Embodiments in accordance with the present invention encompass compositions encompassing a latent catalyst and a thermal or photoactivator along with one or more monomers which undergo ring open metathesis polymerization (ROMP) when said composition is heated to a temperature from 50 C. to 100 C. or higher to form a substantially transparent film. Alternatively the compositions of this invention also undergo polymerization when subjected to suitable radiation. The monomers employed therein have a range of refractive index from 1.4 to 1.6 and thus these compositions can be tailored to form transparent films of varied refractive indices. The compositions of this invention further comprises inorganic nanoparticles which form transparent films and further increases the refractive indices of the compositions. Accordingly, compositions of this invention are useful in various opto-electronic applications, including as coatings, encapsulants, fillers, leveling agents, among others.

A tetraanionic OCO pincer ligand metal-oxo-alkylidene complex is prepared from a trianionic pincer ligand supported metal-alkylidyne. The metal can be tungsten or other group 5-7 transition metal. The tetraanionic pincer ligand metal-oxo-alkylidene complex, a trianionic OCO pincer ligand metal complex, or a trianionic ONO pincer ligand metal complex can be used to polymerize cycloalkenes. The poly(cycloalkene)s are predominantly cis-alkene macrocyclics.

A shaping material contains a crystalline alicyclic structure-containing resin. More specifically, the crystalline alicyclic structure-containing resin in the shaping material has a melting point of 200 C. or higher, and content of chlorobenzene-soluble components in the shaping material is 1,000 ppm or less as an o-dichlorobenzene-equivalent value based on gas chromatography analysis with o-dichlorobenzene as a standard substance.

A manufactured wood based siding or cladding product made from an engineered wood composite including, but not limited to, oriented strand board (OSB), hardboard, plywood, and combinations thereof, with fire-resistant properties (e.g., resistance to flame spread, ignition and combustion) imparted during the manufacturing process. An engineered wood-based composite siding product (in various forms, including lap, panel or trim) possessing such material properties is better suited for meeting the requirements of certain communities or areas where building codes require such protection due to the risk of fires (such as those posed within the boundaries of the wildland-urban interface, WUI).

Engineered or manufactured wood-based composite products are typically manufactured by assembling multiple layers, then consolidating these layers using heat and pressure. A fines layer comprising wood or lignocellulosic wood particles is currently applied to the face of engineered wood-based composite siding products (e.g., lap siding, panel siding, trim) to provide an appropriate outer appearance, or other features, to the product.

In various exemplary embodiments, the present invention treats the particles that make up the fines layer before incorporation of the particles into the manufacturing process (i.e., in-process). The treatment comprises adding ingredients or additives (using appropriate methods) that impart desired protection when exposed to a fire event. Ingredients, for example, include various borate-based chemistries, minerals, or combinations thereof that impart the desired protection.

A material for forming an underlayer film according to the present invention is a material for forming an underlayer film which is used to form a resist underlayer film used in a multi-layer resist process, the material including a cyclic olefin polymer which has a repeating structural unit [A] represented by Formula (1) and a repeating structural unit [B] represented by Formula (2), in which a molar ratio [A]/[B] of the structural unit [A] to the structural unit [B] in the cyclic olefin polymer is greater than or equal to 5/95 and less than or equal to 95/5.

##STR00001##

The invention relates to immobilized metal alkylidene catalysts. The catalysts are useful in olefin metathesis. ##STR00001##

1) Hydrocarbon-based copolymer comprising two end groups preceded by an ester function and chosen from a 2-oxo-1,3-dioxolan-4-yl (or cyclocarbonate), a dithiocyclocarbonate, an exo-vinylene cyclocarbonate and a 2-oxo-1,3-dioxolen-4-yl, the main chain of which comprises units (I) and (II)

##STR00001##

in which R.sup.0 is notably a methyl radical;

and the number-average molecular mass Mn of which is between 400 and 100 000 g/mol.

2) Process for preparing said copolymer, comprising:

(i) a step of heating a statistical bipolymer A chosen from a poly(butadiene-isoprene), a poly(butadiene-myrcene) and a poly(butadiene-farnesene); and then

(ii) a step of heating the product formed, in the presence of a chain-transfer agent.

3) Use as adhesive, as a mixture with an amine compound comprising at least two amine groups.

Macrocyclic polyalkene homopolymers and copolymers can be formed and converted to macrocyclic polyalkanes or macrocyclic poly(alkane-co-alkene) upon hydrogenation or, when the macrocyclic polyalkene is reacted with an alkene in the presence of an olefin metathesis catalyst, to a macrocyclic poly(alkane-co-alkene) comprising vicinal C(CR2)'s. Upon hydrogenation of a macrocyclic poly(alkane-co-alkene) comprising vicinal C(CR2)-'s, macrocyclic poly(alkane)s or poly(alkane-co-alkene)s with isolated C(CR2)- groups can be provided, depending on the degree of hydrogenation. The poly(alkane-co-alkene)s with isolated C(CR2)- units can be used to form poly(macrocyclic poly(alkane-co-alkene))s, poly(macrocyclic poly(alkane))s, and/or bi-, tri-, and/or multi-macrocyclic poly(alkane-co-alkene)s or bi-, tri-, and/or multi-macrocyclic poly(alkane)s.

1) Hydrocarbon-based copolymer comprising two end groups preceded by an ether function and chosen from a 2-oxo-1,3-dioxolan-4-yl (or cyclocarbonate), a dithiocyclocarbonate, and a 2-oxo-1,3-dioxolen-4-yl, the main chain of which comprises units (I) and (II)

##STR00001##

in which R.sup.0 is notably a methyl radical;

and the number-average molecular mass Mn of which is between 400 and 100 000 g/mol.

2) Process for preparing said copolymer, comprising: (i) a step of heating a statistical bipolymer A chosen from a poly(butadiene-isoprene), a poly(butadiene-myrcene) and a poly(butadiene-farnesene); and then (ii) a step of heating the product formed, in the presence of a chain-transfer agent.

3) Use as adhesive, as a mixture with an amine compound comprising at least two amine groups.

A liquid cyclopentene ring-opened polymer having a weight average molecular weight (Mw) of 1,000 to 50,000 and a cis double content of 55% or more in repeating units.