Ex parte WARDLE et al. - Page 5




                  Appeal No.  1996-1529                                                                                                                   
                  Application No.  08/233,219                                                                                                             

                  answer (Paper No. 21, mailed May 30, 1995) for the examiner's reasoning in support of the rejection,                                    

                  and to the appellants’ brief (Paper No. 20, filed March 9, 1995) for the appellants’ arguments                                          
                  thereagainst.  2                                                                                                                        

                                                                 THE INVENTION                                                                            

                           Appellants’ invention is directed to (a) methods for polymerizing cyclic ether monomers having                                 

                  4 or 5 member rings, i.e., substituted or unsubstituted oxetanes or tetrahydrofurans, wherein the                                       

                  polymerization is catalyzed by an alkylating salt together with a co-catalyst alcohol which forms an                                    

                  initiating species together with the salt and (b) polymers formed thereby which                                                         

                  have controlled functionality and high molecular weights (specification, page 24).                                                      

                                                                      OPINION                                                                             

                           Wardle discloses cationic polymerization of 4 and 5 member cyclic ether monomers, e.g.,                                        

                  oxetanes and tetrahydrofurans, using an acid catalyst together with an alcohol which complexes with the                                 

                  acid to form an “initiator adduct,” wherein the acid is used at a molar ratio relative to the hydroxyl                                  

                  groups of the alcohol at between about 0.05:1 to about 0.5:1.  The adduct complexes with a cyclic                                       

                  ether monomer to form an activated cyclic ether.  Uncomplexed alcohol reacts with the activated cyclic                                  

                  ether monomer to open the ring and provide terminal hydroxyl groups on the exposed ends of the ether                                    


                           2Appellants’ reply brief (Paper No. 22, filed June 26, 1995) was denied entry by the examiner in the                           
                  communication mailed October 17, 1995 (Paper No. 23).  Appellants have not filed a petition under 37 C.F.R.                             
                  § 1.181 seeking review of the examiner’s decision to deny entry of the reply brief.  Therefore, the reply brief has not                 
                  been considered in reaching our decision in this appeal.                                                                                

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