1,10-Bis[2-(prop-1-enyl)phenoxy]decane

Maharramov, Abel M.; Bayramov, M. R.; Mehdiyeva, G. M.; Hoseinzadeh, Shahnaz B.; Rashidov, Bahruz A.

doi:10.1107/s1600536811055061

Cited by 2 publications

(1 citation statement)

References 4 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…It is worth noting that alkenylphenol and their derivatives are functionally substituted organic compounds [29][30][31][32][33][34][35][36][37][38][39][40][41][42] that can be applied as effective corrosion inhibitors and biocides [28,[43][44][45]. Furthermore, such compounds can be used as light stabilisers for polymers [46], additives in mineral oils and fuels [47][48][49], to obtain photo-resisting materials [50,51].…”

Section: Introductionmentioning

confidence: 99%

Allylphenoxypiperidinium halides as corrosion inhibitors of carbon steel and biocides

et al. 2020

View full text Add to dashboard Cite

A series of 1-(4-(2-allylphenoxy)butyl)piperidin-1-ium halides (4a-d) was synthesized and characterized via spectroscopic methods (FTIR, 1 H NMR). The corrosion inhibition of the synthesized halides on carbon steel in water-salt-hydrocarbon environment, saturated with H2 S, was investigated. For this purpose, a series of techniques such as gravimetric measurement, potentiodynamic polarisation, and scanning electron microscope (SEM) were used and some thermodynamic parameters of corrosion process (Δ G ads. , ΔH 0 ads. , Δ S 0 ads. ) were evaluated. The steel surface was checked by SEM, and the steel surface showed good surface coverage. The results showed that the synthesized compounds at the concentrations 125, 150 mg ×L -1 have corrosion inhibition activity of 78%–95% by gravimetric measurements and 81%–92% by potentiodynamic measurements at 100, 150 mg ×L -1 . The biological activity was examined against sulphate-reducing bacteria (SRB). It was revealed that at the concentration of compounds 4c and 4d, 100 mg ×L -1 , the antibacterial activity was 100%.

show abstract

Section: Introductionmentioning

confidence: 99%

Allylphenoxypiperidinium halides as corrosion inhibitors of carbon steel and biocides

et al. 2020

View full text Add to dashboard Cite

show abstract

Alkenylphenols: preparation, transformations and applications

Maharramov¹,

Bayramov²,

Agayeva³

et al. 2015

Russ. Chem. Rev.

View full text Add to dashboard Cite

1,10-Bis[2-(prop-1-enyl)phenoxy]decane

Abstract: The complete molecule of the title compound, C28H38O2, is generated by a crystallographic centre of symmetry. The molecular conformation displays an intramolecular C—H⋯π interaction.

Cited by 2 publications

References 4 publications

Allylphenoxypiperidinium halides as corrosion inhibitors of carbon steel and biocides

Allylphenoxypiperidinium halides as corrosion inhibitors of carbon steel and biocides

Alkenylphenols: preparation, transformations and applications

Contact Info

Product

Resources

About

1,10-Bis[2-(prop-1-enyl)phenoxy]decane

Abstract: The complete molecule of the title compound, C28H38O2, is generated by a crystallographic centre of symmetry. The molecular conformation displays an intra­molecular C—H⋯π inter­action.

Cited by 2 publications

References 4 publications

Allylphenoxypiperidinium halides as corrosion inhibitors of carbon steel and biocides

Allylphenoxypiperidinium halides as corrosion inhibitors of carbon steel and biocides

Alkenylphenols: preparation, transformations and applications

Contact Info

Product

Resources

About

Abstract: The complete molecule of the title compound, C28H38O2, is generated by a crystallographic centre of symmetry. The molecular conformation displays an intramolecular C—H⋯π interaction.