crystal X-ray investigations of YPt 2 Al 3 revealed an orthorhombic unit cell (a = 1080.73(6), b = 1871.96(9), c = 413.04(2) pm, wR2 = 0.0780, 942 F 2 values, 46 variables) with space group Cmmm (oC48; q 2 pji 2 hedb). A comparison with the Pearson database indicated that YPt 2 Al 3 forms a new structure type, in which the Pt and Al atoms form a [Pt 2 Al 3 ] δ− polyanion and the Y atoms reside in the cavities within the framework. Via a group-subgroup scheme, the relationship between the PrNi 2 Al 3 -type structure and the new YPt 2 Al 3 -type structure was illustrated. The compounds with RE = Dy-Tm were characterized by powder X-ray diffraction experiments. While YPt 2 Al 3 is a Pauli-paramagnet, the other REPt 2 Al 3 (RE = Dy-Tm) compounds exhibit paramagnetic behavior, which is in line with the rare-earth atoms being in the trivalent oxidation state. DyPt 2 Al 3 and TmPt 2 Al 3 exhibit ferromagnetic ordering at T C = 10.8(1) and 4.7(1) K and HoPt 2 Al 3 antiferromagnetic ordering at T N = 5.5(1) K, respectively. Attempts to synthesize the isostructural lutetium compound resulted in the formation of Lu 2 Pt 3 Al 4 (Ce 2 Ir 3 Sb 4 -type, Pnma, a = 1343.4(2), b = 416.41(8), c = 1141.1(2) pm), which could also be realized with thulium. The structure was refined from single-crystal data (wR2 = 0.0940, 1605 F 2 values, 56 variables). Again, a polyanion with bonding Pt-Al interactions was found, and the two distinct Lu atoms were residing in the cavities of the [Pt 3 Al 4 ] δ-framework. X-ray photoelectron spectroscopy (XPS) measurements were conducted to examine the electron transfer from the rare-earth atoms onto the polyanionic framework.
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