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|Title: ||Investigation into the solid state chemistry of beryllosilicates, sulfimide complexes and nosean compounds|
|Authors: ||MacLucas, Amy|
|Issue Date: ||2013|
|Publisher: ||© Amy MacLucas|
|Abstract: ||The similar chemical properties of sulfur, selenium and tellurium have been used to enable investigation of altering the size of occluded species, AOx (A = sulfur, selenium, tellurium and x = 0, 3 or 4), within sodalite based framework materials.
Geomimetic synthesis of nosean Na8[AlSiO4]6AOx where A = sulfur, selenium, tellurium and x = 0, 3 or 4 has been investigated and a synthesis method for pure nosean selenate has been reported.
Beryllosilicate and beryllogermanate sodalite compounds M8[BeSiO4]6A2 where M = Fe, Mn, Zn, Co, etc. and A = S, Se, Te have also been geomimetically synthesised and the magnetic effect of interchanging the original occluded sulfide for selenide resulted in a change in symmetry from P 3n to P222 at low temperature. Controlled mixed-metal beryllium compounds were targeted in order to investigate the effect of each M and combinations thereof.
Unusual grinding effects have been observed for blue square planar Cu(Ph2SNH)2Cl2, whereby a reversible colour change to green occurs on grinding or application of a sheer force. Evidence points towards the possibility that a sheer effect, induced by way of grinding, causes a twisting of the ligands, inducing a reversible colour change, with properties tending towards those of the pseudo-tetrahedral allogon in the square planar polymorph.
Anion metathesis has been found to occur within a system containing [Cu(Ph2SNH)4]Cl2, Ph2SNH.H2O and NaBF4. There is evidence indicating that, on grinding, an additional Ph2SNH ligand can be coordinated to the copper centre. This would be the first example of a purely solid state reaction in which the maximum coordination number for a ligand could be controlled by the counterion.|
|Description: ||A Doctoral Thesis. Submitted in partial fulfilment of the requirements for the award of Doctor of Philosophy of Loughborough University.|
|Appears in Collections:||PhD Theses (Chemistry)|
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