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Choudhary AS, Patil SR, Sekar N. Study on Synthesis and Fluorescence of Novel Benzofused Phenazine π-Conjugated Skeleton with Coumarin and Isophoron Cores. J Fluoresc. 2015;25(4):1095-102doi: 10.1007/s10895-015-1597-y.
Choudhary, A. S., Patil, S. R., & Sekar, N. (2015). Study on Synthesis and Fluorescence of Novel Benzofused Phenazine π-Conjugated Skeleton with Coumarin and Isophoron Cores. Journal of fluorescence, 25(4), 1095-102. https://doi.org/10.1007/s10895-015-1597-y
Choudhary, Amol S, et al. "Study on Synthesis and Fluorescence of Novel Benzofused Phenazine π-Conjugated Skeleton with Coumarin and Isophoron Cores." Journal of fluorescence vol. 25,4 (2015): 1095-102. doi: https://doi.org/10.1007/s10895-015-1597-y
Choudhary AS, Patil SR, Sekar N. Study on Synthesis and Fluorescence of Novel Benzofused Phenazine π-Conjugated Skeleton with Coumarin and Isophoron Cores. J Fluoresc. 2015 Jul;25(4):1095-102. doi: 10.1007/s10895-015-1597-y. Epub 2015 Jul 03. PMID: 26139529.
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J Fluoresc. 2015 Jul;25(4):1095-102. doi: 10.1007/s10895-015-1597-y. Epub 2015 Jul 03.

Study on Synthesis and Fluorescence of Novel Benzofused Phenazine π-Conjugated Skeleton with Coumarin and Isophoron Cores.

Journal of fluorescence

Amol S Choudhary, Sharad R Patil, Nagaiyan Sekar

Affiliations

  1. Tinctorial Chemistry Group, Department of dyestuff and intermediate Technology, Institute of Chemical Technology, Mumbai, Nathalal Parekh Marg, Matunga, Mumbai, 400 019, India.

PMID: 26139529 DOI: 10.1007/s10895-015-1597-y

Abstract

The novel benzofused phenazine π-conjugated skeleton with a coumarin and isophoron core was synthesized, characterized, and condensed with suitably substituted active methylene compounds by classical Knoevenagel condensation reaction to obtain novel mono-styryl dyes 6a-6d. These novel styryl dyes have hue varying from yellow to violet. The geometries of the styryl dyes were optimized at B3LYP/6-31G (d) level of theory, and their electronic excitation properties were evaluated using density functional theory.

References

  1. J Fluoresc. 2012 Jan;22(1):303-10 - PubMed
  2. J Org Chem. 2012 Jan 6;77(1):432-44 - PubMed
  3. Org Lett. 2011 Oct 7;13(19):5112-5 - PubMed
  4. Chem Commun (Camb). 2009 Apr 28;(16):2198-200 - PubMed
  5. Phys Rev B Condens Matter. 1988 Jan 15;37(2):785-789 - PubMed
  6. Org Lett. 2011 Mar 18;13(6):1454-7 - PubMed
  7. Chem Rev. 2005 Aug;105(8):2999-3093 - PubMed
  8. Beilstein J Org Chem. 2009 Feb 24;5:7 - PubMed
  9. J Org Chem. 2007 Feb 16;72(4):1530-3 - PubMed
  10. J Phys Chem A. 2009 Sep 24;113(38):10238-40 - PubMed
  11. J Phys Chem A. 2012 Dec 20;116(50):12339-48 - PubMed
  12. Angew Chem Int Ed Engl. 2005 Dec 2;44(47):7783-6 - PubMed

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