Styrene using

What is the MM3 enthalpy of formation at 298.15 K of styrene Use the option Mark all pi atoms to take into account the conjugated double bonds in styrene. Is the minimum-energy structure planar, or does the ethylene group move out of the plane of the benzene ring ... 

Phenoxy acetophenone, 46, 94 Phenylacetyleue, oxidative coupling to diphenyldiacetylene, 46, 39 partial reduction to styrene using palladium catalyst, 46, 90 reaction with sodium hypobromite to yield phenylbromoethyne, 46,86... 

Figure 1. Copolymers of acrylonitrile and styrene used for Lopac containers...

Block copolymers were synthesized by a combination of fipase-catalyzed polymerization and atom transfer radical polymerization (ATRE). " " At first, the polymerization of 10-hydroxydecanoic acid was carried out by using lipase CA as catalyst. The terminal hydroxy group was modified by the reaction with a-bromopropionyl bromide, followed by ATRP of styrene using CuCE2,2 -bipyridine as catalyst system to give the polyester-polystyrene block copolymer. Trichloromethyl-terminated poly(e-CL), which was synthesized by lipase CA-catalyzed polymerization with 2,2,2-trichloroethanol initiator, was used as initiator for ATRP of styrene. 

Ratio of divinyl benzene to styrene used in polymerization... 

The styrene storage capacity is given by the scope as 17 days. To convert to a weight basis, the pounds of styrene used for each separate product must be multiplied by the average amount of the product that would be made during the time period. The weight of styrene the storage facilities must be able to contain is ... 

Pounds of styrene used per pound of composite product =... 

Isopropenylferrocene does not homopolymerize under free radical conditions using AIBN as an initiator, but it does copolymerize with styrene.Preliminary results indicate that the IDM monomer also copolymerizes with styrene using AIBN. In benzene solvent at 50°C in 24 h, a 10.6% yield of copolymer (IR vc=0 2020, 1945 cm , vN=0 1675 cm-- -, V q 1601 cm-- -, v 3020 cm-- -) resulted having an M f 5700 and containing 6.8% of IDM as determined by elemental analysis. The initial monomer mixture contained 17% of IDM. 

The Instantaneous values for the initiator efficiencies and the rate constants associated with the suspension polymerization of styrene using benzoyl peroxide have been determined from explicit equations based on the instantaneous polymer properties. The explicit equations for the rate parameters have been derived based on accepted reaction schemes and the standard kinetic assumptions (SSH and LCA). The instantaneous polymer properties have been obtained from the cummulative experimental values by proposing empirical models for the instantaneous properties and then fitting them to the cummulative experimental values. This has circumvented some of the problems associated with differenciating experimental data. The results obtained show that ... 

More recently, a number of different copolymer structures have been prepared from butadiene and styrene, using modified organolithiums as polymerization initiators ( 4). Organolithium initiated polymerizations have gained prominence because stereo-control is combined with excellent polymerization rates, and the absence of a chain termination reaction facilitates control of molecular weights and molecular weight distributions ( 5). 

On each of the curves, the points at lowest X represent swelling in cyclohexane, the next in tetrahydrofuran and the last in benzene. In all cases, the samples were swollen in the pure solvent. The curves are reproduced from Figure 13 of Reference 19. The networks were made from anionically polymerized polyr-styrene using a bifunctional initiator crosslinked subsequently by divinyl benzene. The curves correspond to different ratios of divinyl benzene (DVB) per polystyrene living end (LE),... 

The hydroformylation of styrene using rhodium systems containing the four structurally related diphosphines dppe, dppp, (86), and (87) has been studied. A systematic analysis of the effect of the pressure, temperature, and the ligand metal molar ratio shows that the five- and six-membered ring chelating diphosphines behave differently from one another.347 An analysis of the effect of pressure, temperature, and ligand metal molar ratio on the selectivity of styrene hydroformylation catalyzed... 

Sernetz, F. G. Mulhaupt, R. Fokken, S. Okuda, J. Copolymerization of ethene with styrene using methylalumi-noxane-activated bis(phenolate) complexes. Macromolecules 1997, 30, 1562-1569. 

TABLE 3.1. Asymmetric hydroformylation of styrene using polystyrene supported rhodium catalysts based... 

Linear cooligomerization of butadiene with styrene using ir-allylpalla-dium chloride and BF3 complex of PPh3 as a catalyst at 100°C in nitrobenzene or dichloromethane produced 1 -phenyl-1,4-hexadiene (124) (109) ... 

Table 2 Hydroboration of norbornene, indene, and styrene using catecholborane...

Table 3 Hydroboration of styrene and substituted styrene using ligands 32-34...

Table 5 Hydroboration of styrene using chiral phosphite ligands 48-53... 

Table 6 Hydroboration of substituted styrene using Quinazolinap ligands 66-71...

Table 7 Hydroboration of styrene using pyrazole containing ferrocenyl ligands 80-83...

Table 8 Hydroboration of styrene using ferrocene type ligands...

Brunner, Leitner and others have reported the enantioselective transfer hydrogenation of alpha-, beta-unsaturated alkenes of the acrylate type [50]. The catalysts are usually rhodium phosphine-based and the reductant is formic acid or salts. The rates of reduction of alkenes using rhodium and iridium diamine complexes is modest [87]. An example of this reaction is shown in Figure 35.8. Williams has shown the transfer hydrogenation of alkenes such as indene and styrene using IPA [88]. 

Tanner et al. (58) investigated the use of chelating diaziridines (85) as ligands for transition metals. The cyclopropanation of styrene using CuOTf complexes of phenyl-substituted aziridine (85a) proceeds in modest enantioselectivity and dias-tereoselectivity, but improved enantioselectivity is observed with complexes derived from benzyl-substituted bis(aziridine) (85b), Eq. 42 (59). Complexes derived... 

Suga et al. (63) reported the asymmetric cyclopropanation of styrene using chiral binaphthyl-derived diimines. Diastereoselectivities and enantioselectivities in the cyclopropanation of styrene are moderate, Eq. 45. Improved selectivities are observed using 1,1-diphenylethene, which provides the men thy 1 ester cyclopropane in 96% de. 

Tanner et al. (58) investigated the asymmetric aziridination of styrene using bis(aziridines) such as 85. Low induction is observed with these ligands, Eq. 64. A significant electronic effect was noted with the p-fluoro-phenyl substituted bis(az-iridine) 85c (59). A binaphthyl-derived diamine was used as a ligand for the copper-catalyzed aziridination of dihydronaphthalene (81). The product was formed in 21% ee and 40% yield, Eq. 65. Other structurally related ligands proved to be less selective in this reaction. 

As an inversion of enantioselectivity was observed experimentally for 4-(dimethylamino)styrene, (64% R ee) as compared to styrene (64% S ee), we have recalculated the relative thermodynamic stabilities of endo and exo isomers for each step of the catalytic cycle using this second substrate. These calculations allow us to verify the quality of our findings by checking if an inversion in the relative stabilities of the endo and the exo-ri3-silyl-allyl intermediates (with the endo being more stable than the exo) is observed with 4-(dimethylamino)styrene. Using 4-(dimethylamino)styrene as the substrate, the calculated relative stabilities of the intermediates in the Chalk-Harrod mechanism are shown as parenthetic values in Figure 15. 

Scheme 4 Rh-catalyzed asymmetric hydroformylation of styrene using ligands 2a-c...

Fig. 6 Rhodium-catalyzed asymmetric hydroformylation of styrene using ligands 3 and 23-26. Enantioselectivities obtained at 100 bars of syngas and 60 °C are shown in brackets...

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