pH and temperature responsive redox behavior of biologically important aniline derivatives-Reference-Cited by-同舟云学术

pH and temperature responsive redox behavior of biologically important aniline derivatives

Published:2015 Issue:79 Volume:5 Page:64617-64625
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Subhan Hanif¹²³⁴,Lashin Aref⁵⁶⁷⁸⁹,Rana Usman Ali¹⁰⁵⁷⁸,Al-Arifi Nassir⁵¹¹¹²⁸,Ahmad Khurshid¹²³⁴,Hussain Hidayat¹³¹⁴¹⁵¹⁶,Qureshi Rumana¹²³⁴,Ali Saqib¹²³⁴,Zia Muhammad Abid¹⁷¹⁸¹⁹⁴,Kraatz Heinz-Bernhard²⁰²¹²²²³,Shah Afzal¹²³⁴²⁰

Affiliation:

1. Department of Chemistry

2. Quaid-i-Azam University

3. Islamabad

4. Pakistan

5. King Saud University

6. College of Engineering – Petroleum and Gas Engineering Department

7. Riyadh 11421

8. Saudi Arabia

9. Benha University

10. Sustainable Energy Technologies Center

11. College of Science – Geology and Geophysics Department

12. Riyadh 11451

13. UoN Chair of Oman's Medicinal Plants and Marine Natural Products

14. University of Nizwa

15. Nizwa 616

16. Oman

17. University of Education

18. Attock Campus

19. Attock

20. Department of Physical and Environmental Sciences

21. University of Toronto

22. Toronto

23. Canada

Abstract

The electrochemical oxidation of anilines resulted in azodye formation which was evidenced by the appearance of a new peak in the UV-visible spectra (A) and colour change of the solution (B).

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA10822E

Reference44 articles.

1. DNA-directed alkylating ligands as potential antitumor agents: sequence specificity of alkylation by intercalating aniline mustards

2. Synthesis, biological evaluation, and molecular docking studies of N-((1,3-diphenyl-1H-pyrazol-4-yl)methyl)aniline derivatives as novel anticancer agents

3. Synthesis and biological activity of stable and potent antitumor agents, aniline nitrogen mustards linked to 9-anilinoacridines via a urea linkage

4. Design, synthesis and preliminary SAR studies of novel N-arylmethyl substituted piperidine-linked aniline derivatives as potent HIV-1 NNRTIs

5. Synthesis and biological evaluations of some Schiff-base esters of ferrocenyl aniline and simple aniline

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