Nuclear magnetic resonance study of ligand exchange on hexakis(1,1,3,3-tetramethylurea)yttrium(III)

1981 ◽  
Vol 34 (3) ◽  
pp. 495 ◽  
Author(s):  
DL Pisaniello ◽  
SF Lincoln ◽  
EH Williams ◽  
AJ Jones

The first reported direct study of monodentate ligand exchange on yttrium(III) shows the rate of 1,1,3,3-tetramethylurea exchange on [Y {O=C(NMe2)2}6]3+ to be independent of free ligand concentration consistent with the operation of either a dissociative mechanism or an interchange mechanism where the encounter complex stability constant is ≥ 300. Typical data from this 270-MHz 1H n.m.r. study, where rate of ligand exchange = kex 6[Y {O=C(NMe2)2}63+] are as follows: kex(250 K) = 25�1 s-1, ΔH‡ = 27.1 � 0.5 kJ mol-1 and ΔS‡ = -108 � 2 J K-1 mol-1 for a CD3CN solution in which [Y{O=C(NMe2)2}63+] and free [O=C(NMe2)2] are 0.0039 and 0.028 mol dm-3 respectively. The preparations of [Y(ligand)6] (ClO4)3 where the ligand is O=C(NMe2)2, O=C(Me)(NHMe), O=C(Me)(NMe2), or O=C(Me)(NEt2) are also reported. Solutions of the latter three species and their respective ligands exhibit spectra consistent with ligand exchange being in the fast exchange limit of the n.m.r. time scale down to the lowest accessible temperatures.

1982 ◽  
Vol 35 (12) ◽  
pp. 2393 ◽  
Author(s):  
SF Lincoln ◽  
AM Hounslow ◽  
AJ Jones

A 270-MHz lH n.m.r. study shows the rate of 1,1,3,3-tetramethylurea exchange on [Lu{OC(NMe2)2}6]2+ in CD3CN solution to be independent of [OC(NMe2)2]free consistent with the operation of either a dissociative mechanism or an interchange mechanism characterized by an encounter complex stability constant ≥ 400. For this study ligand exchange rate = 6kex[Lu{OC(NMe2)2}63+] with kex(298.2 K) = 41.9 � 2.7 s-l, ΔH‡ = 41.7 � -0.6 kJmol-1 and ΔS‡ = -74 � JK-1 mol-l. These data are compared with those for the analogous scandium(III) and yttrium(III) systems and also those for some eight-coordinate trivalent lanthanide systems. The preparations of [LuL6] (ClO4)3, where L = OC(NMe2)2, OCMe(NMe2) and OCMe(Net2), are reported.


1972 ◽  
Vol 50 (24) ◽  
pp. 3950-3957 ◽  
Author(s):  
Mrs. G. M. Tanner ◽  
D. G. Tuck ◽  
E. J. Wells

The ligand exchange reaction between InL3 con plexes (L = CF3•CO•CH•CO•R− anion; R = methyl, i-butyl, phenyl, 2-naphthyl, and 2-thienyl) and excess free ligand (HL) has been studied in the solvents diisopropyl ketone, acetonitrile, benzene, and dimethylsulfoxide. Studies of the lifetimes of the reactants as obtained from their 19F n.m.r. line-widths show that the exchange is first order in InL3 concentration, but zero order in free ligand concentration. The coalescence temperature for the collapse of the n.m.r. 19F chemical shift between free and complexed ligand (~50 Hz) yields ΔG≠ for the exchange. The results are in agreement with the known stereochemical properties of indium(III) complexes. The rate-controlling process in the exchange is identified as the. rotation of one monodentate ligand about a partial double bond prior to intramolecular proton transfer to a second monodentate ligand.


1981 ◽  
Vol 34 (2) ◽  
pp. 283 ◽  
Author(s):  
SF Lincoln ◽  
DL Pisaniello ◽  
TM Spotswood ◽  
MN Tkaczuk

31P n.m.r, studies show that the rate of triphenylphosphine oxide exchange on [Zn(O=PPh3)4]2+ in CD2Cl2 solution is independent of [O=PPh3]free. A typical data set is: kex(200 K) = 611 ± 37 s-1, ΔH‡ = 32.0 ± 0.7 kJ mol-1 and ΔS‡ = -28.3 ± 3.4 J K-1 mol-1 for a solution in which [Zn(O=PPh3)42+] and [O=PPh3]free are 0.163 and 0.639 mol dm-3 respectively, where kex = exchange rate/(4[Zn(O=PPh3)42+])= (kBT/h)exp(-ΔH‡/RT)exp(ΔS‡/R) Similarly the rate of ligand exchange on [Mg(O=PPh3)5]2+ is shown to be independent of [O=PPh3]free and a typical data set is kex'(220 K) = 38 ± 4 s-1, ΔH‡ = 73.7 ± 1.8 kJ mol-1 and ΔS‡ = 123 ± 8 J K-1 mol-1 for a solution in which [Mg(O=PPh3)52+] and [O=PPh3]free are 0.0813 and 0.276 mol dm-3 respectively. The ligand exchange process on both species is considered to proceed through a D mechanism. The apparent equilibrium constant K = [Mg(O=PPh3)52+]/ ([Mg(O=PPh3)42+][O=PPh3] ≥ 150 dm3 mol-1 but in contrast [Zn(O=PPh3)2+ appears to be the only stable zinc(II) species in solution. It is concluded that these data probably reflect the hard acid character of magnesium(II) and the intermediate acid characteristics of zinc(II).


1982 ◽  
Vol 35 (7) ◽  
pp. 1489
Author(s):  
AE Bakas ◽  
AM Hounslow ◽  
SF Lincoln ◽  
NJ Maeji

The three species [UO2{OP(OMe)(NMe2)2}4](ClO4)2, [UO2{OP(OMe)2(NMe)}5] (C1O4)2 and [UO2{OPMe2Ph)]5] (ClO4)2 have been isolated and their CD2Cl2 solutions studied by means of 31P n.m.r. An equilibrium between [UO2L52+ and [UO2L4]2+ exists in solutions of the first two species. In solutions of the third species [UO2L5]2+ predominates and ligand exchange proceeds through a dissociative D mechanism for which kex (285 K), characterizing a single ligand, is 1830 � 250 s-1, ΔH‡ 82.15 � 1.8 kJ mol-1 and ΔS‡ 106 � 16 JK-1 mol-1.


Sign in / Sign up

Export Citation Format

Share Document