OXYANIONS CATALYZE GROUP-TRANSFER POLYMERIZATION TO GIVE LIVING POLYMERS

被引:246
作者
DICKER, IB
COHEN, GM
FARNHAM, WB
HERTLER, WR
LAGANIS, ED
SOGAH, DY
机构
[1] Central Research and Development Department, E. I. du Pont de Nemours and Company, Inc., Experimental Station
关键词
D O I
10.1021/ma00220a002
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Oxyanions form a new class of catalysts for group-transfer polymerization (GTP) of acrylic monomers. Active catalysts in this class include aliphatic and aromatic carboxylates, phenolates, sulfinates, phosphinates, sulfonamidates, perfluoroalkoxides, nitrite, and cyanate. Catalytic activity is found in oxyanions whose conjugate acids have ap (in DMSO) within the range 4.5-23. Best results in terms of livingness and polydispersity of the resulting polymers are obtained with the lowest operable concentrations of the most active catalysts and with somewhat higher concentrations of catalysts of moderate activity. Bioxyanions (1:1 complexes of oxyanions with their conjugate acids) also are active but show reduced activity compared to the corresponding monooxyanions. They give better control of molecular weight than is obtained with the corresponding monooxyanions. In contrast to the more potent catalysts, the weaker catalysts show little activity at temperatures substantially below room temperature. Relative catalyst efficiency correlates well with pKa(DMSO) of the conjugate acids of the corresponding catalysts. The stereochemistry of PMMA prepared with oxyanion catalysts does not differ substantially from that of PMMA prepared with bifluoride catalysis. © 1990, American Chemical Society. All rights reserved.
引用
收藏
页码:4034 / 4041
页数:8
相关论文
共 32 条
[1]  
BANDERMANN F, 1985, MAKROMOL CHEM-RAPID, V6, P335
[2]   VOLTAMMETRIC EVALUATION OF THE EFFECTIVE ACIDITIES (PKA') FOR BRONSTED ACIDS IN APROTIC-SOLVENTS [J].
BARRETTE, WC ;
JOHNSON, HW ;
SAWYER, DT .
ANALYTICAL CHEMISTRY, 1984, 56 (11) :1890-1898
[3]   THIOL ACIDITIES AND THIOLATE ION REACTIVITIES TOWARD BUTYL CHLORIDE IN DIMETHYLSULFOXIDE SOLUTION - THE QUESTION OF CURVATURE IN BRONSTED PLOTS [J].
BORDWELL, FG ;
HUGHES, DL .
JOURNAL OF ORGANIC CHEMISTRY, 1982, 47 (17) :3224-3232
[4]   ACIDITIES AND HYDROGEN-BONDING OF PHENOLS IN DIMETHYLSULFOXIDE [J].
BORDWELL, FG ;
MCCALLUM, RJ ;
OLMSTEAD, WN .
JOURNAL OF ORGANIC CHEMISTRY, 1984, 49 (08) :1424-1427
[5]   ACIDITIES OF THE H-C PROTONS IN CARBOXYLIC ESTERS, AMIDES, AND NITRILES [J].
BORDWELL, FG ;
FRIED, HE .
JOURNAL OF ORGANIC CHEMISTRY, 1981, 46 (22) :4327-4331
[6]   EQUILIBRIA INVOLVING ORGANIC-ANIONS IN DIMETHYLSULFOXIDE AND N-METHYLPYRROLIDIN-2-ONE - ACIDITIES, ION-PAIRING, AND HYDROGEN-BONDING [J].
BORDWELL, FG ;
BRANCA, JC ;
HUGHES, DL ;
OLMSTEAD, WN .
JOURNAL OF ORGANIC CHEMISTRY, 1980, 45 (16) :3305-3313
[7]  
BORDWELL FG, 1980, J ORG CHEM, V45, P3295
[8]   KINETICS OF THE ANION-CATALYZED MICHAEL REACTION OF SILYL KETENE ACETALS - INITIATION AND PROPAGATION STEPS OF GROUP TRANSFER POLYMERIZATION [J].
BRITTAIN, WJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (22) :7440-7444
[9]   COMPARISON OF SUBSTITUENT EFFECTS ON DISSOCIATION AND CONJUGATION OF PHENOLS WITH THOSE OF CARBOXYLIC-ACIDS IN ACETONITRILE, N,N-DIMETHYLFORMAMIDE, AND DIMETHYL-SULFOXIDE [J].
CHANTOONI, MK ;
KOLTHOFF, IM .
JOURNAL OF PHYSICAL CHEMISTRY, 1976, 80 (12) :1306-1310
[10]  
CHANTOONI MK, 1970, J AM CHEM SOC, V92, P7025