Published January 1, 2011 | Version v1
Journal article Open

Synthesis, characterization, spectroscopic properties, theoretical calculation, and antimicrobial activity of new aryldisulfonamides

  • 1. Cankiri Karatekin Univ, Dept Chem, Fac Sci, TR-18100 Cankiri, Turkey
  • 2. Gaziantep Univ, Dept Chem, Sci & Art Fac, TR-27310 Gaziantep, Turkey
  • 3. Ahi Evran Univ, Dept Primary Educ, Fac Educ, TR-40100 Kirsehir, Turkey
  • 4. Gazi Univ, Dept Chem, Sci & Art Fac, TR-06500 Ankara, Turkey

Description

New aryldisulfonamides were synthesized and characterized by FTIR, H-1 NMR, C-13 NMR, HETCOR, COSY, LC-MS and elemental analysis techniques. The compounds gave intense emissions, where lambda(max) = 405, 379 and 402 nm, upon irradiation by Ultra-Violet light. The photoluminescence quantum yields and long excited-state lifetimes of the compounds were calculated and were found to have photoluminescence quantum yields 39 +/- 1.8%, 45 +/- 2.2% and 34 +/- 1.4% and long excited-state lifetimes of 3.65 +/- 0.16, 4.17 +/- 0.20 and 3.15 +/- 0.12 ns, respectively. The photoluminescence intensities and quantum yields of compounds varied with the position of substituent on the ring and the chain length between aromatic rings. These novel compounds may be of interest as organic emitting materials for electroluminescent devices. The visible absorption maxima were calculated using time-depended density-functional theory (ID-OFT) and Zerner's intermediate neglect of differential overlap/spectroscopic (ZINDO/S) method in the gas phase. Further, the compounds were evaluated for in vitro antimicrobial activity against various microorganisms by microdilution and disk diffusion methods. (C) 2011 Elsevier B.V. All rights reserved.

Files

bib-b13ad047-fc98-4259-9f97-273030efb3ab.txt

Files (237 Bytes)

Name Size Download all
md5:4fdff1dfbe5e76659d0aa880789cf477
237 Bytes Preview Download