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W. B. Zhang, Y. Tu, R. Ranjan, R. M. V. Horn, S. Leng, J. Wang, M. J. Polce, C. Wesdemiotis, R. P. Quirk, G. R. Newkome and S. Z. D. Cheng, “Clicking Fullerene with Polymers: Synthesis of [60]Fullerene End-Capped Polystyrene,” Macromolecules, Vol. 41, No. 3, 2008, pp. 515-517. http://dx.doi.org/10.1021/ma702345r

has been cited by the following article:

• TITLE: Electrochemical, Photophysical, and Magnetic Properties of Green Emitting bis(2,5-Hexyloxy)-Phenylene-alt-Thiophene Fluorescent Conducting Oligomer Addended Fullerene-Diol Dyad

  AUTHORS: Rachana Singh, Rimpa Jaiswal, Thakohari Goswami

  KEYWORDS: Fullerene-Diol; Fluorescent Conducting Oligomer; Electrochemical Properties; Photophysical Properties; Magnetic Properties

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.3 No.3A, November 28, 2013

  ABSTRACT: Towards the development of potential new organic photovoltaic and optoelectronic materials, a simple route to synthesize flexibly ether linked fullerene-bis[oligo-(phenylene-alt-thiophene)] and evaluation of electrochemical, photophysical and magnetic properties is presented. Flexible ether linking of oligo-phenylene-thiophene chain to 1, 2 C60(OH)2 is achieved employing Williamson’s ether synthesis. 7-chain phenylene-thiophene chain fluorescent conducting oligomer is synthesized using Grignard coupling reaction with preservation of bromo end groups. Oligomer is highly ordered and soluble in all organic solvents while on linking to fullerene-diol, solubility of adduct restricts only to dimethyl sulfoxide (DMSO). All the synthesized materials are characterized through spectroscopic techniques and molecular weight is determined by mass spectrometry and GPC. Properties of the material indicate the substantial effect of fullerene. High quenching in fluorescence intensity and strong paramagnetic property are observed in this material.