The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jun. 28, 2005

Filed:

Dec. 21, 2000
Applicants:

Joseph D. Lichtenhan, San Juan Capistrano, CA (US);

Joseph J. Schwab, Huntington Beach, CA (US);

Yi-zong an, Fountain Valley, CA (US);

William Reinerth, Westminster, CA (US);

Frank J. Feher, Costa Mesa, CA (US);

Inventors:

Joseph D. Lichtenhan, San Juan Capistrano, CA (US);

Joseph J. Schwab, Huntington Beach, CA (US);

Yi-Zong An, Fountain Valley, CA (US);

William Reinerth, Westminster, CA (US);

Frank J. Feher, Costa Mesa, CA (US);

Assignee:

Hybrid Plastics, LLC, Fountain Valley, CA (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C08G077/08 ; C08G077/20 ;
U.S. Cl.
CPC ...
Abstract

Processes have been developed for the manufacture of polyhedral oligomeric silsesquioxanes (POSS), polysilsesquioxanes, polyhedral oligomeric silicates (POS), and siloxane molecules bearing reactive ring-strained cyclic olefins (e.g. norbornenyl, cyclopentenyl, etc. functionalities). The preferred manufacturing processes employ the silation of siloxides (Si—OA, where A=H, alkaline or alkaline earth metals) with silane reagents that contain at least one reactive ring-strained cyclic olefin functionality [e.g., XSi(CH)(CH)where y=1-2 and X=OH, Cl, Br, I, alkoxide OR, acetate OOCR, peroxide OOR, amine NR, isocyanate NCO, and R]. Alternatively, similar products can be prepared through hydrosilation reactions between silanes containing at least one silicon-hydrogen bond (Si—H) with ring-strained cyclic olefin reagents [e.g., 5-vinyl, 2 norbornene CH═CH, cyclopentadiene]. The two processes can be effectively practiced using polymeric silsesquioxanes [RSiO]where ∞=1-1,000,000 or higher and which contain unreacted silanol or silane groups at chain terminus or branch points, on POSS nanostructures of formulas [(RSiO)], homoleptic, [(RSiO)(R'SiO)], heteroleptic, and {(RSiO)(RXSiO)}, functionalized heteroleptic nanostructures, on silanes RSiX, linear, cyclic, oligomeric and polymeric siloxanes (polymeric formula RXSi—(OSiRX)—OSiRXwhere m=0-1000, X=OH, Cl, Br, I, alkoxide OR, acetate OOCR, peroxide OOR, amine NR, isocyanate NCO, and R). Each of the processes result in new chemical species bearing one or more ring strained olefins that can undergo polymerization, grafting, or other desirable chemical reactions to form polymeric products. These polymeric systems are most desirably utilized in polymerizations for the modification of properties of thermoplastic or thermoset resin systems or for the preparation of polymers with utility in electronics, medical devices, sporting goods, and aerospace as coatings and structural components.


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