Polymers functionalized with heterocyclic nitrile compounds

Abstract

A method for preparing a functionalized polymer, the method comprising the steps of preparing a reactive polymer and reacting the reactive polymer with a heterocyclic nitrile compound.

What is claimed is: 
     
         1 . A method for preparing a functionalized polymer, the method comprising the steps of:
 (i) preparing a reactive polymer with a lanthanide-based catalyst system; and   (ii) reacting the reactive polymer with a heterocyclic nitrile compound; where the heterocyclic nitrile compound includes a heterocycle with multiple nitrogen atoms.   
     
     
         2 . The method of  claim 1 , where the heterocycle with multiple nitrogen atoms is selected from the group consisting of pyrazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 3-pyridazinyl, 4-pyridazinyl, N-methyl-2-imidazolyl, N-methyl-4-imidazolyl, N-methyl-5-imidazolyl, N-methyl-3-pyrazolyl, N-methyl-4-pyrazolyl, N-methyl-5-pyrazolyl, N-methyl-2-imidazolin-2-yl, N-methyl-2-imidazolin-4-yl, N-methyl-2-imidazolin-5-yl, N-methyl-2-pyrazolin-3-yl, N-methyl-2-pyrazolin-4-yl, N-methyl-2-pyrazolin-5-yl, 1-phthalazinyl, 2-quinazolinyl, 4-quinazolinyl, 2-quinoxalinyl, 3-cinnolinyl, 4-cinnolinyl, 1-methylindazol-3-yl, 1,5-naphthyridin-2-yl, 1,5-naphthyridin-3-yl, 1,5-naphthyridin-4-yl, 1,8-naphthyridin-2-yl, 1,8-naphthyridin-3-yl, 1,8-naphthyridin-4-yl, 1-methylbenzimidazol-2-yl, N-methyl-β-carbolin-1-yl, N-methyl-β-carbolin-3-yl, N-methyl-β-carbolin-4-yl, 1,7-phenanthrolin-2-yl, 1,7-phenanthrolin-3-yl, 1,7-phenanthrolin-4-yl, 1,10-phenanthrolin-2-yl, 1,10-phenanthrolin-3-yl, 1,10-phenanthrolin-4-yl, 4,7-phenanthrolin-1-yl, 4,7-phenanthrolin-2-yl, 4,7-phenanthrolin-3-yl, and 1-phenazinyl, 2-phenazinyl. 
     
     
         3 . The method of  claim 2 , where the heterocycle with multiple nitrogen atoms is selected from the group consisting pyrazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 3-pyridazinyl, and 4-pyridazinyl. 
     
     
         4 . The method of  claim 1 , where the heterocycle with multiple nitrogen atoms is selected from the group consisting of N-methyl-1,2,3-triazol-4-yl, N-methyl-1,2,3-triazol-5-yl, N-methyl-1,2,4-triazol-3-yl, N-methyl-1,2,4-triazol-5-yl, 1,2,4-triazin-3-yl, 1,2,4-triazin-5-yl, 1,2,4-triazin-6-yl, and 1,3,5-triazinyl. 
     
     
         5 . The method of  claim 1 , where the heterocycle with multiple nitrogen atoms is selected from the group consisting of 2-pteridinyl, 4-pteridinyl, 6-pteridinyl, 7-pteridinyl, N-methyl-2-purinyl, N-methyl-6-purinyl, and N-methyl-8-purinyl. 
     
     
         6 . The method of  claim 1 , where the heterocyclic nitrile compound is defined by the formula θ-C≡V or θ-R—C≡N, where θ is a heterocyclic group with multiple nitrogen atoms and R is a divalent organic group. 
     
     
         7 . The method of  claim 1 , where the heterocyclic nitrile compound is selected from the group consisting of pyrazinecarbonitrile, 2-pyrimidinecarbonitrile, 4-pyrimidinecarbonitrile, 5-pyrimidinecarbonitrile, 3-pyridazinecarbonitrile, 4-pyridazinecarbonitrile, N-methyl-2-imidazolecarbonitrile, N-methyl-4-imidazolecarbonitrile, N-methyl-5-imidazolecarbonitrile, N-methyl-3-pyrazolecarbonitrile, N-methyl-4-pyrazolecarbonitrile, N-methyl-5-pyrazolecarbonitrile, N-methyl-2-imidazoline-2-carbonitrile, N-methyl-2-imidazoline-4-carbonitrile, N-methyl-2-imidazoline-5-carbonitrile, N-methyl-2-pyrazoline-3-carbonitrile, N-methyl-2-pyrazoline-4-carbonitrile, N-methyl-2-pyrazoline-5-carbonitrile, 1-phthalazinecarbonitrile, 2-quinazolinecarbonitrile, 4-quinazolinecarbonitrile, 2-quinoxalinecarbonitrile, 3-cinnolinecarbonitrile, 4-cinnolinecarbonitrile, 1-methylindazole-3-carbonitrile, 1,5-naphthyridine-2-carbonitrile, 1,5-naphthyridine-3-carbonitrile, 1,5-naphthyridine-4-carbonitrile, 1, 8-naphthyridine-2-carbonitrile, 1, 8-naphthyridine-3-carbonitrile, 1,8-naphthyridine-4-carbonitrile, N-methyl-β-carboline-1-carbonitrile, N-methyl-β-carboline-3-carbonitrile, N-methyl-β-carboline-4-carbonitrile, 1,7-phenanthroline-2-carbonitrile, 1,7-phenanthroline-3-carbonitrile, 1,7-phenanthroline-4-carbonitrile, 1,10-phenanthroline-2-carbonitrile, 1,10-phenanthroline-3-carbonitrile, 1,10-phenanthroline-4-carbonitrile, 4,7-phenanthroline-1-carbonitrile, 4,7-phenanthroline-2-carbonitrile, 4,7-phenanthroline-3-carbonitrile, 1-phenazinecarbonitrile, and 2-phenazinecarbonitrile. 
     
     
         8 . The method of  claim 1 , where the heterocyclic nitrile compound is selected from the group consisting of N-methyl-1,2,3-triazole-4-carbonitrile, N-methyl-1,2,3-triazole-5-carbonitrile, N-methyl-1,2,4-triazole-3-carbonitrile, N-methyl-1,2,4-triazole-5-carbonitrile, 1,2,4-triazine-3-carbonitrile, 1,2,4-triazine-5-carbonitrile, 1,2,4-triazine-6-carbonitrile, 1,3,5-triazinecarbonitrile, and 1-methylbenzimidazole-2-carbonitrile. 
     
     
         9 . The method of  claim 1 , where the heterocyclic nitrile compound is selected from the group consisting of 2-pteridinecarbonitrile, 4-pteridinecarbonitrile, 6-pteridinecarbonitrile, 7-pteridinecarbonitrile, N-methyl-2-purinecarbonitrile, N-methyl-6-purinecarbonitrile, and N-methyl-8-purinecarbonitrile. 
     
     
         10 . The method of  claim 1 , where the heterocyclic nitrile compound is 2-pyrimidinecarbonitrile. 
     
     
         11 . The method of  claim 1 , where the heterocyclic nitrile compound is pyrazinecarbonitrile. 
     
     
         12 . The method of  claim 1 , where the reactive polymer has a cis-1,4-linkage content that is greater than 60%.