ChemInform Abstract: Synthesis of Some Novel N-Alkyl/Acyl/Aroyl 2-(Chroman/6-bromochroman-2-yl)-1H-benzimidazoles Using Ionic Liquids and Their Antibacterial Activity.

ChemInform ◽  
2010 ◽  
Vol 41 (42) ◽  
Author(s):  
Changdev Namdev Raut ◽  
Sandeep Madhukar Bagul ◽  
Ravindra Ashok Janrao ◽  
Sanjay Dashrath Vaidya ◽  
Bobba Venkata Siva Kumar ◽  
...  
2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Shihong Liu ◽  
Michael Gonzalez ◽  
Celine Kong ◽  
Scott Weir ◽  
Aaron M. Socha

Abstract Background Ionic liquids (ILs) are promising pretreatment solvents for lignocellulosic biomass, but are largely prepared from petroleum precursors. Benzaldehydes from depolymerized lignin, such as vanillin, syringaldehyde, and 4-methoxy benzaldehyde, represent renewable feedstocks for the synthesis of ionic liquids. We herein report syntheses of novel lignin-derived ionic liquids, with extended N-alkyl chains, and examine their melting points, cellulose dissolution capacities, and toxicity profiles against Daphnia magna and E. coli strain 1A1. The latter organism has been engineered to produce isoprenol, a drop-in biofuel and precursor for commodity chemicals. Results The new N,N-diethyl and N,N-dipropyl methyl benzylammonium ILs were liquids at room temperature, showing 75–100 °C decreased melting points as compared to their N,N,N-trimethyl benzylammonium analog. Extension of N-alkyl chains also increased antibacterial activity threefold, while ionic liquids prepared from vanillin showed 2- to 4-fold lower toxicity as compared to those prepared from syringaldehyde and 4-methoxybenzaldehyde. The trend of antibacterial activity for anions of lignin-derived ILs was found to be methanesulfonate < acetate < hydroxide. Microcrystalline cellulose dissolution, from 2 to 4 wt% after 20 min at 100 °C, was observed in all new ILs using light microscopy and IR spectroscopy. Conclusions Ionic liquids prepared from H-, S- and G-lignin oxidation products provided differential cytotoxic activity against E. coli and D. magna, suggesting these compounds could be tailored for application specificity within a biorefinery.


2021 ◽  
Vol 325 ◽  
pp. 115125
Author(s):  
Md. Abrar Siddiquee ◽  
Juhi Saraswat ◽  
Khalid Imtiyaz ◽  
Ab Raouf Bhat ◽  
Farooq Ahmad Wani ◽  
...  

2016 ◽  
Vol 88 (3) ◽  
pp. 422-433 ◽  
Author(s):  
Diana Hodyna ◽  
Vasyl Kovalishyn ◽  
Sergiy Rogalsky ◽  
Volodymyr Blagodatnyi ◽  
Kirill Petko ◽  
...  

Molecules ◽  
2014 ◽  
Vol 19 (8) ◽  
pp. 11741-11759 ◽  
Author(s):  
Mouslim Messali ◽  
Mohamed Aouad ◽  
Wael El-Sayed ◽  
Adeeb Al-Sheikh Ali ◽  
Taibi Ben Hadda ◽  
...  

2021 ◽  
Author(s):  
Shihong Liu ◽  
Michael Gonzalez ◽  
Celine Kong ◽  
Scott Weir ◽  
Aaron Socha

Abstract Background: Ionic liquids (ILs) are promising pretreatment solvents for lignocellulosic biomass, but are largely prepared from petroleum precursors. Benzaldehydes from depolymerized lignin, such as vanillin, syringaldehyde, and 4-methoxy benzaldehyde, represent renewable feedstocks for the synthesis of ionic liquids. We herein report syntheses of novel lignin-derived ionic liquids, with extended N-alkyl chains, and examine their melting points, cellulose dissolution capacities, and toxicity profiles against Daphnia magna and E. coli strain 1A1. The latter organism has been engineered to produce isoprenol, a drop-in biofuel and precursor for commodity chemicals. Results: The new N,N-diethyl and N,N-dipropyl methyl benzylammonium ILs were liquids at room temperature, showing 75-100oC decreased melting points as compared to their N,N,N-trimethyl benzylammonium analog. Extension of N-alkyl chains also increased antibacterial activity 3-fold, while ionic liquids prepared from vanillin showed 2- to 4-fold lower toxicity as compared to those prepared from syringaldehyde and 4-methoxybenzaldehyde. The trend of antibacterial activity for anions of lignin-derived ILs was found to be methanesulfonate < acetate < hydroxide. Microcrystalline cellulose dissolution, from 2-4 wt% after 20 min at 100oC, was observed in all new ILs using light microscopy and IR spectroscopy.Conclusions: Ionic liquids prepared from H-, S- and G-lignin oxidation products provided differential cytotoxic activity against E.coli and D. magna, suggesting these compounds could be tailored for application specificity within a biorefinery.


2018 ◽  
Vol 4 (7) ◽  
pp. 2370-2379 ◽  
Author(s):  
Kelly N. Ibsen ◽  
Huilin Ma ◽  
Amrita Banerjee ◽  
Eden E. L. Tanner ◽  
Shikha Nangia ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (112) ◽  
pp. 92602-92617 ◽  
Author(s):  
Nassir N. Al-Mohammed ◽  
Yatimah Alias ◽  
Zanariah Abdullah

The incorporated benzenesulfonamide moiety and the active side substituents in di-imidazolium and benzimidazolium cations enhanced both antibacterial activity and miscibility for the synthesized gemini type ILs.


RSC Advances ◽  
2014 ◽  
Vol 4 (9) ◽  
pp. 4301-4307 ◽  
Author(s):  
Ricardo Ferraz ◽  
Vânia Teixeira ◽  
Débora Rodrigues ◽  
Rúben Fernandes ◽  
Cristina Prudêncio ◽  
...  

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