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Basf Aktiengesellschaft

Kabushiki Kaisha Toyota Chuo Kenkyusho

Bruce M Novak

Robert H Grubbs

Timothy J Deming

Mitsuru Nakano

Hong-Zhi Tang

Mark W Ellsworth

Keitaro Seto

Harald Keller

Hiromitsu Tanaka

Hiroaki Kuwahara

Rudolf Zentel

Georg Maxein

Anand Viswanathan

Edward H Haagen

Lisa S Boffa

Described is a cyclobutene polymer comprising: monomeric units of cyclobutene, said cyclobutene having at least one fused ring system substituted thereon, said polymer comprising not more than 10 mol percent ring-opened units of said cyclobutene; and said polymer having a molecular weight of at least 1,000; said polymer optionally copolymerized with a comonomer to form a copolymer therewith. Compositions thereof and methods of making the same are also described.

Cyclobutene polymers and methods of making the same

A polycarbodiimide polymer that is reversibly switchable between two distinct optical orientations is described. The polymer is useful in forming devices such as filters, storage media, actuators, and displays. Methods of making and using such polymers are also described.

Devices containing chiroptical switching materials and methods of making and using the same

The polymerization of polar vinyl monomers in the presence of Lewis acids produces stereoregular vinyl polymers. Polar vinyl monomers may be mixed with Lewis acids to form associations or complexes between the monomers and Lewis acids. The mixtures or monomer-Lewis acid complexes may be polymerized to produce the desire stereoregular vinyl polymers.

Stereoregular polar vinyl polymers and methods of making the same

A method for producing a polymer by coordination polymerization, comprising the steps of (a) reacting an unsaturated polar monomer having a functional group releasing a proton or a salt of the unsaturated polar monomer, with a masking agent comprising a halogenated organometallic compound or a organoaluminum compound capable of masking the functional group to form a corresponding masked monomer; and (b) polymerizing the masked monomer either alone or in combination with another monomer in the presence of the coordination polymerization catalyst to obtain the polymer.

Method for producing a polymer by coordination polymerization

Providing an isomerization process which can isomerize allenes to alkynes less expensively and stably is an assignment to be solved by the present invention and given thereto. The present invention is an isomerization process including the step of reacting an allene-lype hydrocarbon compound (R.sub.1 R.sub.2 C.dbd.C.dbd.CR.sub.3 R.sub.4) in the presence of alkaline-earth metal hydride working as an isomerization catalyst, thereby isomerizing the allene-type hydrocarbon compound to an alkyne-type hydrocarbon compound (R.sub.1 C.ident.C--CR.sub.2 R.sub.3 R.sub.4).

Isomerization of allenes to alkynes with an alkaline-earth metal hydride

Cholesteric copolyisocyanates with repeating units of the formulae: ##STR1## and, where appropriate, of the formula ##STR2## where R.sup.1 is a chiral aliphatic or aromatic radical,

Cholesteric copolyisocyanates

The invention features linear copolymers prepared from mixtures of allenes and alkynes. The new copolymers have the formula: ##STR1## wherein R.sub.1 through R.sub.6 are, independently, H, an alkyl, an aryl, a phenyl or substituted phenyl, an alkoxy, or an aryloxyl, x+n is 1 to 10,000, and m is 1 to 10,000. The invention also features efficient methods of preparing the new copolymers using nickel or palladium catalysts.

Allene/alkyne copolymers

A .pi.-allylnickel/counterion complex is reacted with a hologenated ketone to produce a highly active polymerization initiator.

Highly active .pi.-allynickel-based polymerization initiators

'Living' polymerization methods are described wherein a bimetallic lanthanide complex initiator is reacted with a monomer. Using these methods, link-functionalized polymers can be formed that are capable of being modified after polymerization with various reactants, or to be biodegraded through oxidation or reduction or cleavage. The bimetallic lanthanide complex initiator can be used to polymerize methyl methacrylate in a living fashion. A two-step method of forming a triblock polymer using the bimetallic lanthanide complex initiator is also disclosed.

Polymerization using bimetallic bis-lanthanoid initiators

This invention relates to sol-gel methods for forming non-shrinking, high-glass composite materials and the products. Also taught is an inorganic-organic composite material having a solid interwoven network of an inorganic polymer matrix with interpenetrating polymerized alcohols. The inorganic matrix can be based on either Si or Ti atoms.

Composite materials of interpenetrating inorganic and organic polymer

A .pi.-allylnickel/counterion complex is reacted with a halogenated ketone to product a highly active polymerization initiator.

Highly active .pi.-allylnickel-based polymerization initiators

Photoactive cationic organic polymers are provided which are electrically insulating and which are capable of photolysis to an electrically conductive form. The organic polymer includes a C-A linkage, wherein C is a chalcogenide-sulfide, selenide or telluride-in the polymer backbone chain and A is in aryl or alkyl group. The C-A linkage is capable of being cleaved in the presence of ultraviolet light to release A as a free radical and cause the polymer to become electrically conducting in the presence of the light while the remainder of the polymer remains electrically non-conducting. A thin film of such a polymer containing an electrically insulating region and a photolysed electrically conductive region may be used as a semiconductor. Methods for forming photoactive arylated or alkylated poly(phenylene chalcogenide) polymers involving the step of direct arylation or alkylation of a poly(phenylene chalcogenide) polymer are also provided. In addition, a method is provided for forming a semiconductor. The method involves the steps of selectively exposing at least one region of a photoactive electrically insulating cationic organic polymer to photolytic light to release a radical and convert the exposed region to a stable electrically conducting state.

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El Sobrante, CA, United States of America

Bruce M Novak