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Synthesis of New Benzimidazoles and Their Corrosion Inhibition Performance on Mild Steel in Hydrochloric Acid Solution
| Content Provider | Semantic Scholar |
|---|---|
| Copyright Year | 2015 |
| Abstract | Benzimidazole is a fused aromatic imidazole ring system where a benzene ring is fused to the 4 and 5 positions of an imidazole ring. Benzimidazoles are also known as benziminazoles and 1,3-benzodiazoles. They possess both acidic and basic characteristics. The NH group present in benzimidazoles is relatively strongly acidic and also weakly basic. Another characteristic of benzimidazoles is that they have the capacity to form salts. Benzimidazoles with unsubstituted NH groups exhibit fast prototropic tautomerism which leads to equilibrium mixtures of asymmetrically substituted compounds [1]. Benzimidazole derivatives have been found to be biologically active small molecules, such as vitamin B and a variety of antimicrobial, antiparasitic, and even antitumor agents [1, 2]. Aside from their place in biomedical research, benzimidazoles also have a prominent place in organocatalysis, organometallic [3] and materials chemistry [4] |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | http://ir.inflibnet.ac.in:8080/jspui/bitstream/10603/72595/7/chapter%205.pdf |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |
