Separation of Functionalized 5,6‐Disubstituted‐1,10‐Phenanthroline for Dye‐Sensitized Solar Cell Applications
Author(s) -
Hashem Shahroosvand,
Parisa Abbasi,
Behrouz Notash,
Leyla Najafi
Publication year - 2013
Publication title -
journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.436
H-Index - 50
eISSN - 2090-9063
pISSN - 2090-9071
DOI - 10.1155/2013/475843
Subject(s) - chemistry , phenanthroline , monoclinic crystal system , aryl , epoxy , stoichiometry , dye sensitized solar cell , single crystal , crystal structure , isatin , catalysis , polymer chemistry , crystallography , organic chemistry , electrode , electrolyte , alkyl
5,6-Epoxy-1,10-phenanthroline is used as a convenient starting material for 5-hydroxy-6-Aryl-1,10-phenanthroline ligands containing carboxylic and sulfonic groups useful for further anchoring of the sensitizer on TiO2 for dye-sensitized solar cells (DSCs). Based on the crystal growth of the mixture of products, a convenient separation route for the extension of the p-system on 5,6-disubstituted-1,10-phenanthroline was used to develop a novel series of functionalized 1,10-phenanthroline ligands with electron-withdrawing end-capping group. Also, we report the epoxy opening of 5,6-epoxy-1,10-phenanthroline by aromatic amines stoichiometrically in refluxing water and ethanol in the absence of any catalyst. The dyes were characterized by 1H-NMR, FT-IR, UV-Vis, and X-ray single crystal diffraction analyses. It crystallizes in the monoclinic space group C 2/c, a = 20.920(4) Å, b = 10.340(2) Å, c = 16.187(3) Å, β = 92.30(3)°, V = 3498.6(12) Å3, and Z = 8. The reaction details and features were described in detail
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