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- Lithium salt/amide-based deep eutectic electrolytes for lithium-ion batteries: electrochemical, thermal and computational study. Hideyuki Ogawa, Hideharu Mori
, Phys. Chem. Chem. Phys.
, 2020
, 22
, 8853
- Computer simulation of liquid tetramethylurea and its aqueous solution. Paulo Belletato, Luiz Carlos Gomide Freitas, Elizabeth P. G. Arêas, Paulo Se′rgio Santos
, Phys. Chem. Chem. Phys.
, 1999
, 1
, 4769
- The ultra-violet absorption and chemical constitution of substituted ureas and thioureas. Archibald Clow, N. L. Helmrich
, Trans. Faraday Soc.
, 1940
, 35
, 685
- Photochemistry, spectroscopy, and X-ray structure of an intermolecular charge-transfer complex between an organic substrate and a polyoxometallate, α-H3PMo12O40·6(tetramethylurea). Christina M. Prosser-McCartha, Miryam Kadkhodayan, Michael M. Williamson, Donald A. Bouchard, Craig L. Hill
, J. Chem. Soc., Chem. Commun.
, 1986
, 1747
- A proton magnetic resonance study of ligand exchange on the hexakis(1,1,3,3-tetramethylurea)scandium(III) ion and its NN-dimethylacetamide analogue. Dino L. Pisaniello, Stephen F. Lincoln
, J. Chem. Soc., Dalton Trans.
, 1980
, 699
- Reaction pathways and free energy profiles for spontaneous hydrolysis of urea and tetramethylurea: unexpected substituent effects. Min Yao, Wenlong Tu, Xi Chen, Chang-Guo Zhan
, Org. Biomol. Chem.
, 2013
, 11
, 7595
- A crystallographically characterized salt of self-generated N-protonated tetraethylurea. Marco Bortoluzzi, Fabio Marchetti, Guido Pampaloni, Stefano Zacchini
, Chem. Commun.
, 2015
, 51
, 1323
- Tetramethylurea dimer/lithium salt-based deep eutectics as a novel class of eutectic electrolytes. Hideyuki Ogawa, Yugo Sato, Hideharu Mori
, Mater. Chem. Front.
, 2021
, 5
, 8078
- Kinetics of uncatalysed hydrolysis of 1-benzoyl-3-phenyl-1,2,4-triazole and p-methoxyphenyl dichloroethanoate in aqueous solution containing ureas, carboxamides, sulfonamides, sulfones and sulfoxides. René P. V. Kerstholt, Jan B. F. N. Engberts, Michael J. Blandamer
, J. Chem. Soc., Perkin Trans. 2
, 1993
, 49
- Synthesis of oligosaccharides corresponding to biological repeating units of Shigella flexneri variant Y polysaccharide. Part 1. Overall strategy, synthesis of a key trisaccharide intermediate, and synthesis of a pentasaccharide. B. Mario Pinto, David G. Morissette, David R. Bundle
, J. Chem. Soc., Perkin Trans. 1
, 1987
, 9