Selective and mild oxyfunctionalization of model polyolefins

被引:65
作者
Boaen, NK [1 ]
Hillmyer, MA [1 ]
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
关键词
D O I
10.1021/ma0347621
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The direct oxyfunctionalization of a model polyolefin, polyethylene-alt-propylene (PEP), was achieved utilizing a straightforward, mild process. In the presence of a manganese complex, manganese meso-tetra-2,6-dichlorophenylporphyrin acetate (Mn(TDCPP)OAc), imidazole, a phase transfer agent, and potassium peroxymonosulfate (Oxone), PEP was functionalized under ambient conditions without chain degradation. The primary oxidation products contained tertiary alcohols and ketones based on IR, H-1 NMR, C-13 NMR, and DEPT C-13 NMR spectroscopy of the oxyfunctionalized products. The oxyfunctionalization of squalane, a small molecule, structural analogue of PEP, was also demonstrated. Spectroscopic analyses of the main products from the squalane oxidation were nearly identical with the functional groups identified in the PEP oxidation products. The degree of functionalization was modulated by changing the relative concentration of the oxidant, Oxone. The degree of functionalization and the thermal properties are reported for these new polymeric materials.
引用
收藏
页码:7027 / 7034
页数:8
相关论文
共 61 条
[1]   ON PREPARATION OF METALLOPORPHYRINS [J].
ADLER, AD ;
LONGO, FR ;
KAMPAS, F ;
KIM, J .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1970, 32 (07) :2443-&
[2]   FUNCTIONALIZATION OF SATURATED-HYDROCARBONS .4. THE GIF SYSTEM FOR SELECTIVE OXIDATION USING MOLECULAR-OXYGEN [J].
BARTON, DHR ;
BOIVIN, J ;
GASTIGER, M ;
MORZYCKI, J ;
HAYMOTHERWELL, RS ;
MOTHERWELL, WB ;
OZBALIK, N ;
SCHWARTZENTRUBER, KM .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1986, (06) :947-955
[3]   THE SELECTIVE FUNCTIONALIZATION OF SATURATED-HYDROCARBONS - GIF CHEMISTRY [J].
BARTON, DHR ;
DOLLER, D .
ACCOUNTS OF CHEMICAL RESEARCH, 1992, 25 (11) :504-512
[4]   MONOOXYGENASE-LIKE OXIDATION OF HYDROCARBONS BY H2O2 CATALYZED BY MANGANESE PORPHYRINS AND IMIDAZOLE - SELECTION OF THE BEST CATALYTIC-SYSTEM AND NATURE OF THE ACTIVE OXYGEN SPECIES [J].
BATTIONI, P ;
RENAUD, JP ;
BARTOLI, JF ;
REINAARTILES, M ;
FORT, M ;
MANSUY, D .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (25) :8462-8470
[5]   OXYGEN-TRANSFER FROM PH(4)PHSO(5) TO MANGANESE PORPHYRINS - KINETICS AND MECHANISM OF THE FORMATION OF THE OXO SPECIES IN HOMOGENEOUS SOLUTION [J].
CAMPESTRINI, S ;
DIFURIA, F ;
LABAT, G ;
NOVELLO, F .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1994, (10) :2175-2180
[6]   SYNTHESIS OF FUNCTIONAL HYDROCARBON POLYMERS WITH WELL-DEFINED MOLECULAR-STRUCTURES [J].
CHUNG, TC ;
RAATE, M ;
BERLUCHE, E ;
SCHULZ, DN .
MACROMOLECULES, 1988, 21 (07) :1903-1907
[7]   SHAPE SELECTIVE ALKANE HYDROXYLATION BY METALLOPORPHYRIN CATALYSTS [J].
COOK, BR ;
REINERT, TJ ;
SUSLICK, KS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (23) :7281-7286
[8]   ASPECTS OF METHANE CHEMISTRY [J].
CRABTREE, RH .
CHEMICAL REVIEWS, 1995, 95 (04) :987-1007
[9]  
ESCOVA V, 1972, KINET KATAL, V13, P534
[10]   REACTIONS OF NONHEME IRON(II) CENTERS WITH DIOXYGEN IN BIOLOGY AND CHEMISTRY [J].
FEIG, AL ;
LIPPARD, SJ .
CHEMICAL REVIEWS, 1994, 94 (03) :759-805