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Synthesis, reactions and multinuclear NMR spectroscopic studies of organo bimetallic and trimetallic compounds

The 207Pb and 119Sn NMR chemical shift were used to study the effect of temperature on Ph3MCl
(M= Pb and Sn) adducts in the presence of 10% excess pyridine. The 207Pb and 119Sn chemical
shift indicate a slow exchange at low temperatures below -90 0C and a significant exchange at
higher temperatures above 10 0C. A plot of temperature against 207Pb or 119Sn chemical shift
showed a curve with gentle slope at lower and a steep slope at higher temperatures. A good
linear correlation (coefficient. of 0.95) between Hammett substituent constant and 207Pb or 119Sn
chemical shift of para-substituted derivatives of Ph3MCl.py* (py* = NMe2, OMe, Me, Ph, H, Br,
COPh and COMe; at -90 0C in CD2Cl2/CH2Cl2) was found. Both 207Pb and 119Sn chemical shift
ranges are characteristic of five coordinate systems resolving into trigonal bipyramidal geometry
as shown by X-ray crystal structures.
New complexes of the type [CpFe(CO)(SnPh3)L] (L = PPh3, PBu3, PCy3, PMe3, P(NMe2)3,
PMePh2, PMe2Ph, P(p-FC6H5)3, P(p-OMeC6H4)3, P(p-tolyl)3, P(OMe)3, and P(OPh)3 were
synthesized by ultraviolet irradiation of [CpFe(CO)2(SnPh3)] and the appropriate phosphine or
phosphite ligand. 57Fe NMR studies of the complexes showed an increasing linear relationship
with Tolman’s steric parameter, whereas with Tolman’s electronic parameter the 57Fe chemical
shift showed a decrease. The X-ray crystallographic profile of the selected new piano stool type
complexes shows a significant correlation to the NMR data (solution state), i.e. Fe-Sn, Fe-P bond
length and Sn-Fe-P bond angle against chemical shifts of 207Pb and 119Sn. Disubstituted
complexes of the type [CpFe(SnPh3)L2] (L = PMe3, PMe2Ph, P(OMe)3 and P(OPh)3 were
synthesized under similar conditions as monosubstituted compounds. The correlation trends
between the NMR data and X-ray crystallographic profiles are similar to those found for
monocarbonylated complexes.
Tungsten phosphine complexes of the type [W(CO)5(PR3)] (prepared from [W(CO)6] under
thermal conditions) and [W(CO)4(NCMe)(PR3)] (prepared from [W(CO)5(PR3)] by use of
Me3NO-promoted decarbonylation) were synthesized and characterized by, among other
methods X-ray diffraction techniques (R = Ph, p-tolyl, p-OMeC6H4, p-FC6H4, p-CF3C6H4, and
NMe2). The tungsten complexes [W(CO)4(NCMe)(PR3)] react with [(dppp)Pt{C≡C-C5H4N}2] at
room temperature to form new complexes of the type [(dppe)Pt{C≡C-C5H4N-W(CO)4(PR3)}2] which were characterized unambiguously by NMR spectroscopy. There is a fair correlation
between 195Pt and 183W NMR chemical shifts and Tolman’s electronic parameter which indicates
a fair influence by the substituents of the phosphorus atom on both metal centres.
Tungsten complexes of the type [W(CO)4(NCMe)(L)] (L= PPh3, P(p-FC6H4)3, P(p-OMeC6H4)3,
P(p-tolyl)3, P(p-CF3C6H4)3, PMePh2, and PPh2(C6F5) react with [(PPh3)2Rh(H)2(pytca)] (pytca =
2-(4-pyridyl)thiazole-4-carboxylate) to form new complexes of the type [(PPh3)2Rh(H)2(pytca)-
W(CO)4(L)] under mild conditions. These complexes were characterized principally by NMR
spectroscopy and X-Ray crystallography (L = P(p-tolyl)3). Crystallographic evidence was found
for π-π-π interactions involving two phenyl rings, one of the two phosphines bonded to rhodium
atom, one of the three phosphines bonded to tungsten and the pyridyl ring of the thiazole
corboxylate group. A second π-π interaction is found between a thiazole and a phenyl ring of the
phosphine ligand bonded to the rhodium atom. A fair correlation was found between the rhodium
and tungsten chemical shift measured from this series of complexes as a result of varied paraphenyl
substituent of phosphine ligand bonded to the tungsten atom. This therefore implies the
possible existence of electronic communication between the two bridged metal centres.

Identiferoai:union.ndltd.org:netd.ac.za/oai:union.ndltd.org:wits/oai:wiredspace.wits.ac.za:10539/11990
Date01 October 2012
CreatorsMampa, Richard Mokome
Source SetsSouth African National ETD Portal
LanguageEnglish
Detected LanguageEnglish
TypeThesis
Formatapplication/pdf, application/pdf

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