Patent classifications
C08G2261/13
Catalyst for ring expansion metathesis polymerization of cyclic monomers
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.
Catalyst for ring expansion metathesis polymerization of cyclic monomers
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.
CATALYST FOR RING EXPANSION METATHESIS POLYMERIZATION OF CYCLIC MONOMERS
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.
CATALYST FOR RING EXPANSION METATHESIS POLYMERIZATION OF CYCLIC MONOMERS
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.
Graphene nanoribbon, graphene nanoribbon fabrication method, and semiconductor device
A graphene nanoribbon has a chiral edge to which a dicarbimide structure is bonded. The dicarbimide structure is an electron-withdrawing group. The width and band gap of the graphene nanoribbon are controlled by a precursor molecule used for a polymerization reaction. Furthermore, n-type operation of the graphene nanoribbon is realized by the dicarbimide structure. In addition, with the graphene nanoribbon, an increase in ribbon length and suppression of a polymerization defect by the stabilization of a reaction intermediate of the precursor molecule, as well as improvement in orientation are realized by the dicarbimide structure.
Catalyst for ring expansion metathesis polymerization of cyclic monomers
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.
High density polymers based on norbornadiene
A novel family of cycloalkanes compounds having one or more allylidene functionalities which can be used to create cross-linked thermosets and thermoplastics having thermal stability. An example heptacyclo [6.6.0.0.sup.2,6.0.sup.3,13.0.sup.4,11.0.sup.5,9.0.sup.10,14] tetradecane (HCTD) complex with terminal allylidene groups at the 7- and 12-positions (HCTD-7,12-diallylidene) was generated from norbornadiene via an efficient six-step synthesis. Thermal polymerization at temperatures ranging from 160 to 240? C. yielded a robust cross-linked material with thermal stability up to 485? C. in air, a glass transition temperature of 377? C., and a char yield (600? C.) of 56% in air. Applications include heat resistant composites utilized in the aerospace, electronic, automotive and textile industries.
High mobility polymer organic field-effect transistors by blade-coating semiconductor:insulator blend solutions
Conjugated polymer-based organic field-effect transistors have garnered attention since the solution processability of the semiconductor material raises the possibility of lower device fabrication costs, and considerable progress has been made on achieving high mobility systems. Further improvements in charge carrier mobility while using non-specialized deposition techniques and minimizing the volume of semiconductor used in the fabrication process are important considerations for practical implementation. Here, a method of fabricating devices is disclosed that uses a technique (for example, a scalable blade-coating technique) to cast polymer thin film devices from blend solutions with one component being the polymer semiconductor and the other being a commodity polymer. Even when mixing the semiconducting polymer with 90% polystyrene by weight, an average mobility of 2.70.4 cm.sup.2 V.sup.1 s.sup.1 can be obtained.
Catalyst for Ring Expansion Metathesis Polymerization of Cyclic Monomers
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.
GRAPHENE NANORIBBON, GRAPHENE NANORIBBON FABRICATION METHOD, AND SEMICONDUCTOR DEVICE
A graphene nanoribbon has a chiral edge to which a dicarbimide structure is bonded. The dicarbimide structure is an electron-withdrawing group. The width and band gap of the graphene nanoribbon are controlled by a precursor molecule used for a polymerization reaction. Furthermore, n-type operation of the graphene nanoribbon is realized by the dicarbimide structure. In addition, with the graphene nanoribbon, an increase in ribbon length and suppression of a polymerization defect by the stabilization of a reaction intermediate of the precursor molecule, as well as improvement in orientation are realized by the dicarbimide structure.