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Data on synthesis and characterization of new p-nitro stilbene Schiff bases derivatives as an electrochemical DNA potential spacer

Mohd Izham NZ 1 , Yusoff HM 1 , Ul Haq Bhat I 1 , Endo T 2 , Fukumura H 2 , Kwon E 3 Show all authors , Yoshida SI 3 , Asari A 1 , Osman UM 1 , Mohd Yusof MS 1

Affiliations 

  • 1 Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, Malaysia
  • 2 Sendai National College of Technology, 48 Nodayama, Madeshima-Shiote, Natori-shi, Miyagi 981-1239, Japan
  • 3 Research and Analytical Center for Giant Molecules, Graduate School of Science, Tohoku University, Aramaki Aoba, Aoba-ku, Sendai 980-8578, Miyagi, Japan
Data Brief, 2020 Jun;30:105568.
PMID: 32368595 DOI: 10.1016/j.dib.2020.105568

Abstract

The structural investigation of synthesized compounds can be carried out by various spectroscopic techniques. It is an important prospect in order to elucidate the structure of the desired products before being further utilized. The preparation of new p-nitro stilbene Schiff base derivatives as an electrochemical DNA potential spacer was synthesized using (E)-4-(4-nitrostyryl)aniline from Heck reaction with aldehydes in ethanolic solution. The data presented here in this article contains FTIR, UV-Vis and 1H and 13C NMR of (E)-4-(4-nitrostyryl)aniline and nitrostyryl aniline derivatives.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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