Accession Number : ADA263129


Title :   Synthesis of Oligoimides and Oligoimide Anion Radicals


Descriptive Note : Final technical rept.,


Corporate Author : MINNESOTA UNIV MINNEAPOLIS DEPT OF CHEMISTRY


Personal Author(s) : Miller, Larry L


Full Text : https://apps.dtic.mil/dtic/tr/fulltext/u2/a263129.pdf


Report Date : Jan 1992


Pagination or Media Count : 11


Abstract : Key to the results described in parts B-D are compounds based on naphthalene dianhydride (A) and dimethoxybenzidine (B). It was demonstrated that AB type oligoimides with lengths up to 80 A (8nm) (BABABAB) could be synthesized as single molecular weight, pure and usually soluble compounds. Although rotation about the single bonds along the chain is possible, the chains cannot fold. These oligomers constitute the longest, single molecular weight rigid rods that are known. Various end groups could be attached and unsymmetrical rigid rods (different end groups) could be prepared. The compounds were characterized by NMR, IR, MS and HPLC. In one case a single crystal was obtained which confirmed the linear structure and that the B units were twisted with respect to the A units. Electrochemical studies showed that the naphthalene diimide group (A) formed anion radical (A-) and dianions (A=), which were stable in DMF in the absence of air.


Descriptors :   *OLIGOMERS , LINEAR SYSTEMS , CONDUCTIVITY , SYNTHESIS , POLYMERS , MOLECULAR WEIGHT , ANHYDRIDES , SINGLE CRYSTALS , ELECTRONS , NAPHTHALENES , ROTATION(CHEMICAL BONDS) , CHEMICAL RADICALS , IMIDES , ANISOTROPY , CHAINS , ISOTROPISM , MOLECULAR PROPERTIES , STACKING , ANIONS , FOLDING


Subject Categories : Physical Chemistry
      Polymer Chemistry
      Atomic and Molecular Physics and Spectroscopy


Distribution Statement : APPROVED FOR PUBLIC RELEASE