Introduction of a [5]helicene unit in polyimides by chemical and thermal transformations of precursor polymers

被引:21
作者
Bender, TP [1 ]
Qi, Y [1 ]
Gao, JP [1 ]
Wang, ZY [1 ]
机构
[1] CARLETON UNIV,OTTAWA CARLETON CHEM INST,DEPT CHEM,OTTAWA,ON K1S 5B6,CANADA
关键词
D O I
10.1021/ma961831l
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Several [5]helicene-containing polyimides have been synthesized by chemical and thermal transformation of the precursor polyimides having the tetrahydro[5]helicene unit. The illustrated diamines 4a and 4b were polymerized with two dianhydrides (6FDA and s-BPDA) to form high molecular weight polyimides 5a,b and 6a,b, containing the tetrahydro[5]helicene core. These precursor polyimides showed good solubilities in common solvents and good thermal properties. Chemical transformation in solution or in the film form could be effected by treatment with bromine at elevated temperatures. The resulting [5]helicene-containing polyimides showed a marked increase in thermooxidative stability. The onset temperatures for 5% weight loss in air were over 500 degrees C for the [5]helicene-based polyimides, about 70 degrees C higher than those for the precursor polyimides. Furthermore, the [5]helicene-containing polyimides retained the high tensile (Young's) moduli of the precursor polyimides, indicating that the transformation did not result in any chain cleavage or cross-linking. The transformation to yield [5]helicene-containing polyimides could also be effected by heating at 400 degrees C in air. The thermally induced transformation was supported by the synthesis and transformation of a model compound.
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页码:6001 / 6006
页数:6
相关论文
共 24 条
[1]   N-15-NMR, H-1-NMR, AND C-13-NMR CHEMICAL-SHIFTS AND ELECTRONIC-PROPERTIES OF AROMATIC DIAMINES AND DIANHYDRIDES [J].
ANDO, S ;
MATSUURA, T ;
SASAKI, S .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1992, 30 (11) :2285-2293
[2]  
BECKER KH, 1992, MACROMOLECULES, V25, P2005
[3]   ORGANOMETALLIC MODIFICATION APPROACH TO CONTROL OF POLYMER PROPERTIES - A SOLUBLE, LIQUID-CRYSTALLINE, PI-COMPLEXED AROMATIC POLYAMIDE [J].
DEMBEK, AA ;
BURCH, RR ;
FEIRING, AE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (05) :2087-2089
[4]  
Frimer A. A., 1995, HIGH PERFORM POLYM, V7, P93
[5]   REINVESTIGATION OF THE PHOTOCYCLIZATION OF 1,4-PHENYLENE BIS(PHENYLMALEIC ANHYDRIDE) - PREPARATION AND STRUCTURE OF [5]HELICENE 5,6-9,10-DIANHYDRIDE [J].
FRIMER, AA ;
KINDER, JD ;
YOUNGS, WJ ;
MEADOR, MAB .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (06) :1658-1664
[6]   DEHYDROGENATION OF POLYCYCLIC HYDROAROMATIC COMPOUNDS [J].
FU, PP ;
HARVEY, RG .
CHEMICAL REVIEWS, 1978, 78 (04) :317-361
[7]   TRANSITION-METAL-CATALYZED POLYMERIZATION OF HETEROATOM-FUNCTIONALIZED CYCLOHEXADIENES - STEREOREGULAR PRECURSORS TO POLY(PARA-PHENYLENE) [J].
GIN, DL ;
CONTICELLO, VP ;
GRUBBS, RH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (08) :3167-3169
[8]  
HARRIS FW, 1977, STRUCTURE SOLUBILITY, P183
[9]  
Huang WX, 1997, J POLYM SCI POL CHEM, V35, P143, DOI 10.1002/(SICI)1099-0518(19970115)35:1<143::AID-POLA15>3.0.CO
[10]  
2-K