Jump to main content
Jump to site search

Issue 18, 2017
Previous Article Next Article

Molecular rare earth metal alumosilicates

Author affiliations


The synthesis and stabilization of molecular four-coordinated lanthanide alumosilicates was achieved by the use of a highly encumbered alumosilicate ligand LAl(OH·thf)(μ-O)Si(OH)(OtBu)2 (1, L = HC{C(Me)N(2,6-iPr2C6H3)}2). Reactions between 1 and tris-cyclopentadienyl lanthanides (LnCp3; Ln = Ce, Nd, Sm, Gd, Tb, Dy, Y, Er) derived in the isolation of eight compounds (2–9) where the ligand is observed in three different bonding modes: adducts (2, 3), spirocyclic (4) or cyclic (5–9) coordination compounds. The observed reactivity can be related to the ionic radius of the lanthanide atom and the nature of the oxygen donor-atom from the hydroxide (Al–OH) or hydroxyl (Si–OH) moieties in 1. Compounds 2–9 present general O–Al–O–Si–O–Ln connectivities with different degrees of substitution over the –OH groups in 1 and structural features with only slight variations over the alumosilicate moiety (O–Al–O–Si–O) upon the lanthanide coordination. The spirocyclic samarium derivative presents two tetra-coordinated samarium atoms with a tetrahedral and distorted square planar geometries, respectively, as a result of a highly strained polycyclic architecture.

Graphical abstract: Molecular rare earth metal alumosilicates

Back to tab navigation

Supplementary files

Publication details

The article was received on 10 Mar 2017, accepted on 05 Apr 2017 and first published on 21 Apr 2017

Article type: Paper
DOI: 10.1039/C7DT00874K
Citation: Dalton Trans., 2017,46, 6069-6078
  •   Request permissions

    Molecular rare earth metal alumosilicates

    R. Huerta-Lavorie, D. V. Báez-Rodríguez, J. García-Ríos, E. Martínez-Vollbert, D. Martínez-Otero and V. Jancik, Dalton Trans., 2017, 46, 6069
    DOI: 10.1039/C7DT00874K

Search articles by author