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  • 1
    ISSN: 1434-1948
    Keywords: Dimethyltin salicylaldoximates ; Chiral ligands ; Proton-tin HMQC NMR ; X-ray structure ; Trinuclear microclusters ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complex {[(CH3)2Sn]2[(CH3)2SnO](OCH3)(HONZO)(ONZO)} (3) [ONZOH is the oximate residue, o-(-ON=CH-C6H4-OH), HONZO the corresponding phenolate residue, o-(HON=CH-C6H4-O-), and ONZO the dibasic species o-(-ON=CH-C6H4-O-), all derived from salicylaldoxime, o-(HON=CH-C6H4-OH)] reacts with an excess of racemic (d,l)-2-methyl-1-butanol to afford the μ2-substitution product 5a {[(CH3)2Sn]2[(CH3)2SnO][OCH2CH(CH3)CH2CH3](HONZO)(ONZO)]}. Crystallographic characterisation of the trinuclear microcluster 5a shows the presence of the monobasic HONZO ligand in a tridentate μ2-O,N mode and of the dibasic ONZO ligand in a tridentate O,N,O mode. This coordination mode leads to one seven-coordinate and two five-coordinate tin centers that are linked by a μ3-oxo function. The coordination geometries are distorted pentagonal bipyramidal and trigonal bipyramidal, respectively. The two low-coordinate tin atoms are linked by the alkoxide ion. The corresponding chiral (S)-2-methyl-1-butanol reacts analogously to yield 5b. By contrast, reaction of 3 with chiral secondary alcohols (2-butanol or 1-phenyl-1-ethanol), in various molar ratios, failed to provide the corresponding μ2-alkoxy complex. Instead, pure crystals of {[(CH3)2Sn]2[(CH3)2SnO](OH)(HONZO)(ONZO)} (2a) were isolated.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 5 (1991), S. 1-23 
    ISSN: 0268-2605
    Keywords: Organotin ; carboxylate ; structure ; X-ray ; review ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This review describes the structural chemistry of organotin carboxylates, covering data acquired for mono-, di- and tri-organotin compounds and complexes. A brief discussion is given for organotin amino-acid derivatives.
    Additional Material: 31 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0268-2605
    Keywords: Rhenium ; carbonyl ; terpyridyl ; tris(2-pyridyl)amine ; tris(2-pyridyl)methane ; tris(2-pyridyl)phosphine ; structure ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of [Re(CO)5Cl] with the ligands tpy (2,2′:6′,2″-terpyridine), py3N {tris(2-pyridyl)-amine}, py3CH {tris(2-pyridyl)methane}, and py3P {tris(2-pyridyl)phosphine} in toluene solution realize compounds with the general formulation [Re(ligand)(CO)3Cl] in which the tripyridyl ligands are bidentate. X-ray structural determinations of fac-[Re(typ)(CO)3Cl].H2O and fac-[Re(py3N)(CO)3Cl] confirm these assignments. [Re(tpy)(CO)3Cl].H2O (C18H13ClN3O4Re) is monoclinic, space group P21/n, with cell dimensions a = 7.432(2) Å, b = 17.016(4) Å, c = 14.466(2) Å, β = 93.51(2)°, and Z = 4; full-matrix least-squares refinement on 2435 reflections with I ≥ 2.5σ(I) converged to a final R = 0.028 and Rw = 0.029. [Re(py3N)(CO)3Cl] (C18H12ClN4O3Re) is triclinic, space group P1 with cell dimensions a = 13.761(2) Å, b = 14.636(6)Å, c = 11.110(2) Å, α = 110.70(2)°, β = 102.45(2)°, γ = 107.48(2)°, and Z = 4; full-matrix least-squares refinement on 3459 reflections with I ≥ 2.5σ(I) converged to a final R = 0.038 and Rw = 0.039. If the synthetic procedure is undertaken under irradiation by visible light, for the ligand py3N a species [Re(py3N)(CO)2Cl] (characterized by infrared spectroscopy and conductance measurements) is also formed, in which the ligand py3N is tridentate. No analogous tridentate species is formed with the ligands tpy or py3P, although there is evidence that it also forms for py3CH.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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