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Systematic structural coordination chemistry of p-tert-Butyltetrathiacalix[4]arene: further complexes of Lanthanide Metal Ions

Citation

Bilyk, A and Dunlop, JW and Fuller, RO and Hall, AK and Harrowfield, JM and Hosseini, MW and Koutsantonis, GA and Murray, IW and Skelton, BW and Sobolev, AN and Stamps, RL and White, AH, Systematic structural coordination chemistry of p-tert-Butyltetrathiacalix[4]arene: further complexes of Lanthanide Metal Ions, European Journal of Inorganic Chemistry, 2010, (14) pp. 2127-2152. ISSN 1434-1948 (2010) [Refereed Article]

Copyright Statement

2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

DOI: doi:10.1002/ejic.200901070

Abstract

Extension of previous work on the lanthanide(III) ion complexes of p-tert-butyltetrathiacalix[4]arene has led to a variety of structurally characterised species containing oxo-, hydroxo- and aqua-ligands presumably derived from water present in the preparative medium, along with the thiacalixarene in various stages of deprotonation. The overall stoichiometry of some species is remarkably complicated due to the presence of simple anions and multiple solvents. Simplest is the binuclear complex [(μ-H2O){Ln(O-dmf)2}2(HLdmf)2]nS (dmf = dimethylformamide) [1Ln, Ln = Sm (nS = 2dmf), Eu (nS = 1.5dmf2MeCN)], also the best-defined of all the arrays studied. The heaviest lanthanides give trinuclear Ln(OH)32Ln(LH)xdmfyH2O (2Ln, Ln = Yb, Lu), while both oxo and hydroxo species are isolable with Eu: trinuclear Eu3O(L)(LH)(LH4)13dmf (3) and tetranuclear Eu4O(OH)2(L)(LH2)2(LH4)12dmf (9), both somewhat atypical species containing uncoordinated thiacalixarene molecules within the lattice. Anion (NO3, ClO4) coordination, as in the tri- and tetranuclear species, 46Ln, 9, 10Ln, 11Ln, 12, seems especially favoured for the lighter lanthanides. In these arrays, the Ln3 and Ln4 aggregates are triangular or (quasi-)square-planar, except for Gd4O2(LH2)42H2O2MeOH2dmf3.375CH2Cl2 (12), where there is a Z-disposition. Most common is an Ln3O core, which spans the gamut of Ln in three sets of crystal forms with cells of similar dimensions: for Ln = La...Nd, Ln3(OH)(NO3)4(LH2)24.5dmf (5Ln) (space group C2/m), and Sm...Lu, Ln3O(NO3)(LH)24H2O2dmso2MeCN3py (6Ln) (space group P21/n), conformity with crystallographic symmetryentails disorder of the Ln atoms; in a further form of lowersymmetry Pn, (pyH)Ln3O(NO3)2(LH)22MeCNxH2Oydmso1.5pyMeOH (7Ln, Ln = La, Ce), with no imposed crystallographic symmetry, some disorder persists, but none is found in the crystallographically unrelated form of 8Pr, Pr3O(NO3)(LH)216H2O2MeCN5py. Ln4(OH)(NO3)3(L)28dmf2dmso3H2O (10Ln, Ln = Pr...Gd, previously defined for Nd) has a square-planar Ln4O array sandwiched between a pair of L ligands, with a similar form found for Ln4O(ClO4)2(L2)xdmfyH2O (11Ln, Ln = La...Nd).

Item Details

Item Type:Refereed Article
Keywords:coordination chemistry, lanthanoid, calixarene
Research Division:Chemical Sciences
Research Group:Inorganic chemistry
Research Field:F-block chemistry
Objective Division:Expanding Knowledge
Objective Group:Expanding knowledge
Objective Field:Expanding knowledge in the chemical sciences
UTAS Author:Fuller, RO (Dr Rebecca Fuller)
ID Code:153930
Year Published:2010
Deposited By:Chemistry
Deposited On:2022-10-17
Last Modified:2022-11-03
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