Correlations of Crystal and Electronic Structure via NMR and X-ray Photoelectron Spectroscopies in the RETMAl 2 (RE = Sc, Y, La-Nd, Sm, Gd-Tm, Lu; TM = Ni, Pd, Pt) Series

• Published in: Inorganic chemistry Vol. 58; no. 10; pp. 7010 - 7025
• Main Authors: Radzieowski, Mathis, Stegemann, Frank, Doerenkamp, Carsten, Matar, Samir F, Eckert, Hellmut, Dosche, Carsten, Wittstock, Gunther, Janka, Oliver
• Format: Journal Article
• Language: English
• Published: United States 20-05-2019
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.9b00648

A total of 35 intermetallic aluminum compounds have been synthesized from the elements via arc melting and characterized by powder X-ray diffraction. A total of 15 of them have been previously reported; however, detailed property investigations were missing. Compounds of the RETMAl
(rare earth metal RE = Sc, Y, La-Nd, Sm, Gd-Tm, Lu) series with transition metal TM = Ni, Pd, and Pt crystallize isostructurally in the orthorhombic MgCuAl
type structure ( Cmcm, oC16, fc
). Single-crystal X-ray diffraction investigations were conducted on YNiAl
, LaNiAl
, YPdAl
, ScPtAl
, and YPtAl
. The TM and Al atoms form a [TMAl
]
polyanion, the RE atoms reside in cavities within the framework. While the Sc, Y, La, and Lu compounds exhibit Pauli-paramagnetic behavior, consistent with all atoms being closed shell, the other RETMAl
compounds show paramagnetism along with magnetic ordering at low temperatures, in line with an open-shell trivalent oxidation state for the RE atoms. Solid-state
Al NMR investigations were carried out on the Pauli-paramagnetic samples, all showing only a single central transition, in line with one crystallographic site for the respective atoms. The observed quadrupolar coupling constants and electric-field-gradient asymmetry parameters were found to be in good agreement with the density-functional-theory-calculated values. Isotropic resonance shifts are dominated by the Fermi-contact interactions with s-conduction electron densities at the Fermi edge (Knight shifts). The bonding characteristics mirror the electronic density of states and crystal chemistry of the family of intermetallic compounds under consideration. Both the Knight shifts and quadrupolar coupling constants can be predicted based on element-specific increments.