Solvent effects on the UV-visible absorption spectra of aryl-2,2'-bifuran derivatives | ||||
Mansoura Journal of Chemistry | ||||
Volume 43, Issue 1, February 2019, Page 32-35 PDF (726.82 K) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/mjcc.2019.412966 | ||||
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Authors | ||||
Fatma H. Abdelhamed* 1; Mohamed A. Ismail1; Ehab Abdel-Latif2 | ||||
1Chemistry Department, Faculty of Science, Mansoura University, 35516 Mansoura, Egypt | ||||
2Chemistry Department, Faculty of Science, Mansoura University | ||||
Abstract | ||||
The effect of solvent polarity on absorption spectra of a series of bifuran carbonitriles and their corresponding carboxamidine hydrochloride salts was investigated. Synthesis of the new thienylbifuran-5-carbonitrile 5 was described through a Stille coupling reaction of the precursor 5'-bromo-[2,2'-bifuran]-5-carbonitrile with 2-tri-n-butylstannylthiophene. Cationic thienylbifuran carboxamidine compound 6 was prepared on treatment its corresponding carbonitrile compound 5 with lithium bis-trimethylsilylamide, followed by de-protection step and subsequent hydrochloride salt formation. The relationship between aryl-2,2'-bifuran structure feature and their corresponding absorption in the UV–visible region was studied. The absorption maxima of the tested aryl-2,2'-bifuran derivatives showed that λmax of the amidine derivatives shifted to higher wavelength than their corresponding carbonitrile derivatives. | ||||
Keywords | ||||
2'-bifuran-5-carbonitriles; Stille reaction; 2; 2'-bifuran-5-amidines; UV/Vis absorption; solvent effect | ||||
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