Phosphine electronic properties

As mentioned in Sect. 2.2, phosphine oxides are air-stable compounds, making their use in the field of asymmetric catalysis convenient. Moreover, they present electronic properties very different from the corresponding free phosphines and thus may be employed in different types of enantioselective reactions, m-Chloroperbenzoic acid (m-CPBA) has been showed to be a powerful reagent for the stereospecific oxidation of enantiomerically pure P-chirogenic phos-phine-boranes [98], affording R,R)-97 from Ad-BisP 6 (Scheme 18) [99]. The synthesis of R,R)-98 and (S,S)-99, which possess a f-Bu substituent, differs from the precedent in that deboranation precedes oxidation with hydrogen peroxide to yield the corresponding enantiomerically pure diphosphine oxides (Scheme 18) [99]. 

The catalytic hydroformylation of alkenes has been extensively studied. The selective formation of linear versus branched aldehydes is of capital relevance, and this selectivity is influenced by many factors such as the configuration of the ligands in the metallic catalysts, i.e., its bite angle, flexibility, and electronic properties [152,153]. A series of phosphinous amide ligands have been developed for influencing the direction of approach of the substrate to the active catalyst and, therefore, on the selectivity of the reaction. The use of Rh(I) catalysts bearing the ligands in Scheme 34, that is the phosphinous amides 37 (R ... 

This review has shown that the analogy between P=C and C=C bonds can indeed be extended to polymer chemistry. Two of the most common uses for C=C bonds in polymer science have successfully been applied to P=C bonds. In particular, the addition polymerization of phosphaalkenes affords functional poly(methylenephosphine)s the first examples of macromolecules with alternating phosphorus and carbon atoms. The chemical functionality of the phosphine center may lead to applications in areas such as polymer-supported catalysis. In addition, the first n-conjugated phosphorus analogs of poly(p-phenylenevinylene) have been prepared. Comparison of the electronic properties of the polymers with molecular model compounds is consistent with some degree of n-conjugation in the polymer backbone. 

Carbene ligands can replace phosphines dne to similar electronic properties. The development of NHC design concepts featnring different substituents and backbones eventually culminated in the most prominent derivative, the SIMes (SDVtes = A, A -bis[2,4,6-(trimethyl)phenyl]imidazolidin-2-ylidene) ligand that is nsed in the second and later also third generation catalysts (complexes 72, 73, 74b and 74c in Fig. 3.28) [105, 109, 114,116],... 

Fig. 10 Chelating phosphine ligands (a-g) with varying steric and electronic properties...

The reactivity order Ni>Pd>Pt has been found for the oxidative addition of aryl halides. Steric and electronic properties, and the numbers of L as well as chelate effects, play an important role [65, 194—196]. For example, Pd(0) complexes of basic chelating phosphines react substantially more easily with chlorobenzenes than their nonchelating analogues (see Section 18.2.4) [2, 100, 196]. 

The josiphos ligands arguably constitute the most versatile and successful ferro-cenyl ligand family. Because the two phosphine groups are introduced in consecutive steps with very high yields (as shown in Scheme 25.1), a variety of ligands is readily available with widely differing steric and electronic properties. 

In any case, these first HF attempts to a quantitative study left an approach which is still currently in use, namely the use of model systems. The experimental system is not introduced as such in the calculation because of its large size, but it is replaced by a smaller system which, hopefully, has the same electronic properties. The reaction of the Wilkinson catalyst mentioned above [30, 31] can serve as example. The accepted active species is Rh(PPh3)2Cl, but the calculations were carried out on Rh(PH3)2Cl, as shown in Figure 2. The replacement of the phenyl substituents of the phosphine ligands by hydrogen atoms is certainly a simplification from the experimental system, but it represents an enormous saving in terms of computational time. 

The IR frequencies represent a reliable yardstick of the electronic properties of a series of phosphorus ligands toward a particular metal. The latter restriction is important, because it is clear that the proton basicity scale (considering a proton as a metal) is not the same as a metal phosphine stability series. 

Because of n-electron donation by the heteroatom, these carbene complexes are generally less electrophilic at C than the corresponding non-heteroatom-substituted complexes (Chapter 3). This effect is even more pronounced in bis-heteroatom-substituted carbenes, which are very weak Tt-acceptors and towards low-valent transition metals show binding properties similar to those of phosphines or pyridine. Alkoxycarbenes, on the other hand, have electronic properties similar to those of carbon monoxide, and stable heteroatom-monosubstituted carbene complexes are also usually formed from metals which form stable carbonyl complexes. 

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