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Energy organometallics

Low surface energy substrates, such as polyethylene or polypropylene, are generally difficult to bond with adhesives. However, cyanoacrylate-based adhesives can be effectively utilized to bond polyolefins with the use of the proper primer/activa-tor on the surface. Primer materials include tertiary aliphatic and aromatic amines, trialkyl ammonium carboxylate salts, tetraalkyl ammonium salts, phosphines, and organometallic compounds, which are initiators for alkyl cyanoacrylate polymerization [33-36]. The primer is applied as a dilute solution to the polyolefin surface, solvent is allowed to evaporate, and the specimens are assembled with a small amount of the adhesive. With the use of primers, adhesive strength can be so strong that substrate failure occurs during the course of the shear tests, as shown in Fig. 11. [Pg.862]

Armentrout PB (2003) Threshold Collision-Induced Dissociations for the Determination of Accurate Gas-Phase Binding Energies and Reaction Barriers. 225 227-256 Astruc D, Blais J-C, Cloutet E, Djakovitch L, Rigaut S, Ruiz J, Sartor V, Valerio C (2000) The First Organometallic Dendrimers Design and Redox Functions. 210 229-259 Aug6 J, see Lubineau A (1999) 206 1-39... [Pg.231]

Activation energies of thermal reactions in organometallic compounds have unfortunately not yet been measured. It would seem that the Group VI carbonyls would offer the best possibilities for such measurements, since their reactions are not complicated by competitive reactions. Unfortunately it cannot be said with confidence that these compounds are representative of aU other organometallic compounds as well. [Pg.99]

Investigations of the cobalt-carbon bond energies in organometallic cobalt porphyrins continue to attract interest, originally because of their similarity to coenzyme B 2, and more recently because of their role in the catalysis of free radical... [Pg.283]

Activation energies have been studied in the case of solid ionic compounds, where the target compounds and their side products are somewhat more stable and easier to handle. No measurements of activation energies have as yet been made on organometallic compounds, and unfortunately, very few annealing studies have been done. [Pg.220]

Both PtRu/MgO catalysts prepared from cluster precursor and organometallic mixture were active for ethylene hydrogenation. The apparent activation energy of the former catalyst obtained from the Arrhenius plot during -40 to -25°C was 5.2 kcal/mol and that of the latter catalyst obtained during -50 to -30°C was 6.0 kcal/mol. The catalytic activity in terms of turn over frequency (TOP) was calculated on the assumption that all metal particles were accessible for reactant gas. Lower TOP of catalyst prepared from cluster A at -40°C, 57.3 x lO" s" was observed probably due to Pt-Ru contribution compared to that prepared from acac precursors. [Pg.212]

H2 serves as the alternative energy source relative to fossil fuels and biomass [181] because it is clean and environmentally friendly. Hence, catalytic hydrogen generation from water under mild conditions is one of the goals for the organometallic catalysis. One of the hopeful methods is the electrochemical reduction of protons by a hydrogenase mimic. [Pg.65]

The bond dissociation energy of fluoromethane is 115 kcal mol , which is much higher than the other halides (C-Cl, C-Br and C-1, respectively 84, 72 and 58 kcal mol ) [6], Due to its strength, the carbon-fluorine (C-F) bond is one of the most challenging bonds to activate [7], A variety of C-F bond activation reactions have been carried out with different organometallic complexes [8], Among them, nickel [9] and ruthenium complexes have proven to proceed selectively under mild conditions [10],... [Pg.192]

M. Franklin, K. J. Klabunde, in K. S. Suslick (ed.) High-Energy Processes in Organometallic Chemistry, ACS Symposium Series, 1987, 246. [Pg.248]


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Organometallic compounds bond energies

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