Strained and Reactive Donor/Acceptor-Supported Metallasilanone.

A novel stable donor/acceptor-supported MnI -metallasilanone 3 was synthesized. The intramolecular silanone-MnI interaction induces a highly strained three-membered cyclic structure, leading to an exceptionally high reactivity of 3 as a donor/acceptor complex of silanone. Indeed, metallasilanone 3 readily reacts with various small molecules such as H2 or ethylene gas in mild conditions.

Ferrocene-Containing Tin(IV) Complexes Based on o-Benzoquinone and o-Iminobenzoquinone Ligands. Synthesis, Molecular Structure, and Electrochemical Properties.

The addition of different substituted o-benzoquinones and o-iminobenzoquinones to tin(II) bis(o-iminophenolates) of the types (Fc-IP)2SnII and (Fc-4,6-IP)2SnII (where Fc-IP is anion 2-(ferrocenylmethyleneamino)phenolate [Fc-C(H)═N(C6H4)O-] and Fc-4,6-IP is anion 2-(ferrocenylmethyleneamino)-4,6-di-tert-butylphenolate [Fc-C(H)═N(4,6-tBu-C6H2)O-]) in tetrahydrofuran leads to the oxidation of Sn(II) to Sn(IV) with formation of the corresponding tin(IV) catecholates (Fc-4,6-IP)2SnIV(3,6-Cat) (1), (Fc-IP)2SnIV(3,6-Cat) (2), (Fc-4,6-IP)2SnIV(4-Cl-3,6-Cat) (3), (Fc-IP)2SnIV(4-Cl-3,6-Cat) (4), (Fc-4,6-IP)2SnIV(4,5-Cl2-3,6-Cat) (5), and (Fc-IP)2SnIV(4,5-Cl2-3,6-Cat) (6) or the o-amidophenolates (Fc-4,6-IP)2SnIV(AP-Me) (7), (Fc-IP)2SnIV(AP-iPr) (8), and (Fc-4,6-IP)2SnIV(AP-iPr) (9). Here ligands 3,6-Cat, 4-Cl-3,6-Cat, and 4,5-Cl2-3,6-Cat are dianions 3,6-di-tert-butyl-, 4-chloro-3,6-di-tert-butyl-, and 4,5-dichloro-3,6-di-tert-butylcatecholates, respectively, and AP-Me and AP-iPr are dianions 4,6-di-tert-butyl-N-(2,6-dimethylphenyl)-o-amidophenolate and 4,6-di-tert-butyl-N-(2,6-diisopropylphenyl)-o-amidophenolate, respectively. Complexes 1-9 have been characterized in detail by IR spectroscopy, cyclic voltammetry, and 1H, 13C, and 119Sn NMR spectroscopy. The molecular structures of tin(IV) complexes 5, 7, and 9 in the crystalline state were determined by single-crystal X-ray diffraction analysis. Complexes demonstrate a series of successive oxidations involving alternately catecholato/o-amidophenolato centers and ferrocenyl moieties. The relative oxidation potentials of these redox centers depend on the acceptor properties of the redox-active chelating O,O' or O,N ligand. An increase in the acceptor properties of redox-active o-quinonato-type ligands leads to an increase in the oxidation potentials of redox ligands as well as the following oxidation of ferrocenyl group(s). In two series of complexes, (Fc-4,6-L)2SnL' and (Fc-L)2SnL', where L' is AP-iPr, AP-Me, 3,6-Cat, 4-Cl-3,6-Cat, and 4,5-Cl2-3,6-Cat, a more pronounced convergence of the oxidation potentials of the redox-active o-quinonato ligand and ferrocenyl group occurs in the series (Fc-L)2SnL'.

A Stable N-Hetero-Rh-Metallacyclic Silylene.

A cyclic (amino)metal-substituted dicoordinated silylene derivative has been synthesized and fully characterized. Of particular interest is that the N-hetero-RhI -metallacyclic silylene exhibits a distorted tetrahedral geometry around the rhodium atom and a considerably shortened Si-Rh bond (2.138 Å) compared to classical Si-Rh single bonds (ca. 2.30-2.35 Å). A theoretical investigation reveals that the geometrical deviation around the rhodium center from the classical square-planar to a tetrahedral geometry increases the π-donating and σ-accepting character of the rhodium atom, thereby efficiently stabilizing the silylene moiety.

Bis(formylphenolato)cobalt(II)-Mediated Alternating Radical Copolymerization of tert-Butyl 2-Trifluoromethylacrylate with Vinyl Acetate.

The organometallic-mediated radical polymerization (OMRP) of vinyl acetate (VAc) and its OMR copolymerization (OMRcoP) with tert-butyl 2-trifluoromethylacrylate (MAF-TBE) mediated by Co(SAL)2 (SAL = 2-formylphenolato or deprotonated salicylaldehyde) produced relatively well-defined PVAc and poly(VAc-alt-MAF-TBE) copolymers at moderate temperature (<40 °C) in bulk. The resulting alternating copolymer was characterized by ¹H-, 13C- and 19F-nuclear magnetic resonance (NMR) spectroscopies, and by size exclusion chromatography. The linear first-order kinetic plot, the linear evolutions of the molar mass with total monomer conversion, and the relatively low dispersity (D~1.55) of the resulting copolymers suggest that this cobalt complex provides some degree of control over the copolymerization of VAc and MAF-TBE. Compared to the previously investigated cobalt complex OMRP mediators having a fully oxygen-based first coordination sphere, this study emphasizes a few peculiarities of Co(SAL)2: a lower ability to trap radical chains as compared to Co(acac)2 and the absence of catalytic chain transfer reactions, which dominates polymerizations carried in the presence of 9-oxyphenalenone cobalt derivative.

Catalyzed Chain Transfer in Vinyl Acetate Polymerization Mediated by 9-Oxyphenalenone Cobalt(II) Complexes.

The vinyl acetate (VAc) radical polymerization initiated by V-70 at 30 °C in the presence of [CoII(OPN)2] (OPN = deprotonated 9-oxyphenalenone), 1, leads to PVAc of lower molecular weight (MW) than expected for organometallic-mediated radical polymerization (OMRP), whether reversible termination or degenerate transfer conditions are used. This represents the first clear evidence of catalyzed chain transfer (CCT) in VAc polymerization. The bis-pyridine adduct [CoII(OPN)2(py)2], 2, shows a marginally lower polymerization rate and an increased CCT activity relative to 1, whereas the activity decreases with marginal effect on the polymerization rate upon addition of excess py. However, raising the temperature to 80 °C (with AIBN as initiator) led to a low MW polymer even in the presence of a large py excess. The CCT was confirmed by 1H NMR characterization of the chain ends and by a MALDI-TOF MS analysis of the recovered polymer. The collective trends are consistent with greater CCT activity for the 5-coordinate complex [CoII(OPN)2(py)] relative to 1 and 2. The presence of py association/dissociation equilibria relating these three complexes was confirmed by a 1H NMR investigation.