S. Tirapattur, M. Belletete, N. Drolet, N. Leclerc and G. Durocher, “Steady-State and Time-Resolved Studies of 2,7- Carbazole-Based Conjugated Polymers in Solution and as Thin Films: Determination of Their Solid State Fluorescence Quantum Efficiencies,” Chemical Physics Letters, Vol. 370, No. 5-6, 2003, pp. 799-804. doi:10.1016/S0009-2614(03)00178-7

has been cited by the following article:

• TITLE: Trifuntional Oligoetherols and Polyurethane Foams with Carbazole Ring

  AUTHORS: Renata Lubczak

  KEYWORDS: Oligomers; Ring-Opening Polymerization; Polyurethanes; Thermal Properties

  JOURNAL NAME: Open Journal of Organic Polymer Materials, Vol.2 No.1, January 29, 2012

  ABSTRACT: The method of synthesis of trifuntional oligoetherols with carbazole ring from 9-(2,3-epoxypropyl)carbazole and die- thanolamine and oxiranes like ethylene and propylene oxide was presented. Structure and some physicochemical prope- rties of the products were described. The oligoetherols were demonstrated as good substrates for synthesis of polyure- thane foams of enhanced thermal resistance. It has been found that the obtained foams are rigid at room temperature and their apparent density was 34 kg/m3- 44 kg/m3. The water uptake was low, maximum to 10.5 mass%. Dynamic thermal analysis of this foams showed that 5% mass loss starts at 200?C - 220?C, while temperature of 50% mass loss was 340?C - 370?C. Concomitantly the increase of compression strength was observed.