Carbon bond

Metal-Carbon Bonds. There are three qualitative MO models of the bonding in bent and complexes based on the unit. The essential differ- 

Jezowska-Trzebiatowska, J. Jczierska, A. Jezierski, A. Ozarowski, T. Cukierda, and J. Baranowski, Magn. Reson. Relat. Phenom., (Proc. 18th Ampere Congr., 1974,2,437 (Chem Abs., 1975,83,199891). 

Jezowska-Trzebiatowska and J. Jezierska, Chem Phys. Letters, 1975,34, 237. 

Photodecomposition is a complication in studies of photoexchange in cyclopen tadienylvanadium compounds. The rate of exchange of Cp in ligands is only about one tenth of that for the corresponding titanium dichloride. 

Attempts to prepare compounds of the type CP2VR2 (R = alkyl) have usually afforded CP2VR this has been taken to indicate the inherent instability of the —C 

As part of an ongoing effort to extend the scope of this methodology, we investigated the influence of both the a,/3-unsaturated aldehyde structure and the organo-lithium structure on the formation of the tandem product. Aliphatic a,/3-unsaturated aldehydes as well as aliphatic lithium reagents failed to afford the tandem reaction, 

TABLE 2. Tandem addition-/S-lithiation-electrophilic substitution 

This one-pot sequence readily creates a wide variety of ft-substituted dihydrochalcones besides a new carbon—carbon bond, opening up a new methodology in organic synthesis. As far as we know, this is the only report of this kind of tandem methodology found 

Chiral ligand-mediated lithiation-substitution sequences to promote stereoselectivity in pro-chiral compounds have been exploited widely over the past decade25. An asymmetric deprotonation carried out by the organolithium can be the enantio-determining step, or an asymmetric substitution as a postdeprotonation step. (—)-Sparteine, a readily available alkaloid, has been extensively used in this type of stereoselective transformation, giving high yields of enantiomeric excess. 

The carbolithiation of alkenes and alkynes is a useful transformation for the generation of a new carbon—carbon bond, specially when the alkenes and alkynes are activated by conjugation to carbonyl and related electron-withdrawing groups. Similarly to the intramolecular carbolithiation, it is possible to carry out this reaction with high diastere-o selectivity. 

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Correlations have been found between certain absorption patterns in the infrared and the concentrations of aromatic and paraffinic carbons given by the ndA/method (see article 3.1.3.). The absorptions at 1600 cm due to vibrations of valence electrons in carbon-carbon bonds in aromatic rings and at 720 cm (see the spectrum in Figure 3.8) due to paraffinic chain deformations are directly related to the aromatic and paraffinic carbon concentrations, respectively. )... 

Alkanes from CH to C4gFlg2 typically appear in crude oil, and represent up to 20% of the oil by volume. The alkanes are largely chemically inert (hence the name paraffins, meaning little affinity), owing to the fact that the carbon bonds are fully saturated and therefore cannot be broken to form new bonds with other atoms. This probably explains why they remain unchanged over long periods of geological time, despite their exposure to elevated temperatures and pressures. 

In the longer carbon chains, two double carbon-carbon bonds may exist. Such molecules are called diolefins (or dienes), such as butadiene CH2 = CH - CH = CHj. 

Turro N J, Buchachenko A L and Tarasov V F 1995 How spin stereochemistry severely complicates the formation of a carbon-carbon bond between two reactive radicals in a supercage Acc. Chem. Res. 28 69-80... 

There is the possibility of building up an extensive systematic chemistry of compounds containing boron-nitrogen bonds, analogous to the chemistry of carbon-carbon bonds but the reactivity of the B—bond is much greater than that of the C—C bond, so that we get physical, but not chemical, resemblances between analogous compounds. 

The origin of a torsional barrier can be studied best in simple cases like ethane. Here, rotation about the central carbon-carbon bond results in three staggered and three eclipsed stationary points on the potential energy surface, at least when symmetry considerations are not taken into account. Quantum mechanically, the barrier of rotation is explained by anti-bonding interactions between the hydrogens attached to different carbon atoms. These interactions are small when the conformation of ethane is staggered, and reach a maximum value when the molecule approaches an eclipsed geometry. 

MM2 was, according the web site of the authors, released as MM2 87). The various MM2 flavors are superseded by MM3, with significant improvements in the functional form [10]. It was also extended to handle amides, polypeptides, and proteins [11]. The last release of this series was MM3(%). Further improvements followed by starting the MM4 series, which focuses on hydrocarbons [12], on the description of hyperconjugative effects on carbon-carbon bond lengths [13], and on conjugated hydrocarbons [14] with special emphasis on vibrational frequencies [15]. For applications of MM2 and MM3 in inorganic systems, readers are referred to the literature [16-19]. 

The Wiener index was originally defined only for acyclic graphs and was initially called the path number [6]. "The path number, W, is defined as the sum of the distances between any two carbon atoms in the molecule in terms of carbon-carbon bonds". Hosoya extended the Wiener index and defined it as the half-sum of the off diagonal elements of a distance matrix D in the hydrogen-depleted molecular graph of Eq, (15), where dij is an element of the distance matrix D and gives the shortest path between atoms i and j. 

If you calculate the electrostatic potential for cyclopropane, three minima occur in regions that bisect the carbon-carbon bonds. This result IS consistent with protonalion of cyclopropane occurring along Ih e bond bisector. 

Example I hc reaction coordinate for rotation about the central carbon-carbon bond in rt-bulane has several stationary points.. A, C, H, and G are m in im a and H, D, an d F arc tn axirn a. Only the structures at the m in im a represen t stable species an d of these, the art/[ con form ation is more stable th an ihc nauchc. 

Fig. 2.3 Variation in energy with rotation of the carbon-carbon bond in ethane.

Table 4-1 Bond Lengths for Carbon-Carbon Bonds In Mkanes and /Mkenes...

It has been tentatively suggested that one mechanism underlies the Willgerodt reaction and the Kindler modification of it. A labile intermediate is first formed which has a carbon—carbon bond in the side chain. The scheme is indicated below it postulates a series of steps involving the addition of ammonia or amine (R = H or alkyl), elimination of water, re addition and eUmination of ammonia or amine until the unsaturation appears at the end of the chain then an irreversible oxidation between sulphur and the nitrogen compound may occur to produce a thioamide. 

Periodic acid has a selective oxidising action upon compounds having two hydroxyl groups or a hydroxyl and an amino group attached to adjacent carbon atoms and is characterised by the cleavage of the carbon - carbon bond (Malaprade reaction) ... 

B. Giese Radicals in Organic Synthesis Formation of Carbon-Carbon Bonds (Pergamon Press NY) 1986 Bull. Soc. Chirn. Fr. 1990, 127,675 Tetrahedron 1981, 37, 3073 Tetrahedron 1987, 43, 3541 Advances in Free Radical Chemistry 1990, 1, 121. 

Extensive discussions have focused on the conformation of the alkyl chains in the interior ". It has been has demonstrated that the alkyl chains of micellised surfactant are not fully extended. Starting from the headgroup, the first two or three carbon-carbon bonds are usually trans, whereas gauche conformations are likely to be encountered near the centre of tlie chain ". As a result, the methyl termini of the surfactant molecules can be located near the surface of the micelle, and have even been suggested to be able to protrude into the aqueous phase "". They are definitely not all gathered in the centre of tire micelle as is often suggested in pictorial representations. NMR studies have indicated that the hydrocarbon chains in a micelle are highly mobile, comparable to the mobility of a liquid alkane ... 

Symmetrical diols can be made by a radical reaction. Radical reactions are rarely much use in carbon-carbon bond formation as they often give poor yields and many products They are of course useful in some FGl reactions in things hke altylic bromination and in functionahsing remote carbon atoms. If rou want to read more about this see Tedder, Part 2, Chapter 11 or Carruthers, Chapter 4. One useful radical reaction is the prnacol reduction ... 

O Most synthetic reactions, which produce carbon-carbon bonds, are polar a negatively... 

The combination of two reagents corresponding to one d-synthon and one a-synthon under appropriate conditions yields an additional carbon-carbon bond (exception d°-synthons). The following obvious rules apply to the arrangement offunctionality in the product ("target molecule") ... 

The problem of the synthesis of highly substituted olefins from ketones according to this principle was solved by D.H.R. Barton. The ketones are first connected to azines by hydrazine and secondly treated with hydrogen sulfide to yield 1,3,4-thiadiazolidines. In this heterocycle the substituents of the prospective olefin are too far from each other to produce problems. Mild oxidation of the hydrazine nitrogens produces d -l,3,4-thiadiazolines. The decisive step of carbon-carbon bond formation is achieved in a thermal reaction a nitrogen molecule is cleaved off and the biradical formed recombines immediately since its two reactive centers are hold together by the sulfur atom. The thiirane (episulfide) can be finally desulfurized by phosphines or phosphites, and the desired olefin is formed. With very large substituents the 1,3,4-thiadiazolidines do not form with hydrazine. In such cases, however, direct thiadiazoline formation from thiones and diazo compounds is often possible, or a thermal reaction between alkylideneazinophosphoranes and thiones may be successful (D.H.R. Barton, 1972, 1974, 1975). 

Aldol additions and ester condensations have always been and still are the most popular reactions for the formation of carbon-carbon bonds (A.T. Nielsen, 1968). The earbonyl group acts as an a -synthon, the enoi or enolate as a d -synthon. Both reactions will be treated together here, and arguments, which are given for aldol additions, are also valid for ester condensations. Many famous name reactions belong to this category ). The products of aldol additions may be either /J-hydroxy carbonyl compounds or, after dehydration, or, -unsaturated carbonyl compounds. 

Similar fragmentations to produce S-cyclodecen-l-ones and 1,6-cyclodecadienes have employed l-tosyloxy-4a-decalols and 5-mesyloxy-l-decalyl boranes as educts. The ringfusing carbon-carbon bond was smoothly cleaved and new n-bonds were thereby formed in the macrocycle (P.S. Wharton, 1965 J.A. Marshall, 1966). The mechanism of these reactions is probably E2, and the positions of the leaving groups determine the stereochemistry of the olefinic product. 

Reactive Carbon-Hydrogen and Carbon-Carbon Bonds... 

The most intriguing hydrocarbon of this molecular formula is named buUvalene, which is found in the mixture of products of the reaction given above. G. SchrOder (1963, 1964, 1967) synthesized it by a thermal dimerization presumably via diradicais of cyciooctatetraene and the photolytical cleavage of a benzene molecule from this dimer. The carbon-carbon bonds of buUvalene fluctuate extremely fast by thermal Cope rearrangements. 101/3 = 1,209,6(X) different combinations of the carbon atoms are possible. 

Alkenes coordinated by Pd(II) are attacked by carbon nucleophiles, and carbon-carbon bond formation takes place. The reaction of alkenes with carbon nucleophiles via 7r-allylpalladium complexes is treated in Section 3.1. 

Facile reaction of a carbon nucleophile with an olefinic bond of COD is the first example of carbon-carbon bond formation by means of Pd. COD forms a stable complex with PdCl2. When this complex 192 is treated with malonate or acetoacetate in ether under heterogeneous conditions at room temperature in the presence of Na2C03, a facile carbopalladation takes place to give the new complex 193, formed by the introduction of malonate to COD. The complex has TT-olefin and cr-Pd bonds. By the treatment of the new complex 193 with a base, the malonate carbanion attacks the cr-Pd—C bond, affording the bicy-clo[6.1,0]-nonane 194. The complex also reacts with another molecule of malonate which attacks the rr-olefin bond to give the bicyclo[3.3.0]octane 195 by a transannulation reaction[l2.191]. The formation of 194 involves the novel cyclopropanation reaction of alkenes by nucleophilic attack of two carbanions. 

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