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The preparation of perfectly alternating poly(amide-imide)s via amide unit containing new diamine

Ozarslan, O; Yilmaz, T; Yildiz, E; Fiedeldei, U; Kuyulu, A; Gungor, A


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      {
        "name": "Yilmaz, T"
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      {
        "name": "Yildiz, E"
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      {
        "name": "Fiedeldei, U"
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      {
        "name": "Kuyulu, A"
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        "name": "Gungor, A"
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    "description": "The synthesis of N,N'-bis(4'-amino-4-biphenylene) isophthalamide (BABPI) and its applicability as a new diamine for the preparation of a series of new, high T-g, perfectly alternating poly(amide-imide)s is described. BABPI was synthesized from the catalytic reduction of the corresponding dinitro compound which was prepared by the condensation of isophthaloyl chloride and 4-amino-4'-nitrobiphenyl. The modified selective reduction technique was used for the preparation of 4-amino-4'-nitrobiphenyl from 4,4'-dinitro-biphenyl. Poly(amide-imide)s were synthesized by polycon densation of diamine BABPI with various commercially available aromatic dianhydrides via a conventional two-step procedure. In the first step, poly(amic-acid)s were prepared in a polar aprotic solvent, such as N-methyl pyrrolidone (NMP) at room temperature. Depending on the dianhydride used, intrinsic viscosities of poly(amic-acid)s were found to range between 0.43-0.69 dL/g. Bulk thermal imidization technique was used to obtain fully imidized poly(amide-imide)s at the second step. The synthesized poly(amide-imide)s showed good thermal stability up to 320 degrees C and the 10% weight loss temperatures were recorded in the range of 525-550 degrees C as evidenced by thermogravimetric analysis (TGA). The glass transition temperatures were found to be between 225-235 degrees C from differential scanning calorimeter (DSC) measurements. (C) 1997 John Wiley & Sons, Inc.", 
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      "issue": "6", 
      "pages": "1149-1155", 
      "title": "JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY", 
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    "publication_date": "1997-01-01", 
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