Use of monocarboxylic iron derivatives in the ring-opening polymerization of L-lactide

被引:108
作者
Stolt, M [1 ]
Södergård, A [1 ]
机构
[1] Abo Akad Univ, Lab Polymer Technol, SF-20500 Turku, Finland
关键词
D O I
10.1021/ma9902753
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
L-Lactide was ring-opening polymerized in the melt by using different organic monocarboxylic iron complexes. The complexes were those of iron and acetic acid, butyric acid, isobutyric acid, dichloroacetic acid, and trifluoroacetic acid. The polymerization temperature was in the range 170-210 degrees C, polymerization time between 0.5 and 25 h, and amount of catalyst added varied between 0.12 and 1.20 wt %. Iron butyrate and iron dichloroacetate complexes were low efficient catalysts in the ring-opening polymerization due to hydrolysis during the preparation. Iron acetate, iron trifluoroacetate, and iron isobutyrate complexes were efficient catalysts yielding a high molar mass poly(L-lactide) with a high monomer conversion. Under optimum conditions a poly(L-lactide) with a molar mass (M(w)) of ca. 150 000 g/mol could be prepared. Monomer conversions over 85% were obtained in many experiments. High polymerization temperatures are required though with these kinds of iron catalysts, and some racemization of the polymerization products is evident. The polymerization experiments indicate that the oxidation state of the iron has an influence on the efficiency of the catalysts and that the iron is chemically bound to the polymer.
引用
收藏
页码:6412 / 6417
页数:6
相关论文
共 26 条
[1]   Synthesis and degradability of a novel aliphatic polyester based on L-lactide and sorbitol .3. [J].
Arvanitoyannis, I ;
Nakayama, A ;
Psomiadou, E ;
Kawasaki, N ;
Yamamoto, N .
POLYMER, 1996, 37 (04) :651-660
[2]  
BERO M, 1990, MAKROMOL CHEM, V191, P2287
[3]   CONFIGURATIONAL STRUCTURES OF LACTIC-ACID STEREOCOPOLYMERS AS DETERMINED BY C-13-LABELED (H-1)-NMR [J].
CHABOT, F ;
VERT, M ;
CHAPELLE, S ;
GRANGER, P .
POLYMER, 1983, 24 (01) :53-59
[4]   BIODEGRADABLE POLYMERS .7. ON THE MECHANISM OF RING-OPENING POLYMERIZATION OF CYCLIC ESTERS OF ALIPHATIC HYDROXYCARBOXYLIC ACIDS BY MEANS OF DIFFERENT TIN-COMPOUNDS [J].
DAHLMANN, J ;
RAFLER, G .
ACTA POLYMERICA, 1993, 44 (02) :103-107
[5]   ALUMINUM ALKOXIDES - A FAMILY OF VERSATILE INITIATORS FOR THE RING-OPENING POLYMERIZATION OF LACTONES AND LACTIDES [J].
DUBOIS, P ;
JEROME, R ;
TEYSSIE, P .
MAKROMOLEKULARE CHEMIE-MACROMOLECULAR SYMPOSIA, 1991, 42-3 :103-116
[6]  
EENINK MJD, 1987, THESIS U TWENTE NETH
[7]   INVESTIGATION OF STRUCTURE OF SOLUTION GROWN CRYSTALS OF LACTIDE COPOLYMERS BY MEANS OF CHEMICAL-REACTIONS [J].
FISCHER, EW ;
STERZEL, HJ ;
WEGNER, G .
KOLLOID-ZEITSCHRIFT AND ZEITSCHRIFT FUR POLYMERE, 1973, 251 (11) :980-990
[8]  
HOPPE JO, 1955, AM J MED SCI NOV, P558
[9]   POLYLACTONES .31. SN(II)OCTOATE-INITIATED POLYMERIZATION OF L-LACTIDE - A MECHANISTIC STUDY [J].
KRICHELDORF, HR ;
KREISERSAUNDERS, I ;
BOETTCHER, C .
POLYMER, 1995, 36 (06) :1253-1259
[10]   POLYLACTONES .20. POLYMERIZATION OF EPSILON-CAPROLACTONE WITH TRIBUTYLTIN DERIVATIVES - A MECHANISTIC STUDY [J].
KRICHELDORF, HR ;
SUMBEL, MV ;
KREISERSAUNDERS, I .
MACROMOLECULES, 1991, 24 (08) :1944-1949