New conjugated poly(aryleneethynylenes) with main-chain photochromic units

New photochromic poly(aryleneethynylenes) have been synthesized on the basis of dibromodithienylmaleimide and bisacetylenes under the conditions of the Sonogashira reaction. Molecular masses and polydispersities of the poly(arylene ethynylenes) vary over the following ranges: M _w = 19 150–32 650, M _n = 12 000–19 200, and M _w/M _n = 1.47–1.70; the glass-transition temperatures are in the range 208–230°C; and the 10% weight-loss temperatures in air and argon are in the ranges 330–370 and 550–660°C, respectively. All poly(aryleneethynylenes) exhibit photochromic properties in both solutions and films. It has been shown that, when photochromes are incorporated into a polymer matrix, the efficiency of their photoinduced coloration diminishes, irrespective of whether they are fragments of macromolecular chains or components of polymer solutions.     

Estimate of acidity of bisphenols by NMR spectroscopy method

Conclusions It was established that a correlation exists between the relative acidity of bisphenols in anhydrous isopropanol and the chemical shift of the protons of the hydroxyl groups in DMSO.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2133–2134, September, 1976.     

New photochromic polymers

New photochromic polymers were synthesized by quaternization of amino groups of N-methyldiethanolamine polyterephthalate with a mixture of bis(2,5-dimethyl-4-chloromethyl-3-thienyl)-1,3-dioxol-2-one and p-or m-xylylene dichloride. The spectral-kinetic studies of coatings based on the obtained polymers showed that these coatings have photochromic properties, the efficiency of which decreases with an increase in the sample thickness.     

Poröse Struktur der Polyarylate

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