Sigma-bonded compound

Figure C3.2.7. A series of electron transfer model compounds with the donor and acceptor moieties linked by (from top to bottom) (a) a hydrogen bond bridge (b) all sigma-bond bridge (c) partially unsaturated bridge. Studies with these compounds showed that hydrogen bonds can provide efficient donor-acceptor interactions. From Piotrowiak P 1999 Photoinduced electron transfer in molecular systems recent developments Chem. Soc. Rev. 28 143-50.

Rhodacarborane catalysts have been immobilized by attachment to polystyrene beads with appreciable retention of catalytic activity (227). A 13-vertex /oj iJ-hydridorhodacarborane has also been synthesized and demonstrated to possess catalytic activity similar to that of the icosahedral species (228). Ak-oxidation of closo- >(2- P((Z [) 2 - i- > l[l-Bih(Z, results in a brilliant purple dimer. This compound contains two formal Rh " centers linked by a sigma bond and a pak of Rh—H—B bridge bonds. A number of similar dimer complexes have been characterized and the mechanism of dimer formation in these rhodacarborane clusters have been studied in detail (229). 

Compounds and Other Sigma-Bonded Metal Compounds Based on Metal Vapor as a Reagent. 203... 

A new synthesis for sigma-bonded, metal alkyls and similar compounds, involving a reaction between metal vapor and free radicals generated in a radio-frequency glow-discharge, has been reported (35). 

Attempts to synthesize transition metal alkyl compounds have been continuous since 1952 when Herman and Nelson (1) reported the preparation of the compound C H6>Ti(OPri)3 in which the phenyl group was sigma bonded to the metal. This led to the synthesis by Piper and Wilkinson (2) of (jr-Cpd)2 Ti (CH3)2 in 1956 and a large number of compounds of titanium with a wide variety of ligands such as ir-Cpd, CO, pyridine, halogen, etc., all of which were inactive for polymerization. An important development was the synthesis of methyl titanium halides by Beerman and Bestian (3) and Ti(CH3)4 by Berthold and Groh (4). These compounds show weak activity for ethylene polymerization but are unstable at temperatures above — 70°C. At these temperatures polymerizations are difficult and irreproduceable and consequently the polymerization behavior of these compounds has been studied very little. In 1963 Wilke (5) described a new class of transition metal alkyl compounds—x-allyl complexes,... 

It would appear from the studies on these systems that each metal atom can only accommodate one propagating center. If this were not the case, the metal atom would have attached two sigma-bonded polymer chains with hydrogen atoms on the j8-carbon atoms. The compound Zr(CH2CH2C6HB)4 has been synthesized (19) and found to be unstable above — 80°C, an observation which supports this statement. 

The results of polymerizing ethylene using varying sigma-bonded transition metal alkyl compounds are summarized in Table VII. It is evident that none of the catalysts are very active and are comparable with the simple allyl compounds listed in Table I. 

Sigma-bonded transition metal complexes are able to polymerize a range of vinyl monomers, the only limitation being that the monomer should not have groups that react chemically with the transition metal compound. An important observation is that styrene and its derivatives are polymerized by the sigma complexes. In this respect they differ from the jr-allyl compounds that show no reactivity at all toward these monomers. A reasonable explanation for this is that the mechanism of the initiation is different... 

Compounds with restricted rotation about a sigma bond. 

Sigma (a) bonds Sigma bonds have the orbital overlap on a line drawn between the two nuclei, simple cubic unit cell The simple cubic unit cell has particles located at the corners of a simple cube, single displacement (replacement) reactions Single displacement reactions are reactions in which atoms of an element replace the atoms of another element in a compound, solid A solid is a state of matter that has both a definite shape and a definite volume, solubility product constant (/ p) The solubility product constant is the equilibrium constant associated with sparingly soluble salts and is the product of the ionic concentrations, each one raised to the power of the coefficient in the balanced chemical equation, solute The solute is the component of the solution that is there in smallest amount, solution A solution is defined as a homogeneous mixture composed of solvent and one or more solutes. 

Many reactions may be successfully utilized in the synthesis of compounds with sigma bonds between group IV3 metals and transition metals, but none is of general applicability. Moreover, the problem is complicated in the case of optically active compounds since ... 

The other elements of group 10 and gold do not form stable binary carbonyls. The stabilization of carbonyl complexes of these elements requires the introduction of other ligands, preferably sigma-bonded, that is the compounds [Pd(CO)Cl2] , [Pt(CO)2Cl2] and [Au(CO)Cl] are relatively stable. 

E) A single bond is a sigma bond. All compounds contain at least one sigma bond. 

Metal-Halogen Counpounds. One of the few examples of an olefin insertion into a metal-halogen compound has been reported by Tsuji. The reaction, which also supports the idea that sigma-bonded metal-carbon compounds are intermediates in the palladium chloride-olefin oxidation reaction, was the addition of carbon monoxide to the ethylene palladium chloride 7r-complex in nonaqueous solvents to produce a moderate yield of 3-chloropropionyl chloride (96). 

Palladium (II)-Nucleophile Addition across Olefins. Adding palladium complexes to olefins, either in the presence of an external nucleophile or a ligand which is attached to palladium, produces a palladium-carbon sigma-bonded complex which is not usually isolated in the case of monoolefins. Instead it decomposes and in doing so oxidizes the olefin to an organic carbonyl compound or a vinyl compound, exchanges a substituent group on the olefin, isomerizes the double bond, arylates (alkylates) the olefin, or carboxylates the olefin (2, 3). 

Xlld does not involve the chiral center, so if the reaction takes place by this pathway, the migration of the alkyl group from sulfur to palladium (with the concomitant or subsequent loss of sulfur dioxide) must take place with inversion of configuration at carbon. Inversion of configuration at carbon has been observed in the reverse-type reaction, the sulfur dioxide insertion into a carbon-iron sigma bond (49). Nucleophilic displacement at carbon in compounds of type Xld is unusually difficult, so the reaction via the sulfite intermediate Xlld would appear to be more likely. Conversion of the tosylate of l-phenyl-2,2,2-trifluoroethanol to the corresponding chloride, a reaction which takes place in the presence of tetra- (n-butyl) ajnmonium chloride with inversion of configuration at carbon, requires 100°C for 24 hrs in dimethylsulfoxide. 

---