Li3[ScN2]: the first nitridoscandate(III)-tetrahedral Sc coordination and unusual MX2 framework.

Li(3)[ScN(2)] was prepared from Li(3)N with Sc or ScN in a nitrogen atmosphere at 1020 K as a light yellow powder with an optical band gap of about 2.9 eV. The crystal structure was refined based on X-ray and neutron powder diffraction data (Ia$\bar 3$, Z=16, X-ray diffraction: R(profile)=0.078, R(Bragg)=0.070; Neutron diffraction: R(profile)=0.077, R(Bragg)=0.074; Rietfeld: a=1003.940(8) pm, Guinier: a=1004.50(3) pm). Li(3)[ScN(2)] is an isotype of Li(3)[AlN(2)] and Li(3)[GaN(2)] and crystallizes in an ordered superstructure of the Li(2)O structure type, leading to a three-dimensional framework of all-vertex-sharing tetrahedra 3[infinity[ScN[4/2][3-]]. Li is displaced from the center of a tetrahedron of N atoms in the direction of one trigonal face. Li(3)[ScN(2)] decomposes above 1050 K to form ScN and Li(3)N. Calculations of the periodic nodal surface (PNS) and of the electron localization function (ELF) support the picture of a covalent Sc-N network separated from isolated Li cations, whereby scandium d orbitals are involved in the chemical bonding.