Head to tail dimerization

The ligand group can be introduced either on the meso or on the /5-pyrrole position of the porphyrin ring, but the synthesis of the meso-functionalized derivatives is easier and has been more widely exploited. Balch (50-53) reported that the insertion of trivalent ions such as Fe(III) (32) and Mn(III) (33) into octaethyl porphyrins functionalized at one meso position with a hydroxy group (oxophlorins) leads to the formation of a dimeric head-to-tail complex in solution (Fig. 11a) (50,51). An X-ray crystal structure was obtained for the analogous In(III) complex (34), and this confirmed the head-to-tail geometry that the authors inferred for the other dimers in solution (53) (Fig. lib). The dimers are stable in chloroform but open on addition of protic acids or pyridine (52). The Fe(III) octaethyloxophlorin dimer (52) is easily oxidized by silver salts. The one-electron oxidation is more favorable than for the corresponding monomer or p-oxo dimer, presumably because of the close interaction of the 7r-systems in the self-assembled dimer. 

In most cases, none ofthe following were observed ( )-head-to-head dimers, head-to-tail dimers, or trimers. High regio- and stereo-selectivities set this method apart from Rh(I)-catalyzed dimerization methods. 

Keywords 1,1-diarylethylene, HC1, catalysis, linear dimerization, head-to-tail, waste free, gas-solid reaction, 1,1,3,3-tetraaryl-l-butene... 

Scheme 3. Dipolar species tend to dimerize head to tail.

Rapid formation of polyethylene Catalytic dimerization (head-to-tail) at 80 °C [29]... 

General Considerations. In the well-known photodimerization of anthracenes in liquid solution 9, lO /lO, 9 -dimers (head-to-tail [4 + 4]) are formed in most cases. However, there have also been instances where head-to-head-photodimers (9,9 /10,10 ) are produced [19], and these were overseen previously. The solid phase photoreactions of anthracenes charged the topochemical postulate [7] for decades with hitherto unsolvable difficulties. All examples that contradict this assumption were eliminated without hesitation from the scope of topochemistry and termed to be crystal defect reactions, because the topochemically allowed processes were taken as support for topochemistry without further proof. The later provision, that the dimerizations occur within reaction cavities in the bulk of the crystal [20], did not help in this respect. A summary of the various arguments is given in Ref. 8. From examples 7 to 8 only b and perhaps c formally meet... 

The role of crystal imperfections in the dimerization of substituted anthracenes has been described in the case of l,8-dichloro-9-methylanthracene.178 Similar studies have now been conducted for the 10-methyl isomer.179 In order to explain how the topochemically forbidden / -dimer (head to tail) is produced from irradiation in the solid phase, optical and electron microscopic examinations of the (010) faces of the orthorhombic crystals of the monomer have been carried out, together with differential-enthalpic and dielectric measurements. Again it is shown that the dimer nuclei appear at emergent dislocations. 

The polarization and orientation dependence of plasmon coupling described above is very similar to absorption spectra shifts observed in organic molecules upon their dimerization or aggregation. Organic chromophores dimerized head-to-tail with respect to their transition dipole moment direction (known as J-dimers) show an absorption band that is red-shifted compared to that of the isolated... 

The dimerization of isoprene is possible, but the reaction of isoprene is slower than that of butadiene. Dimerization or telomerization of isoprene, if carried out regioselectively to give a tail-to-liead dimer 18 or a head-to-tail... 

The reaction of isoprene with MeOH catalyzed by Pd(acac)2 and Ph3P is not regioselective, giving a mixture of isomers[37]. However, l-methoxy-2,6-dimethyl-2,7-octadiene (35), the head-to-tail dimer, was obtained in 80% yield, accompanied by the tail-to-tail dimer (15%) using 7r-allylpalladium chloride and BU3P. On heating, 35 was converted into 2.6-dimethyl-1,3,7-octatriene (36) by an elimination reaction[38]. 

Formic acid behaves differently. The expected octadienyl formate is not formed. The reaction of butadiene carried out in formic acid and triethylamine affords 1,7-octadiene (41) as the major product and 1,6-octadiene as a minor product[41-43], Formic acid is a hydride source. It is known that the Pd hydride formed from palladium formate attacks the substituted side of tt-allylpalladium to form the terminal alkene[44] (see Section 2.8). The reductive dimerization of isoprene in formic acid in the presence of Et3N using tri(i)-tolyl)phosphine at room temperature afforded a mixture of dimers in 87% yield, which contained 71% of the head-to-tail dimers 42a and 42b. The mixture was treated with concentrated HCl to give an easily separable chloro derivative 43. By this means, a- and d-citronellol (44 and 45) were pre-pared[45]. 

The reaction of isoprene with CO2 in the presence of oraanotin ethoxide and DBU by the use of dicyclohexyl( 3-pyridylethyl)phosphine (106) affords the isomeric esters 107 and 108 by head-to-tail and tail-to-tail dimerizations. Tin ethoxide forms tin carbonate, which seems to be an effective carrier of CO2[100]. 

Even iV-aryldiaziridines can be obtained. Compound (274) is formed on irradiation of its 1,3-dipolar isomer, which is in thermal equilibrium with its head-to-tail dimer (82TH50800). 

UV irradiation. Indeed, thermal reaction of 1-phenyl-3,4-dimethylphosphole with (C5HloNH)Mo(CO)4 leads to 155 (M = Mo) and not to 154 (M = Mo, R = Ph). Complex 155 (M = Mo) converts into 154 (M = Mo, R = Ph) under UV irradiation. This route was confirmed by a photochemical reaction between 3,4-dimethyl-l-phenylphosphole and Mo(CO)6 when both 146 (M = Mo, R = Ph, R = R = H, R = R" = Me) and 155 (M = Mo) resulted (89IC4536). In excess phosphole, the product was 156. A similar chromium complex is known [82JCS(CC)667]. Complex 146 (M = Mo, R = Ph, r2 = R = H, R = R = Me) enters [4 -H 2] Diels-Alder cycloaddition with diphenylvinylphosphine to give 157. However, from the viewpoint of Woodward-Hoffmann rules and on the basis of the study of UV irradiation of 1,2,5-trimethylphosphole, it is highly probable that [2 - - 2] dimers are the initial products of dimerization, and [4 - - 2] dimers are the final results of thermally allowed intramolecular rearrangement of [2 - - 2] dimers. This hypothesis was confirmed by the data obtained from the reaction of 1-phenylphosphole with molybdenum hexacarbonyl under UV irradiation the head-to-tail structure of the complex 158. 

If weak complexes present in solution consist of dimers alone (Fig. 7), association patterns of homodimers (11 and 13) are of the head-to-tail type, that of heterodimer (72) being of the head-to-head type, since the two acylurea bonds in 1 and 2 extend... 

Maltose, a decomposition product of starch, is a dimer of two glucose molecules. These are combined head-to-tail carbon atom 1 of one molecule is joined through an oxygen atom to carbon atom 4 of the second molecule. To form maltose, the two OH groups on these carbon atoms react, condensing out H20 and leaving the O atom bridge. 

The first step involves a dimerization which can occur by head-to-tail or head-to-head condensation, the former being favoured ... 

Figure 21-2. Fatty acid synthase multienzyme complex. The complex is a dimer of two identical polypeptide monomers, 1 and 2, each consisting of seven enzyme activities and the acyl carrier protein (ACP). (Cys— SH, cysteine thiol.) The— SH of the 4 -phosphopantetheine of one monomer is in close proximity to the— SH of the cysteine residue of the ketoacyl synthase of the other monomer, suggesting a "head-to-tail" arrangement of the two monomers. Though each monomer contains all the partial activities of the reaction sequence, the actual functional unit consists of one-half of one monomer interacting with the complementary half of the other. Thus, two acyl chains are produced simultaneously. The sequence of the enzymes in each monomer is based on Wakil.

The [2 + 2] photodimerization of a, j8-unsaturated sulfones is correctly viewed as a photoreaction of alkenes, rather than the sulfone group, and this aspect has been reviewed recently by Reid, as part of a wider survey of the photoreaction of O- and S-heterocycles. The topic continues to attract considerable interest and a few recent examples, as well as some synthetic applications, will be discussed here. Much of the photodimerization work has been carried out on the benzo[fc]thiophene (thianaphthene) 1,1-dioxide system. For example. Porter and coworkers have shown that both 3-carboxybenzo[i]thiophene 1,1-dioxide (65) and its methyl ester give only the head-to-head (hth), anti dimer (66) on irradiation in ethanol. In a rather unusual finding for such systems, the same dimer was obtained on thermal dimerization of 65. Similar findings for a much wider variety of 3-substituted benzo[fi]thiophene 1,1-dioxides have been reported more recently by Geneste and coworkers . In the 2-substituted analogs, the hth dimer is accompanied by some of the head-to-tail (htt), anti dimer. The formation of the major dimer appears to proceed by way of an excited triplet and the regiochemistry observed is in accord with frontier MO theory. 

Goff (54) synthesized an Fe(III) porphyrin with a 2-hydroxyphenyl group at one meso position (35, Fig. 12a). Under basic conditions, the system spontaneously dimerizes due to phenolate-Fe(III) coordination. The complex is very stable and was isolated and fully characterized. In the solid state, the X-ray crystal structure confirmed the structure of the assembly as a macrocyclic head-to-tail dimer with two intermolecu-... 

---