Ring-opening metathesis polymerization polymers

The sheer activity of these new nickel norbornene polymerization catalysts and their very rapid polymerization rates makes them potential catalysts for a new nor-bornene-RIM (reaction injection molding) technology to afford a saturated, oxidatively stable RIM part rather than the unsaturated ROMP (ring-opening metathesis polymerization) polymer that is the current commercial Telene or Metton . Fig. 4.6 illustrates the concept and also exemplifies the very rapid polymerization rates that are observed. 

Aqueous ring-opening metathesis polymerization (ROMP) was first described in 1989 (90) and it has been appHed to maleic anhydride (91). Furan [110-00-9] reacts in a Diels-Alder reaction with maleic anhydride to give exo-7-oxabicyclo[2.2.1]hept-5-ene-2,3—dicarboxylate anhydride [6118-51 -0] (24). The condensed product is treated with a soluble mthenium(Ill) [7440-18-8] catalyst in water to give upon acidification the polymer (25). Several apphcations for this new copolymer have been suggested (91). 

A drawback to the Durham method for the synthesis of polyacetylene is the necessity of elimination of a relatively large molecule during conversion. This can be overcome by the inclusion of strained rings into the precursor polymer stmcture. This technique was developed in the investigation of the ring-opening metathesis polymerization (ROMP) of benzvalene as shown in equation 3 (31). 

Lu H, Wang J, Lin Y, Oieng J (2009) One-pot synthesis of brush-like polymers via integrated ring-opening metathesis polymerization and polymerization of amino acid N-carboxyanhy-drides. J Am Oiem Soc 131 13582-13583... 

Wolfe and Wagener have developed main-chain boronate polymers (59) (Fig. 38) by the acyclic diene metathesis (ADMET) polymerization of symmetrical ,oj-dienes, containing both methyl- and phenyl-substituted boronate functionalities using Mo and Ru catalysts.84 The ring-opening metathesis polymerization (ROMP) of several norbornene monomers containing methyl- and phenyl-substituted boronates into... 

We have reported the first example of a ring-opening metathesis polymerization in C02 [144,145]. In this work, bicyclo[2.2.1]hept-2-ene (norbornene) was polymerized in C02 and C02/methanol mixtures using a Ru(H20)6(tos)2 initiator (see Scheme 6). These reactions were carried out at 65 °C and pressure was varied from 60 to 345 bar they resulted in poly(norbornene) with similar conversions and molecular weights as those obtained in other solvent systems. JH NMR spectroscopy of the poly(norbornene) showed that the product from a polymerization in pure methanol had the same structure as the product from the polymerization in pure C02. More interestingly, it was shown that the cis/trans ratio of the polymer microstructure can be controlled by the addition of a methanol cosolvent to the polymerization medium (see Fig. 12). The poly(norbornene) prepared in pure methanol or in methanol/C02 mixtures had a very high trans-vinylene content, while the polymer prepared in pure C02 had very high ds-vinylene content. These results can be explained by the solvent effects on relative populations of the two different possible metal... 

Fig.4A,B. Ring-opening metathesis polymerization (ROMP) A Structures of organometal-lic initiators that have been used in ROMP to generate neobiopolymers. B General pathway for polymer synthesis using ROMP. Molybdenum-initiated reactions are typically capped with aldehydes and ruthenium-initiated with end ethers.

See also ROM polymers Ring-opening metathesis polymerization (ROMP) reaction, 20 413 Ring-opening polymerization (ROP), 24 271, 29 816-817, 23 702,... 

Besides the polymerization techniques discussed above, other polymerization methods have been used for the preparation of surface grafts. Recently, ring-opening metathesis polymerization (ROMP) became popular. This polymerization type will be discussed by Buchmeiser in Chapter 8. Recently, interesting accounts have appeared on solventiess polymerization techniques applying (living) ROMP on surfaces to prepare structured brush surfaces of conjugated polymers [331, 332]. 

Olefin metathesis (olefin disproportionation) is the reaction of two alkenes in which the redistribution of the olelinic bonds takes place with the aid of transition metal catalysts (Scheme 7.7). The reaction proceeds with an intermediate formation of a metallacyclobutene. This may either break down to provide two new olefins, or open up to generate a metal alkylidene species which -by multiple alkene insertion- may lead to formation of alkylidenes with a polymeric moiety [21]. Ring-opening metathesis polymerization (ROMP) is the reaction of cyclic olefins in which backbone-unsaturated polymers are obtained. The driving force of this process is obviously in the relief of the ring strain of the monomers. 

Another two polymers, which have been used for the same type of arene-catalyzed lithiation reactions, are compounds 596 and 597, which were prepared by ring-opening metathesis polymerization (ROMP) starting from the corresponding aryl norbonenes 598. ... 

The polymerization of the alkyne triple bond (Secs. 5-7d and 8-6c) and ring-opening metathesis polymerization of a cycloalkene (Secs. 7-8 and 8-6a) yield polymers containing double bonds in the polymer chain. Cis-trans isomerism is possible analogous to the 1,4-polymer-ization of 1,3-dienes. 

Dalphond J, Bazzi H, Kahrim K, Sleiman H. Synthesis and self-assembly of polymers containing dicarboximide groups by living ring-opening metathesis polymerization. Macromol Chem Phys 2002 203 1988-1994. 

Pontrello JK, Allen MJ, Underbakke ES, Kiessling LL. Solid-phase synthesis of polymers using the ring-opening metathesis polymerization. J Am Chem Soc 2005 127 14536-14537. 

The polymerization of cyclic, strained olefins by transition metal alkylidenes of general formula L M = CRR (L = ligand, R, R = H, alkyl, aryl) yields polymers formed via ring-opening that contain unsaturated double bonds within each repetitive unit. Since the mechanism is based on repetitive metathesis steps, this polymerization reaction is known as ring-opening metathesis polymerization (ROMP) (Scheme 1). 

Moore, J. S. Transition Metals in Polymer Synthesis Ring-opening Metathesis Polymerization and Other Transition Metal Polymerization Techniques. In Comprehensive Organometaltic Chemistry // Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds. Elsevier Oxford, 1995 Vol. 12, pp 1209-1232. 

---